cysteine has been researched along with Genetic Predisposition in 119 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 5 (4.20) | 18.2507 |
| 2000's | 80 (67.23) | 29.6817 |
| 2010's | 31 (26.05) | 24.3611 |
| 2020's | 3 (2.52) | 2.80 |
| Authors | Studies |
|---|---|
| Chakraborty, A; Datta, K; Goswami, R; Majumdar, KK; Pramanik, S; Saha, D; Sikdar, N | 1 |
| Abedi, V; Griessenauer, CJ; Hack, RJ; Khan, A; Lesnik Oberstein, SAJ; Li, J; Person, TN; Rutten, JW; Zand, R | 1 |
| Battini, R; Catania, A; Chiapparini, ML; Garavaglia, B; Ghezzi, D; Nardocci, N; Pasquariello, R; Pippucci, T; Seri, M; Tiranti, V; Zorzi, G | 1 |
| Kumar, P; Rai, V | 1 |
| Hua-Lei, L; Jing, C; Li, Z; Qian-Wei, X; Weng-Guang, L; You, W; Yu-Ping, Z | 1 |
| Tao, S; Wang, M; Wang, W; Zhang, J; Zhang, P; Zhou, J | 1 |
| Frolov, SA; Karpukhin, AV; Kashnikov, VN; Liubchenko, LN; Muzaffarova, TA; Pospekhova, NI; Shelygin, IuA; Shubin, VP; Tsukanov, AC | 1 |
| Chen, YB; Frizzell, N; Garg, K; Karamurzin, Y; Nonaka, D; Reyes, C; Soslow, RA | 1 |
| Barbon, G; Casonato, A; Cattini, GM; Daidone, V; Gallinaro, L; Pizzo, P; Pontara, E; Zampese, E | 1 |
| Benito-Vicente, A; Etxebarria, A; Martin, C; Ostolaza, H; Palacios, L; Stef, M | 1 |
| Bienvenu, T; Burgel, PR; Chapron, J; Dusser, D; Gaitch, N; Génin, E; Girodon, E; Honoré, I; Hubert, D; Kanaan, R; Martinez, B; Viel, M | 1 |
| González-Sarmiento, R; Hernández-Martín, A | 1 |
| Frizzell, N; Garg, K; Joseph, NM; Rabban, JT; Solomon, DA; Zaloudek, C | 1 |
| Buelow, B; Cohen, J; Frizzell, N; Garg, K; Joseph, NM; McCalmont, T; Nagymanyoki, Z | 1 |
| Faas, MM; Holwerda, KM; Lely, AT; Nolte, IM; Staff, AC; van Goor, H; Weedon-Fekjær, MS | 1 |
| Brunton, JA; Nosworthy, MG | 1 |
| He, Z; Huang, Z; Liu, S; Liu, X; Wang, Z; Wu, Y; Zhou, J | 1 |
| Ji, L; Jin, F; Qu, Y; Sun, H; Sun, L; Wang, B; Wang, L; Yang, Z; Zhang, C | 1 |
| Cannas, A; Corongiu, D; Cuccu, S; Floris, G; Marrosu, F; Marrosu, MG; Murru, MR; Rolesu, M; Sardu, C; Solla, P; Tranquilli, S | 1 |
| Bertolino, A; Blasi, G; Caforio, G; Callicott, JH; Di Giorgio, A; Gambi, F; Kolachana, B; Latorre, V; Nardini, M; Papazacharias, A; Popolizio, T; Rampino, A; Rizzo, M; Romano, R; Sambataro, F; Weinberger, DR | 1 |
| Gros, P; LaCourse, R; Marquis, JF; North, RJ; Ryan, L | 1 |
| Hagino, H; Kawasaki, Y; Kobayashi, S; Kurachi, M; Maeno, N; Niu, L; Ozaki, N; Sasaoka, T; Seto, H; Suzuki, M; Takahashi, T; Tsuneki, H; Tsunoda, M; Zhou, SY | 1 |
| Cavarra, E; De Cunto, G; Fineschi, S; Giustarini, D; Lungarella, G; Rossi, R | 1 |
| Wu, G; Yan, S | 1 |
| Daimon, M; Jimbu, Y; Kameda, W; Karasawa, S; Kato, T; Kawata, S; Kubota, I; Muramatsu, M; Oizumi, T; Susa, S; Toriyama, S; Wada, K | 1 |
| Mazzei, R; Quattrone, A | 1 |
| Broderick, P; Chandler, I; Houlston, RS; Lubbe, S; Penegar, S; Pittman, AM; Twiss, P | 1 |
| Ganz, T; Nemeth, E; Phatak, PD; Sham, RL | 1 |
| Hogan, KJ; Vladutiu, GD | 1 |
| Aoyagi, Y; Kato, K; Metoki, N; Nozawa, Y; Oguri, M; Satoh, K; Watanabe, S; Yamada, Y; Yokoi, K; Yoshida, H; Yoshida, T | 1 |
| Hida, T; Hosono, S; Ito, H; Kawase, T; Matsuo, K; Mitsudomi, T; Okasaka, T; Suzuki, T; Tajima, K; Tanaka, H; Watanabe, M; Yatabe, Y; Yokoi, K | 1 |
| España-Serrano, L; Hoenicka, J; Huertas, E; Jiménez-Arriero, MA; Koeneke, MA; Palomo, T; Poch, C; Ponce, G | 1 |
| Blasiak, J; Janik-Papis, K; Kaczmarczyk, D; Morawiec-Sztandera, A; Olszewski, J; Pawlowska, E; Rydzanicz, M; Szyfter, K; Zuk, K | 1 |
| Cruchaga, C; Gitcho, MA; Goate, A; Robberecht, W; Seijo-Martínez, M; Van Damme, P; Vidal, JM; Wang, J; Wang, L; Wu, JY | 1 |
| Busto, UE; Kennedy, JL; Yasseen, B; Zawertailo, LA | 1 |
| Bonafé, L; Brenner, RE; Hinrichs, T; Mattes, T; Scheiderer, WD; Superti-Furga, A | 1 |
| Adhikari, A; Bozinoski, M; Gordon, JA; Nason, MW; Role, LW | 1 |
| Chan, LC; Chan, NP; Chan, TL; Fan, YH; Lam, CW; Lam, WW; Leung, TW; Liu, HS; Siu, DY; Wong, KS; Yip, SF | 1 |
| Defesche, JC; Hollak, CE; Holleboom, AG; Hovingh, GK; Kastelein, JJ; Kuivenhoven, JA; Levels, JH; Peter, J; Schimmel, AW; Stroes, ES; Valentijn, RM; van Olden, CC; Vos, P | 1 |
| Haffty, BG; Jiang, L; Li, X; Liang, F; Ma, T; Moran, MS; Tao, K; Yan, S; Yang, Q; Yuan, C; Zhang, N | 1 |
| Ademoğlu, E; Doğru-Abbasoğlu, S; Erbil, Y; Karadağ, B; Ozderya, A; Tanrikulu, S; Uysal, M | 1 |
| Asproudis, I; Bagli, E; Georgiou, I; Giannopoulos, S; Kostoulas, C; Kyritsis, AP; Markoula, S; Nikas, A | 1 |
| Brantley, MA; Cai, J; Li, C; Lu, P; Milne, GL; Osborn, MP; Rezaei, KA; Sanders, BJ; Sternberg, P | 1 |
| Cho, AR; Cho, JW; Ki, CS; Kim, HT; Kim, JS; Lee, WY; Shin, H | 1 |
| Daina, E; Iatropoulos, P; Maranta, R; Mele, C; Noris, M; Remuzzi, G | 1 |
| Campolo, J; Cozzi, L; De Maria, R; Marocchi, A; Parodi, O; Parolini, M; Patrosso, MC; Penco, S | 1 |
| Aguilar-Salinas, CA; Cobos-Bonilla, M; Medina-Santillan, R; Mehta, R; Muñoz-Hernandez, LL; Ordoñez-Sanchez, ML; Ramírez-Márquez, MR; Tusie-Luna, MT | 1 |
| Chiang, AN; Chiang, SC; Chou, SC; Lai, ST; Pan, JP | 1 |
| Gaertner, I; Koehnke, AM; Koehnke, MD; Kolb, W; Lutz, U; Schick, S; Willecke, M | 1 |
| Akahoshi, M; Harada, M; Inoue, Y; Miyake, K; Nakashima, H; Okada, K; Otsuka, T; Shimizu, S; Tanaka, Y | 1 |
| Ahn, SH; Choe, KJ; Choi, JY; Hamajima, N; Han, W; Hirvonen, A; Kang, D; Kim, SU; Lee, KM; Noh, DY; Park, SK; Tajima, K; Yoo, KY; Yoon, KS | 1 |
| Abyholm, FE; Drevon, CA; Jugessur, A; Lie, RT; Murray, JC; Taylor, JA; Ulvik, A; Vindenes, HA; Wilcox, AJ | 1 |
| Ergül, E; Güzelhan, Y; Kara, I; Kaya, G; Sazci, A | 1 |
| Ammar, N; Amouri, R; Barisić, N; Ceuterick, C; De Jonghe, P; Hentati, F; Martin, JJ; Merlini, L; Nelis, E; Timmerman, V | 1 |
| Guo, Y; Han, H; Li, H; Li, T; Liu, X; Ma, C; Shi, J; Tang, M; Wang, Y; Zhang, S; Zhao, J | 1 |
| Corfield, VA; Hemmings, SM; Kinnear, CJ; Knowles, JA; Lochner, C; Moolman-Smook, JC; Niehaus, DJ; Stein, DJ | 1 |
| Cheng, Z; Ding, J; Jiang, X; Lin, R; Lu, X; Turdi, J; Wang, S; Wang, X; Wen, H; Wu, G | 1 |
| Leino-Arjas, P; Luoma, K; Raininko, R; Riihimäki, H; Saarela, J; Solovieva, S | 1 |
| Cha, JH; Choi, MJ; Ham, BJ; Han, CS; Lee, HJ; Lee, MS; Lee, SH; Ryu, SH | 1 |
