proline has been researched along with Genetic Predisposition in 173 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 6 (3.47) | 18.2507 |
| 2000's | 111 (64.16) | 29.6817 |
| 2010's | 52 (30.06) | 24.3611 |
| 2020's | 4 (2.31) | 2.80 |
| Authors | Studies |
|---|---|
| Avramopoulos, D; Bacharaki, S; Dimitrakopoulos, S; Hatzimanolis, A; Maher, BJ; Peng, X; Sobreira, N; Stefanis, NC; Wahbeh, MH; Wohler, E; Yang, X; Yovo, C | 1 |
| Akolkar, B; Butterworth, MD; Fan, S; Fiehn, O; Hagopian, W; Krischer, JP; Lernmark, Å; Li, Q; Parikh, H; Rewers, M; She, JX; Toppari, J; Ziegler, AG | 1 |
| Abbasi, S; Abd El-Wahab, A; Abdallah, M; Abebe, G; Aca-Aca, G; Adama, S; Adefegha, SA; Adidigue-Ndiome, R; Adiseshaiah, P; Adrario, E; Aghajanian, C; Agnese, W; Ahmad, A; Ahmad, I; Ahmed, MFE; Akcay, OF; Akinmoladun, AC; Akutagawa, T; Alakavuklar, MA; Álava-Rabasa, S; Albaladejo-Florín, MJ; Alexandra, AJE; Alfawares, R; Alferiev, IS; Alghamdi, HS; Ali, I; Allard, B; Allen, JD; Almada, E; Alobaid, A; Alonso, GL; Alqahtani, YS; Alqarawi, W; Alsaleh, H; Alyami, BA; Amaral, BPD; Amaro, JT; Amin, SAW; Amodio, E; Amoo, ZA; Andia Biraro, I; Angiolella, L; Anheyer, D; Anlay, DZ; Annex, BH; Antonio-Aguirre, B; Apple, S; Arbuznikov, AV; Arinsoy, T; Armstrong, DK; Ash, S; Aslam, M; Asrie, F; Astur, DC; Atzrodt, J; Au, DW; Aucoin, M; Auerbach, EJ; Azarian, S; Ba, D; Bai, Z; Baisch, PRM; Balkissou, AD; Baltzopoulos, V; Banaszewski, M; Banerjee, S; Bao, Y; Baradwan, A; Barandika, JF; Barger, PM; Barion, MRL; Barrett, CD; Basudan, AM; Baur, LE; Baz-Rodríguez, SA; Beamer, P; Beaulant, A; Becker, DF; Beckers, C; Bedel, J; Bedlack, R; Bermúdez de Castro, JM; Berry, JD; Berthier, C; Bhattacharya, D; Biadgo, B; Bianco, G; Bianco, M; Bibi, S; Bigliardi, AP; Billheimer, D; Birnie, DH; Biswas, K; Blair, HC; Bognetti, P; Bolan, PJ; Bolla, JR; Bolze, A; Bonnaillie, P; Borlimi, R; Bórquez, J; Bottari, NB; Boulleys-Nana, JR; Brighetti, G; Brodeur, GM; Budnyak, T; Budnyk, S; Bukirwa, VD; Bulman, DM; Burm, R; Busman-Sahay, K; Butcher, TW; Cai, C; Cai, H; Cai, L; Cairati, M; Calvano, CD; Camacho-Ordóñez, A; Camela, E; Cameron, T; Campbell, BS; Cansian, RL; Cao, Y; Caporale, AS; Carciofi, AC; Cardozo, V; Carè, J; Carlos, AF; Carozza, R; Carroll, CJW; Carsetti, A; Carubelli, V; Casarotta, E; Casas, M; Caselli, G; Castillo-Lora, J; Cataldi, TRI; Cavalcante, ELB; Cavaleiro, A; Cayci, Z; Cebrián-Tarancón, C; Cedrone, E; Cella, D; Cereda, C; Ceretti, A; Ceroni, M; Cha, YH; Chai, X; Chang, EF; Chang, TS; Chanteux, H; Chao, M; Chaplin, BP; Chaturvedi, S; Chaturvedi, V; Chaudhary, DK; Chen, A; Chen, C; Chen, HY; Chen, J; Chen, JJ; Chen, K; Chen, L; Chen, Q; Chen, R; Chen, SY; Chen, TY; Chen, WM; Chen, X; Chen, Y; Cheng, G; Cheng, GJ; Cheng, J; Cheng, YH; Cheon, HG; Chew, KW; Chhoker, S; Chiu, WN; Choi, ES; Choi, MJ; Choi, SD; Chokshi, S; Chorny, M; Chu, KI; Chu, WJ; Church, AL; Cirrincione, A; Clamp, AR; Cleff, MB; Cohen, M; Coleman, RL; Collins, SL; Colombo, N; Conduit, N; Cong, WL; Connelly, MA; Connor, J; Cooley, K; Correa Ramos Leal, I; Cose, S; Costantino, C; Cottrell, M; Cui, L; Cundall, J; Cutaia, C; Cutler, CW; Cuypers, ML; da Silva Júnior, FMR; Dahal, RH; Damiani, E; Damtie, D; Dan-Li, W; Dang, Z; Dasa, SSK; Davin, A; Davis, DR; de Andrade, CM; de Jong, PL; de Oliveira, D; de Paula Dorigam, JC; Dean, A; Deepa, M; Delatour, C; Dell'Aiera, S; Delley, MF; den Boer, RB; Deng, L; Deng, Q; Depner, RM; Derdau, V; Derici, U; DeSantis, AJ; Desmarini, D; Diffo-Sonkoue, L; Divizia, M; Djenabou, A; Djordjevic, JT; Dobrovolskaia, MA; Domizi, R; Donati, A; Dong, Y; Dos Santos, M; Dos Santos, MP; Douglas, RG; Duarte, PF; Dullaart, RPF; Duscha, BD; Edwards, LA; Edwards, TE; Eichenwald, EC; El-Baba, TJ; Elashiry, M; Elashiry, MM; Elashry, SH; Elliott, A; Elsayed, R; Emerson, MS; Emmanuel, YO; Emory, TH; Endale-Mangamba, LM; Enten, GA; Estefanía-Fernández, K; Estes, JD; Estrada-Mena, FJ; Evans, S; Ezra, L; Faria de, RO; Farraj, AK; Favre, C; Feng, B; Feng, J; Feng, L; Feng, W; Feng, X; Feng, Z; Fernandes, CLF; Fernández-Cuadros, ME; Fernie, AR; Ferrari, D; Florindo, PR; Fong, PC; Fontes, EPB; Fontinha, D; Fornari, VJ; Fox, NP; Fu, Q; Fujitaka, Y; Fukuhara, K; Fumeaux, T; Fuqua, C; Fustinoni, S; Gabbanelli, V; Gaikwad, S; Gall, ET; Galli, A; Gancedo, MA; Gandhi, MM; Gao, D; Gao, K; Gao, M; Gao, Q; Gao, X; Gao, Y; Gaponenko, V; Garber, A; Garcia, EM; García-Campos, C; García-Donas, J; García-Pérez, AL; Gasparri, F; Ge, C; Ge, D; Ge, JB; Ge, X; George, I; George, LA; Germani, G; Ghassemi Tabrizi, S; Gibon, Y; Gillent, E; Gillies, RS; Gilmour, MI; Goble, S; Goh, JC; Goiri, F; Goldfinger, LE; Golian, M; Gómez, MA; Gonçalves, J; Góngora-García, OR; Gonul, I; González, MA; Govers, TM; Grant, PC; Gray, EH; Gray, JE; Green, MS; Greenwald, I; Gregory, MJ; Gretzke, D; Griffin-Nolan, RJ; Griffith, DC; Gruppen, EG; Guaita, A; Guan, P; Guan, X; Guerci, P; Guerrero, DT; Guo, M; Guo, P; Guo, R; Guo, X; Gupta, J; Guz, G; Hajizadeh, N; Hamada, H; Haman-Wabi, AB; Han, TT; Hannan, N; Hao, S; Harjola, VP; Harmon, M; Hartmann, MSM; Hartwig, JF; Hasani, M; Hawthorne, WJ; Haykal-Coates, N; Hazari, MS; He, DL; He, P; He, SG; Héau, C; Hebbar Kannur, K; Helvaci, O; Heuberger, DM; Hidalgo, F; Hilty, MP; Hirata, K; Hirsch, A; Hoffman, AM; Hoffmann, JF; Holloway, RW; Holmes, RK; Hong, S; Hongisto, M; Hopf, NB; Hörlein, R; Hoshino, N; Hou, Y; Hoven, NF; Hsieh, YY; Hsu, CT; Hu, CW; Hu, JH; Hu, MY; Hu, Y; Hu, Z; Huang, C; Huang, D; Huang, DQ; Huang, L; Huang, Q; Huang, R; Huang, S; Huang, SC; Huang, W; Huang, Y; Huffman, KM; Hung, CH; Hung, CT; Huurman, R; Hwang, SM; Hyun, S; Ibrahim, AM; Iddi-Faical, A; Immordino, P; Isla, MI; Jacquemond, V; Jacques, T; Jankowska, E; Jansen, JA; Jäntti, T; Jaque-Fernandez, F; Jarvis, GA; Jatt, LP; Jeon, JW; Jeong, SH; Jhunjhunwala, R; Ji, F; Jia, X; Jia, Y; Jian-Bo, Z; Jiang, GD; Jiang, L; Jiang, W; Jiang, WD; Jiang, Z; Jiménez-Hoyos, CA; Jin, S; Jobling, MG; John, CM; John, T; Johnson, CB; Jones, KI; Jones, WS; Joseph, OO; Ju, C; Judeinstein, P; Junges, A; Junnarkar, M; Jurkko, R; Kaleka, CC; Kamath, AV; Kang, X; Kantsadi, AL; Kapoor, M; Karim, Z; Kashuba, ADM; Kassa, E; Kasztura, M; Kataja, A; Katoh, T; Kaufman, JS; Kaupp, M; Kehinde, O; Kehrenberg, C; Kemper, N; Kerr, CW; Khan, AU; Khan, MF; Khan, ZUH; Khojasteh, SC; Kilburn, S; Kim, CG; Kim, DU; Kim, DY; Kim, HJ; Kim, J; Kim, OH; Kim, YH; King, C; Klein, A; Klingler, L; Knapp, AK; Ko, TK; Kodavanti, UP; Kolla, V; Kong, L; Kong, RY; Kong, X; Kore, S; Kortz, U; Korucu, B; Kovacs, A; Krahnert, I; Kraus, WE; Kuang, SY; Kuehn-Hajder, JE; Kurz, M; Kuśtrowski, P; Kwak, YD; Kyttaris, VC; Laga, SM; Laguerre, A; Laloo, A; Langaro, MC; Langham, MC; Lao, X; Larocca, MC; Lassus, J; Lattimer, TA; Lazar, S; Le, MH; Leal, DB; Leal, M; Leary, A; Ledermann, JA; Lee, JF; Lee, MV; Lee, NH; Leeds, CM; Leeds, JS; Lefrandt, JD; Leicht, AS; Leonard, M; Lev, S; Levy, K; Li, B; Li, C; Li, CM; Li, DH; Li, H; Li, J; Li, L; Li, LJ; Li, N; Li, P; Li, T; Li, X; Li, XH; Li, XQ; Li, XX; Li, Y; Li, Z; Li, ZY; Liao, YF; Lin, CC; Lin, MH; Lin, Y; Ling, Y; Links, TP; Lira-Romero, E; Liu, C; Liu, D; Liu, H; Liu, J; Liu, L; Liu, LP; Liu, M; Liu, T; Liu, W; Liu, X; Liu, XH; Liu, Y; Liuwantara, D; Ljumanovic, N; Lobo, L; Lokhande, K; Lopes, A; Lopes, RMRM; López-Gutiérrez, JC; López-Muñoz, MJ; López-Santamaría, M; Lorenzo, C; Lorusso, D; Losito, I; Lu, C; Lu, H; Lu, HZ; Lu, SH; Lu, SN; Lu, Y; Lu, ZY; Luboga, F; Luo, JJ; Luo, KL; Luo, Y; Lutomski, CA; Lv, W; M Piedade, MF; Ma, J; Ma, JQ; Ma, JX; Ma, N; Ma, P; Ma, S; Maciel, M; Madureira, M; Maganaris, C; Maginn, EJ; Mahnashi, MH; Maierhofer, M; Majetschak, M; Malla, TR; Maloney, L; Mann, DL; Mansuri, A; Marelli, E; Margulis, CJ; Marrella, A; Martin, BL; Martín-Francés, L; Martínez de Pinillos, M; Martínez-Navarro, EM; Martinez-Quintanilla Jimenez, D; Martínez-Velasco, A; Martínez-Villaseñor, L; Martinón-Torres, M; Martins, BA; Massongo, M; Mathew, AP; Mathews, D; Matsui, J; Matsumoto, KI; Mau, T; Maves, RC; Mayclin, SJ; Mayer, JM; Maynard, ND; Mayr, T; Mboowa, MG; McEvoy, MP; McIntyre, RC; McKay, JA; McPhail, MJW; McVeigh, AL; Mebazaa, A; Medici, V; Medina, DN; Mehmood, T; Mei-Li, C; Melku, M; Meloncelli, S; Mendes, GC; Mendoza-Velásquez, C; Mercadante, R; Mercado, MI; Merenda, MEZ; Meunier, J; Mi, SL; Michels, M; Mijatovic, V; Mikhailov, V; Milheiro, SA; Miller, DC; Ming, F; Mitsuishi, M; Miyashita, T; Mo, J; Mo, S; Modesto-Mata, M; Moeller, S; Monte, A; Monteiro, L; Montomoli, J; Moore, EE; Moore, HB; Moore, PK; Mor, MK; Moratalla-López, N; Moratilla Lapeña, L; Moreira, R; Moreno, MA; Mörk, AC; Morton, M; Mosier, JM; Mou, LH; Mougharbel, AS; Muccillo-Baisch, AL; Muñoz-Serrano, AJ; Mustafa, B; Nair, GM; Nakanishi, I; Nakanjako, D; Naraparaju, K; Nawani, N; Neffati, R; Neil, EC; Neilipovitz, D; Neira-Borrajo, I; Nelson, MT; Nery, PB; Nese, M; Nguyen, F; Nguyen, MH; Niazy, AA; Nicolaï, J; Nogueira, F; Norbäck, D; Novaretti, JV; O'Donnell, T; O'Dowd, A; O'Malley, DM; Oaknin, A; Ogata, K; Ohkubo, K; Ojha, M; Olaleye, MT; Olawande, B; Olomo, EJ; Ong, EWY; Ono, A; Onwumere, J; Ortiz Bibriesca, DM; Ou, X; Oza, AM; Ozturk, K; Özütemiz, C; Palacio-Pastrana, C; Palaparthi, A; Palevsky, PM; Pan, K; Pantanetti, S; Papachristou, DJ; Pariani, A; Parikh, CR; Parissis, J; Paroul, N; Parry, S; Patel, N; Patel, SM; Patel, VC; Pawar, S; Pefura-Yone, EW; Peixoto Andrade, BCO; Pelepenko, LE; Peña-Lora, D; Peng, S; Pérez-Moro, OS; Perez-Ortiz, AC; Perry, LM; Peter, CM; Phillips, NJ; Phillips, P; Pia Tek, J; Piner, LW; Pinto, EA; Pinto, SN; Piyachaturawat, P; Poka-Mayap, V; Polledri, E; Poloni, TE; Ponessa, G; Poole, ST; Post, AK; Potter, TM; Pressly, BB; Prouty, MG; Prudêncio, M; Pulkki, K; Pupier, C; Qian, H; Qian, ZP; Qiu, Y; Qu, G; Rahimi, S; Rahman, AU; Ramadan, H; Ramanna, S; Ramirez, I; Randolph, GJ; Rasheed, A; Rault, J; Raviprakash, V; Reale, E; Redpath, C; Rema, V; Remucal, CK; Remy, D; Ren, T; Ribeiro, LB; Riboli, G; Richards, J; Rieger, V; Rieusset, J; Riva, A; Rivabella Maknis, T; Robbins, JL; Robinson, CV; Roche-Campo, F; Rodriguez, R; Rodríguez-de-Cía, J; Rollenhagen, JE; Rosen, EP; Rub, D; Rubin, N; Rubin, NT; Ruurda, JP; Saad, O; Sabell, T; Saber, SE; Sabet, M; Sadek, MM; Saejio, A; Salinas, RM; Saliu, IO; Sande, D; Sang, D; Sangenito, LS; Santos, ALSD; Sarmiento Caldas, MC; Sassaroli, S; Sassi, V; Sato, J; Sauaia, A; Saunders, K; Saunders, PR; Savarino, SJ; Scambia, G; Scanlon, N; Schetinger, MR; Schinkel, AFL; Schladweiler, MC; Schofield, CJ; Schuepbach, RA; Schulz, J; Schwartz, N; Scorcella, C; Seeley, J; Seemann, F; Seinige, D; Sengoku, T; Seravalli, J; Sgromo, B; Shaheen, MY; Shan, L; Shanmugam, S; Shao, H; Sharma, S; Shaw, KJ; Shen, BQ; Shen, CH; Shen, P; Shen, S; Shen, Y; Shen, Z; Shi, J; Shi-Li, L; Shimoda, K; Shoji, Y; Shun, C; Silva, MA; Silva-Cardoso, J; Simas, NK; Simirgiotis, MJ; Sincock, SA; Singh, MP; Sionis, A; Siu, J; Sivieri, EM; Sjerps, MJ; Skoczen, SL; Slabon, A; Slette, IJ; Smith, MD; Smith, S; Smith, TG; Snapp, KS; Snow, SJ; Soares, MCF; Soberman, D; Solares, MD; Soliman, I; Song, J; Sorooshian, A; Sorrell, TC; Spinar, J; Staudt, A; Steinhart, C; Stern, ST; Stevens, DM; Stiers, KM; Stimming, U; Su, YG; Subbian, V; Suga, H; Sukhija-Cohen, A; Suksamrarn, A; Suksen, K; Sun, J; Sun, M; Sun, P; Sun, W; Sun, XF; Sun, Y; Sundell, J; Susan, LF; Sutjarit, N; Swamy, KV; Swisher, EM; Sykes, C; Takahashi, JA; Talmor, DS; Tan, B; Tan, ZK; Tang, L; Tang, S; Tanner, JJ; Tanwar, M; Tarazi, Z; Tarvasmäki, T; Tay, FR; Teketel, A; Temitayo, GI; Thersleff, T; Thiessen Philbrook, H; Thompson, LC; Thongon, N; Tian, B; Tian, F; Tian, Q; Timothy, AT; Tingle, MD; Titze, IR; Tolppanen, H; Tong, W; Toyoda, H; Tronconi, L; Tseng, CH; Tu, H; Tu, YJ; Tung, SY; Turpault, S; Tuynman, JB; Uemoto, AT; Ugurlu, M; Ullah, S; Underwood, RS; Ungell, AL; Usandizaga-Elio, I; Vakonakis, I; van Boxel, GI; van den Beucken, JJJP; van der Boom, T; van Slegtenhorst, MA; Vanni, JR; Vaquera, A; Vasconcellos, RS; Velayos, M; Vena, R; Ventura, G; Verso, MG; Vincent, RP; Vitale, F; Vitali, S; Vlek, SL; Vleugels, MPH; Volkmann, N; Vukelic, M; Wagner Mackenzie, B; Wairagala, P; Waller, SB; Wan, J; Wan, MT; Wan, Y; Wang, CC; Wang, H; Wang, J; Wang, JF; Wang, K; Wang, L; Wang, M; Wang, S; Wang, WM; Wang, X; Wang, Y; Wang, YD; Wang, YF; Wang, Z; Wang, ZG; Warriner, K; Weberpals, JI; Weerachayaphorn, J; Wehrli, FW; Wei, J; Wei, KL; Weinheimer, CJ; Weisbord, SD; Wen, S; Wendel Garcia, PD; Williams, JW; Williams, R; Winkler, C; Wirman, AP; Wong, S; Woods, CM; Wu, B; Wu, C; Wu, F; Wu, P; Wu, S; Wu, Y; Wu, YN; Wu, ZH; Wurtzel, JGT; Xia, L; Xia, Z; Xia, ZZ; Xiao, H; Xie, C; Xin, ZM; Xing, Y; Xing, Z; Xu, S; Xu, SB; Xu, T; Xu, X; Xu, Y; Xue, L; Xun, J; Yaffe, MB; Yalew, A; Yamamoto, S; Yan, D; Yan, H; Yan, S; Yan, X; Yang, AD; Yang, E; Yang, H; Yang, J; Yang, JL; Yang, K; Yang, M; Yang, P; Yang, Q; Yang, S; Yang, W; Yang, X; Yang, Y; Yao, JC; Yao, WL; Yao, Y; Yaqub, TB; Ye, J; Ye, W; Yen, CW; Yeter, HH; Yin, C; Yip, V; Yong-Yi, J; Yu, HJ; Yu, MF; Yu, S; Yu, W; Yu, WW; Yu, X; Yuan, P; Yuan, Q; Yue, XY; Zaia, AA; Zakhary, SY; Zalwango, F; Zamalloa, A; Zamparo, P; Zampini, IC; Zani, JL; Zeitoun, R; Zeng, N; Zenteno, JC; Zepeda-Palacio, C; Zhai, C; Zhang, B; Zhang, G; Zhang, J; Zhang, K; Zhang, Q; Zhang, R; Zhang, T; Zhang, X; Zhang, Y; Zhang, YY; Zhao, B; Zhao, D; Zhao, G; Zhao, H; Zhao, Q; Zhao, R; Zhao, S; Zhao, T; Zhao, X; Zhao, XA; Zhao, Y; Zhao, Z; Zheng, Z; Zhi-Min, G; Zhou, CL; Zhou, HD; Zhou, J; Zhou, W; Zhou, XQ; Zhou, Z; Zhu, C; Zhu, H; Zhu, L; Zhu, Y; Zitzmann, N; Zou, L; Zou, Y | 1 |
