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Keloid

A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues.

Synonyms(1)

Synonym
Keloid

Research Excerpts

Overview

ExcerptReference
"Keloids are medically benign, but often psychologically and cosmetically malignant lesions."( Kelly, AP, 1978)
"Keloids are a benign proliferative growth of dermal collagen usually resulting from an excessive tissue response to skin trauma in predisposed individuals."( Doyle-Lloyd, DJ; White, JA, 1991)
"Keloids are benign cutaneous tumours characterized by excess deposition of collagen, specifically type I collagen."( Peltonen, J; Tan, EM, 1991)
"Keloids are rapidly resolved with the use of flurandrenolide tape covered with positive-pressure chin-strap dressings."( Fulton, JE, 1991)
"Keloid is a disease principally of the human dermis, and occasionally the cornea, appearing as thick scar tissue invading normal skin or cornea and produced by the deposition of excessive amounts of collagen over prolonged periods."( Datubo-Brown, DD, 1990)
"Keloids are benign fibrous growths that result from an abnormal connective tissue response in certain predisposed individuals."( Kelly, AP, 1988)
"Keloids are benign dermal tumors that form during an abnormal wound-healing process in genetically susceptible individuals."( Rodríguez-Eaton, S; Russell, JD; Russell, SB; Trupin, JS; Trupin, KM, 1988)
"Keloids are histologically characterized by an abundance of the extracellular matrix of connective tissue."( Abergel, RP; Chu, ML; Lask, G; Matsuoka, LY; Meeker, CA; Minor, RR; Pizzurro, D; Uitto, J, 1985)
"Keloids are predominantly fibrous tumors which appear as firm, variably pruritic or tender growths near a site of injury."( Murray, JC; Pinnell, SR; Pollack, SV, 1981)
"Linear keloids are an unusual manifestation."( Scott, AM; Scott, MJ, 1994)
"Earlobe keloids are a challenging management problem."( DeWitt, DE; Zuber, TJ, 1994)
"Keloids are disfiguring deformities that occur after trauma or wounding of the skin, most commonly among blacks."( Abrams, BJ; Benedetto, AV; Humeniuk, HM, 1993)
"A keloid is a pathological overgrowth of scar expanding beyond the boundaries of the initiating skin wound."( Banes, AJ; Calderon, M; Lawrence, WT, 1996)
"Keloids are characterized by an overabundant deposition of collagen, and they recur frequently following excision."( Bettinger, DA; Cohen, IK; Diegelmann, RF; Yager, DR, 1996)
"Keloids are pathological lesions characterized by enhanced expression of extracellular matrix molecules including fibronectin."( Eriksson, E; Oliver, N; Sible, JC, 1996)
"Keloids are collagenous lesions acquired as a result of abnormal wound heating."( Appleton, I; Brown, NJ; Willoughby, DA, 1996)
"Keloids are an abnormal response to wound healing distinguished by an overproduction of collagen."( Amsberry, J; Broker, BJ; Keane, WM; Pribitkin, EA; Rosen, D; Sailor, L; Schmidt, R, 1996)
"Keloids are relatively common sequelae of trauma to the skin of the head and neck."( Davis, PT; Lindsey, WH, 1997)
"A keloid is a benign tumor that contains excess collagen, primarily type I collagen."( diLeonardo, M; Kauh, YC; Mondragon, G; Rouda, S; Tan, EM; Tokarek, R; Tuan, RS, 1997)
"Keloids are clinically vexacious scars characterized by a high recurrence rate after excision alone (50-100%)."( Bedane, C; Bonnafoux-Clavere, A; Bonnetblanc, JM; Clavere, P; Rousseau, J, 1997)
"Treatment of keloids is often disappointing and sometime quite difficult to manage."( Bodokh, I; Brun, P, 1996)
"Keloids are the result of a dysregulated wound healing process."( Fivenson, D; Han, X; Hou, Z; Ladin, D; Olson, J; Saed, GM, 1998)
"Keloid is a tissue with an excessive accumulation of collagen."( Katz, EP; Marshall, MK; Tanzawa, H; Uzawa, K; Yamauchi, M; Yeowell, HN, 1998)
"Keloid is a dermal fibroproliferative tissue of unknown etiology."( Akino, K; Fujii, T; Ishihara, H; Ito, M; Kuroda, H; Murakami, R; Namba, H; Ohtsuru, A; Yamashita, S; Yoshimoto, H, 1999)
"Histologically, keloids are composed of excessive collagen with an abnormally large number of partially or totally occluded microvessels."( Chau, D; Chin, G; Gittes, GK; Lee, T; Longaker, MT; Mehrara, BJ; Rowe, NM; Saadeh, PB; Steinbrech, DS, 1999)
"Keloids are exuberant scars, in which collagen, fibronectin and glycosaminoglycans are overdeposited."( Prathiba, V; Suryanarayanan, M, 1999)
"Keloids are typically excluded from palms and soles."( Chipev, CC; Hatch, G; Katz, AE; Siegel, DM; Simman, R; Simon, M, 2000)
"Keloids are characterized by a net accumulation of collagen."( McCauley, RL; Xue, H; Zhang, W, 2000)
"Clinically, keloids are most commonly observed in subjects at ages between 10 and 30 years."( Ishihara, H; Namba, H; Ohtsuru, A; Yamashita, S; Yoshimoto, H, 2000)
"Keloids are benign dermal tumors, characterized by overgrowth of lesions, invasiveness beyond the original boundary of the insult, and recurrence of lesions."( Fujii, T; Fujioka, M; Hirano, A; Ishihara, H; Murakami, R; Namba, H; Ohtsuru, A; Yamashita, S; Yoshimoto, H, 2000)
"Unique to humans, keloids are characterized by an accumulation of extracellular matrix components."( Chin, GS; Hsu, M; Levinson, H; Liu, W; Longaker, MT; Steinbrech, D, 2000)
"Keloid is a dermal fibrotic disease characterized by excessive accumulation of mainly type I collagen in extracellular matrix of the dermis."( Hosokawa, N; Kubota, H; Nagata, K; Naitoh, M; Nishimura, Y; Sawada, M; Shirane, H; Tanaka, T, 2001)
"Keloids are disfiguring, proliferative scars that represent a pathological response to cutaneous injury."( Lim, IJ; Longaker, MT; Phan, TT; Song, C; Tan, WT, 2001)
"Keloids are notoriously difficult to treat."( Gupta, S; Kumar, B, 2001)
"Keloids are a common lesion arising from sites of previous trauma and are a considerable source of morbidity because of continued growth of lesions, pruritus, and physical appearance."( Arbiser, JL; Cohen, C; DiCarlo, J; Johnson, D; Kim, A; McAlpine, B; McCall, C; McLaughlin, ER; Quinn, AG, 2001)
"Keloids are proliferative fibrous growths that result from an excessive tissue response to skin trauma."( Marneros, AG; Norris, JE; Olsen, BR; Reichenberger, E, 2001)
"Keloids are benign lesions that represent an exuberant collagen response to injury."( Porter, JP, 2002)
"Keloids are characterized by the deposition of excessive extracellular-matrix collagen by abnormal fibroblasts in response to cutaneous injury."( Bay, BH; Huynh, HT; Lee, ST; Lim, IJ; Longaker, MT; Phan, TT; Qi, R, 2002)
"Earlobe keloids are benign, fibrous proliferations that show a high rate of recurrence of up to 80% following surgical excision."( Büttemeyer, R; Mall, JW; Müller, JM; Pollmann, C, 2002)
"Keloids are benign tumours of the skin."( Bock, O; Mrowietz, U, 2002)
"Plantar keloids are a management problem as a result of the pain and mechanic restriction with ambulation."( Elston, DM; Osswald, SS; Vogel, PS, 2003)
"Keloids are benign diseases of the skin."( Kutzner, J; Schneider, L; Seegenschmiedt, MH, 2003)
"Keloids are the result of aberrant wound healing of human skin after dermal injury."( Alani, H; Simman, R; Williams, F, 2003)
"Keloids are proliferative dermal growths representing a pathological wound-healing response."( Bay, BH; Huynh, H; Lee, ST; Lim, IJ; Longaker, MT; Phan, TT; Qi, R, 2003)
"Keloids are characterized by abnormal proliferation of fibroblasts and overproduction of collagen."( Chan, SY; Huynh, H; Lee, ST; Nguyen, TT; Phan, TT; See, P; Tran, E, 2003)
"Keloids are benign dermal tumors, characterized by invasive growth of fibroblasts and concomitant increased biosynthesis of extracellular matrix components, with unclear etiology."( Akiyama-Uchida, Y; Daian, T; Fujii, T; Hirano, A; Ishihara, H; Ohtsuru, A; Rogounovitch, T; Saenko, V; Yamashita, S, 2003)
"Keloid is a fibrotic skin disorder that results in an excessive deposition of extracellular matrix, which is associated with altered-expression of or -responses to TGF-beta in dermal fibroblasts."( Hasegawa, T; Nakao, A; Ogawa, H; Sumiyoshi, K; Tsuboi, R, 2003)
"Keloid is a benign, well-demarcated area of fibrous tissue overgrowth that extends beyond the original defect."( Al-Dhalimi, MA; Sharquie, KE, 2003)
"Keloid is an intricate lesion that is probably modulated by interplay of many genes."( Chen, W; Fu, X; Sheng, Z; Sun, T; Sun, X; Zhao, Z, 2003)
"Keloids are benign fibrous growths with characteristic clinical features, whose underlying pathogenic mechanisms are not fully understood."( Aschoff, R; Hackert, I; Sebastian, G, 2003)
"Keloids are benign mesenchymal tumours, usually present at and extending beyond the margins of sites of previous injury."( Berman, B; Jacob, SE; Nassiri, M; Vincek, V, 2003)
"Keloids are characterized as an "overexuberant" healing response in which disequilibrium between production and catabolism of extracellular matrix (ECM) occurs."( Akhondzadeh, A; Ann, DK; Duong, HS; Le, AD; Messadi, DV; Wu, Y; Zhang, Q, 2004)
"Keloids are an excessive accumulation of extracellular matrix."( Ann, DK; Bertolami, CN; Kelly, AP; Le, AD; Messadi, DV; Tuan, TL; Wu, Y; Zhang, Q, 2003)
"Keloids are often resistant to treatment, causing much suffering to the patient."( Chang, SE; Choi, JH; Kim, KJ; Lim, YJ; Moon, KC; Ro, KH; Sung, KJ, 2004)
"Keloids are skin abnormalities that are characterized by excessive deposition of collagen bundles in the dermis."( Harii, K; Kitano, Y; Okazaki, M; Uchida, G; Yoshimura, K, 2003)
"Keloids are skin fibrotic conditions characterized by an excess accumulation of extracellular matrix (ECM) components secondary to trauma or surgical injuries."( Ann, DK; Bertolami, CN; Chau, CH; Le, AD; Wu, Y; Zhang, Q, 2004)
"Keloids are benign, but sometimes painful and/or pruritic, proliferative growths of dermal collagen, usually resulting from excessive tissue response to trauma."( Kelly, AP, 2004)
"Keloids are proliferative fibrous growths that result from an excessive tissue response to skin trauma."( Marneros, AG; Norris, JE; Olsen, BR; Reichenberger, E; Watanabe, S, 2004)
"Keloids are a major cause of morbidity, and arise after operation, injury, or cutaneous infection."( Arbiser, JL; Brown, LF; Cohen, C; Gira, AK; Washington, CV, 2004)
"Keloid is an intricate lesion that is probably regulated by many genes."( Chen, W; Fu, XB; Ge, SL; Sheng, ZY; Sun, XQ; Zhao, ZL; Zhou, G, 2004)
"Keloid is a complicated lesion with many genes involved."( Chen, W; Fu, XB; Ge, SL; Sheng, ZY; Sun, XQ; Zhao, ZL; Zhou, G, 2004)
"Keloids are benign skin tumors that develop following wounding."( Ciarmiello, LF; De Felice, B; Nacca, M; Pinelli, C; Wilson, RR, 2004)
"Earlobe keloids are commonly encountered in dermatological practice and often prove to be recurrent, despite a variety of treatment options."( Dinh, Q; Richards, S; Veness, M, 2004)
"Keloids are characterized as an "over-exuberant" healing response resulting in a disproportionate extracellular matrix (ECM) accumulation and tissue fibrosis."( Doung, HS; Kelly, AP; Le, AD; Messadi, DV; Reichenberger, E; Tuan, TL; Zhang, Q, 2004)
"The blood supply to keloids is inadequate, and this persists."( Furuya, E; Oba, S; Ueda, K; Yasuda, Y, 2004)
"Keloids are characterized by abnormal proliferation and overproduction of extracellular matrix."( Chan, SY; Lee, ST; Lim, IJ; Longaker, MT; Phan, TT; Tan, EK, 2004)
"Keloid is a dermal fibroproliferative lesion of unknown etiology that commonly recurs after surgical excision."( Ghazizadeh, M; Hirai, T; Hyakusoku, H; Kawanami, O; Shimizu, H; Tosa, M, 2005)
"Keloids are more likely to develop when ears are pierced after age 11 than before age 11."( Davis, LS; Lane, JE; Waller, JL, 2005)
"Keloids are common lesions arising from sites of a previous trauma, and are distinguishable from scars by the presence of continuous growth over the borders of the original injury."( Khorshid, FA, 2005)
"Since keloids are common in humans, hypertrophic scars rather than keloids were observed in animal skin wounds."( Khorshid, FA, 2005)
"Keloids are benign skin tumours occurring during wound healing in genetically predisposed patients."( Bayat, A; Bock, O; Ferguson, MW; Mrowietz, U; Yu, H; Zitron, S, 2005)
"A keloid is a specific skin lesion that expands beyond the boundaries of the original injury as it heals."( Fujiwara, M; Muragaki, Y; Ooshima, A, 2005)
"Keloids are disfiguring, proliferative scars that are a pathologic response to cutaneous injury."( Chiu, LL; Karamzadeh, A; Sun, CH; Torkian, B; Tromberg, B; Wong, BJ; Yeh, AT, 2005)
"Keloids are tumor-like lesions that result from excessive scar formation during healing of wounds."( Fujiwara, M; Muragaki, Y; Ooshima, A, 2005)
"Keloids are a dermal fibrotic disease whose etiology remains totally unknown and for which there is no successful treatment."( Ikeda, M; Kubota, H; Nagata, K; Naitoh, M; Shirane, H; Suzuki, S; Tanaka, T, 2005)
"As treatment of keloids is mainly a cosmetic indication, the authors investigated, beyond the recurrence rate, the patients' satisfaction with the result and its correlation with objective medical findings."( Böttcher, HD; Fraunholz, IB; Gerstenhauer, A, 2005)
"Keloids are a hyperproliferative response of connective tissue in response to trauma."( Blazić, TM; Brajac, I, 2006)
"Keloids are defined as excessive scar tissue formation extending beyond the area of the original skin injury and occurring in predisposed individuals."( Krieg, T; Marneros, AG, 2004)
"Keloids are benign cutaneous lesions that result from excessive collagen synthesis and deposition."( Fikrle, T; Pizinger, K, 2005)
"Keloids are proliferative growths of dermal collagen, usually resulting from excessive tissue response during wound healing."( Bay, BH; Lim, D; Phan, TT; Yip, GW, 2006)
"Keloids are exuberant, disfiguring scars that result from an abnormal healing process."( Al-Attar, A; Davison, SP; Kauffman, LC; Mess, S, 2006)
"Keloids are abnormal fibrous growths of the dermis that develop only in response to wounding and represent a form of benign skin tumor."( Longaker, MT; Xia, W; Yang, GP, 2006)
"Keloids are benign and occur secondary to an imbalance between the synthesis of extracellular matrix and its degradation."( Deleuze, JP; Grandjean, FX; Heymans, O; Nickers, P; Schmitz, C; Smeets, L, 2006)
"Keloids are benign tumors that occur only in response to injury, for which there is no effective treatment."( Lim, IJ; Longaker, MT; Phan, TT; Xia, W; Yang, GP, 2006)
"Keloids are common benign tumors of the dermis, typically arising after insult to the skin."( Childs, CC; Fuller, CD; Herman, TS; Jones, K; Luh, JY; Miller, AR; Thomas, CR; Tolcher, AW, 2006)
"Keloids are characterized by increased fibroblast activity in the setting of an altered cytokine profile."( Stashower, ME, 2006)
"Keloids are benign skin tumours occurring during wound healing in genetically predisposed patients."( Bayat, A; Bock, O; Ferguson, MW; Mrowietz, U; Yu, H, 2006)
"Keloids are benign hyperproliferative growths of dermal collagen that usually result from excessive tissue response to skin trauma."( Erdemir, F; Gokce, O; Kadioglu, A; Kilicaslan, I; Parlaktas, BS; Sanli, O; Uluocak, N, 2006)
"Keloids are fibrotic lesions that are a result of an abnormal wound-healing process that lacks control of the mechanisms that regulate tissue repair and regeneration."( Kim, JY; Stewart, CE, 2006)
"Keloids are cosmetically devastating lesions with considerable morbidity."( Uitto, J, 2007)
"Keloids are benign tumors that usually develop as an excessive healing response to injury."( Bukvić-Mokos, Z; Lipozencić, J; Marinović, B, 2006)
"Keloids are defined as dermal fibrotic lesions which are considered an aberration of the wound healing process."( Altmeyer, P; Bechara, FG; Boorboor, P; Hoffmann, K; Mann, B; Sand, D; Sand, M, 2007)
"Keloid is a dermal fibroproliferative disorder characterized by excessive deposition of extracellular matrix (ECM) components such as collagen, glycoproteins and fibronectin."( Aalami, O; Do, DV; Khoo, YT; Lim, IJ; Mukhopadhyay, A; Ong, CT; Phan, TT, 2007)
"Keloids are special type of skin lesions arising from sites of previous trauma."( Brudnik, U; Podolec-Rubiś, M; Wojas-Pelc, A, 2006)
"Keloid is characterized by excessive collagen accumulation, but the mechanism of keloid formation remains unknown, and none of the treatment modalities are consistently effective."( Cen, Y; Chen, JJ; Liu, XX; Wu, DM; Yu, R; Zhao, S, 2007)
"Keloid is characterized with disproportionate extracellular matrix accumulation and fibroblast proliferation."( Cai, J; Xu, B; Zhang, J; Zhao, Y; Zhu, G, 2007)
"Keloids are abnormal wound reactions of connective tissue."( Froelich, K; Hagen, R; Kleinsasser, N; Staudenmaier, R, 2007)
"Keloids are benign fibroproliferative diseases of unknown aetiology."( Bayat, A; Jagadeesan, J, 2007)
"Keloids are benign fibrous growths that appear after surgery, trauma or "spontaneously" as a consequence of microtrauma in predisposed patients."( Karrer, S, 2007)
"Keloid is a hypertrophic scar that may arise within 6 months after injury in susceptible individuals."( Bölke, E; Budach, W; Gripp, S; Matuschek, C; Orth, K; Peiper, M; Schwarz, A, 2007)
"Keloids are proliferative dermal growths representing a pathologic wound healing response."( Kong, W; Lim, IJ; Longaker, MT; Phan, TT; Wang, Z; Xia, W; Yang, GP, 2007)
"Keloids are benign tumors of the dermis that form during a protracted wound healing process."( Boone, BE; Opalenik, SR; Russell, SB; Smith, JC; Williams, SM, 2008)
"Keloids are well-defined fibrous tissue overgrowths extending beyond the original defects."( Bhanot, A; Dewan, SP; Kaur, A; Sharma, S, 2007)
"Keloids are pathologic scars afflicting a large segment of our population and for which there is no definitive therapy."( Butler, PD; Longaker, MT; Ly, DP; Yang, GP, 2008)
"Keloids are a frequent finding after physical trauma."( Chrisostomidis, C; Chrisostomidis, G; Dimitroulis, D; Frangoulis, M; Konofaos, P; Papadopoulos, O; Vasilopoulou, A, 2008)
"Keloid is a benign dermal tumor characterized by proliferation of dermal fibroblasts and overproduction of extracellular matrix (ECM)."( Hirano, A; Makino, S; Mitsutake, N; Nakashima, M; Ohtsuru, A; Saenko, VA; Tanaka, K; Umezawa, K; Yamashita, S, 2008)
"Keloids are benign skin tumors characterized by collagen accumulation and hyperproliferation of fibroblasts."( Jun, EK; Kim, B; Kim, H; Moon, JH; Noh, JY; Oh, C; Oh, S; Park, G; Song, HJ; Yoon, BS; You, S, 2008)
"Reports of corneal keloids are rare, with fewer than 80 cases published since the first case was documented in 1865."( Kai, S; Panda, A; Sen, S; Vanathi, M, 2008)
"Keloids are tumor-like skin scars that grow as a result of the aberrant healing of skin injuries, with no effective treatment."( Benya, PD; Chang, R; Ho, W; Hwu, P; Tuan, TL; Wysocki, A; Yiu, P, 2008)
"Keloids are considered to be benign hyperproliferative growths of dense fibrous tissue and overabundant deposition of disorganized, thick, hyalinized collagen that result from an abnormal tissue response to cutaneous injury."( De Oliveira Moura Cardoso, G; Morosolli, AR; Murilo-Santos, L; Niccoli-Filho, W, 2008)
"The pathogenesis of keloid is poorly understood."( Akino, K; Akita, S; Hayashi, T; Hirano, A; Mineda, T; Yakabe, A, 2008)
"Keloids are benign skin tumors and are the effect of a dysregulated wound-healing process in genetically predisposed patients."( De Felice, B; Garbi, C; Santillo, A; Santoriello, M; Wilson, RR, 2009)
"Keloids are a common presenting complaint in the primary care clinic."( Aziz, N; Davidson, S; Khachemoune, A; Rashid, RM, 2009)
"Keloids are raised reddish nodules that develop at the site of an injury."( Alyanak, A; Guven, E; Yazar, M; Yigit, B, 2009)
"Keloids are characterized by benign proliferation of fibroblasts in the setting of an altered cytokine profile, with a high recurrence rate after surgical treatment."( Cação, FM; Messina, MC; Tanaka, V, 2009)
"Keloid is characterized by excessive deposition of collagen, resulting from aberrant extracellular matrix (ECM) production and degradation."( Akasaka, Y; Imaizumi, R; Inomata, N; Ishikawa, Y; Ito, K; Maruyama, Y; Okada, E, 2009)
"Keloids are distinguished by substantial deposition of collagen in the dermis, resulting in an imbalanced production and aggregation of extra cellular matrix."( Gao, WY; Guo, SZ; Han, Y; Li, X; Li, Y; Lu, KH; Ma, XJ; Xiao, B; Yan, L; Yi, CG; Zhang, GY; Zheng, Y, 2009)
"Keloids are scars, unique to humans, that grow beyond the boundaries of a cutaneous injury, inflammation, burn, or surgical incision."( Kelly, AP, 2009)
"Keloids are a common form of pathologic wound healing characterized by excessive production of extracellular matrix."( Butler, PD; Koong, AC; Longaker, MT; Ly, DP; Wang, Z; Yang, GP, 2011)
"Keloids are benign fibroproliferative tumors but often cause serious cosmetic problems."( Adam, S; Lari, N; Morand, JJ; Salles, F; Thiéry, G, 2009)
"Keloids are recognized as benign tumours characterized by fibroblastic proliferation and accumulation of extracellular matrix, especially collagen deposition."( He, S; Huang, W; Liu, X; Roberts, MS; Xu, S; Yang, S; Yang, Y; Zhang, X, 2010)
"Keloids are benign skin tumors that are the effect of a dysregulated wound-healing process in genetically predisposed patients."( De Felice, B; Nacca, M; Wilson, RR, 2009)
"Keloid is a fibrotic disease characterized by abnormal accumulation of extracellular matrix in the dermis."( Ikeda, M; Ishiko, T; Kubota, H; Kurokawa, M; Nagata, K; Naitoh, M; Nakamura, T; Suzuki, S; Utani, A; Yamawaki, S; Yoshikawa, K, 2009)
"Keloids are associated with small-fiber neuropathy and typically present with itching, pain, and allodynia."( Dave, S; Lippincott, B; Uyesugi, B, 2010)
"Keloids are benign fibroproliferative dermal tumors of unknown etiology."( Cai, LQ; He, SM; Li, Y; Lu, WS; Quan, C; Wang, JF; Wang, ZX; Xiao, FL; Yang, S; Zhang, XJ, 2010)
"These keloids are highly resistant for treatment and are followed by severe cosmetic implications."( Amir, A; Barnea, Y; Ben-Yosef, R; Gur, E; Leshem, D; Miller, E; Shafir, R; Stahl, S; Weiss, J; Zaretski, A, 2010)
"Keloids are fibrous overgrowth induced by cutaneous injury."( Arbiser, JL; Chai, CY; Chen, GS; Govindarajan, B; Hong, CH; Lee, CH; Liao, WT; Lin, YF; Shan, WJ; Yu, HS, 2010)
"Large and multiple keloids are difficult to treat radically and are currently only treatable by multimodal therapies that aim to relieve symptoms."( Ogawa, R, 2010)
"Keloids are pathological scars and, despite numerous available treatment modalities, continue to plague physicians and patients."( Do, DV; Khoo, YT; Lim, IJ; Masilamani, J; Mukhopadhyay, A; Ong, CT; Phan, TT, 2010)
"Keloids are a response to wound healing that occurs due to hyperproliferation of dermal collagen in response to skin injury (Olabanji et al, Surg Pract."( Brown, NA; Ortega, FR, 2010)
"Keloids are common abnormal raised fibroproliferative lesions that can occur following even minor cutaneous trauma."( Cai, LQ; Li, Y; Lu, WS; Sun, LD; Wang, JF; Wang, ZX; Yang, S; Zhang, WY; Zhang, XJ; Zhu, F; Zuo, XB, 2010)
"Keloids are benign dermal tumors that form during wound healing in genetically susceptible individuals."( Broquist, AH; Gayden, AE; Nanney, LB; Opalenik, SR; Raju, L; Russell, JD; Russell, SB; Trupin, KM; Williams, SM, 2010)
"Keloids are the result of a dysfunctional scarring process that leads to excessive deposition of extracellular matrix in susceptible individuals, causing them physical, psychological, and social discomfort."( Bonatti, S; Ferreira, AC; Ferreira, LM; Furtado, F; Hochman, B, 2010)
"Auricular keloids are very frequent and often have a peculiar response to therapy."( Caccialanza, M; Piccinno, R; Recalcati, S, 2011)
"The spontaneous keloids are lesions rarely described in caucasoid subjects."( Boloorchi, A; Gasnier, P; Hu, W; Kerfant, N; Uguen, A, 2011)
"Keloid is a dermal fibroproliferative growth that results from dysfunction of the wound healing processes."( Chung, S; Hosono, N; Kamatani, N; Kawaguchi, T; Kubo, M; Nakamura, Y; Nakashima, M; Takahashi, A; Tsunoda, T; Zembutsu, H, 2010)
"Keloid is a fibrotic disease characterized by abnormal accumulation of extracellular matrix (ECM) in the dermis."( Chang, CC; Chen, MJ; Hsu, YC; Ko, SY; Yu, YM, 2010)
"Keloids are fibroproliferative disorders characterized by increased deposition of extracellular matrix components."( Cao, X; Chan, SY; Do, DV; Khoo, YT; Lim, CP; Lim, IJ; Masilamani, J; Mukhopadhyay, A; Ong, CT; Phan, TT; Vincent, AS; Wong, PK, 2011)
"The progression of keloids is characterized by increased deposition of extracellular matrix proteins, invasion into the surrounding healthy skin and inflammation."( Bayat, A; Dienus, K; Gilmore, BF; Seifert, O, 2010)
"Keloid is a common complication of the wound healing process."( Ayuob, NN; Hajrah, NH; Shaker, SA, 2011)
"Keloids are fibrotic lesions resulting from abnormal wound healing."( Gupta, M; Narang, T, 2011)
"Keloids are fibroproliferative dermal lesions characterized by the proliferation of fibroblasts and the formation of excess scar tissue, for which no effective treatment exists."( Huang, Q; Huang, RL; Liang, J; Peng, Z; Wu, ZX; Zhang, PH, 2011)
"Keloids are found only in humans and the underlying biochemical mechanisms of their pathogenesis remain unknown."( Chua, AW; Fu, Z; Gan, SU; Han, HC; Ma, D; Phan, TT; Sabapathy, K; Song, C, 2011)
"Keloids are common abnormal raised fibroproliferative lesions that can occur following even minor cutaneous trauma."( Cai, LQ; Li, Y; Lu, WS; Sun, LD; Wang, ZX; Yang, S; Zhang, XJ; Zheng, HF; Zhu, F; Zuo, XB, 2011)
"Keloids are a controllable condition when treated with combination therapy, involving surgical excision with postoperative irradiation and early conservative treatment after the detection of recurrence."( Ishiko, T; Muneuchi, G; Naitoh, M; Suzuki, S; Yamawaki, S, 2011)
"Keloids are protrusive claw-like scars that have a propensity to recur even after surgery, and its molecular etiology remains elusive."( Ooi, BN; Phan, TT, 2011)
"Keloids are often refractive to treatment, and recurrences occur quite frequently."( Fruth, K; Gouveris, H; Kuelkens, C; Mann, WJ, 2011)
"A keloid is a fibrous tumor produced by fibroblast hyperproliferation and excessive collagen accumulation due to overproduction of transforming growth factor β1 (TGF-β1)."( Budiyanto, A; Radiono, S; Soebono, H; Wirohadidjojo, YW, 2011)
"Keloids are benign skin tumours occurring during wound healing in genetically predisposed patients."( Cao, J; Chen, H; Li, J; Li, M; Tu, Y; Wang, L; Wu, Z; Xiao, X; Yang, Y; Yu, Y, 2011)
"Keloids are aesthetically disfiguring and severely disabling."( Ghafarian Shirazi, HR; Hatamipour, E; Hatamipour, M; Mehrabi, S, 2011)
"Large and multiple keloids are difficult to treat radically and are currently only treatable by multimodal therapies that aim to relieve symptoms."( Cummings, I; Pai, VB, 2011)
"Keloids are pathologic proliferations of the dermal layer of the skin resulting from excessive collagen production and deposition."( Lee, WJ; Park, SE; Rah, DK, 2011)
"Keloid is a type of scar which extends beyond the boundaries of the original wound."( Gan, SH; Halim, AS; Nurul Syazana, MS; Shamsuddin, S, 2011)
"In the event that a keloid is presented in isolation, chronic osteomyelitis should be considered as a differential diagnosis, and a high index of suspicion is required in order to establish the diagnosis."( Olabanji, JK; Oladele, AO; Orimolade, EA; Yusuf, MB, 2011)
"Keloid is a clinically intractable disease that causes disfigurement, itching, and pain due to abnormal proliferation of fibroblasts and production of collagen."( Maeda, T; Matsumura, H; Saito, M; Setoguchi, Y; Tsuboi, R; Yamazaki, M, 2012)
"Keloid is a common skin condition, especially in people of Asian and African decent."( Nie, Z, 2011)
"Keloids are benign tumours composed of fibrous tissue produced during excessive tissue repair triggered by minor injury, trauma or surgical incision."( Bux, S; Madaree, A, 2012)
"Keloid is regarded as a fibroproliferative disorder with excessive accumulation of extracellular matrix."( Cen, Y; Chen, JJ; Duan, WQ; Jin, PS; Liu, Y; Wang, HS; Xu, XW; Zhao, S, 2011)
"Keloids are manifestations of abnormal wound repair with unresolved clinical complications."( Jayaraman, M; Korrapati, PS; Krishnaswamy, VR; Mogili, NS; Rajaram, R; Venkatraman, A, 2012)
"Keloids are a fibroproliferative disease due to abnormal wound healing process after skin injury."( Hirano, A; Kashiyama, K; Matsuse, M; Mitsutake, N; Ogi, T; Saenko, VA; Ujifuku, K; Utani, A; Yamashita, S, 2012)
"Keloid is a specific skin scar that expands beyond the boundaries of the original injury as it heals."( Bian, D; Dai, Y; Gong, Z; Lu, Q; Song, J; Wei, Z; Xia, Y; Xu, H; Xu, Z, 2012)
"Clinically, keloids are defined as scars that invade adjacent healthy tissue and are caused by tissue injury; however, the clear distinction relating keloids to wound healing or to cancer remains elusive."( Day, PJ; Javad, F, 2012)
"Keloids are characterized by extreme fibroblastic overgrowth of unknown pathogenesis after skin injury."( Bambach, I; Cerroni, L; Heitzer, E; Schmidbauer, U; Seidl, H; Wolf, P, 2012)