| Shizuka, K; Yoneda, H | 1 |
| Agosti, C; Akkawi, N; Archetti, S; Borroni, B; Brambilla, C; Caimi, L; Caltagirone, C; Di Luca, M; Padovani, A | 1 |
| Heikkinen, K; Karppinen, SM; Rapakko, K; Winqvist, R | 1 |
| Deng, G; He, F; Li, S; Li, X; Li, Y; Qiang, B; Shen, Y; Wang, Y; Yao, Z; Zhai, Y; Zhang, R; Zhou, G | 1 |
| Chong, B; Fawkner, M; Hegde, M; Skinner, JR; Webster, DR | 1 |
| Aronson, M; Cleary, SP; Cotterchio, M; Croitoru, ME; Di Nicola, N; Gallinger, S; Gryfe, R; Knight, J; Manno, M; Redston, M; Selander, T | 1 |
| Cabrera, W; Dragani, TA; Falvella, FS; Galbiati, F; Galvan, A; Ibanez, O; Mancuso, MT; Manenti, G; Pazzaglia, S; Pignatiello, C; Saran, A; Spinola, M; Zaffaroni, D | 1 |
| Ignatius, J; Kääriäinen, H; Körkkö, J; Löppönen, T; Lundan, T; Seppänen, U | 1 |
| Heils, A; Hempelmann, A; Höfels, S; Lenzen, KP; Lohoff, FW; Lorenz, S; Sander, T; Schmitz, B | 1 |
| Broich, P; Evert, BO; Fliessbach, K; Hans, VH; Kimonis, V; Mehta, SG; Pauls, K; Schröder, R; Thal, DR; Watts, GD | 1 |
| Beck, SR; Bowden, DW; Burdon, KP; Freedman, BI; Langefeld, CD; Liu, Y; Rich, SS; Wagenknecht, LE | 1 |
| Bolton-Maggs, PH; Bowen, DJ; Collins, PW; Cumming, AM; Enayat, SM; Grundy, P; Hill, FG; Keeling, DM; Keeney, S; Khair, K; Lester, W; Pasi, KJ; Tait, RC; Wilde, JT | 1 |
| Gauthier, S; Gros, P; Malo, D; Mullick, A; Tuite, A; Turcotte, K | 1 |
| Kaji, R; Kawakami, H; Kuno, S; Nishimura, M | 1 |
| Bardsley, V; Fellows, IW; Jennings, BA; Lonsdale, R; Willis, G; Wimperis, JZ | 1 |
| Elikowski, W; Kwaśnikowski, P; Lewandowski, K; Rzeźniczak, M; Swierczyńska, A | 1 |
| Cremonini, F; Saito, YA; Talley, NJ | 1 |
| Csanády, M; Sepp, R | 1 |
| Dávid, M; Habon, T; Keszthelyi, Z; Kovács, N; Losonczy, H; Nagy, A; Tóth, O | 1 |
| Hamanaka, Y; Hashimoto, T; Hinoda, Y; Imate, Y; Okayama, N; Suehiro, Y; Uchida, K; Ueyama, Y; Yamashita, H | 1 |
| Beloqui, O; Belzunce, MS; Orbe, J; Páramo, JA; Rodriguez, JA; Roncal, C | 1 |
| Buyan, N; Gönen, S; Hasanoğlu, E; Kalman, S; Misirlioğlu, M; Ozkaya, O; Söylemezoğlu, O; Tuncer, S | 1 |
| Distante, S | 1 |
| Hamanaka, Y; Hasui, Y; Hinoda, Y; Okayama, N; Shinozaki, F; Suehiro, Y; Ueyama, Y | 1 |
| Abraham, SC; Adams, LA; Angulo, P; Brandhagen, D; Torgerson, H | 1 |
| Cooper, J; Humphries, SE; Kitchen, N; Montgomery, H; Morgan, L | 1 |
| Arias Vásquez, A; Coebergh, JW; González-Zuloeta Ladd, AM; Hofman, A; Stricker, BH; Uitterlinden, AG; van Duijn, CM; Witteman, J | 1 |
| Abe, LM; Carlson, KM; Carpenter, C; Hsia, YE; Marchuk, DA; Perry, AK; Person, DA; Raney, EM; Reinker, KA; Yamaga, KM | 1 |
| Browndyke, J; Ghio, A; Schmechel, DE | 1 |
| Hansen, RD; Overvad, K; Raaschou-Nielsen, O; Sørensen, M; Tjønneland, A; Vogel, U | 1 |
| Boronow, J; Dickerson, F; Origoni, A; Stallings, C; Yolken, R | 1 |
| Burdick, KE; DeRosse, P; Goldman, D; Hodgkinson, CA; Kane, JM; Lencz, T; Malhotra, AK | 1 |
| Houlston, RS; Hubner, RA | 1 |
| Ce, B; Hu, Y; Huang, J; Jiao, X; Luo, C; Lv, M; Su, X; Wu, S | 1 |
| Alenda, C; Andreu, M; Balaguer, F; Bessa, X; Carracedo, A; Castells, A; Castellví-Bel, S; de Cid, R; Gonzalo, V; Jover, R; Llor, X; Muñoz, J; Payá, A; Piqué, JM; Pons, E; Ruiz-Ponte, C; Xicola, RM | 1 |
| Bacci, A; Carlesi, C; Coppedè, F; Lo Gerfo, A; Mancuso, M; Micheli, D; Migliore, L; Murri, L; Nesti, C; Petrozzi, L; Piazza, S; Rocchi, A; Siciliano, G | 1 |
| Assimos, DG; Cantor, DA; Haleblian, GE; Preminger, GM; Sur, RL | 1 |
| Jiang, J; Jin, C; Shentu, X; Tang, X; Wu, R; Yao, K | 1 |
| Alonso, A; Castillo, J; Cayon, A; Monton, F; Oterino, A; Pascual, J; Ruiz-Alegria, C; Ruiz-Lavilla, N; Valle, N | 1 |
| Bowen, G; Cannon-Albright, LA; Chen, W; Eliason, MJ; Florell, SR; Hansen, CB; Harris, RM; Hart, M; Leachman, SA; Porter-Gill, P; Sturm, RA; Swinyer, L | 1 |
| Algar, U; Blokhuis, MM; Goldberg, PA; Govender, D; Pietersen, GE; Ramesar, RS; Vorster, AA | 1 |
| Beppu, Y; Chuman, H; Hirose, H; Kawai, A; Masutani, M; Morioka, H; Nakatani, F; Nakayama, R; Ogino, H; Ohta, T; Sakamoto, H; Sato, Y; Sugimura, H; Toyama, Y; Yabe, H; Yoshida, T | 1 |
| Freiberg, JJ; Jensen, GB; Nordestgaard, BG; Sillesen, H; Tybjaerg-Hansen, A | 1 |
| Anfossi, M; Bernardi, L; Bruni, AC; Colao, R; Costanzo, A; Curcio, SA; Frangipane, F; Gallo, M; Geracitano, S; Iapaolo, D; Maletta, RG; Mirabelli, M; Puccio, G; Smirne, N; Tomaino, C | 1 |
| Faraone, SV; Glatt, SJ; Hwu, HG; Kanazawa, T; Lasky-Su, JA; Tsuang, MT | 1 |
| Goicoechea de Jorge, E; Gomà, M; Montes, T; Pujol, O; Ramos, R; Rodríguez de Córdoba, S; Sánchez-Corral, P | 1 |
| Franz, P; Frey, UH; Grehl, S; Jahnke, K; Lang, S; Lehnerdt, GF; Schmid, KW; Schmitz, KJ; Siffert, W; Zaqoul, A | 1 |
| Hamaguchi, M; Kagami, K; Katsumi, A; Kojima, T; Okamoto, Y; Saito, H; Sugiura, I; Takamatsu, J; Yamazaki, T | 1 |
| Bertina, RM; Landolfi, R; Poort, SR | 1 |
| Ellard, S; Frayling, T; Grove, J; Hattersley, AT; Walker, M | 1 |
| Baeder, S; Baur, C; Calzia, E; Eichinger, HM; Froeba, G; Georgieff, M; Marx, T; Pazhur, J; Radermacher, P | 1 |
| Baba, S; Gao, C; Genka, K; Igarashi, H; Iwamasa, T; Kohno, T; Li, Z; Lum, JK; Martinson, JJ; Morris, BJ; Nagura, K; Ohno, Y; Sawaguchi, T; Shinmura, K; Sugimura, H; Tajima, K; Takezaki, T; Tsugane, S; Varga, T; Wakai, K; Wang, J; Yokota, J | 1 |
| Lilli, R; Lorenzi, C; Serretti, A; Smeraldi, E | 1 |
| Rozen, R | 1 |
| Lin, DX; Song, N; Tan, W; Xing, DY | 1 |
| Amarenco, P; Arveiler, D; Cambien, F; Elbaz, A; Evans, A; Gariepy, J; Grandchamp, B; Hetet, G; Kee, F; Morrison, C; Nicaud, V; Simon, A | 1 |
| Adolfsson, R; Blackwood, D; Blairy, S; Del Favero, J; Dikeos, DG; Kaneva, R; Lerer, B; Lilli, R; Macciardi, F; Massat, I; Mendlewicz, J; Milanova, V; Muir, W; Noethen, M; Oruc, L; Papadimitriou, GN; Petrova, T; Rietschel, M; Segman, RH; Serretti, A; Souery, D; Van Broeckhoven, C; Van Gestel, S | 1 |
| De Bie, S; De Paepe, A; De Vos, M; Delanghe, JR; Leroux-Roels, G; Messiaen, L; Praet, M; Van Vlierberghe, H | 1 |
| Beutler, E; Felitti, V; Gelbart, T; Ho, NJ; Waalen, J | 1 |
14 review(s) available for cysteine and Genetic Predisposition
| Article | Year |
|---|---|
Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19.