| Cappelli, C; Delbarba, A; Di Lodovico, E; Facchetti, F; Facondo, P; Ferlin, A; Fisogni, S; Izzi, C; Maffezzoni, F; Pezzaioli, LC; Scolari, F | 1 |
| Chen, H; Hu, L; Jiang, M; Li, B; Li, Q; Liu, T; Ning, H; Wang, D; Zhang, B | 1 |
| An, SSA; Bagyinszky, E; Giau, VV; Kim, S; Park, J; Shim, K; Youn, YC | 1 |
| Aungraheeta, R; Chen, Q; Gabrielli, S; Hutchinson, JL; Kilo, T; Mackay, J; Morel-Kopp, MC; Mundell, SJ; Rabbolini, D; Stevenson, W; Ward, CM | 1 |
| Massoud, A; Mohammadzadeh, M; Najafi, S; Rezaei, N; Zare Bidoki, A | 1 |
| Dong, Q; Liao, J; Liu, LR; Liu, SZ; Lu, DL; Ren, PW; Ren, ZJ; Yang, B; Yang, LC; Zhang, Q | 1 |
| Idrees, H; Mujtaba, G; Naz, S; Ramzan, M; Sobreira, N; Witmer, PD | 1 |
| Camelo-Santos, J; de Paula Silveira-Lacerda, E; do Prado Barbosa, A; Guillo, LA | 1 |
| Afef, S; Fadhel, NM; Fadoua, N; Khaldoun, BH; Mohamed, N; Naceur, SM; Youssef, SM | 1 |
| Abbasi, ZA; Ajmal, M; Azhar, A; Hameed, A; Khan, MA; Qureshi, NR; Saleem, S | 1 |
| Gong, H; Guan, H; Guo, S; Lang, Z; Liu, B; Liu, L; Wang, H; Zhang, J | 1 |
| Fang, M; Gao, H; Liu, J; Liu, L; Ouyang, Y; Wang, X | 1 |
| Cai, D; Chen, R; Liu, D; Luo, H; Sun, J; Wang, J; Yang, R; Zhang, R | 1 |
| Bae, SC; Lee, YH; Song, GG | 1 |
| Clelland, CL; Clelland, JD; Drouet, V; Duff, KE; Kaon, A; Kelly, A; Nadrich, RH; Rajparia, A; Read, LL | 1 |
| Aldámiz-Echevarria, T; Berenguer, J; Fernández-Rodríguez, A; García-Alvarez, M; García-Broncano, P; Jiménez-Sousa, MÁ; López, JC; Micheloud, D; Miralles, P; Pineda-Tenor, D; Resino, S | 1 |
| Blanchard, E; Samaras, K; Vickers, CR | 1 |
| Black, MH; Buchanan, TA; Haritunians, T; Lawrence, JM; Takayanagi, M; Taylor, KD; Trigo, E; Wang, N; Watanabe, RM; Wu, J; Xiang, AH | 1 |
| He, J; Li, S; Wu, R; Yan, Y | 1 |
| Chen, Y; Li, J; Li, L; Mo, Z | 1 |
| Ampuero, J; Andrade, RJ; Buti, M; Cabezas, J; Calleja, JL; Crespo, J; Del Campo, JA; Fernández, I; Forns, X; Lens, S; Millán, R; Rojas, L; Romero-Gómez, M | 1 |
| Oner, DA; Tastan, H | 1 |
| Ganai, BA; Hameed, I; Kadla, SA; Majid, M; Masood, A | 1 |
| Clelland, CL; Clelland, JD; Drouet, V; Nadrich, RH; Rajparia, A; Read, LL; Rilett, KC; Smeed, JA | 1 |
| Cheng, L; Li, JY; Li, NN; Lu, ZJ; Peng, R; Sun, XY; Tan, EK; Wang, L; Zhang, JH | 1 |
| Crabtree, GW; Gogos, JA; Gordon, JA; Park, AJ | 1 |
| Iyer, S; Kwan, R; Liao, J; Liu, L; Moons, D; Omary, MB; Park, MJ | 1 |
| Campagna, G; Grilli, A; La Fratta, I; Pesce, M; Rizzuto, A; Tatangelo, R | 1 |
| Abbar, M; Al Bouzidi, A; Ameur, A; Ameziane El Hassani, R; Attaleb, M; Dakka, N; El Mzibri, M; Hadami, K | 1 |
| Singh, D; Singh, JR; Sperling, K; Vanita, V; Varon, R | 1 |
| Jiang, JF; Li, HA; Li, XM; Pan, XL; Wang, XL; Yan, LH; Yang, AQ; Zhang, B; Zheng, LL; Zheng, XZ; Zhou, QY | 1 |
| Chang, CT; Chen, RH; Huang, WL; Tsai, CH; Tsai, FJ; Wang, TY | 1 |
| Kang, SJ; Khang, SK; Ki, CS; Kim, DW; Kim, HY; Kim, SH; Koh, SH; Sung, IH | 1 |
| Heun, R; Klockgether, T; Klotz, L; Kölsch, H; Schmidt, S | 1 |
| Almeida, PS; Fraga, AC; Manoel, WJ; Martins, E; Paiva, MV; Reis, AA; Saddi, VA; Silva, ER | 1 |
| Arné-Bes, MC; Delisle, MB; Figarella-Branger, D; Heitz, F; Levade, T; Pellissier, JF; Richard, P; Uro-Coste, E | 1 |
| Li, Y; Lv, XJ; Qian, XP; Qiu, LX; Shen, XK; Song, Y | 1 |
| Dornhoffer, J; Hartzell, LD; McKelvey, KD; Van Hemert, RL | 1 |
| Bhagavati, S; Maccabee, PJ; Xu, W | 1 |
| Gut, I; Hubackova, M; Kodet, R; Kubackova, K; Mrhalova, M; Soucek, P; Vaclavikova, R | 1 |
| Dugi, KA; Schiekofer, S; Schlimmer, P; Schneider, JG; von Eynatten, M | 1 |
| Akrami, SM; Amiri, P; Doosti, M; Golmohammadi, T; Heshmat, R; Mirzaei, H; Nakhjavani, M | 1 |
| Al-Mesfer, S; Aldahmesh, MA; Alkuraya, FS; Ghadhfan, FE; Khan, AO | 1 |
| Gunduz, M; Mita, Y; Naomoto, Y; Ouchida, M; Sakai, A; Shimizu, K; Tanabe, S; Toyooka, S; Yamamoto, H; Yasuda, Y | 1 |
| An, X; Burgunder, JM; Chen, W; Gou, Y; Mao, X; Peng, R; Wang, Y; Wu, Y; Xu, Y; Yuan, G; Zhang, J; Zhang, Z | 1 |
| Bossi, A; De Cosmo, S; Motterlini, N; Pellegrini, F; Prudente, S; Remuzzi, G; Ruggenenti, P; Trevisan, R; Trischitta, V | 1 |
| Cattepoel, S; Eckert, A; Kuehnle, K; Kulic, L; Nitsch, RM; Pagani, L; Rhein, V; Tracy, J; Wollmer, MA | 1 |
| Bamberg, C; Chen, YP; Guthmann, F; Haumann, H; Hocher, B; Kalache, KD; Li, J; Pfab, T; Poralla, C; Schlemm, L | 1 |
| Agarwal, S; Gill, AC; Goldmann, W; Graham, JF; Kirby, L | 1 |
| Burke, W; Crouch, J; Fryer-Edwards, K; Fullerton, SM; Yu, JH | 1 |
| Jiang, P; Li, W; Liu, J; Tang, J; Zeng, X | 1 |
| Dhammawipark, C; Kitkumthorn, N; Mutirangura, A; Rabalert, J; Yanatatsaneejit, P | 1 |
| Afroze, D; Khan, NP; Pandith, AA; Rasool, R; Shah, ZA; Siddiqi, M; Wani, S; Yousuf, A | 1 |
| Choi, JS; Choi, YD; Hwang, JE; Kim, HN; Kim, HR; Kim, SH; Kweon, SS; Park, YK; Piao, JM; Shin, MH; Song, HR; Yoon, JY; Yun, WJ | 1 |
| Cseh, K; Jermendy, A; Körner, A; Kovács, M; Madácsy, L | 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 |
| Guan, J; Su, K; Tao, M; Wu, X; Yi, H; Yin, S | 1 |
| Chen, F; Jiang, DK; Liu, GY; Shen, SQ; Yu, L | 1 |
| Baker, LA; Cost, NG; Khokhar, S; Mitui, M; Rakheja, D; Wickiser, JE | 1 |
| Akhlaghi, S; Dehghan-Manshadi, R; Ferns, GA; Forghanifard, MM; Ghayour-Mobarhan, M; Jamialahmadi, K; Masoudi-Kazemabad, A; Mojarrad, M; Moohebati, M | 1 |
| Thompson, AJ | 1 |
| Chen, H; Chen, J; Hu, H; Mohan, V; Tang, Y; Venkatesan, R; Wang, J; Zhang, H; Zhu, S | 1 |
| Bauer, M; Borte, M; Gräbsch, C; Heinrich, J; Herbarth, O; Illig, T; Klopp, N; Krämer, U; Lehmann, I; Röder, S; Schaaf, B; Schlink, U; von Berg, A | 1 |
| Ma, YY; Shao, CM; Wang, HJ; Ye, ZY; Zhang, J; Zhang, Q | 1 |
| Akbaş, H; Akkus, Z; Atay, AE; Budak, T; Isi, H; Tekes, S; Yalcin, K | 1 |
| Baraban, SC; Choi, M; Coppola, G; Fu, YH; Geschwind, DH; Gibson, G; Hahn, AF; Howard, MA; Huang, A; Kirk, A; Klein, E; Kornberg, Z; Lee, HY; Lifton, RP; Merriman, B; Mirsattari, SM; Nelson-Williams, C; Ptáček, LJ; Russell, JF; Steckley, JL | 1 |
| de Bakker, PI; Elsais, A; Garchon, HJ; Gregersen, PK; Hammarstrom, L; Harbo, HF; Kosoy, R; Lamb, J; Lee, AT; Lie, BA; Maniaol, A; Marx, A; McKee, D; Melms, A; Niks, EH; Pan-Hammarstrom, Q; Piehl, F; Pirskanen-Matell, R; Pütz, M; Raychaudhuri, S; Seldin, MF; Simpfendorfer, KR; Ströbel, P; Sussman, J; Tackenberg, B; Tallaksen, C; Titulaer, MJ; Verschuuren, JJ; Willcox, N | 1 |
| El Hallani, S; Rossetto, M; Sanson, M | 1 |
| Kumar, A; Kumar, S; Mathur, N; Pant, MC; Tilak, AR | 1 |
| Beeson, D; Brydson, M; Chauplannaz, G; Colquhoun, D; Croxen, R; Hatton, C; Newsom-Davis, J; Oosterhuis, H; Shelley, C; Vincent, A | 1 |
| Borch-Johnsen, K; Brødbaek, K; Fenger, M; Frederiksen, L; Jørgensen, T; Madsbad, S; Urhammer, SA | 1 |
| Gallegos-Arreola, MP; Montoya-Fuentes, H; Morán-Moguel, MC; Sánchez-Corona, J; Suárez-Rincón, AE | 1 |
| Bonner, JD; Boyd, J; Chong, G; De La Chapelle, A; Ellis, NA; Farber, D; Figer, A; Foulkes, WD; Friedman, E; Gaff, CL; Gebert, J; Gordon, PH; Greenwood, CM; Gregersen, PK; Gruber, SB; Hamel, N; Hampel, H; Horwitz, M; King, MC; Lee, C; MacNamara, E; Macrae, FA; Marcus, V; Markowitz, A; Nafa, K; Offit, K; Paillerets, BB; Rennert, G; Shia, J; Thiffault, I; Tomsho, L; Walsh, T; Weitzel, JN | 1 |
| Arvanitis, DA; Blennow, K; Palmér, M; Regland, B; Rymo, L; Spandidos, DA; Zafiropoulos, A; Zetterberg, H | 1 |
| Bruno, C; DeFlorio, L; Federico, A; Grieco, GS; Malandrini, A; Mancuso, M; Martini, B; Murri, L; Nappi, G; Petrini, S; Santorelli, FM; Siciliano, G; Tessa, A | 1 |
| Browner, W; Cauley, J; Kahn, A; Morin, P; Saiz, R; Ziv, E | 1 |
| Blennow, K; Boreström, C; Palmér, M; Rymo, L; Zetterberg, H | 1 |
| Diamond, AM; Hu, YJ | 1 |
| Hammar, N; Jartti, L; Järvisalo, MJ; Kaprio, J; Karvonen, MK; Koulu, M; Marniemi, J; Paakkunainen, U; Pesonen, U; Raitakari, OT; Rönnemaa, T; Simell, O | 1 |
| Abba, MC; Dulout, FN; Golijow, CD; Gómez, MA; Laguens, MR; Villaverde, LM | 1 |
| Aoki, M; Fukao, T; Inoue, R; Kaneko, H; Kasahara, K; Kato, Z; Kondo, N; Matsui, E; Suzuki, K; Suzuki, Y; Teramoto, T; Watanabe, M | 1 |
| Bojesen, SE; Nordestgaard, BG; Tybjaerg-Hansen, A | 1 |
| Altshuler, DM; Hankinson, SE; Hu, FB; Hunter, DJ; Liu, S; Manson, JE; Meigs, JB; Memisoglu, A | 1 |
| Huang, Z; Sui, Y; Weng, J; Xiu, L; Yan, J | 1 |
| Frey, J; Klupa, T; Malecki, MT; Mlynarski, W; Sieradzki, J; Skupien, J; Walus, M | 1 |
| Guo, J; Hu, X; Shen, H; Solari, A; Wang, L; Wang, X; Wei, Q; Xu, Y; Zhang, Z | 1 |
| Alderson, D; Farthing, MJ; Feakins, R; Gupta, J; Hollowood, A; Holly, J; Newcomb, P; Storey, A; Zhang, ZW | 1 |
| Abdel-Rahman, WM; Gerdes, AM; Kariola, R; Lönnqvist, KE; Nyström-Lahti, M; Peltomäki, P; Raevaara, TE; Tybjaerg-Hansen, A | 1 |
| Arias, B; Barrantes-Vidal, N; Catalán, R; Fañanás, L; Guitart, M; Papiol, S; Salgado, P | 1 |
| Assumpção, LV; Correa, LA; Granja, F; Morari, EC; Morari, J; Ward, LS | 1 |
| Miyoshi, Y; Noguchi, S; Noma, C; Taguchi, T; Tamaki, Y | 1 |
| Atala, A; Bauer, SB; Deng, FM; Ehrlich, GD; Feather, SA; Gitlin, J; Goldberg, JD; Goodship, JA; Goodship, TH; Hermanns, M; Hu, FZ; Jiang, S; Jones, KE; Lee, A; Liang, FX; Malcolm, S; Mendelsohn, C; Ostrer, H; Preston, RA; Retik, AB; Schneck, FX; Shapiro, E; Sun, TT; Woolf, AS; Wright, V; Wu, XR; Ye, XY; Yu, J | 1 |
| Habuchi, T; Ichimura, Y; Kato, T; Nishiyama, H; Ogawa, O; Oyama, C; Sato, K; Tsuchiya, N; Wang, L | 1 |
| Nakabayashi, A; Ogata, T; Sasagawa, I; Sueoka, K; Watanabe, M; Yoshimura, Y | 1 |
| Allio, G; Bellegou, C; Bou, J; Campion, D; D'Amato, T; Delamillieure, P; Demily, C; Dollfus, S; Fouldrin, G; Frébourg, T; Haouzir, S; Hecketsweiler, B; Houy, E; Jacquet, H; Lerond, J; Ménard, JF; Petit, M; Raux, G; Thibaut, F; Tillaux, A | 1 |
| Aoyagi, Y; Fujisawa, H; Kodama, Y; Kominami, R; Maruyama, M; Mishima, Y; Niwa, O; Obata, M; Schaffner, W; Tamura, Y; Yoshikai, Y | 1 |
| Andel, M; Cerná, M; Cimburová, M; Kolostová, K; Kubena, A; Novota, P; Pintérová, D; Romzová, M | 1 |
| Duan, LH; Guo, W; Kang, S; Li, Y; Wang, N; Zhang, JH | 1 |
| Gao, J; Hu, Z; Lu, F; Luo, S; Zeng, W; Zhao, Y; Zhuo, Y | 1 |
| Fujimoto, M; Fukami, M; Hasegawa, T; Koitabashi, Y; Ogata, T; Soneda, S | 1 |
| Yasuda, K | 1 |
| Charles, MA; Charpentier, G; Clément, K; Froguel, P; Ghoussaini, M; Lobbens, S; Meyre, D; Tauber, M; Weill, J | 1 |
| Chang-Claude, J; Wang-Gohrke, S | 1 |