"Keloids are benign dermal tumors characterized by fibroblastic proliferation and excessive accumulation of collagen."( Fan, DL; Guo, S; Han, SY; Wang, YX; Zhao, WJ, 2012)
"Keloids are defined as excessive scar tissue formation extending beyond the area of the original skin injury and occurring in predisposed individuals."( Guglielmi, G; Parisi, S; Scaramuzzi, G; Simeone, A; Troiano, M, 2011)
"  Keloid is a unique proliferative disorder of fibroblasts resulting from derailment of the typical wound healing process."( Fang, AH; Lan, CC; Wu, CS; Wu, PH, 2012)
"Morbidity of the keloid is high, given the frequent recurrences and unpredictable."( Allah, KC; Assi Djè Bi Djè, V; Kossoko, H; Richard Kadio, M; Yéo, S, 2013)
"The keloid is not a homogenous biological entity."( Allah, KC; Assi Djè Bi Djè, V; Kossoko, H; Richard Kadio, M; Yéo, S, 2013)
"Keloids are thick fibrous scars that are refractory to treatment and unique to humans."( Boyce, ST; Glaser, K; Hahn, JM; McFarland, KL; Supp, DM, 2012)
"Keloid is a complex condition with environmental and genetic risk-contributing factors."( Emami, A; Halim, AS; Kannan, TP; Khoo, TL; Salahshourifar, I; Yussof, SJ, 2012)
"Keloid is the result of excessive deposition of collagen in the dermis and subcutaneous tissues."( Demirdover, C; Oztan, HY; Sahin, B; Vayvada, H, 2013)
"Keloids are the result of excessive scar tissue formation."( Bureik, D; Dombrowski, Y; Gauglitz, GG; Pavicic, T; Ruzicka, T; Schauber, J, 2012)
"Keloids are benign, fibroproliferative growths that occur as a result of dermal injury in ~15% of the population."( Brissett, AE; Naylor, MC, 2012)
"Keloids are characterised by the excessive accumulation of extracellular matrix (ECM), especially overabundant collagen formation."( Bae, GY; Bahk, YY; Cha, HJ; Chin, YW; Kim, JJ; Kim, WS; Lee, JS; Min, HG, 2013)
"Earlobe keloids are benign, fibrous proliferations that occur in predisposed persons at sites of cutaneous injury."( Careta, MF; Fortes, AC; Maruta, CW; Messina, MC, 2013)
"Keloids are a proliferative fibrotic disease characterized by abnormal accumulation of extracellular matrix in the dermis."( Fujita, H; Ikeda, M; Ishiko, T; Kubota, H; Kurahashi, Y; Naitoh, M; Suzuki, S; Yamaguchi, H; Yamawaki, S; Yoshikawa, K, 2013)
"Keloids are managed using a variety of treatments, primarily triamcinolone and excision or destruction of a lesion."( Davis, SA; Feldman, SR; McMichael, AJ, 2013)
"Treatment of keloids is a therapeutic challenge."( Ang, CC; Kwok, C; Tay, YK, 2013)
"Keloid is characterized by fibroblastic cell proliferation and abundant collagen synthesis."( Egawa, S; Ghazizadeh, M; Hyakusoku, H; Igota, S; Murakami, M; Shimizu, H; Tosa, M, 2013)
"Keloids are characterized by the vigorously continuous production of extracellular matrix protein and aberrant cytokine activity in the dermis."( Chen, YL; Chien, HF; Hung, LY; Lee, CW; Liang, CJ; Pu, CM; Tsai, JS; Wang, SH; Yen, FL; Yen, YH, 2013)
"Keloid is a clinically intractable fibro-proliferative disease that spreads beyond the original scar or lesion."( Burm, JS; Lee, KW; Yang, WY, 2013)
"Keloids are considered aberrations of the wound healing process, and various treatment regimens are described depending on the morphology and size of the lesion."( Yüzbaşıoğlu, E, 2013)
"Keloids are common cutaneous pathological scars that are characterised by the histological accumulation of fibroblasts, collagen fibres, and clinically significant invasive growth."( Huang, C; Ogawa, R, 2013)
"Keloids are the result of an overgrowth of dense fibrous tissue that usually develops after healing of a skin injury."( Kundu, RV; Love, PB, 2013)
"Keloid is benign fibroproliferative dermal tumors with unknown etiology."( Cheng, H; Ding, Y; Gao, J; Ha, W; Hou, J; Li, P; Liu, J; Liu, Y; Qian, F; Sheng, Y; Sun, L; Tang, H; Wang, J; Wang, W; Wang, Y; Wu, B; Yang, S; Yuan, X; Zhai, Y; Zhang, X; Zhou, F; Zhu, F; Zuo, X, 2013)
"Keloids are tumor-like skin scars that grow as a result of the aberrant healing of skin injuries, with no effective treatment."( Bai, Y; Cao, M; Li, C; Liu, H; Xu, Y; Yao, H; Zuo, X, 2013)
"Keloids are fibroproliferative disorders that are characterized by histological accumulation of collagens and fibroblasts, refractory clinical symptoms such as itching, topical invasiveness, and frequent postsurgical recurrence."( Huang, C; Ogawa, R, 2013)
"Keloids are tumour-like scars that appear some years after the original wound, and which spread beyond the limits of the scar."( Escudero Nafs, FJ; Pérez-Espadero, A, 2013)
"Keloids are an overgrowth of fibrotic tissue outside the original boundaries of an injury and occur secondary to defective wound healing."( Jagdeo, JR; Lev-Tov, H; Mamalis, AD; Nguyen, DH, 2014)
"Keloids are defined as overgrowths of scar tissue resulting from abnormal wound healing."( Akaishi, S; Aoki, M; Dohi, T; Hyakusoku, H; Miyake, K; Ogawa, R; Shimada, T, 2014)
"Keloid is a disease that is difficult to cure because of its high recurrence rate after chemotherapy or radiotherapy, therefore it is considered as a benign skin tumor."( Chai, G; Liu, W; Qu, M; Song, N; Wu, X, 2013)
"Keloids are scars that extend beyond the borders of the original wound."( Li, W; Liu, Z; Wang, X; Wang, Y, 2014)
"Keloids are fibroproliferative disorders characterized by exuberant extracellular matrix deposition and transforming growth factor (TGF)-β/Smad pathway plays a pivotal role in keloid pathogenesis."( Bian, D; Dai, Y; Dou, Y; Gong, Z; Tan, Q; Wu, X; Xia, Y; Yang, Y; Zhang, J, 2013)
"Keloids are firm rubbery growths that grow beyond the boundaries of human wounds and their treatment has met with limited success."( Biswas, A; Bongso, A; Choolani, M; Fong, CY; Srinivasan, A; Subramanian, A, 2014)
"Keloid is induced by a pathological wound healing response, and hepatocyte growth factor (HGF) is known to be involved in tissue repair via the activation of its primary receptor, c-Met."( Jin, Z, 2014)
"Keloids are slow growing neoplasms characterized by benign proliferation of fibroblasts that is due, at least in part, to altered cytokine profiles."( Bakry, OA; Basha, MA; El Meadawy, I; Samaka, RM; Tharwat, A, 2014)
"Keloid is a kind of pathological scar of skin, which would seriously impair patient's quality of life."( Wang, HM; Xu, JH; Xu, X, 2013)
"Keloids are a burden for patients due to physical, aesthetic and social complaints and treatment remains a challenge because of therapy resistance and high recurrence rates."( Bijlard, E; Busschbach, JJ; Mureau, MA; Niessen, FB; Timman, R; van Neck, JW; Verduijn, GM, 2013)
"Keloids are fibroproliferative extreme variants of an impaired wound healing, developing a tumour-like growth."( Brom, J; Freuschle, A; Hörmann, K; Schultz, JD, 2014)
"Keloid is an inflammatory and fibrotic disease with an unknown pathogenesis."( Funayama, E; Furukawa, H; Hayashi, T; Ikeda, M; Murao, N; Oyama, A; Seino, K; Yamamoto, Y, 2014)
"Keloids are locally exuberant dermal scars characterized by excessive fibroblast proliferation and matrix accumulation."( Desai, T; Martin, G; Muthusubramaniam, L; Paukshto, M; Zaitseva, T, 2014)
"Keloid is a proliferative disease of fibrous tissues."( Cen, Y; Chen, J; Liu, Y; Nicolas, C; Zhao, S, 2016)
"Keloids is a fibroproliferative disease."( Lee, YC; Sun, LM; Wang, KH, 2014)
"Keloids are benign fibro-proliferative skin lesions that very rarely occur on the soles."( Bagot, M; Battistella, M; Cavelier-Balloy, B; Duron, JB; Gorj, M; Hickman, G; Masson, V; May, P; Petit, A; Schneider, P; Vanhaecke, C; Vilmer, C, 2015)
"Keloids are proliferative fibrous growths resulting from excessive tissue response to skin trauma."( de Jong, D; Hennekam, RC; Houge, G; Peters, DJ; Shaw, AC; van Belzen, MJ; van de Kar, AL, 2014)
"The majority of keloids are located on the shoulders and chest."( de Jong, D; Hennekam, RC; Houge, G; Peters, DJ; Shaw, AC; van Belzen, MJ; van de Kar, AL, 2014)
"Keloids are common abnormally raised fibroproliferative lesions that can occur following even minor cutaneous trauma."( Lu, WS; Yao, XH; Zhang, LF; Zheng, XD, 2015)
"Keloids are benign dermal tumors that occur ~20 times more often in African versus Caucasian descent individuals."( Edwards, TL; Russell, SB; Tsosie, KS; Velez Edwards, DR; Williams, SM, 2014)
"Keloids are fibroproliferative dermal lesions characterized by the proliferation of fibroblasts."( Fang, AH; Hu, WP; Kuo, HY; Tien, LY; Wang, JJ; Wu, CS, 2015)
"Keloid is an excessive dermal scar occurring in response to skin injuries."( Chanvorachote, P; Nimmannit, U; Pongrakhananon, V; Sucontphunt, A; Unahabhokha, T; Yongsanguanchai, N, 2015)
"A keloid is pathological scar caused by aberrant response to skin injuries, characterized by excessive accumulation of histological extracellular matrix, and occurs in genetically susceptible individuals."( Long, J; Sun, Y; Wang, X; Wang, Y, 2014)
"A keloid is considered to be a type of benign tumor."( Chen, X; Liu, Y; Wang, X; Xiao, Z; Yang, D, 2014)
"Chest keloids are challenging to surgeons because of their high recurrence rate."( Chen, B; Ding, JP; Wang, LZ; Yang, MY, 2014)
"Keloids are one of the common refractory conditions in dermatology and aesthetic plastic surgery."( Cao, JP; Huan, J; Ji, J; Ji, SJ; Tian, Y; Zhang, LY; Zhou, XZ; Zhu, YQ, 2015)
"Keloids are benign hyper-proliferative growths of fibrous tissue where increased fibroblast activity results in abnormal collagen deposition."( Arbi, S; Bester, MJ; Eksteen, EC; Oberholzer, HM; Taute, H, 2015)
"Keloids are a pathologic condition of the reparative process, which present as excessive scar formation that involves various cells and cytokines."( Chang, CH; Chong, Y; Park, TH; Seo, Sw, 2015)
"Keloid is a protruding hypertrophic fibrous formation of the dermis."( Hermanns-Lê, T; Nizet, JL; Piérard, GE; Piérard-Franchimont, C, 2014)
"Keloid is an overgrowth of scar tissue that develops around a wound."( Li, G; Li, S; Song, R, 2015)
"Keloids are benign fibroproliferative tumors of the skin which commonly occur after injury mainly in darker skinned patients."( Chen, KM; Datta, I; Divine, G; Jones, LR; Ozog, D; Worsham, MJ; Young, W, 2015)
"Keloids are considered benign dermal fibroproliferative tumors."( Chen, G; Li, Q; Liang, X; Liang, Y; Liu, D, 2016)
"Keloids are marked by an overabundance of extracellular matrix."( Ahn, HM; Choi, IK; Jeon, YR; Lee, WJ; Lew, DH; Rah, DK; Yun, CO, 2016)
"Keloid is a fibrotic skin disease for which immune cell infiltration is a primary pathological hallmark."( Cai, J; Dong, P; Fan, J; Gan, C; Jiao, H; Pan, B; Xiao, R; Yan, L; Zong, X, 2015)
"Keloids are progressively expanding scars, mostly prevalent in individuals of African descent."( Frazier, R; Katdare, M; Mantel, A; Newsome, A; Thekkudan, T, 2016)
"Keloids are benign skin tumours and are the effect of a deregulated wound-healing process in genetically predisposed patients."( Boccia, L; De Felice, B; Guida, M; Nacca, M, 2015)
"Keloid is a type of pathological skin scar."( Liang, X; Long, X; Ma, L; Wang, X, 2015)
"Since keloids are a dysfunction of collagen fiber synthesis and organization, this study aimed to evaluate if a 1,210 nm diode laser could have effects in a new animal model of keloid scars."( Andrac-Meyer, L; Bertrand, B; Casanova, D; Kerfant, N; Magalon, G; Mordon, S; Philandrianos, C, 2015)
"Keloids are defined as benign dermal scars invading adjacent healthy tissue, characterized by aberrant fibroblast dynamics and overproduction of extracellular matrix."( Chan, MT; Li, Z; Wu, WK; Yu, X, 2015)
"Keloids are wounding-induced tumor-like human scars."( Benya, PD; Chiu, WC; Choi, A; Hsu, T; Kim, EW; Kulber, DA; Lee, YS; Sarkozy, H; Tuan, TL, 2016)
"Keloids are fibroproliferative lesions of unknown origin that are characterized by increased collagen deposition."( Chen, B; Jia, Y; Liu, Q; Long, X; Wang, X; Wang, Y; Yu, N, 2016)
"The etiology of keloids is unknown but they occur after dermal injury in genetically susceptible individuals, and they cause both physical and psychological distress for the affected individuals."( Andrews, JP; Macarak, E; Marttala, J; Rosenbloom, J; Uitto, J, 2016)
"Keloids are scars that grow beyond the boundaries of a cutaneous injury, inflammation, surgical incision, or burn."( Kaya, H; Polat, M; Şahin, A, 2016)
"Keloid is an abnormal hyperproliferative scarring process with involvement of complex genetic and triggering environmental factors."( Cho, S; Jin, CL; Kim, JE; Kim, M; Kim, Y; Lee, DH; Lee, MJ; Shin, MH, 2016)
"Keloids are common in the Asian population."( Long, X; Wang, X; Wang, Y; Zhang, M; Zhao, R, 2016)
"Keloid is the abnormal wound healing puzzled by the aggressive growth and high recurrence rate due to its unrevealed key pathogenic mechanism."( Cao, R; Jiao, H; Liu, Y; Lv, X; Pan, B; Sun, X; Wang, L; Xiao, R; Yan, L; Zhuang, Q, 2016)
"Keloid is a benign fibrous growth, which presents in scar tissue of predisposed individuals."( Kesh, F; Khaddam, J; Shaheen, A, 2016)
"Keloid is one of the most frustrating problems related to wounding healing and presents a great challenge in clinic."( An, G; Liang, S; Liu, Y; Sheng, C; Yao, W, 2017)
"Keloids are difficult to treat due to their poor response and high recurrence rate."( Behera, B; Kumari, R; Malathi, M; Thappa, DM, 2016)
"Keloids are characterized by the formation of excessive scar tissue that extends beyond the area of the initial wound."( Akaishi, S; Aoki, M; Dohi, T; Hyakusoku, H; Nakao, J; Ogawa, R, 2016)
"Keloids are fibroproliferative scars that develop as a result of a dysregulated wound healing process; however, the molecular mechanisms of keloid pathogenesis remain unclear."( Gao, Z; Jiang, Z; Wang, X; Wu, X; Xia, L; Yu, Q; Zhang, Y, 2016)
"Keloids are difficult to remove successfully and there is no universally accepted treatment."( Lee, NH; Roh, SG; Shin, JY; Yang, KM; Yun, SK, 2017)
"Keloid is conventionally treated with intra-lesional (IL) triamcinolone, which is highly operator dependent and has its own adverse effects."( Imran, FH; Ismail, R; Jamil, A; Nor, NM; Shah, SA, 2017)
"Keloids are fibrous overgrowths induced by cutaneous injury."( Cui, F; Pang, QY; Rang, Z; Wang, YW; Wang, ZY; Yang, G, 2016)
"Keloid is a benign tumor that is characterized by the hyperproliferation of dermal fibroblasts and excessive deposition of extracellular matrix (ECM) especially the collagen."( Jiang, RH; Kim, CD; Lee, JH; Yin, WT; Yoon, TJ; Zhou, MW; Zhu, MJ, 2017)
"Keloids are pathologic scars defined as dermal fibrotic tumors resulting from a disturbance of skin wound healing process."( Binda, D; Humbert, P; Mankhetkorn, S; Pazart, L; Rolin, G; Suttho, D, 2017)
"Keloids are benign fibroproliferative tumors more frequently found among African Americans."( Bonifacio, KM; Cruz, T; Fuentes-Duculan, J; Garcet, S; Gilleadeau, P; Krueger, JG; Kunjravia, N; Suárez-Fariñas, M; Sullivan-Whalen, M; Tirgan, MH; Wang, CQF; Xu, H, 2017)
"At present, keloids are classified as strongly inflammatory scars, while hypertrophic scars are considered to be mildly inflammatory scars."( Akaishi, S; Ogawa, R, 2016)
"Auricularis keloids are the keloids locating on the earlobe and helix which often caused by ear piercing, burn wound and skin injury."( Liu, K; Wang, PH; Wu, XL, 2016)
"Keloids are fibroproliferative skin disorders characterised clinically by continuous horizontal progression and post-surgical recurrence and histologically by the accumulation of collagen and fibroblast ingredients."( Du, Y; Huang, C; Liu, L; Ogawa, R; Wang, B; You, Z, 2017)
"The literature on keloids is replete with authors expressing frustration with treatment results."( Aluko-Olokun, B; Olaitan, AA, 2016)
"Keloids are abnormal overgrowth of collagen fibers, and the first-line treatment includes intralesional injection of triamcinolone acetonide (TA), which is associated with pain."( Burusapat, C; Usanakornkul, A, 2017)
"Keloids are fibroproliferative diseases characterized by the accumulation of an extracellular matrix including collagen."( Horinaka, M; Kawarazaki, A; Nishino, K; Numajiri, T; Sakai, T; Yasuda, S, 2017)
"Keloid is a pathologic fibro-proliferative disorder and is characterized by hyper-proliferation of fibroblasts and excess extracellular matrix (ECM) deposition."( Li, ZM; Lin, XH; Zhang, L; Zhang, QY; Zhang, Y, 2017)
"Keloid is a common and refractory disease characterized by abnormal fibroblast proliferation and excessive deposition of extracellular matrix components."( Han, G; Hu, Y; Jiao, Y; Li, S; Qi, T; Wei, G; Zhang, C, 2017)
"Keloid is a skin fibrosis disease that characterised by invasive growth of fibroblasts and aberrant deposition of extracellular matrix."( Bogari, M; Chai, G; Chen, W; Chen, X; Lin, L; Mar Aung, Z; Qu, M; Wang, X; Xin, Y; Zhang, Y; Zhu, M, 2017)
"Keloid is a benign fibroproliferative growths resulting from an overexuberant healing response."( Li, ZG, 2017)
"Keloids are benign dermal fibroproliferative tumors that develop as a result of several dysregulated processes."( Cui, F; Feng, J; Pang, Q; Rang, Z; Xue, S, 2017)
"Keloids are developed as fibrotic scar at the site of surgery or trauma and often enlarge beyond the original scar margins."( Bhusari, P; Chhabra, A; De, D; Handa, S; Kumar, M; Kumaran, S; Mittal, BR; Palarwar, K; Rathore, Y; Shukla, J; Vatsa, R, 2017)
"Keloids are characterized by excessive collagen deposition and growth beyond the edges of the initial injury, and cytokines may be related to their formation."( Carneiro, CAX; da Silva, IR; da Silva, MV; Dos Reis, MA; Furtado, PC; Peixoto, AB; Rodrigues, BR; Rodrigues, DBR; Rodrigues, V; Tiveron, LCRDC, 2017)
"Keloid is a disorder of fibroproliferative diseases that occurs in wounds, characterized by an exaggerated response to injury."( Cai, Y; Pan, M; Wang, C; Wu, W; Yang, W; Zhu, S, 2017)
"Keloid is one kind of benign skin disease caused by hyperplasia of fibroblasts and collagen fibrils."( Gong, H; Jiang, D; Jiao, Y; Qi, Y; Wang, X; Zhang, J, 2017)
"Keloids are abnormal fibroproliferative scars that pose a significant challenge to patients and clinicians."( Hahn, JM; Supp, DM, 2017)
"Keloids are benign cutaneous lesions, arising from proliferating fibroblasts."( Hoffmann, TK; Rotter, N; Scheithauer, MO; Thierauf, J; Veit, JA; Walther, M, 2017)
"Keloids are pathological scars characterized by excessive extracellular matrix production that are prone to form in body sites with increased skin tension."( Chen, WR; Cheng, CM; Harn, HI; Ho, YT; Hsu, CK; Lee, JY; Lee, YC; Lin, HH; McGrath, JA; Ogawa, R; Shieh, SJ; Tang, MJ; Wang, YK, 2018)
"Keloids are fibrous growths that occur as a result of abnormal response to dermal injury."( Ho, D; Jagdeo, J; Kraeva, E, 2017)
"Keloids are an exuberant response to cutaneous wound healing."( Glass, DA, 2017)
"Keloid is characterized by hyper-proliferation of fibroblasts and excess extracellular matrix (ECM) deposition."( Cui, S; Lu, F; Si, E; Wang, W; Yuan, Z; Zhang, X; Zhao, H, 2017)
"Keloids are reportedly rare at the extremes of life."( Adebayo, W; Ademola, SA; Iyun, AO; Michael, AI; Olawoye, OA; Oluwatosin, OM, 2017)
"Keloids are mysterious soft-tissue tumors that are characterized by excessive reparative processes composed of collagen-forming fibroblasts and inflammatory cells."( Chang, CH; Chong, Y; Kim, CW; Kim, YS; Park, TH, 2018)
"Keloid is a cutaneous fibroproliferative disorder."( Kubota, Y; Noishiki, C; Ogawa, R; Takagi, G, 2017)
"Keloids are characterized by abnormal fibrosis, caused by fibroblasts in response to inflammation."( Funayama, E; Furukawa, H; Hosono, H; Kawakubo, K; Murao, N; Ohnishi, S; Oyama, A; Sakamoto, N; Sato, C; Yamamoto, Y, 2018)
"Keloids are a burden for patients due to physical, aesthetic and social consequences."( Bijlard, E; Hovius, SER; Mureau, MAM; Niessen, FB; Timman, R; Verduijn, GM, 2018)
"A keloid is a fibroproliferative disorder occurring in wounds characterized by an exaggerated response to injury."( Gao, Z; Ma, Y; Wang, X; Yang, J, 2018)
"Keloids are benign dermal tumors occurring approximately 20 times more often in individuals of African descent as compared to individuals of European descent."( Edwards, TL; Hellwege, JN; Russell, SB; Velez Edwards, DR; Williams, SM, 2018)
"Keloids are benign skin tumors that develop in individuals who have a positive family history of keloid disorders."( De Felice, B; Garbi, C; Manfellotto, F; Nacca, M; Santoriello, M, 2018)
"Auricular keloids are common following ear piercing, infection, trauma, burns, or spontaneously, and they are highly resistant for treatment and are followed by severe cosmetic problems, especially for patients with bulky auricular keloids."( Jiang, C; Xu, Q; Yang, Y, 2019)
"Keloid is a fibro-proliferative skin disorder with tumor-like behavior and dependence on anaerobic glycolysis (the Warburg effect), but its exact pathogenesis is unknown."( Eid, N; Ito, Y; Kondo, Y; Okuno, R; Otsuki, Y; Ueda, K, 2018)
"Keloids are a type of abnormal scar tissue."( Chang, P; Guo, B; Hui, Q; Li, W; Tao, K; Zhang, Y, 2018)
"Keloids are skin fibroproliferative tumors characterized by locally invasive growth of fibroblasts and excessive collagen deposition."( Cai, L; Huang, Y; Ke, X; Wang, M; Zhang, Q; Zhao, X, 2018)
"Keloid is characterized by tumor-like invasive growth, high incidence, and low remission rate."( Guo, QG; Yao, M, 2018)
"Treatment of keloids is a challenge as a result of paucity of effective treatment modalities, significant side effects, and their recurrent nature."( Aggarwal, A; Raghukumar, S; Ravikumar, BC; Vinay, KN; Yashovardhana, DP, 2018)
"The pathogenesis of keloid is largely unknown."( Lu, CC; Lu, YY; Wang, QR; Wu, CH; Yu, WW; Zhang, CL; Zhang, L, 2018)
"Keloid is a common abnormal cutaneous fibroproliferative disorder."( Bian, L; Jin, H; Liu, Z; Lu, D; Lyu, J; Lyu, L; Zhong, L, 2018)
"Keloids are benign fibroproliferative tumors that extend beyond the original wound."( Alajmi, A; Jfri, A, 2018)
"Spontaneous keloids are diagnosed clinically based on the patient's history, and it is challenging to confirm since they might be triggered by minimal injury or inflammation especially if it is a single lesion."( Alajmi, A; Jfri, A, 2018)
"Keloids are defined as highly inflamed, hyperproliferative pathological scars."( da Cunha Colombo Tiveron, LR; da Silva, IR; da Silva, MV; Peixoto, AB; Rodrigues, DBR; Rodrigues, V, 2018)
"Penile and genital keloids are uncommon despite frequent surgeries in the genital area."( Alyami, F; Ferandez, N; Koyle, MA; Salle, JP, 2019)
"Genital keloids are rare and difficult to treat."( Alyami, F; Ferandez, N; Koyle, MA; Salle, JP, 2019)
"Keloids are a fibroproliferative disorder of the skin resulted from abnormal healing of injured or irritated skin and are characterized by the ability to spread beyond the original boundary of the wound."( Gao, Z; Liu, K; Ruan, M; Wang, X; Yang, J, 2018)
"Keloid is a fibrous benign tumor of the skin caused by increased fibroblast proliferation and overproduction of extracellular matrix (ECM) in the dermis."( Peng, W; Qiu, X; Shi, K; Yan, D; Zheng, W, 2018)
"Keloids are exuberant responses to cutaneous wound healing."( Glass, DA; Tan, A, 2019)
"Keloids are associated with significant morbidity related to disfigurement and/or symptoms (e."( Bakhshaeekia, A; Feily, A; Gianfaldoni, S; Hadibarhaghtalab, M; Lange, CS; Lotti, T; Matta, J; Pazyar, N; Ramirez-Fort, MK; Ramirez-Pacheco, LA; Rasaii, S; Seifi, V; Sohrabian, N, 2019)
"Keloid is a healing disorder that occurs exclusively in humans."( Brito, MJA; Ferreira, LM; Filho, AG; Isoldi, FC; Motoki, THC, 2019)
"Keloids are benign fibroproliferative skin tumors that can cause disfigurement and disability."( Chong, T; Costa, C; Karimpour-Fard, A; LaRanger, R; Mathes, D; Wright, WE, 2019)
"Keloid is characterized by excessive proliferation of scar tissue following trauma."( Fu, S; Huang, H; Liu, D, 2018)
"Keloids are a dermal fibrotic disease whose etiology remains totally unknown and for which there is no successful treatment."( Cao, T; Liu, T; Lv, Y; Ma, B; Pang, H; Song, H; Wang, W; Zhai, D; Zhang, H; Zhang, Y; Zhou, Z, 2019)
"Keloids are a common dermal pathological disorder characterized by the excessive deposition of extracellular matrix components; however, the exact pathogenesis of the disease is still not clear."( Guo, J; Li, X; Liu, Z; Lu, D; Lu, H; Lyu, L; Zhao, Y, 2019)
"Keloids are the most common pathological form of trauma healing, with features that seriously affect appearance and body function, are difficult to treat and have a high recurrence rate."( Lei, R; Pang, Q; Shen, Y; Wang, Y; Xu, J; Xu, M; Xu, S, 2019)
"Keloid is a dermal proliferative disorder characterized by the excessive proliferation and migration of keratinocytes and fibroblasts."( Chen, J; Liu, K; Liu, Y; Wang, X; Zhang, Z, 2019)
"A keloid is a type of unusually raised scar."( Hur, JK; Kang, S; Kim, D, 2019)
"Keloids are defined histopathologically as an inflammatory disorder characterized by exhibiting numerous fibroblasts, abnormal vascularization, increased number of proinflammatory immune cells as well as uncontrolled cell proliferation, and exacerbated and disorganized deposition of extracellular matrix (ECM) molecules."( Arciniegas, E; Carrillo, LM; Chopite, M; Ramírez, R; Rojas, H, 2019)
"Helical rim keloids are difficult to excise because of the complex, three-dimensional, cartilaginous structure of the helix and its thin and tightly adherent covering layer of skin."( Hayashi, T; Maeda, T; Murao, N; Yamamoto, Y, 2019)
"The aetiology of keloids is becoming clearer, but many questions remain, including about the most optimal treatment."( Du, Y; Huang, C; Liu, L; Ogawa, R; You, Z, 2019)
"Keloids are wounding-induced fibroproliferative human tumor-like skin scars of complex genetic makeup and poorly defined pathogenesis."( Chuong, CM; Kulber, DA; Lee, YS; Liang, YC; Tanabe, K; Tuan, TL; Widelitz, R; Wu, P, 2019)
"Keloids are characterized by excessive proliferation of fibroblasts and invasion of surrounding healthy skin."( Chang, CH; Chen, YW; Feng, CH; Hsieh, SC; Huang, SW; Lai, CS; Li, ZY; Yen, JH, 2019)
"Keloids are benign fibrous overgrowths that occur as a result of abnormal wound healing following cutaneous injury."( Chen, H; Chen, S; Gao, X; He, C; Jian, X; Qu, L; Wang, Y; Zhao, Q; Zou, Q, 2019)
"A keloid is a benign fibroproliferative skin tumor that results from abnormal wound healing after injury and tends to grow beyond the boundary of the original wound; the mechanism of keloid formation is still unclear."( Cen, Y; Chen, J; Fang, L; Li, Z; Qing, Y; Wu, J, 2019)
"Keloids are debilitating skin lesions that develop often as a result of minor skin lesions."( Modarressi, A; Petrou, IG; Pittet-Cuénod, B; Rüegg, EM, 2019)
"Keloids are composed of stiff tissue, which displays a fibrotic phenotype with relatively low proliferation."( Akaishi, S; Dohi, T; Gurtner, GC; Matsumoto, NN; Ogawa, R; Padmanabhan, J; Terashima, M; Than, PA, 2019)
"Keloid is characterized by overactive fibroblasts."( Cheng, C; Wang, S; Xu, M; Zeng, W; Zhang, D; Zhang, Y, 2019)
"The formation of keloid is associated with accumulation of extracellular matrix (ECM) formed mainly of collagen and fibronectin."( Abdu Allah, AMK; Essam, M; Farag, AGA; Hagag, MM; Mohammed, KI; Tayel, NR, 2019)
"Keloids are characterized by an overabundance of collagen deposition due to elevated activity and proliferation of fibroblasts, which lead to hypoxic conditions."( Hardiany, NS; Jusman, SWA; Ningsih, SS; Sadikin, M; Sari, DH, 2019)
"Keloid is characterized by benign overgrowth of dermal collagen in response to skin injury in genetically predisposed individuals."( Khan, HA; Paracha, MM; Sahibzada, MN, 2019)
"Keloids are pathologic scars, defined as fibroproliferative diseases resulting from abnormal wound responses, which grow beyond the original wound margins."( Chambert, J; Chatelain, B; Humbert, P; Jacquet, E; Joly, S; Lihoreau, T; Rolin, G; Sandoz, P, 2019)
"Keloid is a dermal tumor with high recurrence rate."( Chen, Y; Fu, X; Jin, Q; Niu, F; Qiao, J, 2019)
"Keloid is a major complication of wound healing."( Belie, O; Mofikoya, BO; Ugburo, AO, 2019)
"Keloids are hard nodules or plaques formed by excessive proliferation of connective tissue."( Fu, J; Li, H; Shao, Y; Sun, Y; Yang, X; Yu, W; Zhang, L; Zhang, X, 2019)
"Keloids are a common presenting complaint in Black Africans but remain poorly documented in these populations."( Akpadjan, F; Kouotou, EA; Mendouga Menye, CR; Nansseu, JR; Ndjitoyap Ndam, EC; Omona Guissana, E; Tounkara, TM; Zoung-Kanyi Bissek, AC, 2019)
"Keloids are considered as benign fibroproliferative skin tumors growing beyond the site of the original dermal injury."( Bayat, A; Khumalo, N; Tan, S, 2019)
"Keloid is a benign fibroblastic tumor which is most often secondary to a scar, but it can occur spontaneously in a subject with black skin."( Mallé, M; Touré, S, 2019)
"Keloids are benign skin tumors with a high recurrence rate following surgical excision."( Gao, Z; Huang, J; Lin, M; Liu, W; Tu, T; Wang, W; Wu, X; Zhang, W; Zhou, G, 2019)
"Severe keloids are currently treated with surgical resection followed by radiation."( Akaishi, S; Aoki, M; Dohi, T; Ogawa, R; Tsuge, T; Yamamoto, H, 2020)