Topics: Actin Cytoskeleton; Actins; Adaptor Proteins, Signal Transducing; Adenocarcinoma; Adenosine Triphosphate; Adsorption; Adult; Africa, Eastern; Aged; Air Pollutants; Air Pollution; Air Pollution, Indoor; Alcohol Drinking; Allergens; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Animals; Anti-Bacterial Agents; Antibodies; Antibodies, Immobilized; Antigen Presentation; Antigens, CD; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Apoptosis; Aptamers, Nucleotide; Asthma; Asthma, Exercise-Induced; Atrophy; Autophagy; Azoospermia; Bacillus cereus; Bacterial Infections; Beclin-1; Bile Duct Neoplasms; Bile Ducts, Intrahepatic; Biofouling; Biological Monitoring; Biomarkers; Biomarkers, Tumor; Biosensing Techniques; Blastocyst; Bone Neoplasms; Bone Regeneration; Bronchoconstriction; Burkitt Lymphoma; C9orf72 Protein; Campylobacter; Campylobacter Infections; Campylobacter jejuni; Carcinogenesis; Carcinoma, Hepatocellular; Carcinoma, Pancreatic Ductal; Carcinoma, Squamous Cell; Cardiomyopathies; Caregivers; Carmine; Case-Control Studies; Catalysis; Cattle; Cause of Death; CCAAT-Enhancer-Binding Protein-alpha; CD8-Positive T-Lymphocytes; Cefepime; Cell Differentiation; Cell Line, Tumor; Cell Nucleus; Cell Transdifferentiation; Chelating Agents; Chemical and Drug Induced Liver Injury, Chronic; Chemoradiotherapy, Adjuvant; Child; Child, Preschool; China; Chlorquinaldol; Cholangiocarcinoma; Cholera; Chromatin; Clinical Trials as Topic; Cognitive Dysfunction; Cohort Studies; Colonic Neoplasms; Colorectal Neoplasms; Colorimetry; Cooking; Coordination Complexes; COVID-19; Creatinine; CRISPR-Cas Systems; Critical Care; Critical Illness; Cross-Sectional Studies; Cryopreservation; Cryoprotective Agents; Cysteine; Cytokines; Device Removal; Diet; Diet, High-Fat; Diet, Mediterranean; Dietary Supplements; Dimethyl Sulfoxide; Dipeptides; Disease Models, Animal; Dithiothreitol; DNA; DNA Repeat Expansion; DNA, Bacterial; DNA, Complementary; Dopamine; Electrochemical Techniques; Electrodes; Endocannabinoids; Environmental Exposure; Environmental Monitoring; Environmental Pollutants; Enzyme-Linked Immunosorbent Assay; Erlotinib Hydrochloride; Escherichia coli; Escherichia coli O157; Esophageal Neoplasms; Esophagitis, Peptic; Ethylene Glycol; Europium; Exanthema; Fallopian Tubes; Feces; Female; Fertilization in Vitro; Fluoresceins; Fluorescent Dyes; Follicle Stimulating Hormone; Follow-Up Studies; Food Microbiology; Forced Expiratory Volume; Forkhead Transcription Factors; Frontotemporal Dementia; G-Quadruplexes; Galactose; Gastroenteritis; Gastrointestinal Diseases; Gastrointestinal Microbiome; Gastrointestinal Neoplasms; Gastrointestinal Tract; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genital Neoplasms, Female; Genome-Wide Association Study; Genome, Viral; Genomics; Genotype; Glucose; Glutathione; Glycerol; Gold; Graphite; GTPase-Activating Proteins; Heat-Shock Proteins; Heme Oxygenase-1; Hepacivirus; Hepatitis C; Hepatocytes; Histamine; Histocompatibility Antigens Class II; Hoarseness; Hospice and Palliative Care Nursing; Humans; Hydrogen; Hydrogen Peroxide; Hydrogen Sulfide; Hydroxybenzoates; Hydroxyl Radical; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hyperthermia, Induced; Hysteroscopy; Immunoassay; Indigo Carmine; Inflammation; Inflammatory Bowel Diseases; Insulin Resistance; Intensive Care Units; Interleukin-11; Interleukin-6; Interleukins; Iodine Radioisotopes; Iran; Iridium; Islets of Langerhans; Kinetics; Lactation; Lactobacillus; Lactobacillus plantarum; Lamins; Latin America; Lead; Lectins; Leukopenia; Ligands; Limit of Detection; Lipopolysaccharides; Lipoprotein Lipase; Liver; Liver Cirrhosis; Liver Neoplasms; Lolium; Luminescent Measurements; Luminol; Lung; Luteinizing Hormone; Macrophages; Magnetic Phenomena; Magnetic Resonance Imaging; Male; Malnutrition; Maltose; Manganese Compounds; Maternal Nutritional Physiological Phenomena; Melatonin; Metabolic Engineering; Metal Nanoparticles; Metallocenes; Metaplasia; Methicillin-Resistant Staphylococcus aureus; Methylation; Mevalonic Acid; Mexico; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microbial Sensitivity Tests; Microbiota; MicroRNAs; Milk; Mitomycin; Molecular Diagnostic Techniques; Molecular Docking Simulation; Monte Carlo Method; Moringa oleifera; Multiple Sclerosis; Muscle Strength; Muscle, Skeletal; Nanocomposites; Nanotubes, Carbon; Neoadjuvant Therapy; Neoplasms; Neurodegenerative Diseases; Neurotransmitter Agents; NF-E2-Related Factor 2; Nickel; Nitrogen Dioxide; Non-alcoholic Fatty Liver Disease; Nucleic Acid Amplification Techniques; Nucleic Acid Hybridization; Nucleocapsid Proteins; Nutritional Status; Obesity; Osteogenesis; Osteosarcoma; Oxidation-Reduction; Oxides; Oxygen; Oxyquinoline; Pain; Palliative Care; Pancreatic Neoplasms; Pandemics; Particulate Matter; Peroxidase; Peroxidases; Phagocytosis; Phaseolus; Photothermal Therapy; Point-of-Care Systems; Polyethyleneimine; Polymers; Polymorphism, Single Nucleotide; Polysomnography; Postoperative Complications; Pregnancy; Pregnant Women; Prenatal Exposure Delayed Effects; Prevalence; Printing, Three-Dimensional; Probability; Probiotics; Prognosis; Prophages; Prospective Studies; Proteomics; Proto-Oncogene Proteins; Pseudomonas aeruginosa; Pseudomonas putida; Pulmonary Disease, Chronic Obstructive; Pulmonary Embolism; Pyridines; Pyrroles; Quality of Life; Quinolones; Rabbits; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; Real-Time Polymerase Chain Reaction; Receptors, Histamine; Receptors, Histamine H2; Recombinases; Rectal Neoplasms; Reperfusion Injury; Respiration; Respiratory Function Tests; Respiratory Rate; Respiratory Sounds; Retrospective Studies; rho GTP-Binding Proteins; Risk Assessment; Risk Factors; RNA; RNA, Messenger; RNA, Ribosomal, 16S; Robotic Surgical Procedures; Running; Rural Population; Saccharomyces cerevisiae; Salpingectomy; Sarcopenia; SARS-CoV-2; Seeds; Semen; Sensitivity and Specificity; Sepsis; Shock, Septic; Signal Transduction; Silicon Dioxide; Silver; Sirtuin 1; Skin Neoplasms; Sleep Apnea, Obstructive; Soil; Spain; Spectrum Analysis, Raman; Sperm Retrieval; Spermatozoa; Spirometry; Staphylococcus aureus; STAT3 Transcription Factor; Stereoisomerism; Sterilization, Tubal; Stroke Volume; Sulfadiazine; Sulfites; Superoxide Dismutase; Surface Plasmon Resonance; tau Proteins; Testis; Testosterone; Thioredoxin-Disulfide Reductase; Thyroid Neoplasms; Thyroidectomy; Trans-Activators; Transcription Factor AP-1; Treatment Outcome; Triazoles; Triclosan; Trifluridine; Tumor Microenvironment; Tumor Necrosis Factor-alpha; United States; Uracil; Vagina; Vegetables; Ventricular Function, Left; Ventricular Pressure; Vibrio cholerae; Vietnam; Virulence; Vital Capacity; Vitrification; Walking; Water; Water Pollutants, Radioactive; Whole Genome Sequencing; Wind; YAP-Signaling Proteins; Zeolites; Zinc Oxide | 2023 |
Methylenetetrahydrofolate reductase C677T polymorphism and susceptibility to epilepsy.
Topics: Cysteine; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2); Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Threonine | 2018 |
MTHFR C677T and A1298C polymorphisms were associated with bladder cancer risk and disease progression: a meta-analysis.
Topics: Alanine; Amino Acid Substitution; Carcinoma; Case-Control Studies; Cysteine; Disease Progression; Genetic Predisposition to Disease; Humans; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Urinary Bladder Neoplasms | 2013 |
A meta-analysis of the association between the hOGG1 Ser326Cys polymorphism and the risk of esophageal squamous cell carcinoma.
Topics: Aged; Alleles; Carcinoma, Squamous Cell; Case-Control Studies; Cysteine; DNA Glycosylases; Esophageal Neoplasms; Esophageal Squamous Cell Carcinoma; Esophagus; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Models, Genetic; Odds Ratio; Polymorphism, Genetic; Risk; Serine | 2013 |
Recent advances in congenital ichthyoses.
Topics: Administration, Topical; Cysteine; Dermatologic Agents; Gene Expression Regulation; Genes, Dominant; Genes, Recessive; Genetic Predisposition to Disease; Genetic Therapy; Humans; Ichthyosiform Erythroderma, Congenital; Mutation; Phenotype; Practice Guidelines as Topic; Randomized Controlled Trials as Topic | 2015 |
Lack of association between MTHFR A1298C variant and Alzheimer's disease: evidence from a systematic review and cumulative meta-analysis.
Topics: Alanine; Alzheimer Disease; Cysteine; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Single Nucleotide | 2017 |
[Outcome of genetic studies on atypical psychoses].
Topics: Chromosomes, Human, Pair 1; Cysteine; Genetic Predisposition to Disease; Haplotypes; Humans; Membrane Proteins; Microsatellite Repeats; Molecular Diagnostic Techniques; Mutation; Polymorphism, Genetic; Presenilin-1; Psychotic Disorders; Receptor, Serotonin, 5-HT2A; Receptors, Dopamine D2; Serine; Taq Polymerase | 2004 |
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1).
Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome | 2004 |
[The long QT syndrome from the bedside to molecular genetic laboratory. The history of the first described Hungarian family].
Topics: Cysteine; Electrocardiography; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Genetic Linkage; Genetic Predisposition to Disease; Humans; Hungary; Lod Score; Long QT Syndrome; Mutation, Missense; Pedigree; Tryptophan | 2005 |
[Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].
Topics: Adult; C-Reactive Protein; Cholesterol; Cysteine; Female; Fibrin; Genetic Predisposition to Disease; Homocysteine; Humans; Male; Pedigree; Plasminogen Activator Inhibitor 1; Polymorphism, Genetic; Risk Factors; Threonine; Thrombophilia; Thrombosis; Venous Thrombosis; von Willebrand Factor | 2005 |
Genetic predisposition to iron overload: prevalence and phenotypic expression of hemochromatosis-associated HFE-C282Y gene mutation.
Topics: Cysteine; Genetic Predisposition to Disease; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron Overload; Membrane Proteins; Mutation; Prevalence; Scandinavian and Nordic Countries; Tyrosine | 2006 |
MTHFR C677T and colorectal cancer risk: A meta-analysis of 25 populations.
