leucine and Genetic Predisposition

leucine has been researched along with Genetic Predisposition in 123 studies

Research

Studies (123)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (0.81)	18.2507
2000's	81 (65.85)	29.6817
2010's	37 (30.08)	24.3611
2020's	4 (3.25)	2.80

Authors

Authors	Studies
Adan, R; Alkema, A; Antel, J; Cahn, W; Hebebrand, J; Hinney, A; Libuda, L; Lin, BD; Luykx, JJ; Peters, T; Zinkstok, J	1
Alhan, A; Beysel, S; Bozkurt, E; Cakal, E; Caliskan, M; Eyerci, N; Hepsen, S; Kan, S; Kizilgul, M; Pinarli, FA	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
Bararpour, N; Darrous, L; Froguel, P; Gasser, M; Gilardi, F; Kutalik, Z; Marques-Vidal, P; Porcu, E; Thomas, A; Waeber, G; Yengo, L	1
An, SSA; Bagyinszky, E; Giau, VV; Kim, S; Park, J; Shim, K; Youn, YC	1
Hirschey, MD; Hu, X; Huynh, FK; Johnson, JD; Lin, Z	1
Idrees, H; Mujtaba, G; Naz, S; Ramzan, M; Sobreira, N; Witmer, PD	1
Feng, Y; Geng, X; Jia, W; Jiang, Z; Li, F; Lu, H; Wang, C; Wei, X; Yan, J; Zhang, Y	1
Sun, HM; Wang, ZZ; Zhang, Y	1
Lv, J; You, T; Zhou, L	1
Anfossi, M; Bernardi, L; Bruni, AC; Clodomiro, A; Colao, R; Conidi, ME; Curcio, SA; Di Lorenzo, R; Frangipane, F; Gallo, M; Maletta, R; Mirabelli, M; Puccio, G; Smirne, N; Vasso, F	1
Alexander, D; Alonso, A; Boerwinkle, E; Manolio, TA; Nettleton, JA; Yu, B; Zheng, Y	1
Liu, HL; Liu, LZ; Wu, EP	1
Cakir, OO; Demir, E; Ersoy, N; Incekara, K; Kose, MO; Yilmaz, A	1
Oner, DA; Tastan, H	1
Ehmen, C; Horstmann, RD; Meyer, CG; Owusu-Dabo, E; Reiling, N; Ruge, G; Thye, T	1
Ye, B; Ye, X	1
Cheng, L; Li, JY; Li, NN; Lu, ZJ; Peng, R; Sun, XY; Tan, EK; Wang, L; Zhang, JH	1
Jin, AL; Xie, XR; Yang, YM	1
Abbar, M; Al Bouzidi, A; Ameur, A; Ameziane El Hassani, R; Attaleb, M; Dakka, N; El Mzibri, M; Hadami, K	1
Kang, SJ; Khang, SK; Ki, CS; Kim, DW; Kim, HY; Kim, SH; Koh, SH; Sung, IH	1
Berthold, HK; Giannakidou, E; Gouni-Berthold, I; Krone, W; Mantzoros, CS	1
Gholami, L; Hajilooi, M; Houshmand, B; Mani-Kashani, K; Rafiei, A	1
Armamento-Villareal, R; Bucchieri, S; Camarda, L; Camarda, MR; Di Fede, G; Giri, T; Jain, S; Mumm, S; Napoli, N; Rini, GB; Serber, D; Yarramaneni, J	1
Arné-Bes, MC; Delisle, MB; Figarella-Branger, D; Heitz, F; Levade, T; Pellissier, JF; Richard, P; Uro-Coste, E	1
Bové, A; Cervera, R; de la Red, G; Espinosa, G; Monteagudo, J; Plaza, J; Reverter, JC; Tàssies, D	1
Accili, E; Armstrong, L; Chapman, K; Demos, MK; Farrell, K; Macri, V; Nelson, TN	1
Dornhoffer, J; Hartzell, LD; McKelvey, KD; Van Hemert, RL	1
Caron-Dorval, D; Couture, P; Lemieux, S; Paquet, P; Paradis, AM; Rudkowska, I; Vohl, MC	1
Ataç, FB; Gökmen, Z; Gülcan, H; Ince, DA; Ozbek, N; Sezgin, E; Taneri, A; Tarcan, A; Verdi, H; Yazici, AC	1
Cattepoel, S; Eckert, A; Kuehnle, K; Kulic, L; Nitsch, RM; Pagani, L; Rhein, V; Tracy, J; Wollmer, MA	1
Agarwal, S; Gill, AC; Goldmann, W; Graham, JF; Kirby, L	1
Abbamondi, N; Anfossi, M; Bernardi, L; Bruni, AC; Bugiani, O; Clodomiro, A; Colao, R; Curcio, SA; Di Lorenzo, R; Foncin, JF; Forloni, G; Frangipane, F; Gallo, M; Geracitano, S; Giaccone, G; Leotta, A; Lio, SG; Maletta, R; Milan, G; Mirabelli, M; Muraca, MG; Nee, L; Pappatà, S; Pinessi, L; Postiglione, A; Puccio, G; Rainero, I; Rogaeva, E; Rubino, E; Smirne, N; Sorbi, S; Spillantini, MG; St George Hyslop, P; Terni, B; Tomaino, C	1
Baelde, HJ; Bakker, SJ; Bilo, HJ; Böhringer, S; Bruijn, JA; De Heer, E; Dekker, FW; Grootendorst, DC; Janssen, B; Kleefstra, N; Mooyaart, AL; Navis, G; van Valkengoed, IG; Zutinic, A	1
Chen, B; Li, Y; Qiu, LX; Wang, XL; Wu, JQ; Xu, W; Zhao, WH	1
Chang, PY; Hsia, KT; Huang, SH; Lin, MW; Liu, CJ	1
Einav, Y; Hauschner, H; Koren, A; Mansour, W; Rosenberg, N; Seligsohn, U	1
de Jongh, RT; Dekkers, OM; Kramer, MH; Lips, P; Rijs, KJ; van Schoor, NM; Vandenbroucke, JP	1
Hsiao, HH; Hsu, JF; Lee, CP; Lin, SF; Liu, YC; Tsai, HJ	1
Li, J; Miao, R; Shen, H; Sun, Z; Xu, F	1
Bahman, I; Bhatia, KP; Brüggemann, N; Erogullari, A; Kaiser, FJ; Klein, C; Lohmann, K; Najmabadi, H; Osmanovic, A; Ramirez, A; Schneider, SA; Shafa, MA; Shafiee, K; Winkler, S	1
Bal-dit-Sollier, C; Barthélémy, O; Bellemain-Appaix, A; Beygui, F; Cayla, G; Collet, JP; Drouet, L; Galier, S; Hulot, JS; Montalescot, G; Pena, A; Silvain, J; Vignalou, JB; Weisel, JW	1
Archacki, S; Cui, X; Du, R; Liu, J; Liu, M; Liu, Y; Tang, Z; Wang, QK; Zeng, F; Zhan, T; Zhang, J	1
Biasin, M; Cagliani, R; Caruz, A; Clerici, M; De Luca, M; Forni, D; Lo Caputo, S; Macías, J; Mazzotta, F; Pineda, JA; Saulle, I; Sironi, M	1
Akhlaghi, S; Dehghan-Manshadi, R; Ferns, GA; Forghanifard, MM; Ghayour-Mobarhan, M; Jamialahmadi, K; Masoudi-Kazemabad, A; Mojarrad, M; Moohebati, M	1
Choi, SJ; Ji, JD; Lee, YH; Song, GG	1
Ghaffari, SH; Ghaffarpor, M; Ghlichnia, HA; Kollaee, A; Zamani, M	1
Aggerbeck, LP; Aparicio, T; Bligny, D; Chétiveaux, M; Kasbi-Chadli, F; Krempf, M; Magot, T; Nazih, H; Ouguerram, K; Samson-Bouma, ME; Schmitz, J; Zaïr, Y	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
Bautista, JM; Belohradsky, BH; de Boer, M; Gómez-Gallego, F; Hartwig, NG; Mason, PJ; Petropoulou, T; Roos, D; Stevens, D; van Bruggen, R; van Zwieten, R	1
Beeson, D; Brydson, M; Chauplannaz, G; Colquhoun, D; Croxen, R; Hatton, C; Newsom-Davis, J; Oosterhuis, H; Shelley, C; Vincent, A	1
