glutamine has been researched along with Genetic Predisposition in 128 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 7 (5.47) | 18.2507 |
| 2000's | 66 (51.56) | 29.6817 |
| 2010's | 54 (42.19) | 24.3611 |
| 2020's | 1 (0.78) | 2.80 |
| Authors | Studies |
|---|---|
| Amos, CI; Bloomer, W; Chen, K; Lee, JE; Li, X; Liu, H; Liu, Z; Nan, H; Wei, Q | 1 |
| Daly, E; Gudbrandsen, M; Hathway, P; Howes, O; Jauhar, S; McCutcheon, RA; Rogdaki, M | 1 |
| Bussink, J; Kaanders, JHAM; Lok, J; Looijen-Salamon, MG; Meijer, TWH; Span, PN; Tops, B; van den Heuvel, M | 1 |
| Aasen, T; Abdul Moin, NI; Abdul Wafi, S; Aboukameel, A; Abu-Bakar, N; Acharya, A; Ackermans, L; Adaramoye, O; Adarsh, KV; Adeosun, WA; Ahmad, NH; Ahmadi, F; Akanni, O; Akbar, M; Akbulak, RO; Akev, N; Akkaya, Ö; Al-Rashed, S; AlAbbad, S; Alabi, O; Alappat, BJ; Alcalá, S; Alcoutlabi, M; Aleppo, G; Alexander Ross, JB; Alexander, JH; Alexander, R; Alias, A; Alimba, C; Alken, FA; Allan, R; Alpers, M; Alsbou, EM; Amarasiri, SS; An, T; Anastasiadis, F; Anastassiadou, M; Anderson, KC; Andronikos, P; Anheyer, D; Annapurna, K; Anorlu, RI; Anten, MM; Anthopoulos, TD; Araujo-Castillo, RV; Aravamudhan, S; Arawwawala, LDAM; Arulsamy, N; Arunamata, A; Asghar, A; Asiri, AM; Aslanidou, T; Astrakhantseva, IV; Astutik, E; Attanayake, AP; Atwater, BD; Audureau, E; Augusto, S; Bakare, A; Banach, M; Bandelier, P; Banerjee, S; Barral, M; Bascuñán, J; Bates, FS; Bauer, NJC; Bayrak, BB; Beck, RW; Beckervordersantforth, J; Beeri, R; Begum, R; Beldi-Ferchiou, A; Bellingham, G; Ben-Tal, N; Bendib, I; Bergenstal, RM; Berger, MF; Bernasconi, G; Berry, S; Beuvon, F; Bi, WJ; Bi, Z; Bianconi, V; Bibi, I; Blank, BR; Bliemeister, E; Bobkowski, W; Bode, AM; Booth, CM; Bose, U; Boyd, K; Brancato, A; Brenmoehl, J; Brogi, E; Bronzo, P; Brooks, T; Brown, D; Brown, DN; Bruce, D; Buan, MEM; Bueno-Hernández, F; Bugielski, B; Bulavaitė, A; Buscagan, TM; Buxton, R; Caffaro, MM; Cai, Q; Cai, X; Cai, Y; Calhoun, P; Callander, N; Cambier, S; Camparo, P; Canales-Vargas, EJ; Canham, K; Cantu, J; Cao, J; Cao, JW; Cao, P; Cao, T; Cao, X; Caravella, BA; Carcadea, E; Carè, J; Carmichael, P; Carrasco Cabrera, L; Carteaux, G; Carvalho, PDS; Casarez, E; Cazorla, M; Celestrin, CP; Chakraborty, NK; Chan, B; Chandarlapaty, S; Chandgude, AL; Chang, CC; Chang, JH; Chang, X; Chang, Y; Chankhanittha, T; Chantanis, S; Chapovetsky, A; Chavan, S; Chen, B; Chen, D; Chen, F; Chen, G; Chen, H; Chen, J; Chen, K; Chen, KJ; Chen, KP; Chen, L; Chen, MA; Chen, Q; Chen, S; Chen, W; Chen, WF; Chen, X; Chen, Y; Cheng, D; Cheng, J; Cheng, Q; Cheon, GJ; Chiu, SC; Cho, CH; Cho, J; Choi, H; Choi, JS; Choi, YH; Christie, P; Chu, CH; Chu, Y; Chung, DH; Chung, F; Cline, JP; Cohen, A; Cohen, AD; Cohen, NJ; Comen, E; Compter, I; Cong, J; Cong, Z; Cooper, A; Cornud, F; Costa, C; Costa, S; Covey, A; Cowan, AM; Cramer, H; Cruz-Rivera, C; Cui, J; Cui, M; Cui, Y; Cui, YH; Culquichicón, C; Cushman, T; D'Auria, SJ; da Silva, J; Dalgediene, I; Danenberg, HD; Das, S; Dasgupta, K; Daubit, IM; de Oliveira, PD; de Prost, N; De Ruysscher, D; Dearman, K; Decato, D; Delfau-Larue, MH; Deng, L; Dhakate, SR; Dharuman, V; Di Costanzo, N; Dickler, MN; Dinehart, EE; Ding, D; Dinh, TK; Divya, KP; Djifack Tadongfack, T; Do, T; Domínguez-Roldan, R; Domínguez-Zambrano, E; Dömling, A; Donato, MD; Dong, JH; Dong, W; Dong, X; Dong, XR; Dong, Y; Dong, Z; Downs, M; Drutskaya, MS; Du, B; Du, F; Du, H; Du, L; Du, X; Duan, Z; Duangthip, D; Dunstand-Guzmán, E; Duong, F; Eckert, DJ; Edelhäuser, BAH; Eekers, DBP; Efendi, F; Efraimidis, P; Ehrenberg, H; Ehsanbakhsh, Z; Eickholt, C; Eksterowicz, J; El Mobadder, M; El-Araby, IE; El-Magd, MA; El-Tarabany, MS; Elgorban, AM; Engelmann, D; English, KL; Esfandiari, H; Eslami, B; Espinosa-Cuevas, A; Eswara, S; Faber, E; Fan, XH; Fan, Y; Fang, J; Fang, Z; Fantin, VR; Fei, P; Feng, G; Feng, H; Feng, J; Feng, X; Feng, XJ; Fennell, TR; Fernández-Moreira, V; Ferraz, ABF; Ferreras, KN; Flores, K; Flores-Pérez, I; Flox, C; Fluharty, FL; Fokouong Tchoffo, E; Folefack, GO; Foroutan, T; Fort, D; Fourati, S; Fousas, S; Frapard, T; Freguia, S; Friedman, DJ; Friedman, LS; Fu, D; Fu, Q; Fu, Y; Fujinami, S; Furihata, K; Gal, RL; Gan, H; Gao, C; Gao, F; Gao, R; Gao, SS; Gao, W; Gao, XC; Gao, Y; Gao, Z; Garozi, L; Ge, J; Georgiopoulos, A; Gerakiou, K; Ghazimirsaeed, SM; Ghazimirsaeed, ST; Gimeno, MC; Gjestad, R; Glurich, I; Goetchius, E; Goland, S; Goldstein, S; Gonçalves, CM; Gonçalves, H; Gong, Q; Gonzalez, D; Goplen, FK; Gorshkova, EN; Gotsman, I; Govindasamy, V; Granger, CB; Greco, L; Grigoriadou-Skouta, E; Grigoropoulos, P; Grivicich, I; Gromov, NV; Gruber, S; Grytczuk, M; Grzech-Leśniak, K; Gu, L; Gu, S; Gu, Z; Guadagnini, D; Guan, H; Guilliams, M; Guo, J; Guo, L; Gupta, A; Gupta, SK; Gurzu, S; Gutleb, AC; Haban, A; Hablitz, JJ; Hadisuyatmana, S; Hahn, S; Haiges, R; Hallal-Calleros, C; Hamed, M; Hammad, N; Hammer, N; Han, C; Hao, Y; Harnett, J; Has, EMM; Hassanpour, K; Hatzopoulos, D; Hawaldar, R; He, X; He, Y; He, YY; He, Z; Heberman, D; Heckl, D; Hegde, H; Henson, MA; Hernández-Velázquez, VM; Herrera, E; Hijazi, Z; Hirayama, K; Hirth, JM; Hoeben, A; Hohnloser, SH; Hong, M; Hood, K; Hoplock, LB; Hopman, WM; Horlbogen, LM; Hossein Rashidi, B; Hou, G; Hou, H; Hou, J; Hou, Y; Hu, J; Hu, W; Hu, X; Hua, W; Huang, G; Huang, H; Huang, J; Huang, T; Huang, W; Huang, Y; Huang, YD; Huang, Z; Hudis, CA; Hue, S; Huo, J; Hussain, M; Hvas, AM; Ichii, T; Ide Zeuna, J; Ilyas, S; Inoue, T; Iranzo, A; Irfan, M; Iwasa, Y; Iwashita, Y; Izgorodina, EI; J R, A; Jaber, WA; Jaborek, JR; Jacobus, SJ; Jadeja, SD; Jafarabadi, M; Jalan, D; Jamil, MI; Jarrah, S; Jarvis, D; Jayatilaka, KAPW; Jemal-Turki, A; Jeon, YK; Jeong, N; Jeong, SH; Jeong, SY; Jermy, M; Jhaveri, K; Ji, H; Ji, K; Ji, RY; Jiang, F; Jiang, J; Jiang, X; Jiang, Y; Jiao, Q; Jilani, K; Jiménez-Guerrero, P; Jin, L; Jo, YH; Johnson, JG; Johnson, ML; Jones, WS; Jose, S; Jularic, M; Jung, I; Jung, YJ; Jungen, C; Junttila, MR; Kache, S; Kahanovitch, U; Kalantzi, KI; Kallio, T; Kamnoedboon, P; Kang, CH; Kang, H; Kang, J; Kang, KW; Kapoor, P; Karmakar, D; Kartalis, A; Kauranen, P; Kazocina, A; Keikha, F; Keltai, M; Kershaw, SV; Kettani, M; Khalvati, S; Khandhar, S; Khosla, N; Kiely, CJ; Kim, CC; Kim, H; Kim, MJ; Kim, Y; Kim, YH; Kim, YT; Kimoto, E; Kiyu, A; Klatt, N; Kobayashi, M; Koh, J; Köhler, R; Kondadasula, SV; Kong, H; Kong, W; Kong, X; Kotidis, A; Kotwal, A; Kouvari, M; Kozhinov, AN; Kruger, D; Kuang, S; Kuang, Y; Kubota, M; Kuklik, P; Kumar, P; Kumar, SK; Kuo, YF; Kurup, SP; Kusuhara, H; Kuswanto, H; Lacouture, ME; Lambin, P; Lang, CC; Langroudi, FH; Lanman, RB; Larsen, OH; Laskin, J; Le, VH; Leach, M; Lee, BG; Lee, DF; Lee, DS; Lee, HJ; Lee, SB; Lee, YA; Lei, Y; Lekashvili, O; Lelj, F; Lemin, AS; Lemoine, J; Leuschner, R; Li, B; Li, BT; Li, C; Li, D; Li, F; Li, G; Li, H; Li, HW; Li, J; Li, M; Li, P; Li, Q; Li, S; Li, W; Li, X; Li, XY; Li, Y; Li, Z; Lian, Y; Liang, C; Liao, J; Liao, W; Liao, Y; Lin, D; Lin, W; Lin, YL; Lindbäck, J; Lindsay, AP; Ling, J; Linser, PJ; Liu, C; Liu, H; Liu, JJ; Liu, L; Liu, Q; Liu, SF; Liu, X; Liu, Y; Liu, Z; Liu, ZM; Lo Sterzo, C; Lo, ECM; Lobchuk, MM; Lodge, TP; Logotheti, S; Lonial, S; Lopes, G; Lopes, RD; Lopez, J; Lopez, SA; López-Santos, AL; López-Sendón, JL; Loring, Z; Louis, C; Lovita, AND; Lu, DZ; Lu, H; Lu, J; Lu, K; Lu, TT; Lu, Y; Luengo, A; Lum, LG; Luna, JM; Luo, L; Luo, R; Luo, T; Luo, X; Luo, Z; Lv, B; Lymperopoulos, N; Lyras, A; Lyu, Y; M Kannan, A; Ma, H; Ma, M; Ma, Q; Ma, S; Ma, WY; Ma, Y; Maalouf, E; Machado, FA; Maeda, K; Magrans, JO; Maharani, A; Maia, G; Mainwaring, RD; Maji, TK; Majumdar, K; Mannarino, MR; Mansuri, MS; Marinescu, SC; Markatos, G; Marquardt, S; Marraiki, N; Martens, C; Martínez, TJ; Marumo, K; Maruyama, H; Marwani, HM; Marzo, I; Masrati, G; Matamba, P; Mathialagan, S; Matys, J; Mayatra, JM; Mboua, PC; McArthur, T; McCrimmon, RJ; McIntosh, S; McSpadden, S; Medina-Campos, ON; Medvedovsky, AT; Mei, Z; Mekontso-Dessap, A; Menezes, AMB; Meng, J; Meng, P; Meng, Y; Menter, A; Mets, MB; Mets-Halgrimson, R; Metzger, T; Metzler-Nolte, N; Meyer, C; Mi, Y; Michailoviene, V; Mikrogeorgiou, A; Militz, H; Miller Iii, TF; Minarowska, A; Mir, S; Miron, I; Miyake, T; Moayer, F; Modi, S; Moeller, SJ; Mohamad, MN; Mohammed, EHM; Mokhonov, VV; Mondal, A; Moore, J; Moravcova, M; Mordi, IR; Mordi, NA; Mortensen, NP; Moscariello, C; Moser, J; Moynahan, ME; Mu, J; Mu, W; Mudduwa, LKB; Mukherjee, S; Mukhtar, A; Mulkey, DK; Murr, N; Mushtaq, Z; Muthuswamy, N; Mutlu, O; Muto, C; Myroforou, I; Na, KJ; Nabi, M; Nagornov, KO; Nagy, RJ; Naik, A; Nakajima, K; Nam, KT; Nam, YW; Namburath, M; Nammour, S; Namour, A; Namour, M; Nanan, S; Natsume, H; Nave, S; Naveed, A; Nazir, H; Ndubaku, C; Nedospasov, SA; Neradilek, MB; Newcomb, C; Nguépy