Topics: Adult; Aged; Aged, 80 and over; Colorectal Neoplasms; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Incidence; Male; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Polymorphism, Genetic; Risk; Threonine | 2007 |
Genetic association study and meta-analysis of the HTR2C Cys23Ser polymorphism and migraine.
Topics: Adult; Amino Acid Substitution; Brain; Case-Control Studies; Chromosomes, Human, X; Cysteine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Humans; Male; Middle Aged; Migraine Disorders; Point Mutation; Polymorphism, Genetic; Receptor, Serotonin, 5-HT2C; Risk Factors; Serine; Serotonin | 2007 |
Genetic modulation of homocysteinemia.
Topics: Amino Acid Substitution; Cardiovascular Diseases; Cystathionine beta-Synthase; Cysteine; Folic Acid; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Methyltransferases; Mutation, Missense; Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Polymorphism, Genetic; Sulfur; Tetrahydrofolates | 2000 |
3 trial(s) available for cysteine and Genetic Predisposition
| Article | Year |
|---|---|
Effect of 12-week of aerobic exercise on hormones and lipid profile status in adolescent girls with polycystic ovary syndrome: A study during COVID-19.
Topics: Actin Cytoskeleton; Actins; Adaptor Proteins, Signal Transducing; Adenocarcinoma; Adenosine Triphosphate; Adsorption; Adult; Africa, Eastern; Aged; Air Pollutants; Air Pollution; Air Pollution, Indoor; Alcohol Drinking; Allergens; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Animals; Anti-Bacterial Agents; Antibodies; Antibodies, Immobilized; Antigen Presentation; Antigens, CD; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Apoptosis; Aptamers, Nucleotide; Asthma; Asthma, Exercise-Induced; Atrophy; Autophagy; Azoospermia; Bacillus cereus; Bacterial Infections; Beclin-1; Bile Duct Neoplasms; Bile Ducts, Intrahepatic; Biofouling; Biological Monitoring; Biomarkers; Biomarkers, Tumor; Biosensing Techniques; Blastocyst; Bone Neoplasms; Bone Regeneration; Bronchoconstriction; Burkitt Lymphoma; C9orf72 Protein; Campylobacter; Campylobacter Infections; Campylobacter jejuni; Carcinogenesis; Carcinoma, Hepatocellular; Carcinoma, Pancreatic Ductal; Carcinoma, Squamous Cell; Cardiomyopathies; Caregivers; Carmine; Case-Control Studies; Catalysis; Cattle; Cause of Death; CCAAT-Enhancer-Binding Protein-alpha; CD8-Positive T-Lymphocytes; Cefepime; Cell Differentiation; Cell Line, Tumor; Cell Nucleus; Cell Transdifferentiation; Chelating Agents; Chemical and Drug Induced Liver Injury, Chronic; Chemoradiotherapy, Adjuvant; Child; Child, Preschool; China; Chlorquinaldol; Cholangiocarcinoma; Cholera; Chromatin; Clinical Trials as Topic; Cognitive Dysfunction; Cohort Studies; Colonic Neoplasms; Colorectal Neoplasms; Colorimetry; Cooking; Coordination Complexes; COVID-19; Creatinine; CRISPR-Cas Systems; Critical Care; Critical Illness; Cross-Sectional Studies; Cryopreservation; Cryoprotective Agents; Cysteine; Cytokines; Device Removal; Diet; Diet, High-Fat; Diet, Mediterranean; Dietary Supplements; Dimethyl Sulfoxide; Dipeptides; Disease Models, Animal; Dithiothreitol; DNA; DNA Repeat Expansion; DNA, Bacterial; DNA, Complementary; Dopamine; Electrochemical Techniques; Electrodes; Endocannabinoids; Environmental Exposure; Environmental Monitoring; Environmental Pollutants; Enzyme-Linked Immunosorbent Assay; Erlotinib Hydrochloride; Escherichia coli; Escherichia coli O157; Esophageal Neoplasms; Esophagitis, Peptic; Ethylene Glycol; Europium; Exanthema; Fallopian Tubes; Feces; Female; Fertilization in Vitro; Fluoresceins; Fluorescent Dyes; Follicle Stimulating Hormone; Follow-Up Studies; Food Microbiology; Forced Expiratory Volume; Forkhead Transcription Factors; Frontotemporal Dementia; G-Quadruplexes; Galactose; Gastroenteritis; Gastrointestinal Diseases; Gastrointestinal Microbiome; Gastrointestinal Neoplasms; Gastrointestinal Tract; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genital Neoplasms, Female; Genome-Wide Association Study; Genome, Viral; Genomics; Genotype; Glucose; Glutathione; Glycerol; Gold; Graphite; GTPase-Activating Proteins; Heat-Shock Proteins; Heme Oxygenase-1; Hepacivirus; Hepatitis C; Hepatocytes; Histamine; Histocompatibility Antigens Class II; Hoarseness; Hospice and Palliative Care Nursing; Humans; Hydrogen; Hydrogen Peroxide; Hydrogen Sulfide; Hydroxybenzoates; Hydroxyl Radical; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hyperthermia, Induced; Hysteroscopy; Immunoassay; Indigo Carmine; Inflammation; Inflammatory Bowel Diseases; Insulin Resistance; Intensive Care Units; Interleukin-11; Interleukin-6; Interleukins; Iodine Radioisotopes; Iran; Iridium; Islets of Langerhans; Kinetics; Lactation; Lactobacillus; Lactobacillus plantarum; Lamins; Latin America; Lead; Lectins; Leukopenia; Ligands; Limit of Detection; Lipopolysaccharides; Lipoprotein Lipase; Liver; Liver Cirrhosis; Liver Neoplasms; Lolium; Luminescent Measurements; Luminol; Lung; Luteinizing Hormone; Macrophages; Magnetic Phenomena; Magnetic Resonance Imaging; Male; Malnutrition; Maltose; Manganese Compounds; Maternal Nutritional Physiological Phenomena; Melatonin; Metabolic Engineering; Metal Nanoparticles; Metallocenes; Metaplasia; Methicillin-Resistant Staphylococcus aureus; Methylation; Mevalonic Acid; Mexico; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microbial Sensitivity Tests; Microbiota; MicroRNAs; Milk; Mitomycin; Molecular Diagnostic Techniques; Molecular Docking Simulation; Monte Carlo Method; Moringa oleifera; Multiple Sclerosis; Muscle Strength; Muscle, Skeletal; Nanocomposites; Nanotubes, Carbon; Neoadjuvant Therapy; Neoplasms; Neurodegenerative Diseases; Neurotransmitter Agents; NF-E2-Related Factor 2; Nickel; Nitrogen Dioxide; Non-alcoholic Fatty Liver Disease; Nucleic Acid Amplification Techniques; Nucleic Acid Hybridization; Nucleocapsid Proteins; Nutritional Status; Obesity; Osteogenesis; Osteosarcoma; Oxidation-Reduction; Oxides; Oxygen; Oxyquinoline; Pain; Palliative Care; Pancreatic Neoplasms; Pandemics; Particulate Matter; Peroxidase; Peroxidases; Phagocytosis; Phaseolus; Photothermal Therapy; Point-of-Care Systems; Polyethyleneimine; Polymers; Polymorphism, Single Nucleotide; Polysomnography; Postoperative Complications; Pregnancy; Pregnant Women; Prenatal Exposure Delayed Effects; Prevalence; Printing, Three-Dimensional; Probability; Probiotics; Prognosis; Prophages; Prospective Studies; Proteomics; Proto-Oncogene Proteins; Pseudomonas aeruginosa; Pseudomonas putida; Pulmonary Disease, Chronic Obstructive; Pulmonary Embolism; Pyridines; Pyrroles; Quality of Life; Quinolones; Rabbits; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; Real-Time Polymerase Chain Reaction; Receptors, Histamine; Receptors, Histamine H2; Recombinases; Rectal Neoplasms; Reperfusion Injury; Respiration; Respiratory Function Tests; Respiratory Rate; Respiratory Sounds; Retrospective Studies; rho GTP-Binding Proteins; Risk Assessment; Risk Factors; RNA; RNA, Messenger; RNA, Ribosomal, 16S; Robotic Surgical Procedures; Running; Rural Population; Saccharomyces cerevisiae; Salpingectomy; Sarcopenia; SARS-CoV-2; Seeds; Semen; Sensitivity and Specificity; Sepsis; Shock, Septic; Signal Transduction; Silicon Dioxide; Silver; Sirtuin 1; Skin Neoplasms; Sleep Apnea, Obstructive; Soil; Spain; Spectrum Analysis, Raman; Sperm Retrieval; Spermatozoa; Spirometry; Staphylococcus aureus; STAT3 Transcription Factor; Stereoisomerism; Sterilization, Tubal; Stroke Volume; Sulfadiazine; Sulfites; Superoxide Dismutase; Surface Plasmon Resonance; tau Proteins; Testis; Testosterone; Thioredoxin-Disulfide Reductase; Thyroid Neoplasms; Thyroidectomy; Trans-Activators; Transcription Factor AP-1; Treatment Outcome; Triazoles; Triclosan; Trifluridine; Tumor Microenvironment; Tumor Necrosis Factor-alpha; United States; Uracil; Vagina; Vegetables; Ventricular Function, Left; Ventricular Pressure; Vibrio cholerae; Vietnam; Virulence; Vital Capacity; Vitrification; Walking; Water; Water Pollutants, Radioactive; Whole Genome Sequencing; Wind; YAP-Signaling Proteins; Zeolites; Zinc Oxide | 2023 |
The R230C variant of the ATP binding cassette protein A1 (ABCA1) gene is associated with a decreased response to glyburide therapy in patients with type 2 diabetes mellitus.
Topics: Adult; Aged; Amino Acid Substitution; Arginine; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters; Cysteine; Diabetes Mellitus, Type 2; Dose-Response Relationship, Drug; Drug Resistance; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glyburide; Humans; Hypoglycemic Agents; Male; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Single-Blind Method; Young Adult | 2013 |
hOGG1 Ser326Cys polymorphism and breast cancer risk among Asian women.
Topics: Adult; Aged; Amino Acid Substitution; Asian People; Breast Neoplasms; Case-Control Studies; Cysteine; DNA Glycosylases; DNA, Neoplasm; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Japan; Korea; Logistic Models; Middle Aged; Polymorphism, Genetic; Risk Factors; Serine | 2003 |
103 other study(ies) available for cysteine and Genetic Predisposition
| Article | Year |
|---|---|
Possible Association Between Polymorphisms in ESR1, COL1A2, BGLAP, SPARC, VDR, and MMP2 Genes and Dental Fluorosis in a Population from an Endemic Region of West Bengal.