"A keloid is defined as an overgrowth of the dense fibrous tissues that form around a wound."( Chu, X; Lei, R; Li, J; Li, W; Liu, F; Wang, Y; Xu, J; Zhang, S, 2019)
"Keloids are very resistant to treatment in dermatology and plastic surgical practice."( Fan, F; Hou, Z; Liu, P, 2019)
"Keloids are a skin disorder where the skin goes beyond the original border of the wound or trauma, resulting in functional and cosmetic deformities, displeasure, itching, pain, psychological stress, and patient dissatisfaction."( Ge, P; Huang, GB; Shi, CK; Zhao, YP, 2019)
"Keloids are caused by an imbalance between collagen matrix decomposition and production during wound repair."( Dong, W; Huang, J; Long, X; Wang, X; Zhang, W, 2020)
"Keloid is a common and frequently-occurring disease in plastic surgery, and its ugly appearance and itching symptoms bring mental and life pain to patients."( Hu, Z; Lu, X; Pan, B; Sun, P, 2021)
"Keloids are benign fibroproliferative dermal scars of unknown etiopathogenesis resulting in an exophytic protuberant growth with persistent and progressive peri-lesional expansile behavior."( Bayat, A; Ud-Din, S, 2020)
"Keloids are dermal fibroproliferative disorders that characterized by over deposition of components of the extracellular matrix."( Khattab, FM; Samir, MA, 2020)
"Keloids are benign fibro-proliferative growths occurring after skin injury or spontaneously."( Hegab, DS; Hewedy, ES; Mohamed, WS; Sabaa, BEI, 2022)
"Keloids are a major complication related to surgical wound healing and very challenging condition to treat."( Hietanen, KE; Huhtala, H; Järvinen, TAH; Kaartinen, IS; Tolonen, TT, 2020)
"Keloids are dermal fibroproliferative tumors that arise beyond the boundary of the original wound edges and invades adjacent tissue."( Aya, R; Ishiko, T; Katayama, Y; Kubota, H; Morimoto, N; Naitoh, M; Yamawaki, S, 2020)
"Keloid is a benign dermal tumor with excessive hyperplasia and deposition of collagen."( Huang, Y; Jiang, L; Lin, L; Liu, J; Wang, P; Wang, X; Wang, Y, 2020)
"Keloids are reactive or spontaneous fibroproliferative dermal tumors characterized by the exaggerated and uncontrolled accumulation of extracellular collagen."( Kang, Y; Kumar, R; Njauw, CN; Rajadurai, A; Rajadurai, S; Roh, MR; Tsao, H; Zheng, Z, 2020)
"Keloids are firm, fibrous nodules that form on an individual's skin and are associated with difficult symptoms as well as high recurrence rates."( Ma, J; Shen, H; Wang, Y; Zhang, Z, 2020)
"Keloids are induced by skin injuries such as surgeries, skin piercings, burns, and trauma."( Kim, YC; Park, J, 2021)
"Keloids are fibroproliferative skin disorders characterized by the progressive deposition of collagen."( Choi, YS; Han, SH; Kim, DH; Suh, HS, 2020)
"Keloid is a disease that is difficult to cure and has a high recurrence rate."( Cao, ZD; Liu, W, 2020)
"A keloid is characterized by red, tickling, hard, and irregular raised tissues, and it tends to outgrow its origin."( Guan, E; Han, Q; Huang, J; Liu, Y; Liu, Z; Long, F; Long, X; Si, L; Wang, X; Zhang, H; Zhang, M; Zhao, R; Zhao, RC, 2020)
"Keloid is a fibrous tissue proliferative disease in which proliferative scars grow beyond the boundary of the original wound skin."( Gao, YK; Jiang, H; Jie, X; Nie, B; Zhao, X, 2020)
"Keloids are considered as benign fibroproliferative skin tumors, and rare cases of malignancies have been reported."( Chen, A; Kuo, YR; Lin, SD; Ramachandran, S; Yang, CK, 2020)
"Management of keloid is difficult, so there is always a need for adequate and effective therapy."( Brar, BK; Kaushal, V; Kumar, S; Singh, A, 2020)
"A keloid is a type of pathological scar often caused by abnormal tissue repair after a skin injury and is more common in genetically susceptible individuals."( Bao, X; Feng, Y; Liu, S; Lv, W; Ren, Y; Yi, Z; Zhang, Q, 2021)
"Keloids are described as benign dermal fibroproliferative lesions, and vascularization may play a significant role in their pathogenesis."( Chen, C; Long, X; Wang, X; Wang, Y; Yu, N; Zhang, M; Zhang, W, 2021)
"Keloids are any unpleasant, non-compliant comorbidity affecting a major section of people around the globe who acquire it either genetically or by pathological means as a result of a skin injury."( Kamalasanan, K; Kumar, AS, 2021)
"Keloids are benign tumours caused by abnormal wound healing driven by increased expression of cytokines, including activin A."( de Kretser, D; Ham, S; Harrison, C; Southwick, G; Temple-Smith, P; Wallace, EM, 2021)
"Keloid is a representative chronic fibroproliferative condition that occurs after tissue injury."( Kang, H; Kim, JE; Kim, SK; Lee, DG; Lee, KJ; Lee, S; Lee, YJ; Park, H; Park, SH, 2020)
"Keloid is a benign fibroproliferative tumor of the skin caused by abnormal wound healing process after skin injury."( Chen, F; Deng, P; Feng, X; Qi, Y; Wen, H; Yang, J, 2021)
"Keloids are characterized by fibroblast activation and altered architecture of extracellular matrix (ECM)."( Gao, Z; Liu, W; Tu, T; Wang, W; Wu, X; Zhou, B, 2021)
"Keloids are a skin fibrotic disease that cause a number of problems for reconstructive surgeons."( Jiang, S; Xu, Q, 2021)
"Keloids are a skin fibroproliferative condition characterized by the hyperproliferation of fibroblasts and the excessive deposition of extracellular matrix (ECM) components."( Hu, W; Luo, X; Lv, W; Ren, Y; Wu, M; Wu, Y; Zhang, Q, 2021)
"Keloids are benign lesions arising from overproduction of the extracellular matrix and abnormal collagen deposition by dermal fibroblasts."( Bakus, AD; Garden, BC; Garden, JM; Jones, VA; Lai, O; Patel, PM, 2021)
"Keloids are a common condition with variable rates of treatment satisfaction."( Bakus, AD; Garden, BC; Garden, JM; Jones, VA; Lai, O; Patel, PM, 2021)
"Keloid is troublesome for patients' skin appearance and mental health, although it is a benign tumor."( Gao, Y; Ma, Y; Su, X; Wang, Q, 2021)
"Keloid is a type of skin fibroproliferative disease, characterized by excessive deposition of collagen in the extracellular matrix, myofibroblast activation and invasive growth to the surrounding normal skin tissue."( Luo, X; Lv, W; Ren, Y; Wu, M; Wu, Y; Yu, J; Zhang, Q, 2021)
"Keloid is a skin disease characterized by fibrous hyperplasia, which is often difficult to cure."( Li, G; Liu, L; Sun, N; Xu, L, 2021)
"Keloid is a kind of pathological skin scar with unclear molecular pathology."( Liu, N; Ma, J; Song, N; Wu, P; Wu, X; Zhang, J, 2021)
"Keloids are characterized by disturbance of fibroblast proliferation and apoptosis, deposition of collagen, and upregulation of dermal inflammation cells."( Lu, CC; Lu, YY; Qin, H; Wu, CH; Zhang, CL; Zhang, ZH, 2021)
"Keloids are characterized by increased deposition of fibrous tissue in the skin and subcutaneous tissue following an abnormal wound healing process."( Chatelain, B; Dirand, Z; Humbert, P; Isidoro, C; Lihoreau, T; Marty, P; Rolin, G; Secomandi, E; Senez, C; Tissot, M, 2021)
"Keloids are a type of aberrant skin scarring characterized by excessive accumulation of collagen and extracellular matrix (ECM), arising from uncontrolled wound healing responses."( Choi, SJ; Jeon, BH; Kim, CS; Kim, S; Lee, I; Nagar, H; Oh, SH; Piao, S, 2021)
"Chest keloids are a difficult sub-group of scars to treat, likely secondary to the high wound tension in the area that promotes excessive fibroblast proliferation and collagen deposition."( Fua, T; Miles, OJ; Paleri, S; Ramakrishnan, A; Zhou, J, 2021)
"Keloids are fibroproliferative disorders characterized by high recurrence rates, with few factors known to influence the same."( Agak, GW; Anzala, O; Nangole, FW; Ogeng'o, J; Ouyang, K; Zuriel, D, 2021)
"Keloids are characterized by abnormal proliferation of fibroblasts and continuous deposition of extracellular matrix (ECM) components."( Guo, G; Niu, T; Shi, Y; Tian, Y; Tong, Y; Wang, G, 2021)
"Keloids are a type of disordered scar formation which not only show heterogeneity between individuals and within the scar itself, but also share common features of hyperproliferation, abnormal extra-cellular matrix deposition and degradation, as well as altered expression of the molecular markers of wound healing."( Alishahedani, ME; Freeman, AF; McCann, KJ; Myles, IA; Yadav, M, 2021)
"Keloid is a benign tumor characterized by persistent inflammation, increased fibroblast proliferation, and abnormal deposition of collagen in the wound."( Chen, J; Cheng, B; Guo, J; He, QY; Lin, X; Wang, T; Xu, P; Yan, Z; Zhang, W; Zheng, W; Zhong, J; Zhou, J, 2021)
"Keloids are fibroproliferative dermal tumors of unknown origin that are characterized by the overabundant accumulation of extracellular matrix (ECM) components."( Chai, M; Gao, D; Leng, L; Li, M; Liu, B; Lv, L; Ma, J; Wang, W; Wu, Z; Zhang, S; Zhu, Y, 2021)
"Keloid is a benign well-demarcated overgrowth of fibrotic tissue which extends beyond the original boundaries of a defect."( Ali, SM; Hafiz, HSA; Mamdouh, M; Omar, GA, 2022)
"Keloids are essentially different from other types of scars in terms of energy metabolism."( Chen, Y; Fan, J; Gan, C; Jiao, H; Liu, L; Su, Z; Tian, J; Yang, Z; Zhang, T, 2022)
"Keloids are abnormal fibroproliferative scars with aggressive dermal growth expanding beyond the borders of the original injury."( Memariani, H; Memariani, M; Moravvej, H; Shahidi-Dadras, M, 2021)
"Keloids are fibroproliferative lesions resulting from an abnormal wound healing process due to pathological mechanisms that remain incompletely understood."( Anness, MC; Combs, KA; Hahn, JM; McFarland, KL; Supp, DM, 2021)
"Keloid is a unique refractory syndrome characterized by a proliferation disorder of the fibroblasts."( Li, H; Li, Y; Liu, Z; Nie, Y; Shi, L; Wang, H; Wu, H; Zheng, W, 2021)
"Keloid is a skin disease characterized by exaggerated scar formation, excessive fibroblast proliferation, and excessive collagen deposition."( Chang, KL; Hong, CH; Lee, CH; Lu, YY; Tu, HP; Wu, CH; Yang, HJ; Yang, KC, 2021)
"Keloids are benign fibroproliferative skin tumors."( Tan, M; Wu, D; Zhou, J; Zhou, Y, 2021)
"Keloids are common fibroproliferative tumors, and their treatment still represents a dilemma."( Gamea, MM; Hegab, DS; Mahmoud, WH; Serag-Eldin, YMA, 2021)
"Keloid is a hyperplastic pathological scar of body caused by infection, trauma, and surgery or formed spontaneously for unknown reasons."( Lei, JA; Qin, ZL; Zhou, Y, 2021)
"Keloids are disfiguring pathological scars that could cause pain and pruritus."( Hu, T; Liu, W; Ning, X; Xia, L; Xu, C; Yang, Y, 2021)
"Keloids are a benign dermal fibrotic disorder with features similar to malignant tumors."( Chen, J; Chen, W; Li, Z; Liu, X; Long, X; Ma, B; Meng, T; Yu, N; Zeng, Q; Zhou, Z, 2022)
"Keloids are focal fibrotic responses to cutaneous trauma characterized by disordered collagen, which may be associated with elevated systemic fibrocyte levels and/or wound bed chemokine expression."( Burdick, MD; Campbell, CA; Strieter, RM, 2021)
"Keloid is a fibroproliferative disorder of dermal origin, common and severe in the dark-skinned individuals."( Belie, MF; Belie, O; Mofikoya, BO; T Omidiji, OA; Ugburo, AO, 2021)
"Ear keloids are benign, fibrous proliferations due to excessive collagen synthesis and deposition."( Chandrashekar, BS; Madura, C; Nayak, PB; Raj, PR, 2021)
"Keloids are a benign fibroproliferative disease with a high tendency of recurrence."( Lee, JW; Seol, KH, 2021)
"Keloid is a fibroproliferative disorder resulting from trauma, characterized by abnormal activation of keloid fibroblasts and excessive deposition of extracellular matrix (ECM)."( Deng, X; Liu, J; Qi, F; Qian, L; Wang, L; Wang, Q; Wei, C; Yang, Y, 2022)
"Keloids are the result of aberrant tissue scarring typically occurring in injured skin, and are caused by the overgrowth of granulation tissue or collagen type III during the healing process."( Naik, PP, 2022)
"Keloids are benign skin tumors characterized by aggressive growth."( Huang, S; Liao, J; Liu, F; Luo, X; Shi, G; Wen, W, 2021)
"Keloid is an aberrant scarring process of the skin, characterized by excessive extracellular matrix synthesis and deposition."( Bauerschmitz, J; Baur, AS; Fröhlich, W; Kirr, M; Ostalecki, C; Pitiot, A; Plosnita, B; Rath, M; Schliep, S, 2021)
"Keloids are scars that extend beyond the margins of an insulting cutaneous injury."( Hawash, AA; Ingrasci, G; Nouri, K; Yosipovitch, G, 2021)
"Keloid is a type of unusually raised scar."( Dai, X; Lei, TC, 2021)
"Keloid is a benign fibro-proliferative dermal tumor formed by an abnormal scarring response to injury and characterized by excessive collagen accumulation and invasive growth."( Jin, M; Jin, Z; Li, C; Luo, Y; Pi, L, 2021)
"Keloids are a common form of pathologic wound healing and are characterized by an excessive production of extracellular matrix."( Jun, S; Kang, YE; Kim, CS; Kim, S; Lee, SE; Nagar, H; Oh, SH; Shin, C; Yeo, MK; Yi, S; Yi, YS, 2021)
"Keloid is considered as a tumor-like skin disease with multiple aetiologies including immunological factors and mechanical microenvironment."( Gao, Z; Liu, W; Wang, W; Wu, X; Zhou, B, 2022)
"Keloids are pathological wound healing responses to dermal injuries."( Dilogo, IH; Harsono, AD; Prasetyono, TOH, 2022)
"Keloids are benign fibrous tumors derived by excessive proliferation of fibroblasts and collagen synthesis after an injury, and they do not regress spontaneously."( Bovani, B; Clementoni, MT; Conforti, C; Crisman, G; Gennai, A; Melfa, F; Piccolo, D, 2022)
"Keloids are skin lesions which result from an aberration in the physiological healing process marked with overgrowth of collagen fibers."( Abrego, I; Hamdan, S; Lindsey, JT; Nejat, AH; Vitter, R, 2022)
"Keloids are laterally growing fibroproliferative skin disorders."( Cho, H; Dohi, T; Fukumitsu, K; Hayakawa, S; Kamegai, M; Karasawa, K; Ogawa, R; Shimizuguchi, T, 2023)
"The etiology of keloid is largely unknown; however, AD and keloid share inflammatory pathways characterized by T-helper cell 2 cytokines and increased dermal fibroblast activity."( Ahn, HJ; Jeong, SJ; Kwon, HE; Shin, MK, 2021)
"Keloid is a benign fibroproliferative skin tumor."( Lin, G; Wang, Z; Zheng, W, 2021)
"Keloids are intractable scar diseases and sometimes undergo hospitalization."( Gan, L; Kong, W; Shi, Y; Sun, Y; Tang, H; Wang, H; Xia, Z; Xiao, Y; Zhu, Z, 2022)
"Keloid is a benign dermal tumor characterized by abnormal proliferation and invasion of fibroblasts."( Huang, Z; Jiang, R; Jin, H; Li, X, 2022)
"Ear keloids are abnormal continuously growing healing process following cutaneous injury."( Al-Gendi, R; Al-Mohsen, S; Elawadi, AA; Mohamed, R; Wafa, A; Wani, S, 2022)
"Keloid is a skin disease marked by fibroplasia, and fibroblasts viability plays a considerable part in keloid."( Li, T; Liu, F; Zhan, X, 2022)
"Keloid is a skin fibroproliferative disease currently having no uniformly successful treatment."( Chen, L; Cheng, X; He, Y; Jia, C; Li, S; Su, Y; Yin, B, 2022)
"Keloids are disfiguring, hypertrophic scars with yet poorly understood pathomechanisms, which could lead to severe functional impairments."( Ankersmit, HJ; Bormann, D; Copic, D; Direder, M; Farlik, M; Golabi, B; Haslik, W; Hoetzenecker, K; Klas, K; Laggner, M; Mildner, CS; Mildner, M; Pfisterer, K; Radtke, C; Shaw, L; Tschachler, E; Vorstandlechner, V; Weiss, T, 2022)
"Keloids are benign fibrous growths that are caused by excessive tissue build-up."( Cen, Y; Deng, K; Li, W; Liu, R; Wang, R; Xiao, H; Xu, X, 2022)
"Keloid is commonly regarded as a benign skin tumour."( Gao, Z; Li, Q; Liu, W; Tu, T; Wang, W; Wu, X, 2022)
"Keloids are an excessive tissue response to dermal damage, characterized by uncontrolled growth and a high recurrence rate after various treatments."( Bi, J; Huo, R; Li, J; Li, Z; Wang, S, 2022)
"Keloids are benign fibroproliferative skin disorders characterized by chronic inflammation."( Ansai, SI; Ogawa, R; Tosa, M, 2022)
"Keloid is a pathological skin scar formation with complex and unclear molecular pathology mechanism."( Bergquist, J; Chi, X; Deng, T; Hu, W; Liu, J; Mi, J; Wang, H; Wang, Y; Yang, C; Yang, X; Zhang, C; Zhang, H; Zhu, Y, 2022)
"Keloids are "tumor-like" scars that grow beyond the boundary of injury."( Li, B; Yan, Q, 2022)
"Keloids are a fibrotic skin disorder caused by abnormal wound healing and featuring the activation and expansion of fibroblasts beyond the original wound margin."( Chan, H; Chen, TC; Hong, YK; Hsu, CK; Huang, YL; Hung, KS; Lin, YC; Liu, YT; Pai, TP; Wu, CH, 2022)
"Keloids are a chronic disease and cause pain, pruritus, and limitation of motion."( Cho, MY; Chung, KY; Roh, MR; Song, A, 2022)
"Keloids are benign fibroproliferative diseases with abnormally proliferated bulges beyond the edge of the skin lesions, and they are characterized by uncontrolled fibroblast proliferation and excessive extracellular matrix deposition in the dermis."( Chen, JY; Deng, CC; Feng, QL; Gu, JJ; Pan, HH; Xu, XY; Yang, B; Zheng, WY, 2022)
"Keloids are benign fibroproliferative tumors that display many cancer-like characteristics, such as progressive uncontrolled growth, lack of spontaneous regression, and extremely high rates of recurrence."( Fu, R; Huang, RL; Li, Q; Liu, C; Wang, X; Yan, Y; Yang, J, 2022)
"Keloid is a benign proliferative disease characterized by excessive deposition of extracellular matrix collagen during skin wound healing."( Chen, L; Liu, Y; Qi, S; Tang, J; Wang, H; Wang, P; Xie, J; Zhou, Z, 2022)
"BACKGROUND A keloid is a pathological scar hyperplasia that is affected by genetic and environmental factors."( Du, H; Guo, Y; Hao, X; Wang, J; Wen, X, 2022)
"Keloids are benign fibroproliferative skin tumors."( Li, X; Li, Y; Liu, Y; Ni, Z; Song, J; Wang, X; Zhu, F, 2022)
"Keloid is an abnormal fibrotic disease after cutaneous injury characterized by exaggerated scar tissue formation, which often extends beyond the boundaries of the original wound."( Cho, KH; Cho, ML; Choi, JW; Lee, AR; Lee, CR; Lee, JH; Lee, SY, 2022)
"Keloids are pathological scars extending beyond the initial wound's natural borders."( Andersen, PS; Schønfeldt, T, 2022)
"Relapse of keloids is common after corticosteroid injection in patients with oily skin."( Fan, H; Min, P; Peng, Y; Zhang, S; Zhang, Y, 2022)
"Keloids are the result of abnormal wound healing, and they differ from the normal skin of the patient in the level of blood perfusion and the degrees of inflammation, hypoxia, regeneration of vessels, and expression of sensory receptors."( Li, S; Long, X; Wang, X; Zhang, M, 2022)
"Keloids are considered disorders of fibroproliferation characterized by accumulation of collagen fibers in hypodermis and dermis, caused by inflammation, surgery, and trauma."( Bessar, H; Khater, EM; Khattab, FM, 2022)
"Keloids are a common type of pathological scar as a result of skin healing, which are extremely difficult to prevent and treat without recurrence."( Shao, J; Shen, Z; Sun, J; Xu, J, 2022)
"A keloid is a fibroproliferative disorder of unknown etiopathogenesis that requires ill-defined treatment."( Chen, X; Li, J; Liang, B; Pi, X; Wang, X; Yang, R; Zhang, P; Zhou, S; Zhou, X, 2022)
"Background: A keloid is a benign skin tumor that extends beyond the initial injury area, and its pathologic mechanism remains unclear."( Feng, C; Hao, Y; Liu, H; Shan, M; Song, K; Wang, Y, 2022)
"Keloid is a common dermis tumor, occurring repeatedly, affecting the quality of patients' life."( Gao, F; Li, L; Liang, ZH; Lin, SS; Lin, X; Liu, Y; Qiu, ZY; Wang, JY, 2023)
"Keloids are chronic dermal fibro-proliferative disorders resulting from excessive collagen deposition."( Ajani, AA; Akinboro, AO; Alo, AG; Olanrewaju, FO; Olasode, OA; Oripelaye, MM, 2022)
"Keloids are benign dermal tumors that arise from abnormal wound healing processes following skin lesions."( Chen, S; Hong, M; Li, X; Liu, Y; Mo, W; Shi, B; Shi, Y; Yan, T; Yu, D; Zhang, S, 2023)
"Keloids are skin fibroproliferative disorders, resulting from abnormal healing of deep cutaneous injuries."( Ioannou, E; Karalis, V; Kikionis, S; Koromvoki, M; Kyritsi, A; Panagiotopoulos, A; Polichronaki, E; Rallis, M; Roussis, V; Stratigos, A; Tagka, A; Vitsos, A, 2022)
"Keloids are a fibroproliferative disease characterized by unsatisfactory therapeutic effects and a high recurrence rate."( Chen, H; Chen, K; Chen, L; Hu, Y; Huang, D; Jin, S; Ju, M; Li, R; Liu, L; Luan, C; Wang, Z; Zhang, J; Zhou, X, 2022)
"Keloids are pathological scars that invade normal surrounding tissue without self-limitation, causing pain, itching, cosmetic disfigurement, etc."( Nurzat, Y; Xu, H; Zhang, Y; Zhu, Z, 2023)
"Keloid is a type of benign tumor of the skin with abnormal proliferation of fibrous tissue."( Hao, Y; Li, W; Liu, H; Qiu, J; Shan, M; Wang, Y, 2022)
"Treatment of chest keloids is challenging."( Ha, B; Im, S; Kim, SJ; Lee, YJ; Park, TH, 2023)
"Keloid is a common pathological scar, which involves the regulation of immune microenvironment."( Hu, Z; Wang, X, 2022)
"Since keloids are driven by skin injuries, the existence of keloidal dermatofibroma has been suggested to support the injury hypothesis of dermatofibroma etiology."( Akaishi, S; Ansai, SI; Dohi, T; Nishimoto, A; Ogawa, R, 2023)
"Keloids are common and have significant negative effects on quality of life."( Banner, L; Cohen, AJ; Gleason, L; Lazarevic, B; Malkani, K; Nikbakht, N; Talasila, S; Uitto, J, 2023)
"Keloids are common and have significant negative effects on quality of life."( Banner, L; Cohen, AJ; Gleason, L; Lazarevic, B; Malkani, K; Nikbakht, N; Talasila, S; Uitto, J, 2023)
"Keloids are common and have significant negative effects on quality of life."( Banner, L; Cohen, AJ; Gleason, L; Lazarevic, B; Malkani, K; Nikbakht, N; Talasila, S; Uitto, J, 2023)
"A keloid is a benign fibroproliferative skin tumor whose formation is regulated by circular RNAs (circRNAs)."( Cai, M; Hu, Z; Liu, L; Su, J, 2023)
"A keloid is a benign fibroproliferative skin tumor whose formation is regulated by circular RNAs (circRNAs)."( Cai, M; Hu, Z; Liu, L; Su, J, 2023)
"A keloid is a benign fibroproliferative skin tumor whose formation is regulated by circular RNAs (circRNAs)."( Cai, M; Hu, Z; Liu, L; Su, J, 2023)
"Keloid is a benign tumor with high recurrence rate; accordingly, complete surgical excision with adjuvant radiotherapy is one of the most effective treatments."( Chen, F; Chiang, CH; Huang, CJ; Huang, MY; Kuo, YR; Tang, JY, 2022)
"Keloid is a benign tumor with high recurrence rate; accordingly, complete surgical excision with adjuvant radiotherapy is one of the most effective treatments."( Chen, F; Chiang, CH; Huang, CJ; Huang, MY; Kuo, YR; Tang, JY, 2022)
"Keloid is a benign tumor with high recurrence rate; accordingly, complete surgical excision with adjuvant radiotherapy is one of the most effective treatments."( Chen, F; Chiang, CH; Huang, CJ; Huang, MY; Kuo, YR; Tang, JY, 2022)
"Keloids are chronic progressive dermal pseudo-tumors that can grow considerably in volume and surface area but do not invade other tissues."( Charvet, E; Delaleu, J; Petit, A, 2023)
"Keloids are chronic progressive dermal pseudo-tumors that can grow considerably in volume and surface area but do not invade other tissues."( Charvet, E; Delaleu, J; Petit, A, 2023)
"Keloid is a benign fibro-proliferative dermal tumour formed by an abnormal scarring response to injury and characterised by excessive collagen accumulation and invasive growth."( Hu, Z; Wang, Z; Xu, H; Yang, H; Zhu, J, 2023)
"Keloid is a benign fibro-proliferative dermal tumour formed by an abnormal scarring response to injury and characterised by excessive collagen accumulation and invasive growth."( Hu, Z; Wang, Z; Xu, H; Yang, H; Zhu, J, 2023)
"Keloids are fibroproliferative disorders, which seriously affect the quality of life of patients with keloids."( Guo, F; Hu, H; Mao, G; Zheng, J, 2022)
"Keloids are fibroproliferative disorders, which seriously affect the quality of life of patients with keloids."( Guo, F; Hu, H; Mao, G; Zheng, J, 2022)
"Auricular keloids are difficult to treat, and recurrent keloids are more aggressive and more likely to develop aural deformities."( Dong, G; Hu, J; Jin, Q; Liu, Y; Qu, C; Wang, L; Wang, M; Wu, H, 2023)
"The incidence of keloids is higher in the case of darker skin."( Abe, Y; Hashimoto, I; Ishida, S; Minami, K; Mineda, K; Nakahara, T; Sato, K; Yamashita, Y, 2023)
"Keloid is a pathological dermatological condition that manifests as an overgrowth scar secondary to skin trauma."( Qi, S; Tang, J; Wang, H; Xie, J; Zhou, Z, 2023)
"Keloids are defined as overrepairing products that develop after skin lesions."( Li, ZJ; Long, X; Qiu, ZK; Si, LB; Wang, XJ; Yu, NZ; Zhang, MZ; Zhang, WC, 2023)
"Keloids are considered the manifestation of a fibroproliferative disease characterized by chronic inflammation that is induced following skin injury."( Chao, H; He, J; Hsu, P; Liu, H; Ma, H; Tang, Q; Wu, R; Xu, S; Zeng, R; Zheng, L; Zhou, Y, 2023)
"Keloids are a fibroproliferative skin disorder with a high recurrence rate."( Chen, ZA; Gao, Z; Lin, X; Ma, QY; Wang, WB; Wu, XL; Xia, LL; Xie, CH; Yang, YT; Zhao, Q, 2023)
"Keloids are formed due to abnormal hyperplasia of the skin connective tissue."( Chen, W; Chen, X; Gan, W; Huang, J; Qin, X; Wang, X; Yang, R; Zheng, W; Zhou, S, 2023)
"Keloids are pathologic scars that pose a significant functional and cosmetic burden."( Kundu, RV; Kwan, KR; Miller, CH; Pontes, D; Poondru, S; Walsh, LA; Wu, E, 2023)
"Keloids are pathological scars from exuberant fibroproliferative collagen response and excessive extracellular matrix production usually extending beyond the original wound margins."( Martinez, F; Nguyen, A; Nguyen, BD, 2023)
"A keloid is a classic fibrotic skin disease characterized by excessive deposition of extracellular matrix (ECM)."( Bi, J; Chen, H; Li, Q; Liu, Y, 2023)
"Keloids are skin tumours caused by aberrant growth of dermal fibroblasts."( Chung, JH; Darmawan, CC; Hur, K; Kusumaningrum, N; Lee, SH; Mun, JH, 2023)
"Ear keloid is one of the more common forms of keloid, which may cause pain and itching, and is aesthetically unappealing."( Cai, XN; Ji, YC; Wang, MM, 2023)
"Keloid is a type of disfiguring pathological scarring unique to human skin."( Chen, CB; Chen, CH; Chung, WH; Lee, CC; Tsai, CH; Yeh, YC, 2023)
"Keloid is a type of benign fibrous proliferative tumor characterized by excessive scarring."( Dou, H; He, L; Jia, J; Shu, M; Yu, X; Zhu, C, 2023)
"Ear keloids are disfiguring disorders resistant to various treatments."( Ahmednaji, NM; Chen, XD; Wang, YX; Wu, XY, 2023)
"Usually, keloids are considered and treated as a single entity but clinical observations suggest heterogeneity in keloid morphologies with distinction of superficial/extensive and nodular entities."( Benssussan, A; Boccara, D; Boismal, F; Bouaziz, JD; DE LA Grange, P; Ferrero, L; Gentien, D; Henry, E; Michel, L; Mimoun, M; Serror, K; Sintes, M; Thery, M; Vianay, B, 2023)
"Keloid is a pathological scar formed by abnormal wound healing, characterized by the persistence of local inflammation and excessive collagen deposition, where the intensity of inflammation is positively correlated with the size of the scar formation."( Chen, G; Chen, L; Chi, H; Cui, Z; Du, Y; Gao, B; Song, B; Yu, Z; Zheng, Y; Zhu, Y, 2023)
"Keloids are an exuberant response to skin wound healing in which abundant scar tissue grows beyond the boundaries of the inciting insult."( Glass, DA; Knowles, A, 2023)
"Keloid is a heterogeneous disease featured by the excessive production of extracellular matrix."( Guo, C; Huang, J; Liang, L; Qiu, X; Tan, G; Wang, L; Xie, Y; Zheng, J, 2023)
"Keloid is a highly aggressive fibrotic disease resulting from excessive extracellular matrix deposition after dermal injury."( Hao, Y; Kuang, X; Liang, Z; Liu, H; Shan, M; Wang, Y; Xia, Y, 2023)
"Keloids are known to recur and can cause severe cosmetic, functional, and psychological impairments."( Datema, FR; Rothuizen, LT; Saridin, J; Timmer, FCA; van Zijl, FVWJ, 2023)
"Keloids are benign skin lesions that gradually invade the surrounding normal tissue, and no treatment has proven curative."( Han, X; Hu, SD; Ji, DS; Liu, Y; Zhao, YM, 2023)
"Keloids are a fibroproliferative skin disorder that develops in people of all ages."( Chen, H; Qian, H; Wang, C; Zhang, M, 2023)
"Keloids are benign skin tumors resulting from the excessive proliferation of connective tissue in wound skin."( Li, Z; Liang, H; Tian, B, 2023)
"Keloids are pathologic conditions characterized by fibroblast hyper-proliferation and excess collagen deposition."( Eltahlawy, S; Hamada Mohamed, B; Marzouk, WA; Mohamad, NE, 2023)
"Keloids are fibroproliferative disorders described by excessive growth of fibrotic tissue, which also invades adjacent areas (beyond the original wound borders)."( Adebayo, OE; Bordas, SPA; Chouly, F; Eftimie, R; Rolin, G; Urcun, S, 2023)
"Keloids are a type of fibrotic disease characterized by excessive collagen production and extracellular matrix (ECM) deposition."( Li, D; Wu, X; Zhang, X, 2023)
"Patients with keloids are often younger than 30 years old and have darker skin."( Bonan, P; Conforti, C; Crisman, G; Fusco, I; Piccolo, D, 2023)