Keubo, FR; Nguyen, M; Ning, J; Ning, Q; Noguchi, S; Nordahl, SHG; Nordfalk, KF; Norton, L; Noupoue, EM; Nouri, SS; Nowak, JK; Núñez, K; Oakes, K; Odegaard, JI; Ogorodnikova, OL; Ogunsuyi, O; Oh, HK; Oh, HR; Oh, KH; Ohgi, K; Okunade, KS; Oliveira, AG; Olorunfemi, G; Olsen, ML; Olson, BA; Omari, KW; Ondruschka, B; Orfali, R; Orkopoulos, A; Orlowski, RZ; Oser, SM; Oser, TK; Özcan, M; Padilla, V; Paeng, JC; Pajuelo-Lozano, N; Pal, SK; Palmieri, S; Palomeque, E; Pan, W; Panagiotakos, DB; Pandey, M; Pang, D; Pang, Q; Pangarah, CA; Panny, A; Paparella, A; Papirio, S; Papouskova, K; Parang, K; Park, HJ; Park, IK; Park, S; Parker, TL; Parkhomenko, A; Parmon, VN; Parsons, B; Parsons, J; Patel, PR; Patil, S; Patsourakos, NG; Patterson, KC; Pavlidis, P; Pedernera, M; Pedersen, R; Pedraza-Chaverri, J; Pellegrini, M; Peña-Chora, G; Pereira, EDM; Pereira, MADS; Peretz, A; Perez-Padilla, R; Perlman, GY; Perona, R; Petras, C; Phuntsho, S; Picada, JN; Pinder, TA; Piper, LFJ; Pirozzi, F; Pirro, M; Pleckaityte, M; Ploutz-Snyder, LL; Ploutz-Snyder, R; Pogorzelski, A; Poles, L; Postma, AA; Prager, A; Prakash, J; Punn, R; Pützer, BM; Qi, J; Qi, MC; Qi, Y; Qian, J; Qian, Y; Qiang, L; Qiu, J; Qu, Y; Rabiu, KA; Rahighi, S; Rahman, MM; Rahmani, B; Rajkumar, SV; Ramanathan, R; Raras, TYM; Rashi, Y; Rasool, G; Rathore, MG; Ratnawati, R; Ratola, N; Raucci, U; Ray, SK; Razavi, P; Razazi, K; Razek, S; Razi, SS; Reback, M; Reddy, K; Rees, DC; Reginatto, FH; Reich, H; Reis-Filho, JS; Ren, X; Ren, Y; Renner, G; Rey, G; Reymen, B; Riaz, M; Ricci, A; Richardson, PG; Richter, C; Riga, M; Ritchie, C; Rivoal, S; Roberts, W; Robson, ME; Rocha, GZ; Rodrigues, AD; Rogach, AL; Rojas, A; Rosenberg, A; Rosenberg, E; Rosenheck, RA; Roslan, K; Rothenberger, C; Rouschop, KMA; Rubagumya, F; Ryan, CM; Ryder, JW; Saad, MJA; Sacan, O; Sacchi, A; Sahebkar, A; Saini, A; Sainz, B; Sajo, EA; Sakizadeh, J; Saleh, AA; Salgado Júnior, IB; Salvi, R; Samoylova, YV; Samuni, A; Sanchez, DM; Sanchez-Perez, I; Santos, M; Sarapulova, A; Sardot, T; Saud, N; Sauerbier, P; Scaltriti, M; Schaeffer, B; Schalk, DL; Scherschel, K; Schijven, MP; Schreuder, HWR; Schuhmacher, M; Schultz-Lebahn, A; Schwarzl, J; Scott, JM; Sebayang, SK; Seeger, ZL; Segabinazi Peserico, C; Selenica, P; Serio, A; Seruga, B; Shah, A; Shah, C; Shah, PD; Shahrokh Tehraninezhad, E; Shan, A; Shao, Z; Sharma, AMR; Sharma, RK; Shen, J; Shen, R; Shi, X; Shi, Y; Shi, ZE; Shih, YC; Shimohata, H; Shimpi, N; Shin, SH; Shon, HK; Shuvy, M; Siddique, AB; Siegbahn, A; Sikandar, M; Silvani, Y; Singh, A; Singh, AK; Singh, D; Singh, JS; Singh, KP; Singh, M; Situ, B; Skipper, MT; Skouloudi, M; Sloane, BF; Smyrnioudis, N; Snyder, MA; Söhnchen, C; Solis Condor, R; Solit, DB; Someya, S; Song, H; Song, J; Song, W; Song, Y; Sorokina, KN; Soshi, S; Soyer, P; Spitschak, A; Sreekrishnan, TR; Srinivasan, M; Staruschenko, A; Steel, A; Stefan-van Staden, RI; Stein, AM; Strayer, H; Struthers, AD; Su, H; Su, Q; Su, X; Sudore, RL; Sugimura, H; Sugiyama, Y; Sujuti, H; Sumner, SJ; Sun, B; Sun, D; Sun, H; Sun, J; Sun, JY; Sun, X; Sun, Y; Sun, Z; Sung, YC; Surenaud, M; Sutimantanapi, D; Suwandaratne, NS; Swaroop, S; Sychrova, H; Syed, A; Szczepanik, M; Szederjesi, J; Szodorai, R; Tacy, TA; Tadelle, RM; Takayasu, M; Tammeveski, K; Tan, H; Tan, M; Tang, HX; Tang, S; Tang, X; Tanokura, M; Tao, F; Tao, H; Tarafdari, A; Tarín-Carrasco, P; Tasson Tatang, C; Teixeira, JP; Thakur, A; Theobald, A; Thevenot, P; Thomaidis, K; Tian, J; Tillib, SV; Toma, C; Tomita, M; Tonchev, I; Tong, F; Toy, W; Trypuć, M; Tselepis, AD; Tsetseris, L; Tsikouri, GE; Tsikouris, EI; Tsoplifack, CB; Tsoumani, ME; Tsujimoto, R; Tsybin, YO; Tu, J; Tu, TM; Turco, M; Turkyilmaz, IB; Uddin, MJ; Ung, J; Unsihuay, D; Utsunomiya, T; Vagenende, B; Vaishnav, J; Valdes, C; Validad, MH; Valle, J; van Ginkel, MPH; van Grevenstein, WMU; Vanderpuye, V; Vasan, N; Vasilenko, EA; Vasques, GJ; Vavoulis, P; Verani, A; Veziroglu, E; Viegas, A; Vitali, MG; Vitsas, G; Voccio, JP; Vogiatzidis, C; Volow, A; Volpin, F; Vourvahis, M; Wagner, LI; Walkowiak, J; Wallace, R; Wallentin, L; Wan, D; Wan, L; Wan, T; Wang, C; Wang, F; Wang, FN; Wang, H; Wang, J; Wang, L; Wang, Q; Wang, S; Wang, T; Wang, W; Wang, X; Wang, XW; Wang, Y; Wang, YS; Wang, Z; Ward, J; Ward, L; Waseem, R; Watson, DF; Weber, P; Wehrmeister, FC; Wei, CH; Wei, H; Wei, L; Wei, Q; Wei, Y; Weinstock, RS; Weiss, M; Welborn, M; Wen, L; Wen, LM; Wen, Q; Wen, Z; Wesseling, P; Westerbergh, J; White, K; Wick, MP; Willems, S; Wiyasa, IWA; Wójciak, R; Wolkenhauer, O; Won, HH; Wong, J; Woo, YC; Wood, LS; Wu, CT; Wu, CY; Wu, D; Wu, G; Wu, J; Wu, K; Wu, M; Wu, Q; Wu, T; Wu, W; Wu, X; Wu, XT; Wu, Y; Xi, D; Xi, J; Xiang, W; Xiang, Y; Xiao, M; Xiao, Z; Xie, H; Xie, Q; Xie, S; Xie, X; Xing, M; Xing, YL; Xu, C; Xu, X; Xu, Y; Xu, Z; Xue, F; Xue, XD; Yaglioglu, HG; Yamada, H; Yamashita, M; Yan, W; Yan, Z; Yanardag, R; Yang, D; Yang, H; Yang, K; Yang, QQ; Yang, R; Yang, S; Yang, T; Yang, X; Yang, Y; Yao, H; Yao, Y; Yari, D; Yassin, MT; Ye, C; Ye, J; Ye, Q; Yildiz, EA; Ying, S; Yoon, H; Yu, D; Yu, K; Yu, N; Yu, PL; Yuan, C; Yuan, D; Yuan, LJ; Yuan, Z; Yuen, N; Zagatto, AM; Zakaria, Y; Zalewski, AM; Zamora, S; Zavorotinskaya, T; Zeid, JL; Zeinoun, T; Zeng, C; Zerby, HN; Zhan, X; Zhang, A; Zhang, D; Zhang, E; Zhang, F; Zhang, H; Zhang, J; Zhang, L; Zhang, M; Zhang, P; Zhang, Q; Zhang, QY; Zhang, RG; Zhang, S; Zhang, T; Zhang, X; Zhang, Y; Zhang, YY; Zhao, CK; Zhao, H; Zhao, J; Zhao, K; Zhao, Q; Zhao, S; Zhao, T; Zhao, XQ; Zhao, Y; Zhao, Z; Zheng, J; Zheng, L; Zheng, Y; Zhou, B; Zhou, G; Zhou, L; Zhou, T; Zhou, X; Zhu, C; Zhu, J; Zhu, Y; Zhu, ZQ; Zhuang, T; Zimmermannova, O; Zin, NNINM; Zisimos, K; Zoghebi, KA; Zonder, JA; Zou, C; Zwirner, J | 1 |
| Barrère, C; Barrère-Lemaire, S; Boisguérin, P; Covinhes, A; Delgado-Betancourt, V; Gallot, L; Lattuca, B; Nargeot, J; Piot, C; Solecki, K; Sportouch, C; Vincent, A | 1 |
| Allasia, A; Deutz, NEP; Engelen, MPKJ; Klimberg, VS | 1 |
| Costeas, PA; Gerasimou, P; Monos, D; Nicolaidou, V; Picolos, M; Skordis, N | 1 |
| Behjati, M; Karimian, M; Mobasseri, N; Nikzad, H; Noureddini, M | 1 |
| Gomez, GVB; Lima, CSP; Lourenço, GJ; Moraes, AM; Oliveira, C; Rinck-Junior, JA; Torricelli, C | 1 |
| Abe, K; Hishikawa, N; Huang, Y; Liu, X; Morihara, R; Ohta, Y; Sato, K; Shang, J; Shi, X; Takemoto, M; Yamashita, T | 1 |
| Bănescu, C; Dobreanu, M; Duicu, C; Trifa, AP | 1 |
| Hammami, B; Hamza-Chaffai, A; Kallel, I; Khlifi, R; Rebai, A | 1 |
| Boussaada, R; Finsterer, J; Mehri, S; Ouarda, F; Zarrouk-Mahjoub, S | 1 |
| Chitnis, T; De Jager, PL; Frohlich, IY; Guttmann, CR; Hafler, DA; Healy, BC; Keenan, BT; Khoury, SJ; Lee, M; Ottoboni, L; Weiner, HL; Xia, Z | 1 |
| Attili, VS; Jamil, K; Madireddy, UR; Natukula, K; Pingali, UR | 1 |
| Alcais, A; Beldjord, C; Bouazza, N; Carel, JC; Chabadel, O; Chaussain, C; Courson, F; Davit-Béal, T; Droz, D; Gasse, B; Hennequin, M; Laboux, O; Laffont, AG; Moulis, E; Opsahl Vital, S; Sire, JY; Tassery, H; Treluyer, JM; Vaysse, F | 1 |
| Gao, CY; Li, BH; Li, JC; Liao, SQ; Liu, Y; Yin, YW; Zhang, LL; Zhang, M; Zhang, MJ | 1 |
| Abotalib, Z; Al-Hakeem, MM; Alharbi, KK; Khan, IA | 1 |
| Dong, WG; Guo, XF; Lei, XF; Wang, J; Zeng, YP | 1 |
| Deng, J; Fang, W; Lu, J; Qiu, F; Yang, L; Zhang, H; Zhang, L; Zhou, Y | 1 |
| Chen, SQ; Chen, Y; Hou, X; Jing, ZH; Liu, Y; Lv, WS; Song, XJ; Wang, R; Wang, YG | 1 |
| Akkad, DA; Antiguedad, A; Bedri, SK; Butzkueven, H; Dutertre, S; Field, J; Glaser, A; Graham, CA; Gresle, M; Gu, BJ; Hawkins, S; Hillert, J; Hoffjan, S; Kilpatrick, TJ; Laws, SM; Lea, R; Lechner-Scott, J; Matute, C; Ou, A; Petrou, S; Scott, R; Stankovich, J; Taylor, BV; Wiley, JS | 1 |
| Bargalló, N; Falcon, C; Gassó, P; Lafuente, A; Lázaro, L; Mas, S; Ortiz, AE | 1 |
| Aldashev, AA; Asambaeva, DA; Isakova, ZhT; Makieva, KB; Sultangazieva, BB | 1 |
| Egerton, A; Kempton, MJ; McGuire, PK; Merritt, K; Taylor, MJ | 1 |
| Boer, VO; Cahn, W; Kahn, RS; Klomp, DW; Neggers, SF; Rösler, L; Thakkar, KN; Wijnen, JP | 1 |
| Du, H; Lv, J; Yang, J; Zhang, L | 1 |
| Jin, AL; Xie, XR; Yang, YM | 1 |
| Campagna, G; Grilli, A; La Fratta, I; Pesce, M; Rizzuto, A; Tatangelo, R | 1 |
| Liu, MT; Meng, T; Ren, Q; Shi, H; Wang, JM; Zhang, ST | 1 |
| Lieberman, AP; Robins, DM | 1 |
| Singh, D; Singh, JR; Sperling, K; Vanita, V; Varon, R | 1 |
| Chang, KW; Chang, SS; Ku, TH; Liu, CJ; Shieh, TM; Tu, HF | 1 |
| Mate, A; Nagy, G; Nemoda, Z; Rahman, OA; Ronai, Z; Sasvari-Szekely, M; Somogyi, A; Varga, T | 1 |
| Lamnissou, K; Stefanakis, N; Trygonis, S; Ziroyiannis, P | 1 |
| Inoue, N; Kasahara, M; Miyaishi, A; Osawa, K; Osawa, Y; Shimada, E; Tabuchi, Y; Takahashi, J; Tanaka, K; Tsutou, A; Yamamoto, M; Yoshida, K | 1 |
| De Vivo, G; Gentile, V | 1 |
| Anyanwu, SN; Bunker, CH; Ezeome, ER; Ferrell, RE; Garte, SJ; Kuller, LH; Okobia, MN; Taioli, E; Uche, EE; Zmuda, JM | 1 |
| Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pellkofer, H; Pöllmann, W | 1 |
| Galán, JJ; Jover, M; Romero-Gómez, M; Ruiz, A | 1 |
| Bertolacini, CD; Ribeiro-Bicudo, LA; Richieri-Costa, A | 1 |
| Pinheiro, TJ; Robinson, PJ | 1 |
| Gunduz, M; Mita, Y; Naomoto, Y; Ouchida, M; Sakai, A; Shimizu, K; Tanabe, S; Toyooka, S; Yamamoto, H; Yasuda, Y | 1 |
| Donglan, S; Na, W; Rongmiao, Z; Yan, L; Yanan, D; Zhifeng, C | 1 |
| Kalela, A; Kortelainen, ML; Kunnas, T; Lahtio, R; Nikkari, ST | 1 |
| Constantin, A; Costache, G; Glavce, CS; Popov, DL; Sima, AV; Vladica, M | 1 |