Topics: Cysteine; Estrogen Receptor alpha; Fluorides; Fluorosis, Dental; Genetic Predisposition to Disease; Humans; Matrix Metalloproteinase 2; Minerals; Osteocalcin; Osteonectin; Polymorphism, Single Nucleotide; Receptors, Calcitriol | 2022 |
Cysteine-Altering
Topics: Adult; Age Factors; Aged; CADASIL; Cerebral Small Vessel Diseases; Cysteine; Female; Genetic Predisposition to Disease; Humans; Ischemic Attack, Transient; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Proportional Hazards Models; Protein Domains; Receptor, Notch3; Stroke | 2020 |
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome.
Topics: Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Cells, Cultured; Child; Child, Preschool; Consanguinity; Cysteine; Female; Follow-Up Studies; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation, Missense; Neuroaxonal Dystrophies; Pedigree; Proteins; Siblings; Spastic Paraplegia, Hereditary | 2018 |
[Molecular genetics study of hereditary predisposition to diffuse gastric cancer in Russian patients].
Topics: Adult; Antigens, CD; Cadherins; Carcinoma, Signet Ring Cell; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Molecular Biology; Pedigree; Polymorphism, Single Nucleotide; Russia; Sequence Deletion; Stomach Neoplasms; Threonine | 2013 |
Uterine smooth muscle tumors with features suggesting fumarate hydratase aberration: detailed morphologic analysis and correlation with S-(2-succino)-cysteine immunohistochemistry.
Topics: Adult; Cysteine; Female; Fumarate Hydratase; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Immunohistochemistry; Middle Aged; Smooth Muscle Tumor; Uterine Neoplasms | 2014 |
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor.
Topics: Adult; Aged; Amino Acid Substitution; Culture Media, Conditioned; Cysteine; DNA Mutational Analysis; Endoplasmic Reticulum; Female; Genetic Predisposition to Disease; Golgi Apparatus; HEK293 Cells; Hemostasis; Humans; Male; Mutation, Missense; Phenotype; Phenylalanine; Protein Multimerization; Protein Transport; Transfection; von Willebrand Diseases; von Willebrand Factor; Weibel-Palade Bodies | 2014 |
Activity-associated effect of LDL receptor missense variants located in the cysteine-rich repeats.
Topics: Amino Acid Motifs; Animals; CHO Cells; Computer Simulation; Cricetulus; Cysteine; Flow Cytometry; Genetic Predisposition to Disease; Hyperlipoproteinemia Type II; Lipoproteins; Microscopy, Confocal; Models, Molecular; Mutagenesis, Site-Directed; Mutation, Missense; Phenotype; Protein Binding; Protein Interaction Domains and Motifs; Receptors, LDL; Repetitive Sequences, Amino Acid; Structure-Activity Relationship; Transfection | 2015 |
DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
Topics: Adolescent; Adult; Child; Child, Preschool; Cysteine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dynactin Complex; Female; Genetic Predisposition to Disease; Humans; Incidence; Infant; Male; Middle Aged; Mutation, Missense; Pseudomonas aeruginosa; Pseudomonas Infections; Retrospective Studies; Sex Factors; Tyrosine; Young Adult | 2016 |
Morphology and Immunohistochemistry for 2SC and FH Aid in Detection of Fumarate Hydratase Gene Aberrations in Uterine Leiomyomas From Young Patients.
Topics: Adult; Age Factors; Biomarkers, Tumor; Biopsy; Cysteine; DNA Mutational Analysis; Female; Fumarate Hydratase; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Leiomyomatosis; Mutation; Neoplastic Syndromes, Hereditary; Phenotype; Predictive Value of Tests; Prognosis; Skin Neoplasms; Uterine Neoplasms; Young Adult | 2015 |
Immunohistochemistry for 2-Succinocysteine (2SC) and Fumarate Hydratase (FH) in Cutaneous Leiomyomas May Aid in Identification of Patients With HLRCC (Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome).
Topics: Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Cysteine; DNA Mutational Analysis; Female; Fumarate Hydratase; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Humans; Immunohistochemistry; Leiomyomatosis; Male; Middle Aged; Neoplastic Syndromes, Hereditary; Polymerase Chain Reaction; Skin Neoplasms; Uterine Neoplasms | 2016 |
The association of single nucleotide polymorphisms of the maternal cystathionine-β-synthase gene with early-onset preeclampsia.
Topics: Adult; Biomarkers; Blood Pressure; Case-Control Studies; Cystathionine; Cystathionine beta-Synthase; Cysteine; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Gestational Age; Homocysteine; Humans; Phenotype; Polymorphism, Single Nucleotide; Pre-Eclampsia; Pregnancy; Protective Factors; Risk Factors | 2016 |
Cysteinyl-glycine reduces mucosal proinflammatory cytokine response to fMLP in a parenterally-fed piglet model.
Topics: Animals; Cysteine; Cytokines; Dipeptides; Disease Models, Animal; Genetic Predisposition to Disease; Glycine; Inflammation; Interleukin-10; Intestinal Mucosa; Mannitol; Mucous Membrane; N-Formylmethionine Leucyl-Phenylalanine; Parenteral Nutrition; Perfusion; Peroxidase; Random Allocation; Swine; Time Factors | 2016 |
The Ser311Cys variation in the paraoxonase 2 gene increases the risk of type 2 diabetes in northern Chinese.
Topics: Amino Acid Substitution; Aryldialkylphosphatase; Asian People; Blood Pressure; Case-Control Studies; China; Cysteine; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Hypertension; Male; Middle Aged; Multivariate Analysis; Regression Analysis; Serine | 2008 |
Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.
Topics: Adult; Age Factors; Aged; Aged, 80 and over; Arginine; Cysteine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glycine; Humans; Italy; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Population Groups; Protein Serine-Threonine Kinases; Serine; Tomography, Emission-Computed, Single-Photon | 2009 |
Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding.
Topics: Adult; Alleles; Amino Acid Sequence; Amino Acid Substitution; Cysteine; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Memory; Memory Disorders; Nerve Tissue Proteins; Neural Pathways; Polymorphism, Genetic; Prefrontal Cortex; Schizophrenia; Serine; Young Adult | 2008 |
Disseminated and rapidly fatal tuberculosis in mice bearing a defective allele at IFN regulatory factor 8.
Topics: Alleles; Amino Acid Substitution; Animals; Arginine; Cysteine; Female; Genetic Predisposition to Disease; Interferon Regulatory Factors; Interferons; Liver; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred DBA; Mutation; Mycobacterium tuberculosis; Spleen; Tuberculosis, Pulmonary; Virulence | 2009 |
The Disrupted-in-Schizophrenia-1 Ser704Cys polymorphism and brain morphology in schizophrenia.
Topics: Adult; Brain; Cognition Disorders; Cysteine; Female; Frontal Lobe; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homozygote; Humans; Magnetic Resonance Imaging; Male; Nerve Tissue Proteins; Neuropsychological Tests; Polymorphism, Genetic; Schizophrenia; Schizophrenic Psychology; Serine | 2009 |
Differential thiol status in blood of different mouse strains exposed to cigarette smoke.
Topics: Animals; Cysteine; Dipeptides; Emphysema; Genetic Predisposition to Disease; Glutathione; Glutathione Disulfide; Homocysteine; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Inbred ICR; Oxidative Stress; Sulfhydryl Compounds; Tobacco Smoke Pollution | 2009 |
Descriptively quantitative relationship between mutated N-acetylgalactosamine-6-sulfatase and mucopolysaccharidosis IVA.
Topics: Chondroitinsulfatases; Cysteine; Genetic Predisposition to Disease; Humans; Mucopolysaccharidosis IV; Mutation | 2009 |
Association of the Ser326Cys polymorphism in the OGG1 gene with type 2 DM.
Topics: Aged; Amino Acid Substitution; Asian People; Cysteine; Diabetes Mellitus, Type 2; DNA Glycosylases; Female; Genetic Predisposition to Disease; Humans; Insulin; Insulin Secretion; Male; Middle Aged; Polymorphism, Genetic; Serine | 2009 |
Cysteine-sparing notch3 mutations: cadasil or cadasil variants?
Topics: CADASIL; Cysteine; Exons; Genetic Predisposition to Disease; Genetic Variation; Humans; Introns; Muscle, Smooth, Vascular; Mutation; Phenotype; Polymorphism, Single Nucleotide; Receptor, Notch3; Receptors, Notch | 2009 |
The CDH1-160C>A polymorphism is a risk factor for colorectal cancer.
Topics: Aged; Alanine; Antigens, CD; Cadherins; Case-Control Studies; Colorectal Neoplasms; Cysteine; Female; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Risk Assessment; Risk Factors; United Kingdom; White People | 2009 |
Hereditary hemochromatosis due to resistance to hepcidin: high hepcidin concentrations in a family with C326S ferroportin mutation.
Topics: Adolescent; Antimicrobial Cationic Peptides; Cation Transport Proteins; Child; Cysteine; Female; Genetic Predisposition to Disease; Hemochromatosis; Hepcidins; Humans; Male; Middle Aged; Mutation | 2009 |
Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation.
Topics: Amino Acid Substitution; Anesthetics, Inhalation; Arginine; Carnitine O-Palmitoyltransferase; Child, Preschool; Cysteine; Female; Genetic Predisposition to Disease; Halothane; Heterozygote; Humans; Malignant Hyperthermia; Metabolism, Inborn Errors; Mutation; Neuromuscular Depolarizing Agents; Risk Factors; Succinylcholine; Syndrome | 2009 |
Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.
Topics: Aged; Alanine; Asian People; Cell Adhesion Molecules; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Glycine; GTPase-Activating Proteins; Humans; Hypertension; Logistic Models; Male; Middle Aged; Nerve Tissue Proteins; Oligonucleotide Array Sequence Analysis; Polymorphism, Genetic | 2010 |
hOGG1 Ser326Cys polymorphism and risk of lung cancer by histological type.
Topics: Adenocarcinoma; Adult; Aged; Carcinoma, Small Cell; Carcinoma, Squamous Cell; Case-Control Studies; Cysteine; DNA Glycosylases; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Lung Neoplasms; Male; Meta-Analysis as Topic; Middle Aged; Multivariate Analysis; Mutation, Missense; Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Serine; Smoking | 2009 |
The D2 dopamine receptor gene variant C957T affects human fear conditioning and aversive priming.