| Brismar, K; Ding, B; Efendic, S; Gu, HF; Kärvestedt, L; Nordman, S; Ostenson, CG | 1 |
| Blakemore, AI; El Nahas, AM; Khalil, MS | 1 |
| Alvarez, V; Batalla, A; Coto, E; García-Castro, M; González, P; Lozano, I; Montes, M; Ordóñez, AG; Palop, RL; Reguero, JR | 1 |
| Axelsson, CK; Bojesen, SE; Nordestgaard, BG; Tybjaerg-Hansen, A | 1 |
| Bhattacharya, P; Sengupta, S | 2 |
| Coutlée, F; Duarte-Franco, E; Forest, P; Franco, EL; Ghosh, A; Koushik, A; Matlashewski, G; Voyer, H | 1 |
| Arnold, ML; Brandt, T; Grond-Ginsbach, C; Hausser, I | 1 |
| Blaakaer, J; Bojesen, SE; Høgdall, CK; Høgdall, EV; Kjaer, SK; Nordestgaard, BG; Thomsen, BL; Tybjaerg-Hansen, A | 1 |
| Ambrosone, CB; Chang-Claude, J; Haase, W; Helmbold, I; Kropp, S; Popanda, O; Sautter-Bihl, ML; Schmezer, P; Tan, XL; von Fournier, D; Wenz, F | 1 |
| Aasly, JO; Farrer, MJ; Pielsticker, L; Ross, OA; Toft, M | 1 |
| Borg, A; Dziadziuszko, R; Jassem, E; Jassem, J; Kobierska-Gulida, G; Limon, J; Rzyman, W; Szymanowska, A | 1 |
| Chen, Y; Jiang, D; Sun, X; Wan, B; Yu, L | 1 |
| Abate, N; Babu, HN; Chandalia, M; Deepa, R; Ghosh, S; Grundy, SM; Majumder, PP; Mohan, V; Radha, V; Rao, SM; Satija, P; Vimaleswaran, KS | 1 |
| Xie, J; Yu, Y; Zhang, A; Zhang, J; Zhang, M | 1 |
| Beutler, B; Dahiyat, BI; Du, X; Hoebe, K; Mann, N; Rutschmann, S; Steed, P; Zalevsky, J | 1 |
| Adamiec, R; Bednarska-Chabowska, D; Dobosz, T; Gacka, M; Szymaniec, S | 1 |
| Aiso, S; Kanekura, K; Matsuoka, M; Nishimoto, I | 1 |
| Caplan, L; Danilov, SM; Klockgether, T; Linnebank, M; Semmler, A; Stein, RW | 1 |
| Bar-Shira, A; Mabjeesh, NJ; Matzkin, H; Orr-Urtreger, A | 1 |
| Coulam, CB; Jeyendran, RS; Kay, C | 1 |
| Carvalho, MA; Edelman, L; Friedman, E; Kaufman, B; Laitman, Y; Menachem, TD; Monteiro, AN; Zidan, J | 1 |
| Allen-Auerbach, M; Doostzadeh, J; Langston, JW; Schüle, B; Tetrud, JW | 1 |
| Brandjes, DP; Büller, HR; de Kruif, MD; Florquin, S; Gerdes, VE; Keller, TT; Levi, M; Meijers, JC; van der Poll, T; van der Sluijs, KF; van Gorp, EC | 1 |
| Chung, JH; Lee, BC; Lee, HJ | 1 |
| Alvarez, V; Calatayud, MT; Corao, AI; Coto, E; García-Castro, M; González, P; Lahoz, CH; Martínez, C; Menéndez, M; Peña, J | 1 |
| Alexandre, CO; Damin, AP; Damin, DC; Frazzon, AP; Hermes, V; Roehe, A; Zettler, C | 1 |
| Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J | 1 |
| Chen, S; Deng, X; Ding, X; Dong, H; Li, W; Li, X; Ma, G; Wu, T; Yao, J; Zeng, Y; Zhang, X | 1 |
| Byrski, T; Edler, L; Górski, B; Gronwald, J; Hamann, U; Huzarski, T; Jakubowska, A; Lubinski, J; Menkiszak, J; Scott, RJ | 1 |
| Accardo, A; Bongiovanni, A; Candore, G; Caruso, C; Crivello, A; Di Noto, L; Forte, GI; Giacalone, A; Lio, D; Macaluso, MC; Palmeri, L; Palmeri, S; Raimondi, C; Scola, L; Vaglica, M; Verna, R | 1 |
| Bach-Mortensen, P; Bojesen, SE; Hyldstrup, L; Nordestgaard, BG; Tofteng, CL; Tybjaerg-Hansen, A | 1 |
| Ahn, SY; Ahn, YM; Byun, SH; Doo, HK; Ha, E; Hong, M; Kim, SI; Lee, BC; Leem, KH; Park, HK; Yim, SV; Yin, C | 1 |
| Bugert, P; Pabinger, I; Panzer, S; Skeate, RC; Stamer, K; Vormittag, R; Wahi, MM | 1 |
| Ardovino, M; Bontempo, P; Cioffi, M; Cobellis, L; Colacurci, N; Iannella, I; Molinari, AM; Scaffa, C; Vietri, MT | 1 |
| Cannella, C; Corbo, RM; De Stefano, GF; Pacella, A; Pinto, A; Rickards, O; Scacchi, R | 1 |
| Adeli, K; Bahrami, Y; Ghaemi, A; Khatami, S; Khoshbin, E; Larijani, B; Meshkani, R; Mirkhani, F; Molapour, A; Sadeghi, S; Taghikhani, M | 1 |
| Benz, CC; Bruno, M; Calistri, D; Casadei, S; Eppenberger-Castori, S; Fedele, V; Giannelli, G; Ginzinger, D; Lacalamita, R; Longo, S; Paradiso, A; Pilato, B; Schittulli, F; Scott, G; Seymour, I; Simone, G; Tommasi, S | 1 |
| Curatolo, P; Gagliano, A; Galasso, C; Gloria-Bottini, F; Lalli, C; Refice, F; Rizzo, R; Saccucci, P; Verrotti, A | 1 |
| Ishida, T; Kashima, T; Makino, K; Soemantri, A | 1 |
| Asaka, T; Hirohata, M; Komai, K; Motozaki, Y; Ono, K; Yamada, M | 1 |
| Altshuler, D; Bell, DW; Daly, MB; Freedman, ML; Garber, JE; Godwin, AK; Haber, DA; Haiman, CA; Harris, PL; Haserlat, SM; Henderson, BE; Kim, SH; Le Marchand, L; Niendorf, KB; Olopade, OI; Schiripo, TA; Sgroi, DC; Smith, MR; Wahrer, DC | 1 |
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| Brismar, K; Dahlquist, G; Efendic, S; Falhammar, H; Gu, HF; Ma, J; Möllsten, A; Nordman, S | 1 |
| Amorim, J; Costa, S; Lima-Ramos, V; Lopes, JM; Pacheco-Figueiredo, L; Pardal, F; Reis, RM; Silva, A | 1 |
| Annesi, F; Annesi, G; Carrideo, S; Cirò Candiano, IC; Civitelli, D; Condino, F; De Marco, EV; Messina, D; Morelli, M; Nicoletti, G; Novellino, F; Provenzano, G; Quattrone, A; Rocca, FE; Tarantino, P | 1 |
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| Bird, TD; Griffith, A; Leis, BC; Leverenz, JB; Mata, IF; Roberts, JW; Samii, A; Schellenberg, GD; Schneer, SH; Sidransky, E; Tsuang, D; Zabetian, CP | 1 |
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| Cuajungco, MP; Samie, MA | 1 |
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| Goto, J; Harada, A; Hase, M; Ikeda, K; Kanematsu, M; Miyauchi, A; Okuizumi, H; Takagi, Y; Takai, H; Yamada, Y | 1 |
| Buys, CH; Hayes, VM; Hofstra, RM; Hollema, H; van der Zee, AG | 1 |
| Brown, MG; Du, Y; Scalzo, AA; Stoll, J; Yokoyama, WM; Zhang, J | 1 |
| Giannoudis, A; Graham, DA; Herrington, CS; Southern, SA | 1 |
| Keshava, C; McCanlies, EC; Sharp, DS; Sun, Y; Weston, A | 1 |
| Baek, WK; Cha, SD; Cho, CH; Cho, JW; Lee, TS; Shin, DH; Suh, MH; Suh, SI | 1 |
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| Yamada, Y | 1 |
| Dokianakis, DN; Papadakis, EN; Spandidos, DA | 1 |
| Beilby, JP; Chapman, CM; Hung, J; McQuillan, BM; Swarbrick, MM; Thompson, PL | 1 |
| Baker, DW; Bradley, JF; Huelsman, KM; Rothberg, PG | 1 |
| Christiani, DC; Fan, R; Liu, G; Lynch, TJ; Miller, DP; Su, L; Thurston, SW; Wain, JC; Xu, LL; Zhou, W | 1 |
| Brice, A; Campion, D; Durr, A; Frebourg, T; Hahn, V; Jacquemont, ML; Tallaksen, C | 1 |
| He, Z; Lin, D; Xing, D; Zhang, L | 1 |
15 review(s) available for proline and Genetic Predisposition
| Article | Year |
|---|---|
Topics: 3T3-L1 Cells; A Kinase Anchor Proteins; Acetates; Achilles Tendon; Acute Kidney Injury; Acute Pain; Acyclic Monoterpenes; Adenine Nucleotides; Adhesins, Escherichia coli; Adipocytes; Adipocytes, Brown; Adipogenesis; Administration, Inhalation; Administration, Oral; Adrenal Cortex Hormones; Adsorption; Adult; Aeromonas hydrophila; Africa; Aged; Aged, 80 and over; Agrobacterium tumefaciens; Air; Air Pollutants; Air Pollution; Air Pollution, Indoor; Algorithms; Alkaloids; Alkynes; Allosteric Regulation; Amines; Amino Acid Sequence; Amino Acids; Amino Acids, Branched-Chain; Aminoisobutyric Acids; Aminopyridines; Amyotrophic Lateral Sclerosis; Anaerobic Threshold; Angiography; Angiotensin II Type 1 Receptor Blockers; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Animal Distribution; Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Ankle Joint; Anti-Bacterial Agents; Anti-HIV Agents; Anti-Inflammatory Agents; Antibodies, Bacterial; Antifungal Agents; Antimalarials; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Antioxidants; Antiretroviral Therapy, Highly Active; Antiviral Agents; Aotidae; Apelin; Apoptosis; Arabidopsis Proteins; Argentina; Arginine; Artemisinins; Arthritis, Experimental; Arthritis, Rheumatoid; Arthroscopy; Aspergillus; Aspergillus niger; Asteraceae; Asthma; ATP Binding Cassette Transporter, Subfamily B, Member 1; ATP Binding Cassette Transporter, Subfamily G, Member 2; Auditory Cortex; Autoantibodies; Autophagy; Bacteria; Bacterial Infections; Bacterial Proteins; Bacterial Typing Techniques; Base Composition; Base Sequence; Basketball; Beclin-1; Benzhydryl Compounds; Benzimidazoles; Benzo(a)pyrene; Benzofurans; Benzoxazines; Bereavement; beta Catenin; beta-Lactamase Inhibitors; beta-Lactamases; beta-Lactams; Betacoronavirus; Betaine; Binding Sites; Biofilms; Biological Assay; Biological Availability; Biological Evolution; Biomarkers; Biomechanical Phenomena; Biopolymers; Biopsy; Bismuth; Blood Glucose; Blood Platelets; Blood Pressure; Body Composition; Body Weight; Bone Marrow; Bone Marrow Cells; Bone Regeneration; Boron; Botrytis; Brain Ischemia; Brain Neoplasms; Brain-Derived Neurotrophic Factor; Brazil; Breast Neoplasms; Breath Tests; Bronchoalveolar Lavage Fluid; Burkholderia; C-Reactive Protein; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Calcification, Physiologic; Calcium; Calcium Signaling; Calorimetry, Differential Scanning; Cameroon; Camptothecin; Candida; Candida albicans; Capillaries; Carbapenem-Resistant Enterobacteriaceae; Carbapenems; Carbohydrate Conformation; Carbon; Carbon Dioxide; Carbon Isotopes; Carcinoma, Ovarian Epithelial; Cardiac Output; Cardiomyopathy, Hypertrophic; Cardiotonic Agents; Cardiovascular Diseases; Caregivers; Carps; Case-Control Studies; Catalase; Catalysis; Cats; CD4 Lymphocyte Count; Cell Culture Techniques; Cell Differentiation; Cell Line, Tumor; Cell Membrane; Cell Movement; Cell Proliferation; Cell Survival; Cells, Cultured; Cellulose; Centrosome; Ceratopogonidae; Chickens; Child; China; Cholera Toxin; Choline; Cholinesterases; Chromatography, High Pressure Liquid; Chromatography, Liquid; Chromatography, Micellar Electrokinetic Capillary; Chromatography, Reverse-Phase; Chronic Disease; Cinnamates; Cities; Citrates; Climate Change; Clinical Trials, Phase III as Topic; Coal; Coal Mining; Cohort Studies; Coinfection; Colchicine; Colony Count, Microbial; Colorectal Neoplasms; Coloring Agents; Common Cold; Complement Factor H; Computational Biology; Computer Simulation; Continuous Positive Airway Pressure; Contrast Media; Coordination Complexes; Coronary Artery Bypass; Coronavirus 3C Proteases; Coronavirus Infections; Coronavirus Protease Inhibitors; Corynebacterium glutamicum; Cosmetics; COVID-19; Creatinine; Cross-Sectional Studies; Crotonates; Crystallography, X-Ray; Cues; Culicidae; Culture Media; Curcuma; Cyclopentanes; Cyclopropanes; Cymbopogon; Cystine; Cytochrome P-450 CYP2B6; Cytochrome P-450 CYP2C19; Cytochrome P-450 CYP2C19 Inhibitors; Cytokines; Databases, Genetic; Death; Dendritic Cells; Density Functional Theory; Depsides; Diabetes Mellitus, Type 2; Diamond; Diarylheptanoids; Dibenzofurans; Dibenzofurans, Polychlorinated; Diclofenac; Diet; Dietary Carbohydrates; Dietary Supplements; Diffusion Magnetic Resonance Imaging; Dioxins; Diphenylamine; Disease Outbreaks; Disease Susceptibility; Disulfides; Dithiothreitol; Dizocilpine Maleate; DNA Methylation; DNA-Binding Proteins; DNA, Bacterial; Dogs; Dose-Response Relationship, Drug; Double-Blind Method; Doublecortin Protein; Drosophila melanogaster; Droughts; Drug Carriers; Drug Combinations; Drug Delivery Systems; Drug Liberation; Drug Resistance; Drug Resistance, Bacterial; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Dust; Dynactin Complex; Dysferlin; Echo-Planar Imaging; Echocardiography; Edaravone; Egypt; Elasticity; Electrodes; Electrolytes; Emodin; Emtricitabine; Endometriosis; Endothelium, Vascular; Endotoxins; Energy Metabolism; Energy Transfer; Enterobacteriaceae; Enterococcus faecalis; Enterotoxigenic Escherichia coli; Environmental Monitoring; Enzyme Inhibitors; Epidemiologic Factors; Epigenesis, Genetic; Erythrocytes; Escherichia coli; Escherichia coli Infections; Escherichia coli Vaccines; Esophageal Neoplasms; Esophagectomy; Esophagogastric Junction; Esterases; Esterification; Ethanol; Ethiopia; Ethnicity; Eucalyptus; Evidence-Based Practice; Exercise; Exercise Tolerance; Extracorporeal Membrane Oxygenation; Family; Fatty Acids; Feedback; Female; Ferric Compounds; Fibrin Fibrinogen Degradation Products; Filtration; Fish Diseases; Flavonoids; Flavonols; Fluorodeoxyglucose F18; Follow-Up Studies; Food Microbiology; Food Preservation; Forests; Fossils; Free Radical Scavengers; Freund's Adjuvant; Fruit; Fungi; Gallium; Gender Identity; Gene Expression Regulation; Gene Expression