Context

ExcerptReference
"No keloid has ever been noted to recur before epithelial migration is complete."( Shaw, GY; Stucker, FJ, 1992)
"Eight of the nine keloids have recurred to their original or close to original size as early as 10 months following treatment and as late as 22 months."( Apfelberg, DB; Lash, H; Maser, MR; White, DN, 1989)
"The treatment of keloids has always been a formidable task and no definitive treatment method has yet been established."( Arai, K, 1999)
"Keloids have been treated with flashlamp pulsed dye lasers (PDLs) with good results."( Chang, PR; Chen, TH; Huang, HC; Jeng, SF; Kuo, YR; Wang, FS; Yang, KD, 2004)
"For centuries, keloids have been an enigma and despite considerable research to unravel this phenomenon no universally accepted treatment protocol currently exists."( Louw, L, 2007)
"Since keloids have hypersecretion of extracellular matrix, we hypothesized that keloid fibroblasts (KFs) may have enhanced activation of the UPR compared with normal fibroblasts (NFs)."( Butler, PD; Koong, AC; Longaker, MT; Ly, DP; Wang, Z; Yang, GP, 2011)
"Familial keloids have been reported, having either autosomal dominant or autosomal recessive inheritance."( Clark, JA; Howard, L; Kleta, R; Kopp, JB; Stanescu, H; Turner, ML, 2009)
"Keloids have been treated by using radiation for over a century, and it is currently suggested that keloids are best treated by a combination of surgery and postoperative radiation therapy, although randomized controlled trials testing this are still lacking."( Miyashita, T; Ogawa, R; Yoshida, K; Yoshitatsu, S, 2009)
"Keloids have a predilection for the aural region because of the special shape of the pinna."( Cen, Y; Liu, XX; Xu, XW; Yu, R; Zhang, YG, 2009)
"Keloids have a tendency to recur after surgical excision as a single treatment."( Chang, CH; Kim, JK; Park, TH; Seo, SW, 2011)
"Management of keloids has remained a conundrum, because an optimum treatment regimen has yet to be elucidated."( Bennett, KG; Brown, DL; Hayman, JA; Kung, TA, 2017)
"The etiology of keloids has not been resolved but previous studies suggest that keloids are a genetically heterogeneous disorder."( Ademola, S; Bamshad, MJ; Benahmed-Miniuk, F; Fadiora, S; Hu, Y; Kanaujiya, JK; Leal, SM; Nickerson, DA; Odesina, V; Olaitan, PB; Oluwatosin, OM; Reichenberger, EJ; Santos-Cortez, RLP; Sun, F; Tao, J, 2017)
"Keloids have been one of the most concerning problems in cosmetic surgery."( Burusapat, C; Pruksapong, C; Yingtaweesittikul, S, 2017)
"Spontaneous keloids have been reported mainly in association with syndromes such as Rubinstein-Taybi syndrome, Dubowitz syndrome, Noonan syndrome, Goeminne syndrome, Bethlem myopathy, conjunctivocorneal dystrophy, X-linked recessive polyfibromatosis and a novel X-linked syndrome with flamin A mutation."( Alajmi, A; Jfri, A, 2018)
"Keloids have high recurrence rates."( Hietanen, KE; Huhtala, H; Järvinen, TA; Kaartinen, IS; Kuokkanen, HO; Tolonen, TT, 2019)
"Keloids have been assessed by numerous methods and severity indices resulting in a lack of standardization across published research."( Braunberger, TL; Lyons, AB; Ozog, DM; Peacock, A; Viola, KV, 2019)
"The pathogenesis of keloids has not been elucidated, and the disease is thought to be caused by abnormal secretion of proinflammatory mediators and irregular responses to other inflammatory signals mediated by keloid fibroblasts (KFs)."( Cho, ML; Choi, JW; Jung, KA; Kim, DS; Kim, EK; Lee, JH; Lee, SY; Moon, SJ; Seo, HB; Yang, SC; Yoo, JH, 2020)
"Although keloids have been empirically treated with steroids and radiation, evidence-based radiation parameters for keloid therapy are lacking."( Cohen, GF; Gunjan, A; Om, A; Phillips, EON; Price, KM; Rosenberg, LZ; Shaath, TS; Son, Y; Stefanovic, B; Wolfe, CM, 2020)
"Recurrence rates of keloids have generally been reported at one time point."( Funayama, E; Hayashi, T; Ishikawa, K; Maeda, T; Murao, N; Osawa, M; Yamamoto, Y, 2021)
"Patients with keloids have increased odds risk of arthrofibrosis following primary TKA."( Flick, TR; Hodo, TW; Patel, AH; Sanchez, FL; Sherman, WF; Wang, CX, 2021)
"The prevalence of keloids has been reported to increase in patients with AD, but it remains controversial."( Ahn, HJ; Jeong, SJ; Kwon, HE; Shin, MK, 2021)
"Keloids have always been a difficult problem in the clinic."( Fan, J; Gan, C; Huang, R; Jiao, H; Liu, L; Su, Z; Tian, J; Yang, Z, 2022)
"The pathogenesis of keloids has not been definitively clarified and treatment is often protracted and less than satisfactory."( Haubner, F; Oettgen, F, 2022)
"Keloid has brought great trouble to people and currently has no uniformly successful treatment."( He, Y; Jia, C; Lan, J; Li, S; Lian, W; Wang, P; Yin, B; Zhang, Z, 2022)
"In addition, keloids have not been reported in albinism patients of any race, and those with darker skin in the same race are more likely to develop this disease (LaRanger et al."( Shao, J; Shen, Z; Sun, J; Xu, J, 2022)
"The pathogenesis of keloids has not been definitively clarified and treatment is often protracted and less than satisfactory."( Haubner, F; Oettgen, F, 2022)
"Post-acne keloids have become a serious problem affecting the physical and mental health of adolescents."( Li, J; Liu, J; Wang, X; Wang, Y; Zhang, W; Zhang, Z, 2023)

Actions

ExcerptReference
"Keloids affects predominantly young adults with single anatomical site being the commonest presentation, with the chest mostly affected and the flat pattern commonly observed."( Ajani, AA; Akinboro, AO; Alo, AG; Olanrewaju, FO; Olasode, OA; Oripelaye, MM, 2022)

Treatment

ExcerptReference
"Here we report our method of treating recurrent keloid and hypertrophic scars."( Tang, YW, 1992)
"The optimal treatment for keloids remains undefined."( Lawrence, WT, 1991)
"The use of radiations for the treatment of keloids was the topic of debate for years."( Deka, AC; Deka, BC; Rao, SM; Supe, SJ; Supe, SS, 1991)
"Silicone gel is effective in the treatment of keloid scars."( Mercer, NS, 1989)
"Several methods for the treatment of scar keloids have been reported."( Ohmori, S, 1988)
"We report on the treatment of keloids and scars by means of topical application and injection of active substances."( Landes, E, 1987)
"Atrophic scars resulted after 1 to 8 treatments."( Mende, B, 1987)
"A report is given on the treatment of keloids and hypertrofic scars using an argon laser."( Hulsbergen Henning, JP; Roskam, Y; van Gemert, MJ, 1986)
"The results of treatment of keloids are still very disappointing."( Oluwasanmi, JO, 1974)
"In other situations, as in the treatment of keloids, physicians may wish to introduce drugs known to reduce scar formation into the biologic environment in which wound healing ensues."( Pollack, SV, 1982)
"A report is given on the treatment of keloids and hypertrophic scars using ordinary zinc tape."( Bartholdson, L; Hallmans, G; Söderberg, T, 1982)
"Morphologic changes in steroid-treated keloids were established using light and electron microscopy."( Boyadjiev, C; Mazgalova, J; Popchristova, E, 1995)
"In the treatment of keloids surgical excision followed by radiation therapy provides the highest reported control rates of 72% to 92%."( Anscher, M; Klumpar, DI; Murray, JC, 1994)
"Traditional treatment of keloids by surgery or surgery combined with other techniques has met with limited success."( Mincer, FR; Ship, AG; Weiss, PR; Wolkstein, W, 1993)
"There is no one right way to treat all keloids and hypertrophic scars."( Nemeth, AJ, 1993)
"Numerous approaches are used to treat keloids, but none is ideal for all scars and recurrence after treatment is frequent."( Bono, R; Rossi, G; Rusciani, L, 1993)
"A review of the surgical treatment of keloids with emphasis on surgery combined with nonsurgical therapies is presented."( Berman, B; Bieley, HC, 1996)
"Various lasers have been used in the treatment of keloids with great variability in the recurrence rate but in general result in similar recurrence rates as conventional surgery."( Berman, B; Bieley, HC, 1996)
"However, the results in treating keloid are variable."( Chang, CH; Chen, JS; Chiu, HC; Lin, LJ; Liu, CC; Wong, TW, 1996)
"Six patients with previously untreated keloids were studied."( diLeonardo, M; Kauh, YC; Mondragon, G; Rouda, S; Tan, EM; Tokarek, R; Tuan, RS, 1997)
"Although optimal treatment for keloids remains undefined, successful treatment can be obtained through a multimodality approach."( English, RS; Shenefelt, PD, 1999)
"As a surgical treatment for keloids, we have been using the intralesional technique which we think gives better results."( Egloff, DV; Gailloud-Matthieu, MC; Raffoul, W, 1999)
"Hence, it becomes important to treat keloids as a separate entity different from hypertrophic scars and enhancement of Fas-sensitivity could be a promising therapeutic target."( Chodon, T; Funayama, E; Furukawa, H; Igawa, HH; Sugihara, T, 2000)
"The authors treated 24 keloids of the ear, trunk, face, and genitalia with keloid core excision."( Baek, RM; Hong, JJ; Lee, Y; Minn, KW, 2001)
"HDR brachytherapy is an effective treatment for keloid scars."( Andrés, A; Finestres, F; Guix, B; Henríquez, I; Martínez, A; Tello, JI, 2001)
"The current treatment of keloids is based on surgery, medical therapy and physical treatment."( Baroni, A; Brongo, S; D'Andrea, F; Ferraro, G, 2002)
"Successful treatment of keloids is difficult."( Bock, O; Mrowietz, U, 2002)
"Ten patients with previously untreated keloidal or hypertrophic median sternotomy scars at least 6 months after surgery that were considered problematic by the patients."( Fitzpatrick, RE; Manuskiatti, W, 2002)
"We have treated 41 keloides of earlobes in 28 cases, and analyzed the factors."( Li, B; Liu, D; Tian, J; Zhou, C, 1999)
"Participants (n = 80) were treated for 80 keloid scars (59 percent female patients, 76 percent nonwhite), and 44 percent of keloids were located on earlobes."( Cornes, PG; Glees, JP; Moss, AL; Ragoowansi, R, 2003)
"Fibroblasts were cultured from nontreated earlobe keloids and burn hypertrophic scars."( Bay, BH; Chan, SY; Lee, ST; Phan, TT; Sun, L, 2003)
"We investigated whether PDL treatments induced keloid regression by decreasing growth factor-beta(1) (TGF-beta(1)) induction, thereby reducing fibroblast proliferation and collagen deposition."( Chang, PR; Chen, TH; Huang, HC; Jeng, SF; Kuo, YR; Wang, FS; Yang, KD, 2004)
"Twelve months after final PDL treatments, keloid regression ( >/= 50%) had occurred in 26/30 patients in whom erythema and surface irregularities had been reduced and pliability had been increased."( Chang, PR; Chen, TH; Huang, HC; Jeng, SF; Kuo, YR; Wang, FS; Yang, KD, 2004)
"By use of integrated methods to treat keloid, if the wound can be sutured directly, skin grafting should not be adopted."( Cen, Y; Cui, ZJ; Liu, XX, 2004)
"Biopsies from ten untreated keloids (duration of disease 3 - 30 years) and ten hypertrophic scars (duration of disease 6 - 10 months) and five normal adult skin specimens."( Han, CM; He, XJ; Peng, JP, 2004)
"As no specific effective treatment for keloid is currently available, utilization of this readily available therapeutic agent may improve treatment outcome."( Kronenberg, J; Orenstein, A; Talmi, YP; Wolf, M, 2005)
"Given the difficulty and cost of treating keloids, prevention remains the best approach."( Davis, LS; Lane, JE; Waller, JL, 2005)
"Between 1985 and 2003, we treated 109 keloid scars in 94 patients by injecting 1 to 10?mg of triamcinolone acetonide depending on the size of the lesion at four week intervals."( Hata, Y; Igawa, HH; Ito, O; Muneuchi, G; Onodera, M; Suzuki, S, 2006)
"This pilot study suggests that treatment of keloid and hypertrophic scars with intra-lesional injections of collagenase is ineffective."( Gault, D; Kang, N; Nduka, C; Sanders, R; Sivakumar, B, 2006)
"Several options are described to treat keloid scars, none of them being 100% successful."( Boeckx, WD; De Lorenzi, F; Lutgens, LC; Nieman, FH; Rhemrev, R; Tielemans, HJ; van der Hulst, RR, 2007)
"This new treatment of keloids has been shown to be effective in the majority of patients but further studies are required to confirm this benefit."( Bailey, JN; Clayton, WJ; Rustin, MH; Waite, AE, 2007)
"In all the treated keloids, the defect healed in 6-8 weeks, and no recurrence was seen while on imiquimod application; however, all keloids completely recurred within 4 weeks of stopping imiquimod."( Gupta, S; Khaitan, BK; Malhotra, AK; Sharma, VK, 2007)
"The basic treatment of keloids changed, radiotherapy was combined with the above mentioned methods because of its high recurrence rate."( Kelemen, O; Kollár, L, 2007)
"Ten of the treated keloids recurred (28."( Chuangsuwanich, A; Gunjittisomram, S, 2007)
"The primary protocol presented for the treatment of ear keloids produces durable results, with an acceptably low recurrence rate."( Freeman, K; Patel, MK; Rosen, DJ; Weiss, PR, 2007)
"The authors present their experience of treating earlobe keloids using the "sandwich" technique protocol; extralesional excision and external-beam radiotherapy are given a day before and a day after the operation."( Amir, A; Barnea, Y; Ben-Yosef, R; Gur, E; Leshem, D; Miller, E; Shafir, R; Stahl, S; Weiss, J; Zaretski, A, 2010)
"A deep core biopsy of the treated keloid performed three months following the last electrochemotherapy session showed no evidence of chronic lymphocytic leukaemia."( Allison, KP; Muir, T; Sainsbury, DC, 2010)
"In both treatment groups, keloids responded well without any major side effect."( Dastgheib, L; Emad, M; Ghaem, H; Mortazavi, A; Omidvari, S, 2010)
"A silicone gel sheet is effective for treating keloid scars following median sternotomy."( Akahoshi, T; Miyasaka, Y; Sakuraba, M; Suzuki, K; Takahashi, N, 2010)
"Successful treatment of keloids remains a challenge because this disease process has a high propensity for recurrence."( Gupta, M; Narang, T, 2011)
"We have treated keloids using a combination of surgical excision and postoperative irradiation."( Ishiko, T; Muneuchi, G; Naitoh, M; Suzuki, S; Yamawaki, S, 2011)
"The authors treated 58 chest keloid patients with surgical excision followed by intraoperative and postoperative intralesional steroid injection."( Chang, CH; Kim, JK; Park, TH; Seo, SW, 2011)
"Of course, the best treatment for keloids remains prevention."( Berman, B; Caperton, CV; Viera, MH, 2011)
"Currently, there is no gold standard treatment for keloids and hypertrophic scars (HTS)."( Seo, SH; Sung, HW, 2012)
"Patients with a history of previous treatment and keloids in the perioral region should be monitored closely for signs of recurrence and managed cautiously during treatment."( Chang, CH; Kim, JK; Park, TH; Seo, SW, 2012)
"The authors treated 1436 ear keloids in 883 patients with surgical excision followed by pressure therapy using magnets at Kangbuk Samsung Hospital over the 7."( Chang, CH; Kim, JK; Park, TH; Seo, SW, 2011)
"An established treatment for keloids is surgery and radiotherapy, using a single applied field."( Barber, E; Collis, CH; Eaton, DJ; Ferguson, L; Mark Simpson, G, 2012)
"Pulsed dye laser treatment of keloids significantly down-regulates the expression of CTGF in most cases."( Avram, MM; Guan, M; Huang, G; Lu, Z; Ma, Y; Yang, Q; Zhu, R, 2012)
"The percentage of after-treatment keloids and hypertrophic scars observed was very low (~1%) especially upon the usage of lower parameters."( Arunachalam, M; Bassi, A; Bonan, P; Bruscino, N; Campolmi, P; Cannarozzo, G; Lotti, T; Moretti, S; Troiano, M, 2012)
"There are no set guidelines for the treatment of keloids and the most common treatments are individualized and depended on the distribution, size, thickness, and consistency of lesions."( Accardo, M; Brongo, S; Cataldo, C; D'Andrea, F; De Francesco, F; Ferraro, GA; Grella, R; Mele, CM; Nicoletti, G, 2013)
"Evaluation of perioperative treatment of keloid scars with electron beam therapy or iridium 192 low dose rate brachytherapy."( Autret, D; Cellier, P; Fernandez, L; Jadaud, E; Krhili, S; Mahé, MA; Mesgouez-Nebout, N; Paumier, A; Poirier, AL; Rio, E; Tuchais, C; Vinchon-Petit, S; Yossi, S, 2013)
"To determine the main treatments used for keloids in the United States and demographics of patient visits for keloids."( Davis, SA; Feldman, SR; McMichael, AJ, 2013)
"At present, to treat or prevent keloids, new drugs are currently being designed and the pharmaceutical indications of known drugs are being expanded."( Huang, C; Ogawa, R, 2013)
"Numerous modalities have been used to treat keloids and hypertrophic scars; however, optimal treatment has not yet been established."( Kwon, SY; Park, K; Park, SD, 2014)
"In the prevention and treatment of keloids and hypertrophic scars, ointments containing heparin and onion extract are very popular."( Krauze-Baranowska, M; Pikuła, M; Pobłocka-Olech, L; Sznitowska, M; Trzonkowski, P; Żebrowska, ME, 2014)
"All patients referred for treatment of an ear keloid and undergoing subsequent surgical excision followed by immediate freezing of the postoperative wound using cryosurgery were included."( Boullie, MC; De Barros, A; Dehesdin, D; Joly, P; Litrowski, N, 2014)
"On Days 3, 6, and 9 treated keloid cells showed linear decreases in cell proliferation (BrdU), increases in Annexin V-FITC and TUNEL-positive cells, interruptions of the cell cycle and inhibition of migration in scratch-wound assays."( Biswas, A; Bongso, A; Choolani, M; Fong, CY; Srinivasan, A; Subramanian, A, 2014)
"The WJ-MSC-CM-treated keloid fibroblasts showed higher proliferation rates than their control keloid fibroblasts with no significant change in apoptosis rate or migration ability."( Al-Shehab, M; Amini-Nik, S; Arno, AI; Belo, C; Blit, PH; Herer, E; Jeschke, MG, 2014)
"Although there was a report about treating keloid with topical captopril, the further investigation about captopril affecting keloid has not been performed so far."( Cen, Y; Chen, J; Liu, Y; Nicolas, C; Zhao, S, 2016)
"A variety of therapeutic procedures for treating keloids have been previously reported, with varying success and recurrence rates."( Babic, D; Dunda, S; Eppstein, RJ; Har-Shai, Y; Pallua, N; Stromps, JP, 2014)
"Finally, additional treatment of keloid scars previously unresponsive to IL cryotherapy is predisposed to a high recurrence rate."( Bulstra, AE; Niessen, FB; van Leeuwen, MC; van Leeuwen, PA, 2014)
"Cryosurgery is a safe and effective treatment of keloids."( Abdel-Meguid, AM; Awad, SM; Refaiy, AE; Sayed, DS; Weshahy, AH, 2015)
"Intralesional cryotherapy is a novel treatment for keloid scars in which the scar is frozen from inside."( Bulstra, AJ; Galindo-Garre, F; Molier, J; Niessen, FB; van der Wal, MBA; van Leeuwen, MCE; van Leeuwen, PAM; van Zuijlen, PPM, 2015)
"Intralesional cryotherapy for the treatment of keloid scars shows favorable results in terms of reduction of volume and complaints of pain and pruritus."( Bulstra, AJ; Galindo-Garre, F; Molier, J; Niessen, FB; van der Wal, MBA; van Leeuwen, MCE; van Leeuwen, PAM; van Zuijlen, PPM, 2015)
"Glucocorticoids (GCs) are first-line treatment for keloid disease (KD) but are limited by high incidence of resistance, recurrence and undesirable side-effects."( Bayat, A; Matthews, LC; McGrouther, DA; Ray, DW; Rutkowski, D; Syed, F; Watson, RE, 2015)
"The untreated cultured keloid fibroblasts served as controls."( Avram, MM; Guan, M; Huang, G; Lu, Z; Ma, Y; Yang, Q; Yue, B; Zhu, R, 2015)
"Radiation therapy is considered to be a treatment for keloid scarring; however, radioresistance has been shown to be a serious impediment to treatment efficacy."( Long, F; Long, X; Si, L; Wang, X; Yang, B; Zhang, F, 2016)
"None of therapeutic options for the treatment of keloids has been found completely effective and satisfactory."( Abdel Hay, RM; El Hawary, MS; Nour-Edin, F; Sayed, K; Weshay, AH, 2015)
"The authors successfully treated pediatric keloids selecting proper regimen according to anatomic locations."( Chang, CH; Park, TH, 2015)
"The 17-AAG-treated keloid fibroblasts showed significantly decreased proliferation, promotion of apoptosis, and decreased expression of Akt."( Lee, MH; Lee, WJ; Lew, DH; Park, JC; Rah, DK; Yun, IS, 2015)
"Effective treatment of keloid scars is important because patients are often confronted with major cosmetic, psychological, and social consequences."( Colla, C; Erends, M; Piatkowski de Grzymala, AA; Van den Kerckhove, E; van der Aa, T; van der Hulst, RR; Verhiel, SH, 2015)
"In addition, in 17-AAG-treated keloid spheroids, the collagen deposition and expression of major extracellular matrix proteins were investigated by means of Masson trichrome staining and immunohistochemistry."( Ahn, HM; Kim, YO; Lee, JH; Lee, WJ; Lew, DH; Song, SY; Yun, CO, 2015)
"Currently, the treatment of keloids remains a challenge for high recurrence rates."( Boccia, L; De Felice, B; Guida, M; Nacca, M, 2015)
"PDL and long-pulsed Nd:YAG laser treatments for keloid and hypertrophic scar provide significant improvement with insignificant difference between both modalities."( Al-Mohamady, Ael-S; Ibrahim, SM; Muhammad, MM, 2016)
"Twenty-one patients with 61 untreated keloids were enrolled into this study."( Chen, B; Jia, Y; Liu, Q; Long, X; Wang, X; Wang, Y; Yu, N, 2016)
"Five patients underwent treatment; two had keloids involving the superior helix of the ear (average area, 2."( Bastidas, N; Kasabian, AK; Nguyen, KT; Shikowitz, L, 2016)
"Sorafenib is a promising agent for the treatment of keloids and hypertrophic scars."( Chen, YL; Ding, X; Gao, Z; Gu, T; Liu, W; Qu, M; Wang, W; Wu, X; Xu, L; Zhang, W, 2016)
"It is difficult to find an ideal treatment for keloids in this area due to the limit of local soft tissues and higher recurrence rate."( Long, X; Wang, X; Wang, Y; Zhang, M; Zhao, R, 2016)
"The color of 33 untreated keloids from 30 patients was measured with a narrow-band reflectance colorimeter."( Akaishi, S; Aoki, M; Dohi, T; Hyakusoku, H; Nakao, J; Ogawa, R, 2016)
"Hence, it may be used as an alternative treatment for keloid particularly in patients with low pain threshold, needle phobia and those who prefers home-based treatment."( Imran, FH; Ismail, R; Jamil, A; Nor, NM; Shah, SA, 2017)
"After treatment, the mean keloid VSS score was decreased on both sides (4."( Chun, JY; Lee, JH; Park, JH, 2017)
"Impact statement Effective treatment of keloid that is a commonly recurrent dermatosis is very difficult, even after standard treatment."( Alencar, AP; da Silva, BB; Filho, LL; Soares-Lopes, IM; Soares-Lopes, LR, 2017)
"The radioactive patch treatment of keloids is noninvasive, painless and safe with prolonged outcome."( Bhusari, P; Chhabra, A; De, D; Handa, S; Kumar, M; Kumaran, S; Mittal, BR; Palarwar, K; Rathore, Y; Shukla, J; Vatsa, R, 2017)
"Patient cohorts from 3 centers treated with keloid excision followed by 2 × 9 Gy, 3 × 6 Gy, or 2 × 6 Gy high-dose-rate brachytherapy were retrospectively compared regarding recurrence (after at least 12 months' follow-up) and complications (after at least 1 month's follow-up), using logistic regression analyses."( Bijlard, E; Dehnad, H; Harmeling, JX; Meijer, OWM; Mureau, MAM; Niessen, FB; Verduijn, GM, 2018)
"Effective treatment of keloids is challenging because the recurrence rate after surgical excision is high."( Gold, DA; Jacobsen, G; Jones, LR; Ozog, DM; Sheinin, R, 2018)
"After conventional treatments, keloid scars show varying degrees of recurrence."( Ezzedine, K; Hermeziu, O; Hersant, B; Meningaud, JP; Picard, F; Rodriguez, AM; SidAhmed-Mezi, M, 2018)
"Previous treatments for keloids include surgery, drugs, lasers and so on."( Guo, QG; Yao, M, 2018)
"First-line treatment of formed keloids involves topical or intralesional steroids."( Bakhshaeekia, A; Feily, A; Gianfaldoni, S; Hadibarhaghtalab, M; Lange, CS; Lotti, T; Matta, J; Pazyar, N; Ramirez-Fort, MK; Ramirez-Pacheco, LA; Rasaii, S; Seifi, V; Sohrabian, N, 2019)
"The OSI-027 treatment of keloid keratinocytes showed more effectively inhibited cell proliferation and migration compared to the mTORC1 inhibitor, rapamycin."( Chen, J; Liu, K; Liu, Y; Wang, X; Zhang, Z, 2019)
"One of the first-line options to treat keloid scars is corticosteroid injection after excision of the existing scar."( Chua, SC; Gidaszewski, B; Khajehei, M, 2019)
"Current understanding of steroid treatments for keloids is in regards to modulation of inflammation, proliferation, and apoptosis, with no in vivo study on the latter."( Chen, AD; Chen, RF; Huang, YT; Kuo, YR; Lai, CS; Li, YT; Lin, SD, 2019)
"However, the clinical treatment of keloid, such as drug injection treatment, surgical resection, cryotherapy, laser treatment and other therapeutic effects are poor."( Hu, Z; Lu, X; Pan, B; Sun, P, 2021)
"Stiffness in post-treated keloids and normal skins was significantly different (P < 0."( Cheng, S; Guo, RQ; Huang, SY; Qiu, L; Wang, LY; Xiang, X, 2020)
"We used microneedles to treat keloid because this method has the feasibility of self-administration without pain."( Kim, YC; Park, J, 2021)
"Concerning the treatment of keloids and hypertrophic scars, even though verapamil was safer than TAC, TAC worked faster than verapamil."( Deng, Z; Liu, L; Liu, R; Yang, B; Zhao, X, 2020)
"IL verapamil is effective in the treatment of keloids which is possibly attributed to suppression of MMP9 and VEGF."( Abou-Taleb, DAE; Badary, DM, 2021)
"After treatment, the mean keloid VSS of the injection side became 2."( Abd El-Dayem, DH; Elsaie, ML; Hanafy, NS; Nada, HA, 2021)
"A total of 59 patients with 110 untreated keloids on the anterior chest were enrolled in this study."( Chen, C; Long, X; Wang, X; Wang, Y; Yu, N; Zhang, M; Zhang, W, 2021)
"All patients treated for keloids at the authors' institution were included."( Breton, P; Daurade, M; Ibrahim, B; Lorchel, F; Rouard, N; Sigaux, N, 2020)
"Cryotherapy is used to treat keloid scars; however, the molecular and pathological mechanisms are not clearly understood."( Kim, J; Kim, SM; Lee, JH; Lee, WJ; Lee, YI; Song, SY, 2020)
"There are numerous strategies to treat keloid."( Kamalasanan, K; Kumar, AS, 2021)
"Autophagy induction by rapamycin treatment in keloid fibroblasts effectively suppressed expression levels of Notch1 and NLRP3 inflammasome proteins."( Kang, H; Kim, JE; Kim, SK; Lee, DG; Lee, KJ; Lee, S; Lee, YJ; Park, H; Park, SH, 2020)
"Recently, successful treatment of keloids has been reported using the Nd:YAG laser in conjunction with 5-fluorouracil and intralesional corticosteroids."( Bakus, AD; Garden, BC; Garden, JM; Jones, VA; Lai, O; Patel, PM, 2021)
"The successful treatment of keloids is a great challenge in the plastic surgery field."( Chen, ZY; Liu, XM; Wang, XM; Wang, Y, 2021)
"At present, the consensus on the best treatment for keloids is the combination of clinical and surgical therapies, if necessary, associated with adjuvant radiotherapy like brachytherapy."( Wang, T; Wen, P; Wu, C; Yu, Y; Zhou, Y, 2021)
"There are few means to treat large keloid scars, as exeresis-even if partial-impedes direct closure without tension in the absence of a flap or a skin graft."( Azoulay, L; Boccara, D; Chaouat, M; Chatelain, S; Mimoun, M; Serror, K, 2021)
"A retrospective study of patients treated for keloid scars by using the new therapeutic protocol."( Azoulay, L; Boccara, D; Chaouat, M; Chatelain, S; Mimoun, M; Serror, K, 2021)
"Although clinical case studies for the treatment of keloid or hypertrophic scars are limited, it is necessary and helpful to understand the effectiveness of corticosteroid combined with botulinum toxin type A in the treatment of keloid or hypertrophic scars."( Liu, XG; Zhang, D, 2021)
"Despite numerous existing treatments for keloids, the responses in the clinic have been disappointing, due to either low efficacy or side effects."( Chen, LM; Feng, HC; Friedrich, RE; Fu, LL; Gosau, M; Nada, OA; Smeets, R; Yan, M, 2021)
"Kynurenine shows promise as a topical treatment for keloids and hypertrophic scars."( Arnold, D; Berman, B; Fischer, DL; Gade, A; Han, H; Lawson, A; Nestor, MS, 2021)
"Coupled with few effective treatments in keloid at present, we have focused on the immunological mechanisms of keloids with an aim to unravel some new therapeutic approaches in the future."( Fu, S; Ogawa, R; Wu, H; Yu, Y; Zhang, Q, 2021)
"Of the 40 patients for a total of 41 treated keloids in the first group, 85."( Bovani, B; Clementoni, MT; Conforti, C; Crisman, G; Gennai, A; Melfa, F; Piccolo, D, 2022)
"Cryosurgery, the most common treatment for keloids, causes skin traumas."( Ioannou, E; Karalis, V; Kikionis, S; Koromvoki, M; Kyritsi, A; Panagiotopoulos, A; Polichronaki, E; Rallis, M; Roussis, V; Stratigos, A; Tagka, A; Vitsos, A, 2022)
"Six patients with recurred keloid were treated with keloid surgery and radiotherapy for the second time."( Hao, Y; Li, W; Liu, H; Qiu, J; Shan, M; Wang, Y, 2022)
"Many methods have been used for the treatment of keloids and hypertrophic scars, there is no standardized method so far."( Li, X; Zhang, W, 2023)
"Concerning the treatment of keloids and hypertrophic scars, TAC was more effective than verapamil for improving vascularity; TAC was superior to verapamil in improving height within 9 weeks of treatment; TAC produced superior result for improving pliability within 18 weeks of treatment, whereas verapamil produced superior result between 18 and 24 weeks of treatment."( Li, X; Zhang, W, 2023)
"A standardized and sequential treatment plan for keloids with different morphology and anatomical locations can achieve remodeling of the auricular morphology and maintain long-term results."( Dong, G; Hu, J; Jin, Q; Liu, Y; Qu, C; Wang, L; Wang, M; Wu, H, 2023)
"Standard treatment for keloids includes combination intralesional therapy with triamcinolone and fluorouracil."( Frazier, WT; Proddutur, S; Swope, K, 2023)
"Intralesional treatments for keloid and hypertrophic scars may be the most reliable treatment option to improve pathologic scars, while laser treatment may have specific benefits for Fitzpatrick skin types I-III over types IV-VI."( Alam, M; Anvery, N; Asadbeigi, SN; Christensen, RE; Dirr, MA; Hisham, FI; Ibrahim, SA; Jain-Poster, K; Kang, BY; Kim, K; Merkel, EA; Poon, E; Reynolds, KA; Worley, B, 2023)
"In addition, dasatinib-treated keloid fibroblasts conditioned medium reduced procollagen and p16 expression in cultured keloid fibroblasts."( Chung, JH; Darmawan, CC; Hur, K; Kusumaningrum, N; Lee, SH; Mun, JH, 2023)
"(2) After drug injection treatment, the keloid began to shrink, some of the keloids disappeared."( Luo, QF, 2023)
"First-line treatment of keloids consists of intralesional needle injections with corticosteroids, but generally entails multiple painful sessions, resulting in variable clinical outcomes."( Bik, L; Elmzoon, I; Prens, EP; van Doorn, MBA; Wolkerstorfer, A, 2023)
"Among 56 treated keloids, 89."( Alessandro, G; Bruno, B; Claudio, C; Daniele, B; Domenico, P; Fabrizio, M; Giuliana, C; Matteo, TC, 2023)
"Dermatologists may want to consider treating keloids that cover a large area with systemic dupilumab, a therapy with an established, reassuring safety profile."( Cobos, G; LaChance, AH; Lee, MS; Mazori, DR; Merola, JF; Min, MS; Vleugels, RA, 2023)