Aoki, S; Itoh, S; Iwata, T; Katagiri, T; Mukae, S; Nishio, K; Sato, R	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
Boyle, P; English, DR; Giles, GG; Hopper, JL; McCredie, MR; Morris, H; Neufing, P; Severi, G; Southey, MC; Tesoriero, A; Tilley, W	1
Brooks, SA; Fellers, JP; Gill, BS; Huang, L; Li, W; Trick, HN	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
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
Backer, CB; Buyon, JP; Clancy, RM; Kapur, RP; Molad, Y; Yin, X	1
Huang, Z; Sui, Y; Weng, J; Xiu, L; Yan, J	1
Arinami, T; Hamano, K; Iwasaki, N; Matsui, A; Nakahara, S; Nakayama, J; Ohta, M	1
Adler, D; Fick, G; Hughes, RM; Kanji, N; Trpkov, K	1
Habuchi, T; Ichimura, Y; Kato, T; Nishiyama, H; Ogawa, O; Oyama, C; Sato, K; Tsuchiya, N; Wang, L	1
Goebeler, S; Ilveskoski, E; Kajander, O; Karhunen, PJ; Lehtimäki, T; Mikkelsson, J; Penttilä, A; Perola, M; Rontu, R	1
Clarimon, J; Eerola, J; Hellström, O; Singleton, A; Tienari, PJ	1
Inokuchi, A; Kageshita, T; Monji, M; Nakatsura, T; Nishimura, Y; Ono, T; Sawatsubashi, M; Senju, S; Shinohara, M; Yoshitake, Y	1
Colditz, GA; De Vivo, I; Hankinson, SE; Hunter, DJ	1
Barontini, M; Levin, G; Rudaz, MC; Sansó, G	1
Brooks, WS; Gregory, G; Halliday, GM; Kersaitis, C; Kril, JJ; Kwok, JB; Lepar, G; Rahimi, F; Schofield, PR; Shepherd, CE; Song, YJ	1
Kawabe, M; Sakaue, M; Taniguchi, H	1
Chang-Claude, J; Wang-Gohrke, S	1
Brismar, K; Ding, B; Efendic, S; Gu, HF; Kärvestedt, L; Nordman, S; Ostenson, CG	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
Bresso, F; D'Amato, M; Halfvarson, J; Järnerot, G; Pettersson, S; Tysk, C	1
Abrahamsson, PA; Ahlgren, G; Gadaleanu, V; Giwercman, A; Giwercman, YL	1
Baelde, H; Bakker, SJ; Bartram, CR; Brinkkoetter, P; Cerna, M; de Heer, E; Fischer, C; Hammes, HP; Hohenadel, D; Janssen, B; Köppel, H; Mathieson, P; Meyer, J; Nawroth, P; Peters, V; Rind, N; Romzova, M; Rondeau, E; Rychlik, I; Saleem, MA; Sauerhoefer, S; van der Woude, FJ; Yard, BA; Zirie, M; Zschocke, J	1
Frisén, L; Kalbasi, M; Kockum, I; Lagerstedt, K; Nordenskjöld, A; Thai, HT	1
Mitchell, BD; O'Connell, JR; Pollin, TI; Shuldiner, AR; Steinle, NI	1
Blaakaer, J; Bojesen, SE; Høgdall, CK; Høgdall, EV; Kjaer, SK; Nordestgaard, BG; Thomsen, BL; Tybjaerg-Hansen, A	1
Alvarez, L; Arranz, JJ; San Primitivo, F	1
Cao, Y; Chen, S; Chen, Y; Du, Z; Li, L; Lin, Z; Liu, B; Liu, Z; Wu, Y; Xu, A; Zhang, Y	1
Aasly, JO; Farrer, MJ; Pielsticker, L; Ross, OA; Toft, M	1
Bilge, AK; Diz-Kucukkaya, R; Ergen, G; Hancer, VS; Nalcaci, M; Oncul, A; Ozben, B	1
Chen, Y; Jiang, D; Sun, X; Wan, B; Yu, L	1
Almasy, L; Dassori, A; Escamilla, M; Leach, RJ; Lew, DF; Liu, W; Montero, P; Raventos, H; Villegas, R; Walss-Bass, C	1
Anderson, JL; Doucette, SP; Gagnon, F; Scarvelis, DK; Wells, PS	1
Caplan, L; Danilov, SM; Klockgether, T; Linnebank, M; Semmler, A; Stein, RW	1
Anderson, JL; Carson, N; Doucette, SP; Grimwood, RL; Rodger, MA; Wells, PS	1
Alvarez, V; Calatayud, MT; Corao, AI; Coto, E; García-Castro, M; González, P; Lahoz, CH; Martínez, C; Menéndez, M; Peña, 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
Bowden, DW; Freedman, BI; Hicks, PJ; Janssen, B; Langefeld, CD; McDonough, C; Pierson, ED; Rich, SS; Sale, MM; van der Woude, FJ; Xu, J; Yard, BA	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
Adány, R; Bereczky, Z; Katona, E; Muszbek, L; Vokó, Z	1
Anderson, JL; Doucette, SP; Gagnon, F; Scarvelis, D; Shafey, M; Wells, PS	1
Honmyo, R; Ishikawa, M; Kokaze, A; Masuda, Y; Matsunaga, N; Satoh, M; Takashima, Y; Teruya, K; Uchida, Y; Yoshida, M	1
Ivanov, VP; Khoroshaia, IV; Kozhukhov, MA; Panfilov, VI; Polonikov, AV; Solodilova, MA	1
Ghandour, K; Krajewski, KM; Li, J; Nicholson, GA; Radovanovic, D; Shy, ME; Shy, RR	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
Bernat, R; Bronić, A; Ferencak, G; Stavljenić-Rukavina, A; Zadro, R	1
Chaparro, JX; Comstock, JC; Dang, PM; Glynn, NC; Sood, SG	1
Brismar, K; Dahlquist, G; Efendic, S; Falhammar, H; Gu, HF; Ma, J; Möllsten, A; Nordman, S	1
Ampuero, I; García de Yébenes, J; Ros, R	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
Fan, YM; Kivelä, SL; Lehtimäki, T; Salminen, M; Vahlberg, T	1
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
Ahari, SE; Bahar, M; Banoei, MM; Houshmand, M; Kasraie, S; Moin, M; Panahi, MS; Shariati, P	1
Mazzeo, A; Messina, C; Muglia, M; Patitucci, A; Quattrone, A; Rodolico, C; Toscano, A; Vita, G	1
Acharya, M; Banerjee, A; Banerjee, D; Bhattacharjee, A; Mookherjee, S; Ray, A; Ray, K; Sen, A	1
Goto, J; Harada, A; Hase, M; Ikeda, K; Kanematsu, M; Miyauchi, A; Okuizumi, H; Takagi, Y; Takai, H; Yamada, Y	1
Houlston, RS	1
Bhakta, AV; Hwang, CF; Pudlo, WM; Truesdell, GM; Williamson, VM	1
Yamada, Y	1
Baker, DW; Bradley, JF; Huelsman, KM; Rothberg, PG	1
Hashiramoto, M; Iwamoto, K; Kasuga, M; Maeda, E; Mori, H; Okazawa, H	1
Almer, S; Belaiche, J; Binder, V; Cézard, JP; Chamaillard, M; Colombel, JF; Cortot, A; Finkel, Y; Gassull, M; Gower-Rousseau, C; Hugot, JP; Laurent-Puig, P; Lesage, S; Macry, J; Modigliani, R; O'Morain, CA; Sahbatou, M; Thomas, G; Tysk, C; Zouali, H	1
Slow, E	1
Brice, A; Campion, D; Durr, A; Frebourg, T; Hahn, V; Jacquemont, ML; Tallaksen, C	1