Regulation, Neoplastic; Gene Expression Regulation, Plant; Gene Knockdown Techniques; Genes, Bacterial; Genes, Plant; Genetic Predisposition to Disease; Genitalia; Genotype; Glomerulonephritis, IGA; Glottis; Glucocorticoids; Glucose; Glucuronides; Glutathione Transferase; Glycogen Synthase Kinase 3 beta; Gram-Negative Bacterial Infections; Gram-Positive Bacterial Infections; Grassland; Guinea Pigs; Half-Life; Head Kidney; Heart Atria; Heart Rate; Heart Septum; HEK293 Cells; Hematopoietic Stem Cells; Hemodynamics; Hep G2 Cells; Hepacivirus; Hepatitis C; Hepatitis C, Chronic; Hepatocytes; Hesperidin; High-Frequency Ventilation; High-Temperature Requirement A Serine Peptidase 1; Hippocampus; Hirudins; History, 20th Century; History, 21st Century; HIV Infections; Homeostasis; Hominidae; Housing, Animal; Humans; Hydrocarbons, Brominated; Hydrogen Bonding; Hydrogen Peroxide; Hydrogen-Ion Concentration; Hydroxybutyrates; Hydroxyl Radical; Hypertension; Hypothyroidism; Image Interpretation, Computer-Assisted; Immunoconjugates; Immunogenic Cell Death; Indoles; Infant, Newborn; Infant, Premature; Infarction, Middle Cerebral Artery; Inflammation; Inflammation Mediators; Infrared Rays; Inhibitory Concentration 50; Injections, Intravenous; Interferon-gamma; Interleukin-23; Interleukin-4; Interleukin-6; Intermediate Filaments; Intermittent Claudication; Intestine, Small; Iridoid Glucosides; Iridoids; Iron; Isomerism; Isotope Labeling; Isoxazoles; Itraconazole; Kelch-Like ECH-Associated Protein 1; Ketoprofen; Kidney Failure, Chronic; Kinetics; Klebsiella pneumoniae; Lactams, Macrocyclic; Lactobacillus; Lactulose; Lakes; Lamivudine; Laparoscopy; Laparotomy; Laryngoscopy; Leucine; Limit of Detection; Linear Models; Lipid A; Lipopolysaccharides; Listeria monocytogenes; Liver; Liver Cirrhosis; Logistic Models; Longitudinal Studies; Losartan; Low Back Pain; Lung; Lupinus; Lupus Erythematosus, Systemic; Machine Learning; Macular Degeneration; Madin Darby Canine Kidney Cells; Magnetic Phenomena; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Magnetics; Malaria, Falciparum; Male; Mannans; MAP Kinase Signaling System; Mass Spectrometry; Melatonin; Membrane Glycoproteins; Membrane Proteins; Meniscectomy; Menisci, Tibial; Mephenytoin; Mesenchymal Stem Cells; Metal Nanoparticles; Metal-Organic Frameworks; Methionine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Nude; Mice, Obese; Mice, Transgenic; Microbial Sensitivity Tests; Microcirculation; MicroRNAs; Microscopy, Video; Microtubules; Microvascular Density; Microwaves; Middle Aged; Minimally Invasive Surgical Procedures; Models, Animal; Models, Biological; Models, Molecular; Models, Theoretical; Molecular Docking Simulation; Molecular Structure; Molecular Weight; Morus; Mouth Floor; Multicenter Studies as Topic; Multiple Sclerosis; Multiple Sclerosis, Relapsing-Remitting; Muscle, Skeletal; Myocardial Ischemia; Myocardium; NAD; NADP; Nanocomposites; Nanoparticles; Naphthols; Nasal Lavage Fluid; Nasal Mucosa; Neisseria meningitidis; Neoadjuvant Therapy; Neoplasm Invasiveness; Neoplasm Recurrence, Local; Neoplasms, Experimental; Neural Stem Cells; Neuroblastoma; Neurofilament Proteins; Neurogenesis; Neurons; New York; NF-E2-Related Factor 2; NF-kappa B; Nicotine; Nitriles; Nitrogen; Nitrogen Fixation; North America; Observer Variation; Occupational Exposure; Ochrobactrum; Oils, Volatile; Olea; Oligosaccharides; Omeprazole; Open Field Test; Optimism; Oregon; Oryzias; Osmolar Concentration; Osteoarthritis; Osteoblasts; Osteogenesis; Ovarian Neoplasms; Ovariectomy; Oxadiazoles; Oxidation-Reduction; Oxidative Stress; Oxygen; Ozone; p38 Mitogen-Activated Protein Kinases; Pakistan; Pandemics; Particle Size; Particulate Matter; Patient-Centered Care; Pelargonium; Peptides; Perception; Peripheral Arterial Disease; Peroxides; Pets; Pharmaceutical Preparations; Pharmacogenetics; Phenobarbital; Phenols; Phenotype; Phosphates; Phosphatidylethanolamines; Phosphines; Phospholipids; Phosphorus; Phosphorylation; Photoacoustic Techniques; Photochemotherapy; Photosensitizing Agents; Phylogeny; Phytoestrogens; Pilot Projects; Plant Components, Aerial; Plant Extracts; Plant Immunity; Plant Leaves; Plant Oils; Plants, Medicinal; Plasmodium berghei; Plasmodium falciparum; Platelet Activation; Platelet Function Tests; Pneumonia, Viral; Poaceae; Pogostemon; Poloxamer; Poly I; Poly(ADP-ribose) Polymerase Inhibitors; Polychlorinated Biphenyls; Polychlorinated Dibenzodioxins; Polycyclic Compounds; Polyethylene Glycols; Polylysine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Population Dynamics; Portasystemic Shunt, Transjugular Intrahepatic; Positron Emission Tomography Computed Tomography; Postoperative Complications; Postprandial Period; Potassium Cyanide; Predictive Value of Tests; Prefrontal Cortex; Pregnancy; Prepulse Inhibition; Prevalence; Procalcitonin; Prodrugs; Prognosis; Progression-Free Survival; Proline; Proof of Concept Study; Prospective Studies; Protein Binding; Protein Conformation; Protein Domains; Protein Folding; Protein Multimerization; Protein Sorting Signals; Protein Structure, Secondary; Proton Pump Inhibitors; Protozoan Proteins; Psychometrics; Pulse Wave Analysis; Pyridines; Pyrrolidines; Quality of Life; Quantum Dots; Quinoxalines; Quorum Sensing; Radiopharmaceuticals; Rain; Random Allocation; Randomized Controlled Trials as Topic; Rats; Rats, Sprague-Dawley; Rats, Wistar; RAW 264.7 Cells; Reactive Oxygen Species; Receptor, Angiotensin, Type 1; Receptor, PAR-1; Receptors, CXCR4; Receptors, Estrogen; Receptors, Glucocorticoid; Receptors, Interleukin-1; Receptors, Interleukin-17; Receptors, Notch; Recombinant Fusion Proteins; Recombinant Proteins; Reducing Agents; Reflex, Startle; Regional Blood Flow; Regression Analysis; Reperfusion Injury; Reproducibility of Results; Republic of Korea; Respiratory Tract Diseases; Retrospective Studies; Reverse Transcriptase Inhibitors; Rhinitis, Allergic; Risk Assessment; Risk Factors; Rituximab; RNA, Messenger; RNA, Ribosomal, 16S; ROC Curve; Rosmarinic Acid; Running; Ruthenium; Rutin; Sarcolemma; Sarcoma; Sarcopenia; Sarcoplasmic Reticulum; SARS-CoV-2; Scavenger Receptors, Class A; Schools; Seasons; Seeds; Sequence Analysis, DNA; Severity of Illness Index; Sex Factors; Shock, Cardiogenic; Short Chain Dehydrogenase-Reductases; Signal Transduction; Silver; Singlet Oxygen; Sinusitis; Skin; Skin Absorption; Small Molecule Libraries; Smoke; Socioeconomic Factors; Soil; Soil Microbiology; Solid Phase Extraction; Solubility; Solvents; Spain; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared; Speech; Speech Perception; Spindle Poles; Spleen; Sporothrix; Staphylococcal Infections; Staphylococcus aureus; Stereoisomerism; Stomach Neoplasms; Stress, Physiological; Stroke Volume; Structure-Activity Relationship; Substrate Specificity; Sulfonamides; Surface Properties; Surface-Active Agents; Surveys and Questionnaires; Survival Rate; T-Lymphocytes, Cytotoxic; Tandem Mass Spectrometry; Temperature; Tenofovir; Terpenes; Tetracycline; Tetrapleura; Textiles; Thermodynamics; Thiobarbituric Acid Reactive Substances; Thrombin; Thyroid Hormones; Thyroid Neoplasms; Tibial Meniscus Injuries; Time Factors; Tissue Distribution; Titanium; Toluidines; Tomography, X-Ray Computed; Tooth; Tramadol; Transcription Factor AP-1; Transcription, Genetic; Transfection; Transgender Persons; Translations; Treatment Outcome; Triglycerides; Ubiquinone; Ubiquitin-Specific Proteases; United Kingdom; United States; Up-Regulation; Vascular Stiffness; Veins; Ventricular Remodeling; Viral Load; Virulence Factors; Virus Replication; Vitis; Voice; Voice Quality; Wastewater; Water; Water Pollutants, Chemical; Water-Electrolyte Balance; Weather; Wildfires; Wnt Signaling Pathway; Wound Healing; X-Ray Diffraction; Xenograft Model Antitumor Assays; Young Adult; Zoogloea | 2022 |
TP53 gene Arg72Pro polymorphism and male infertility risk: A meta-analysis.
Topics: Arginine; Asian People; Genetic Predisposition to Disease; Humans; Infertility, Male; Male; Polymorphism, Single Nucleotide; Proline; Tumor Suppressor Protein p53 | 2018 |
Polymorphisms of ERBB2 and breast cancer risk: a meta-analysis of 26 studies involving 35,088 subjects.
Topics: Adult; Aged; Alanine; Alleles; Asian People; Black People; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Proline; Receptor, ErbB-2; Risk Factors; Valine; White People | 2013 |
Effects of Pro12Ala polymorphism in peroxisome proliferator-activated receptor-γ2 gene on metabolic syndrome risk: a meta-analysis.
Topics: Alanine; Case-Control Studies; Genetic Predisposition to Disease; Humans; Metabolic Syndrome; Polymorphism, Genetic; PPAR gamma; Proline | 2014 |
Meta-analysis of associations between the peroxisome proliferator-activated receptor-γ Pro12Ala polymorphism and susceptibility to nonalcoholic fatty liver disease, rheumatoid arthritis, and psoriatic arthritis.
Topics: Alanine; Arthritis, Psoriatic; Arthritis, Rheumatoid; Genetic Predisposition to Disease; Humans; Non-alcoholic Fatty Liver Disease; Polymorphism, Genetic; PPAR gamma; Proline | 2014 |
Meta-analysis of association between the TP53 Arg72Pro polymorphism and risk of endometriosis based on case-control studies.
Topics: Arginine; Asian People; Case-Control Studies; Endometriosis; Female; Genetic Predisposition to Disease; Humans; Polymorphism, Single Nucleotide; Proline; Tumor Suppressor Protein p53; White People | 2015 |
TP53 Arg72Pro polymorphism (rs1042522) and risk of endometriosis among Asian and Caucasian populations.
Topics: Arginine; Asian People; Endometriosis; Female; Genetic Predisposition to Disease; Humans; Linkage Disequilibrium; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53; White People | 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 |
A meta-analysis of TP53 codon 72 polymorphism and lung cancer risk: evidence from 15,857 subjects.
Topics: Asian People; Codon; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Humans; Lung Neoplasms; Polymorphism, Single Nucleotide; Proline; Smoking; White People | 2009 |
Population description and its role in the interpretation of genetic association.
Topics: Alanine; Diabetes Mellitus, Type 2; Gene Frequency; Genetic Predisposition to Disease; Humans; Patient Selection; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Racial Groups; Reproducibility of Results; Validation Studies as Topic; White People | 2010 |
Meta-analysis shows significant association of the TP53 Arg72Pro with ovarian cancer risk.
Topics: Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Homozygote; Humans; Ovarian Neoplasms; Polymorphism, Single Nucleotide; Proline; Publication Bias; Risk Factors; Tumor Suppressor Protein p53 | 2012 |
Peroxisome proliferator-activated receptor γ polymorphism Pro12Ala Is associated with nephropathy in type 2 diabetes: evidence from meta-analysis of 18 studies.
Topics: Alanine; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Female; Genetic Predisposition to Disease; Genotype; Humans; Insulin Resistance; Kidney Failure, Chronic; Male; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; PPAR gamma; Proline | 2012 |
Meta-analysis of the association between P53 codon 72 polymorphisms and gastric cancer.
Topics: Arginine; Asian People; Codon; Genetic Predisposition to Disease; Genotype; Humans; Odds Ratio; Polymorphism, Single Nucleotide; Proline; Risk Factors; Stomach Neoplasms; Tumor Suppressor Protein p53; White People | 2013 |
[PPARgamma gene Pro12Ala polymorphism in diabetes mellitus].
Topics: Alanine; Alleles; Amino Acid Substitution; Animals; Diabetes Mellitus; Environment; Genetic Predisposition to Disease; Humans; Life Style; Pharmacogenetics; Polymorphism, Single Nucleotide; PPAR gamma; Proline | 2005 |
The varitint-waddler mouse phenotypes and the TRPML3 ion channel mutation: cause and consequence.