Research

Studies (3,808)

TimeframeStudies, This Condition (%)All Conditions %
pre-1990921 (24.19)23.3326
1990's397 (10.43)12.5806
2000's728 (19.12)18.1394
2010's1097 (28.81)28.8240
2020's665 (17.46)9.53
DrugIndicatedRelationship StrengthStudiesTrials
dinitrochlorobenzene0low20
aminolevulinic acid0low100
allantoin0medium103
ammonium hydroxide0low10
betaine0low10
citric acid, anhydrous0low10
hydrochloric acid0low10
salicylic acid0low160
phloroglucinol0low10
gallic acid0low10
cytosine0low10
lactic acid0low50
dimethyl sulfoxide0medium41
glycine0low10
glycerol0low10
glycolic acid0medium21
hydrogen cyanide0low10
dalteparin0low10
histamine0low40
methanol0low10
nickel0medium41
niacinamide0low10
niacin0low10
phenol0low10
phosphorylcholine0low20
putrescine0medium11
urea0low20
aminopropionitrile0low20
phenytoin0low10
aspirin0low10
azathioprine0low10
bupivacaine0low20
busulfan0low10
verapamil0medium338
chloroquine0low20
chlorpyrifos0low10
clioquinol0low10
clofazimine0low10
dapsone0low10
deferoxamine0low20
eflornithine0low10
diphenyleneiodonium0low10
fluorouracil0medium8520
miltefosine0low10
hydroxychloroquine0low10
ibuprofen0low10
lidocaine0medium111
indomethacin0low10
1-methyl-3-isobutylxanthine0low10
2-propanol0low20
khellin0medium3,836170
losartan0medium11
2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one0low30
mechlorethamine0low10
metformin0low50
minoxidil0low10
mitoxantrone0low40
activins0low10
nicardipine0low10
niclosamide0low10
oxybutynin0medium41
pd 980590low40
pentoxifylline0low50
pheniramine0low10
prilocaine0low20
procaine0low10
propranolol0low10
protoporphyrin ix0low20
pyroxamide0low10
sevoflurane0low10
sulfamethoxypyridazine0low10
sulforaphane0low10
thalidomide0low10
troglitazone0low10
hydrocortisone acetate0low30
mitomycin0medium152
prednisolone0low80
thymidine0low30
hydroxyproline0low140
spironolactone0low10
aldosterone0low10
penicillamine0medium71
prednisone0medium41
estrone0low20
methylprednisolone acetate0low10
oxandrolone0low10
chloramphenicol0low10
glutamine0low10
lysine0low30
sucrose0low10
2,3,4,6-tetrachlorophenol0low10
bromodeoxyuridine0low10
carbostyril0low10
edetic acid0low20
tributyrin0low10
methylene blue0low10
colchicine0low80
cycloheximide0low10
ficusin0low10
fluocinolone acetonide0medium73
ampicillin0low10
mannitol0low10
histidine0low10
arginine0low20
ethane0low10
ethyl chloride0low10
isoprene0low30
methylprednisolone0low50
lawsone0low10
thymol0low10
benzoyl peroxide0low10
pyrroles0low20
framycetin0low40
pyrazolanthrone0low30
1,2-dihydroxybenzene-3,5-disulfonic acid disodium salt0low10
catechin0low30
perylene0low20
isoxazoles0low10
thiazoles0low20
perfluorodecalin0low10
dexamethasone 21-phosphate0low10
azacitidine0low30
betamethasone0medium91
alpha-aminopyridine0low10
cyanogen bromide0low10
oleanolic acid0low10
podophyllotoxin0low10
dihydrotestosterone0low10
malondialdehyde0low30
phenalen-1-one0low10
hematoporphyrin0low40
3-hydroxyflavone0low10
acetylcysteine0low10
durapatite0medium11
ferrous oxide0low10
glycyrrhizic acid0low20
d-alpha tocopherol0medium72
tocopherols0low10
flurandrenolone0low20
2,5-dichloro-4-bromophenol0low10
sabinene0low10
mannose0low10
dithiothreitol0low10
triamcinolone hexacetonide0medium11
enbucrilate0low10
octyl 2-cyanoacrylate0low30
iridium0low30
neodymium0medium61
neon0low20
rhenium0low10
silver0low10
titanium0low10
tungsten0low30
argon0medium72
cerium0low10
erbium0low10
gold0medium21
helium0low20
yttrium0medium51
hypochlorous acid0low10
camptothecin0medium21
zinc sulfate0low10
silver nitrate0low30
potassium dichromate0low10
galactose0low20
trolamine salicylate0low20
tiletamine hydrochloride0low20
daunorubicin0low20
phosphotyrosine0low10
phenyl acetate0low10
paclitaxel0low10
etoposide0low10
promegestone0low10
phorbol 12,13-dibutyrate0low10
propiconazole0low30
captopril0low20
colforsin0low20
simvastatin0low10
mifepristone0low10
itraconazole0low30
acridine orange0low10
isothiocyanic acid0low10
halofuginone0low20
dexamethasone 21-methanesulfonate0low10
thiazolyl blue0low10
thymine arabinoside0low10
epigallocatechin gallate0low30
betamethasone sodium phosphate0low10
tomatidine0low10
solanidine0low10
iridium radioisotopes0low110
2-methoxyestradiol0low10
pinocembrin0low10
fluorodeoxyglucose f180medium31
voriconazole0low10
10,11-methylenedioxy-20-camptothecin0low10
2-(methylamino)isobutyric acid0low20
adipostatin a0low10
clarithromycin0low10
diprotin a0low10
glucuronic acid0low10
diosgenin0low10
cobalt0low10
yttrium radioisotopes0low30
arginyl-glycyl-aspartic acid0low10
artesunic acid0low10
pyridinoline0low20
deoxypyridinoline0low10
asiaticoside0medium51
deoxyglucose0low10
tanshinone0low10
asiatic acid0low10
delta-hydroxylysylnorleucine0low10
imatinib mesylate0low10
5,5'-dihydroxylysylnorleucine0low10
diprofos0low10
methotrexate0low60
xylose0low10
proline0low110
methyl 5-aminolevulinate0low40
potassium titanylphosphate0low10
tetraphenylphosphonium0low10
histidinohydroxymerodesmosine0low10
angiotensin ii0low30
ropivacaine0low10
sb 2035800low20
organophosphonates0low20
cortisone0low130
2-(4-aminophenyl)benzothiazole0low10
pheophorbide a0low10
taurochenodeoxycholic acid0low10
n-acetylneuraminic acid0low10
fibrin0low40
elastin0low110
inositol 3-phosphate0medium61
iduronate0low10
griseofulvin0low10
eplerenone0low10
trichostatin a0low40
tretinoin0low150
arachidonic acid0low40
resveratrol0low10
retinol0low20
oleic acid0low10
tacrolimus0low40
ferric hydroxide0low10
cocaine0low10
eicosapentaenoic acid0low20
brivudine0low10
prostaglandin d20low10
diethylstilbestrol0low10
decitabine0low20
dactinomycin0low10
enkephalin, leucine0low10
shikonin0low10
bromochloroacetic acid0medium81
glycosides0medium31
isomethyleugenol0low10
squalene0low10
sesquiterpenes0low10
curcumin0low40
hypocrellin b0low10
allylthiourea0low10
thiourea0low10
tamoxifen0low40
u 01260low10
zinc oxide0low10
cobaltous chloride0low10
hydroxylysine0low10
cystine0low10
dasatinib0low10
ginsenosides0low20
blister0low10
alpha-chymotrypsin0low10
17-ketosteroids0low10
naphthoquinones0low20
cathepsin g0low10
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1h-imidazol-2-yl)benzamide0low30
sphingosine0low40
quercetin0low80
dinoprostone0low50
apigenin0low10
luteolin0low10
linoleic acid0low40
calcitriol0low20
alprostadil0low10
kaempferol0low10
9-deoxy-delta-9-prostaglandin d20low10
amphotericin b0low20
cucurbitacin i0low10
tranilast0low100
isotretinoin0low90
sphingosine 1-phosphate0low10
ceramide 1-phosphate0low10
cholesteryl oleate0low10
phenylephrine hydrochloride0medium71
sirolimus0low50
fenretinide0low10
clobetasol0medium11
lysophosphatidic acid0low20
su 112480low10
aluminum0low20
strontium0low10
gallium0low10
enalapril0low30
silicon0low20
strontium radioisotopes0medium81
cefotaxime0low10
selenocysteine0low10
radium0low80
beta-aminopropionitrile fumarate0low10
1-oleoyl-2-acetylglycerol0low10
involucrin0low10
tanespimycin0low20
pep0050low20
staurosporine0low20
midostaurin0low10
sincalide0low10
dehydroxymethylepoxyquinomicin0low10
psd 5020low10
ginsenoside rg30low10
tofacitinib0medium11
sr 113020low10
aluminum oxide0low10
jte 0130low10
oxadiazoles0low10
nystatin a10low10
vialinin a0low10
pf 5732280low10
ly21097610low10
palmitoylcarnitine0low10
calcimycin0low10
indocyanine green0low20
podophyllin0low10
palomid 5290low10
acid phosphatase0low30
curcumol0low10
hypocrellin a0low10
nad0low10
desmosine0low10
thymosin beta(4)0low10
tannins0low20
oligonucleotides0low10
endothelin-10low10
phosphatidylcholines0low10
(9R)-9-chloro-11,17-dihydroxy-17-(2-hydroxy-1-oxoethyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one0low10
chlorophyll a0low10
ku 00637940low10
sphingosine kinase0low10
chitosan0low40
15-deoxyprostaglandin j20low10
madecassoside0low10
oxymatrine0low20
incb-0184240medium11
piperidines0low20
thymosin0low10
interleukin-80low50
calcipotriene0low10
3-amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acid0low10
cudc-9070low10
ascorbic acid0low100
tetracycline0low10
salicylates0low10
metastat0low10
epidermal growth factor0low70
kaolinite0low10
transforming growth factor beta0medium1362
miravirsen0low10
hirudin0low10
cyclin d10low60
histidinohydroxylysinonorleucine0low10
oligomycins0low10
1 alpha,24-dihydroxyvitamin d30low10
hyaluronoglucosaminidase0medium212
vitamin b 120low10
cyclosporine0low20
silybin0low20
digitonin0low10
icg 0010low10
tomatine0low10
chondroitin sulfates0low80
exudates0low30
angiogenin0low10
acyclovir0low10
osi 0270low10
cyclic gmp0low30
guanine0low10
folic acid0medium21
allopurinol0low10
2,2'-(hydroxynitrosohydrazono)bis-ethanamine0low10
alcian blue0low10
eye0low10
metallothionein0low20
phosphorus radioisotopes0low10
leptin0low10
pyrimidinones0low10

Protein Targets (2,596)