Reviews

14 review(s) available for leucine and Genetic Predisposition

Article	Year
Zeitschrift fur Gesundheitswissenschaften = Journal of public health, 2022, Volume: 30, Issue:2 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
A meta-analysis of the relationship of the Parkin p.Val380Leu polymorphism to Parkinson's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2013, Volume: 162B, Issue:3 Topics: Adult; Age of Onset; Aged; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Leucine; Male; Middle Aged; Odds Ratio; Parkinson Disease; Polymorphism, Genetic; Ubiquitin-Protein Ligases; Valine	2013
PON1 Q192R and L55M polymorphisms and organophosphate toxicity risk: a meta-analysis. DNA and cell biology, 2013, Volume: 32, Issue:5 Topics: Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Case-Control Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Methionine; Organophosphate Poisoning; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; White People	2013
Association between the Val34Leu polymorphism in blood coagulation factor XIII-A and intracerebral hemorrhage: a meta-analysis. Genetics and molecular research : GMR, 2016, Jul-25, Volume: 15, Issue:3 Topics: Amino Acid Substitution; Cerebral Hemorrhage; Factor XIIIa; Genetic Predisposition to Disease; Humans; Leucine; Polymorphism, Single Nucleotide; Valine	2016
The CYP1B1 Leu432Val polymorphism contributes to lung cancer risk: evidence from 6501 subjects. Lung cancer (Amsterdam, Netherlands), 2010, Volume: 70, Issue:3 Topics: Adenocarcinoma; Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 CYP1B1; Ethnicity; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Lung Neoplasms; Penetrance; Polymorphism, Genetic; Risk; Smoking; Valine	2010
Meta-analysis on the association of TIRAP S180L variant and tuberculosis susceptibility. Tuberculosis (Edinburgh, Scotland), 2011, Volume: 91, Issue:3 Topics: Black People; Case-Control Studies; Confidence Intervals; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Membrane Glycoproteins; Mutation, Missense; Odds Ratio; Receptors, Interleukin-1; Risk Factors; Serine; Tuberculosis; Tuberculosis, Pulmonary	2011
Association between the valine/leucine247 polymorphism of β2-glycoprotein I and susceptibility to anti-phospholipid syndrome: a meta-analysis. Lupus, 2012, Volume: 21, Issue:8 Topics: Alleles; Antibodies; Antiphospholipid Syndrome; beta 2-Glycoprotein I; Genetic Predisposition to Disease; Humans; Leucine; Polymorphism, Genetic; Thrombosis; Valine	2012
ELAC2/HPC2 polymorphisms, prostate-specific antigen levels, and prostate cancer. Journal of the National Cancer Institute, 2003, Jun-04, Volume: 95, Issue:11 Topics: Aged; Alanine; Case-Control Studies; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Leucine; Linear Models; Logistic Models; Male; Middle Aged; Neoplasm Proteins; Odds Ratio; Polymorphism, Genetic; Prostate-Specific Antigen; Prostatic Neoplasms; Research Design; Risk Assessment; Risk Factors; Serine; Threonine	2003
[Polymorphisms of uncoupling protein-1 gene in type 2 diabetes]. Nihon rinsho. Japanese journal of clinical medicine, 2005, Volume: 63 Suppl 2 Topics: 5' Untranslated Regions; Alleles; Amino Acid Substitution; Animals; Carrier Proteins; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Humans; Ion Channels; Leucine; Membrane Proteins; Methionine; Mitochondrial Proteins; Mutation, Missense; Polymorphism, Genetic; Promoter Regions, Genetic; Uncoupling Protein 1	2005
Factor XIII Val34Leu variant is protective against venous thromboembolism: a HuGE review and meta-analysis. American journal of epidemiology, 2006, Jul-15, Volume: 164, Issue:2 Topics: Amino Acid Substitution; Factor XIII; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Leucine; Point Mutation; Polymorphism, Genetic; Risk Factors; Thromboembolism; Valine; Venous Thrombosis	2006
Factor XIII Val34Leu variant protects against coronary artery disease. A meta-analysis. Thrombosis and haemostasis, 2007, Volume: 97, Issue:3 Topics: Amino Acid Substitution; Bayes Theorem; Coronary Artery Disease; Factor VIII; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Leucine; Male; Odds Ratio; Polymorphism, Genetic; Risk Assessment; Risk Factors; Valine	2007
Factor XIII Val34Leu variant and the risk of myocardial infarction: a meta-analysis. Thrombosis and haemostasis, 2007, Volume: 97, Issue:4 Topics: Adult; Factor XIII; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Myocardial Infarction; Odds Ratio; Risk Assessment; Risk Factors; Valine	2007
CYP1A1 polymorphisms and lung cancer risk: a meta-analysis. Pharmacogenetics, 2000, Volume: 10, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Cytochrome P-450 CYP1A2; Deoxyribonuclease HpaII; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Leucine; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Risk Factors	2000
Identification of a Crohn's disease susceptibility gene. Clinical genetics, 2001, Volume: 60, Issue:3 Topics: Carrier Proteins; Chromosomes, Human, Pair 16; Cloning, Molecular; Crohn Disease; Frameshift Mutation; Genetic Predisposition to Disease; Humans; Intracellular Signaling Peptides and Proteins; Leucine; Models, Biological; Nod2 Signaling Adaptor Protein; Proteins	2001