Topics: Alanine; Animals; Calcium; Genetic Predisposition to Disease; Genotype; Hair Color; Hearing; Hearing Disorders; Isoleucine; Membrane Potentials; Mice; Mice, Mutant Strains; Models, Molecular; Mutation; Phenotype; Proline; Protein Conformation; Protein Structure, Tertiary; Skin Pigmentation; Threonine; Transient Receptor Potential Channels; TRPM Cation Channels | 2008 |
3 trial(s) available for proline and Genetic Predisposition
| Article | Year |
|---|---|
Topics: 3T3-L1 Cells; A Kinase Anchor Proteins; Acetates; Achilles Tendon; Acute Kidney Injury; Acute Pain; Acyclic Monoterpenes; Adenine Nucleotides; Adhesins, Escherichia coli; Adipocytes; Adipocytes, Brown; Adipogenesis; Administration, Inhalation; Administration, Oral; Adrenal Cortex Hormones; Adsorption; Adult; Aeromonas hydrophila; Africa; Aged; Aged, 80 and over; Agrobacterium tumefaciens; Air; Air Pollutants; Air Pollution; Air Pollution, Indoor; Algorithms; Alkaloids; Alkynes; Allosteric Regulation; Amines; Amino Acid Sequence; Amino Acids; Amino Acids, Branched-Chain; Aminoisobutyric Acids; Aminopyridines; Amyotrophic Lateral Sclerosis; Anaerobic Threshold; Angiography; Angiotensin II Type 1 Receptor Blockers; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Animal Distribution; Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Ankle Joint; Anti-Bacterial Agents; Anti-HIV Agents; Anti-Inflammatory Agents; Antibodies, Bacterial; Antifungal Agents; Antimalarials; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Antioxidants; Antiretroviral Therapy, Highly Active; Antiviral Agents; Aotidae; Apelin; Apoptosis; Arabidopsis Proteins; Argentina; Arginine; Artemisinins; Arthritis, Experimental; Arthritis, Rheumatoid; Arthroscopy; Aspergillus; Aspergillus niger; Asteraceae; Asthma; ATP Binding Cassette Transporter, Subfamily B, Member 1; ATP Binding Cassette Transporter, Subfamily G, Member 2; Auditory Cortex; Autoantibodies; Autophagy; Bacteria; Bacterial Infections; Bacterial Proteins; Bacterial Typing Techniques; Base Composition; Base Sequence; Basketball; Beclin-1; Benzhydryl Compounds; Benzimidazoles; Benzo(a)pyrene; Benzofurans; Benzoxazines; Bereavement; beta Catenin; beta-Lactamase Inhibitors; beta-Lactamases; beta-Lactams; Betacoronavirus; Betaine; Binding Sites; Biofilms; Biological Assay; Biological Availability; Biological Evolution; Biomarkers; Biomechanical Phenomena; Biopolymers; Biopsy; Bismuth; Blood Glucose; Blood Platelets; Blood Pressure; Body Composition; Body Weight; Bone Marrow; Bone Marrow Cells; Bone Regeneration; Boron; Botrytis; Brain Ischemia; Brain Neoplasms; Brain-Derived Neurotrophic Factor; Brazil; Breast Neoplasms; Breath Tests; Bronchoalveolar Lavage Fluid; Burkholderia; C-Reactive Protein; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Calcification, Physiologic; Calcium; Calcium Signaling; Calorimetry, Differential Scanning; Cameroon; Camptothecin; Candida; Candida albicans; Capillaries; Carbapenem-Resistant Enterobacteriaceae; Carbapenems; Carbohydrate Conformation; Carbon; Carbon Dioxide; Carbon Isotopes; Carcinoma, Ovarian Epithelial; Cardiac Output; Cardiomyopathy, Hypertrophic; Cardiotonic Agents; Cardiovascular Diseases; Caregivers; Carps; Case-Control Studies; Catalase; Catalysis; Cats; CD4 Lymphocyte Count; Cell Culture Techniques; Cell Differentiation; Cell Line, Tumor; Cell Membrane; Cell Movement; Cell Proliferation; Cell Survival; Cells, Cultured; Cellulose; Centrosome; Ceratopogonidae; Chickens; Child; China; Cholera Toxin; Choline; Cholinesterases; Chromatography, High Pressure Liquid; Chromatography, Liquid; Chromatography, Micellar Electrokinetic Capillary; Chromatography, Reverse-Phase; Chronic Disease; Cinnamates; Cities; Citrates; Climate Change; Clinical Trials, Phase III as Topic; Coal; Coal Mining; Cohort Studies; Coinfection; Colchicine; Colony Count, Microbial; Colorectal Neoplasms; Coloring Agents; Common Cold; Complement Factor H; Computational Biology; Computer Simulation; Continuous Positive Airway Pressure; Contrast Media; Coordination Complexes; Coronary Artery Bypass; Coronavirus 3C Proteases; Coronavirus Infections; Coronavirus Protease Inhibitors; Corynebacterium glutamicum; Cosmetics; COVID-19; Creatinine; Cross-Sectional Studies; Crotonates; Crystallography, X-Ray; Cues; Culicidae; Culture Media; Curcuma; Cyclopentanes; Cyclopropanes; Cymbopogon; Cystine; Cytochrome P-450 CYP2B6; Cytochrome P-450 CYP2C19; Cytochrome P-450 CYP2C19 Inhibitors; Cytokines; Databases, Genetic; Death; Dendritic Cells; Density Functional Theory; Depsides; Diabetes Mellitus, Type 2; Diamond; Diarylheptanoids; Dibenzofurans; Dibenzofurans, Polychlorinated; Diclofenac; Diet; Dietary Carbohydrates; Dietary Supplements; Diffusion Magnetic Resonance Imaging; Dioxins; Diphenylamine; Disease Outbreaks; Disease Susceptibility; Disulfides; Dithiothreitol; Dizocilpine Maleate; DNA Methylation; DNA-Binding Proteins; DNA, Bacterial; Dogs; Dose-Response Relationship, Drug; Double-Blind Method; Doublecortin Protein; Drosophila melanogaster; Droughts; Drug Carriers; Drug Combinations; Drug Delivery Systems; Drug Liberation; Drug Resistance; Drug Resistance, Bacterial; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Dust; Dynactin Complex; Dysferlin; Echo-Planar Imaging; Echocardiography; Edaravone; Egypt; Elasticity; Electrodes; Electrolytes; Emodin; Emtricitabine; Endometriosis; Endothelium, Vascular; Endotoxins; Energy Metabolism; Energy Transfer; Enterobacteriaceae; Enterococcus faecalis; Enterotoxigenic Escherichia coli; Environmental Monitoring; Enzyme Inhibitors; Epidemiologic Factors; Epigenesis, Genetic; Erythrocytes; Escherichia coli; Escherichia coli Infections; Escherichia coli Vaccines; Esophageal Neoplasms; Esophagectomy; Esophagogastric Junction; Esterases; Esterification; Ethanol; Ethiopia; Ethnicity; Eucalyptus; Evidence-Based Practice; Exercise; Exercise Tolerance; Extracorporeal Membrane Oxygenation; Family; Fatty Acids; Feedback; Female; Ferric Compounds; Fibrin Fibrinogen Degradation Products; Filtration; Fish Diseases; Flavonoids; Flavonols; Fluorodeoxyglucose F18; Follow-Up Studies; Food Microbiology; Food Preservation; Forests; Fossils; Free Radical Scavengers; Freund's Adjuvant; Fruit; Fungi; Gallium; Gender Identity; Gene Expression Regulation; Gene Expression Regulation, Neoplastic; Gene Expression Regulation, Plant; Gene Knockdown Techniques; Genes, Bacterial; Genes, Plant; Genetic Predisposition to Disease; Genitalia; Genotype; Glomerulonephritis, IGA; Glottis; Glucocorticoids; Glucose; Glucuronides; Glutathione Transferase; Glycogen Synthase Kinase 3 beta; Gram-Negative Bacterial Infections; Gram-Positive Bacterial Infections; Grassland; Guinea Pigs; Half-Life; Head Kidney; Heart Atria; Heart Rate; Heart Septum; HEK293 Cells; Hematopoietic Stem Cells; Hemodynamics; Hep G2 Cells; Hepacivirus; Hepatitis C; Hepatitis C, Chronic; Hepatocytes; Hesperidin; High-Frequency Ventilation; High-Temperature Requirement A Serine Peptidase 1; Hippocampus; Hirudins; History, 20th Century; History, 21st Century; HIV Infections; Homeostasis; Hominidae; Housing, Animal; Humans; Hydrocarbons, Brominated; Hydrogen Bonding; Hydrogen Peroxide; Hydrogen-Ion Concentration; Hydroxybutyrates; Hydroxyl Radical; Hypertension; Hypothyroidism; Image Interpretation, Computer-Assisted; Immunoconjugates; Immunogenic Cell Death; Indoles; Infant, Newborn; Infant, Premature; Infarction, Middle Cerebral Artery; Inflammation; Inflammation Mediators; Infrared Rays; Inhibitory Concentration 50; Injections, Intravenous; Interferon-gamma; Interleukin-23; Interleukin-4; Interleukin-6; Intermediate Filaments; Intermittent Claudication; Intestine, Small; Iridoid Glucosides; Iridoids; Iron; Isomerism; Isotope Labeling; Isoxazoles; Itraconazole; Kelch-Like ECH-Associated Protein 1; Ketoprofen; Kidney Failure, Chronic; Kinetics; Klebsiella pneumoniae; Lactams, Macrocyclic; Lactobacillus; Lactulose; Lakes; Lamivudine; Laparoscopy; Laparotomy; Laryngoscopy; Leucine; Limit of Detection; Linear Models; Lipid A; Lipopolysaccharides; Listeria monocytogenes; Liver; Liver Cirrhosis; Logistic Models; Longitudinal Studies; Losartan; Low Back Pain; Lung; Lupinus; Lupus Erythematosus, Systemic; Machine Learning; Macular Degeneration; Madin Darby Canine Kidney Cells; Magnetic Phenomena; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Magnetics; Malaria, Falciparum; Male; Mannans; MAP Kinase Signaling System; Mass Spectrometry; Melatonin; Membrane Glycoproteins; Membrane Proteins; Meniscectomy; Menisci, Tibial; Mephenytoin; Mesenchymal Stem Cells; Metal Nanoparticles; Metal-Organic Frameworks; Methionine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Nude; Mice, Obese; Mice, Transgenic; Microbial Sensitivity Tests; Microcirculation; MicroRNAs; Microscopy, Video; Microtubules; Microvascular Density; Microwaves; Middle Aged; Minimally Invasive Surgical Procedures; Models, Animal; Models, Biological; Models, Molecular; Models, Theoretical; Molecular Docking Simulation; Molecular Structure; Molecular Weight; Morus; Mouth Floor; Multicenter Studies as Topic; Multiple Sclerosis; Multiple Sclerosis, Relapsing-Remitting; Muscle, Skeletal; Myocardial Ischemia; Myocardium; NAD; NADP; Nanocomposites; Nanoparticles; Naphthols; Nasal Lavage Fluid; Nasal Mucosa; Neisseria meningitidis; Neoadjuvant Therapy; Neoplasm Invasiveness; Neoplasm Recurrence, Local; Neoplasms, Experimental; Neural Stem Cells; Neuroblastoma; Neurofilament Proteins; Neurogenesis; Neurons; New York; NF-E2-Related Factor 2; NF-kappa B; Nicotine; Nitriles; Nitrogen; Nitrogen Fixation; North America; Observer Variation; Occupational Exposure; Ochrobactrum; Oils, Volatile; Olea; Oligosaccharides; Omeprazole; Open Field Test; Optimism; Oregon; Oryzias; Osmolar Concentration; Osteoarthritis; Osteoblasts; Osteogenesis; Ovarian Neoplasms; Ovariectomy; Oxadiazoles; Oxidation-Reduction; Oxidative Stress; Oxygen; Ozone; p38 Mitogen-Activated Protein Kinases; Pakistan; Pandemics; Particle Size; Particulate Matter; Patient-Centered Care; Pelargonium; Peptides; Perception; Peripheral Arterial Disease; Peroxides; Pets; Pharmaceutical Preparations; Pharmacogenetics; Phenobarbital; Phenols; Phenotype; Phosphates; Phosphatidylethanolamines; Phosphines; Phospholipids; Phosphorus; Phosphorylation; Photoacoustic Techniques; Photochemotherapy; Photosensitizing Agents; Phylogeny; Phytoestrogens; Pilot Projects; Plant Components, Aerial; Plant Extracts; Plant Immunity; Plant Leaves; Plant Oils; Plants, Medicinal; Plasmodium berghei; Plasmodium falciparum; Platelet Activation; Platelet Function Tests; Pneumonia, Viral; Poaceae; Pogostemon; Poloxamer; Poly I; Poly(ADP-ribose) Polymerase Inhibitors; Polychlorinated Biphenyls; Polychlorinated Dibenzodioxins; Polycyclic Compounds; Polyethylene Glycols; Polylysine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Population Dynamics; Portasystemic Shunt, Transjugular Intrahepatic; Positron Emission Tomography Computed Tomography; Postoperative Complications; Postprandial Period; Potassium Cyanide; Predictive Value of Tests; Prefrontal Cortex; Pregnancy; Prepulse Inhibition; Prevalence; Procalcitonin; Prodrugs; Prognosis; Progression-Free Survival; Proline; Proof of Concept Study; Prospective Studies; Protein Binding; Protein Conformation; Protein Domains; Protein Folding; Protein Multimerization; Protein Sorting Signals; Protein Structure, Secondary; Proton Pump Inhibitors; Protozoan Proteins; Psychometrics; Pulse Wave Analysis; Pyridines; Pyrrolidines; Quality of Life; Quantum Dots; Quinoxalines; Quorum Sensing; Radiopharmaceuticals; Rain; Random Allocation; Randomized Controlled Trials as Topic; Rats; Rats, Sprague-Dawley; Rats, Wistar; RAW 264.7 Cells; Reactive Oxygen Species; Receptor, Angiotensin, Type 1; Receptor, PAR-1; Receptors, CXCR4; Receptors, Estrogen; Receptors, Glucocorticoid; Receptors, Interleukin-1; Receptors, Interleukin-17; Receptors, Notch; Recombinant Fusion Proteins; Recombinant Proteins; Reducing Agents; Reflex, Startle; Regional Blood Flow; Regression Analysis; Reperfusion Injury; Reproducibility of Results; Republic of Korea; Respiratory Tract Diseases; Retrospective Studies; Reverse Transcriptase Inhibitors; Rhinitis, Allergic; Risk Assessment; Risk Factors; Rituximab; RNA, Messenger; RNA, Ribosomal, 16S; ROC Curve; Rosmarinic Acid; Running; Ruthenium; Rutin; Sarcolemma; Sarcoma; Sarcopenia; Sarcoplasmic Reticulum; SARS-CoV-2; Scavenger Receptors, Class A; Schools; Seasons; Seeds; Sequence Analysis, DNA; Severity of Illness Index; Sex Factors; Shock, Cardiogenic; Short Chain Dehydrogenase-Reductases; Signal Transduction; Silver; Singlet Oxygen; Sinusitis; Skin; Skin Absorption; Small Molecule Libraries; Smoke; Socioeconomic Factors; Soil; Soil Microbiology; Solid Phase Extraction; Solubility; Solvents; Spain; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared; Speech; Speech Perception; Spindle Poles; Spleen; Sporothrix; Staphylococcal Infections; Staphylococcus aureus; Stereoisomerism; Stomach Neoplasms; Stress, Physiological; Stroke Volume; Structure-Activity Relationship; Substrate Specificity; Sulfonamides; Surface Properties; Surface-Active Agents; Surveys and Questionnaires; Survival Rate; T-Lymphocytes, Cytotoxic; Tandem Mass Spectrometry; Temperature; Tenofovir; Terpenes; Tetracycline; Tetrapleura; Textiles; Thermodynamics; Thiobarbituric Acid Reactive Substances; Thrombin; Thyroid Hormones; Thyroid Neoplasms; Tibial Meniscus Injuries; Time Factors; Tissue Distribution; Titanium; Toluidines; Tomography, X-Ray Computed; Tooth; Tramadol; Transcription Factor AP-1; Transcription, Genetic; Transfection; Transgender Persons; Translations; Treatment Outcome; Triglycerides; Ubiquinone; Ubiquitin-Specific Proteases; United Kingdom; United States; Up-Regulation; Vascular Stiffness; Veins; Ventricular Remodeling; Viral Load; Virulence Factors; Virus Replication; Vitis; Voice; Voice Quality; Wastewater; Water; Water Pollutants, Chemical; Water-Electrolyte Balance; Weather; Wildfires; Wnt Signaling Pathway; Wound Healing; X-Ray Diffraction; Xenograft Model Antitumor Assays; Young Adult; Zoogloea | 2022 |
Impact of the PPAR-gamma2 Pro12Ala polymorphism and ACE inhibitor therapy on new-onset microalbuminuria in type 2 diabetes: evidence from BENEDICT.
Topics: Adult; Aged; Alanine; Albuminuria; Alleles; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Diabetes Complications; Diabetes Mellitus, Type 2; Double-Blind Method; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Hypertension; Incidence; Italy; Kaplan-Meier Estimate; Male; Middle Aged; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Prospective Studies; Research Design; Risk Factors | 2009 |
Hyperprolinemia is a risk factor for schizoaffective disorder.
Topics: Adult; Analysis of Variance; Antimanic Agents; Bipolar Disorder; Case-Control Studies; Chromosomes, Human, Pair 22; Female; Gene Deletion; Genetic Predisposition to Disease; Humans; Male; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Reference Values; Risk Factors; Schizophrenia; Sex Factors; Statistics, Nonparametric; Valproic Acid | 2005 |
156 other study(ies) available for proline and Genetic Predisposition
| Article | Year |
|---|---|
A Missense Variant in CASKIN1's Proline-Rich Region Segregates with Psychosis in a Three-Generation Family.
Topics: Adaptor Proteins, Signal Transducing; Bipolar Disorder; Genetic Predisposition to Disease; Humans; Nerve Tissue Proteins; Proline; Psychotic Disorders; Schizophrenia | 2023 |
Longitudinal Metabolome-Wide Signals Prior to the Appearance of a First Islet Autoantibody in Children Participating in the TEDDY Study.
Topics: Alanine; Amino Acids, Branched-Chain; Autoantibodies; Child, Preschool; Dehydroascorbic Acid; Diabetes Mellitus, Type 1; Fatty Acids; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamate Decarboxylase; Humans; Infant; Infant, Newborn; Insulin Antibodies; Longitudinal Studies; Male; Metabolome; Methionine; Phosphatidylethanolamines; Prodromal Symptoms; Proline; Risk; Triglycerides | 2020 |
Testicular Involvement is a Hallmark of Apo A-I Leu75Pro Mutation Amyloidosis.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Amyloidosis; Apolipoprotein A-I; Cohort Studies; Databases, Factual; Genetic Predisposition to Disease; Humans; Italy; Leucine; Male; Middle Aged; Mutation, Missense; Proline; Retrospective Studies; Testicular Diseases; Testis; Young Adult | 2020 |
Identification of a novel functional JAK1 S646P mutation in acute lymphoblastic leukemia.
Topics: Adolescent; Adult; Animals; Cell Line, Tumor; Cell Proliferation; Exome Sequencing; Female; Genetic Predisposition to Disease; Humans; Janus Kinase 1; Male; Mice; Mice, Nude; Neoplasm Transplantation; Point Mutation; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Prognosis; Proline; Serine; Signal Transduction; Young Adult | 2017 |
Identification of a novel PSEN1 mutation (Leu232Pro) in a Korean patient with early-onset Alzheimer's disease and a family history of dementia.
Topics: Adult; Alzheimer Disease; Asian People; Atrophy; Codon; Dementia; Exons; Genetic Association Studies; Genetic Predisposition to Disease; Helix-Loop-Helix Motifs; Humans; Leucine; Magnetic Resonance Imaging; Mutation, Missense; Neuroimaging; Parietal Lobe; Presenilin-1; Proline | 2017 |
Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding.
Topics: Adolescent; Blood Platelet Disorders; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; HEK293 Cells; Hemorrhage; Heredity; High-Throughput Nucleotide Sequencing; Humans; Male; Middle Aged; Models, Molecular; Mutation; Pedigree; Phenotype; Platelet Aggregation; Platelet Function Tests; Proline; Protein Multimerization; Protein Structure, Quaternary; Receptors, Purinergic P2Y12; Severity of Illness Index; Structure-Activity Relationship; White People; Young Adult | 2018 |
Autosomal dominant deficiency of the interleukin-17F in recurrent aphthous stomatitis: Possible novel mutation in a new entity.
Topics: Algorithms; Case-Control Studies; Female; Gene Frequency; Genes, Dominant; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Inflammation; Interleukin-17; Iran; Male; Mutation, Missense; Polymerase Chain Reaction; Probability; Proline; Sequence Analysis, DNA; Software; Stomatitis, Aphthous; Threonine | 2018 |
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss.
Topics: Age of Onset; Consanguinity; Deafness; Exome Sequencing; Female; Genetic Heterogeneity; Genetic Predisposition to Disease; Humans; KCNQ Potassium Channels; Leucine; Male; Mutation, Missense; Pedigree; Proline | 2019 |
Arginine homozygosity in codon 72 of p53 correlates with failure to imatinib response in chronic myeloid leukemia.
Topics: Adult; Alleles; Antineoplastic Agents; Arginine; Benzamides; Codon; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Male; Piperazines; Polymorphism, Genetic; Proline; Pyrimidines; Tumor Suppressor Protein p53 | 2013 |
A Pro 12 Ala substitution in the PPARγ2 polymorphism may decrease the number of diseased vessels and the severity of angiographic coronary artery.
Topics: Adult; Aged; Aged, 80 and over; Alanine; Amino Acid Substitution; Biomarkers; Blood Glucose; Case-Control Studies; Chi-Square Distribution; Coronary Angiography; Coronary Artery Disease; Coronary Vessels; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Insulin; Insulin Resistance; Male; Middle Aged; Odds Ratio; Phenotype; Polymorphism, Genetic; PPAR gamma; Predictive Value of Tests; Proline; Risk Factors; Severity of Illness Index | 2013 |
P53 (Pro72Arg) polymorphism associated with the risk of oral squamous cell carcinoma in gutka, niswar and manpuri addicted patients of Pakistan.