| Bonaldo, P; Bovolenta, M; Ferlini, A; Franchella, A; Gualandi, F; Martoni, E; Mercuri, E; Merlini, L; Messina, S; Sabatelli, P; Squarzoni, S; Urciuolo, A | 1 |
| Eerola, J; Luoma, PT; Paisan-Ruiz, C; Peuralinna, T; Scholz, S; Singleton, AB; Suomalainen, A; Tienari, PJ | 1 |
| Dooijes, D; Jongbloed, JD; Paulus, WJ; van den Berg, MP; van der Werf, R; van Spaendonck-Zwarts, KY; van Tintelen, JP; van Veldhuisen, DJ | 1 |
| Einav, Y; Hauschner, H; Koren, A; Mansour, W; Rosenberg, N; Seligsohn, U | 1 |
| Catamo, E; Crovella, S; Fabris, A; Pontillo, A; Vendramin, A | 1 |
| Cakir, E; Dalgic, N; Kayaalti, Z; Kilic, B; Kutlubay, B; Odabasi, M; Sancar, M; Soylemezoglu, T; Tekin, D | 1 |
| Alam, F; Chua, SC; Duggal, P; Gilchrist, CA; Guo, X; Haque, R; Houpt, E; Leduc, CA; Leibel, RL; Marie, C; Mondal, D; Myers, MG; Noor, Z; Peterson, KM; Petri, WA; Porcella, SF; Ricklefs, S; Sher, A; Verkerke, HP | 1 |
| Bradley, DT; Hughes, AE; Mullan, GM | 1 |
| Azechi, M; Fukumoto, M; Hashimoto, R; Ikezawa, K; Iwase, M; Kamino, K; Kasai, K; Kazui, H; Ohi, K; Takeda, M; Umeda-Yano, S; Yamamori, H; Yasuda, Y | 1 |
| Acosta, MT; Arbelaez, A; Arcos-Burgos, M; Bailey-Wilson, JE; Balog, J; Castellanos, FX; Elia, J; Freitag, CM; Hakonarson, H; Hemminger, U; Jacob, C; Jain, M; Lesch, KP; Londoño, AC; Lopera, F; Meyer, J; Muenke, M; Palacio, JD; Palacio, LG; Palmason, H; Pineda, D; Renner, T; Roessler, E; Romanos, J; Romanos, M; Seitz, C; Swanson, J; Vélez, JI; Walitza, S; Warnke, A | 1 |
| Dai, LM; Fang, LZ; Fu, WP; Liu, L; Shu, JK; Sun, C; Wang, L; Wang, XM; Zhang, JQ; Zhao, ZH; Zhong, L | 1 |
| Al-Mohanna, F; Al-Saif, A; Bohlega, S | 1 |
| Feng, S; Li, Z; Lu, B; Shao, L; Shuai, Y; Wang, J; Wang, L; Zhao, Y; Zhong, Y | 1 |
| Bhowmik, AD; Chaudhuri, K; Mukherjee, S; Mukhopadhyay, K; Ray, JG; Roychoudhury, P | 1 |
| Breman, C; Delanghe, J; Gahutu, JB; Masaisa, F; Mukiibi, J; Philippé, J | 1 |
| Bergseng, E; Bodd, M; Lundin, KE; Sollid, LM; Tollefsen, S | 1 |
| Ghanizadeh, A; Mohammadynejad, P; Saadat, I; Saadat, M | 1 |
| Cavalli, IJ; de Oliveira, BV; de Souza Fonseca Ribeiro, EM; de Syllos Cólus, IM; Dos Reis, MB; Losi-Guembarovski, R; Mizuno, LT; Morita, MC; Ramos, GH; Rogatto, SR | 1 |
| Adamski, J; Giegling, I; Hartmann, AM; He, Y; Illig, T; Kahn, R; Li, Y; Prehn, C; Rujescu, D; Wang-Sattler, R; Xie, L; Yu, Z | 1 |
| Doecke, JD; Fozzard, N; Jones, G; Morrison, NA; Nicholson, GC; Osato, M; Pasco, J; Polly, P; Prince, RL; Ralston, SH; Sambrook, PN; Stephens, AA; Tan, TC; Yamashita, N | 1 |
| Czerwinski, M; Duk, M; Grodecka, M; Jaskiewicz, E; Kaczmarek, R; Laskowska, A; Lisowska, E; Lukasiewicz, J; Majorczyk, E; Smolarek, D; Suchanowska, A; Wasniowska, K | 1 |
| Li, SW; Li, Y; Liu, F; Tan, SQ; Wang, Y | 1 |
| Chen, Y; Hong, XS; Jing, X; Lei, M; Liu, X; Luo, XP; Xiong, XD; Zeng, LQ | 1 |
| Colagiuri, S; Duarte, NL; Palu, T; Wang, XL; Wilcken, DE | 1 |
| Christiani, DC; Lee, BW; London, L; Myers, J; Paulauskis, J | 1 |
| Calabuig, J; Macho-Azcarate, T; Marti, A; Martinez, JA | 1 |
| Ariza, A; Beyer, K; Fernández-Figueras, MT; Lao, JI; Latorre, P; Mate, JL; Matute, B; Riutort, N | 1 |
| Corbalán, MS; Forga, L; Marti, A; Martínez, JA; Martínez-González, MA; Sánchez-Villegas, A | 1 |
| Abate, N; Cabo-Chan, A; Carulli, L; Chandalia, M; Grundy, SM; Snell, PG | 1 |
| Barrack, ER; Ding, D; Menon, M; Reddy, GP; Xu, L | 1 |
| Amarenco, P; Arveiler, D; Cambien, F; Courbon, D; Ducimetière, P; Elbaz, A; Evans, A; Gariépy, J; Kee, F; Morrison, C; Nicaud, V; Poirier, O | 1 |
| Cilli, A; Coskun, M; Keser, I; Ogus, AC; Olcen, S; Ozdemir, T; Uguz, A; Yegin, O; Yoldas, B | 1 |
| Benke, KS; Damasceno, BP; Loscalzo, J; Panhuysen, CI; Voetsch, B | 1 |
| Hamajima, N; Ito, H; Kang, D; Lee, KM; Matsuo, K; Mitsudomi, T; Saito, T; Sato, S; Sugiura, T; Tajima, K; Ueda, R; Yasue, T; Yoo, KY | 1 |
| Allen, P; Hanstock, C; Tibbo, P; Valiakalayil, A | 1 |
| Clarimon, J; Eerola, J; Hellström, O; Singleton, A; Tienari, PJ | 1 |
| Béziel, A; Blanc, MC; Cynober, L; Darquy, S; De Bandt, JP; Moinard, C | 1 |
| Heliö, T; Jääskeläinen, P; Kaartinen, M; Kärkkäinen, S; Kuusisto, J; Laakso, M; Miettinen, R; Nieminen, MS; Peuhkurinen, K; Reissell, E; Toivonen, L; Tuomainen, P; Ylitalo, K | 1 |
| Bresolin, N; Comi, GP; Del Bo, R; Dominici, R; Fenoglio, C; Forloni, G; Galbiati, S; Galimberti, D; Gatti, A; Guidi, I; Lovati, C; Mariani, C; Pomati, S; Scarpini, E; Venturelli, E; Virgilio, R | 1 |
| Jeon, YT; Kang, SB; Kim, JW; Lee, HP; Park, NH; Song, YS | 1 |
| Bowden, G; Burren, O; Cooper, JD; Godfrey, LM; Guja, C; Ionescu-Tîrgovişte, C; Lam, AC; Masters, J; Nutland, S; Pask, R; Payne, F; Rance, H; Rønningen, KS; Smink, LJ; Smyth, DJ; Szeszko, J; Todd, JA; Twells, RC; Undlien, DE; Walker, NM; Wang, WY | 1 |
| Abrahamsson, PA; Ahlgren, G; Gadaleanu, V; Giwercman, A; Giwercman, YL | 1 |
| Burmester, GR; Diterich, I; Draing, C; Eckert, J; Göbel, UB; Hahn, K; Hartung, T; Hassler, D; Hermann, C; Michelsen, KS; Priem, S; Schröder, NW; Schumann, RR; von Baehr, V; Zinke, A | 1 |
| Mitchell, BD; O'Connell, JR; Pollin, TI; Shuldiner, AR; Steinle, NI | 1 |
| Braunwald, E; DelMonte, T; Devlin, JJ; Dracopoli, NC; Hui, L; Iakoubova, OA; Kirchgessner, TG; Ranade, K; Sabatine, MS; Sacks, FM; Shaw, PM; Tsuchihashi, Z; Vishnupad, P; White, TJ | 1 |
| Heinonen, S; Helisalmi, S; Hiltunen, M; Laakso, M; Saarela, T | 1 |
| Itokawa, M; Yoshikawa, T | 1 |
| Burke, GL; Chang, JM; Durda, JP; Heckbert, SR; Kuller, LH; Lemaitre, RN; Lumley, TS; Psaty, BM; Rea, TD; Siscovick, DS; Sotoodehnia, N; Towbin, JA; Tracy, RP; Vatta, M | 1 |
| Chen, J; Lipska, BK; Weinberger, DR | 1 |
| Alpsoy, E; Bacanli, A; Sallakci, N; Yavuzer, U; Yegin, O | 1 |
| Arici, M; Bakkaloglu, A; Berdeli, A; Besbas, N; Kutlay, S; Ozen, S; Türel, B; Yalcinkaya, F; Yilmaz, E | 1 |
| Allan, JM; Smith, AG; Worrillow, LJ | 1 |
| Milutinović, A; Petrovic, D | 1 |
| Aasly, JO; Adler, CH; Blazquez, M; Farrer, MJ; Gibson, JM; Gwinn-Hardy, K; Haugarvoll, K; Hulihan, MM; Kachergus, J; Lynch, T; Mata, IF; Ross, OA; Stone, JT; Toft, M; White, LR | 1 |
| Böcker, U; Haas, SL; Ruether, A; Schreiber, S; Singer, MV | 1 |
| Bahar, R; Dubinsky, MC; Dutridge, D; Katzir, L; Mengesha, E; Picornell, Y; Quiros, A; Rotter, JI; Silber, G; Targan, SR; Taylor, KD; Wahbeh, G; Wang, D; Wrobel, I | 1 |
| Chen, H; Li, X; Pan, F; Xu, J; Ye, D; Zhang, K | 1 |
| Eberly, SW; Glazko, G; Goldenberg, I; Mathew, J; McNitt, S; Morray, B; Moss, AJ; Ryan, D; Zareba, W | 1 |
| Guo, Y; Lin, D; Miao, X; Sun, T; Tan, W; Zhang, X; Zhao, D | 1 |
| Christiani, DC; Gonzalez, E; Mahiuddin, G; McCarty, KM; Quamruzzaman, Q; Rahman, M; Ryan, L; Smith, TJ; Su, L; Zhou, W | 1 |
| Barbato, D; Di Angelantonio, E; Evangelista, A; Marchitti, S; Pirisi, A; Quarta, G; Rubattu, S; Stanzione, R; Volpe, M; Zanda, B | 1 |
| Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pöllmann, W; Rübsamen, H | 1 |
| Bastholm, IA; Melø, TM; Nehlig, A; Sonnewald, U | 1 |
| Adali, O; Arinç, E; Bek, S; Can Demirdöğen, B; Demirkaya, S; Sanisoğlu, Y; Türkanoğlu, A; Vural, O | 1 |
| Arnold, S; Brown, MA; Buchanan, D; Chenevix-Trench, G; Couch, FJ; Farrugia, DJ; Goldgar, DE; Healey, S; Henderson, BR; Lakhani, SR; Lovelock, PK; Mok, MT; Spurdle, AB; Tavtigian, SV | 1 |
| Akbari, MR; Bismar, TA; Darnel, A; Fafard, E; Foulkes, WD; Ghadirian, P; Giroux, S; Hamel, N; Martin, G; Narod, SA; Poll, A; Robidoux, A; Rousseau, F; Royer, R; Sabbaghian, N; Tischkowitz, M | 1 |
| Berkovic, SF; Freeman, JL; Harvey, AS; Izzillo, PA; Mulley, JC; Rosenfeld, JV; Shouri, MR; Wallace, RH | 1 |
| Bermejo, JL; Gurzau, E; Hemminki, K; Koppova, K; Kumar, R; Rudnai, P; Scherer, D | 1 |
| Bass, NJ; Choudhury, K; Curtis, D; Gurling, HM; Kosmin, M; Lawrence, J; McQuillin, A; Puri, V | 1 |
| Lv, Z; Ma, X; Wang, B; Wang, J; Xie, YC; Yang, Z; Zhang, P; Zheng, C; Zhou, S | 1 |
| Kloos, A; Weller, EB; Weller, RA | 1 |
| Cooper, CM; Da Costa, M; Detwiler, L; Jenny, AL; Neuman, S; Prusiner, SB; Westaway, D; Zuliani, V | 1 |
| Dahlbäck, B; He, X; Svensson, PJ; Zöller, B | 1 |
| Grohmann, J; Koch, HG; Nowak-Göttl, U; Schneppenheim, R; Vielhaber, H | 1 |
| Bertina, RM; Doggen, CJ; Manger Cats, V; Reitsma, PH; Rosendaal, FR; Vandenbroucke, JP | 1 |
| D'amato, M; di Pietro, A; Ferrigno, L; Matricardi, PM; Petrelli, G; Trezza, R; Vitiani, LR | 1 |
| Dybdahl, M; Frentz, G; Nexø, BA; Vogel, U; Wallin, H | 1 |
| Akahoshi, M; Arinobu, Y; Inoue, H; Nagano, S; Nakashima, H; Niho, Y; Niiro, H; Ogami, E; Otsuka, T; Tanaka, Y; Yamaoka, K | 1 |
| Belinsky, SA; Bocklage, TJ; Cook, DL; Crowell, RE; Divine, KK; Gilliland, FD; Stidley, CA | 1 |
| Barth, C; Ehren, M; Enderle, MD; Hering, S; Koch, M; Pfohl, M | 1 |
| Baylis, M; Bostock, CJ; Chihota, CM; Evans, JC; Goldmann, W; Gravenor, MB; Kao, RR; McLean, AR; Smith, AJ | 1 |
| Benjafield, AV; Ericsson, JO; Morris, BJ | 1 |
13 review(s) available for glutamine and Genetic Predisposition
| Article | Year |
|---|---|
Psychological distress among health care professionals of the three COVID-19 most affected Regions in Cameroon: Prevalence and associated factors.