Trials

2 trial(s) available for leucine and Genetic Predisposition

Article

Year

Zeitschrift fur Gesundheitswissenschaften = Journal of public health, 2022, Volume: 30, Issue:2

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

A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2007, Volume: 22, Issue:4

Topics: Adult; Aged; Alleles; Carnosine; Case-Control Studies; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Dipeptidases; Europe; Female; Genetic Linkage; Genetic Predisposition to Disease; Genotype; Humans; Kidney Failure, Chronic; Leucine; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Trinucleotide Repeats; United States; White People

2007

Other Studies

108 other study(ies) available for leucine and Genetic Predisposition

Article	Year
Assessing causal links between metabolic traits, inflammation and schizophrenia: a univariable and multivariable, bidirectional Mendelian-randomization study. International journal of epidemiology, 2019, 10-01, Volume: 48, Issue:5 Topics: Bayes Theorem; Biomarkers; C-Reactive Protein; Genetic Predisposition to Disease; Humans; Inflammation; Leucine; Lipids; Lipoproteins, VLDL; Mendelian Randomization Analysis; Phenotype; Polymorphism, Single Nucleotide; Risk Factors; Schizophrenia; Triglycerides	2019
HNF1A gene p.I27L is associated with co-existing preeclampsia in gestational diabetes mellitus. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 2020, Volume: 36, Issue:6 Topics: Adult; Amino Acid Substitution; Case-Control Studies; Comorbidity; Diabetes, Gestational; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hepatocyte Nuclear Factor 1-alpha; Humans; Isoleucine; Leucine; Polymorphism, Single Nucleotide; Pre-Eclampsia; Pregnancy; Turkey; Young Adult	2020
Testicular Involvement is a Hallmark of Apo A-I Leu75Pro Mutation Amyloidosis. The Journal of clinical endocrinology and metabolism, 2020, 12-01, Volume: 105, Issue:12 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
Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes. Scientific reports, 2021, 03-18, Volume: 11, Issue:1 Topics: Adult; Aged; Betaine; Biomarkers; Carnitine; Case-Control Studies; Diabetes Mellitus, Type 2; Early Diagnosis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Lysine; Male; Mannose; Mendelian Randomization Analysis; Metabolome; Middle Aged; Valine	2021
Identification of a novel PSEN1 mutation (Leu232Pro) in a Korean patient with early-onset Alzheimer's disease and a family history of dementia. Neurobiology of aging, 2017, Volume: 56 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
Loss of sirtuin 4 leads to elevated glucose- and leucine-stimulated insulin levels and accelerated age-induced insulin resistance in multiple murine genetic backgrounds. Journal of inherited metabolic disease, 2018, Volume: 41, Issue:1 Topics: Age Factors; Animals; Biomarkers; Blood Glucose; Female; Genetic Predisposition to Disease; In Vitro Techniques; Insulin; Insulin Resistance; Leucine; Lipid Metabolism; Lysine; Male; Metabolism, Inborn Errors; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Proteins; Phenotype; Protein Processing, Post-Translational; Sirtuins; Up-Regulation	2018
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss. Gene, 2019, Jul-15, Volume: 705 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
De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome. Journal of diabetes research, 2019, Volume: 2019 Topics: Adenosine Triphosphate; Adult; Aged; Aged, 80 and over; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Family Health; Female; Genetic Predisposition to Disease; Humans; Leucine; Leukocytes, Mononuclear; Magnetic Resonance Imaging; Male; Middle Aged; Mitochondrial Diseases; Mutation; Pedigree; Phenotype; Point Mutation; Reactive Oxygen Species; RNA, Transfer; Sequence Analysis, DNA	2019
Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation. Journal of Alzheimer's disease : JAD, 2013, Volume: 37, Issue:2 Topics: Adult; Age of Onset; Alzheimer Disease; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Membrane Transport Proteins; Memory Disorders; Methionine; Middle Aged; Mitochondrial Precursor Protein Import Complex Proteins; Mutation; Neuropsychological Tests; Polymorphism, Genetic; Presenilin-1	2013
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study. Genetic epidemiology, 2013, Volume: 37, Issue:8 Topics: Acetyltransferases; Alleles; Atherosclerosis; Black or African American; Chromosomes, Human, Pair 2; Chromosomes, Human, Pair 5; Cohort Studies; Fatty Acids, Unsaturated; Female; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study; Heart Failure; Humans; Incidence; Isoleucine; Leucine; Male; Metabolome; Metabolomics; Middle Aged; Polymorphism, Single Nucleotide; Pyrrolidonecarboxylic Acid; Risk Factors	2013
Relation between K469E gene polymorphism of ICAM-1 and recurrence of ACS and cardiovascular mortality. Asian Pacific journal of tropical medicine, 2013, Volume: 6, Issue:11 Topics: Acute Coronary Syndrome; Aged; Alleles; Asian People; Blood Glucose; Blood Pressure; China; Cholesterol, HDL; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Intercellular Adhesion Molecule-1; Leucine; Lipids; Logistic Models; Male; Middle Aged; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors; Risk Reduction Behavior; Secondary Prevention	2013
Association of the BsmI, ApaI, TaqI, Tru9I and FokI Polymorphisms of the Vitamin D Receptor Gene with Nephrolithiasis in the Turkish Population. Urology journal, 2016, Mar-05, Volume: 13, Issue:1 Topics: Adult; Alleles; Deoxyribonucleases, Type II Site-Specific; DNA; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Nephrolithiasis; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Receptors, Calcitriol; Turkey	2016
Association Between the Transforming Growth Factor Beta 1 Gene Polymorphisms and Turkish Patients with Nonsyndromic Cleft Lip With/Without Cleft Palate. Genetic testing and molecular biomarkers, 2016, Volume: 20, Issue:5 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
TLR1 Variant H305L Associated with Protection from Pulmonary Tuberculosis. PloS one, 2016, Volume: 11, Issue:5 Topics: Amino Acid Substitution; Case-Control Studies; Disease Resistance; Gene Frequency; Genes, Recessive; Genetic Association Studies; Genetic Predisposition to Disease; Ghana; Histidine; Humans; Leucine; Polymorphism, Single Nucleotide; Toll-Like Receptor 1; Tuberculosis, Pulmonary	2016
Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171, Issue:8 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