Topics: Areca; Arginine; Base Sequence; Carcinoma, Squamous Cell; Cocarcinogenesis; DNA Primers; Genes, p53; Genetic Predisposition to Disease; Humans; Mouth Neoplasms; Pakistan; Polymerase Chain Reaction; Polymorphism, Genetic; Proline | 2013 |
The association between the Pro12Ala variant in the PPARγ2 gene and type 2 diabetes mellitus and obesity in a Chinese population.
Topics: Adult; Alanine; Amino Acid Substitution; Asian People; Blood Glucose; Body Mass Index; China; Diabetes Mellitus, Type 2; Fasting; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin; Male; Middle Aged; Obesity; Odds Ratio; Polymorphism, Genetic; PPAR gamma; Proline | 2013 |
Vitamin D insufficiency and schizophrenia risk: evaluation of hyperprolinemia as a mediator of association.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Fasting; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Models, Statistical; Mutation; Proline; Proline Oxidase; Risk Factors; Schizophrenia; Vitamin D; Vitamin D Deficiency; Young Adult | 2014 |
PPARγ2 Pro12Ala polymorphism was associated with favorable cardiometabolic risk profile in HIV/HCV coinfected patients: a cross-sectional study.
Topics: Adult; Alanine; Amino Acid Substitution; Cardiovascular Diseases; Coinfection; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Hepatitis C; HIV Infections; HIV-1; Humans; Male; Metabolic Diseases; Metabolome; Middle Aged; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Risk Factors | 2014 |
Not so sweet: autoimmune diabetes mellitus on triple therapy for chronic hepatitis C infection.
Topics: Adult; Antiviral Agents; Autoimmune Diseases; Diabetes Mellitus, Type 1; Drug Therapy, Combination; Female; Genetic Predisposition to Disease; Hepatitis C, Chronic; Humans; Interferon-alpha; Interferons; Interleukins; Oligopeptides; Polyethylene Glycols; Polymorphism, Single Nucleotide; Proline; Protease Inhibitors; Ribavirin; Young Adult | 2015 |
Variation in PPARG is associated with longitudinal change in insulin resistance in Mexican Americans at risk for type 2 diabetes.
Topics: Adult; Alanine; Amino Acid Substitution; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Humans; Insulin Resistance; Longitudinal Studies; Male; Mexican Americans; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Young Adult | 2015 |
Role of ITPA and SLC28A2 genes in the prediction of anaemia associated with protease inhibitor plus ribavirin and peginterferon in hepatitis C treatment.
Topics: Adolescent; Adult; Aged; Anemia; Antiviral Agents; Drug Therapy, Combination; Female; Genetic Predisposition to Disease; Hepatitis C, Chronic; Humans; Incidence; Male; Membrane Transport Proteins; Middle Aged; Oligopeptides; Proline; Prospective Studies; Protease Inhibitors; Pyrophosphatases; Ribavirin; Risk Assessment; Young Adult | 2015 |
Association Between the Transforming Growth Factor Beta 1 Gene Polymorphisms and Turkish Patients with Nonsyndromic Cleft Lip With/Without Cleft Palate.
Topics: Amino Acid Substitution; Arginine; Case-Control Studies; Child; Child, Preschool; Cleft Lip; Cleft Palate; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Leucine; Polymorphism, Single Nucleotide; Proline; Transforming Growth Factor beta1; Turkey | 2016 |
Association of Pro12Ala Polymorphism of Peroxisome Proliferator-Activated Receptor gamma 2 (PPARγ2) Gene with Type 2 Diabetes Mellitus in Ethnic Kashmiri Population.
Topics: Adult; Alanine; Asian People; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Polymorphism, Genetic; PPAR gamma; Proline | 2017 |
Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder.
Topics: Adult; Alleles; Bipolar Disorder; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Proline; Schizophrenia; Schizophrenic Psychology | 2016 |
Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Asian People; China; DNA-Binding Proteins; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Leucine; Male; Middle Aged; Mitochondrial Proteins; Mutation; Parkinson Disease; Proline; Risk Factors; Transcription Factors | 2016 |
Cytosolic Accumulation of L-Proline Disrupts GABA-Ergic Transmission through GAD Blockade.
Topics: Animals; Central Nervous System; Cytosol; Disease Models, Animal; Gamma Rhythm; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamate Decarboxylase; Humans; Mice; Proline; Proline Oxidase; Schizophrenia; Vigabatrin | 2016 |
Clusterin and Pycr1 alterations associate with strain and model differences in susceptibility to experimental pancreatitis.
Topics: Amylases; Animals; Ceruletide; Choline; Clusterin; delta-1-Pyrroline-5-Carboxylate Reductase; Disease Models, Animal; Ethionine; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Male; Mice; Mice, Inbred BALB C; Pancreatitis; Proline; Protein Processing, Post-Translational; Proteome; Pyrroline Carboxylate Reductases; Species Specificity | 2017 |
Association between GPX1 Pro189Leu polymorphism and the occurrence of bladder cancer in Morocco.
Topics: Adult; Aged; Alleles; Base Sequence; Case-Control Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Humans; Leucine; Male; Middle Aged; Morocco; Polymorphism, Genetic; Proline; Risk Factors; Urinary Bladder Neoplasms | 2016 |
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 |
Ethnicity determines association of p53Arg72Pro alleles with cervical cancer in China.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Arginine; Base Sequence; Carcinoma; Case-Control Studies; China; Female; Genes, p53; Genetic Linkage; Genetic Predisposition to Disease; Humans; Middle Aged; Molecular Sequence Data; Polymorphism, Single Nucleotide; Proline; Uterine Cervical Neoplasms | 2008 |
p53 codon 72 proline/arginine polymorphism and autoimmune thyroid diseases.
Topics: Adolescent; Adult; Aged; Arginine; Codon; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genotype; Hashimoto Disease; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Thyroiditis, Autoimmune; Tumor Suppressor Protein p53 | 2008 |
A novel LMNA gene mutation Leu162Pro and the associated clinical characteristics in a family with autosomal-dominant emery-dreifuss muscular dystrophy.
Topics: Adult; Age of Onset; Amino Acid Substitution; Chromatin; Chromosome Disorders; DNA Mutational Analysis; Endothelial Cells; Female; Genes, Recessive; Genetic Markers; Genetic Predisposition to Disease; Humans; Lamin Type A; Leucine; Male; Muscle, Skeletal; Muscular Dystrophy, Emery-Dreifuss; Nuclear Envelope; Pedigree; Point Mutation; Proline | 2008 |
Association of the PPARgamma gene polymorphism Pro12Ala with delayed onset of multiple sclerosis.
Topics: Adolescent; Adult; Age of Onset; Aged; Alanine; Case-Control Studies; Community Health Planning; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Multiple Sclerosis; Polymorphism, Genetic; PPAR gamma; Proline; Young Adult | 2009 |
TP53 codon 72 polymorphism in adult soft tissue sarcomas.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Codon; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Sarcoma; Tumor Suppressor Protein p53; Young Adult | 2008 |
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.
Topics: Amino Acid Substitution; Cardiac Myosins; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart; Humans; Leucine; Middle Aged; Muscle Hypotonia; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Myosin Heavy Chains; Phenotype; Proline; Young Adult | 2009 |
Cerebellopontine angle tumor in a patient with a maternally inherited SDHD gene mutation.
Topics: Alleles; Amino Acid Substitution; Base Sequence; Cerebellar Neoplasms; Cerebellopontine Angle; Chromosome Deletion; Codon; Diagnosis, Differential; DNA Mutational Analysis; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Neoplasms, Multiple Primary; Neuroma, Acoustic; Paraganglioma; Proline; Radiography; Radiosurgery; Succinate Dehydrogenase | 2008 |
The neurofilament light chain gene (NEFL) mutation Pro22Ser can be associated with mixed axonal and demyelinating neuropathy.
Topics: Adolescent; Amino Acid Sequence; Amino Acid Substitution; Axons; Charcot-Marie-Tooth Disease; Demyelinating Diseases; DNA Mutational Analysis; Electrodiagnosis; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Male; Mutation; Mutation, Missense; Neural Conduction; Neurofilament Proteins; Peripheral Nerves; Phenotype; Proline; Serine | 2009 |
NAD(P)H:quinone oxidoreductase 1 Pro187Ser polymorphism and expression do not cosegregate with clinico-pathological characteristics of human mammary tumors.
Topics: Breast Neoplasms; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Middle Aged; NAD(P)H Dehydrogenase (Quinone); Polymorphism, Single Nucleotide; Proline; RNA, Messenger; Serine | 2009 |
The proline 12 alanine substitution in the PPARgamma2 gene is associated with increased extent of coronary artery disease in men.
Topics: Age Factors; Aged; Alanine; Alleles; Angiography; Coronary Artery Disease; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin Resistance; Male; Middle Aged; Polymorphism, Genetic; PPAR gamma; Proline; Protein Isoforms; Regression Analysis | 2009 |
Polymorphism of Pro12Ala in the peroxisome proliferator-activated receptor gamma2 gene in Iranian diabetic and obese subjects.
Topics: Alanine; Asian People; Body Mass Index; Case-Control Studies; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Iran; Logistic Models; Male; Obesity; Odds Ratio; Polymorphism, Single Nucleotide; PPAR gamma; Proline; Risk Assessment; Risk Factors | 2009 |
Founder heterozygous P23T CRYGD mutation associated with cerulean (and coralliform) cataract in 2 Saudi families.
Topics: Amino Acid Substitution; Asian People; Base Sequence; Cataract; Child; Child, Preschool; Family; Female; Founder Effect; gamma-Crystallins; Genetic Predisposition to Disease; Haplotypes; Heterozygote; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Proline; Saudi Arabia; Threonine | 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 |
LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Asian People; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Protein Serine-Threonine Kinases; Young Adult | 2009 |
Combined expression of tau and the Harlequin mouse mutation leads to increased mitochondrial dysfunction, tau pathology and neurodegeneration.
Topics: Adenosine Triphosphate; Age Factors; Animals; Apoptosis; Apoptosis Inducing Factor; Brain; Caspase 3; Electron Transport Complex I; Gene Expression Regulation; Genetic Predisposition to Disease; Humans; In Situ Nick-End Labeling; Leucine; Lipid Peroxidation; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Mitochondria; Mitochondrial Diseases; Movement Disorders; Mutation; Nerve Degeneration; Nerve Tissue Proteins; Oxidative Stress; Proline; Proton Pumps; Silver Staining; Statistics, Nonparametric; tau Proteins; Tauopathies | 2011 |
Interaction of maternal peroxisome proliferator-activated receptor gamma2 Pro12Ala polymorphism with fetal sex affects maternal glycemic control during pregnancy.
Topics: Adult; Alanine; Amino Acid Substitution; Blood Glucose; Female; Fetus; Genetic Predisposition to Disease; Humans; Male; Polymorphism, Single Nucleotide; PPAR gamma; Pregnancy; Proline; Sex Characteristics | 2010 |
Inverse correlation of thermal lability and conversion efficiency for five prion protein polymorphic variants.
Topics: Amino Acid Substitution; Animals; Cell-Free System; Deer; Genetic Predisposition to Disease; Genetic Variation; Immunity, Innate; Leucine; Mice; Peptide Fragments; Polymorphism, Genetic; Prion Diseases; Prions; Proline; Protein Conformation; Protein Denaturation; Protein Folding; Protein Stability; Sheep; Temperature | 2010 |
Association of TP53 codon 72 polymorphism with cervical cancer risk in Chinese women.
Topics: Adult; Arginine; Case-Control Studies; Chi-Square Distribution; China; Codon; Cohort Studies; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms | 2010 |
Association of P53 codon 72 polymorphism and ameloblastoma.
Topics: Alleles; Ameloblastoma; Arginine; Codon; Cytosine; Double-Blind Method; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Guanine; Homozygote; Humans; Male; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proline; Sex Factors; Thailand; Tumor Suppressor Protein p53 | 2010 |
Role of TP53 Arg72Pro polymorphism in urinary bladder cancer predisposition and predictive impact of proline related genotype in advanced tumors in an ethnic Kashmiri population.
Topics: Adult; Arginine; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Proline; Risk Factors; Smoking; Tumor Suppressor Protein p53; Urinary Bladder Neoplasms | 2010 |
p53 codon 72 polymorphism in patients with gastric and colorectal cancer in a Korean population.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; Codon; Colon; Colorectal Neoplasms; DNA; Female; Follow-Up Studies; Gastric Mucosa; Genetic Predisposition to Disease; Genotype; Humans; Intestinal Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Proline; Real-Time Polymerase Chain Reaction; Rectum; Republic of Korea; Risk Factors; Stomach; Stomach Neoplasms; Tumor Suppressor Protein p53; Young Adult | 2011 |
PPAR-gamma2 pro12Ala polymorphism is associated with post-challenge abnormalities of glucose homeostasis in children and adolescents with obesity.
Topics: Adolescent; Alanine; Amino Acid Substitution; Child; Cohort Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Glucose; Glucose Metabolism Disorders; Glucose Tolerance Test; Homeostasis; Humans; Male; Obesity; Polymorphism, Single Nucleotide; PPAR gamma; Proline | 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 |
Pro12Ala polymorphism in human peroxisome proliferator activated receptor gamma is associated with hyperlipidaemia in obstructive sleep apnoea hypopnoea syndrome.
Topics: Adult; Alanine; Amino Acid Substitution; Body Mass Index; Case-Control Studies; China; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Hyperlipidemias; Linear Models; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; PPAR gamma; Proline; Severity of Illness Index; Sleep Apnea, Obstructive | 2011 |
TP53 codon 72 polymorphisms in favorable histology Wilms tumors.
Topics: Alleles; Arginine; Bone Neoplasms; Child; Child, Preschool; Codon; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Humans; Infant; Male; Neoplasm Recurrence, Local; Neoplasm Staging; Polymorphism, Single Nucleotide; Proline; Retrospective Studies; Risk Factors; Tumor Suppressor Protein p53; Wilms Tumor | 2012 |
High frequency of Neuropeptide Y Leu7Pro polymorphism in an Iranian population and its association with coronary artery disease.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Coronary Artery Disease; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genetics, Population; Humans; Iran; Leucine; Male; Middle Aged; Neuropeptide Y; Polymorphism, Single Nucleotide; Prevalence; Proline; Young Adult | 2012 |
Genetic factors and hepatitis C virus infection.
Topics: Antiviral Agents; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Hepatitis C, Chronic; Humans; Interferon-alpha; Interferons; Interleukins; Oligopeptides; Polyethylene Glycols; Polymorphism, Single Nucleotide; Predictive Value of Tests; Proline; Recombinant Proteins; Ribavirin; Risk Factors; Treatment Outcome | 2012 |
Genetic association between obstructive bronchitis and enzymes of oxidative stress.
Topics: Adult; Arginine; Aryldialkylphosphatase; Bronchitis; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Cohort Studies; Epoxide Hydrolases; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Germany; Histidine; Humans; Leucine; Lung Diseases, Obstructive; Male; Methionine; NAD(P)H Dehydrogenase (Quinone); Oxidative Stress; Polymorphism, Single Nucleotide; Pregnancy; Pregnancy Complications; Prenatal Exposure Delayed Effects; Proline; Prospective Studies; Risk Factors; Serine; Smoking; Valine | 2012 |
Role of p53 codon 72 polymorphism in chromosomal aberrations and mitotic index in patients with chronic hepatitis B.
Topics: Adult; Arginine; Case-Control Studies; Chromosome Aberrations; Codon; Female; Genetic Predisposition to Disease; Genotype; Hepatitis B, Chronic; Humans; Male; Mitotic Index; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53 | 2012 |
Familial cortical myoclonus with a mutation in NOL3.
Topics: Adolescent; Adult; Age of Onset; Animals; Apoptosis Regulatory Proteins; Canada; Cell Line, Transformed; Chromosome Mapping; Chromosomes, Human, Pair 16; Electroencephalography; Family Health; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mice; Middle Aged; Muscle Proteins; Mutation; Myoclonus; Phenotype; Proline; Transfection | 2012 |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
Topics: Adult; Age of Onset; Alanine; Case-Control Studies; DNA-Binding Proteins; Europe; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; HLA-B8 Antigen; Humans; Male; Meta-Analysis as Topic; Myasthenia Gravis; Polymorphism, Single Nucleotide; Proline; White People; Young Adult | 2012 |
The Pro/Pro genotype at TP53 codon 72 polymorphism is associated with early onset glioblastoma.
Topics: Adult; Age of Onset; Codon; Genetic Predisposition to Disease; Genotype; Glioblastoma; Humans; Polymorphism, Single Nucleotide; Proline; Young Adult | 2012 |
Polymorphism Arg72Pro of p53 confers susceptibility to squamous cell carcinoma of lungs in a North Indian population.
Topics: Aged; Amino Acid Substitution; Arginine; Asian People; Carcinoma, Squamous Cell; Case-Control Studies; Female; Genes, p53; Genetic Predisposition to Disease; Genetics, Population; Genotype; Humans; India; Lung Neoplasms; Male; Middle Aged; Polymorphism, Single Nucleotide; Proline | 2013 |
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
Topics: Adolescent; Adult; Amino Acid Sequence; Case-Control Studies; DNA Mutational Analysis; Electromyography; Genetic Predisposition to Disease; Humans; Leucine; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense; Myasthenia Gravis; Phenylalanine; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Proline; Receptors, Nicotinic | 2002 |
Comment: studies of the Pro12Ala polymorphism of the PPAR-gamma gene in the Danish MONICA cohort: homozygosity of the Ala allele confers a decreased risk of the insulin resistance syndrome.
Topics: Adult; Aged; Alanine; Cohort Studies; Denmark; Disease Susceptibility; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Male; Metabolic Syndrome; Middle Aged; Phenotype; Polymorphism, Single Nucleotide; Proline; Receptors, Cytoplasmic and Nuclear; Risk Factors; Transcription Factors | 2002 |
[Polymorphism in codon 72 of the p53 gene and cervico-uterine cancer risk in Mexico].