ProteinPotency MeasurementsInhibition MeasurementsActivation MeasurementsDrugs
IDH1410041
chromobox protein homolog 1580058
geminin980098
Chain A, High-affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A0101
Chain A, cAMP-specific 3',5'-cyclic phosphodiesterase 4D0101
Chain A, Phosphodiesterase 9A0101
Chain A, JmjC domain-containing histone demethylation protein 3A250025
Chain A, Class I phosphodiesterase PDEB10101
Chain A, High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A0101
Chain A, cGMP-dependent 3',5'-cyclic phosphodiesterase0101
Chain A, cGMP-specific 3',5'-cyclic phosphodiesterase catalytic domain, Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha chimera0101
Chain A, cGMP-specific 3',5'-cyclic phosphodiesterase catalytic domain, Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha chimera0101
Chain A, High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A0101
Chain A, High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A0101
glp-1 receptor, partial300030
thyroid stimulating hormone receptor400040
estrogen-related nuclear receptor alpha970097
Phosphodiesterase 0202
mitogen-activated protein kinase 1370037
cytochrome P450 3A4 isoform 1490049
histone acetyltransferase KAT2A isoform 1370037
cGMP-dependent 3',5'-cyclic phosphodiesterase0303
Gamma-aminobutyric acid receptor subunit pi493254
Monocarboxylate transporter 40101
High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A0202
cGMP-specific 3',5'-cyclic phosphodiesterase0505
High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A0101
Renin0303
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A 0202
cAMP-specific 3',5'-cyclic phosphodiesterase 4D 0101
cAMP-specific 3',5'-cyclic phosphodiesterase 4C0101
cAMP-specific 3',5'-cyclic phosphodiesterase 4B0101
Gamma-aminobutyric acid receptor subunit beta-1493254
Gamma-aminobutyric acid receptor subunit delta493254
Gamma-aminobutyric acid receptor subunit gamma-2493254
Gamma-aminobutyric acid receptor subunit alpha-5493254
Gamma-aminobutyric acid receptor subunit alpha-3493254
Gamma-aminobutyric acid receptor subunit gamma-1494255
Gamma-aminobutyric acid receptor subunit alpha-2493254
Adenosine receptor A1110114
Gamma-aminobutyric acid receptor subunit alpha-4493254
Gamma-aminobutyric acid receptor subunit gamma-3493254
Adenosine receptor A30202
Adenosine receptor A2a012215
Adenosine receptor A2b0102
Adenosine receptor A2b0202
Gamma-aminobutyric acid receptor subunit alpha-6493254
Adenosine receptor A109112
Adenosine receptor A2a012115
Sodium-dependent serotonin transporter011012
Adenosine receptor A2a0101
Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha'0101
cAMP-specific 3',5'-cyclic phosphodiesterase 4A0101
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A0101
Gamma-aminobutyric acid receptor subunit alpha-1494255
Gamma-aminobutyric acid receptor subunit beta-3493254
Gamma-aminobutyric acid receptor subunit beta-2493254
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B0202
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B0101
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B0202
cAMP-specific 3',5'-cyclic phosphodiesterase 4B0506
cAMP-specific 3',5'-cyclic phosphodiesterase 4D0606
cGMP-inhibited 3',5'-cyclic phosphodiesterase B0404
Voltage-dependent L-type calcium channel subunit alpha-1C0909
High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A0202
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C0101
cGMP-inhibited 3',5'-cyclic phosphodiesterase A0505
Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C0202
Phosphodiesterase 0101
GABA theta subunit493254
Phosphodiesterase 0202
Gamma-aminobutyric acid receptor subunit epsilon493254
cAMP-specific 3',5'-cyclic phosphodiesterase 7B0101
phosphopantetheinyl transferase360036
regulator of G-protein signaling 4430043
Histone H2A.x400040
nuclear factor erythroid 2-related factor 2 isoform 1760076
Cellular tumor antigen p53800080
DNA topoisomerase 106215
Amyloid-beta precursor protein318123
72 kDa type IV collagenase0707
Matrix metalloproteinase-90404
Neutrophil collagenase0202
Collagenase 30404
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10101
Chain A, Proto-oncogene serine/threonine-protein kinase Pim-10101
Chain A, HADH2 protein400040
Chain B, HADH2 protein400040
Chain A, 2-oxoglutarate Oxygenase390039
Chain A, Cruzipain270027
Chain A, Methyltransferase Wbdd0101
thioredoxin reductase490049
15-lipoxygenase, partial270027
ATAD5 protein, partial490049
NFKB1 protein, partial170017
TDP1 protein10500105
Thrombopoietin170017
aldehyde dehydrogenase 1 family, member A1700070
hypoxia-inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)300030
EWS/FLI fusion protein550056
67.9K protein390039
Parkin200020
euchromatic histone-lysine N-methyltransferase 2900090
cytochrome P450 2D6 isoform 1210021
cellular tumor antigen p53 isoform a320032
cytochrome P450 2C19 precursor190019
cytochrome P450 2C9 precursor180018
flap endonuclease 1320032
serine/threonine-protein kinase mTOR isoform 1220022
survival motor neuron protein isoform d450045
M-phase phosphoprotein 8210021
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform06714
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha0101
Serine/threonine-protein kinase PLK4031114
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta0178
Polyunsaturated fatty acid lipoxygenase ALOX15B222024
Bromodomain-containing protein 40101
5-hydroxytryptamine receptor 4014014
Integrin beta-3264030
Cytochrome P450 1A2017119
Integrin alpha-IIb263029
Neuronal acetylcholine receptor subunit alpha-42406
Serine/threonine-protein kinase pim-1071119
Neuronal acetylcholine receptor subunit beta-22406
Casein kinase II subunit alpha'071017
Proteinase-activated receptor 10001
Bromodomain-containing protein 20101
Phosphatidylinositol 3-kinase regulatory subunit alpha0304
5-hydroxytryptamine receptor 2A013114
5-hydroxytryptamine receptor 2C015116
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform0101
Type-1 angiotensin II receptor0213
5-hydroxytryptamine receptor 2B023124
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform08817
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform 0101
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform06715
Serine/threonine-protein kinase mTOR09817
Serine/threonine-protein kinase mTOR0101
Histamine H2 receptor322135
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform 07715
Glycogen synthase kinase-3 beta0101020
D(1A) dopamine receptor110011
Serine/threonine-protein kinase PLK106915
Casein kinase II subunit beta0707
Casein kinase II subunit alpha08816
DNA-dependent protein kinase catalytic subunit0909
Mu-type opioid receptor0538
Serine-protein kinase ATM0202
Serine/threonine-protein kinase ATR0336
Bromodomain-containing protein 30101
Serine/threonine-protein kinase pim-30189
Phosphoinositide 3-kinase regulatory subunit 50101
Serine/threonine-protein kinase PLK304812
Serine/threonine-protein kinase PLK203710
ATP-dependent phosphofructokinase330033
Proton-coupled amino acid transporter 10505
Chain A, Beta-lactamase260026
GLS protein350035
PPM1D protein340034
glucocerebrosidase230023
lysosomal alpha-glucosidase preproprotein120012
interferon gamma precursor0004
nuclear factor erythroid 2-related factor 2 isoform 2370037
atrial natriuretic peptide receptor 2 precursor120012
urokinase-type plasminogen activator precursor280028
plasminogen precursor280028
urokinase plasminogen activator surface receptor precursor280028
DNA dC->dU-editing enzyme APOBEC-3G isoform 17108
lamin isoform A-delta10750075
Interferon beta650065
Tubulin alpha-1A chain0539
Tubulin beta chain0538
Sex hormone-binding globulin0167
Cytochrome P450 1A1013114
TAR DNA-binding protein 43231024
Cytochrome P450 1B1015116
Tubulin beta-2B chain0619
Similar to alpha-tubulin isoform 1 0518
Similar to alpha-tubulin isoform 1 0507
hypoxia-inducible factor 1 alpha subunit350035
RAR-related orphan receptor gamma730073
GLI family zinc finger 3880088
AR protein11400114
retinoic acid nuclear receptor alpha variant 1800080
retinoid X nuclear receptor alpha750075
estrogen nuclear receptor alpha12000120
peroxisome proliferator-activated receptor delta580058
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a680068
activating transcription factor 6440044
v-jun sarcoma virus 17 oncogene homolog (avian)370037
thyroid hormone receptor beta isoform a390039
heat shock protein beta-1400040
Voltage-dependent calcium channel gamma-2 subunit500050
Glutamate receptor 2510051
Luciferase400040
interleukin 8220022
estrogen receptor 2 (ER beta)540054
nuclear receptor subfamily 1, group I, member 3620062
progesterone receptor570057
glucocorticoid receptor [Homo sapiens]940094
farnesoid X nuclear receptor590059
pregnane X nuclear receptor660066
peroxisome proliferator activated receptor gamma640064
aryl hydrocarbon receptor470047
15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 1330033
thyroid hormone receptor beta isoform 2810081
Nuclear receptor ROR-gamma271129
Peroxisome proliferator-activated receptor alpha3015
ATPase family AAA domain-containing protein 5450045
Ataxin-2540054
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASE610061
USP1 protein, partial580058
Smad3260026
apical membrane antigen 1, AMA1170017
importin subunit beta-1 isoform 1170017
snurportin-1170017
GTP-binding nuclear protein Ran isoform 1110011
DNA polymerase eta isoform 1150015
DNA polymerase iota isoform a (long)440044
nuclear receptor ROR-gamma isoform 1400040
Carbonic anhydrase 12010013
Carbonic anhydrase 1022027
Carbonic anhydrase 2024232
ATP-dependent translocase ABCB1027749
Calmodulin-10213
Androgen receptor116629
Pyruvate kinase PKM0404
Polyunsaturated fatty acid lipoxygenase ALOX150303
Polyunsaturated fatty acid lipoxygenase ALOX120202
Xanthine dehydrogenase/oxidase013013
Fatty acid synthase0303
Carbonic anhydrase 9012116
Aurora kinase B091019
Dipeptidyl peptidase 30606
HSP40, subfamily A [Plasmodium falciparum 3D7]0004
Chain A, TYROSYL-DNA PHOSPHODIESTERASE370037
Chain A, TGF-beta receptor type-10101
tyrosine-protein kinase Yes150015
lethal factor (plasmid)320032
Serine/threonine-protein kinase 250088
Citron Rho-interacting kinase011011
Serine/threonine-protein kinase RIO30088
Serine/threonine-protein kinase Chk1021113
Aurora kinase A051116
Cyclin-G-associated kinase021113
Serine/threonine-protein kinase DCLK10088
Muscle, skeletal receptor tyrosine-protein kinase0088
3-phosphoinositide-dependent protein kinase 101910
Death-associated protein kinase 30099
Receptor-interacting serine/threonine-protein kinase 2041014
NUAK family SNF1-like kinase 102810
Tyrosine-protein kinase JAK2061119
Ribosomal protein S6 kinase alpha-5021113
Ribosomal protein S6 kinase alpha-4001010
Serine/threonine-protein kinase 16001111
Serine/threonine-protein kinase PAK 30088
Serine/threonine-protein kinase 17B0088
Serine/threonine-protein kinase 10001010
Serine/threonine-protein kinase D3021114
Cyclin-dependent kinase 140088
Mitogen-activated protein kinase kinase kinase kinase 4001010
Serine/threonine-protein kinase LATS1001010
Serine/threonine-protein kinase PAK 4021012
Tyrosine-protein kinase ABL10131429
Epidermal growth factor receptor0181028
RAF proto-oncogene serine/threonine-protein kinase07815
Receptor tyrosine-protein kinase erbB-208816
High affinity nerve growth factor receptor001010
Insulin receptor041014
Tyrosine-protein kinase Lck0101021
Tyrosine-protein kinase Fyn081018
Tyrosine-protein kinase Fes/Fps001010
Macrophage colony-stimulating factor 1 receptor05813
Tyrosine-protein kinase Yes041014
Tyrosine-protein kinase Lyn021012
Proto-oncogene tyrosine-protein kinase receptor Ret051015
Insulin-like growth factor 1 receptor021012
Hepatocyte growth factor receptor05914
Tyrosine-protein kinase HCK041014
Proto-oncogene tyrosine-protein kinase ROS0189
Platelet-derived growth factor receptor beta071017
Tyrosine-protein kinase Fgr0099
Mast/stem cell growth factor receptor Kit08917
Fibroblast growth factor receptor 1051015
Myosin light chain kinase, smooth muscle0077
Proto-oncogene tyrosine-protein kinase Src0111022
Insulin receptor-related protein0088
Serine/threonine-protein kinase B-raf071118
Phosphorylase b kinase gamma catalytic chain, liver/testis isoform001111
Platelet-derived growth factor receptor alpha06915
Tyrosine-protein kinase Fer001010
cAMP-dependent protein kinase catalytic subunit alpha031013
Vascular endothelial growth factor receptor 1 03811
Interferon-induced, double-stranded RNA-activated protein kinase0189
Cyclin-dependent kinase 11B0088
Ephrin type-A receptor 10099
Fibroblast growth factor receptor 20088
Fibroblast growth factor receptor 40088
Fibroblast growth factor receptor 30088
cAMP-dependent protein kinase catalytic subunit beta021012
Tyrosine-protein kinase JAK1051219
Protein kinase C eta type031014
Cyclin-dependent kinase 2061218
Activin receptor type-2A0088
Mitogen-activated protein kinase 3 011012
MAP/microtubule affinity-regulating kinase 3001010
Mitogen-activated protein kinase 1061016
Ephrin type-A receptor 2011011
Ephrin type-A receptor 30099
Ephrin type-A receptor 80088
Ephrin type-B receptor 2021012
Leukocyte tyrosine kinase receptor0088
Non-receptor tyrosine-protein kinase TYK2051219
Wee1-like protein kinase001010
Tyrosine-protein kinase receptor UFO02810
Mitogen-activated protein kinase 40088
RAC-alpha serine/threonine-protein kinase081018
RAC-beta serine/threonine-protein kinase011011
Dual specificity protein kinase TTK011011
Tyrosine-protein kinase receptor Tie-10088
Vascular endothelial growth factor receptor 303811
Vascular endothelial growth factor receptor 209919
Dual specificity mitogen-activated protein kinase kinase 2031013
Receptor-type tyrosine-protein kinase FLT30111022
Bone morphogenetic protein receptor type-1A001010
Activin receptor type-1B001010
TGF-beta receptor type-1041115
Serine/threonine-protein kinase receptor R30099
TGF-beta receptor type-2021012
Tyrosine-protein kinase CSK031013
Tyrosine-protein kinase Tec021012
Tyrosine-protein kinase TXK02810
Tyrosine-protein kinase ABL2011011
Tyrosine-protein kinase FRK001010
Tyrosine-protein kinase ZAP-700088
Tyrosine-protein kinase SYK051318
Mitogen-activated protein kinase 8031114
Mitogen-activated protein kinase 9021113
Dual specificity mitogen-activated protein kinase kinase 40189
Dual specificity mitogen-activated protein kinase kinase 3001010
Casein kinase I isoform delta011011
MAP kinase-activated protein kinase 2021012
Cyclin-dependent kinase 80189
Casein kinase I isoform epsilon011112
Dual specificity protein kinase CLK1001010
Dual specificity protein kinase CLK2001111
Dual specificity protein kinase CLK30099
Glycogen synthase kinase-3 alpha041014
Cyclin-dependent kinase 7011011
Cyclin-dependent kinase 9001010
Tyrosine-protein kinase Blk02810
Ribosomal protein S6 kinase alpha-3031013
Cytoplasmic tyrosine-protein kinase BMX02810
cAMP-dependent protein kinase catalytic subunit PRKX0088
Serine/threonine-protein kinase Nek2021012
Tyrosine-protein kinase JAK306918
Dual specificity mitogen-activated protein kinase kinase 6001010
Death-associated protein kinase 106814
LIM domain kinase 1011011
LIM domain kinase 2011011
Mitogen-activated protein kinase 12031013
Mitogen-activated protein kinase 10081119
5'-AMP-activated protein kinase catalytic subunit alpha-201810
Ephrin type-B receptor 3001010
Ephrin type-A receptor 5001010
Ephrin type-B receptor 4031013
Ephrin type-B receptor 10088
Ephrin type-A receptor 4001010
Serine/threonine-protein kinase SIK102810
Tubulin alpha-1A chain0077
Phosphatidylinositol 5-phosphate 4-kinase type-2 beta0088
SRSF protein kinase 20088
Casein kinase I isoform gamma-2001010
Mitogen-activated protein kinase kinase kinase 90088
Inositol monophosphatase 1190019
Cyclin-dependent kinase 30099
Cyclin-dependent-like kinase 5 051015
Cyclin-dependent kinase 16001111
Cyclin-dependent kinase 170099
Protein kinase C epsilon type031014
Dual specificity mitogen-activated protein kinase kinase 1061016
Angiopoietin-1 receptor04913
Mitogen-activated protein kinase kinase kinase 100088
Protein kinase C theta type031216
Activin receptor type-1001010
Focal adhesion kinase 1041014
Protein kinase C delta type041217
Tyrosine-protein kinase BTK041014
Tyrosine-protein kinase receptor TYRO30088
Cyclin-dependent kinase 180099
Activated CDC42 kinase 1011011
Epithelial discoidin domain-containing receptor 1031013
Tyrosine-protein kinase ITK/TSK02810
Myotonin-protein kinase0189
Tyrosine-protein kinase Mer02911
Serine/threonine-protein kinase 4001111
5'-AMP-activated protein kinase catalytic subunit alpha-1011012
Serine/threonine-protein kinase PAK 102810
Mitogen-activated protein kinase 7001010
Serine/threonine-protein kinase PAK 2001010
Serine/threonine-protein kinase 3001010
cGMP-dependent protein kinase 20088
Non-receptor tyrosine-protein kinase TNK1001010
Receptor-interacting serine/threonine-protein kinase 10189
Calcium/calmodulin-dependent protein kinase type II subunit beta0189
Calcium/calmodulin-dependent protein kinase type II subunit gamma001010
Calcium/calmodulin-dependent protein kinase type II subunit delta001010
Activin receptor type-2B001010
Bone morphogenetic protein receptor type-2001010
Protein-tyrosine kinase 6011011
cGMP-dependent protein kinase 1 001010
Calcium/calmodulin-dependent protein kinase type 10099
Inhibitor of nuclear factor kappa-B kinase subunit epsilon001010
Protein-tyrosine kinase 2-beta011011
Maternal embryonic leucine zipper kinase001010
Serine/threonine-protein kinase D102912
Ribosomal protein S6 kinase alpha-20099
Ephrin type-A receptor 70099
Ribosomal protein S6 kinase alpha-1021012
Dual specificity testis-specific protein kinase 10099
Myosin light chain kinase, smooth muscle001010
Mitogen-activated protein kinase 11031114
Serine/threonine-protein kinase STK11001010
NT-3 growth factor receptor0088
Serine/threonine-protein kinase N1011011
Serine/threonine-protein kinase N2011011
Mitogen-activated protein kinase 140171330
Calcium/calmodulin-dependent protein kinase type IV001010
Mitogen-activated protein kinase kinase kinase 11001010
BDNF/NT-3 growth factors receptor0088
Mitogen-activated protein kinase 60088
Phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform0088
Discoidin domain-containing receptor 2041014
AP2-associated protein kinase 1031114
Serine/threonine-protein kinase TNNI3K0189
Serine/threonine-protein kinase MRCK alpha001010
Serine/threonine-protein kinase MRCK gamma001010
Serine/threonine-protein kinase Nek50088
Serine/threonine-protein kinase MARK2001111
Serine/threonine-protein kinase tousled-like 20088
Serine/threonine-protein kinase 32C0088
Myosin light chain kinase family member 40088
Calcium/calmodulin-dependent protein kinase type 1D0099
Mitogen-activated protein kinase kinase kinase kinase 3001010
MAP kinase-activated protein kinase 5031013
Serine/threonine-protein kinase BRSK20088
Serine/threonine-protein kinase DCLK20088
Calcium/calmodulin-dependent protein kinase kinase 10088
Casein kinase I isoform alpha-like0088
Myosin-IIIa0088
Ankyrin repeat and protein kinase domain-containing protein 10088
Atypical kinase COQ8A, mitochondrial001010
Mitogen-activated protein kinase 15001010
Serine/threonine-protein kinase Nek9001010
Serine/threonine-protein kinase BRSK10088
Serine/threonine-protein kinase Nek70088
Myosin-IIIb0088
Mitogen-activated protein kinase kinase kinase kinase 1001010
Atypical kinase COQ8B, mitochondrial0088
MAP/microtubule affinity-regulating kinase 4001010
Calcium/calmodulin-dependent protein kinase type 1G001010
Serine/threonine-protein kinase Nek1001010
Calcium/calmodulin-dependent protein kinase kinase 2001111
SRSF protein kinase 10088
Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase021012
Mitogen-activated protein kinase kinase kinase 5001010
Phosphatidylinositol 4-phosphate 5-kinase type-1 alpha0088
Serine/threonine-protein kinase RIO10088
MAP kinase-interacting serine/threonine-protein kinase 10189
Cyclin-dependent kinase 190189
Testis-specific serine/threonine-protein kinase 10088
Serine/threonine-protein kinase 330088
Serine/threonine-protein kinase D2001010
Serine/threonine-protein kinase DCLK30088
NUAK family SNF1-like kinase 20099
Serine/threonine-protein kinase SIK2011011
Myosin light chain kinase 2, skeletal/cardiac muscle0088
STE20-like serine/threonine-protein kinase 001111
Tyrosine-protein kinase Srms0088
Dual specificity protein kinase CLK4001111
MAP kinase-interacting serine/threonine-protein kinase 203912
Serine/threonine-protein kinase Nek60189
Casein kinase I isoform gamma-1001111
Serine/threonine-protein kinase PAK 60189
Serine/threonine-protein kinase LATS20088
Serine/threonine-protein kinase 360189
BMP-2-inducible protein kinase001111
Serine/threonine-protein kinase 32B0088
Mitogen-activated protein kinase kinase kinase 20001010
Serine/threonine-protein kinase MARK10088
Serine/threonine-protein kinase pim-2001010
Serine/threonine-protein kinase PAK 50189
Serine/threonine-protein kinase 26001010
eIF-2-alpha kinase GCN20088
Serine/threonine-protein kinase NLK011011
Serine/threonine-protein kinase 17A0099
Ephrin type-A receptor 60088
Death-associated protein kinase 20099
Ribosomal protein S6 kinase alpha-6001010
TRAF2 and NCK-interacting protein kinase011112
Serine/threonine-protein kinase tousled-like 10088
ALK tyrosine kinase receptor03811
Cyclin-dependent kinase 11A0088
Aurora kinase C0099
Calcium/calmodulin-dependent protein kinase type II subunit alpha0088
RAC-gamma serine/threonine-protein kinase011011
Serine/threonine-protein kinase 38-like0099
Dual specificity tyrosine-phosphorylation-regulated kinase 1B0099
Mitogen-activated protein kinase kinase kinase kinase 5001010
Serine/threonine-protein kinase MRCK beta001010
Interleukin-1 receptor-associated kinase 3001010
Serine/threonine-protein kinase 24001010
Casein kinase I isoform gamma-3001010
Mitogen-activated protein kinase kinase kinase 4001010
Chain A, Putative fructose-1,6-bisphosphate aldolase180018
acetylcholinesterase270027
Microtubule-associated protein tau540054
cytochrome P450 family 3 subfamily A polypeptide 4580058
G360036
cytochrome P450 2D6320032
thyroid stimulating hormone receptor340034
nuclear receptor subfamily 1, group I, member 2190019
vitamin D3 receptor isoform VDRA470047
histone deacetylase 9 isoform 3100010
DNA polymerase kappa isoform 1400040
peripheral myelin protein 22490049
HLA class I histocompatibility antigen, B alpha chain 360036
Inositol hexakisphosphate kinase 1360036
cytochrome P450 2C9, partial360036
Ubiquitin carboxyl-terminal hydrolase isozyme L30101
Chain A, ATP-DEPENDENT DNA HELICASE Q1190019
dopamine D1 receptor8008
pregnane X receptor200020
vitamin D (1,25- dihydroxyvitamin D3) receptor550055
arylsulfatase A290029
Bloom syndrome protein isoform 1350035
D(1A) dopamine receptor110011
muscarinic acetylcholine receptor M1190019
Histone deacetylase 3010114
Solute carrier family 22 member 60607
Histone deacetylase 409114
Guanine nucleotide-binding protein G170017
Histone deacetylase 1012318
Histone deacetylase 709012
Histone deacetylase 2011216
Polyamine deacetylase HDAC1009012
Histone deacetylase 11 09012
Histone deacetylase 8012015
Histone deacetylase 6012217
Histone deacetylase 909012
Histone deacetylase 5010013
Telomerase reverse transcriptase0303
Reverse transcriptase/RNaseH 0606
Chain E, Purine nucleoside phosphorylase0101
Chain A, Ferritin light chain360036
Thymidine kinase 0304
hemoglobin subunit beta8008
atrial natriuretic peptide receptor 1 precursor100010
ubiquitin carboxyl-terminal hydrolase 2 isoform a110011
Solute carrier family 22 member 1 07010
ATP-binding cassette sub-family C member 3051051
Multidrug resistance-associated protein 4052057
Bile salt export pump011012
Bile salt export pump073074
Purine nucleoside phosphorylase0303
Thymidine kinase, cytosolic0508
POU domain, class 2, transcription factor 20001
Cytochrome P450 2C9 028231
Cytochrome P450 2J20707
Disintegrin and metalloproteinase domain-containing protein 1792011
Purine nucleoside phosphorylase0022
Solute carrier family 22 member 60407
Thymidine kinase 0101
Solute carrier family 22 member 80408
Canalicular multispecific organic anion transporter 1051052
Thymidine kinase0304
Prostaglandin G/H synthase 1014217
Prostaglandin G/H synthase 2019929
Corticosteroid-binding globulin0606
Mineralocorticoid receptor 110518
Androgen receptor017119
Mineralocorticoid receptor0404
Solute carrier organic anion transporter family member 1A10205
RGS123003
Alpha-synuclein128121
transcriptional regulator ERG isoform 3120012
ras-related protein Rab-9A190019
Polyphenol oxidase 209012
Hypoxanthine-guanine phosphoribosyltransferase0002
Xanthine dehydrogenase/oxidase [Includes: Xanthine dehydrogenase 0101
Nuclear receptor ROR-gamma0101
Xanthine dehydrogenase/oxidase09113
Shiga toxin subunit A0202
Histamine H3 receptor0204
bromodomain adjacent to zinc finger domain 2B200020
parathyroid hormone/parathyroid hormone-related peptide receptor precursor190019
Heat shock protein HSP 90-alpha0336
Botulinum neurotoxin type A 0303
Neutrophil cytosol factor 10202
Nitric oxide synthase, endothelial0101
Nitric oxide synthase, brain0102
Nitric oxide synthase, brain 0102
Nitric oxide synthase, inducible0215
Kappa-type opioid receptor07210
Phosphatidylinositol 4-kinase alpha0101
Tyrosine-protein kinase 0011
Phosphatidylinositol 4-kinase type 2-beta0101
Phosphatidylinositol 4-kinase type 2-alpha0101
Phosphatidylinositol 4-kinase beta0178
Thromboxane-A synthase 0707
Prostaglandin E2 receptor EP3 subtype0303
Prostaglandin E2 receptor EP4 subtype0314
Prostaglandin E2 receptor EP1 subtype0303
Prostacyclin receptor0325
Nuclear receptor subfamily 4 group A member 20066
Solute carrier organic anion transporter family member 2A10104
Nuclear receptor subfamily 4 group A member 20011
Nuclear receptor subfamily 4 group A member 20011
Prostaglandin E2 receptor EP2 subtype0314
Solute carrier organic anion transporter family member 2A10104
Solute carrier organic anion transporter family member 2B10102
Solute carrier organic anion transporter family member 3A10001
Gamma-aminobutyric acid receptor subunit rho-10101
Glutamate receptor 10101
Glutamate receptor 20101
Glutamate receptor 30101
Glutamate receptor ionotropic, kainate 30101
Solute carrier family 15 member 10505
Glutamate receptor 40101
Solute carrier family 15 member 10404
Solute carrier family 15 member 20303
Lysyl oxidase homolog 20101
Protein-lysine 6-oxidase0101
Protein-lysine 6-oxidase0101
Lysyl oxidase homolog 20101
Lysyl oxidase homolog 30101
Lysyl oxidase homolog 40101
Lysyl oxidase homolog 20101
tumor necrosis factor2002
Cytochrome P450 3A4027232
Cytochrome P450 2D6011112
Cytochrome P450 2C19016117
Potassium voltage-gated channel subfamily H member 2024024
Broad substrate specificity ATP-binding cassette transporter ABCG2019224
Chain A, Mutant Al2 6e7p9g0011
Beta-lactamase 0002
acid sphingomyelinase8008
Beta-lactamase 0102
Beta-lactamase 0002
Metallo-beta-lactamase type 20114
Metallo-beta-lactamase VIM-11 0002
Metallo-beta-lactamase VIM-20002
Beta-lactamase 0002
Metallo-beta-lactamase0002
Beta-lactamase 0102
DNA polymerase beta170017
60 kDa heat shock protein, mitochondrial0909
Beta-lactamase OXA-70001
Spike glycoprotein392748
10 kDa heat shock protein, mitochondrial0909
Beta-lactamase 0002
Beta-lactamase 0002
Beta-lactamase 0002
Solute carrier family 15 member 20202
Thiosulfate sulfurtransferase0808
Metallo-beta-lactamase VIM-130103
Efflux transporter 0001
Beta-lactamase 0002
Beta-lactamase Toho-10002
Beta-lactamase 0001
Class D beta-lactamase0001
60 kDa chaperonin 0909
Metallo-beta-lactamase0002
Beta-lactamase 0002
Beta-lactamase 0001
10 kDa chaperonin 0909
Metallo-b-lactamase 0002
Carbapenem-hydrolyzing beta-lactamase KPC0002
Beta-lactamase class B VIM-2 0114
Beta-lactamase VIM-1 0103
Atrial natriuretic peptide receptor 30202
Type-1A angiotensin II receptor 0426
Type-1 angiotensin II receptor0011
Type-1B angiotensin II receptor0404
Type-1 angiotensin II receptor05411
Type-2 angiotensin II receptor0505
Type-2 angiotensin II receptor0303
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain A, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain B, (3R)-hydroxymyristoyl-acyl carrier protein dehydratase0202
Chain A, Transthyretin0033
Chain A, Transthyretin0033
Chain A, Transthyretin0033
Chain A, Transthyretin0033
Chain B, Transthyretin0033
Chain A, Transthyretin0033
Chain B, Transthyretin0033
Chain A, Casein kinase II subunit alpha0202
Chain A, Casein kinase II subunit alpha0202
Chain A, Casein Kinase Ii Subunit Alpha0202
endonuclease IV120012
BRCA16006
Neuraminidase 0909
pyruvate kinase8008
heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)180018
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_a320032
Replicase polyprotein 1ab04711
NPC intracellular cholesterol transporter 1 precursor160016
peripheral myelin protein 22 isoform 1250025
guanine nucleotide-binding protein G(i) subunit alpha-1 isoform 12002
glycogen synthase kinase-3 beta isoform 10044
peptidyl-prolyl cis-trans isomerase NIMA-interacting 1110011
pyruvate kinase PKM isoform b6006
neuropeptide S receptor isoform A140014
Gamma-aminobutyric acid receptor subunit pi0303
Gamma-aminobutyric acid receptor subunit delta0303
Aldo-keto reductase family 1 member B100606
G2/mitotic-specific cyclin-B20404
Poly [ADP-ribose] polymerase tankyrase-10202
Lysozyme C-10202
Cationic trypsin0404
Transthyretin0358
Estrogen receptor117727
Glucocorticoid receptor128647
Myeloperoxidase0606
Cyclin-dependent kinase 107815
Beta-glucuronidase0303
Aldo-keto reductase family 1 member B1016016
Seed linoleate 13S-lipoxygenase-107013
Neutrophil elastase0808
Ornithine decarboxylase6209
Poly [ADP-ribose] polymerase 10303
Replicase polyprotein 1a06713
Replicase polyprotein 1ab03710
Replicase polyprotein 1ab012820
Replicase polyprotein 1ab013821
Sialidase0505
Aromatase014015
Angiotensin-converting enzyme011012
Cystic fibrosis transmembrane conductance regulator0134
17-beta-hydroxysteroid dehydrogenase type 10506
G2/mitotic-specific cyclin-B10606
Gamma-aminobutyric acid receptor subunit alpha-10314
Urease subunit alpha0606
Aldo-keto reductase family 1 member B1012013
G2/mitotic-specific cyclin-B0404
Mucin-10101
Glycogen synthase kinase-3 beta0505
Gamma-aminobutyric acid receptor subunit beta-10303
Gamma-aminobutyric acid receptor subunit gamma-20314
Amine oxidase [flavin-containing] A010010
Acetylcholinesterase014014
Carbonic anhydrase 4012015
Amine oxidase [flavin-containing] B011011
Dipeptidyl peptidase 4011011
Proteasome subunit beta type-50808
Gamma-aminobutyric acid receptor subunit beta-30303
Substance-P receptor010010
Gamma-aminobutyric acid receptor subunit alpha-50303
Multidrug resistance-associated protein 1 09113
Gamma-aminobutyric acid receptor subunit alpha-30303
Mu-type opioid receptor09213
Testosterone 17-beta-dehydrogenase 30404
17-beta-hydroxysteroid dehydrogenase type 20505
Acetylcholinesterase0202
Peroxisome proliferator-activated receptor gamma0033
Delta-type opioid receptor010315
Kappa-type opioid receptor08212
Homeobox protein Nkx-2.5 0202
Gamma-aminobutyric acid receptor subunit alpha-20303
Gamma-aminobutyric acid receptor subunit beta-20314
Gamma-aminobutyric acid receptor subunit alpha-40303
Estrogen receptor0011
Beta-secretase 109010
Urease subunit beta0606
Gamma-aminobutyric acid receptor subunit epsilon0303
Lactoperoxidase0204
MO15-related protein kinase Pfmrk 0303
Cyclin-dependent kinase 605813
Cyclin homolog0404
Transcription factor GATA-4 0202
Cyclin-dependent kinase 5 activator 10404
Gamma-aminobutyric acid receptor subunit alpha-60303
Carbonic anhydrase 30606
Substance-K receptor0505
Integrase 010010
Gamma-aminobutyric acid receptor subunit gamma-10303
Casein kinase II subunit alpha 30606
Inositol polyphosphate multikinase0404
G2/mitotic-specific cyclin-B30404
Estrogen receptor beta114723
Enoyl-acyl-carrier protein reductase 0808
NACHT, LRR and PYD domains-containing protein 3 0202
Gamma-aminobutyric acid receptor subunit gamma-30303
Myocilin0011
Cyclin-dependent kinase 10404