Genetic polymorphisms in extracellular superoxide dismutase Leu53Leu, Arg213Gly, and Ala40Thr and susceptibility to type 2 diabetes mellitus. Genetics and molecular research : GMR, 2016, Dec-02, Volume: 15, Issue:4 Topics: Adult; Alanine; Arginine; Asian People; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Male; Middle Aged; Polymorphism, Single Nucleotide; Regression Analysis; Superoxide Dismutase; Threonine	2016
Association between GPX1 Pro189Leu polymorphism and the occurrence of bladder cancer in Morocco. Cellular and molecular biology (Noisy-le-Grand, France), 2016, Dec-30, Volume: 62, Issue:14 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 novel LMNA gene mutation Leu162Pro and the associated clinical characteristics in a family with autosomal-dominant emery-dreifuss muscular dystrophy. Muscle & nerve, 2008, Volume: 38, Issue:4 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
The Leu72Met polymorphism of the ghrelin gene is associated with a decreased risk for type 2 diabetes. Clinica chimica acta; international journal of clinical chemistry, 2009, Volume: 399, Issue:1-2 Topics: Aged; Atherosclerosis; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Ghrelin; Humans; Leucine; Male; Methionine; Middle Aged; Polymorphism, Genetic; Reference Values; White People	2009
E-selectin and L-selectin polymorphisms in patients with periodontitis. Journal of periodontal research, 2009, Volume: 44, Issue:1 Topics: Adenine; Adolescent; Adult; Aggressive Periodontitis; Alleles; Arginine; Chronic Periodontitis; Cytosine; Dental Plaque; E-Selectin; Female; Genetic Predisposition to Disease; Gingival Hemorrhage; Humans; L-Selectin; Leucine; Male; Middle Aged; Periodontal Attachment Loss; Periodontal Pocket; Periodontitis; Phenylalanine; Polymorphism, Genetic; Serine; Socioeconomic Factors; Thymine; Young Adult	2009
The Val432Leu polymorphism of the CYP1B1 gene is associated with differences in estrogen metabolism and bone density. Bone, 2009, Volume: 44, Issue:3 Topics: Aryl Hydrocarbon Hydroxylases; Bone Density; Cytochrome P-450 CYP1B1; Estrogens; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Middle Aged; Polymorphism, Genetic; Risk Factors; Valine	2009
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation. Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:2 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
Factor XIII-A subunit Val34Leu polymorphism is associated with the risk of thrombosis in patients with antiphospholipid antibodies and high fibrinogen levels. Thrombosis and haemostasis, 2009, Volume: 101, Issue:2 Topics: Adult; Antiphospholipid Syndrome; Case-Control Studies; Factor XIII; Female; Fibrinogen; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Odds Ratio; Polymorphism, Genetic; Protein Subunits; Risk Assessment; Risk Factors; Thrombosis; Up-Regulation; Valine	2009
A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. Movement disorders : official journal of the Movement Disorder Society, 2009, Apr-15, Volume: 24, Issue:5 Topics: Adult; Animals; Cerebellar Diseases; Child, Preschool; CHO Cells; Cricetinae; Cricetulus; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Kv1.1 Potassium Channel; Leucine; Magnetic Resonance Imaging; Male; Membrane Potentials; Mutation; Transfection; Valine	2009
Cerebellopontine angle tumor in a patient with a maternally inherited SDHD gene mutation. The international tinnitus journal, 2008, Volume: 14, Issue:2 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
Effect of the PPAR-Alpha L162V polymorphism on the cardiovascular disease risk factor in response to n-3 polyunsaturated fatty acids. Journal of nutrigenetics and nutrigenomics, 2008, Volume: 1, Issue:4 Topics: Adult; Amino Acid Substitution; Cardiovascular Diseases; Fatty Acids, Omega-3; Fatty Acids, Unsaturated; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Middle Aged; Polymorphism, Single Nucleotide; PPAR alpha; Risk Factors; Valine; Young Adult	2008
Lack of association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor beta1 (915G/T) gene polymorphisms and bronchopulmonary dysplasia: a single-center study. DNA and cell biology, 2010, Volume: 29, Issue:1 Topics: Amino Acid Substitution; Bronchopulmonary Dysplasia; Factor VII; Factor VIII; Female; Genetic Predisposition to Disease; Humans; INDEL Mutation; Infant, Newborn; Leucine; Male; Polymorphism, Genetic; Transforming Growth Factor beta1; Turkey; Valine	2010
Combined expression of tau and the Harlequin mouse mutation leads to increased mitochondrial dysfunction, tau pathology and neurodegeneration. Neurobiology of aging, 2011, Volume: 32, Issue:10 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
Inverse correlation of thermal lability and conversion efficiency for five prion protein polymorphic variants. Biochemistry, 2010, Feb-23, Volume: 49, Issue:7 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
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation. Neurology, 2010, Mar-09, Volume: 74, Issue:10 Topics: Adult; Alzheimer Disease; Brain; Cognition Disorders; Family Health; Female; Fluorodeoxyglucose F18; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Global Health; History, 17th Century; History, 21st Century; Humans; International Cooperation; Italy; Leucine; Male; Memory Disorders; Methionine; Middle Aged; Mutation; Phenotype; Positron-Emission Tomography; Presenilin-1	2010
Association between CNDP1 genotype and diabetic nephropathy is sex specific. Diabetes, 2010, Volume: 59, Issue:6 Topics: Age of Onset; Aged; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Dipeptidases; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Leucine; Male; Middle Aged; Reference Values; Repetitive Sequences, Amino Acid; Sex Characteristics; White People	2010
O6-methylguanine-DNA methyltransferase gene coding region polymorphisms and oral cancer risk. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2010, Volume: 39, Issue:8 Topics: Age Factors; Carcinoma, Squamous Cell; Case-Control Studies; Codon; Cytosine; Disease-Free Survival; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Haplotypes; Humans; Leucine; Linkage Disequilibrium; Male; Middle Aged; Mouth Neoplasms; O(6)-Methylguanine-DNA Methyltransferase; Phenylalanine; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Precancerous Conditions; Retrospective Studies; Risk Factors; Sequence Analysis, DNA; Survival Rate; Taiwan; Thymine	2010
An αIIb mutation in patients with Glanzmann thrombasthenia located in the N-terminus of blade 1 of the β-propeller (Asn2Asp) disrupts a calcium binding site in blade 6. Journal of thrombosis and haemostasis : JTH, 2011, Volume: 9, Issue:1 Topics: Adolescent; Amino Acid Sequence; Animals; Arabs; Asparagine; Aspartic Acid; Binding Sites; Blood Platelets; Calcium; Cell Line; Child; Child, Preschool; Cricetinae; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamine; Hemostasis; Heredity; Humans; Hydrogen Bonding; Integrin alpha2; Integrin beta3; Israel; Leucine; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Thrombasthenia; Transfection	2011