Topics: Adult; Arginine; Case-Control Studies; Codon; DNA Mutational Analysis; DNA-Binding Proteins; Exons; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Mexico; Oncogene Proteins, Viral; Papillomaviridae; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Repressor Proteins; Risk Factors; Substrate Specificity; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms | 2002 |
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.
Topics: Alanine; Case-Control Studies; Chromosomes, Human, Pair 2; Colorectal Neoplasms, Hereditary Nonpolyposis; Crystallography, X-Ray; DNA-Binding Proteins; Female; Founder Effect; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Heterozygote; Humans; Israel; Jews; Male; Microsatellite Repeats; Mutation, Missense; MutS Homolog 2 Protein; Neoplasms; Pedigree; Point Mutation; Polymorphism, Genetic; Proline; Protein Conformation; Proto-Oncogene Proteins | 2002 |
The transcobalamin codon 259 polymorphism influences the risk of human spontaneous abortion.
Topics: Abortion, Spontaneous; Alleles; Arginine; Codon; Female; Gene Frequency; Genetic Predisposition to Disease; Gestational Age; Homozygote; Humans; Polymorphism, Genetic; Pregnancy; Proline; Transcobalamins | 2002 |
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.
Topics: Adenine Nucleotide Translocator 1; Adult; Biopsy; Bipolar Disorder; Blotting, Western; Electron Transport Complex IV; Female; Genes, Dominant; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Leucine; Molecular Sequence Data; Muscle, Skeletal; Mutation, Missense; Myosins; Ophthalmoplegia; Pedigree; Proline | 2003 |
No association between the TGF-beta 1 Leu10Pro polymorphism and osteoporosis among white women in the United States.
Topics: Aged; Amino Acid Sequence; Bone Density; Cohort Studies; Female; Fractures, Bone; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Multivariate Analysis; Osteoporosis; Polymorphism, Genetic; Proline; Proportional Hazards Models; Risk Factors; Transforming Growth Factor beta; Transforming Growth Factor beta1; United States; White People | 2003 |
The transcobalamin codon 259 polymorphism should be designated 776C>G, not 775G>C.
Topics: Adult; Aged; Arginine; Codon; Deoxyribonucleases, Type II Site-Specific; Genetic Predisposition to Disease; Humans; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Terminology as Topic; Transcobalamins; Vitamin B 12 Deficiency | 2003 |
Role of glutathione peroxidase 1 in breast cancer: loss of heterozygosity and allelic differences in the response to selenium.
Topics: Adenocarcinoma; Alanine; Alleles; Amino Acid Substitution; Breast Neoplasms; Codon; DNA, Neoplasm; Enzyme Induction; Gene Expression Regulation, Neoplastic; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Leucine; Loss of Heterozygosity; Neoplasm Proteins; Polymorphism, Genetic; Proline; Recombinant Fusion Proteins; Repetitive Sequences, Amino Acid; Selenium; Structure-Activity Relationship; Tumor Cells, Cultured | 2003 |
Enhanced endothelium-dependent vasodilation in subjects with Proline7 substitution in the signal peptide of neuropeptide Y.
Topics: Adult; Age Factors; Aged; Analysis of Variance; Blood Pressure Determination; Brachial Artery; Child; Coronary Disease; Endothelium, Vascular; Female; Genetic Predisposition to Disease; Humans; Hypercholesterolemia; Leucine; Male; Middle Aged; Neuropeptide Y; Polymorphism, Genetic; Probability; Proline; Prospective Studies; Protein Sorting Signals; Reference Values; Risk Factors; Sampling Studies; Statistics, Nonparametric; Vasodilation | 2003 |
The p53 codon 72 genotypes in HPV infection and cervical disease.
Topics: Alleles; Arginine; Codon; DNA, Viral; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53; Uterine Cervical Diseases; Vaginal Smears | 2003 |
A novel single-nucleotide substitution, Leu 467 Pro, in the interferon-gamma receptor 1 gene associated with allergic diseases.
Topics: Adolescent; Adult; Amino Acid Substitution; Asthma; Case-Control Studies; Cells, Cultured; Child; Dermatitis, Atopic; DNA-Binding Proteins; Female; Genetic Linkage; Genetic Predisposition to Disease; Humans; Hypersensitivity; Immunoglobulin E; Interferon gamma Receptor; Interferon-gamma; Interleukin-12; Interleukin-18; Leucine; Male; Neutrophils; Pedigree; Phosphorylation; Point Mutation; Proline; Receptors, Interferon; Rhinitis, Allergic, Perennial; STAT1 Transcription Factor; Trans-Activators | 2003 |
Integrin beta3 Leu33Pro homozygosity and risk of cancer.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Animals; Cytosine; Denmark; Disease Progression; Female; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Genotype; Humans; Incidence; Integrin beta3; Leucine; Male; Middle Aged; Neoplasm Invasiveness; Neoplasms; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Proportional Hazards Models; Prospective Studies; Registries; Risk Assessment; Risk Factors; Thymine | 2003 |
Prospective study of the association between the proline to alanine codon 12 polymorphism in the PPARgamma gene and type 2 diabetes.
Topics: Alanine; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Incidence; Middle Aged; Polymorphism, Genetic; Proline; Prospective Studies; Receptors, Cytoplasmic and Nuclear; Risk Factors; Transcription Factors | 2003 |
Missense mutation of Pro387Leu in protein tyrosine phosphatase-1B (PTP-1B) is not associated with type 2 diabetes in a Chinese Han population.
Topics: Asian People; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Humans; Leucine; Mutation, Missense; Proline; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Protein Tyrosine Phosphatases | 2003 |
The Pro12Ala polymorphism of PPARgamma2 gene and susceptibility to type 2 diabetes mellitus in a Polish population.
Topics: Age of Onset; Alanine; Amino Acid Substitution; Body Mass Index; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Genotype; Glycated Hemoglobin; Humans; Middle Aged; Poland; Polymorphism, Restriction Fragment Length; Proline; Protein Isoforms; Receptors, Cytoplasmic and Nuclear; Reference Values; Transcription Factors; White People | 2003 |
P53 codon 72 polymorphism and risk of gastric cancer in a Chinese population.
Topics: Adult; Aged; Asian People; China; Codon; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Stomach Neoplasms; Tumor Suppressor Protein p53 | 2004 |
A comparison study of gastric cancer risk in patients with duodenal and gastric ulcer: roles of gastric mucosal histology and p53 codon 72 polymorphism.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Codon; Duodenal Ulcer; Gastric Mucosa; Gastritis; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Risk Factors; Stomach Neoplasms; Stomach Ulcer | 2004 |
HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1.
Topics: Adaptor Proteins, Signal Transducing; Amino Acid Substitution; Carrier Proteins; Cell Line, Tumor; Child; Colorectal Neoplasms, Hereditary Nonpolyposis; Female; Genetic Predisposition to Disease; Germ-Line Mutation; HCT116 Cells; Homozygote; Humans; Male; MutL Protein Homolog 1; Neoplasm Proteins; Neurofibromatosis 1; Nuclear Proteins; Proline; Serine | 2004 |
Analysis of polymorphisms at the tumor suppressor gene p53 (TP53) in contributing to the risk for schizophrenia and its associated neurocognitive deficits.
Topics: Adult; Alleles; Arginine; Chi-Square Distribution; Cognition Disorders; DNA Transposable Elements; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Polymorphism, Genetic; Proline; Risk; Schizophrenia; Tumor Suppressor Protein p53 | 2004 |
Proline homozygosity in codon 72 of p53 is a factor of susceptibility for thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adenoma; Adolescent; Adult; Aged; Aged, 80 and over; Carcinogens; Carcinoma, Papillary; Case-Control Studies; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Germ-Line Mutation; Homozygote; Humans; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Thyroid Diseases; Thyroid Neoplasms | 2004 |
Association of p53 genetic polymorphism (Arg72Pro) with estrogen receptor positive breast cancer risk in Japanese women.
Topics: Adult; Aged; Arginine; Breast Neoplasms; Case-Control Studies; Codon; DNA Mutational Analysis; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Japan; Menopause; Middle Aged; Polymorphism, Genetic; Proline; Receptors, Estrogen; Risk Factors | 2004 |
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.
Topics: Alanine; Amino Acid Substitution; Animals; Base Sequence; Case-Control Studies; Chromosome Mapping; Cytosine; Embryo, Mammalian; Exons; Gene Expression; Genetic Predisposition to Disease; Genotype; Guanine; Humans; Introns; Membrane Glycoproteins; Membrane Proteins; Mice; Mice, Inbred BALB C; Molecular Sequence Data; Mutation, Missense; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Proline; Thymine; Uroplakin Ia; Uroplakin Ib; Uroplakin II; Uroplakin III; Urothelium; Vesico-Ureteral Reflux | 2004 |
Increased risk of bladder cancer associated with a glutathione peroxidase 1 codon 198 variant.
Topics: Aged; Alanine; Asian People; Carcinoma, Transitional Cell; Female; Genetic Predisposition to Disease; Genotype; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Humans; Leucine; Logistic Models; Male; Middle Aged; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Superoxide Dismutase; Urinary Bladder Neoplasms; Valine | 2004 |
Association of male infertility with Pro185Ala polymorphism in the aryl hydrocarbon receptor repressor gene: implication for the susceptibility to dioxins.
Topics: Adult; Alanine; Alleles; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Dioxins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Infertility, Male; Male; Middle Aged; Oligospermia; Polymorphism, Genetic; Proline; Receptors, Aryl Hydrocarbon; Repressor Proteins; Trinucleotide Repeats | 2004 |
Predisposition to mouse thymic lymphomas in response to ionizing radiation depends on variant alleles encoding metal-responsive transcription factor-1 (Mtf-1).
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Cell Line, Tumor; Disease Models, Animal; DNA Primers; DNA-Binding Proteins; Genetic Markers; Genetic Predisposition to Disease; Genetic Variation; Immunity, Innate; Lymphoma; Mice; Mice, Inbred BALB C; Neoplasms, Radiation-Induced; Polymorphism, Single Nucleotide; Proline; Serine; Thymus Neoplasms; Transcription Factor MTF-1; Transcription Factors; Transfection | 2005 |
The frequency of alleles of the Pro12Ala polymorphism in PPARgamma2 is different between healthy controls and patients with type 2 diabetes.
Topics: Adult; Aged; Alanine; Alleles; Case-Control Studies; Czech Republic; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Lipids; Male; Middle Aged; Polymorphism, Restriction Fragment Length; PPAR gamma; Proline | 2004 |
[Association of p53 gene polymorphism with susceptibility to ovarian cancer].
Topics: Adult; Arginine; Asian People; China; Codon; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Neoplasm Staging; Ovarian Neoplasms; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Risk Factors | 2004 |
[p53 gene codon 72 polymorphism and susceptibility to keloid in Chinese population].
Topics: Alleles; Arginine; Asian People; China; Codon; Exons; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Keloid; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53 | 2005 |
Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signaling.
Topics: Adolescent; Alanine; Arginine; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Child; Child, Preschool; Congenital Abnormalities; Dioxins; Gene Frequency; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Lysine; Male; Penis; Polymorphism, Genetic; Proline; Receptors, Aryl Hydrocarbon; Repressor Proteins; Signal Transduction | 2005 |
Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population.
Topics: Adolescent; Adult; Alanine; Amino Acid Substitution; Case-Control Studies; Child; Diabetes Mellitus, Type 2; Female; France; Gene Frequency; Genetic Predisposition to Disease; Humans; Insulin; Insulin Resistance; Male; Middle Aged; Obesity; Phenotype; Polymorphism, Single Nucleotide; PPAR gamma; Proline; White People | 2005 |
Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer.
Topics: Case-Control Studies; Codon; Denmark; Female; Gene Expression Regulation, Neoplastic; Gene Frequency; Genetic Predisposition to Disease; Germany; Homozygote; Humans; Incidence; Integrin beta3; Leucine; Neoplasm Invasiveness; Odds Ratio; Ovarian Neoplasms; Polymorphism, Genetic; Proline; Risk Assessment; Risk Factors; Up-Regulation | 2005 |
Leu7Pro polymorphism in the neuropeptide Y (NPY) gene is associated with impaired glucose tolerance and type 2 diabetes in Swedish men.
Topics: Adult; Alleles; Blood Glucose; Body Mass Index; Diabetes Mellitus, Type 2; Fasting; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glucose Intolerance; Heterozygote; Humans; Insulin; Leucine; Male; Middle Aged; Neuropeptide Y; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Sex Characteristics; Sweden | 2005 |
Transforming growth factor-beta1 SNPs: genetic and phenotypic correlations in progressive kidney insufficiency.
Topics: Adult; Aged; Aged, 80 and over; Arginine; Case-Control Studies; Cytosine; Disease Progression; Female; Fibrosis; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glomerulosclerosis, Focal Segmental; Haplotypes; Homozygote; Humans; Immunohistochemistry; Kidney; Kidney Failure, Chronic; Male; Middle Aged; Phenotype; Polymorphism, Single Nucleotide; Proline; Severity of Illness Index; Staining and Labeling; Thymine; Transforming Growth Factor beta; Transforming Growth Factor beta1 | 2005 |
The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction.
Topics: Alleles; Case-Control Studies; Exons; Genetic Predisposition to Disease; Genotype; Humans; Leucine; MADS Domain Proteins; Male; MEF2 Transcription Factors; Middle Aged; Mutation; Myocardial Infarction; Myogenic Regulatory Factors; Polymorphism, Single Nucleotide; Polymorphism, Single-Stranded Conformational; Proline | 2006 |
No association of breast cancer risk with integrin beta3 (ITGB3) Leu33Pro genotype.
Topics: Adult; Aged; Aged, 80 and over; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Integrin beta3; Leucine; Middle Aged; Proline | 2005 |
Lack of evidence that proline homozygosity at codon 72 of p53 and rare arginine allele at codon 31 of p21, jointly mediate cervical cancer susceptibility among Indian women.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Arginine; Cell Cycle Proteins; Codon; Cyclin-Dependent Kinase Inhibitor p21; DNA, Neoplasm; DNA, Viral; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; India; Middle Aged; Papillomaviridae; Papillomavirus Infections; Polymorphism, Restriction Fragment Length; Proline; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms | 2005 |
The p53 codon 72 polymorphism and risk of high-grade cervical intraepithelial neoplasia.
Topics: Adult; Arginine; Canada; Case-Control Studies; Codon; DNA, Neoplasm; Female; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Odds Ratio; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Proline; Risk Factors; Sequence Analysis, DNA; Tumor Suppressor Protein p53; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms | 2005 |
Collagen morphology is not associated with the Ala549Pro polymorphism of the COL1A2 gene.
Topics: Alanine; Collagen; Collagen Type I; DNA Mutational Analysis; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Peptides; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Proline; Skin; Vertebral Artery Dissection | 2005 |
Increased risk of ovarian cancer in integrin beta3 Leu33Pro homozygotes.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Female; Genetic Predisposition to Disease; Homozygote; Humans; Integrin beta3; Leucine; Middle Aged; Odds Ratio; Ovarian Neoplasms; Proline; Risk Factors | 2005 |
Association between TP53 and p21 genetic polymorphisms and acute side effects of radiotherapy in breast cancer patients.
Topics: Arginine; Body Mass Index; Breast Neoplasms; Cyclin-Dependent Kinase Inhibitor p21; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Linkage Disequilibrium; Middle Aged; Polymorphism, Genetic; Proline; Proportional Hazards Models; Radiodermatitis; Radiotherapy; Retrospective Studies; Serine; Tumor Suppressor Protein p53 | 2006 |
Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population.
Topics: Adult; Aged; Aged, 80 and over; Asparagine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Glucosylceramidase; Heterozygote; Humans; Leucine; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Serine | 2006 |
Increased risk of non-small cell lung cancer and frequency of somatic TP53 gene mutations in Pro72 carriers of TP53 Arg72Pro polymorphism.
Topics: Adenocarcinoma; Arginine; Carcinoma, Large Cell; Carcinoma, Non-Small-Cell Lung; Carcinoma, Squamous Cell; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Lung Neoplasms; Male; Middle Aged; Mutation; Polymorphism, Genetic; Proline; Risk Factors; Tumor Suppressor Protein p53 | 2006 |
Presymptomatic genetic diagnosis for consulters from a large Chinese family with juvenile open angle glaucoma.
Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Asian People; Cytoskeletal Proteins; Eye Proteins; Female; Genes, Dominant; Genetic Predisposition to Disease; Glaucoma, Open-Angle; Glycoproteins; Heterozygote; Humans; Leucine; Male; Middle Aged; Mutation; Pedigree; Phenotype; Proline | 2006 |
Role of genetic polymorphism peroxisome proliferator-activated receptor-gamma2 Pro12Ala on ethnic susceptibility to diabetes in South-Asian and Caucasian subjects: Evidence for heterogeneity.
Topics: Absorptiometry, Photon; Adult; Aged; Alanine; Amino Acid Substitution; Asian People; DNA Primers; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Molecular Sequence Data; Polymerase Chain Reaction; Polymorphism, Genetic; PPAR gamma; Proline; Reference Values; White People | 2006 |
The influence of the Pro12Ala mutation of PPARgamma2 receptor gene on beta-cells restoration and insulin resistance in type 2 diabetes with hypertension.
Topics: Alanine; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Hypertension; Insulin Resistance; Insulin-Secreting Cells; Mutation; PPAR gamma; Proline | 2005 |
PanR1, a dominant negative missense allele of the gene encoding TNF-alpha (Tnf), does not impair lymphoid development.
Topics: Alleles; Amino Acid Substitution; Animals; Ethylnitrosourea; Female; Genes, Dominant; Genetic Predisposition to Disease; Germ-Line Mutation; Listeriosis; Male; Membrane Proteins; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Knockout; Mutation, Missense; Peyer's Patches; Proline; Protein Binding; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Solubility; Spleen; Threonine; Tumor Necrosis Factor Decoy Receptors; Tumor Necrosis Factor-alpha | 2006 |
[Influence of polymorphism pro12Ala of PPARgamma gene on endothelium destruction in patients with diabetes mellitus t. 2].
Topics: Adult; Aged; Alanine; Amino Acid Substitution; Blood Pressure; Body Mass Index; Diabetes Mellitus, Type 2; Endothelium; Female; Genetic Predisposition to Disease; Humans; Hypertension; Male; Middle Aged; Polymorphism, Genetic; PPAR gamma; Proline; Transcription Factors | 2005 |
Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8).