Topics: 3' Untranslated Regions; 5'-Nucleotidase; A549 Cells; Accidental Falls; Acetylcholinesterase; Acrylic Resins; Actinobacillus; Acute Disease; Acute Kidney Injury; Adaptor Proteins, Signal Transducing; Adenosine; Adenosine Triphosphate; Administration, Inhalation; Administration, Oral; Adolescent; Adult; Advance Care Planning; Africa, Northern; Age Factors; Aged; Aged, 80 and over; Air Pollutants; Air Pollution; Air Pollution, Indoor; Albendazole; Aluminum Oxide; Anastomosis, Surgical; Ancylostoma; Ancylostomiasis; Androstadienes; Angiogenesis Inhibitors; Angiotensin II; Animals; Anti-Bacterial Agents; Anti-Infective Agents; Antibodies, Bispecific; Antibodies, Viral; Anticoagulants; Antihypertensive Agents; Antinematodal Agents; Antineoplastic Agents; Antineoplastic Agents, Immunological; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Antiporters; Antiviral Agents; Apoptosis; Aptamers, Nucleotide; Aromatase Inhibitors; Asian People; Astrocytes; Atrial Fibrillation; Auditory Threshold; Aurora Kinase B; Australia; Autophagy; Autophagy-Related Protein 5; Autotrophic Processes; Bacillus cereus; Bacillus thuringiensis; Bacterial Proteins; Beclin-1; Belgium; Benzene; Benzene Derivatives; Benzhydryl Compounds; beta Catenin; beta-Arrestin 2; Biliary Tract Diseases; Biofilms; Biofuels; Biomarkers; Biomarkers, Tumor; Biomass; Biomechanical Phenomena; Bioreactors; Biosensing Techniques; Biosynthetic Pathways; Bismuth; Blood Platelets; Bone and Bones; Bone Regeneration; Bortezomib; Botulinum Toxins, Type A; Brain; Brain Injuries; Brain Ischemia; Brain Neoplasms; Breast Neoplasms; Breath Tests; Bronchodilator Agents; Calcium Phosphates; Cannabis; Carbon Dioxide; Carbon Isotopes; Carcinogenesis; Carcinoma, Hepatocellular; Carcinoma, Non-Small-Cell Lung; Carcinoma, Squamous Cell; Cardiac Resynchronization Therapy; Cardiac Resynchronization Therapy Devices; Cardiomyopathies; Cardiovascular Diseases; Cariostatic Agents; Case Managers; Case-Control Studies; Catalysis; Cation Transport Proteins; CD8-Positive T-Lymphocytes; Cecropia Plant; Cell Adhesion; Cell Count; Cell Differentiation; Cell Division; Cell Line; Cell Line, Tumor; Cell Membrane; Cell Movement; Cell Proliferation; Cell Self Renewal; Cell Survival; Cells, Cultured; Cellular Reprogramming; Cellulose; Charcoal; Chemical and Drug Induced Liver Injury; Chemical Phenomena; Chemokines; Chemoradiotherapy; Chemoreceptor Cells; Child; Child Abuse; Child, Preschool; China; Chlorogenic Acid; Chloroquine; Chromatography, Gas; Chronic Disease; Clinical Competence; Coated Materials, Biocompatible; Cochlea; Cohort Studies; Color; Comorbidity; Computer Simulation; Computer-Aided Design; Contraception; Contraceptive Agents, Female; Contrast Media; COP-Coated Vesicles; Coronavirus Infections; Cost of Illness; Coturnix; COVID-19; Creatinine; Cross-Over Studies; Cross-Sectional Studies; Culex; Curriculum; Cyclic N-Oxides; Cytokines; Cytoplasm; Cytotoxicity, Immunologic; Cytotoxins; Databases, Factual; Deep Learning; Delivery, Obstetric; Denitrification; Dental Caries; Denture, Complete; Dexamethasone; Diabetes Complications; Diabetes Mellitus; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Dielectric Spectroscopy; Diet, High-Fat; Dietary Fiber; Disease Models, Animal; Disease Progression; DNA; DNA Copy Number Variations; DNA, Mitochondrial; Dog Diseases; Dogs; Dopaminergic Neurons; Double-Blind Method; Down-Regulation; Doxorubicin; Drug Carriers; Drug Design; Drug Interactions; Drug Resistance, Bacterial; Drug Resistance, Neoplasm; Drug-Related Side Effects and Adverse Reactions; Drugs, Chinese Herbal; Dry Powder Inhalers; Dust; E2F1 Transcription Factor; Ecosystem; Education, Nursing; Education, Nursing, Baccalaureate; Electric Impedance; Electricity; Electrocardiography; Electrochemical Techniques; Electrochemistry; Electrodes; Electrophoresis, Polyacrylamide Gel; Endoplasmic Reticulum; Endothelial Cells; Environmental Monitoring; Enzyme Inhibitors; Epithelial Cells; Epithelial-Mesenchymal Transition; Esophageal Neoplasms; Esophageal Squamous Cell Carcinoma; Estrogen Receptor Modulators; Europe; Evoked Potentials, Auditory, Brain Stem; Exosomes; Feasibility Studies; Female; Ferricyanides; Ferrocyanides; Fibrinogen; Finite Element Analysis; Fistula; Fluorescent Dyes; Fluorides, Topical; Fluorodeoxyglucose F18; Fluticasone; Follow-Up Studies; Food Contamination; Food Microbiology; Foods, Specialized; Forensic Medicine; Frail Elderly; France; Free Radicals; Fresh Water; Fungi; Fungicides, Industrial; Galactosamine; Gastrointestinal Neoplasms; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Gene Frequency; Genetic Predisposition to Disease; Genotype; Gingival Hemorrhage; Glioblastoma; Glioma; Glomerular Filtration Rate; Glomerulosclerosis, Focal Segmental; Glucose; Glucose Transport Proteins, Facilitative; Glucosides; Glutamine; Glycolysis; Gold; GPI-Linked Proteins; Gram-Negative Bacteria; Gram-Positive Bacteria; Graphite; Haplotypes; HCT116 Cells; Healthy Volunteers; Hearing Loss; Heart Failure; Hedgehog Proteins; HEK293 Cells; HeLa Cells; Hemodynamics; Hemorrhage; Hepatocytes; Hippo Signaling Pathway; Histone Deacetylases; Homeostasis; Hospital Mortality; Hospitalization; Humans; Hydantoins; Hydrazines; Hydrogen Peroxide; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Hydroxylamines; Hypoglycemic Agents; Immunity, Innate; Immunoglobulin G; Immunohistochemistry; Immunologic Factors; Immunomodulation; Immunophenotyping; Immunotherapy; Incidence; Indazoles; Indonesia; Infant; Infant, Newborn; Infarction, Middle Cerebral Artery; Inflammation; Injections, Intramuscular; Insecticides; Insulin-Like Growth Factor I; Insurance, Health; Intention to Treat Analysis; Interleukin-1 Receptor-Associated Kinases; Interleukin-6; Intrauterine Devices; Intrauterine Devices, Copper; Iron; Ischemia; Jordan; Keratinocytes; Kidney; Kidney Diseases; Kir5.1 Channel; Klebsiella Infections; Klebsiella pneumoniae; Lab-On-A-Chip Devices; Laparoscopy; Lasers; Lasers, Semiconductor; Lenalidomide; Leptin; Lethal Dose 50; Levonorgestrel; Limit of Detection; Lipid Metabolism; Lipid Metabolism Disorders; Lipogenesis; Lipopolysaccharides; Liquid Biopsy; Liver; Liver Abscess, Pyogenic; Liver Cirrhosis; Liver Diseases; Liver Neoplasms; Longevity; Lung Neoplasms; Luteolin; Lymph Nodes; Lymphocyte Activation; Macaca fascicularis; Macrophages; Mad2 Proteins; Magnetic Resonance Imaging; Male; Mammary Glands, Human; Manganese; Manganese Compounds; MAP Kinase Signaling System; Materials Testing; Maternal Health Services; MCF-7 Cells; Medicaid; Medicine, Chinese Traditional; Melanoma; Membrane Proteins; Mental Health; Mercury; Metal Nanoparticles; Metals, Heavy; Metformin; Methionine Adenosyltransferase; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred CBA; Mice, Knockout; Mice, Nude; Microalgae; Microbial Sensitivity Tests; Microglia; MicroRNAs; Microscopy, Atomic Force; Microscopy, Electron, Scanning; Middle Aged; Mitochondria; Mitochondrial Proteins; Mitral Valve; Mitral Valve Insufficiency; Models, Anatomic; Molecular Structure; Molybdenum; Monocarboxylic Acid Transporters; Moths; MPTP Poisoning; Multigene Family; Multiparametric Magnetic Resonance Imaging; Multiple Myeloma; Muscle, Skeletal; Mutagens; Mutation; Myeloid Cells; Nanocomposites; Nanofibers; Nanomedicine; Nanoparticles; Nanowires; Neoadjuvant Therapy; Neomycin; Neoplasm Grading; Neoplasm Recurrence, Local; Neoplasms; Neoplastic Stem Cells; Neostriatum; Neovascularization, Pathologic; Netherlands; Neuromuscular Agents; Neurons; NF-E2-Related Factor 2; NF-kappa B; Nickel; Nitrogen Oxides; Non-alcoholic Fatty Liver Disease; Nucleosides; Nucleotidyltransferases; Nutritional Status; Obesity, Morbid; Ofloxacin; Oils, Volatile; Oligopeptides; Oncogene Protein v-akt; Optical Imaging; Organic Cation Transport Proteins; Organophosphonates; Osteoarthritis; Osteoarthritis, Hip; Osteoarthritis, Knee; Osteoblasts; Osteogenesis; Oxidation-Reduction; Oxidative Stress; Oxides; Oxygen Isotopes; Pancreas; Pancreaticoduodenectomy; Pandemics; Particle Size; Particulate Matter; Patient Acceptance of Health Care; Patient Compliance; PC-3 Cells; Peptide Fragments; Peptides; Periodontal Attachment Loss; Periodontal Index; Periodontal Pocket; Periodontitis; Peroxides; Peru; Pest Control, Biological; Phosphatidylinositol 3-Kinase; Phosphatidylinositol 3-Kinases; Phylogeny; Pilot Projects; Piperidines; Plant Bark; Plant Extracts; Plant Leaves; Plasmids; Platelet Function Tests; Pneumonia, Viral; Podocytes; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerase Inhibitors; Polyethylene Terephthalates; Polymers; Polymorphism, Single Nucleotide; Porosity; Portugal; Positron-Emission Tomography; Postoperative Complications; Postural Balance; Potassium Channels, Inwardly Rectifying; Povidone; Powders; Precancerous Conditions; Precision Medicine; Predictive Value of Tests; Pregnancy; Prenatal Care; Prognosis; Promoter Regions, Genetic; Prospective Studies; Prostatectomy; Prostatic Neoplasms; Proteasome Inhibitors; Protective Agents; Protein Binding; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Protein Transport; Proto-Oncogene Proteins B-raf; Proto-Oncogene Proteins c-akt; Psychiatric Nursing; PTEN Phosphohydrolase; Pulmonary Embolism; Pyrimethamine; Radiopharmaceuticals; Rats; Rats, Sprague-Dawley; Rats, Wistar; Reactive Oxygen Species; Receptor, ErbB-2; Receptor, IGF Type 1; Receptors, Estrogen; Receptors, G-Protein-Coupled; Recombinational DNA Repair; Recovery of Function; Regional Blood Flow; Renal Dialysis; Renin; Renin-Angiotensin System; Reperfusion Injury; Reproducibility of Results; Republic of Korea; Respiratory Distress Syndrome; Retrospective Studies; Rhodamines; Risk Assessment; Risk Factors; RNA, Long Noncoding; RNA, Messenger; Running; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Salinity; Salmeterol Xinafoate; Sarcoma; Seasons; Shoulder Injuries; Signal Transduction; Silicon Dioxide; Silver; Sirtuin 1; Sirtuins; Skull Fractures; Social Determinants of Health; Sodium; Sodium Fluoride; Sodium Potassium Chloride Symporter Inhibitors; Sodium-Glucose Transporter 2 Inhibitors; Soil; Soil Pollutants; Spain; Spectrophotometry; Spectroscopy, Fourier Transform Infrared; Staphylococcal Protein A; Staphylococcus aureus; Stem Cells; Stereoisomerism; Stomach Neoplasms; Streptomyces; Strontium; Structure-Activity Relationship; Students, Nursing; Substance-Related Disorders; Succinic Acid; Sulfur; Surface Properties; Survival Rate; Survivin; Symporters; T-Lymphocytes; Temozolomide; Tensile Strength; Thiazoles; Thiobacillus; Thiohydantoins; Thiourea; Thrombectomy; Time Factors; Titanium; Tobacco Mosaic Virus; Tobacco Use Disorder; Toll-Like Receptor 4; Toluene; Tomography, X-Ray Computed; TOR Serine-Threonine Kinases; Toxicity Tests, Acute; Toxicity Tests, Subacute; Transcriptional Activation; Treatment Outcome; Troponin I; Tumor Cells, Cultured; Tumor Escape; Tumor Hypoxia; Tumor Microenvironment; Tumor Necrosis Factor Inhibitors; Tumor Necrosis Factor-alpha; Tyrosine; Ubiquitin-Protein Ligases; Ubiquitination; Ultrasonic Waves; United Kingdom; United States; United States Department of Veterans Affairs; Up-Regulation; Urea; Uric Acid; Urinary Bladder Neoplasms; Urinary Bladder, Neurogenic; Urine; Urodynamics; User-Computer Interface; Vemurafenib; Verbenaceae; Veterans; Veterans Health; Viral Load; Virtual Reality; Vitiligo; Water Pollutants, Chemical; Wildfires; Wnt Signaling Pathway; Wound Healing; X-Ray Diffraction; Xenograft Model Antitumor Assays; Xylenes; Young Adult; Zinc; Zinc Oxide; Zinc Sulfate; Zoonoses | 2021 |
Association between intercellular adhesion molecule-1 gene K469E polymorphism and the risk of stroke in a Chinese population: a meta-analysis.
Topics: Asian People; Confidence Intervals; Databases, Bibliographic; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Intercellular Adhesion Molecule-1; Lysine; Male; Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Stroke | 2015 |
XPD Lys751Gln polymorphisms and the risk of esophageal cancer: an updated meta-analysis.
Topics: Case-Control Studies; DNA Repair; Esophageal Neoplasms; Genetic Predisposition to Disease; Glutamine; Humans; Lysine; Odds Ratio; Polymorphism, Single Nucleotide; Prognosis; Risk Factors; Xeroderma Pigmentosum Group D Protein | 2015 |
The functional polymorphism of NBS1 p.Glu185Gln is associated with an increased risk of lung cancer in Chinese populations: case-control and a meta-analysis.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Cell Cycle Proteins; China; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Lung Neoplasms; Male; Middle Aged; Nuclear Proteins; Polymorphism, Single Nucleotide; Risk Factors | 2014 |
Association of LEPR Gln223Arg polymorphism with T2DM: A meta-analysis.
Topics: Amino Acid Substitution; Arginine; Diabetes Mellitus, Type 2; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Polymorphism, Single Nucleotide; Receptors, Leptin | 2015 |
The progression of coeliac disease: its neurological and psychiatric implications.
Topics: Adult; Celiac Disease; Cognitive Dysfunction; Diet, Gluten-Free; Disease Progression; Edible Grain; Environment; Female; Genetic Predisposition to Disease; Glutamine; Humans; Immune System Diseases; Immunity; Male; Mental Disorders; Middle Aged; Nervous System Diseases; Plant Proteins; Proline | 2017 |
Transglutaminase-catalyzed post-translational modifications of proteins in the nervous system and their possible involvement in neurodegenerative diseases.
Topics: Animals; Brain; Brain Chemistry; Genetic Predisposition to Disease; Glutamine; Humans; Inclusion Bodies; Nerve Tissue Proteins; Neurodegenerative Diseases; Protein Processing, Post-Translational; Transglutaminases; Trinucleotide Repeat Expansion | 2008 |
Gut ammonia production and its modulation.
Topics: Ammonia; Animals; Genetic Predisposition to Disease; Glutaminase; Glutamine; Hepatic Encephalopathy; Humans; Hyperammonemia; Intestine, Small; Liver Circulation; Liver Failure, Acute; Mutation | 2009 |
Complement factor B polymorphism 32W protects against age-related macular degeneration.
Topics: Aged; Aged, 80 and over; Arginine; Case-Control Studies; Complement Activation; Complement Factor B; Complement Factor H; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; High-Temperature Requirement A Serine Peptidase 1; Humans; Linkage Disequilibrium; Macular Degeneration; Male; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Retina; Risk Factors; Serine Endopeptidases; Smoking; Tryptophan | 2011 |
X-ray repair cross-complementing group 1 (XRCC1) genetic polymorphisms and cervical cancer risk: a huge systematic review and meta-analysis.