Prenyltransferase homolog0003
Poly [ADP-ribose] polymerase tankyrase-20336
Carboxylic ester hydrolase 0203
NADPH oxidase 40404
Estrogen receptor beta0011
Inositol hexakisphosphate kinase 20404
Short transient receptor potential channel 50404
Gamma-aminobutyric acid receptor subunit theta0303
Sialidase-20606
2,3-bisphosphoglycerate-independent phosphoglycerate mutase3003
Chain A, ADIPOCYTE LIPID-BINDING PROTEIN0011
Chain A, SERUM ALBUMIN0022
Chain A, SERUM ALBUMIN0022
thioredoxin glutathione reductase150015
lethal(3)malignant brain tumor-like protein 1 isoform I4004
caspase-1 isoform alpha precursor8008
Fatty-acid amide hydrolase 10202
Prostaglandin G/H synthase 1 0709
Trypsin0404
Coagulation factor VII0707
60 kDa chaperonin0707
Tissue factor0909
Fatty acid-binding protein, adipocyte0516
Calmodulin 0012
Prostaglandin G/H synthase 2011012
Fatty acid-binding protein 50303
Fatty acid-binding protein 50011
Lanosterol 14-alpha demethylase0202
Solute carrier organic anion transporter family member 1B3016018
Cytosolic phospholipase A2 gamma0202
Transient receptor potential cation channel subfamily V member 20202
Solute carrier organic anion transporter family member 1B1017017
Chain E, LYSINE, ARGININE, ORNITHINE-BINDING PROTEIN0022
Chain E, LYSINE, ARGININE, ORNITHINE-BINDING PROTEIN0022
Chain E, LYSINE, ARGININE, ORNITHINE-BINDING PROTEIN0022
alpha-galactosidase9009
Nitric oxide synthase, endothelial0002
Nitric oxide synthase, inducible0506
Cationic amino acid transporter 30202
Integrin beta-10101
Integrin alpha-V 0202
Integrin alpha-50101
Integrin beta-50101
Chain A, Hyaluronidase, phage associated0101
Pancreatic alpha-amylase0202
Albumin0203
Urease0304
Prolyl 4-hydroxylase subunit alpha-10001
Tyrosinase0606
Alpha-2B adrenergic receptor010213
Hyaluronate lyase0101
Prolyl hydroxylase EGLN20012
Egl nine homolog 10012
Prolyl hydroxylase EGLN30012
Hypoxia-inducible factor 1-alpha inhibitor0102
Solute carrier family 23 member 10101
Glycogen phosphorylase, muscle form0303
Pancreatic alpha-amylase0305
Polyunsaturated fatty acid 5-lipoxygenase010010
Tyrosine-protein phosphatase non-receptor type 20202
Tyrosine-protein phosphatase non-receptor type 1010012
DNA repair protein RAD52 homolog0202
G-protein coupled bile acid receptor 10044
Chain A, Phospholipase A2 isoform 30011
GTP-binding protein (rab7)0011
ras protein, partial0011
hypothetical protein, conserved5005
Rac1 protein0011
cell division cycle 42 (GTP binding protein, 25kDa), partial0011
Prostaglandin-H2 D-isomerase0202
Prostaglandin G/H synthase 2 0304
Fatty acid-binding protein, liver0404
Glutathione hydrolase 1 proenzyme0101
Prostaglandin G/H synthase 1017017
Urotensin-2 receptor0101
4-aminobutyrate aminotransferase, mitochondrial0202
Ras-related protein Rab-2A0011
Rho-associated protein kinase 20303
Nicotinate phosphoribosyltransferase0303
Solute carrier family 22 member 200505
Solute carrier family 22 member 60505
Sigma non-opioid intracellular receptor 1013114
Sigma non-opioid intracellular receptor 10011
Fumarate hydratase260026
polyprotein260026
huntingtin isoform 2170017
Adenosine receptor A3014115
DNA (cytosine-5)-methyltransferase 10404
Multidrug and toxin extrusion protein 1010010
Histone-lysine N-methyltransferase EHMT20202
SMAD family member 2320032
SMAD family member 3320032
P537007
muscleblind-like protein 1 isoform 1190019
Protein-arginine deiminase type-40303
Chain A, Betaine ABC transporter permease and substrate binding protein0011
Chain A, Osmoprotection protein (ProX)0011
Chain A, Glycine betaine/carnitine/choline-binding protein0011
Chain A, Glycine betaine/carnitine/choline-binding protein0011
Chain A, Glycine betaine/carnitine/choline-binding protein0011
Chain A, Glycine betaine/carnitine/choline-binding protein0011
galanin receptor type 30101
Glycine receptor subunit alpha-1024024
Glycine receptor subunit beta024024
Glycine receptor subunit alpha-2024024
Glycine receptor subunit alpha-3024024
ORF730022
Myosin-2 heavy chain, non muscle0101
Myosin-2 heavy chain0101
Myosin IC heavy chain0101
Myosin-90101
Myosin-100156
Unconventional myosin-X0101
Myosin-70101
Unconventional myosin-Ib0101
Myosin-40101
Myosin-140101
Nonmuscle myosin heavy chain0101
Unconventional myosin-Va0101
Myosin heavy chain, non-muscle0101
Unconventional myosin-XV0101
Thymidine kinase0304
Nuclear hormone receptor family member daf-120011
oxysterols receptor LXR-beta isoform 10011
Thymidine phosphorylase0013
Thymidylate kinase0202
Thymidine kinase0002
Thymidylate kinase0303
Potassium channel subfamily K member 30303
Potassium channel subfamily K member 30101
Potassium channel subfamily K member 20112
Potassium channel subfamily K member 90101
ClpP4004
electroneutral potassium-chloride cotransporter KCC20011
TSHR protein3003
nonstructural protein 1140014
LacZ protein (plasmid)0011
XBP10101
serine-protein kinase ATM isoform a5005
hexokinase-4 isoform 14004
type-1 angiotensin II receptor0101
potassium voltage-gated channel subfamily H member 2 isoform d210021
glucokinase regulatory protein4004
serine/threonine-protein kinase PLK1100010
apelin receptor0202
heat shock protein HSP 90-alpha isoform 20206
DNA damage-inducible transcript 3 protein0101
Vpr7007
streptokinase A precursor0077
Rap guanine nucleotide exchange factor 3110011
heat shock protein 90, putative0004
Chain A, Vitamin D Nuclear Receptor0011
Vitamin D3 receptor0011
Vitamin D-binding protein0011
Vitamin D3 receptor0225
Vitamin D3 receptor0113
Retinoic acid receptor RXR-alpha0448
Vitamin D3 receptor0011
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial0011
Vitamin D3 receptor0112
Transporter0101
Vitamin D3 receptor A0022
DNA topoisomerase 0101
putative alpha-glucosidase1001
eukaryotic translation initiation factor 2-alpha kinase 3 isoform 1 precursor0011
relaxin receptor 1 isoform 13003
Type-2 restriction enzyme ScaI0101
Deoxyribonuclease-2-alpha0101
Tyrosyl-DNA phosphodiesterase 20101
Deoxyribonuclease-10101
Type-2 restriction enzyme PstI0101
Type-2 restriction enzyme EcoRI0101
Prothrombin0327
DNA ligase0202
Heterogeneous nuclear ribonucleoprotein A10022
DNA topoisomerase 2-alpha05720
Type-2 restriction enzyme BamHI0101
Somatostatin receptor type 10101
Somatostatin receptor type 20101
Somatostatin receptor type 40101
Somatostatin receptor type 30101
Somatostatin receptor type 50101
Type-2 restriction enzyme HindIII0101
Ribonuclease pancreatic0101
DNA topoisomerase 2-beta02919
DNA topoisomerase 10102
DNA topoisomerase 10101
DNA topoisomerase type IB small subunit 0011
Tyrosyl-DNA phosphodiesterase 10202
Chain A, angiotensin converting enzyme0101
Chain A, angiotensin converting enzyme0101
transient receptor potential cation channel subfamily V member 11001
Neprilysin0101
Neprilysin0202
Leukotriene A-4 hydrolase0415
EEF1AKMT4-ECE2 readthrough transcript protein0101
Angiotensin-converting enzyme 0819
Leukotriene A-4 hydrolase0101
Endothelin-converting enzyme 10101
Succinyl-diaminopimelate desuccinylase0404
Angiotensin-converting enzyme0314
Beta-lactamase TEM0101
Beta-lactamase 0304
Beta-lactamase 0303
Angiotensin-converting enzyme 2 04711
Chain A, serum paraoxonase0101
Carbonic anhydrase 30609
Carbonic anhydrase 6010013
Carbonic anhydrase 5A, mitochondrial08011
Carbonic anhydrase 7011014
Carbonic anhydrase 130305
Carbonic anhydrase 140609
Carbonic anhydrase 5B, mitochondrial08010
Arginase 0404
Pancreatic triacylglycerol lipase0505
Sucrase-isomaltase, intestinal0202
Melatonin receptor type 1A0011
Melatonin receptor type 1B0011
Dihydroorotate dehydrogenase 0202
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Metallo-beta-lactamase VIM-19 0001
Beta-lactamase 0001
Albumin0358
Beta-lactamase SHV-10001
Beta-lactamase SHV-10001
Beta-lactamase0001
B2 metallo-beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Metallo-beta-lactamase VIM-20001
Beta-lactamase 0001
Solute carrier family 22 member 70104
Beta-lactamase 0001
BlaVIM-1 0001
Beta-lactamase 0001
Beta-lactamase 0001
Beta-lactamase 0001
Solute carrier family 22 member 110104
Solute carrier family 22 member 80101
Solute carrier family 22 member 70103
Dihydroxyacetone phosphate acyltransferase0002
30S ribosomal protein S60303
30S ribosomal protein S70303
50S ribosomal protein L150303
50S ribosomal protein L100303
50S ribosomal protein L110303
50S ribosomal protein L7/L120303
50S ribosomal protein L190303
50S ribosomal protein L10303
50S ribosomal protein L200303
50S ribosomal protein L270303
50S ribosomal protein L280303
50S ribosomal protein L290303
50S ribosomal protein L310303
50S ribosomal protein L31 type B0303
50S ribosomal protein L320303
50S ribosomal protein L330303
50S ribosomal protein L340303
50S ribosomal protein L350303
50S ribosomal protein L360303
30S ribosomal protein S100303
30S ribosomal protein S110303
30S ribosomal protein S120303
30S ribosomal protein S130303
30S ribosomal protein S160303
30S ribosomal protein S180303
30S ribosomal protein S190303
30S ribosomal protein S200303
30S ribosomal protein S20303
30S ribosomal protein S30303
30S ribosomal protein S40303
30S ribosomal protein S50303
30S ribosomal protein S80303
30S ribosomal protein S90303
50S ribosomal protein L130303
50S ribosomal protein L140303
50S ribosomal protein L160303
50S ribosomal protein L230303
30S ribosomal protein S150303
50S ribosomal protein L170303
50S ribosomal protein L210303
50S ribosomal protein L300303
50S ribosomal protein L60303
30S ribosomal protein S140303
30S ribosomal protein S170303
30S ribosomal protein S10303
50S ribosomal protein L180303
50S ribosomal protein L20303
50S ribosomal protein L30303
50S ribosomal protein L240303
50S ribosomal protein L40303
50S ribosomal protein L220303
50S ribosomal protein L50303
30S ribosomal protein S210303
50S ribosomal protein L250303
50S ribosomal protein L36 20303
Methionine--tRNA ligase, mitochondrial0011
glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase0202
Spike glycoprotein0279
glucose-6-phosphate 1-dehydrogenase isoform b0202
Transmembrane protease serine 20279
Dihydrofolate reductase 0303
Riboflavin-binding protein0123
Major prion protein0011
Histidine-rich protein PFHRP-II0102
Procathepsin L03710
Muscarinic acetylcholine receptor M2011214
Muscarinic acetylcholine receptor M40808
Muscarinic acetylcholine receptor M50606
Alpha-2A adrenergic receptor09212
Spike glycoprotein0325
Muscarinic acetylcholine receptor M1013115
Ribosyldihydronicotinamide dehydrogenase [quinone]03912
Alpha-2C adrenergic receptor0528
DNA ligase 10101
Muscarinic acetylcholine receptor M309110
Calcium-dependent protein kinase 10011
DNA ligase A0101
Sigma intracellular receptor 20202
Phosphoethanolamine N-methyltransferase0101
Cysteine proteinase falcipain 2a 0101
Cysteine proteinase falcipain 2a 0101
PINK14004
Caspase-78008
polyunsaturated fatty acid lipoxygenase ALOX127007
prostaglandin E2 receptor EP2 subtype1002
caspase-38008
Acetylcholinesterase 0101
Carboxylic ester hydrolase 0101
Rap guanine nucleotide exchange factor 46006
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, Proto-oncogene Tyrosine-protein Kinase Src0101
Chain A, N5-carboxyaminoimidazole ribonucleotide mutase0011
Chain B, N5-carboxyaminoimidazole ribonucleotide mutase0011
Chain A, N5-carboxyaminoimidazole ribonucleotide mutase0011
Chain B, N5-carboxyaminoimidazole ribonucleotide mutase0011
hepatocyte nuclear factor 4-alpha isoform 20101
perilipin-50202
perilipin-10202
1-acylglycerol-3-phosphate O-acyltransferase ABHD5 isoform a0202
Beta-lactamase0101
3-dehydroquinate dehydratase0011
ATP-citrate synthase 0001
Ribonuclease T0001
Cell death-related nuclease 40001
3-dehydroquinate dehydratase0011
Prolyl 4-hydroxylase0101
Alpha-ketoglutarate-dependent dioxygenase FTO0101
mu opioid receptor, partial0011
90-kda heat shock protein beta HSP90 beta, partial0202
LAP40011
MEP20011
delta-type opioid receptor0112
kappa-type opioid receptor isoform 10101
nuclear factor NF-kappa-B p105 subunit isoform 16017
DNA dC->dU-editing enzyme APOBEC-3F isoform a2002
Alpha-1B adrenergic receptor017219
Catechol O-methyltransferase0101
Alpha-1D adrenergic receptor0729
Alpha-1A adrenergic receptor016218
Beta-galactosidase0011
Carbonic anhydrase 150406
Carbonic anhydrase 130609
mitogen-activated protein kinase kinase kinase kinase 2 isoform 10011
eyes absent homolog 2 isoform a1001
mitogen-activated protein kinase kinase kinase 3 isoform 10011
Estrogen receptor0045
5-hydroxytryptamine receptor 1A016220
Cruzipain0404
C-terminal-binding protein 11001
Estrogen receptor beta0045
Chain A, CHIMERA OF IG KAPPA CHAIN: HUMAN CONSTANT REGION AND MOUSE VARIABLE REGION0011
Chain B, CHIMERA OF IG GAMMA-1 CHAIN: HUMAN CONSTANT REGION AND MOUSE VARIABLE REGION0011
Chain H, Fab M82G2, Heavy chain0011
Chain L, Fab M82G2, Light chain0011
Chain H, Fab M82g2, Heavy Chain0011
Chain L, Fab M82g2, Light Chain0011
Fatty acid-binding protein, heart0303
Muscarinic acetylcholine receptor M20112
Muscarinic acetylcholine receptor M10213
5-hydroxytryptamine receptor 2C0315
Tryptophan 5-hydroxylase 10101
5-hydroxytryptamine receptor 2A0426
D0101
Alpha-2B adrenergic receptor0112
Alpha-2C adrenergic receptor0112
Alpha-2A adrenergic receptor0112
Liver carboxylesterase 10203
Sodium-dependent noradrenaline transporter 012517
Sodium-dependent dopamine transporter0415
cAMP-specific 3',5'-cyclic phosphodiesterase 4A0404
5-hydroxytryptamine receptor 1B0707
5-hydroxytryptamine receptor 1D0101
5-hydroxytryptamine receptor 1F0101
5-hydroxytryptamine receptor 2B0213
5-hydroxytryptamine receptor 60101
Sodium-dependent serotonin transporter013114
5-hydroxytryptamine receptor 7 0101
5-hydroxytryptamine receptor 5A0101
5-hydroxytryptamine receptor 5B0101
Glutamate receptor ionotropic, NMDA 1 0418
5-hydroxytryptamine receptor 3A0101
Lysosomal Pro-X carboxypeptidase0101
D(2) dopamine receptor0325
Glutamate receptor ionotropic, NMDA 2A 0317
Glutamate receptor ionotropic, NMDA 2B0418
Glutamate receptor ionotropic, NMDA 2C0317
Sodium-dependent dopamine transporter 010010
Leukotriene B4 receptor 10101
Sodium-dependent dopamine transporter0202
Glutamate receptor ionotropic, NMDA 2D0317
5-hydroxytryptamine receptor 4 0101
Glutamate receptor ionotropic, NMDA 3B0317
5-hydroxytryptamine receptor 3B0101
Leukotriene B4 receptor 20101
Glutamate receptor ionotropic, NMDA 3A0317
Transporter0202
PAX80002
nuclear receptor subfamily 0 group B member 10303
steroidogenic factor 10303
Solute carrier family 22 member 30506
Plasma kallikrein0205
Tubulin beta-4A chain04411
ATP-dependent translocase ABCB10404
Tubulin beta chain04411
Tubulin alpha-3C chain04411
ATP-dependent translocase ABCB10528
Tubulin alpha-1B chain04411
Tubulin alpha-4A chain04411
Tubulin beta-4B chain04411
Vesicular acetylcholine transporter0101
Tubulin beta-3 chain05412
Tubulin beta-2A chain04411
Tubulin polymerization-promoting protein0011
Tubulin beta-8 chain04411
Tubulin alpha-3E chain04411
Tubulin alpha-1A chain04411
CREB-binding protein1203
Tubulin alpha-1C chain04411
Tubulin beta-6 chain04411
Tubulin beta-2B chain04411
Tubulin beta-1 chain04411
histone-lysine N-methyltransferase 2A isoform 2 precursor180018
relaxin receptor 2 isoform 11001
Nuclear receptor subfamily 1 group I member 20156
5-hydroxytryptamine receptor 1A0314
Solute carrier family 2, facilitated glucose transporter member 10314
Adenylate cyclase type 20011
Adenylate cyclase type 80011
Adenylate cyclase type 10112
Relaxin receptor 10011
Nuclear receptor subfamily 1 group I member 20022
Potassium voltage-gated channel subfamily A member 10011
Integrin alpha-L0101
Phosphatidylinositol 3-kinase catalytic subunit type 30101
Nuclear receptor corepressor 20303
Chain A, Breast cancer type 1 susceptibility protein3003
Nrf22002
alkaline phosphatase, intestinal0101
caspase 7, apoptosis-related cysteine protease150015
toll-like receptor 90101
caspase-3150015
TPA: protein transporter TIM100202
thyrotropin-releasing hormone receptor6006
alkaline phosphatase, tissue-nonspecific isozyme isoform 1 preproprotein0101
intestinal alkaline phosphatase precursor0101
pyruvate kinase PKM isoform a3003
tumor susceptibility gene 101 protein2002
alkaline phosphatase, germ cell type preproprotein0101
hypothetical protein SA14220101
Prostaglandin E synthase0303
Acetylcholinesterase0505
Lysine-specific histone demethylase 1A0404
D-amino-acid oxidase0101
Phospholipase A20303
Sarcoplasmic/endoplasmic reticulum calcium ATPase 10707
Neuronal proto-oncogene tyrosine-protein kinase Src 0102
Cholinesterase0404
Heme oxygenase 1 0303
Glutathione S-transferase P0202
Microtubule-associated protein tau0315
Sarcoplasmic/endoplasmic reticulum calcium ATPase 2 0101
Aminopeptidase N0101
Aminopeptidase N0101
Sarcoplasmic/endoplasmic reticulum calcium ATPase 20202
Voltage-dependent L-type calcium channel subunit alpha-1C0505
Heme oxygenase 20303
Voltage-dependent L-type calcium channel subunit alpha-1D0303
Caspase-76006
Cholinesterase0404
Voltage-dependent L-type calcium channel subunit alpha-1S0303
Lactoylglutathione lyase0606
Histone acetyltransferase p3000202
5-hydroxytryptamine receptor 40011
Sodium/bile acid cotransporter0112
Nuclear factor erythroid 2-related factor 20158
Thioredoxin reductase 1, cytoplasmic0203
Thioredoxin reductase 30101
Sortase A0101
Sarcoplasmic/endoplasmic reticulum calcium ATPase 30202
Cysteine protease 0202
Thioredoxin reductase 2, mitochondrial0101
CDGSH iron-sulfur domain-containing protein 10404
Lymphocyte antigen 960011
Beta lactamase (plasmid)0101
Multidrug resistance-associated protein 50001
RPL19A0011
transactivating tegument protein VP16 [Human herpesvirus 1]0404
COUP transcription factor 2 isoform a0101
Glucose transporter0101
Hexose transporter 1 0101
Eukaryotic initiation factor 4A-I0101
Peptidyl-prolyl cis-trans isomerase FKBP1A0628
Peptidyl-prolyl cis-trans isomerase FKBP30101
Peptidyl-prolyl cis-trans isomerase FKBP40101
Peptidyl-prolyl cis-trans isomerase NIMA-interacting 10415
Hypoxia-inducible factor 1-alpha0213
Endothelial PAS domain-containing protein 10202
Peptidyl-prolyl cis-trans isomerase FKBP140101
Peptidyl-prolyl cis-trans isomerase NIMA-interacting 40101
Deoxycytidine kinase0001
Alpha-tocopherol transfer protein0011
RAD510202
Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 10101
Growth factor receptor-bound protein 20102
Pantothenate synthetase0101
Growth factor receptor-bound protein 2 0101
Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase0011
6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase 0101
Dihydrofolate reductase0303
5-hydroxytryptamine receptor 60819
Leukotriene C4 synthase0077
GALC protein110011
Bone morphogenetic protein receptor type-1B0099
Membrane-associated progesterone receptor component 10055
ATP-dependent RNA helicase DDX3X0088
Pyridoxal kinase0088
Dual specificity mitogen-activated protein kinase kinase 70178
Inhibitor of nuclear factor kappa-B kinase subunit beta0179
Peripheral plasma membrane protein CASK0077
Inhibitor of nuclear factor kappa-B kinase subunit alpha0178
Ephrin type-B receptor 60099
Peroxisomal acyl-coenzyme A oxidase 30088
Mitogen-activated protein kinase 1303811
Mitogen-activated protein kinase kinase kinase 130077
Mitogen-activated protein kinase kinase kinase 70077
Mitotic checkpoint serine/threonine-protein kinase BUB10077
Dynamin-like 120 kDa protein, mitochondrial0088
Phosphatidylinositol 4-phosphate 5-kinase type-1 gamma0077
Voltage-dependent L-type calcium channel subunit alpha-1F0606
Eukaryotic translation initiation factor 5B0066
Rho-associated protein kinase 203912
Serine/threonine-protein kinase ULK10099
Serine/threonine-protein kinase/endoribonuclease IRE101910
U5 small nuclear ribonucleoprotein 200 kDa helicase0088
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma0077
Cyclin-dependent kinase-like 50088
Structural maintenance of chromosomes protein 20077
Mitogen-activated protein kinase kinase kinase 60099
Serine/threonine-protein kinase OSR10077
Serine/threonine-protein kinase Chk20178
Tyrosine-protein kinase ABL10202
Proto-oncogene tyrosine-protein kinase Src0213
Guanine nucleotide-binding protein G(i) subunit alpha-20055
ADP/ATP translocase 20088
Protein kinase C beta type031014
Proto-oncogene tyrosine-protein kinase LCK 0202
Glycogen phosphorylase, liver form0189
Adenine phosphoribosyltransferase0055
Signal recognition particle receptor subunit alpha0055
Cytochrome c1, heme protein, mitochondrial0088
Quinolone resistance protein NorA0202
Wee1-like protein kinase 20077
Uncharacterized serine/threonine-protein kinase SBK30077
Serine/threonine-protein kinase A-Raf0189
Glycogen phosphorylase, brain form0088
Breakpoint cluster region protein061119
Cytochrome P450 2A60303
Cyclin-dependent kinase 403912
ADP/ATP translocase 30088
Inosine-5'-monophosphate dehydrogenase 20066
cAMP-dependent protein kinase type II-alpha regulatory subunit0077
Potassium voltage-gated channel subfamily E member 10202
Tyrosine-protein kinase Blk0101
Protein kinase C alpha type071121
General transcription and DNA repair factor IIH helicase subunit XPD0088
Ras-related protein Rab-6A0077
Serine/threonine-protein kinase MAK0077
Cytochrome P450 2B60404
Receptor tyrosine-protein kinase erbB-30077
Multifunctional protein ADE20088
cAMP-dependent protein kinase catalytic subunit gamma0279
Ferrochelatase, mitochondrial0088
Ribosomal protein S6 kinase beta-101910
Beta-adrenergic receptor kinase 10088
Probable ATP-dependent RNA helicase DDX60088
Deoxycytidine kinase0088
UMP-CMP kinase 0044
Phosphatidylethanolamine-binding protein 10066
Heme oxygenase 20088
S-adenosylmethionine synthase isoform type-20088
DnaJ homolog subfamily A member 10088
G protein-coupled receptor kinase 40077
DNA replication licensing factor MCM40077
Electron transfer flavoprotein subunit beta0077
Glycine--tRNA ligase0088
Protein kinase C iota type021012
Exosome RNA helicase MTR40088
Megakaryocyte-associated tyrosine-protein kinase0077
G protein-coupled receptor kinase 60055
26S proteasome regulatory subunit 6B0088
Casein kinase I isoform alpha03912
Elongation factor Tu, mitochondrial0088
Choline-phosphate cytidylyltransferase A0044
Cysteine--tRNA ligase, cytoplasmic0077
Very long-chain specific acyl-CoA dehydrogenase, mitochondrial0088
Ras-related protein Rab-27A0066
Interleukin-1 receptor-associated kinase 10099
Potassium voltage-gated channel subfamily KQT member 10202
Serine/threonine-protein kinase Nek30099
Serine/threonine-protein kinase Nek40077
Tyrosine--tRNA ligase, cytoplasmic0088
5'-AMP-activated protein kinase subunit gamma-10089
Adenylate kinase 2, mitochondrial0088
Adenosine kinase0088
Hormonally up-regulated neu tumor-associated kinase0077
Receptor-interacting serine/threonine-protein kinase 40077
Ras-related protein Rab-100088
Cell division control protein 2 homolog0077
Actin-related protein 30088
Actin-related protein 20077
Calcium-dependent protein kinase 10077
GTP-binding nuclear protein Ran0088
Serine/threonine-protein kinase PknB0077
Cyclin-dependent kinase-like 10077
Myelin transcription factor 10101
Voltage-dependent L-type calcium channel subunit alpha-1D 0606
ATP-dependent 6-phosphofructokinase, platelet type0088
Macrophage-stimulating protein receptor0099
Protein kinase C zeta type0369
Mitogen-activated protein kinase kinase kinase kinase 20099
Mitogen-activated protein kinase kinase kinase 120077
Dual specificity mitogen-activated protein kinase kinase 50099
Mitogen-activated protein kinase kinase kinase 10099
Integrin-linked protein kinase0088
Rho-associated protein kinase 102911
Serine/threonine-protein kinase PRP4 homolog0077
Dual specificity tyrosine-phosphorylation-regulated kinase 1A01910
Voltage-dependent L-type calcium channel subunit alpha-1S0606
Cyclin-dependent kinase 130099
Sodium channel protein type 5 subunit alpha0606
Structural maintenance of chromosomes protein 1A0077
Chromodomain-helicase-DNA-binding protein 40077
Peroxisomal acyl-coenzyme A oxidase 10066
Serine/threonine-protein kinase 380077
Receptor tyrosine-protein kinase erbB-40178
Delta(24)-sterol reductase0077
Rhodopsin kinase GRK10077
Myosin light chain kinase 30099
Uncharacterized aarF domain-containing protein kinase 50044
Serine/threonine-protein kinase SBK10077
Mitogen-activated protein kinase kinase kinase 190077
Putative heat shock protein HSP 90-beta 20088
Leucine-rich repeat serine/threonine-protein kinase 20178
Acyl-CoA dehydrogenase family member 100066
Serine/threonine-protein kinase N30055
Breakpoint cluster region protein0101
Serine/threonine-protein kinase ULK30099
Dual serine/threonine and tyrosine protein kinase0077
Mitogen-activated protein kinase kinase kinase 150077
Uncharacterized protein FLJ452520088
Acyl-CoA dehydrogenase family member 110066
Serine/threonine-protein kinase/endoribonuclease IRE20077
Serine/threonine-protein kinase TAO10099
STE20-related kinase adapter protein alpha0088
Myosin-140088
AarF domain-containing protein kinase 10088
ATP-dependent RNA helicase DDX420033
Serine/threonine-protein kinase VRK20077
Homeodomain-interacting protein kinase 10178
Cyclin-dependent kinase-like 30077
Serine/threonine-protein kinase NIM10077
Eukaryotic peptide chain release factor GTP-binding subunit ERF3B0033
Serine/threonine-protein kinase ULK20077
Misshapen-like kinase 10088
Homeodomain-interacting protein kinase 40178
Serine/threonine-protein kinase Nek110077
Phosphatidylinositol 5-phosphate 4-kinase type-2 gamma0099
Serine/threonine-protein kinase 350077
Rhodopsin kinase GRK70077
Serine/threonine-protein kinase 32A0077
ATP-dependent RNA helicase DDX10088
Dual specificity tyrosine-phosphorylation-regulated kinase 20077
Cyclin-dependent kinase-like 20077
Serine/threonine-protein kinase Sgk30077
Cyclin-dependent kinase 150077
PAS domain-containing serine/threonine-protein kinase0077
EKC/KEOPS complex subunit TP53RK0088
Dual specificity testis-specific protein kinase 20044
Protein cereblon0428
Mitogen-activated protein kinase kinase kinase 30099
Eukaryotic translation initiation factor 2-alpha kinase 10099
Serine/threonine-protein kinase RIO20077
Transient receptor potential cation channel subfamily M member 60077
Nucleolar GTP-binding protein 10077
RNA cytidine acetyltransferase0088
Serine/threonine-protein kinase TAO30099
Homeodomain-interacting protein kinase 20178
Homeodomain-interacting protein kinase 30178
dCTP pyrophosphatase 10088
SNF-related serine/threonine-protein kinase0077
Phenylalanine--tRNA ligase beta subunit0088
Isoleucine--tRNA ligase, mitochondrial0066
Obg-like ATPase 10066
Midasin0088
Interleukin-1 receptor-associated kinase 40099
Cyclin-dependent kinase 120088
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 130077
Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial0088
STE20/SPS1-related proline-alanine-rich protein kinase0077
5'-AMP-activated protein kinase subunit gamma-20089
Serine/threonine-protein kinase TBK102911
Septin-90088
Potassium voltage-gated channel subfamily D member 30202
Serine/threonine-protein kinase TAO20099
Long-chain-fatty-acid--CoA ligase 50055
SRSF protein kinase 30077
Serine/threonine-protein kinase ICK0099
Microtubule-associated serine/threonine-protein kinase 10077
Serine/threonine-protein kinase SIK301910
Mitogen-activated protein kinase kinase kinase 20099
Thyroid hormone receptor-associated protein 30077
Receptor-interacting serine/threonine-protein kinase 30189
NF-kappa-B essential modulator0101
runt-related transcription factor 1 isoform AML1b2002
core-binding factor subunit beta isoform 22002
NADH-ubiquinone oxidoreductase chain 40001
Carbonyl reductase [NADPH] 10001
Glutamate receptor 12002
Glutamate receptor 32002
Glutamate receptor 42002
Platelet-activating factor receptor1001
exodeoxyribonuclease V subunit RecD0101
exodeoxyribonuclease V subunit RecB0101
exodeoxyribonuclease V subunit RecC0101
Lysine-specific demethylase 4A0101
Methylcytosine dioxygenase TET20101
Deoxyhypusine hydroxylase0101
high affinity choline transporter 1 isoform a0101
Beta-1 adrenergic receptor0617
Polyunsaturated fatty acid lipoxygenase ALOX150808
D(2) dopamine receptor0516
Substance-K receptor0808
D(1A) dopamine receptor0516
Alpha-1D adrenergic receptor08110
D(3) dopamine receptor0808
Vasopressin V1a receptor0314
Estrogen-related receptor gamma0112
Aldehyde oxidase0202
UDP-glucose 4-epimerase0101
Cysteinyl leukotriene receptor 10202
Chain A, Sex Hormone-Binding Globulin0011
Progesterone receptor0101
Progesterone receptor011620
Glucocorticoid receptor0326
Sex hormone-binding globulin0101
Androgen receptor0112
Cannabinoid receptor 20101
Muscarinic acetylcholine receptor0112
Neuropeptide FF receptor 20001
Cereblon isoform 40404
Insulin-like growth factor-binding protein 50011
Choline O-acetyltransferase 0101
Glutathione S-transferase omega-10101
Solute carrier family 22 member 20204
Solute carrier organic anion transporter family member 1A50002
Prostaglandin E2 receptor EP1 subtype0213
Prostaglandin E2 receptor EP4 subtype0213
Prostaglandin F2-alpha receptor0011
Prostaglandin E2 receptor EP4 subtype0112
Prostaglandin E2 receptor EP3 subtype0213
Prostaglandin E2 receptor EP2 subtype0213
Prostaglandin E2 receptor EP2 subtype0112
Solute carrier family 22 member 70001
Solute carrier organic anion transporter family member 1B20103
UDP-glucuronosyltransferase 1A40104
signal transducer and activator of transcription 6, interleukin-4 induced2002
Single-stranded DNA cytosine deaminase4004
Dipeptidyl peptidase 40101
Tripeptidyl-peptidase 20101
Dipeptidyl peptidase 80101
Eyes absent homolog 20101
Mitochondrial 2-oxodicarboxylate carrier0101
Chain A, Protein (peroxisome Proliferator Activated Receptor (ppar-delta))0101
Peroxisome proliferator-activated receptor gamma0236
Oxoeicosanoid receptor 10101
Endothelin-1 receptor0213
Opioid receptor, delta 1b 0101
Opioid receptor homologue0101
Proenkephalin-B0011
Delta-type opioid receptor0427
Delta-type opioid receptor0203
Kappa-type opioid receptor0101
Mu-type opioid receptor0426
Kappa-type opioid receptor0202
Mu-type opioid receptor0101
Mu-type opioid receptor0101
Chain A, Troponin C, slow skeletal and cardiac muscles0011
Chain A, Peptidyl-prolyl cis-trans isomerase NIMA-interacting 10011
Chain A, POLYMERASE PA0101
Chain A, Polymerase Pa0101
Chain A, Polymerase Pa0101
Chain A, Polymerase Pa0101
Chain A, Polymerase Pa0101
Genome polyprotein 0303
galactokinase3003
POsterior Segregation0055
Polycomb protein EED0112
NAD kinase0213
Dihydrofolate reductase0406
Urokinase-type plasminogen activator0303
Tissue-type plasminogen activator0202
Polymerase acidic protein0112
Plasminogen activator inhibitor 10202
Urokinase-type plasminogen activator0202
Heat shock protein HSP 90-beta0327
Matrilysin0202
Enoyl-[acyl-carrier-protein] reductase [NADH] FabI0303
Alpha-amylase 1A 0303
Apoptosis regulator Bcl-20303
Glucose-6-phosphate 1-dehydrogenase0101
Fatty acid synthase0202
CPG DNA methylase0101
Lethal factor0202
Phosphoglycerate mutase 10101
Cannabinoid receptor 10101
Cannabinoid receptor 2 0101
Signal transducer and activator of transcription 1-alpha/beta0011
Matrix metalloproteinase-140101
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT60202
Squalene monooxygenase 0203
6-phosphogluconate dehydrogenase, decarboxylating0202
BH3-interacting domain death agonist0101
Bcl-2-like protein 10303
Induced myeloid leukemia cell differentiation protein Mcl-10303
Alpha-(1,3)-fucosyltransferase 70202
CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 10202
Bcl-2-related protein A10101
Sigma non-opioid intracellular receptor 10213
Dual specificity tyrosine-phosphorylation-regulated kinase 1A0101
3-oxoacyl-[acyl-carrier-protein] reductase 0101
Histone acetyltransferase KAT2B0101
Bcl-2-like protein 20101
Bcl2-associated agonist of cell death 0101
Histone acetyltransferase KAT50101
3-oxoacyl-acyl-carrier protein reductase 0505
Beta-hydroxyacyl-ACP dehydratase precursor (Fatty acid synthesis protein)0505
Bcl-2-like protein 100101
Zinc finger protein mex-50055
Steryl-sulfatase0101
Ghrelin O-acyltransferase0101
LMP1 [Human herpesvirus 4]0001
nuclear receptor coactivator 1 isoform 1 [Homo sapiens]0202
nuclear receptor coactivator 3 isoform a0202
Regulatory protein E20022