Topics: Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Animals; Cell Line, Tumor; Endoplasmic Reticulum; Genetic Linkage; Genetic Predisposition to Disease; Humans; Mice; Proline; Protein Folding; Serine; Solubility; Vesicular Transport Proteins | 2006 |
Hereditary hyper-ACE-emia due to the Pro1199Leu mutation of somatic ACE as a potential pitfall in diagnosis: a first family outside Europe.
Topics: Cytosine; Europe; Female; Genetic Predisposition to Disease; Granuloma; Humans; Leucine; Male; Peptidyl-Dipeptidase A; Point Mutation; Proline; Thymine | 2006 |
The homozygous P582S mutation in the oxygen-dependent degradation domain of HIF-1 alpha is associated with increased risk for prostate cancer.
Topics: Adult; Aged; Aged, 80 and over; Cell Hypoxia; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Jews; Male; Middle Aged; Oxygen; Point Mutation; Proline; Prostatic Neoplasms; Protein Structure, Tertiary; Risk Factors; Serine | 2007 |
p53 tumour suppressor gene polymorphism is associated with recurrent implantation failure.
Topics: Abortion, Habitual; Adult; Case-Control Studies; Codon; Embryo Implantation; Female; Fertilization in Vitro; Gene Frequency; Genetic Predisposition to Disease; Humans; Polymorphism, Genetic; Pregnancy; Proline; Recurrence; Treatment Failure; Tumor Suppressor Protein p53 | 2006 |
The P1812A and P25T BRCA1 and the 5164del4 BRCA2 mutations: occurrence in high-risk non-Ashkenazi Jews.
Topics: Adult; Aged; Alanine; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; BRCA1 Protein; BRCA2 Protein; Female; Genetic Predisposition to Disease; Humans; Jews; Male; Middle Aged; Molecular Sequence Data; Pedigree; Proline; Sequence Deletion; Threonine | 2006 |
Novel features in a patient homozygous for the L347P mutation in the PINK1 gene.
Topics: Adult; Aged; Aged, 80 and over; Cohort Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Lysine; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Protein Kinases | 2007 |
Effects on coagulation and fibrinolysis induced by influenza in mice with a reduced capacity to generate activated protein C and a deficiency in plasminogen activator inhibitor type 1.
Topics: Animals; Blood Coagulation; Female; Fibrinolysis; Genetic Predisposition to Disease; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Orthomyxoviridae; Orthomyxoviridae Infections; Plasminogen Activator Inhibitor 1; Proline; Protein C; Thrombomodulin; Thrombosis | 2006 |
Peroxisome proliferator-activated receptor-gamma2 Pro12Ala polymorphism is associated with reduced risk for ischemic stroke with type 2 diabetes.
Topics: Aged; Alanine; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Multivariate Analysis; Peroxisome Proliferator-Activated Receptors; Polymorphism, Genetic; Proline; Retrospective Studies; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Stroke | 2006 |
Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Apolipoprotein E4; DNA Mutational Analysis; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; MADS Domain Proteins; Male; MEF2 Transcription Factors; Middle Aged; Myogenic Regulatory Factors; Odds Ratio; Peptides; Polymorphism, Genetic; Proline | 2007 |
Evidence for an association of TP53 codon 72 polymorphism with breast cancer risk.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Arginine; Brazil; Breast Neoplasms; Carcinoma, Ductal; Carcinoma, Lobular; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Risk Factors | 2006 |
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors | 2007 |
A novel P755L mutation in LRRK2 gene associated with Parkinson's disease.
Topics: Adult; Aged; Aged, 80 and over; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Protein Serine-Threonine Kinases; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger | 2006 |
Integrin beta3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk.
Topics: Adult; Aged; Aged, 80 and over; Alleles; BRCA1 Protein; Breast Neoplasms; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Integrin beta3; Leucine; Middle Aged; Ovarian Neoplasms; Polymorphism, Genetic; Proline | 2007 |
Regulatory cytokine gene polymorphisms and risk of colorectal carcinoma.
Topics: Alleles; Amino Acid Substitution; Carcinoma; Case-Control Studies; Colorectal Neoplasms; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Interleukin-10; Italy; Leucine; Male; Polymorphism, Single Nucleotide; Proline; Risk; Transforming Growth Factor beta1 | 2006 |
Integrin beta3 Leu33Pro polymorphism and risk of hip fracture: 25 years follow-up of 9233 adults from the general population.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Bone Density; Denmark; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Hip Fractures; Homozygote; Humans; Integrin beta3; Leucine; Male; Middle Aged; Polymorphism, Genetic; Proline; Prospective Studies; Risk Factors | 2007 |
Peroxisome proliferator-activated receptor-gamma Pro12Ala polymorphism is associated with the susceptibility to ischemic stroke in Taeeumin classified by Sasang medicine.
Topics: Aged; Alanine; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Medicine, East Asian Traditional; Middle Aged; Philosophy, Medical; Polymorphism, Genetic; PPAR gamma; Proline; Stroke | 2007 |
The risk for thromboembolic disease in lupus anticoagulant patients due to pathways involving P-selectin and CD154.
Topics: Adult; CD40 Ligand; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Lupus Coagulation Inhibitor; Male; Membrane Glycoproteins; Middle Aged; Odds Ratio; P-Selectin; Polymorphism, Single Nucleotide; Predictive Value of Tests; Proline; Risk Assessment; Risk Factors; Threonine; Thromboembolism; Thrombosis; Venous Thrombosis | 2007 |
Arg72Pro p53 polymorphism in Italian women: no association with endometriosis.
Topics: Adolescent; Adult; Arginine; Endometriosis; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Italy; Middle Aged; Polymorphism, Genetic; Proline | 2007 |
An analysis of peroxisome proliferator-activated receptor gamma (PPAR-gamma 2) Pro12Ala polymorphism distribution and prevalence of type 2 diabetes mellitus (T2DM) in world populations in relation to dietary habits.
Topics: Adult; Aged; Aged, 80 and over; Alanine; Benin; Climate; Diabetes Mellitus, Type 2; Dietary Fats; Ecuador; Environment; Ethiopia; Feeding Behavior; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Italy; Male; Middle Aged; Polymorphism, Genetic; PPAR gamma; Prevalence; Proline | 2007 |
Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-gamma2 (PPARgamma-2) gene is associated with greater insulin sensitivity and decreased risk of type 2 diabetes in an Iranian population.
Topics: Alanine; Base Sequence; Diabetes Mellitus, Type 2; DNA Primers; Genetic Predisposition to Disease; Humans; Insulin Resistance; Iran; Polymorphism, Genetic; PPAR gamma; Proline | 2007 |
655Val and 1170Pro ERBB2 SNPs in familial breast cancer risk and BRCA1 alterations.
Topics: Adult; Age Distribution; Aged; BRCA1 Protein; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Polymorphism, Single Nucleotide; Proline; Receptor, ErbB-2; Valine | 2007 |
Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation.
Topics: Adolescent; Child; Child, Preschool; Codon; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Intellectual Disability; Male; Odds Ratio; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53 | 2007 |
TP53 codon 72 polymorphism in 12 populations of insular Southeast Asia and Oceania.
Topics: Amino Acid Substitution; Arginine; Asia, Southeastern; Codon; Gene Frequency; Genetic Predisposition to Disease; Humans; Neoplasms; Oceania; Polymorphism, Genetic; Population; Proline; Tumor Suppressor Protein p53 | 2007 |
Hereditary inclusion body myopathy with a novel mutation in the GNE gene associated with proximal leg weakness and necrotizing myopathy.
Topics: Adult; Creatine Kinase; Genetic Predisposition to Disease; Histidine; Humans; Leg; Male; Multienzyme Complexes; Mutation; Myelitis, Transverse; Myositis, Inclusion Body; Proline | 2007 |
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.
Topics: Adult; Age of Onset; Aged; Asian People; Black or African American; Breast Neoplasms; Case-Control Studies; Checkpoint Kinase 2; DNA Mutational Analysis; DNA, Complementary; Female; Gene Frequency; Genetic Predisposition to Disease; Germ-Line Mutation; Hawaii; Hispanic or Latino; Histidine; Humans; Isoleucine; Leucine; Male; Middle Aged; Mutation; Mutation, Missense; Predictive Value of Tests; Proline; Prostatic Neoplasms; Protein Serine-Threonine Kinases; Risk Assessment; Risk Factors; Threonine; Tyrosine; United States; White People | 2007 |
Predisposition to HPV16/18-related cervical cancer because of proline homozygosity at codon 72 of p53 among Indian women is influenced by HLA-B*07 and homozygosity of HLA-DQB1*03.
Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; Cohort Studies; Female; Genes, p53; Genetic Predisposition to Disease; HLA-B Antigens; HLA-B7 Antigen; HLA-DQ Antigens; HLA-DQ beta-Chains; Homozygote; Human papillomavirus 16; Humans; India; Logistic Models; Middle Aged; Papillomavirus Infections; Proline; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms | 2007 |
Frequency of TP53 mutations in relation to Arg72Pro genotypes in non small cell lung cancer.
Topics: Aged; Alleles; Arginine; Carcinoma, Non-Small-Cell Lung; Cell Transformation, Neoplastic; Codon; DNA Mutational Analysis; Female; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Lung Neoplasms; Male; Middle Aged; Norway; Polymorphism, Single Nucleotide; Proline; Smoking; Tumor Suppressor Protein p53 | 2007 |
Distribution of neuropeptide Y Leu7Pro polymorphism in patients with type 1 diabetes and diabetic nephropathy among Swedish and American populations.
Topics: Adult; Diabetes Mellitus, Type 1; Diabetic Nephropathies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Neuropeptide Y; Polymorphism, Single Nucleotide; Proline; Sweden; United States | 2007 |
TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
Topics: Adult; Arginine; Brain Neoplasms; Case-Control Studies; Codon; Combined Modality Therapy; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Glioma; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Retrospective Studies; Survival Rate; Treatment Outcome | 2008 |
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
Topics: Aged; Asparagine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glucosylceramidase; Humans; Italy; Leucine; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Serine | 2008 |
FGFR mutations and plagiocephaly.
Topics: Acrocephalosyndactylia; Arginine; Craniofacial Dysostosis; Craniosynostoses; Electrophoresis; Exons; Genetic Predisposition to Disease; Genetic Variation; Humans; Infant; Mutation; Plagiocephaly, Nonsynostotic; Proline; Receptor, Fibroblast Growth Factor, Type 1; Receptor, Fibroblast Growth Factor, Type 2; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor | 2008 |
Leucine 7 to proline 7 polymorphism in the neuropeptide Y gene and changes in serum lipids during a family-based counselling intervention among school-aged children with a family history of CVD.
Topics: Adolescent; Adolescent Nutritional Physiological Phenomena; Alleles; Cardiovascular Diseases; Child; Child Nutritional Physiological Phenomena; Cholesterol, LDL; Female; Finland; Genetic Predisposition to Disease; Genotype; Health Education; Humans; Leucine; Lipids; Male; Neuropeptide Y; Overweight; Polymorphism, Genetic; Proline; Public Health; Risk Factors; Sex Factors; Thinness | 2008 |
Association of missense variants of the PRKC, apoptosis, WT1, regulator (PAWR) gene with schizophrenia.
Topics: 5' Untranslated Regions; Adult; Apoptosis Regulatory Proteins; Arginine; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Methionine; Middle Aged; Mutation, Missense; Polymorphism, Genetic; Proline; Schizophrenia; Sex Factors; Taiwan | 2008 |
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
Topics: Aged; Asparagine; Case-Control Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glucosylceramidase; Humans; Leucine; Lewy Body Disease; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Risk Factors; Serine | 2008 |
Evaluation of the transforming growth factor beta1 codon 25 (Arg-->Pro) polymorphism in alcoholic liver disease.
Topics: Adult; Alcohol Drinking; Arginine; Codon; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Liver Cirrhosis, Alcoholic; Liver Diseases, Alcoholic; Liver Transplantation; Male; Middle Aged; Multivariate Analysis; Polymorphism, Genetic; Proline; Transforming Growth Factor beta1 | 2008 |
Glutathione-S-Transferase M1 and codon 72 p53 polymorphisms in a northwestern Mediterranean population and their relation to lung cancer susceptibility.
Topics: Adenocarcinoma; Adult; Age Factors; Aged; Aged, 80 and over; Alleles; Amino Acid Sequence; Arginine; Carcinoma; Carcinoma, Small Cell; Codon; Female; Gene Deletion; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Proline; Risk Factors; Smoking; Spain | 1996 |
Association of a polymorphism of the transforming growth factor-beta1 gene with genetic susceptibility to osteoporosis in postmenopausal Japanese women.
Topics: Adult; Aged; Amino Acid Substitution; Female; Genetic Predisposition to Disease; Genotype; Humans; Japan; Leucine; Middle Aged; Osteoporosis; Polymorphism, Genetic; Postmenopause; Proline; Protein Sorting Signals; Sequence Analysis, DNA; Transforming Growth Factor beta | 1998 |
Homozygous arginine-72 in wild type p53 and risk of cervical cancer.
Topics: Alleles; Arginine; Cell Transformation, Neoplastic; Female; Genetic Predisposition to Disease; Homozygote; Humans; Neoplasm Staging; Papillomaviridae; Papillomavirus Infections; Proline; Risk Factors; Tumor Suppressor Protein p53; Tumor Virus Infections; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms | 1998 |
Localization on a physical map of the NKC-linked Cmv1 locus between Ly49b and the Prp gene cluster on mouse chromosome 6.
Topics: Animals; Antigens, Ly; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 6; Genes, Overlapping; Genetic Markers; Genetic Predisposition to Disease; Humans; Killer Cells, Natural; Lectins, C-Type; Membrane Glycoproteins; Mice; Mice, Congenic; Mice, Inbred A; Mice, Inbred BALB C; Mice, Inbred C57BL; Multigene Family; Muromegalovirus; NK Cell Lectin-Like Receptor Subfamily A; Peptides; Physical Chromosome Mapping; Proline; Proline-Rich Protein Domains; Receptors, NK Cell Lectin-Like | 1999 |
p53 codon 72 ARG/PRO polymorphism is not related to HPV type or lesion grade in low- and high-grade squamous intra-epithelial lesions and invasive squamous carcinoma of the cervix.
Topics: Arginine; Carcinoma, Squamous Cell; Condylomata Acuminata; Female; Genes, p53; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Oncogene Proteins, Viral; Papillomaviridae; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Risk Factors; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms | 1999 |
DNA sequence variants of p53: cancer and aging.
Topics: Aged; Aged, 80 and over; Aging; Arginine; Codon; Genes, p53; Genetic Predisposition to Disease; Genetic Variation; Genotype; Haplotypes; Humans; Middle Aged; Neoplasms; Odds Ratio; Polymorphism, Genetic; Proline | 1999 |
p53 codon 72 polymorphism and risk of cervical carcinoma in Korean women.
Topics: Alleles; Arginine; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Papillomaviridae; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Risk Factors; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms | 2000 |
Association between alpha-1-antichymotrypsin polymorphism and susceptibility to chronic obstructive pulmonary disease.
Topics: Adult; Alanine; Alleles; alpha 1-Antichymotrypsin; Amino Acid Substitution; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Lung Diseases, Obstructive; Male; Polymorphism, Genetic; Proline; Protein Sorting Signals | 2000 |
Association of a Leu(10)-->Pro polymorphism of the transforming growth factor-beta1 with genetic susceptibility to osteoporosis and spinal osteoarthritis.
Topics: Animals; Bone Density; Disease Susceptibility; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Osteoarthritis; Osteoporosis; Polymorphism, Genetic; Proline; Radius; Transforming Growth Factor beta; Transforming Growth Factor beta1; Treatment Outcome | 2000 |
p53 codon 72 polymorphism as a risk factor in the development of breast cancer.
Topics: Adult; Alleles; Amino Acid Substitution; Arginine; Breast Neoplasms; Codon; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Middle Aged; Neoplasm Staging; Polymorphism, Genetic; Proline; Receptors, Estrogen; Receptors, Progesterone; Tumor Suppressor Protein p53 | 2000 |
A Pro12Ala polymorphism in the human peroxisome proliferator-activated receptor-gamma 2 is associated with combined hyperlipidaemia in obesity.
Topics: Aging; Alanine; Alleles; Amino Acid Substitution; Anthropometry; Australia; Blood Pressure; Cholesterol, HDL; Diabetes Mellitus; Female; Genetic Predisposition to Disease; Genotype; Humans; Hyperlipidemias; Male; Middle Aged; Obesity; Odds Ratio; Polymorphism, Genetic; Proline; Receptors, Cytoplasmic and Nuclear; Sex Characteristics; Smoking; Thinness; Transcription Factors; Triglycerides; White People | 2001 |
Is the P25L a "real" VHL mutation?
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; DNA Mutational Analysis; Female; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Humans; Leucine; Ligases; Male; Point Mutation; Polymorphism, Genetic; Proline; Proteins; Tumor Suppressor Proteins; Ubiquitin-Protein Ligases; von Hippel-Lindau Disease; Von Hippel-Lindau Tumor Suppressor Protein | 2001 |
Differential association of the codon 72 p53 and GSTM1 polymorphisms on histological subtype of non-small cell lung carcinoma.
Topics: Adenocarcinoma; Aged; Alleles; Arginine; Carcinoma, Squamous Cell; Case-Control Studies; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Logistic Models; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Proline | 2001 |
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease.
Topics: Alzheimer Disease; Amino Acid Substitution; Dementia; Genetic Predisposition to Disease; Humans; Leucine; Male; Membrane Proteins; Middle Aged; Mutation; Paraparesis, Spastic; Presenilin-1; Proline | 2002 |
[p53 gene codon 72 polymorphism and susceptibility to esophageal squamous cell carcinoma in a Chinese population].
Topics: Alleles; Arginine; Asian People; Carcinoma, Squamous Cell; Codon; Confidence Intervals; Esophageal Neoplasms; Genetic Predisposition to Disease; Genotype; Humans; Odds Ratio; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53 | 2002 |