Topics: Arginine; Asian People; DNA Damage; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamine; Humans; Odds Ratio; Polymorphism, Genetic; Risk; Risk Factors; Tryptophan; Uterine Cervical Neoplasms; X-ray Repair Cross Complementing Protein 1 | 2012 |
[Susceptibility genes for schizophrenia].
Topics: Animals; Carrier Proteins; Dopamine; Dysbindin; Dystrophin-Associated Proteins; Genetic Linkage; Genetic Predisposition to Disease; Glutamine; Humans; Intracellular Signaling Peptides and Proteins; Nerve Tissue Proteins; Neuregulin-1; Polymorphism, Single Nucleotide; Schizophrenia | 2005 |
Genetic mouse models of schizophrenia: from hypothesis-based to susceptibility gene-based models.
Topics: Animals; Behavior, Animal; Disease Models, Animal; Dopamine; Genetic Predisposition to Disease; Glutamine; Mice; Models, Genetic; Schizophrenia | 2006 |
Biologic basis of bipolar disorder in children and adolescents.
Topics: Adolescent; Antimanic Agents; Aspartic Acid; Bipolar Disorder; Brain; Brain-Derived Neurotrophic Factor; Child; Energy Metabolism; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Lithium Compounds; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Neuropsychological Tests | 2008 |
2 trial(s) available for glutamine and Genetic Predisposition
| Article | Year |
|---|---|
Psychological distress among health care professionals of the three COVID-19 most affected Regions in Cameroon: Prevalence and associated factors.
Topics: 3' Untranslated Regions; 5'-Nucleotidase; A549 Cells; Accidental Falls; Acetylcholinesterase; Acrylic Resins; Actinobacillus; Acute Disease; Acute Kidney Injury; Adaptor Proteins, Signal Transducing; Adenosine; Adenosine Triphosphate; Administration, Inhalation; Administration, Oral; Adolescent; Adult; Advance Care Planning; Africa, Northern; Age Factors; Aged; Aged, 80 and over; Air Pollutants; Air Pollution; Air Pollution, Indoor; Albendazole; Aluminum Oxide; Anastomosis, Surgical; Ancylostoma; Ancylostomiasis; Androstadienes; Angiogenesis Inhibitors; Angiotensin II; Animals; Anti-Bacterial Agents; Anti-Infective Agents; Antibodies, Bispecific; Antibodies, Viral; Anticoagulants; Antihypertensive Agents; Antinematodal Agents; Antineoplastic Agents; Antineoplastic Agents, Immunological; Antineoplastic Combined Chemotherapy Protocols; Antioxidants; Antiporters; Antiviral Agents; Apoptosis; Aptamers, Nucleotide; Aromatase Inhibitors; Asian People; Astrocytes; Atrial Fibrillation; Auditory Threshold; Aurora Kinase B; Australia; Autophagy; Autophagy-Related Protein 5; Autotrophic Processes; Bacillus cereus; Bacillus thuringiensis; Bacterial Proteins; Beclin-1; Belgium; Benzene; Benzene Derivatives; Benzhydryl Compounds; beta Catenin; beta-Arrestin 2; Biliary Tract Diseases; Biofilms; Biofuels; Biomarkers; Biomarkers, Tumor; Biomass; Biomechanical Phenomena; Bioreactors; Biosensing Techniques; Biosynthetic Pathways; Bismuth; Blood Platelets; Bone and Bones; Bone Regeneration; Bortezomib; Botulinum Toxins, Type A; Brain; Brain Injuries; Brain Ischemia; Brain Neoplasms; Breast Neoplasms; Breath Tests; Bronchodilator Agents; Calcium Phosphates; Cannabis; Carbon Dioxide; Carbon Isotopes; Carcinogenesis; Carcinoma, Hepatocellular; Carcinoma, Non-Small-Cell Lung; Carcinoma, Squamous Cell; Cardiac Resynchronization Therapy; Cardiac Resynchronization Therapy Devices; Cardiomyopathies; Cardiovascular Diseases; Cariostatic Agents; Case Managers; Case-Control Studies; Catalysis; Cation Transport Proteins; CD8-Positive T-Lymphocytes; Cecropia Plant; Cell Adhesion; Cell Count; Cell Differentiation; Cell Division; Cell Line; Cell Line, Tumor; Cell Membrane; Cell Movement; Cell Proliferation; Cell Self Renewal; Cell Survival; Cells, Cultured; Cellular Reprogramming; Cellulose; Charcoal; Chemical and Drug Induced Liver Injury; Chemical Phenomena; Chemokines; Chemoradiotherapy; Chemoreceptor Cells; Child; Child Abuse; Child, Preschool; China; Chlorogenic Acid; Chloroquine; Chromatography, Gas; Chronic Disease; Clinical Competence; Coated Materials, Biocompatible; Cochlea; Cohort Studies; Color; Comorbidity; Computer Simulation; Computer-Aided Design; Contraception; Contraceptive Agents, Female; Contrast Media; COP-Coated Vesicles; Coronavirus Infections; Cost of Illness; Coturnix; COVID-19; Creatinine; Cross-Over Studies; Cross-Sectional Studies; Culex; Curriculum; Cyclic N-Oxides; Cytokines; Cytoplasm; Cytotoxicity, Immunologic; Cytotoxins; Databases, Factual; Deep Learning; Delivery, Obstetric; Denitrification; Dental Caries; Denture, Complete; Dexamethasone; Diabetes Complications; Diabetes Mellitus; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Dielectric Spectroscopy; Diet, High-Fat; Dietary Fiber; Disease Models, Animal; Disease Progression; DNA; DNA Copy Number Variations; DNA, Mitochondrial; Dog Diseases; Dogs; Dopaminergic Neurons; Double-Blind Method; Down-Regulation; Doxorubicin; Drug Carriers; Drug Design; Drug Interactions; Drug Resistance, Bacterial; Drug Resistance, Neoplasm; Drug-Related Side Effects and Adverse Reactions; Drugs, Chinese Herbal; Dry Powder Inhalers; Dust; E2F1 Transcription Factor; Ecosystem; Education, Nursing; Education, Nursing, Baccalaureate; Electric Impedance; Electricity; Electrocardiography; Electrochemical Techniques; Electrochemistry; Electrodes; Electrophoresis, Polyacrylamide Gel; Endoplasmic Reticulum; Endothelial Cells; Environmental Monitoring; Enzyme Inhibitors; Epithelial Cells; Epithelial-Mesenchymal Transition; Esophageal Neoplasms; Esophageal Squamous Cell Carcinoma; Estrogen Receptor Modulators; Europe; Evoked Potentials, Auditory, Brain Stem; Exosomes; Feasibility Studies; Female; Ferricyanides; Ferrocyanides; Fibrinogen; Finite Element Analysis; Fistula; Fluorescent Dyes; Fluorides, Topical; Fluorodeoxyglucose F18; Fluticasone; Follow-Up Studies; Food Contamination; Food Microbiology; Foods, Specialized; Forensic Medicine; Frail Elderly; France; Free Radicals; Fresh Water; Fungi; Fungicides, Industrial; Galactosamine; Gastrointestinal Neoplasms; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Gene Frequency; Genetic Predisposition to Disease; Genotype; Gingival Hemorrhage; Glioblastoma; Glioma; Glomerular Filtration Rate; Glomerulosclerosis, Focal Segmental; Glucose; Glucose Transport Proteins, Facilitative; Glucosides; Glutamine; Glycolysis; Gold; GPI-Linked Proteins; Gram-Negative Bacteria; Gram-Positive Bacteria; Graphite; Haplotypes; HCT116 Cells; Healthy Volunteers; Hearing Loss; Heart Failure; Hedgehog Proteins; HEK293 Cells; HeLa Cells; Hemodynamics; Hemorrhage; Hepatocytes; Hippo Signaling Pathway; Histone Deacetylases; Homeostasis; Hospital Mortality; Hospitalization; Humans; Hydantoins; Hydrazines; Hydrogen Peroxide; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Hydroxylamines; Hypoglycemic Agents; Immunity, Innate; Immunoglobulin G; Immunohistochemistry; Immunologic Factors; Immunomodulation; Immunophenotyping; Immunotherapy; Incidence; Indazoles; Indonesia; Infant; Infant, Newborn; Infarction, Middle Cerebral Artery; Inflammation; Injections, Intramuscular; Insecticides; Insulin-Like Growth Factor I; Insurance, Health; Intention to Treat Analysis; Interleukin-1 Receptor-Associated Kinases; Interleukin-6; Intrauterine Devices; Intrauterine Devices, Copper; Iron; Ischemia; Jordan; Keratinocytes; Kidney; Kidney Diseases; Kir5.1 Channel; Klebsiella Infections; Klebsiella pneumoniae; Lab-On-A-Chip Devices; Laparoscopy; Lasers; Lasers, Semiconductor; Lenalidomide; Leptin; Lethal Dose 50; Levonorgestrel; Limit of Detection; Lipid Metabolism; Lipid Metabolism Disorders; Lipogenesis; Lipopolysaccharides; Liquid Biopsy; Liver; Liver Abscess, Pyogenic; Liver Cirrhosis; Liver Diseases; Liver Neoplasms; Longevity; Lung Neoplasms; Luteolin; Lymph Nodes; Lymphocyte Activation; Macaca fascicularis; Macrophages; Mad2 Proteins; Magnetic Resonance Imaging; Male; Mammary Glands, Human; Manganese; Manganese Compounds; MAP Kinase Signaling System; Materials Testing; Maternal Health Services; MCF-7 Cells; Medicaid; Medicine, Chinese Traditional; Melanoma; Membrane Proteins; Mental Health; Mercury; Metal Nanoparticles; Metals, Heavy; Metformin; Methionine Adenosyltransferase; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred CBA; Mice, Knockout; Mice, Nude; Microalgae; Microbial Sensitivity Tests; Microglia; MicroRNAs; Microscopy, Atomic Force; Microscopy, Electron, Scanning; Middle Aged; Mitochondria; Mitochondrial Proteins; Mitral Valve; Mitral Valve Insufficiency; Models, Anatomic; Molecular Structure; Molybdenum; Monocarboxylic Acid Transporters; Moths; MPTP Poisoning; Multigene Family; Multiparametric Magnetic Resonance Imaging; Multiple Myeloma; Muscle, Skeletal; Mutagens; Mutation; Myeloid Cells; Nanocomposites; Nanofibers; Nanomedicine; Nanoparticles; Nanowires; Neoadjuvant Therapy; Neomycin; Neoplasm Grading; Neoplasm Recurrence, Local; Neoplasms; Neoplastic Stem Cells; Neostriatum; Neovascularization, Pathologic; Netherlands; Neuromuscular Agents; Neurons; NF-E2-Related Factor 2; NF-kappa B; Nickel; Nitrogen Oxides; Non-alcoholic Fatty Liver Disease; Nucleosides; Nucleotidyltransferases; Nutritional Status; Obesity, Morbid; Ofloxacin; Oils, Volatile; Oligopeptides; Oncogene Protein v-akt; Optical Imaging; Organic Cation Transport Proteins; Organophosphonates; Osteoarthritis; Osteoarthritis, Hip; Osteoarthritis, Knee; Osteoblasts; Osteogenesis; Oxidation-Reduction; Oxidative Stress; Oxides; Oxygen Isotopes; Pancreas; Pancreaticoduodenectomy; Pandemics; Particle Size; Particulate Matter; Patient Acceptance of Health Care; Patient Compliance; PC-3 Cells; Peptide Fragments; Peptides; Periodontal Attachment Loss; Periodontal Index; Periodontal Pocket; Periodontitis; Peroxides; Peru; Pest Control, Biological; Phosphatidylinositol 3-Kinase; Phosphatidylinositol 3-Kinases; Phylogeny; Pilot Projects; Piperidines; Plant Bark; Plant Extracts; Plant Leaves; Plasmids; Platelet Function Tests; Pneumonia, Viral; Podocytes; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerase Inhibitors; Polyethylene Terephthalates; Polymers; Polymorphism, Single Nucleotide; Porosity; Portugal; Positron-Emission Tomography; Postoperative Complications; Postural Balance; Potassium Channels, Inwardly Rectifying; Povidone; Powders; Precancerous Conditions; Precision Medicine; Predictive Value of Tests; Pregnancy; Prenatal Care; Prognosis; Promoter Regions, Genetic; Prospective Studies; Prostatectomy; Prostatic Neoplasms; Proteasome Inhibitors; Protective Agents; Protein Binding; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Protein Transport; Proto-Oncogene Proteins B-raf; Proto-Oncogene Proteins c-akt; Psychiatric Nursing; PTEN Phosphohydrolase; Pulmonary Embolism; Pyrimethamine; Radiopharmaceuticals; Rats; Rats, Sprague-Dawley; Rats, Wistar; Reactive Oxygen Species; Receptor, ErbB-2; Receptor, IGF Type 1; Receptors, Estrogen; Receptors, G-Protein-Coupled; Recombinational DNA Repair; Recovery of Function; Regional Blood Flow; Renal Dialysis; Renin; Renin-Angiotensin System; Reperfusion Injury; Reproducibility of Results; Republic of Korea; Respiratory Distress Syndrome; Retrospective Studies; Rhodamines; Risk Assessment; Risk Factors; RNA, Long Noncoding; RNA, Messenger; Running; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Salinity; Salmeterol Xinafoate; Sarcoma; Seasons; Shoulder Injuries; Signal Transduction; Silicon Dioxide; Silver; Sirtuin 1; Sirtuins; Skull Fractures; Social Determinants of Health; Sodium; Sodium Fluoride; Sodium Potassium Chloride Symporter Inhibitors; Sodium-Glucose Transporter 2 Inhibitors; Soil; Soil Pollutants; Spain; Spectrophotometry; Spectroscopy, Fourier Transform Infrared; Staphylococcal Protein A; Staphylococcus aureus; Stem Cells; Stereoisomerism; Stomach Neoplasms; Streptomyces; Strontium; Structure-Activity Relationship; Students, Nursing; Substance-Related Disorders; Succinic Acid; Sulfur; Surface Properties; Survival Rate; Survivin; Symporters; T-Lymphocytes; Temozolomide; Tensile Strength; Thiazoles; Thiobacillus; Thiohydantoins; Thiourea; Thrombectomy; Time Factors; Titanium; Tobacco Mosaic Virus; Tobacco Use Disorder; Toll-Like Receptor 4; Toluene; Tomography, X-Ray Computed; TOR Serine-Threonine Kinases; Toxicity Tests, Acute; Toxicity Tests, Subacute; Transcriptional Activation; Treatment Outcome; Troponin I; Tumor Cells, Cultured; Tumor Escape; Tumor Hypoxia; Tumor Microenvironment; Tumor Necrosis Factor Inhibitors; Tumor Necrosis Factor-alpha; Tyrosine; Ubiquitin-Protein Ligases; Ubiquitination; Ultrasonic Waves; United Kingdom; United States; United States Department of Veterans Affairs; Up-Regulation; Urea; Uric Acid; Urinary Bladder Neoplasms; Urinary Bladder, Neurogenic; Urine; Urodynamics; User-Computer Interface; Vemurafenib; Verbenaceae; Veterans; Veterans Health; Viral Load; Virtual Reality; Vitiligo; Water Pollutants, Chemical; Wildfires; Wnt Signaling Pathway; Wound Healing; X-Ray Diffraction; Xenograft Model Antitumor Assays; Xylenes; Young Adult; Zinc; Zinc Oxide; Zinc Sulfate; Zoonoses | 2021 |
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients.