Associations between vitamin D receptor genotypes and mortality in a cohort of older Dutch individuals. European journal of endocrinology, 2011, Volume: 164, Issue:1 Topics: Aged; Aged, 80 and over; Cardiovascular Diseases; CDX2 Transcription Factor; Cohort Studies; Deoxyribonucleases, Type II Site-Specific; Female; Genetic Predisposition to Disease; Genotype; Haplotypes; Homeodomain Proteins; Humans; Leucine; Male; Middle Aged; Mortality; Neoplasms; Netherlands; Odds Ratio; Polymorphism, Genetic; Receptors, Calcitriol; Risk Assessment; Risk Factors; White People	2011
JAK2V617F mutation is associated with special alleles in essential thrombocythemia. Leukemia & lymphoma, 2011, Volume: 52, Issue:3 Topics: Alleles; Amino Acid Substitution; DNA Mutational Analysis; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genetic Testing; Humans; Janus Kinase 2; Leucine; Lysine; Mutation, Missense; Phenylalanine; Polymorphism, Single Nucleotide; Receptors, Thrombopoietin; Thrombocythemia, Essential; Tryptophan; Valine	2011
Homozygous THAP1 mutations as cause of early-onset generalized dystonia. Movement disorders : official journal of the Movement Disorder Society, 2011, Volume: 26, Issue:5 Topics: Adult; Apoptosis Regulatory Proteins; Carcinoma; Cell Line, Tumor; Consanguinity; DNA-Binding Proteins; Dystonia; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Histidine; Homozygote; Humans; Iran; Leucine; Male; Middle Aged; Mutation; Nuclear Proteins; Pedigree	2011
FXIII-A Leu34 genetic variant in premature coronary artery disease: a genotype--phenotype case control study. Thrombosis and haemostasis, 2011, Volume: 106, Issue:3 Topics: Adult; Age Factors; Case-Control Studies; Coronary Artery Disease; Coronary Thrombosis; DNA Mutational Analysis; Factor XIII; Female; Follow-Up Studies; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Hemodynamics; Humans; Leucine; Male; Myocardial Infarction; Polymorphism, Genetic; Recurrence; Survival Analysis	2011
A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family. Neuroscience letters, 2011, Sep-26, Volume: 503, Issue:1 Topics: Adolescent; Adult; Aged; Asian People; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy, Generalized; Family Health; Female; Genetic Linkage; Genetic Predisposition to Disease; Humans; Leucine; Male; Middle Aged; Models, Molecular; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Phenylalanine; Seizures, Febrile; Sodium Channels	2011
A common polymorphism in TLR3 confers natural resistance to HIV-1 infection. Journal of immunology (Baltimore, Md. : 1950), 2012, Jan-15, Volume: 188, Issue:2 Topics: Cells, Cultured; Cohort Studies; Genetic Predisposition to Disease; Genetic Variation; HIV Infections; HIV Seronegativity; Humans; Italy; Leucine; Male; Phenylalanine; Polymorphism, Genetic; Prospective Studies; Spain; Toll-Like Receptor 3	2012
High frequency of Neuropeptide Y Leu7Pro polymorphism in an Iranian population and its association with coronary artery disease. Gene, 2012, Mar-15, Volume: 496, Issue:1 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
The influence of the HLA-DRB1 and HLA-DQB1 allele heterogeneity on disease risk and severity in Iranian patients with multiple sclerosis. International journal of immunogenetics, 2012, Volume: 39, Issue:5 Topics: Adult; Alleles; Case-Control Studies; Female; Gene Frequency; Genetic Association Studies; Genetic Heterogeneity; Genetic Predisposition to Disease; Haplotypes; HLA-DQ beta-Chains; HLA-DRB1 Chains; Humans; Iran; Leucine; Male; Middle Aged; Multiple Sclerosis; Odds Ratio; Risk Factors; Severity of Illness Index; White People; Young Adult	2012
Low rate of production of apolipoproteins B100 and AI in 2 patients with Anderson disease (chylomicron retention disease). Arteriosclerosis, thrombosis, and vascular biology, 2012, Volume: 32, Issue:6 Topics: Adult; Apolipoprotein A-I; Apolipoprotein B-100; Biomarkers; Carbon Isotopes; Cholesterol; Down-Regulation; Female; Genetic Predisposition to Disease; Humans; Hypobetalipoproteinemias; Kinetics; Leucine; Lipoproteins, VLDL; Malabsorption Syndromes; Male; Models, Biological; Monomeric GTP-Binding Proteins; Mutation; Phenotype; Triglycerides	2012
Genetic association between obstructive bronchitis and enzymes of oxidative stress. Metabolism: clinical and experimental, 2012, Volume: 61, Issue:12 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
Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections. Blood, 2002, Aug-01, Volume: 100, Issue:3 Topics: Adolescent; Anemia, Hemolytic, Congenital Nonspherocytic; Bacterial Infections; Base Sequence; Child, Preschool; Chronic Disease; DNA Mutational Analysis; Erythrocytes; Family Health; Genetic Predisposition to Disease; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Granulocytes; Humans; Leucine; Male; Mutation; Respiratory Burst; RNA, Messenger; Sequence Deletion	2002
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes. Neurology, 2002, Jul-23, Volume: 59, Issue:2 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
Mitochondrial 5178A/C genotype is associated with acute myocardial infarction. Circulation journal : official journal of the Japanese Circulation Society, 2003, Volume: 67, Issue:1 Topics: Aged; Aging; Alleles; Amino Acid Substitution; Diabetes Complications; DNA, Mitochondrial; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Hypercholesterolemia; Hypertension; Leucine; Male; Methionine; Middle Aged; Myocardial Infarction; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors	2003
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene. Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:2 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. The American journal of medicine, 2003, Feb-15, Volume: 114, Issue:3 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
Map-based cloning of leaf rust resistance gene Lr21 from the large and polyploid genome of bread wheat. Genetics, 2003, Volume: 164, Issue:2 Topics: Blotting, Southern; Chromosome Mapping; Cloning, Molecular; Cosmids; DNA, Complementary; Gene Library; Genetic Complementation Test; Genetic Predisposition to Disease; Genome, Plant; Leucine; Models, Genetic; Molecular Sequence Data; Open Reading Frames; Phenotype; Plant Diseases; Plants, Genetically Modified; Protein Structure, Tertiary; Recombination, Genetic; Reverse Transcriptase Polymerase Chain Reaction; Sequence Tagged Sites; Triticum	2003