Topics: Adult; Attention; Conditioning, Psychological; Cysteine; Electroshock; Extinction, Psychological; Face; Fear; Female; Galvanic Skin Response; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Learning; Male; Mental Disorders; Pattern Recognition, Visual; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Receptors, Dopamine D2; Threonine; Young Adult | 2010 |
The Cys326 allele of the 8-oxoguanine DNA N-glycosylase 1 gene as a risk factor in smoking- and drinking-associated larynx cancer.
Topics: Aged; Aged, 80 and over; Alcohol Drinking; Alleles; Case-Control Studies; Cysteine; DNA Glycosylases; Female; Genetic Predisposition to Disease; Humans; Laryngeal Neoplasms; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Smoking | 2009 |
Pathogenic cysteine mutations affect progranulin function and production of mature granulins.
Topics: Animals; Arginine; Axons; Brain; Cell Enlargement; Cell Line, Transformed; Cysteine; Dithiothreitol; Embryo, Mammalian; Enzyme-Linked Immunosorbent Assay; Family Health; Frontotemporal Dementia; Gene Expression Regulation; Genetic Predisposition to Disease; Green Fluorescent Proteins; Humans; Intercellular Signaling Peptides and Proteins; Motor Neurons; Mutation; Neurites; Pancreatic Elastase; Progranulins; Rats; Rats, Wistar; RNA, Messenger; Transfection; Tyrosine | 2010 |
Comorbidity between bipolar disorder and alcohol use disorder: association of dopamine and serotonin gene polymorphisms.
Topics: Adult; Alcohol-Related Disorders; Bipolar Disorder; Chi-Square Distribution; Comorbidity; Cysteine; Databases, Genetic; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Neurotransmitter Transport Proteins; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Receptors, Dopamine; Receptors, Serotonin; Serine; Severity of Illness Index; Sex Factors | 2010 |
Recessive multiple epiphyseal dysplasia (rMED) with homozygosity for C653S mutation in the DTDST gene--phenotype, molecular diagnosis and surgical treatment of habitual dislocation of multilayered patella: case report.
Topics: Adult; Amino Acid Substitution; Anion Transport Proteins; Cysteine; Genes, Recessive; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Knee Dislocation; Male; Mutation; Orthopedic Procedures; Osteochondrodysplasias; Patella; Phenotype; Serine; Sulfate Transporters; Treatment Outcome | 2010 |
Disrupted activity in the hippocampal-accumbens circuit of type III neuregulin 1 mutant mice.
Topics: Action Potentials; Animals; Cysteine; Genetic Predisposition to Disease; Hippocampus; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Neural Pathways; Neuregulin-1; Neurons; Nucleus Accumbens; Protein Isoforms; Protein Structure, Tertiary | 2011 |
Genetic predisposition of white matter infarction with protein S deficiency and R355C mutation.
Topics: Adolescent; Adult; Aged; Arginine; Brain; Cerebral Infarction; Child; Cysteine; Female; Genetic Predisposition to Disease; Haplotypes; Hong Kong; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Molecular Sequence Annotation; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Protein S; Protein S Deficiency; Risk Factors; Young Adult | 2010 |
Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.
Topics: Adolescent; Anemia, Hemolytic; Angiotensin-Converting Enzyme Inhibitors; Animals; Child; Child, Preschool; Chlorocebus aethiops; Cholesterol, HDL; Corneal Opacity; COS Cells; Cysteine; Disulfides; Diuretics; Female; Genetic Predisposition to Disease; Homozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Male; Mutation; Phosphatidylcholine-Sterol O-Acyltransferase; Proteinuria; Transfection; Treatment Outcome; Tyrosine | 2011 |
BCL-2 (-938C > A) polymorphism is associated with breast cancer susceptibility.
Topics: Adult; Aged; Alanine; Biomarkers, Tumor; Blotting, Western; Breast Neoplasms; Case-Control Studies; Cell Line, Tumor; Cysteine; Female; Gene Expression Regulation, Neoplastic; Genes, bcl-2; Genetic Predisposition to Disease; Genotype; Humans; Immunohistochemistry; Logistic Models; Lymphatic Metastasis; Middle Aged; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Proto-Oncogene Proteins c-bcl-2; Risk Assessment; Risk Factors | 2011 |
The 8-oxoguanine DNA N-glycosylase 1 (hOGG1) Ser326Cys variant affects the susceptibility to Graves' disease.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Biomarkers; Cysteine; DNA; DNA Damage; DNA Glycosylases; DNA Repair; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Graves Disease; Guanine; Humans; Male; Middle Aged; Oxidative Stress; Polymorphism, Genetic; Reactive Oxygen Species; Risk; Serine; Young Adult | 2011 |
Renin-angiotensin-aldosterone system genes and nonarteritic anterior ischemic optic neuropathy.
Topics: Age Factors; Aged; Aged, 80 and over; Alanine; Alleles; Angiotensinogen; Confidence Intervals; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Odds Ratio; Optic Neuropathy, Ischemic; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Sex Factors; Threonine | 2011 |
Plasma biomarkers of oxidative stress and genetic variants in age-related macular degeneration.
Topics: Aged; Biomarkers; Case-Control Studies; Chromatography, High Pressure Liquid; Complement Factor H; Cysteine; Cystine; Female; Furans; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutathione; Humans; Isoprostanes; Lipid Peroxidation; Macular Degeneration; Male; Oxidative Stress; Polymorphism, Single Nucleotide; Prospective Studies; Proteins | 2012 |
A Korean Parkinson's disease family with the LRRK2 p.Tyr1699Cys mutation showing clinical heterogeneity.
Topics: Age of Onset; Aged; Cysteine; DNA Mutational Analysis; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinson Disease; Protein Serine-Threonine Kinases; Republic of Korea; Tyrosine | 2012 |
Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutation.
Topics: Amino Acid Substitution; Child, Preschool; Coloboma; Cysteine; Disease Progression; Diseases in Twins; Environment; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Mutation; PAX2 Transcription Factor; Phenotype; Renal Insufficiency; Risk Factors; Twins, Monozygotic; Vesico-Ureteral Reflux; Young Adult | 2012 |
Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis.
Topics: Alleles; Aryldialkylphosphatase; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Glutathione; Homocysteine; Humans; Hypertension; Ischemic Attack, Transient; Lipid Peroxidation; Lipids; Male; Malondialdehyde; Middle Aged; Myocardial Infarction; Oxidative Stress; Polymorphism, Single Nucleotide; Risk Factors; Stroke; Thrombosis | 2013 |
The risk of coronary artery disease in population of Taiwan is associated with Cys-Ser 311 polymorphism of human paraoxonase (PON)-2 gene.
Topics: Adult; Aged; Aryldialkylphosphatase; Coronary Disease; Cysteine; Esterases; Female; Genetic Predisposition to Disease; Genotype; Humans; Lipids; Male; Middle Aged; Polymorphism, Genetic; Risk; Serine; Taiwan | 2002 |
Severity of alcohol withdrawal symptoms and the T1128C polymorphism of the neuropeptide Y gene.
Topics: Adult; Alcohol Withdrawal Delirium; Alcoholism; Alleles; Case-Control Studies; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Neuropeptide Y; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Severity of Illness Index; Substance Withdrawal Syndrome; Threonine | 2002 |
Influence of interleukin-12 receptor beta1 polymorphisms on tuberculosis.
Topics: Adult; Aged; Alanine; Asian People; Blotting, Western; Case-Control Studies; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Glycine; Haplotypes; Humans; Interferon-gamma; Japan; Killer Cells, Natural; Male; Middle Aged; Mutation, Missense; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Receptors, Interleukin; Receptors, Interleukin-12; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Threonine; Tuberculosis | 2003 |
Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads.
Topics: Adolescent; Adult; Alanine; Case-Control Studies; Cleft Lip; Cleft Palate; Cysteine; Female; Folic Acid; Genetic Predisposition to Disease; Genetic Variation; Haplotypes; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2); Norway; Oxidoreductases Acting on CH-NH Group Donors; Polymerase Chain Reaction; Registries; Risk Factors; Threonine | 2003 |
Methylenetetrahydrofolate reductase gene polymorphisms in patients with schizophrenia.
Topics: Alanine; Alleles; Chi-Square Distribution; Cysteine; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Lymphocytes; Methylenetetrahydrofolate Reductase (NADPH2); Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Schizophrenia; Threonine | 2003 |
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Analysis; Electrophysiology; Family Health; Female; Genetic Predisposition to Disease; Glycine; Histidine; Humans; Male; Microscopy, Electron; Mutation; Nerve Tissue Proteins; Neural Conduction; Pedigree; Peripheral Nerves; Sequence Analysis, DNA; Tryptophan | 2003 |
Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer's disease in Chinese.
Topics: Aged; Aged, 80 and over; Alleles; Alzheimer Disease; Apolipoproteins E; Aryldialkylphosphatase; Asian People; Chi-Square Distribution; Cysteine; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Polymerase Chain Reaction; Polymorphism, Genetic; Serine | 2004 |
Gender in obsessive-compulsive disorder: clinical and genetic findings.
Topics: Adolescent; Adult; Age of Onset; Aged; Case-Control Studies; Comorbidity; Cysteine; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glycine; Humans; Interviews as Topic; Male; Middle Aged; Monoamine Oxidase; Obsessive-Compulsive Disorder; Polymorphism, Genetic; Pregnancy; Psychiatric Status Rating Scales; Quality of Life; Receptor, Serotonin, 5-HT1D; Serotonin; Sex Characteristics; South Africa | 2004 |
GNB3 gene C825T and ACE gene I/D polymorphisms in essential hypertension in a Kazakh genetic isolate.
Topics: Adult; Blood Pressure; Case-Control Studies; China; Cysteine; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Genotype; Heterotrimeric GTP-Binding Proteins; Humans; Hypertension; Kazakhstan; Logistic Models; Male; Middle Aged; Peptidyl-Dipeptidase A; Polymerase Chain Reaction; Polymorphism, Genetic; Threonine | 2004 |
Possible association of interleukin 1 gene locus polymorphisms with low back pain.
Topics: Adult; Alanine; Alleles; Cohort Studies; Cysteine; Finland; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Interleukin-1; Intervertebral Disc Displacement; Low Back Pain; Lumbar Vertebrae; Magnetic Resonance Imaging; Male; Middle Aged; Pain Measurement; Polymerase Chain Reaction; Polymorphism, Genetic; Receptors, Interleukin; Regression Analysis; Risk; RNA; Surveys and Questionnaires; Threonine | 2004 |
Association between norepinephrine transporter gene polymorphism and major depression.