Topics: Age Distribution; Age of Onset; Aged; Aged, 80 and over; Alzheimer Disease; Amino Acid Substitution; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Homocysteine; Humans; Italy; Male; Middle Aged; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Polymorphism, Genetic; Risk Assessment; Risk Factors; Statistics as Topic | 2005 |
114 other study(ies) available for glutamine and Genetic Predisposition
| Article | Year |
|---|---|
Genetic variants in glutamine metabolic pathway genes predict cutaneous melanoma-specific survival.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Disease-Free Survival; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamine; Histidine Ammonia-Lyase; Humans; Male; Melanoma; Melanoma, Cutaneous Malignant; Metabolic Networks and Pathways; Middle Aged; Polymorphism, Single Nucleotide; Pyrroline Carboxylate Reductases; Skin Neoplasms | 2019 |
Glutamatergic function in a genetic high-risk group for psychosis: A proton magnetic resonance spectroscopy study in individuals with 22q11.2 deletion.
Topics: Adolescent; Adult; Corpus Striatum; Cross-Sectional Studies; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Gyrus Cinguli; Humans; Magnetic Resonance Spectroscopy; Male; Psychotic Disorders; Risk Factors; Thalamus; Young Adult | 2019 |
Glucose and glutamine metabolism in relation to mutational status in NSCLC histological subtypes.
Topics: Biomarkers, Tumor; Carcinoma, Non-Small-Cell Lung; Fluorescent Antibody Technique; Genetic Association Studies; Genetic Predisposition to Disease; Glucose; Glutamine; Humans; Lung Neoplasms; Mutation; Neoplasm Staging | 2019 |
Cardiac mGluR1 metabotropic receptors in cardioprotection.
Topics: Animals; Disease Models, Animal; Excitatory Amino Acid Agonists; Excitatory Amino Acid Antagonists; Genetic Predisposition to Disease; Glutamine; Mice, Inbred C57BL; Mice, Knockout; Myocardial Infarction; Myocardial Reperfusion Injury; Myocardium; Phenotype; Phosphatidylinositol 3-Kinase; Proto-Oncogene Proteins c-akt; Receptors, Metabotropic Glutamate; Signal Transduction; Time Factors; Ventricular Function, Left | 2017 |
Major surgery diminishes systemic arginine availability and suppresses nitric oxide response to feeding in patients with early stage breast cancer.
Topics: Adult; Arginine; Breast Neoplasms; Citrulline; Female; Genetic Predisposition to Disease; Glutamine; Humans; Mastectomy; Metabolic Clearance Rate; Middle Aged; Nitric Oxide; Postoperative Complications; Postprandial Period | 2018 |
Combined effect of glutamine at position 70 of HLA-DRB1 and alanine at position 57 of HLA-DQB1 in type 1 diabetes: An epitope analysis.
Topics: Age of Onset; Alanine; Binding Sites; Cohort Studies; Cyprus; Diabetes Mellitus, Type 1; Epitope Mapping; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Haplotypes; HLA-DQ beta-Chains; HLA-DRB1 Chains; Humans; Linkage Disequilibrium; Male | 2018 |
Arg399Gln substitution in XRCC1 as a prognostic and predictive biomarker for prostate cancer: Evidence from 8662 subjects and a structural analysis.
Topics: Alleles; Amino Acid Substitution; Arginine; Case-Control Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Iran; Male; Meta-Analysis as Topic; Odds Ratio; Polymorphism, Single Nucleotide; Prognosis; Prostatic Neoplasms; Risk Factors; X-ray Repair Cross Complementing Protein 1 | 2018 |
Influence of functional variants Asp312Asn and Lys751Gln of Xeroderma Pigmentosum Group D (XPD) and Glutathione S-transferase Mu 1 (GSTM1) and Theta 1 (GSTT1) genes on cutaneous melanoma susceptibility and prognosis.
Topics: Aged; Asparagine; Aspartic Acid; Cell Survival; Disease-Free Survival; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Glutathione Transferase; Humans; Lysine; Melanoma; Middle Aged; Prognosis; Proportional Hazards Models; Skin Neoplasms; Treatment Outcome; Xeroderma Pigmentosum | 2019 |
Twendee X Ameliorates Phosphorylated Tau, α-Synuclein and Neurovascular Dysfunction in Alzheimer's Disease Transgenic Mice With Chronic Cerebral Hypoperfusion.
Topics: alpha-Synuclein; Alzheimer Disease; Amyloid beta-Protein Precursor; Animals; Antioxidants; Ascorbic Acid; Brain; Cerebrovascular Disorders; Cystine; Dietary Supplements; Disease Models, Animal; Female; Genetic Predisposition to Disease; Glutamine; Male; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurovascular Coupling; Phenotype; Phosphorylation; tau Proteins | 2019 |
XRCC1 Arg194Trp and Arg399Gln polymorphisms are significantly associated with shorter survival in acute myeloid leukemia.
Topics: Acute Disease; Adult; Aged; Amino Acid Substitution; Arginine; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leukemia, Myeloid; Male; Middle Aged; Polymorphism, Genetic; Risk Factors; Survival Analysis; Tryptophan; X-ray Repair Cross Complementing Protein 1 | 2014 |
DNA repair gene polymorphisms and risk of head and neck cancer in the Tunisian population.
Topics: Adenine; Adolescent; Adult; Aged; Aged, 80 and over; Alcohol Drinking; Arginine; Case-Control Studies; DNA Helicases; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Glutamine; Guanine; Head and Neck Neoplasms; Humans; Lysine; Male; Middle Aged; Occupational Exposure; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Smoking; X-ray Repair Cross Complementing Protein 1; Xeroderma Pigmentosum Group D Protein; Young Adult | 2014 |
Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy.
Topics: Adolescent; Base Sequence; Cardiomyopathy, Hypertrophic; DNA, Mitochondrial; Genetic Markers; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Humans; Male; Molecular Sequence Data; Polymorphism, Single Nucleotide; RNA, Transfer | 2015 |
Clinical relevance and functional consequences of the TNFRSF1A multiple sclerosis locus.
Topics: Animals; Arginine; Chemokine CXCL10; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Genotype; Glutamine; HEK293 Cells; Humans; Immunologic Factors; Longitudinal Studies; Male; Monocytes; Multiple Sclerosis; Mutation; Phorbol Esters; Receptors, Tumor Necrosis Factor, Type I; RNA Isoforms; Signal Transduction; Tumor Necrosis Factor-alpha | 2013 |
The codon 399 Arg/Gln XRCC1 polymorphism is associated with lung cancer in Indians.
Topics: Adenocarcinoma; Arginine; Carcinoma, Non-Small-Cell Lung; Carcinoma, Squamous Cell; Case-Control Studies; Codon; DNA; DNA-Binding Proteins; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; India; Lung Neoplasms; Male; Middle Aged; Neoplasm Staging; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Prognosis; Risk Factors; Survival Rate; X-ray Repair Cross Complementing Protein 1 | 2013 |
Dental caries and enamelin haplotype.
Topics: Amino Acid Substitution; Arginine; Child; Dental Caries; Dental Caries Susceptibility; DMF Index; Exons; Extracellular Matrix Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Haplotypes; Humans; Introns; Isoleucine; Linkage Disequilibrium; Male; Mutation, Missense; Polymorphism, Single Nucleotide; Proteins; Threonine; Young Adult | 2014 |
Relationship between the paraoxonase 1 gene glutamine 192 to arginine polymorphism and gestational diabetes mellitus in Saudi women.
Topics: Adult; Amino Acid Substitution; Aryldialkylphosphatase; Diabetes, Gestational; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Pregnancy; Risk Factors; Saudi Arabia | 2014 |
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis.
Topics: Adenosine Triphosphate; Amino Acid Substitution; Arginine; Australasia; Binding Sites; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Models, Molecular; Multiple Sclerosis; Receptors, Purinergic P2X7; White People | 2015 |
Association between genetic variants of serotonergic and glutamatergic pathways and the concentration of neurometabolites of the anterior cingulate cortex in paediatric patients with obsessive-compulsive disorder.
Topics: Child; Comorbidity; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Gyrus Cinguli; Humans; Magnetic Resonance Spectroscopy; Male; Mental Disorders; Neural Pathways; Neurons; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Serotonergic Neurons; Statistics as Topic; Young Adult | 2016 |
[Association of the Arg399Gln polymorphisms of the XRCC1 gene with breast cancer risk in Kyrgiz women].
Topics: Adult; Aged; Alleles; Arginine; Breast Neoplasms; DNA-Binding Proteins; DNA, Neoplasm; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Heterozygote; Humans; Kyrgyzstan; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Risk Assessment; Risk Factors; X-ray Repair Cross Complementing Protein 1 | 2015 |
Nature of Glutamate Alterations in Schizophrenia: A Meta-analysis of Proton Magnetic Resonance Spectroscopy Studies.
Topics: Brain; Brain Mapping; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Proton Magnetic Resonance Spectroscopy; Reference Values; Risk Factors; Schizophrenia; Synaptic Transmission | 2016 |
7T Proton Magnetic Resonance Spectroscopy of Gamma-Aminobutyric Acid, Glutamate, and Glutamine Reveals Altered Concentrations in Patients With Schizophrenia and Healthy Siblings.
Topics: Adult; Brain; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Male; Proton Magnetic Resonance Spectroscopy; Schizophrenia; Siblings | 2017 |
Association of rs1137101 polymorphism in LEPR and susceptibility to knee osteoarthritis in a Northwest Chinese Han population.
Topics: Aged; Amplified Fragment Length Polymorphism Analysis; Arginine; Asian People; Biomarkers; Case-Control Studies; Ethnicity; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Middle Aged; Osteoarthritis, Knee; Polymorphism, Single Nucleotide; Receptors, Leptin; Sequence Analysis, DNA; Sex Factors | 2016 |
Genetic polymorphisms in extracellular superoxide dismutase Leu53Leu, Arg213Gly, and Ala40Thr and susceptibility to type 2 diabetes mellitus.
Topics: Adult; Alanine; Arginine; Asian People; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Male; Middle Aged; Polymorphism, Single Nucleotide; Regression Analysis; Superoxide Dismutase; Threonine | 2016 |
Association between COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population.
Topics: Adult; Arginine; Asian People; Case-Control Studies; Collagen Type IX; Female; Genetic Predisposition to Disease; Glutamine; Humans; Intervertebral Disc Degeneration; Intervertebral Disc Displacement; Male; Middle Aged; Mutation | 2016 |
The androgen receptor's CAG/glutamine tract in mouse models of neurological disease and cancer.
Topics: Alleles; Animals; Crosses, Genetic; Disease Models, Animal; Gene Targeting; Genetic Predisposition to Disease; Glutamine; Humans; Male; Mice; Mice, Knockout; Mice, Transgenic; Motor Neurons; Muscle, Skeletal; Muscular Atrophy, Spinal; Phenotype; Prostatic Neoplasms; Receptors, Androgen; Spinal Cord; Trinucleotide Repeats | 2008 |
A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
Topics: Amino Acid Substitution; Base Sequence; Cataract; Child; Connexins; DNA Mutational Analysis; Eye Proteins; Family; Female; Genetic Predisposition to Disease; Glutamine; Humans; India; Male; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Proline; United Kingdom | 2008 |
Association between lysyl oxidase polymorphisms and oral submucous fibrosis in older male areca chewers.
Topics: Adenine; Age Factors; Alleles; Amino Acid Sequence; Areca; Arginine; Genetic Predisposition to Disease; Genotype; Glutamine; Guanine; Heterozygote; Humans; Male; Middle Aged; Oral Submucous Fibrosis; Polymorphism, Single Nucleotide; Precancerous Conditions; Protein-Lysine 6-Oxidase; Risk Factors | 2009 |
P2RX7 Gln460Arg polymorphism is associated with depression among diabetic patients.
Topics: Arginine; Brain-Derived Neurotrophic Factor; Depression; Diabetes Complications; Diabetes Mellitus; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Multivariate Analysis; Polymorphism, Genetic; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Serotonin Plasma Membrane Transport Proteins; Tryptophan Hydroxylase | 2008 |
Modifier effect of the Glu298Asp polymorphism of endothelial nitric oxide synthase gene in autosomal-dominant polycystic kidney disease.
Topics: Adult; Effect Modifier, Epidemiologic; Female; Genetic Predisposition to Disease; Glutamine; Greece; Humans; Incidence; Male; Middle Aged; Nitric Oxide Synthase Type III; Polycystic Kidney, Autosomal Dominant; Polymorphism, Single Nucleotide | 2008 |
Association of MUTYH Gln324His and APEX1 Asp148Glu with colorectal cancer and smoking in a Japanese population.
Topics: Aged; Asian People; Aspartic Acid; Case-Control Studies; Colorectal Neoplasms; DNA Glycosylases; DNA-(Apurinic or Apyrimidinic Site) Lyase; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Histidine; Humans; Male; Middle Aged; Polymorphism, Genetic; Smoking | 2008 |
Leptin receptor Gln223Arg polymorphism and breast cancer risk in Nigerian women: a case control study.
Topics: Arginine; Breast Neoplasms; Carcinoma, Ductal, Breast; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Nigeria; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Postmenopause; Premenopause; Receptors, Leptin; Risk Factors; Signal Transduction | 2008 |
Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases.
Topics: Adult; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Arginine; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Glatiramer Acetate; Glutamine; HLA-D Antigens; Humans; Immunosuppressive Agents; Male; Middle Aged; Mitoxantrone; Multiple Sclerosis; Mutation; Natalizumab; Penetrance; Peptides; Phenotype; Receptors, Tumor Necrosis Factor, Type I; Sequence Analysis, DNA; Young Adult | 2008 |
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly.
Topics: DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamine; Hedgehog Proteins; Histidine; Holoprosencephaly; Humans; Magnetic Resonance Imaging; Male; Mutation | 2010 |
The unfolding of the prion protein sheds light on the mechanisms of prion susceptibility and species barrier.
Topics: Animals; Arginine; Cricetinae; Genetic Predisposition to Disease; Glutamine; Mice; Mutagenesis, Site-Directed; Prion Diseases; Prion Proteins; Prions; Protein Denaturation; Protein Folding; Species Specificity; Thermodynamics; Tryptophan | 2009 |
Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Biomarkers, Tumor; Case-Control Studies; Colorectal Neoplasms; Esophageal Neoplasms; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Head and Neck Neoplasms; Humans; Incidence; Isoleucine; Japan; Lung Neoplasms; Male; Methionine; Middle Aged; Neoplasms; Polymorphism, Single Nucleotide; Proline; Protein Tyrosine Phosphatase, Non-Receptor Type 13; Receptor-Like Protein Tyrosine Phosphatases, Class 3; Risk Factors | 2010 |
Polymorphisms of XRCC1 gene and risk of gastric cardiac adenocarcinoma.