DNA topoisomerase 20002
UDP-glucuronosyltransferase 1A1 0204
Serum paraoxonase/arylesterase 10303
Caspase-30202
DNA topoisomerase 2-alpha 0001
Glycoprotein hormones alpha chain5005
Retinol-binding protein 40033
Prosaposin0011
Retinoic acid receptor gamma 0339
Alpha-1A adrenergic receptor0202
Retinoic acid receptor RXR-beta0325
Indoleamine 2,3-dioxygenase 10404
Retinoic acid receptor RXR-gamma0325
Indoleamine 2,3-dioxygenase 20303
Nuclear factor NF-kappa-B p105 subunit0303
Chain A, Uracil Phosphoribosyltransferase0101
Skn7p0001
Solute carrier family 22 member 80001
Thymidylate synthase0405
Chain A, Dihydrofolate reductase0011
Thymidylate synthase0404
Dihydrofolate reductase0235
Folylpolyglutamate synthase, mitochondrial0104
Solute carrier organic anion transporter family member 1A30203
Folylpolyglutamate synthase, mitochondrial0104
Multidrug resistance associated protein0103
Menin0011
Lecithin retinol acyltransferase0101
Protein Rev 0011
Aminoglycoside 3'-phosphotransferase 0001
Beta-galactosidase0101
Lipopolysaccharide heptosyltransferase 10101
PA-I galactophilic lectin0011
Jacalin0011
fructose-bisphosphate aldolase A1001
glyceraldehyde-3-phosphate dehydrogenase isoform 11001
L-selectin0101
P-selectin0101
E-selectin0101
Prolyl 4-hydroxylase subunit alpha-10202
Autoinducer 2-binding periplasmic protein LuxP0101
Anthrax toxin receptor 20202
Polypeptide N-acetylgalactosaminyltransferase 20112
Carbonic anhydrase0303
Toll-like receptor 2 0101
Chain A, Estrogen receptor 1 (alpha)0101
Chain A, Transthyretin0011
Chain A, Transthyretin0011
Alpha-mannosidase0101
Maltase-glucoamylase, intestinal0303
Steroid hormone receptor ERR20101
Triosephosphate isomerase0101
Tyrosinase0505
Steroid hormone receptor ERR10303
Ornithine decarboxylase0202
Solute carrier family 2, facilitated glucose transporter member 40101
Dipeptidyl peptidase 40101
Amine oxidase [flavin-containing] A 0202
Amine oxidase [flavin-containing] A 0202
G1/S-specific cyclin-D10303
Cystic fibrosis transmembrane conductance regulator0011
Alpha-glucosidase MAL320101
Signal transducer and activator of transcription 30303
Quinone oxidoreductase0004
Oxysterols receptor LXR-beta0202
Amine oxidase [flavin-containing] B0202
Oxysterols receptor LXR-alpha0101
Tissue alpha-L-fucosidase0101
DNA (cytosine-5)-methyltransferase 3-like0101
DNA (cytosine-5)-methyltransferase 3A0101
Chain A, Glutamine Binding Protein0011
Neutral amino acid transporter A0303
Asc-type amino acid transporter 10202
Neutral amino acid transporter B(0)0303
Carbonic anhydrase-like protein, putative0003
Amino acid transporter0303
Chain B, EUKARYOTIC TRANSLATION INITIATION FACTOR 4E0011
Glycine receptor subunit alpha-10011
Sodium- and chloride-dependent GABA transporter 20101
Sodium- and chloride-dependent GABA transporter 30101
Sodium- and chloride-dependent glycine transporter 10101
Large neutral amino acids transporter small subunit 10202
Serine racemase0101
Olfactory receptor 51E20123
Sodium- and chloride-dependent glycine transporter 20202
Beta-glucuronidase0101
High mobility group protein B10033
Corticosteroid 11-beta-dehydrogenase isozyme 10112
Corticosteroid 11-beta-dehydrogenase isozyme 10112
High mobility group protein B10001
Corticosteroid 11-beta-dehydrogenase isozyme 20112
Canalicular multispecific organic anion transporter 10203
Solute carrier family 22 member 10306
Solute carrier family 22 member 20305
Ricin0101
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase0011
Purine nucleoside phosphorylase 0012
Guanine deaminase0001
Chain A, CARBONIC ANHYDRASE II0011
Chain A, Protein (female-specific Histamine Binding Protein 2)0011
aryl hydrocarbon receptor nuclear translocator0001
transforming acidic coiled-coil-containing protein 30001
Macrophage migration inhibitory factor0303
Histamine H2 receptor0729
5-hydroxytryptamine receptor 1D0002
Histamine H1 receptor0134
Histamine H1 receptor0213
Metabotropic glutamate receptor 50112
Histamine H1 receptor0224
Carbonic anhydrase0204
Carbonic anhydrase0003
Histamine H3 receptor0101
Histamine N-methyltransferase 0101
Glutaminyl-peptide cyclotransferase0202
Carbonic anhydrase 0104
Carbonic anhydrase0205
Carbonic anhydrase0104
Carbonic anhydrase 0003
Equilibrative nucleoside transporter 40001
Histamine H4 receptor0123
Histamine H4 receptor0123
Histamine H4 receptor 0101
Carbonic anhydrase 40002
Histamine H4 receptor0123
Histamine H3 receptor0123
Chain A, HISTIDINE-BINDING PROTEIN0011
Histidine-binding periplasmic protein0011
Carbonic anhydrase 0202
Carbonic anhydrase0202
Carbonic anhydrase, alpha family 0101
Cyclic GMP-AMP synthase0101
Toll-like receptor 90101
Toll-like receptor 70112
Glutamine synthetase0101
Genome polyprotein0101
Small conductance calcium-activated potassium channel protein 30101
Sorbitol dehydrogenase0202
Oleandomycin glycosyltransferase0001
Estrogen receptor beta0013
Protein kinase C gamma type0326
Estrogen receptor0013
Acid-sensing ion channel 30101
Solute carrier organic anion transporter family member 1A40102
Albumin0022
Fatty acid-binding protein, intestinal0101
Polyunsaturated fatty acid 5-lipoxygenase0305
UDP-glucuronosyltransferase 2B70103
Prostaglandin G/H synthase 10202
Caspase-10102
Prostaglandin G/H synthase 2 0304
UDP-glucuronosyltransferase 1A30001
Aldo-keto reductase family 1 member C30404
Caspase-40101
Caspase-50101
Caspase-90101
Acid-sensing ion channel 10101
Fatty-acid amide hydrolase 10303
Prostaglandin G/H synthase 20304
Prostaglandin G/H synthase 1 0304
Dehydrogenase/reductase SDR family member 90101
DNA repair protein RAD52 homolog isoform a0004
Cytochrome P450 2C80506
Cytochrome P450 3A50203
7,8-dihydro-8-oxoguanine triphosphatase0101
Toll-like receptor 80011
Cell division cycle 7-related protein kinase0044
Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha0055
Tyrosine-protein kinase JAK2 0011
Chain A, membrane-associated prostaglandin E synthase-20101
3',5'-cyclic-AMP phosphodiesterase 0101
Solute carrier organic anion transporter family member 2B1 0202
Cytochrome c oxidase subunit 20101
Phospholipase A2, major isoenzyme0101
Interleukin-80101
Aldo-keto reductase family 1 member B10404
Aldo-keto reductase family 1 member C40101
Sodium- and chloride-dependent GABA transporter 10202
Sodium- and chloride-dependent GABA transporter 20202
Sodium- and chloride-dependent GABA transporter 30202
Bifunctional epoxide hydrolase 20404
Sodium- and chloride-dependent betaine transporter0202
C-X-C chemokine receptor type 30101
Aldo-keto reductase family 1 member C2 0101
Prostaglandin D2 receptor 0202
Aldo-keto reductase family 1 member C10101
Uracil nucleotide/cysteinyl leukotriene receptor0101
Sigma intracellular receptor 20202
Dehydrogenase/reductase SDR family member 90101
P2Y purinoceptor 120101
Prostaglandin D2 receptor 20112
Ornithine decarboxylase0002
Retinoic acid receptor alpha0224
Retinoic acid receptor gamma0224
Retinoic acid receptor beta0224
Cellular retinoic acid-binding protein 20022
Retinoic acid receptor RXR-alpha0224
Retinoic acid receptor RXR-beta0224
Retinoic acid receptor RXR-gamma0224
Cellular retinoic acid-binding protein 10203
Cellular retinoic acid-binding protein 10022
Cytochrome P450 1440022
Steroid C26-monooxygenase0022
Steroid C26-monooxygenase0022
Sphingosine 1-phosphate receptor 20225
Sphingosine 1-phosphate receptor 40213
Sphingosine 1-phosphate receptor 10213
Sphingosine 1-phosphate receptor 20101
Sphingosine 1-phosphate receptor 30213
Sphingosine 1-phosphate receptor 50213
dual specificity tyrosine-phosphorylation-regulated kinase 1A0002
rac GTPase-activating protein 1 isoform a0202
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 10101
Protein E60202
Neuraminidase0101
Interstitial collagenase0314
Beta-glucuronidase0101
Aryl hydrocarbon receptor0101
Prolyl endopeptidase0202
E3 ubiquitin-protein ligase XIAP0101
Histone-lysine N-methyltransferase SETD70404
Rapamycin-insensitive companion of mTOR0101
Regulatory-associated protein of mTOR0202
Target of rapamycin complex 2 subunit MAPKAP10101
Target of rapamycin complex subunit LST80202
Dihydroorotate dehydrogenase 0101
Indoleamine 2,3-dioxygenase 10202
Genome polyprotein 0101
Protease 0202
Tyrosine-protein phosphatase non-receptor type 220101
P2X purinoceptor 70101
Sodium channel protein type 1 subunit alpha0101
Sodium channel protein type 2 subunit alpha0202
Sodium channel protein type 3 subunit alpha0101
Potassium voltage-gated channel subfamily A member 50101
Sodium channel protein type 4 subunit alpha0203
Sodium channel protein type 9 subunit alpha0202
Potassium voltage-gated channel subfamily D member 20101
Potassium channel subfamily K member 180101
Sodium channel protein type 3 subunit alpha0202
Free fatty acid receptor 10011
Sterol O-acyltransferase 10202
Tyrosine-protein phosphatase non-receptor type 70101
Sterol O-acyltransferase 10303
Dual specificity protein phosphatase 30202
Free fatty acid receptor 40011
Thromboxane A2 receptor 0102
Squalene synthase0202
cAMP-specific 3',5'-cyclic phosphodiesterase 4C0202
Platelet glycoprotein VI0113
Type-1 angiotensin II receptor0112
histidine kinase 0101
WRN3003
integrase, partial0202
lens epithelium-derived growth factor p750202
cystic fibrosis transmembrane conductance regulator ATP-binding cassette sub-family C member 70001
Chemotaxis protein CheA0101
Stromelysin-10314
Cytosol aminopeptidase0202
ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 10303
Macrophage metalloelastase0202
1-deoxy-D-xylulose 5-phosphate reductoisomerase0202
Protein polybromo-10011
G-protein coupled receptor 350224
DNA topoisomerase 10101
phosphoglycerate kinase5005
M1-family alanyl aminopeptidase0101
large T antigen0213
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplast0101
Chain A, Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplast0101
Glutathione reductase, mitochondrial0405
Lysophosphatidic acid receptor 60011
Ectonucleotide pyrophosphatase/phosphodiesterase family member 20202
Lysophosphatidic acid receptor 4 0011
Lysophosphatidic acid receptor 10022
Lysophosphatidic acid receptor 40011
Lysophosphatidic acid receptor 50011
Lysophosphatidic acid receptor 20011
Lysophosphatidic acid receptor 30011
Alpha-mannosidase 2C10101
Fucose-binding lectin PA-IIL0101
CD209 antigen0101
Chain B, DIHYDROFOLATE REDUCTASE0011
Chain B, DIHYDROFOLATE REDUCTASE0011
Chain B, DIHYDROFOLATE REDUCTASE0011
Thymidylate synthase 0101
Thymidylate synthase 0101
Toll-like receptor 40101
Fatty-acid amide hydrolase 10101
ATP-binding cassette sub-family C member 30102
Dihydrofolate reductase0203
Dihydrofolate reductase0101
Dihydrofolate reductase0101
Dihydrofolate reductase0203
Thymidylate synthase0101
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Dihydrofolate reductase0101
Thymidylate synthase0101
Glucose-6-phosphate 1-dehydrogenase0303
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Folate receptor beta0101
Cytochrome P450 11B1, mitochondrial 0101
Folate receptor alpha0101
Histidine decarboxylase0101
Trifunctional purine biosynthetic protein adenosine-30101
Bifunctional purine biosynthesis protein ATIC0202
Reduced folate transporter0202
Dihydrofolate reductase0101
Pteridine reductase 10101
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Bifunctional dihydrofolate reductase-thymidylate synthase0101
Trifunctional purine biosynthetic protein adenosine-30101
Dihydrofolate reductase 0101
Dihydrofolate reductase0101
ATP-binding cassette sub-family C member 110001
Proton-coupled folate transporter0101
Chain E, Fibrin beta chain0101
T cell receptor, partial1001
luteinizing hormone receptor1001
chaperonin-containing TCP-1 beta subunit homolog2002
Caspase 6, apoptosis-related cysteine peptidase0001
Apoptotic peptidase activating factor 10101
isocitrate dehydrogenase 1, partial3003
luciferase1001
neutrophil cytosol factor 10101
caspase-9 isoform alpha precursor0101
caspase-3 isoform a preproprotein0101
protein AF-9 isoform a0002
replicative DNA helicase0001
recombinase A0011
Glutathione reductase0101
Dihydrolipoyl dehydrogenase, mitochondrial0102
Dihydrolipoyl dehydrogenase 0102
Protein delta homolog 10134
Aspartyl/asparaginyl beta-hydroxylase0101
Rab-like protein 30055
Chain A, PROGESTERONE RECEPTOR0101
Glucocorticoid receptor 0101
Tegument protein VP160011
Glucocorticoid receptor0112
Thyroid hormone receptor alpha0101
Thyroid hormone receptor beta0101
Steroid 17-alpha-hydroxylase/17,20 lyase 0101
Progesterone receptor0011
Glucocorticoid receptor0101
Platelet-activating factor receptor0101
M-phase inducer phosphatase 10202
Chain A, Probable serine/threonine-protein kinase pknB0101
DNA polymerase III, partial3003
nonstructural protein 10101
LANA0001
phospholipase A2, group III0101
histone-lysine N-methyltransferase NSD2 isoform 10001
NEDD8-activating enzyme E1 regulatory subunit0011
Nuclear receptor subfamily 3 group C member 3 0606
Multidrug and toxin extrusion protein 20101
NEDD8-activating enzyme E1 catalytic subunit0011
P2Y purinoceptor 120202
Sialidase-40101
Sialidase-10101
Sialidase-30101
Chain B, Exotoxin A0011
Chain B, Exotoxin A0011
Chain B, Exotoxin A0011
Cholesteryl ester transfer protein0213
D-amino-acid oxidase0101
Hydroxycarboxylic acid receptor 30011
Nicotinamidase0101
Hydroxycarboxylic acid receptor 20011
Hydroxycarboxylic acid receptor 20213
D-aspartate oxidase0101
Hydroxycarboxylic acid receptor 20112
Chain A, NAD-dependent deacetylase0101
Poly [ADP-ribose] polymerase 20101
NAD-dependent histone deacetylase SIR20101
NAD-dependent protein deacetylase HST20101
Protein mono-ADP-ribosyltransferase PARP150101
NAD(+) hydrolase SARM10101
NAD-dependent protein deacetylase sirtuin-20213
NAD-dependent protein deacetylase sirtuin-60213
NAD-dependent protein deacetylase sirtuin-10114
NAD-dependent protein deacetylase sirtuin-3, mitochondrial0112
NAD-dependent protein deacylase sirtuin-5, mitochondrial0202
NAD-dependent protein deacetylase 0101
Voltage-dependent L-type calcium channel subunit alpha-1C0404
Equilibrative nucleoside transporter 10101
B2 bradykinin receptor0202
Chymotrypsinogen A0202
Beta-lactamase0202
Malate dehydrogenase, cytoplasmic0101
Transient receptor potential cation channel subfamily A member 10011
Anoctamin-10101
Phosphotyrosine protein phosphatase 0101
Hemagglutinin [Cleaved into: Hemagglutinin HA1 chain; Hemagglutinin HA2 chain]0011
DNA polymerase beta0101
DNA polymerase beta0101
Receptor-type tyrosine-protein phosphatase C0101
Receptor-type tyrosine-protein phosphatase F0101
Receptor-type tyrosine-protein phosphatase alpha0101
Receptor-type tyrosine-protein phosphatase epsilon0101
Low molecular weight phosphotyrosine protein phosphatase0101
Tyrosine-protein phosphatase non-receptor type 60202
M-phase inducer phosphatase 20202
Transcription factor p650202
Tyrosine-protein phosphatase non-receptor type 110203
Env polyprotein 0011
Transmembrane prolyl 4-hydroxylase0011
Protease 0202
Chain A, Adipocyte Lipid-binding Protein0011
Chain A, MUSCLE FATTY ACID BINDING PROTEIN0011
Chain A, MUSCLE FATTY ACID BINDING PROTEIN0011
Chain A, MUSCLE FATTY ACID BINDING PROTEIN0011
Chain A, BCL-2-RELATED PROTEIN A10011
putative potassium channel subunit0011
bcl-2-like protein 11 isoform 10011
Fatty acid-binding protein, liver0011
Peroxisome proliferator-activated receptor delta0001
MAP kinase-activated protein kinase 30022
ATP-dependent RNA helicase DHX300055
Muscarinic acetylcholine receptor M30112
Muscarinic acetylcholine receptor M20112
MBT domain-containing protein 10101
Lethal(3)malignant brain tumor-like protein 40101
Lethal(3)malignant brain tumor-like protein 30101
Lethal(3)malignant brain tumor-like protein 10101
Genome polyprotein 0202
UDP-glucuronosyltransferase 1-60202
Cholecystokinin receptor type A0538
Melanocortin receptor 50404
UDP-glucuronosyltransferase 2B10 0101
Beta-tubulin 0101
Nucleotide-binding oligomerization domain-containing protein 20101
Luciferin 4-monooxygenase0202
Amine oxidase [flavin-containing] B0404
Dual specificity mitogen-activated protein kinase kinase 2 0101
Dual specificity mitogen-activated protein kinase kinase 1 0101
Cystathionine gamma-lyase0202
vasopressin V1b receptor1001
Tumor necrosis factor0101
Chitotriosidase-10213
Endochitinase B10213
Focal adhesion kinase 1 0001
Cyclin-H0101
CDK-activating kinase assembly factor MAT10101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Penicillin Amidohydrolase0101
Chain B, Penicillin Amidohydrolase0101
Chain A, Lysozyme0011
Chain A, Lysozyme0011
Chain A, Lysozyme0011
Chain A, Lysozyme0011
Chain A, Ferritin light chain0011
Chain A, Ferritin light chain0011
Chain A, Ferritin light chain0011
Chain A, Ferritin light chain0011
Chain A, Ferritin light chain0011
Chain A, Ferritin light chain0011
Chain A, Ferritin light chain0011
Endolysin0011
Sulfotransferase 1A1 0001
Cannabinoid receptor 10101
Carbonic anhydrase 0101
Beta-carbonic anhydrase 10101
beta-2 adrenergic receptor1001
mu-type opioid receptor isoform MOR-10011
5-hydroxytryptamine receptor 2A0011
Gamma-aminobutyric acid 0101
Gamma-aminobutyric acid receptor subunit alpha-60101
Gamma-aminobutyric acid receptor subunit gamma-20101
Gamma-aminobutyric acid receptor subunit delta0101
Gamma-aminobutyric acid receptor subunit alpha-20101
Gamma-aminobutyric acid receptor subunit alpha-30101
Gamma-aminobutyric acid receptor subunit gamma-30101
Sodium channel protein type 1 subunit alpha0101
Gamma-aminobutyric acid receptor subunit beta-10101
Gamma-aminobutyric acid receptor subunit alpha-10101
Gamma-aminobutyric acid receptor subunit beta-30101
Gamma-aminobutyric acid receptor subunit alpha-50101
Gamma-aminobutyric acid receptor subunit pi0101
Sodium channel protein type 2 subunit alpha0101
Gamma-aminobutyric acid receptor subunit alpha-40101
Gamma-aminobutyric acid receptor subunit theta0101
Gamma-aminobutyric acid receptor subunit gamma-10101
Protein kinase C alpha type0101
Proto-oncogene vav0011
Protein kinase C delta type0112
Transient receptor potential cation channel subfamily V member 4 0011
4-hydroxyphenylpyruvate dioxygenase0101
Transforming growth factor beta-1 proprotein0101
Mothers against decapentaplegic homolog 3 0101
Regulatory protein E20011
Regulatory protein E20011
Calcium-activated potassium channel subunit alpha-10101
luciferase0001
Glutamine synthetase0011
Nociceptin receptor0011
Glutamate 5-kinase0001
Beta-1 adrenergic receptor 0113
Beta-2 adrenergic receptor0213
Beta-2 adrenergic receptor0203
Beta-3 adrenergic receptor0415
Beta-1 adrenergic receptor0214
D(3) dopamine receptor0202
Beta-3 adrenergic receptor0202
5-hydroxytryptamine receptor 1B0213
Neuromedin-K receptor0011
5-hydroxytryptamine receptor 70213
Beta-1 adrenergic receptor0101
Alpha-1A adrenergic receptor0124
Alpha-1B adrenergic receptor0012
5-hydroxytryptamine receptor 70202
Beta-2 adrenergic receptor0101
Beta-2 adrenergic receptor0113
Nuclear receptor subfamily 2 group E member 10022
Solute carrier organic anion transporter family member 2A10101
Chain A, RNA-directed RNA polymerase NS50101
SUMO-10101
chaperonin GroEL1001
Exoribonuclease H 0101
Coproheme decarboxylase0011
Chain A, PUTRESCINE-BINDING PROTEIN0011
Chain A, S-ADENOSYLMETHIONINE DECARBOXYLASE ALPHA CHAIN0101
Chain B, S-ADENOSYLMETHIONINE DECARBOXYLASE BETA CHAIN0101
Chain A, S-ADENOSYLMETHIONINE DECARBOXYLASE ALPHA CHAIN0101
Chain B, S-ADENOSYLMETHIONINE DECARBOXYLASE BETA CHAIN0101
S-adenosylmethionine decarboxylase proenzyme0001
Chain A, Mitogen-activated protein kinase 100101
Chain A, Mitogen-activated protein kinase 100101
Chain A, Mitogen-activated protein kinase 100101
TPA: protein transporter TIM230101
polyadenylate-binding protein 10101
Serine/threonine-protein kinase ULK30022
Serine/threonine-protein kinase 30022
Chain A, APH(2')-Id0101
glucose-6-phosphate dehydrogenase0101
hexokinase0101
Prothrombin 0101
Chymotrypsin-like elastase family member 10101
Neuraminidase0101
Beta-lactamase0101
Epoxide hydrolase 1 0101
Trypsin-10101
Trypsin-20101
Lysosomal alpha-glucosidase0101
Malate dehydrogenase0202
Solute carrier family 2, facilitated glucose transporter member 20101
Sucrase-isomaltase, intestinal0101
Cytochrome P450 11B1, mitochondrial0101
Chymotrypsinogen B0202
Solute carrier family 2, facilitated glucose transporter member 4 0101
5'-nucleotidase0101
D(4) dopamine receptor0303
Glyceraldehyde-3-phosphate dehydrogenase, glycosomal0101
C-X-C chemokine receptor type 10101
Vasopressin V2 receptor0101
Trypsin-30101
Glutathione reductase0101
Aldo-keto reductase family 1 member A10101
Aldo-keto reductase family 1 member A10101
C-C chemokine receptor type 40101
Oligo-1,6-glucosidase IMA10101
Monocarboxylate transporter 10101
Aldo-keto reductase family 1 member B10101
Heat shock factor protein 10101
cGMP-dependent 3',5'-cyclic phosphodiesterase0101
ELAV-like protein 30101
ELAV-like protein 10101
Probable maltase-glucoamylase 20101
Monocarboxylate transporter 20101
Aldo-keto reductase family 1 member C210202
Chymotrypsin-C0101
Chain A, Troponin C, slow skeletal and cardiac muscles0011
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
Chain A, Leukotriene A-4 hydrolase0101
M18 aspartyl aminopeptidase0101
cathepsin L10101
FAD-linked sulfhydryl oxidase ALR0001
Vif0101
transcription factor p65 isoform 10011
serine/threonine-protein kinase 33 isoform a0011
Aryl hydrocarbon receptor0101
Transient receptor potential cation channel subfamily A member 10224
Myc proto-oncogene protein0102
Cathepsin D0101
DNA polymerase alpha catalytic subunit0101
Endothelin receptor type B1001
Endothelin-1 receptor1001
Cannabinoid receptor 10202
Alpha-glucosidase MAL120101
Nuclear factor NF-kappa-B p100 subunit 0101
N1L 0101
NAD(P)H dehydrogenase [quinone] 10004
Lysosomal alpha-glucosidase0101
Transient receptor potential cation channel subfamily A member 10213
Chain A, PLASMA RETINOL-BINDING PROTEIN PRECURSOR0011
Beta-lactoglobulin0011
Chain A, 6,7-Dimethyl-8-ribityllumazine Synthase0011
Chain B, 6,7-Dimethyl-8-ribityllumazine Synthase0011
Chain H, Immunoglobulin Igg1 Heavy chain0011
Chain L, Immunoglobulin Igg1 Lambda Light Chain0011
Chain A, DODECIN0011
Chain A, DODECIN0011
Chain C, DODECIN0011
Chain E, DODECIN0011
NPYLR7B0011
Chain A, Lysr-type Regulatory Protein0011
Chain A, Lysr-type Regulatory Protein0011
Chain A, Lysr-type Regulatory Protein0011
Chain A, 146aa long hypothetical transcriptional regulator0011
Chain A, Anthranilate phosphoribosyltransferase0101
Chain A, Anthranilate phosphoribosyltransferase0101
Chain A, Anthranilate phosphoribosyltransferase0101
Chain B, Anthranilate phosphoribosyltransferase0101
Chain C, Anthranilate phosphoribosyltransferase0101
Chain A, Anthranilate phosphoribosyltransferase0101
Anthranilate phosphoribosyltransferase0101
5'-AMP-activated protein kinase subunit beta-20001
Tyrosine-protein phosphatase YopH0101
Ubiquitin-like domain-containing CTD phosphatase 10101
5'-AMP-activated protein kinase subunit gamma-30001
5'-AMP-activated protein kinase subunit beta-10001
Chain A, Erk20101
Mitogen-activated protein kinase 20101
Mitogen-activated protein kinase 14 0112
Mitogen-activated protein kinase 10101
P2X purinoceptor 70101
P2X purinoceptor 70101
Sterol O-acyltransferase 20101
Tyrosine-protein phosphatase 10101
Pyruvate kinase PKLR0101
Neuraminidase0101
Class A sortase SrtA 0101
photoreceptor-specific nuclear receptor0101
3-hydroxy-3-methylglutaryl-coenzyme A reductase0202
Insulin receptor 0101
3-hydroxy-3-methylglutaryl-coenzyme A reductase 0101
3-hydroxy-3-methylglutaryl-coenzyme A reductase0101
Cholecystokinin receptor type A0101
Cholecystokinin receptor type A0202
Gastrin/cholecystokinin type B receptor0112
Gastrin/cholecystokinin type B receptor0224
Gastrin/cholecystokinin type B receptor0202
Cholecystokinin receptor type A0202
Eukaryotic translation initiation factor 4E0011
Peptidyl-prolyl cis-trans isomerase FKBP1A0101
Peptidyl-prolyl cis-trans isomerase FKBP1B0022
Peptidyl-prolyl cis-trans isomerase FKBP50202
Programmed cell death protein 40011
Serine/threonine-protein kinase mTOR 0101
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, Mitogen-activated protein kinase 140011
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
Chain A, VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 20101
melanocortin receptor 40112
Platelet-derived growth factor receptor beta0202
Cyclin-C0112
Serine/threonine-protein kinase B-raf 0101
Vascular endothelial growth factor receptor 30101
Vascular endothelial growth factor receptor 20101
5-hydroxytryptamine receptor 5A0101
Vascular endothelial growth factor receptor 20101
RuvB-like 20112
RuvB-like 10101
C-X-C chemokine receptor type 5 isoform 10101
ubiquitin-conjugating enzyme E2 N0202
C-C chemokine receptor type 60101
bcl-2-related protein A10101
Endoglycoceramidase II 0001
Protein kinase C alpha type0303
Protein kinase C delta type0303
Protein kinase C epsilon type0303
Protein kinase C zeta type0303
cAMP-dependent protein kinase catalytic subunit alpha 0101
Protein kinase C gamma type0303
Protein kinase C beta type0303
Protein kinase C eta type0303
Sphingosine kinase 20101
Sphingosine kinase 10101
Protein kinase C theta type0303
Chain A, Mineralocorticoid receptor0101
Chain A, Mineralocorticoid receptor0101
Retinoic acid receptor alpha0238
Retinoic acid receptor beta0238
Chain A, Ribosomal protein S6 kinase alpha-10101
Chain X, Tyrosine-protein kinase Lyn0101
Chain A, Dual specificity protein kinase TTK0011
Chain A, Dual specificity protein kinase TTK0011
Mast/stem cell growth factor receptor Kit0101
Translocator protein0101
Beta-adrenergic receptor kinase 10101
Platelet-derived growth factor receptor alpha 0101
G protein-coupled receptor kinase 50101
Cyclin-dependent kinase 100011
Bromodomain-containing protein 90011
Bromodomain-containing protein 70011
Substance-P receptor0202
Neuromedin-K receptor0011
Substance-K receptor0112
Substance-P receptor0415
Neuromedin-K receptor0112
Substance-K receptor0101
Substance-K receptor0101
Growth hormone secretagogue receptor type 10011
Mas-related G-protein coupled receptor member X20011
Chain A, MALTOPORIN0011
Chain B, MALTOPORIN0011
Transcription regulator protein BACH10101
Transcription factor MafK 0101
NAD0001
Kelch-like ECH-associated protein 10123
Nuclear factor erythroid 2-related factor 20001
Kelch-like ECH-associated protein 10001
Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform0202
Splicing factor 3B subunit 30202
Chain A, CES1 protein0101
Lysosomal acid glucosylceramidase0011
Transcriptional activator protein LuxR0101
B2 bradykinin receptor0202
Melanocortin receptor 40202
C-8 sterol isomerase0202
Melanocortin receptor 30202
Phospholipase D1 0101
Platelet-activating factor acetylhydrolase0101
Phospholipase D10101
3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase0314
Emopamil-binding protein-like0202
7-dehydrocholesterol reductase0112
Corticotropin releasing hormone receptor 20101
Lysine-specific demethylase 6B0101
Lysine-specific demethylase 4B0101
ATP-dependent molecular chaperone HSP820101
ATP-dependent molecular chaperone HSC820101
Lysine-specific demethylase 5A0101
Endoplasmin0112
Heat shock protein 75 kDa, mitochondrial0101
Heat-shock protein0101
Putative heat shock protein HSP 90-alpha A40101
Lysine-specific demethylase 4C0101
Cocaine esterase0101
Polycomb protein SUZ120101
Histone-lysine N-methyltransferase EZH20101
Sodium/bile acid cotransporter0001
Ileal sodium/bile acid cotransporter0101
Bile acid receptor0011
Bile salt export pump0001
estrogen receptor beta isoform 10101
tyrosine-protein phosphatase non-receptor type 7 isoform 20101
Tetracycline resistance protein, class B0001
Multidrug transporter MdfA0101
Chain A, Multidrug-efflux Transporter 1 Regulator Bmrr0011
DNA-binding protein Ikaros0001
DNA damage-binding protein 10112
Cytochrome P450 2B10101
Alcohol dehydrogenase E chain0101
Alcohol dehydrogenase S chain0101
Urease subunit alpha0101
Urease subunit beta 0101
Thymidine phosphorylase0001
Thymidine kinase, cytosolic 0002
Thymidine kinase 0102
Sterol O-acyltransferase 10101
Thymidine kinase0001
Thymidine kinase 2, mitochondrial0101
Thymidine kinase0101
Deoxynucleoside kinase0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain B, Odorant-binding Protein0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain A, ODORANT-BINDING PROTEIN0101
Chain A, ODORANT-BINDING PROTEIN0101
Secreted chorismate mutase0101
Heat sensitive channel TRPV30011
Transient receptor potential cation channel subfamily M member 80112
Chain A, Tyrosine-protein kinase0101
Chain A, Tyrosine-protein kinase0101
Chain A, Tyrosine-protein kinase JAK20101
Serine/threonine-protein kinase Sgk10101
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial0101
Tyrosine-protein kinase JAK30101
Tyrosine-protein kinase JAK20101
Tyrosine-protein kinase JAK30101
MSH0001
Hematopoietic prostaglandin D synthase0101
NACHT, LRR and PYD domains-containing protein 3 0101
Transient receptor potential cation channel subfamily V member 20101
Chain A, Nuclear Receptor ROR-beta0101
Nuclear receptor ROR-alpha0101
Nuclear receptor ROR-beta0101
procathepsin L isoform 1 preproprotein0101
Chain A, HDLP (HISTONE DEACETYLASE-LIKE PROTEIN)0101
Chain B, HDLP (HISTONE DEACETYLASE-LIKE PROTEIN)0101
Chain A, Histone deacetylase 7a0101
Chain A, Histone deacetylase 7a0101
Histone deacetylase 80101
Histone deacetylase 0101
Lysine-specific demethylase 4E0101
unnamed protein product0001
Histone deacetylase 10202
5-hydroxytryptamine receptor 3A0101
Histone deacetylase 30101
Adenosine receptor A10101
Histone deacetylase 20101
Histone deacetylase 10101
Adenosine receptor A10101
Histone deacetylase 0101
Histone deacetylase 40101
Polyamine deacetylase HDAC100101
Histone deacetylase 30101
Histone deacetylase-like amidohydrolase0202
Histone deacetylase 70101
Histone deacetylase 80101
Histone deacetylase 110101
HD2 type histone deacetylase HDA106 0202
Histone deacetylase 90101
Histone deacetylase 70101
Histone deacetylase 6 0101
Histone deacetylase 40101
Histone deacetylase 0101
Histone deacetylase 60101
Histone deacetylase 50101
Histone deacetylase 0101
NADPH oxidase 10101
Snq2p0001
Ubiquitin carboxyl-terminal hydrolase 10101
Trypanothione reductase0202
Pleiotropic ABC efflux transporter of multiple drugs0102
Calcium-dependent protein kinase 40101
WD repeat-containing protein 480101
Muscarinic acetylcholine receptor M40011
Muscarinic acetylcholine receptor M50011
Forkhead box protein M10202
ATP-binding cassette sub-family C member 80101
ATP-sensitive inward rectifier potassium channel 110101
UDP-glucuronosyltransferase 1A100001
Glycoprotein0101
Catechol O-methyltransferase0101
Potassium voltage-gated channel subfamily A member 30101
Chloroquine resistance transporter0101
Ubiquitin carboxyl-terminal hydrolase isozyme L10101
Ubiquitin carboxyl-terminal hydrolase 50202
Ubiquitin carboxyl-terminal hydrolase 40101
Sentrin-specific protease 10202
Sterol 14-alpha-demethylase0011
14-alpha sterol demethylase 0011
Cholesterol side-chain cleavage enzyme, mitochondrial 0011
Lanosterol 14-alpha demethylase0011
Sterol 14-alpha demethylase0011
14-alpha sterol demethylase 0011
14-alpha sterol demethylase 0011
Cholesterol 24-hydroxylase0213
Hsf1 protein0011
Chain E, cAMP-dependent protein kinase, alpha-catalytic subunit0101
Chain I, cAMP-dependent protein kinase inhibitor, alpha form0101
Chain B, Rho-associated protein kinase 10101
Chain A, Rho-associated protein kinase 10101
Chain A, Rho-associated protein kinase 10101
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0101
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0101
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0101
Chain I, cAMP-dependent protein kinase inhibitor alpha0101
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0101
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit0101
Chain I, cAMP-dependent protein kinase inhibitor alpha0101
Chain A, Rho-associated protein kinase 10101
cAMP-dependent protein kinase catalytic subunit alpha0101
cAMP-dependent protein kinase catalytic subunit alpha 0101
C-C motif chemokine 20101
Rho-associated protein kinase 20101
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]