Topics: Adult; Cysteine; Depressive Disorder, Major; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Norepinephrine Plasma Membrane Transport Proteins; Polymorphism, Genetic; Psychiatric Status Rating Scales; Random Allocation; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Symporters; Threonine | 2004 |
Intronic CYP46 polymorphism along with ApoE genotype in sporadic Alzheimer Disease: from risk factors to disease modulators.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Analysis of Variance; Apolipoproteins E; Case-Control Studies; Chi-Square Distribution; Cholesterol 24-Hydroxylase; Cysteine; Female; Follow-Up Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Introns; Male; Mental Status Schedule; Odds Ratio; Polymorphism, Genetic; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; RNA, Messenger; Steroid Hydroxylases; Time Factors; Tyrosine | 2004 |
Mutation screening of the BARD1 gene: evidence for involvement of the Cys557Ser allele in hereditary susceptibility to breast cancer.
Topics: Alleles; Amino Acid Sequence; Breast Neoplasms; Cysteine; DNA Mutational Analysis; Female; Finland; Genetic Predisposition to Disease; Genetic Testing; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Ovarian Neoplasms; Pedigree; Serine; Tumor Suppressor Proteins; Ubiquitin-Protein Ligases | 2004 |
Association of estrogen receptor alpha polymorphisms with susceptibility to chronic hepatitis B virus infection.
Topics: Adult; Alanine; Alleles; Asian People; Chromosome Mapping; Cysteine; Estrogen Receptor alpha; Female; Genetic Predisposition to Disease; Haplotypes; Hepatitis B, Chronic; Heterozygote; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Estrogen; Threonine | 2004 |
Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsy.
Topics: Arginine; Autopsy; Child; Cysteine; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Genetic Predisposition to Disease; Humans; Infant, Newborn; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Male; Molecular Diagnostic Techniques; Mutation, Missense; Neonatal Screening; Pedigree; Potassium Channels, Voltage-Gated | 2004 |
Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.
Topics: Adenomatous Polyposis Coli; Aspartic Acid; Base Pair Mismatch; Biomarkers, Tumor; Case-Control Studies; Colorectal Neoplasms; Colorectal Neoplasms, Hereditary Nonpolyposis; Cysteine; DNA Glycosylases; DNA Mutational Analysis; DNA, Neoplasm; Gene Frequency; Genetic Predisposition to Disease; Germ-Line Mutation; Glycine; Humans; Loss of Heterozygosity; Ontario; Phenotype; Risk Factors; Tyrosine | 2004 |
Met proto-oncogene juxtamembrane rare variations in mouse and humans: differential effects of Arg and Cys alleles on mouse lung tumorigenesis.
Topics: Adenocarcinoma; Alleles; Amino Acid Sequence; Animals; Arginine; Carcinoma, Non-Small-Cell Lung; Cell Transformation, Neoplastic; Cysteine; Disease Models, Animal; DNA Mutational Analysis; Genetic Linkage; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Lung Neoplasms; Mice; Mice, Inbred Strains; Molecular Sequence Data; Multifactorial Inheritance; Proto-Oncogene Mas; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-met; Receptors, Growth Factor; Receptors, Thrombin; Reverse Transcriptase Polymerase Chain Reaction | 2005 |
Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.
Topics: Alleles; Arginine; Case-Control Studies; Chi-Square Distribution; Cysteine; DNA Mutational Analysis; Epilepsy, Generalized; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Mutation, Missense; Polymorphism, Genetic; Potassium Channels, Inwardly Rectifying | 2005 |
Mutant valosin-containing protein causes a novel type of frontotemporal dementia.
Topics: Adenosine Triphosphatases; Amyloid beta-Protein Precursor; Arginine; Blotting, Western; Brain; Cell Cycle Proteins; Cysteine; Dementia; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glial Fibrillary Acidic Protein; Humans; Immunohistochemistry; Middle Aged; Mutation, Missense; Staining and Labeling; tau Proteins; Ubiquitin; Valosin Containing Protein | 2005 |
T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study.
Topics: Aged; Albuminuria; Aspartic Acid; Creatinine; Cysteine; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Exons; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Homozygote; Humans; Linkage Disequilibrium; Male; Middle Aged; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Odds Ratio; Polymorphism, Genetic; Promoter Regions, Genetic; Threonine | 2005 |
The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotype.
Topics: ABO Blood-Group System; ADAM Proteins; ADAMTS13 Protein; Cohort Studies; Cysteine; Enzyme-Linked Immunosorbent Assay; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Male; Metalloendopeptidases; Pedigree; Phenotype; Polymorphism, Genetic; von Willebrand Diseases | 2005 |
A mutation in the Icsbp1 gene causes susceptibility to infection and a chronic myeloid leukemia-like syndrome in BXH-2 mice.
Topics: Amino Acid Substitution; Animals; Arginine; Chromosomes, Mammalian; Cysteine; Genetic Predisposition to Disease; Immunologic Deficiency Syndromes; Interferon Regulatory Factors; Interferon-gamma; Interleukin-12; Leukemia, Myeloid; Mice; Mutagenesis, Insertional; Mycobacterium bovis; Point Mutation; Quantitative Trait Loci; Repressor Proteins; Retroviridae; RNA, Messenger; Spleen; Tuberculosis; Virus Replication | 2005 |
Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Brain-Derived Neurotrophic Factor; Cysteine; Female; Genetic Predisposition to Disease; Humans; Japan; Male; Methionine; Middle Aged; Multiple System Atrophy; Parkinson Disease; Polymorphism, Genetic; Threonine; Valine | 2005 |
Hepatocellular carcinoma and the penetrance of HFE C282Y mutations: a cross sectional study.
Topics: Aging; Carcinoma, Hepatocellular; Case-Control Studies; Cross-Sectional Studies; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Liver Neoplasms; Male; Membrane Proteins; Middle Aged; Mutation; Penetrance; Tyrosine | 2005 |
The prevalence of C807T mutation of glycoprotein Ia gene among young male survivors of myocardial infarction: a relation with coronary angiography results.
Topics: Adult; Alanine; Case-Control Studies; Coronary Angiography; Cysteine; Gene Expression; Gene Frequency; Genetic Predisposition to Disease; Humans; Integrin alpha2; Male; Middle Aged; Mutation; Myocardial Infarction; Polymorphism, Genetic; Threonine | 2005 |
Association of the 1438G/A and 102T/C polymorphism of the 5-HT2A receptor gene with irritable bowel syndrome 5-HT2A gene polymorphism in irritable bowel syndrome.
Topics: Alanine; Case-Control Studies; Cysteine; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Irritable Bowel Syndrome; Polymorphism, Genetic; Receptor, Serotonin, 5-HT2A; Threonine | 2005 |
Interaction of OGG1 Ser326Cys polymorphism with cigarette smoking in head and neck squamous cell carcinoma.
Topics: Adult; Aged; Aged, 80 and over; Alcohol Drinking; Carcinoma, Squamous Cell; Cysteine; DNA Glycosylases; Female; Genetic Predisposition to Disease; Genotype; Head and Neck Neoplasms; Humans; Lymphatic Metastasis; Male; Middle Aged; Polymorphism, Genetic; Serine; Smoking | 2006 |
Protective effect of the G-765C COX-2 polymorphism on subclinical atherosclerosis and inflammatory markers in asymptomatic subjects with cardiovascular risk factors.
Topics: Atherosclerosis; Biomarkers; Cholesterol; Cyclooxygenase 2; Cysteine; Female; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Glycine; Humans; Inflammation; Male; Middle Aged; Monocytes; Polymorphism, Genetic | 2006 |
Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement.
Topics: Adolescent; Alanine; Angiotensinogen; Child; Child, Preschool; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; IgA Vasculitis; Kidney Diseases; Male; Methionine; Nephrotic Syndrome; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Proteinuria; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Severity of Illness Index; Threonine | 2006 |
Association of the OGG1 Ser326Cys polymorphism with tooth loss.
Topics: Aged; Aged, 80 and over; Cysteine; DNA Glycosylases; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Regression Analysis; Serine; Tooth Loss | 2006 |
The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosis.
Topics: Adult; Aged; Aspartic Acid; Cysteine; Fatty Liver; Female; Genetic Predisposition to Disease; Glucose Intolerance; Hemochromatosis; Hepatitis; Heterozygote; Histidine; Homozygote; Humans; Iron Overload; Liver Cirrhosis; Male; Metabolic Syndrome; Middle Aged; Multivariate Analysis; Predictive Value of Tests; Prospective Studies; Risk Factors; Tyrosine | 2006 |
The interleukin-6 gene -174G>C and -572G>C promoter polymorphisms are related to cerebral aneurysms.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Guanine; Humans; Interleukin-6; Intracranial Aneurysm; Male; Middle Aged; Polymorphism, Genetic; Promoter Regions, Genetic; Risk Factors | 2006 |
Interleukin 6 G-174 C polymorphism and breast cancer risk.
Topics: Aged; Aged, 80 and over; Breast Neoplasms; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Interleukin-6; Middle Aged; Polymorphism, Genetic; Risk Factors | 2006 |
Precocious osteoarthritis in a family with recurrent COL2A1 mutation.
Topics: Arginine; Collagen Type II; Cysteine; Family Health; Female; Genetic Predisposition to Disease; Genetic Testing; Humans; Male; Microsatellite Repeats; Mutation, Missense; Osteoarthritis, Hip; Osteoarthritis, Knee; Osteochondrodysplasias; Pedigree; Polymerase Chain Reaction; Radiography | 2006 |
Strategies for dissecting genetic-environmental interactions in neurodegenerative disorders.
Topics: Adult; Age Factors; Age of Onset; Aged; Aged, 80 and over; Aging; alpha 1-Antitrypsin; Analysis of Variance; Apolipoprotein E4; Apolipoproteins E; Chi-Square Distribution; Cysteine; DNA Mutational Analysis; Environment; Female; Gene Frequency; Genetic Predisposition to Disease; Hemochromatosis; Humans; Male; Middle Aged; Mutation; Neurodegenerative Diseases; Phenotype; Retrospective Studies; Tryptophan | 2006 |
Interactions between the OGG1 Ser326Cys polymorphism and intake of fruit and vegetables in relation to lung cancer.