Topics: Adenine; Adenocarcinoma; Adult; Aged; Arginine; Cardia; Case-Control Studies; Codon; Cytosine; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; Histidine; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Smoking; Stomach Neoplasms; Thymine; Tryptophan; X-ray Repair Cross Complementing Protein 1 | 2009 |
Gln27Glu variant of Beta2-adrenoceptor gene affects male type fat accumulation in women.
Topics: Adolescent; Adult; Body Mass Index; Coronary Artery Disease; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Intra-Abdominal Fat; Male; Middle Aged; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Young Adult | 2009 |
Leptin G-2548A and leptin receptor Q223R gene polymorphisms are not associated with obesity in Romanian subjects.
Topics: Adult; Arginine; Body Mass Index; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Leptin; Male; Middle Aged; Obesity; Polymorphism, Single Nucleotide; Receptors, Leptin; Romania; White People | 2010 |
Autosomal recessive Bethlem myopathy.
Topics: Adult; Cells, Cultured; Codon, Nonsense; Collagen Diseases; Collagen Type VI; Female; Fibroblasts; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscle, Skeletal; Muscular Diseases; Tomography, X-Ray Computed | 2009 |
POLG1 polyglutamine tract variants associated with Parkinson's disease.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Male; Middle Aged; Parkinson Disease; Peptides; Trinucleotide Repeats; White People | 2010 |
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy.
Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Cardiomyopathies; Cardiomyopathy, Dilated; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Humans; Myocardium; Pedigree; Pregnancy; Pregnancy Complications; Puerperal Disorders; Troponin C | 2010 |
An αIIb mutation in patients with Glanzmann thrombasthenia located in the N-terminus of blade 1 of the β-propeller (Asn2Asp) disrupts a calcium binding site in blade 6.
Topics: Adolescent; Amino Acid Sequence; Animals; Arabs; Asparagine; Aspartic Acid; Binding Sites; Blood Platelets; Calcium; Cell Line; Child; Child, Preschool; Cricetinae; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamine; Hemostasis; Heredity; Humans; Hydrogen Bonding; Integrin alpha2; Integrin beta3; Israel; Leucine; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Thrombasthenia; Transfection | 2011 |
The missense variation Q705K in CIAS1/NALP3/NLRP3 gene and an NLRP1 haplotype are associated with celiac disease.
Topics: Adaptor Proteins, Signal Transducing; Adolescent; Apoptosis Regulatory Proteins; Carrier Proteins; Celiac Disease; Child; Child, Preschool; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; Humans; Inflammasomes; Italy; Lysine; Male; Mutation, Missense; NLR Family, Pyrin Domain-Containing 3 Protein; NLR Proteins; Polymorphism, Single Nucleotide | 2011 |
Arg753Gln polymorphism of the human Toll-like receptor 2 gene from infection to disease in pediatric tuberculosis.
Topics: Adolescent; Arginine; Child; Child, Preschool; Disease Progression; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Mutation; Polymorphism, Genetic; Toll-Like Receptor 2; Tuberculosis, Pulmonary; Turkey | 2011 |
A mutation in the leptin receptor is associated with Entamoeba histolytica infection in children.
Topics: Alleles; Apoptosis; Child, Preschool; Cohort Studies; Entamoeba histolytica; Entamoebiasis; Female; Genetic Predisposition to Disease; Glutamine; Homozygote; Humans; Liver Abscess; Male; Mutation; Prospective Studies; Receptors, Leptin | 2011 |
The SIGMAR1 gene is associated with a risk of schizophrenia and activation of the prefrontal cortex.
Topics: Adult; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Meta-Analysis as Topic; Middle Aged; Polymorphism, Single Nucleotide; Prefrontal Cortex; Proline; Receptors, sigma; Schizophrenia; Sigma-1 Receptor; Spectroscopy, Near-Infrared; Speech Disorders | 2011 |
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.
Topics: Aspartic Acid; Attention Deficit Disorder with Hyperactivity; Brain; Case-Control Studies; Choline; Chromosomes, Human, Pair 11; Genetic Linkage; Genetic Predisposition to Disease; Glutamine; Humans; Inositol; Magnetic Resonance Spectroscopy; Methylphenidate; Polymorphism, Single Nucleotide; Protons; Receptors, G-Protein-Coupled; Receptors, Peptide | 2012 |
Relationship between polymorphisms in the 5' leader cistron, positions 16 and 27 of the adrenergic β2 receptor gene and asthma in a Han population from southwest China.
Topics: Adrenergic beta-2 Receptor Agonists; Albuterol; Arginine; Asian People; Asthma; Bronchodilator Agents; Case-Control Studies; China; Female; Forced Expiratory Volume; Gene Expression Regulation; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Adrenergic, beta-2 | 2011 |
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Cell Line; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 9; Cloning, Molecular; Enzyme Inhibitors; Family Health; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; In Situ Nick-End Labeling; Infant; Male; Mice; Motor Neurons; Mutagenesis, Site-Directed; Phenotype; Polymorphism, Single Nucleotide; Receptors, sigma; Saudi Arabia; Sigma-1 Receptor; Thapsigargin; Transfection | 2011 |
Schizophrenia susceptibility gene dysbindin regulates glutamatergic and dopaminergic functions via distinctive mechanisms in Drosophila.
Topics: Animals; Carrier Proteins; DNA-Binding Proteins; Dopamine; Dopaminergic Neurons; Drosophila melanogaster; Drosophila Proteins; Dysbindin; Dystrophin-Associated Proteins; Genetic Predisposition to Disease; Glutamine; Humans; Models, Biological; Mutation; Neurons; Neurotransmitter Agents; Schizophrenia; Tissue Distribution | 2011 |
Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population.
Topics: Adult; Areca; Arginine; Arylamine N-Acetyltransferase; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Heterozygote; Homozygote; Humans; India; Lysine; Male; Methionine; Multifactor Dimensionality Reduction; Oral Submucous Fibrosis; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tobacco, Smokeless; Tryptophan; X-ray Repair Cross Complementing Protein 1 | 2012 |
Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating serum hepcidin levels in Rwandese HIV-positive women.
Topics: Adolescent; Adult; Amino Acid Substitution; Antimicrobial Cationic Peptides; Cation Transport Proteins; Cross-Sectional Studies; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Hepcidins; Histidine; HIV Infections; HIV Seropositivity; HIV-1; Humans; Middle Aged; Mutation, Missense; Osmolar Concentration; Rwanda; Young Adult | 2012 |
Evidence that HLA-DQ9 confers risk to celiac disease by presence of DQ9-restricted gluten-specific T cells.
Topics: Amino Acid Sequence; Antigen Presentation; Celiac Disease; Epitopes, T-Lymphocyte; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glutens; HLA-DQ Antigens; Humans; Molecular Sequence Data; Peptides; Protein Binding; Risk; T-Lymphocytes | 2012 |
Genetic polymorphisms (at codons 194 and 399) in the DNA repair gene XRCC1 and susceptibility to bipolar disorder.
Topics: Bipolar Disorder; Case-Control Studies; DNA-Binding Proteins; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Linkage Disequilibrium; Male; Polymorphism, Genetic; Tryptophan; X-ray Repair Cross Complementing Protein 1 | 2012 |
Allelic variants of XRCC1 and XRCC3 repair genes and susceptibility of oral cancer in Brazilian patients.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Arginine; Carcinoma, Squamous Cell; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Humans; Lymphatic Metastasis; Male; Methionine; Middle Aged; Mouth Neoplasms; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tryptophan; X-ray Repair Cross Complementing Protein 1; Young Adult | 2013 |
Schizophrenia shows a unique metabolomics signature in plasma.
Topics: Adult; Aged; Analysis of Variance; Antipsychotic Agents; Arginine; Biomarkers; Case-Control Studies; Female; Genetic Markers; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamine; Humans; Least-Squares Analysis; Logistic Models; Male; Mass Spectrometry; Metabolomics; Middle Aged; Schizophrenia | 2012 |
Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivation.
Topics: Adult; Aged; Aged, 80 and over; Animals; Bone Density; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Female; Femoral Neck Fractures; Femur Neck; Genetic Predisposition to Disease; Glutamine; HEK293 Cells; Humans; Mice; Monte Carlo Method; Mutation; NIH 3T3 Cells; Receptors, Calcitriol; Repetitive Sequences, Amino Acid; Transcriptional Activation; Ultrasonography | 2012 |
A single point mutation in the gene encoding Gb3/CD77 synthase causes a rare inherited polyagglutination syndrome.
Topics: Amino Acid Substitution; Carbohydrate Sequence; Cell Line, Tumor; Embryonal Carcinoma Stem Cells; Flow Cytometry; Galactosyltransferases; Genetic Predisposition to Disease; Genotype; Globosides; Glutamic Acid; Glutamine; Hemagglutination; Humans; Molecular Sequence Data; Phenotype; Point Mutation; Polymorphism, Single Nucleotide; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Syndrome | 2012 |
The MBD4 Glu346Lys polymorphism is associated with the risk of cervical cancer in a Chinese population.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Asian People; Carcinoma, Squamous Cell; Case-Control Studies; Endodeoxyribonucleases; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genetics, Population; Glutamine; Humans; Lysine; Middle Aged; Mutation, Missense; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Uterine Cervical Neoplasms | 2012 |
Obesity, Type II diabetes and the beta 2 adrenoceptor gene Gln27Glu polymorphism in the Tongan population.
Topics: Adult; Blood Glucose; Body Constitution; Body Mass Index; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Genotype; Glutamic Acid; Glutamine; Humans; Male; Middle Aged; Obesity; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Tonga | 2003 |
Association between human paraoxonase gene polymorphism and chronic symptoms in pesticide-exposed workers.
Topics: Adult; Agriculture; Arginine; Aryldialkylphosphatase; Chronic Disease; Cross-Sectional Studies; Esterases; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Occupational Exposure; Pesticides; Polymorphism, Genetic | 2003 |
Basal fat oxidation and after a peak oxygen consumption test in obese women with a beta2 adrenoceptor gene polymorphism.
Topics: Adipose Tissue; Adult; Alleles; Calorimetry, Indirect; Exercise; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Glycerol; Humans; Lipolysis; Obesity; Oxidation-Reduction; Oxygen Consumption; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Receptors, Adrenergic, beta-2; Triglycerides | 2003 |
Methionine synthase polymorphism is a risk factor for Alzheimer disease.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Age of Onset; Aged; Aged, 80 and over; Aging; Alanine; Alzheimer Disease; Apolipoproteins E; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Logistic Models; Male; Middle Aged; Mutation; Polymorphism, Genetic; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; RNA, Messenger; Sex Characteristics | 2003 |
Obesity risk is associated with carbohydrate intake in women carrying the Gln27Glu beta2-adrenoceptor polymorphism.
Topics: Adult; Case-Control Studies; Dietary Carbohydrates; Dose-Response Relationship, Drug; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Insulin; Male; Middle Aged; Obesity; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Sex Characteristics | 2003 |
Genetic polymorphism PC-1 K121Q and ethnic susceptibility to insulin resistance.
Topics: Adult; Asian People; Female; Gene Frequency; Genetic Predisposition to Disease; Glucose Clamp Technique; Glucose Tolerance Test; Glutamine; Humans; Hyperinsulinism; India; Insulin Resistance; Lysine; Male; Middle Aged; Phosphoric Diester Hydrolases; Polymorphism, Genetic; Pyrophosphatases; White People | 2003 |
Effect of a short CAG (glutamine) repeat on human androgen receptor function.
Topics: Blotting, Western; Cell Line, Tumor; Genetic Predisposition to Disease; Glutamine; Humans; Luciferases; Male; Microsatellite Repeats; Neoplasms, Hormone-Dependent; Plasmids; Polymorphism, Genetic; Prostate-Specific Antigen; Prostatic Neoplasms; Receptors, Androgen; Transfection | 2004 |
Polymorphism R92Q of the tumour necrosis factor receptor 1 gene is associated with myocardial infarction and carotid intima-media thickness--the ECTIM, AXA, EVA and GENIC Studies.
Topics: Adult; Aged; Antigens, CD; Arginine; Arteriosclerosis; Brain Infarction; Carotid Arteries; Cross-Sectional Studies; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamine; Humans; Introns; Male; Middle Aged; Mutation; Myocardial Infarction; Odds Ratio; Polymorphism, Genetic; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Tunica Intima; Tunica Media; Ultrasonography | 2004 |
The Arg753GLn polymorphism of the human toll-like receptor 2 gene in tuberculosis disease.
Topics: Adult; Alleles; Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Immune Tolerance; Immunogenetics; Male; Membrane Glycoproteins; Middle Aged; Mycobacterium tuberculosis; Phenotype; Polymorphism, Single Nucleotide; Receptors, Cell Surface; Retrospective Studies; Toll-Like Receptor 2; Toll-Like Receptors; Tuberculosis, Lymph Node; Tuberculosis, Pleural; Tuberculosis, Pulmonary; Turkey | 2004 |
The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults.
Topics: Adult; Arginine; Aryldialkylphosphatase; Case-Control Studies; Confidence Intervals; Demography; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Logistic Models; Male; Odds Ratio; Open Reading Frames; Polymerase Chain Reaction; Polymorphism, Genetic; Promoter Regions, Genetic; Risk; Sequence Analysis, DNA; Stroke | 2004 |
Gene-environment interactions between the smoking habit and polymorphisms in the DNA repair genes, APE1 Asp148Glu and XRCC1 Arg399Gln, in Japanese lung cancer risk.
Topics: Adult; Aged; Alleles; Arginine; Aspartic Acid; Codon; DNA Repair; DNA-(Apurinic or Apyrimidinic Site) Lyase; DNA-Binding Proteins; Environment; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Risk; Risk Factors; Smoking; X-ray Repair Cross Complementing Protein 1 | 2004 |
3-T proton MRS investigation of glutamate and glutamine in adolescents at high genetic risk for schizophrenia.
Topics: Adolescent; Child of Impaired Parents; Cohort Studies; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Glutamine; Humans; Magnetic Resonance Spectroscopy; Male; Prefrontal Cortex; Psychiatric Status Rating Scales; Schizophrenia; Social Class | 2004 |
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Aryldialkylphosphatase; Case-Control Studies; DNA Mutational Analysis; Female; Finland; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic | 2004 |
Arginine and glutamine availability and macrophage functions in the obese insulin-resistant Zucker rat.
Topics: Animals; Arginine; Cells, Cultured; Disease Models, Animal; Dose-Response Relationship, Drug; Down-Regulation; Genetic Predisposition to Disease; Glutamine; Immune System; Immunity, Innate; Infections; Insulin Resistance; Lipopolysaccharides; Macrophages; Male; Nitric Oxide; Obesity; Rats; Rats, Zucker; Signal Transduction; Tumor Necrosis Factor-alpha | 2005 |
Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
Topics: Adolescent; Adult; Aged; Arginine; Blood Pressure; Cardiomyopathy, Dilated; Child; Female; Finland; Follow-Up Studies; Genetic Predisposition to Disease; Glutamine; Heart Failure; Humans; Hypertrophy, Left Ventricular; Male; Middle Aged; Mutation; Myosin Heavy Chains; Pedigree; Phenotype; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sarcomeres; Stroke Volume; Tropomyosin; Troponin C; Troponin I; Troponin T; Tryptophan; Ventricular Myosins | 2004 |
DNA repair gene XRCC1 Arg399Gln polymorphism is associated with increased risk of uterine leiomyoma.
Topics: Adult; Arginine; Asian People; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamine; Heterozygote; Humans; Korea; Leiomyoma; Middle Aged; Polymorphism, Genetic; Uterine Neoplasms; X-ray Repair Cross Complementing Protein 1 | 2005 |
No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes.
Topics: Chromosomes, Human, Pair 6; Diabetes Mellitus, Type 1; DNA, Intergenic; Genetic Predisposition to Disease; Glutamine; Humans; Microsatellite Repeats; Polymorphism, Genetic; Repetitive Sequences, Amino Acid; TATA-Box Binding Protein | 2005 |
The 5alpha-reductase type II A49T and V89L high-activity allelic variants are more common in men with prostate cancer compared with the general population.
Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Aged; Alanine; Alleles; Arginine; Biomarkers, Tumor; Case-Control Studies; Dihydrotestosterone; Disease Progression; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Luteinizing Hormone; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Prostatic Hyperplasia; Prostatic Neoplasms; Receptors, Androgen; Risk Factors; Sex Hormone-Binding Globulin; Sweden; Terminal Repeat Sequences; Testosterone; Threonine; Valine | 2005 |
Heterozygous Arg753Gln polymorphism of human TLR-2 impairs immune activation by Borrelia burgdorferi and protects from late stage Lyme disease.
Topics: Adult; Alleles; Animals; Arginine; Borrelia burgdorferi; Cell Line; Cells, Cultured; Cytokines; Genetic Carrier Screening; Genetic Predisposition to Disease; Glutamine; Humans; Incidence; Lyme Disease; Mice; Mice, Inbred C57BL; Mice, Knockout; Middle Aged; Polymorphism, Single Nucleotide; Toll-Like Receptor 2 | 2005 |
Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish.
Topics: Adult; Arginine; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genetics, Population; Genotype; Ghrelin; Glutamine; Heterozygote; Humans; Hunger; Leucine; Male; Metabolic Syndrome; Methionine; Middle Aged; Peptide Hormones; United States | 2005 |
Evaluation of the paraoxonases as candidate genes for stroke: Gln192Arg polymorphism in the paraoxonase 1 gene is associated with increased risk of stroke.
Topics: Arginine; Aryldialkylphosphatase; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Genotype; Glutamine; Heterozygote; Homozygote; Humans; Lipoproteins, LDL; Male; Multivariate Analysis; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Pravastatin; Risk; Risk Factors; Stroke | 2005 |
Plasma cell membrane glycoprotein-1 K121Q polymorphism in preeclampsia.
Topics: Adult; Case-Control Studies; Female; Finland; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Lysine; Phosphoric Diester Hydrolases; Polymorphism, Genetic; Pre-Eclampsia; Pregnancy; Pyrophosphatases | 2006 |
Beta2-adrenergic receptor genetic variants and risk of sudden cardiac death.
Topics: Aged; Black People; Case-Control Studies; Death, Sudden, Cardiac; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Haplotypes; Homozygote; Humans; Male; Polymorphism, Single Nucleotide; Receptors, Adrenergic, beta-2; Reproducibility of Results; White People | 2006 |
Toll-like receptor 2 Arg753Gln gene polymorphism in Turkish patients with Behçet's disease.
Topics: Adult; Arginine; Behcet Syndrome; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Toll-Like Receptor 2; Turkey | 2006 |
Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease.
Topics: Amyloidosis; Arginine; Environment; Familial Mediterranean Fever; Genetic Predisposition to Disease; Glutamine; Humans; Phenotype; Point Mutation; Polymorphism, Restriction Fragment Length; Toll-Like Receptor 2 | 2006 |
A common genetic variant in XPD associates with risk of 5q- and 7q-deleted acute myeloid leukemia.
Topics: Acute Disease; Chromosome Deletion; Chromosomes, Human, Pair 5; Chromosomes, Human, Pair 7; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Humans; Leukemia, Myeloid; Prognosis; Xeroderma Pigmentosum Group D Protein | 2007 |
The K469E polymorphism of the intracellular adhesion molecule 1 (ICAM-1) gene is not associated with myocardial infarction in Caucasians with type 2 diabetes.
Topics: Aged; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Intercellular Adhesion Molecule-1; Lysine; Male; Middle Aged; Myocardial Infarction; Polymorphism, Single Nucleotide; White People | 2006 |
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.
Topics: Aged; Aged, 80 and over; Arginine; Case-Control Studies; Female; Genetic Predisposition to Disease; Glutamine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Mutation; Parkinson Disease; Protein Serine-Threonine Kinases | 2007 |
Functional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease.
Topics: Alanine; Amino Acid Substitution; Arginine; Case-Control Studies; Crohn Disease; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Histidine; Humans; Male; Polymorphism, Single Nucleotide; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Tyrosine | 2007 |
IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease.
Topics: Adolescent; Child; Child, Preschool; Colitis, Ulcerative; Crohn Disease; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Infant; Jews; Linkage Disequilibrium; Nod2 Signaling Adaptor Protein; Polymorphism, Single Nucleotide; Receptors, Interleukin | 2007 |
Gln50Ter polymorphism of Fcgamma receptor IIB gene associated with genetic susceptibility to human systemic lupus erythematosus in Chinese populations.
Topics: Adult; Antigens, CD; Asian People; China; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Lupus Erythematosus, Systemic; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, IgG | 2007 |
Polymorphisms in the paraoxonase and endothelial nitric oxide synthase genes and the risk of early-onset myocardial infarction.
Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Arginine; Aryldialkylphosphatase; Aspartic Acid; Cohort Studies; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Male; Middle Aged; Myocardial Infarction; Nitric Oxide Synthase Type III; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors | 2007 |
Platelet 12-lipoxygenase Arg261Gln polymorphism: functional characterization and association with risk of esophageal squamous cell carcinoma in combination with COX-2 polymorphisms.
Topics: Adult; Aged; Aged, 80 and over; Arachidonate 12-Lipoxygenase; Arginine; Base Sequence; Blood Platelets; Carcinoma, Squamous Cell; Case-Control Studies; Cyclooxygenase 2; DNA Mutational Analysis; Esophageal Neoplasms; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Male; Membrane Proteins; Middle Aged; Molecular Sequence Data; Polymorphism, Single Nucleotide; Risk | 2007 |
Polymorphisms in XPD (Asp312Asn and Lys751Gln) genes, sunburn and arsenic-related skin lesions.
Topics: Adult; Amino Acid Substitution; Arsenic; Asparagine; Aspartic Acid; Case-Control Studies; Female; Genetic Predisposition to Disease; Glutamine; Humans; Lysine; Male; Polymorphism, Single Nucleotide; Skin Diseases; Sunburn; Water Supply; Xeroderma Pigmentosum Group D Protein | 2007 |
Beta2-adrenergic receptor gene polymorphisms and risk of ischemic stroke.
Topics: Aged; Aged, 80 and over; Alleles; Case-Control Studies; DNA; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Italy; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Risk Factors; Stroke | 2007 |
Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation.
Topics: Adult; Arginine; Diagnosis, Differential; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Heterozygote; Humans; Hypergammaglobulinemia; Male; Middle Aged; Multiple Sclerosis; Mutation; Pedigree; Prospective Studies; Receptors, Tumor Necrosis Factor, Type I | 2007 |
Astrocytes may play a role in the etiology of absence epilepsy: a comparison between immature GAERS not yet expressing seizures and adults.
Topics: Acetic Acid; Aging; Animals; Astrocytes; Brain; Cell Communication; Cell Differentiation; Disease Models, Animal; Energy Metabolism; Epilepsy; Epilepsy, Absence; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glucose; Glutamine; Magnetic Resonance Spectroscopy; Male; Mitochondria; Neural Inhibition; Neurons; Rats; Up-Regulation | 2007 |
Paraoxonase/arylesterase ratio, PON1 192Q/R polymorphism and PON1 status are associated with increased risk of ischemic stroke.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Carboxylic Ester Hydrolases; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Hypoxia-Ischemia, Brain; Male; Middle Aged; Polymorphism, Genetic; Risk; Stroke | 2008 |
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?
Topics: Alanine; Arginine; Biomarkers, Tumor; Breast Neoplasms; Centrosome; DNA, Complementary; Factor Analysis, Statistical; Female; Genes, BRCA1; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Humans; Immunohistochemistry; Keratins; Mutation, Missense; Nucleic Acid Amplification Techniques; Plasmids; Polymorphism, Single Nucleotide; Predictive Value of Tests; Receptors, Estrogen; Risk Assessment; Risk Factors; Sequence Analysis, DNA; Valine | 2007 |
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women.
Topics: Adult; Age of Onset; Breast Neoplasms; Fanconi Anemia Complementation Group N Protein; Female; Founder Effect; France; Genetic Predisposition to Disease; Glutamine; Humans; Infant, Newborn; Middle Aged; Mutation; Nuclear Proteins; Quebec; Tumor Suppressor Proteins | 2007 |
Somatic mutations in GLI3 can cause hypothalamic hamartoma and gelastic seizures.
Topics: Adolescent; Adult; Child; Child, Preschool; DNA Mutational Analysis; Epilepsies, Partial; Genetic Predisposition to Disease; Glutamine; Hamartoma; Humans; Hypothalamic Diseases; Kruppel-Like Transcription Factors; Magnetic Resonance Imaging; Nerve Tissue Proteins; Polymorphism, Single-Stranded Conformational; Zinc Finger Protein Gli3 | 2008 |
MC1R variants associated susceptibility to basal cell carcinoma of skin: interaction with host factors and XRCC3 polymorphism.
Topics: Adult; Aged; Arginine; Carcinoma, Basal Cell; Case-Control Studies; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Hungary; Male; Methionine; Middle Aged; Polymorphism, Genetic; Receptor, Melanocortin, Type 1; Risk Factors; Romania; Sequence Analysis, DNA; Skin Neoplasms; Slovakia; Threonine | 2008 |
Case-control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipolar-affective disorders.
Topics: Amino Acid Substitution; Arginine; Bipolar Disorder; Case-Control Studies; Chromosomes, Human, Pair 12; Depressive Disorder; Gene Frequency; Genes, Dominant; Genetic Predisposition to Disease; Glutamine; Haplotypes; Heterozygote; Homozygote; Humans; Linkage Disequilibrium; Microsatellite Repeats; Receptors, Purinergic P2; Receptors, Purinergic P2X7 | 2009 |
Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease.
Topics: Aged; Alzheimer Disease; Apolipoprotein E4; Arginine; Chi-Square Distribution; China; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamine; Humans; Male; Polymorphism, Genetic; tau Proteins; Tumor Necrosis Factor-alpha | 2008 |
Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie.
Topics: Alleles; Amino Acid Sequence; Animals; Base Sequence; Cloning, Molecular; Exons; Female; Genetic Predisposition to Disease; Glutamine; Homozygote; Male; Models, Genetic; Molecular Sequence Data; Polymorphism, Genetic; Promoter Regions, Genetic; PrPSc Proteins; Scrapie; Sequence Analysis, DNA; Sheep; Species Specificity; United States | 1994 |
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C.
Topics: Arginine; Base Sequence; Drug Resistance; Enzyme Activation; Factor V; Female; Genetic Predisposition to Disease; Glutamine; Heterozygote; Homozygote; Humans; Male; Molecular Sequence Data; Point Mutation; Protein C; Risk Factors; Survival Analysis; Sweden; Thrombophlebitis | 1994 |
Arginine506 to glutamin mutation in the factor V gene in infancy and childhood: evidence of fibrinolytic impairment.
Topics: Adolescent; Arginine; Child; Child, Preschool; DNA Mutational Analysis; Factor V; Female; Fibrin Fibrinogen Degradation Products; Fibrinolysis; Genetic Carrier Screening; Genetic Predisposition to Disease; Glutamine; Homozygote; Humans; Infant; Infant, Newborn; Male; Oligopeptides; Protein C; Thrombin; Thrombophlebitis | 1997 |
A genetic propensity to high factor VII is not associated with the risk of myocardial infarction in men.
Topics: Adult; Aged; Antigens; Arginine; Case-Control Studies; Factor VII; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Middle Aged; Myocardial Infarction; Polymorphism, Genetic; Risk Factors | 1998 |
Association of persistent bronchial hyperresponsiveness with beta2-adrenoceptor (ADRB2) haplotypes. A population study.
Topics: Adolescent; Adult; Allergens; Amino Acid Sequence; Asthma; Bronchial Hyperreactivity; Bronchial Provocation Tests; Bronchoconstrictor Agents; Confounding Factors, Epidemiologic; Environment; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Glycine; Haplotypes; Humans; Immunoglobulin E; Male; Methacholine Chloride; Polymorphism, Genetic; Population Surveillance; Receptors, Adrenergic, beta-2; Risk Factors | 1998 |
Polymorphisms in the DNA repair gene XPD: correlations with risk and age at onset of basal cell carcinoma.
Topics: Adenine; Adult; Age Factors; Age of Onset; Alleles; Carcinoma, Basal Cell; Confidence Intervals; Cytosine; DNA Helicases; DNA Repair; DNA-Binding Proteins; Exons; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Humans; Lysine; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Proteins; Psoriasis; Risk Factors; Transcription Factors; Transcription, Genetic; Xeroderma Pigmentosum Group D Protein | 1999 |
The combination of polymorphisms within interferon-gamma receptor 1 and receptor 2 associated with the risk of systemic lupus erythematosus.
Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Interferon gamma Receptor; Lupus Erythematosus, Systemic; Male; Methionine; Middle Aged; Molecular Sequence Data; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Receptors, Interferon; Reverse Transcriptase Polymerase Chain Reaction; Valine | 1999 |
The XRCC1 399 glutamine allele is a risk factor for adenocarcinoma of the lung.
Topics: Adenocarcinoma; Adult; Aged; Aged, 80 and over; Alleles; DNA-Binding Proteins; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Glutamine; Humans; Lung Neoplasms; Middle Aged; Risk Factors; X-ray Repair Cross Complementing Protein 1 | 2001 |
Paraoxonase 1 192 Gln/Arg gene polymorphism and cerebrovascular disease: interaction with type 2 diabetes.
Topics: Aged; Alleles; Arginine; Aryldialkylphosphatase; Cerebrovascular Disorders; Diabetes Mellitus, Type 2; Esterases; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Smoking | 2001 |
The potential size and duration of an epidemic of bovine spongiform encephalopathy in British sheep.
Topics: Age Factors; Animal Feed; Animal Husbandry; Animals; Cattle; Cohort Studies; Disease Outbreaks; Disease Transmission, Infectious; Eating; Encephalopathy, Bovine Spongiform; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Infectious Disease Transmission, Vertical; Logistic Models; Models, Biological; Models, Statistical; Prevalence; Prions; Probability; Scrapie; Sheep; Sheep Diseases; Time Factors; United Kingdom | 2002 |
Association of beta2-adrenoceptor Gln27Glu variant with body weight but not hypertension.
Topics: Body Weight; Case-Control Studies; Chromosomes, Human, Pair 5; Cohort Studies; Genetic Markers; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Hypertension; Obesity; Receptors, Adrenergic, beta-2; Risk Factors | 2001 |