Topics: Cysteine; Diet; DNA Glycosylases; Female; Fruit; Genetic Predisposition to Disease; Humans; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Prospective Studies; Serine; Smoking; Vegetables | 2006 |
The lymphotoxin Cys13Arg polymorphism and cognitive functioning in individuals with schizophrenia.
Topics: Adult; Antibodies, Viral; Arginine; Bipolar Disorder; Cognition Disorders; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Herpesvirus 1, Human; Humans; Intelligence; Lymphotoxin-alpha; Male; Middle Aged; Neuropsychological Tests; Polymorphism, Genetic; Schizophrenia | 2007 |
Disrupted in schizophrenia 1 genotype and positive symptoms in schizophrenia.
Topics: Cysteine; Delusions; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Hallucinations; Haplotypes; Homozygote; Humans; Nerve Tissue Proteins; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Serine | 2007 |
hOGG1 Ser326Cys polymorphism and susceptibility to gallbladder cancer in a Chinese population.
Topics: Asian People; Case-Control Studies; China; Cysteine; DNA Glycosylases; Female; Gallbladder Neoplasms; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Polymorphism, Genetic; Serine | 2007 |
Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer.
Topics: ADP-Ribosylation Factors; Amino Acid Substitution; Arginine; Base Sequence; Case-Control Studies; Colorectal Neoplasms; Cysteine; Genetic Predisposition to Disease; Genetic Variation; Humans; Incidence; Middle Aged; Molecular Sequence Data; Risk Factors; Spain | 2007 |
Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.
Topics: Age Factors; Aged; Amino Acid Sequence; Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Cysteine; Disease Progression; DNA Glycosylases; DNA Mutational Analysis; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Middle Aged; Mutation; Phenotype; Polymorphism, Genetic; Serine; Sex Factors | 2007 |
Nephrolithiasis in identical twins: the impact of nature vs nurture.
Topics: Adult; Aged; Calcium Oxalate; Cohort Studies; Cysteine; Diseases in Twins; Female; Genetic Predisposition to Disease; Humans; Male; Metabolic Diseases; Middle Aged; Nephrolithiasis; Retrospective Studies; Twins, Monozygotic | 2007 |
Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients.
Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Asian People; Base Sequence; Child; Cysteine; DNA Mutational Analysis; Ectopia Lentis; Female; Fibrillin-1; Fibrillins; Genetic Predisposition to Disease; Humans; Male; Marfan Syndrome; Microfilament Proteins; Molecular Sequence Data; Mutation; Pedigree | 2007 |
Multiple primary melanomas in a CDKN2A mutation carrier exposed to ionizing radiation.
Topics: 5' Untranslated Regions; Adult; Arginine; Cysteine; Environmental Exposure; Female; Genes, p16; Genetic Predisposition to Disease; Hair Color; Heterozygote; Humans; Melanoma; Mutation; Neoplasms, Multiple Primary; Neoplasms, Radiation-Induced; Nuclear Weapons; Receptor, Melanocortin, Type 1; Skin Neoplasms | 2007 |
The extracolonic cancer spectrum in females with the common 'South African' hMLH1 c.C1528T mutation.
Topics: Adaptor Proteins, Signal Transducing; Adult; Alleles; Case-Control Studies; Cohort Studies; Colorectal Neoplasms, Hereditary Nonpolyposis; Cysteine; Female; Genetic Predisposition to Disease; Humans; Incidence; Microsatellite Instability; Middle Aged; Mutation; MutL Protein Homolog 1; Neoplasms; Neoplasms, Multiple Primary; Nuclear Proteins; Phenotype; Population Surveillance; Risk Factors; Sex Factors; Siblings; South Africa; Threonine | 2008 |
Association of a missense single nucleotide polymorphism, Cys1367Arg of the WRN gene, with the risk of bone and soft tissue sarcomas in Japan.
Topics: Adult; Alleles; Arginine; Base Sequence; Bone Neoplasms; Case-Control Studies; Cysteine; Exodeoxyribonucleases; Female; Genetic Predisposition to Disease; Genotype; Humans; Japan; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense; Polymorphism, Single Nucleotide; RecQ Helicases; Sarcoma; Werner Syndrome Helicase | 2008 |
Promotor polymorphisms in leukotriene C4 synthase and risk of ischemic cerebrovascular disease.
Topics: Adult; Aged; Aged, 80 and over; Carotid Artery Diseases; Case-Control Studies; Cerebrovascular Disorders; Cross-Sectional Studies; Cysteine; Female; Follow-Up Studies; Gene Frequency; Genetic Predisposition to Disease; Glutathione Transferase; Humans; Leukotrienes; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Genetic; Predictive Value of Tests; Prospective Studies; Risk Factors; Stroke; Venous Thrombosis | 2008 |
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
Topics: Adult; Arginine; Cysteine; DNA Mutational Analysis; Family Health; Female; Fluorodeoxyglucose F18; Frontotemporal Dementia; Genetic Predisposition to Disease; Humans; Intercellular Signaling Peptides and Proteins; Male; Microtubule-Associated Proteins; Middle Aged; Mutation; Presenilin-1; Progranulins; Radionuclide Imaging | 2009 |
Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.
Topics: Asian People; Case-Control Studies; Cysteine; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Linkage Disequilibrium; Male; Polymorphism, Single Nucleotide; Receptors, Dopamine D2; Risk; Schizophrenia; Serine; Taiwan | 2009 |
Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis.
Topics: Amino Acid Substitution; Animals; Base Sequence; Blotting, Western; Chlorocebus aethiops; Complement Factor H; COS Cells; Cysteine; Eye; Genetic Predisposition to Disease; Glomerulonephritis, Membranoproliferative; Humans; Kidney; Macular Degeneration; Mass Spectrometry; Middle Aged; Molecular Sequence Data; Mutation; Recombinant Proteins; Tyrosine | 2008 |
Overall and relapse-free survival in oropharyngeal and hypopharyngeal squamous cell carcinoma are associated with genotypes of T393C polymorphism of the GNAS1 gene.
Topics: Adult; Aged; Amino Acid Substitution; Biomarkers, Tumor; Carcinoma, Squamous Cell; Chromogranins; Cysteine; Disease-Free Survival; Female; Genetic Predisposition to Disease; Genotype; GTP-Binding Protein alpha Subunits, Gs; Humans; Hypopharyngeal Neoplasms; Male; Middle Aged; Oropharyngeal Neoplasms; Polymorphism, Single Nucleotide; Prognosis; Recurrence; Survival Analysis; Threonine | 2008 |
Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474.
Topics: Androgen-Binding Protein; Animals; Arginine; Base Sequence; Binding Sites; Cattle; Cell Line, Transformed; Chlorocebus aethiops; CHO Cells; Consanguinity; Cricetinae; Cysteine; DNA, Complementary; Female; Genetic Predisposition to Disease; Genetic Vectors; Humans; Laminin; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Protein S; Protein S Deficiency; Rabbits; Rats; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Thrombosis | 1996 |
Compound heterozygosity for two novel missense mutations in the prothrombin gene in a patient with a severe bleeding tendency.
Topics: Blood Coagulation Factors; Cysteine; Female; Genetic Predisposition to Disease; Genetic Variation; Hemorrhage; Heterozygote; Humans; Hypoprothrombinemias; Infant, Newborn; Point Mutation; Prothrombin; Reference Values; Sequence Analysis, DNA; Tryptophan; Tyrosine | 1997 |
C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes.
Topics: Adult; Codon; Cysteine; Diabetes Mellitus, Type 2; England; Female; Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Humans; Male; Middle Aged; Mutation; Polymerase Chain Reaction; Prevalence; Tyrosine | 1998 |
Xenon does not trigger malignant hyperthermia in susceptible swine.
Topics: Amino Acid Substitution; Anesthesia, General; Anesthetics, Inhalation; Animals; Arginine; Blood Pressure; Cardiac Output; Cysteine; Genetic Predisposition to Disease; Halothane; Heart Rate; Homozygote; Malignant Hyperthermia; Mutation; Ryanodine Receptor Calcium Release Channel; Swine; Xenon | 1999 |
hOGG1 Ser326Cys polymorphism and lung cancer susceptibility.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Carcinoma, Squamous Cell; Case-Control Studies; Cysteine; DNA Damage; Genetic Predisposition to Disease; Guanine; Humans; Japan; Lung Neoplasms; Male; Middle Aged; N-Glycosyl Hydrolases; Polymorphism, Genetic; Risk Assessment; Serine | 1999 |
Further evidence supporting the association between the dopamine receptor D2 Ser/Cys311 variant and disorganized symptomatology of schizophrenia.
Topics: Amino Acid Substitution; Cysteine; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Polymorphism, Genetic; Receptors, Dopamine D2; Schizophrenia, Disorganized; Serine | 2000 |
Ser326Cys polymorphism in hOGG1 gene and risk of esophageal cancer in a Chinese population.
Topics: Amino Acid Substitution; Asian People; Cysteine; DNA-Formamidopyrimidine Glycosylase; Esophageal Neoplasms; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; N-Glycosyl Hydrolases; Polymorphism, Genetic; Risk Factors; Serine | 2001 |
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arteriosclerosis; Aspartic Acid; Brain Infarction; Cardiovascular Diseases; Case-Control Studies; Cysteine; Female; France; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; HLA Antigens; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Myocardial Infarction; Northern Ireland; Polymorphism, Genetic; Prevalence; Prospective Studies; Tyrosine; Ultrasonography; United Kingdom | 2001 |
Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder.
Topics: Amino Acid Substitution; Bipolar Disorder; Cysteine; Depressive Disorder; Ethnicity; Europe; Female; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genetic Variation; Humans; Israel; Least-Squares Analysis; Likelihood Functions; Male; Polymorphism, Genetic; Receptor, Serotonin, 5-HT2C; Receptors, Serotonin; Reference Values; Serine; White People | 2001 |
Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C.
Topics: Adult; Aged; Alleles; Case-Control Studies; Chi-Square Distribution; Cohort Studies; Cysteine; Female; Genetic Predisposition to Disease; Genetic Testing; Haptoglobins; Hepatitis C, Chronic; Humans; Male; Middle Aged; Mutation, Missense; Phenotype; Polymorphism, Genetic; Prevalence; Probability; Reference Values; Risk Assessment; Tyrosine | 2001 |
Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene.
Topics: Adult; Aged; Aspartic Acid; Case-Control Studies; Cysteine; Double-Blind Method; Female; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hispanic or Latino; Histidine; Homozygote; Humans; Male; Middle Aged; Mutation; Prevalence; Surveys and Questionnaires; Transferrin; Tyrosine; United States; White People | 2002 |