Role of glutathione peroxidase 1 in breast cancer: loss of heterozygosity and allelic differences in the response to selenium. Cancer research, 2003, Jun-15, Volume: 63, Issue:12 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. Atherosclerosis, 2003, Volume: 167, Issue:2 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
A novel single-nucleotide substitution, Leu 467 Pro, in the interferon-gamma receptor 1 gene associated with allergic diseases. International journal of molecular medicine, 2003, Volume: 12, Issue:2 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. Journal of the National Cancer Institute, 2003, Aug-06, Volume: 95, Issue:15 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
Cytokine polymorphisms and histologic expression in autopsy studies: contribution of TNF-alpha and TGF-beta 1 to the pathogenesis of autoimmune-associated congenital heart block. Journal of immunology (Baltimore, Md. : 1950), 2003, Sep-15, Volume: 171, Issue:6 Topics: Arginine; Autoimmune Diseases; Autopsy; Child; Cytokines; Exanthema; Female; Fetal Diseases; Gene Frequency; Genetic Predisposition to Disease; Heart Block; Humans; Leucine; Mothers; Polymorphism, Genetic; RNA, Messenger; Transforming Growth Factor beta; Transforming Growth Factor beta1; Tumor Necrosis Factor-alpha	2003
Missense mutation of Pro387Leu in protein tyrosine phosphatase-1B (PTP-1B) is not associated with type 2 diabetes in a Chinese Han population. Diabetes care, 2003, Volume: 26, Issue:10 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
Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients. Neuropediatrics, 2003, Volume: 34, Issue:5 Topics: Alleles; Brain; Case-Control Studies; DNA Mutational Analysis; Epilepsy, Temporal Lobe; Gene Expression; Genetic Predisposition to Disease; Genetic Variation; Humans; Intracellular Signaling Peptides and Proteins; Introns; Japan; Leucine; Point Mutation; Polymorphism, Genetic; Proteins; Seizures, Febrile	2003
HPC2/ELAC2 gene variants associated with incident prostate cancer. Journal of human genetics, 2003, Volume: 48, Issue:12 Topics: Age Factors; Alleles; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heterozygote; Homozygote; Humans; Leucine; Logistic Models; Male; Neoplasm Proteins; Prostate; Prostatic Neoplasms; Risk; Serine; Threonine	2003
Increased risk of bladder cancer associated with a glutathione peroxidase 1 codon 198 variant. The Journal of urology, 2004, Volume: 172, Issue:2 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 paraoxonase-1 M55L genotype and alcohol consumption with coronary atherosclerosis: the Helsinki Sudden Death Study. Pharmacogenetics, 2004, Volume: 14, Issue:8 Topics: Adult; Aged; Alcohol Drinking; Amino Acid Substitution; Aryldialkylphosphatase; Autopsy; Coronary Artery Disease; Coronary Vessels; Finland; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Methionine; Middle Aged; Prospective Studies; Risk Factors	2004
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population. Neuroscience letters, 2004, Sep-02, Volume: 367, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Aryldialkylphosphatase; Case-Control Studies; DNA Mutational Analysis; Female; Finland; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic	2004
Identification of a novel human cancer/testis antigen, KM-HN-1, recognized by cellular and humoral immune responses. Clinical cancer research : an official journal of the American Association for Cancer Research, 2004, Sep-15, Volume: 10, Issue:18 Pt 1 Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Antigens, Neoplasm; Blotting, Northern; Cell Line; Cell Line, Tumor; Cell Nucleus; Cloning, Molecular; COS Cells; DNA, Complementary; Enzyme-Linked Immunosorbent Assay; Epitopes; Fluorescent Antibody Technique, Indirect; Gene Library; Genetic Predisposition to Disease; Glutathione Transferase; HLA-A Antigens; HLA-A24 Antigen; Humans; Immune System; Immunoglobulin G; Immunohistochemistry; Immunotherapy; Interferon-gamma; Leucine; Male; Microscopy, Fluorescence; Molecular Sequence Data; Nuclear Proteins; Peptides; Protein Structure, Tertiary; Recombinant Proteins; RNA, Messenger; T-Lymphocytes, Cytotoxic; Testis; Tissue Distribution	2004
The progesterone receptor Val660-->Leu polymorphism and breast cancer risk. Breast cancer research : BCR, 2004, Volume: 6, Issue:6 Topics: Breast Neoplasms; Case-Control Studies; Genetic Predisposition to Disease; Humans; Leucine; Middle Aged; Polymorphism, Single Nucleotide; Postmenopause; Premenopause; Receptors, Progesterone; Valine	2004
Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene. American journal of hypertension, 2004, Volume: 17, Issue:12 Pt 1 Topics: Adrenal Gland Neoplasms; Adult; Arginine; Child; Follow-Up Studies; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Leucine; Magnetic Resonance Imaging; Male; Pedigree; Pheochromocytoma; Point Mutation; Proto-Oncogenes; Sequence Analysis, DNA; von Hippel-Lindau Disease; Von Hippel-Lindau Tumor Suppressor Protein	2004
Pick bodies in a family with presenilin-1 Alzheimer's disease. Annals of neurology, 2005, Volume: 57, Issue:1 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Blotting, Western; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Leucine; Male; Membrane Proteins; Methionine; Middle Aged; Mutation; Neurofibrillary Tangles; Pick Disease of the Brain; Plaque, Amyloid; Postmortem Changes; Presenilin-1; tau Proteins	2005
Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer. Journal of the National Cancer Institute, 2005, May-18, Volume: 97, Issue:10 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. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association, 2005, Volume: 113, Issue:5 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
The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction. Journal of medical genetics, 2006, Volume: 43, Issue:2 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. British journal of cancer, 2005, Jul-11, Volume: 93, Issue:1 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
CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2005, Volume: 37, Issue:10 Topics: Adolescent; Adult; Arginine; Case-Control Studies; Child; Crohn Disease; Female; Frameshift Mutation; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Intracellular Signaling Peptides and Proteins; Leucine; Male; Middle Aged; Nod2 Signaling Adaptor Protein; Polymorphism, Genetic; Sweden; Tryptophan; Twins, Monozygotic	2005
The 5alpha-reductase type II A49T and V89L high-activity allelic variants are more common in men with prostate cancer compared with the general population. European urology, 2005, Volume: 48, Issue:4 Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Aged; Alanine; Alleles; Arginine; Biomarkers, Tumor; Case-Control Studies; Dihydrotestosterone; Disease Progression; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Luteinizing Hormone; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Prostatic Hyperplasia; Prostatic Neoplasms; Receptors, Androgen; Risk Factors; Sex Hormone-Binding Globulin; Sweden; Terminal Repeat Sequences; Testosterone; Threonine; Valine	2005
Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP1. Diabetes, 2005, Volume: 54, Issue:8 Topics: Aged; Carnosine; Cells, Cultured; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Dipeptidases; Female; Gene Expression; Genetic Predisposition to Disease; Glucose; Humans; Kidney; Leucine; Male; Middle Aged; Repetitive Sequences, Amino Acid; RNA, Messenger; Sequence Alignment	2005
The valine allele of the V89L polymorphism in the 5-alpha-reductase gene confers a reduced risk for hypospadias. The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:12 Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Alleles; Base Sequence; Case-Control Studies; DNA; Gene Frequency; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Hypospadias; Infant, Newborn; Leucine; Male; Molecular Sequence Data; Polymorphism, Genetic; Valine	2005
Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish. The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:12 Topics: Adult; Arginine; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genetics, Population; Genotype; Ghrelin; Glutamine; Heterozygote; Humans; Hunger; Leucine; Male; Metabolic Syndrome; Methionine; Middle Aged; Peptide Hormones; United States	2005
Increased risk of ovarian cancer in integrin beta3 Leu33Pro homozygotes. Endocrine-related cancer, 2005, Volume: 12, Issue:4 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
Identification of a new leucine haplotype (ALQ) at codon 154 in the ovine prion protein gene in Spanish sheep. Journal of animal science, 2006, Volume: 84, Issue:2 Topics: Alleles; Animals; Codon; DNA Primers; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Leucine; Male; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; PrPSc Proteins; Scrapie; Sequence Analysis, DNA; Sheep; Spain	2006
Polymorphic amino acids at codons 9 and 37 of HLA-DQB1 alleles may confer susceptibility to cervical cancer among Chinese women. International journal of cancer, 2006, Jun-15, Volume: 118, Issue:12 Topics: Amino Acid Sequence; Amino Acids; Aspartic Acid; Case-Control Studies; China; Codon; DNA, Viral; Female; Gene Frequency; Genetic Predisposition to Disease; HLA-DQ Antigens; HLA-DQ beta-Chains; Human papillomavirus 16; Humans; Isoleucine; Leucine; Papillomavirus Infections; Phenylalanine; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Sequence Analysis, DNA; Tyrosine; Uterine Cervical Neoplasms	2006
Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population. Neurology, 2006, Feb-14, Volume: 66, Issue:3 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
The association between factor XIII Val34Leu polymorphism and early myocardial infarction. Circulation journal : official journal of the Japanese Circulation Society, 2006, Volume: 70, Issue:3 Topics: Adult; Age Factors; Alleles; Case-Control Studies; Coronary Thrombosis; DNA; Factor XIII; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Myocardial Infarction; Polymerase Chain Reaction; Polymorphism, Genetic; Regression Analysis; Valine	2006
Presymptomatic genetic diagnosis for consulters from a large Chinese family with juvenile open angle glaucoma. Molecular vision, 2006, Apr-17, Volume: 12 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
A novel missense mutation in the transmembrane domain of neuregulin 1 is associated with schizophrenia. Biological psychiatry, 2006, Sep-15, Volume: 60, Issue:6 Topics: Animals; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Mutation, Missense; Neuregulin-1; Pedigree; Protein Structure, Tertiary; Schizophrenia; Sequence Homology; Valine	2006
Hereditary hyper-ACE-emia due to the Pro1199Leu mutation of somatic ACE as a potential pitfall in diagnosis: a first family outside Europe. Clinical chemistry and laboratory medicine, 2006, Volume: 44, Issue:9 Topics: Cytosine; Europe; Female; Genetic Predisposition to Disease; Granuloma; Humans; Leucine; Male; Peptidyl-Dipeptidase A; Point Mutation; Proline; Thymine	2006
The factor XIII Val34Leu polymorphism: is it protective against idiopathic venous thromboembolism? Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2006, Volume: 17, Issue:7 Topics: Amino Acid Substitution; Case-Control Studies; Factor XIII; Female; Genetic Predisposition to Disease; Genotype; Humans; Leucine; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Risk Assessment; Thromboembolism; Valine; Venous Thrombosis; White People	2006
Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms. Neuroscience letters, 2007, Jan-03, Volume: 411, Issue:1 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
A novel P755L mutation in LRRK2 gene associated with Parkinson's disease. Neuroreport, 2006, Dec-18, Volume: 17, Issue:18 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. Journal of medical genetics, 2007, Volume: 44, Issue:6 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. Annals of the New York Academy of Sciences, 2006, Volume: 1089 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. Pharmacogenetics and genomics, 2007, Volume: 17, Issue:1 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
NADH dehydrogenase subunit-2 237 Leu/Met polymorphism modifies the effects of alcohol consumption on risk for hypertension in middle-aged Japanese men. Hypertension research : official journal of the Japanese Society of Hypertension, 2007, Volume: 30, Issue:3 Topics: Alcohol Drinking; Asian People; Blood Pressure; Cross-Sectional Studies; Genetic Predisposition to Disease; Genotype; Humans; Hypertension; Japan; Leucine; Male; Methionine; Middle Aged; NADH Dehydrogenase; Polymorphism, Restriction Fragment Length; Protein Subunits; Risk Factors	2007
[Heterozygosity of 198LEU mutant allele in glutathione peroxidase-1 gene as a risk factor of bronchial asthma associated with smoking]. Terapevticheskii arkhiv, 2007, Volume: 79, Issue:3 Topics: Alleles; Asthma; Female; Genetic Predisposition to Disease; Glutathione Peroxidase; Glutathione Peroxidase GPX1; Heterozygote; Humans; Leucine; Male; Mutation; Sex Characteristics; Smoking	2007
Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies. Archives of neurology, 2007, Volume: 64, Issue:7 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Child; DNA Mutational Analysis; Down-Regulation; Electrodiagnosis; Female; Frameshift Mutation; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Heredodegenerative Disorders, Nervous System; Humans; Leucine; Male; Middle Aged; Myelin Proteins; Neural Conduction; Peripheral Nerves; Peripheral Nervous System Diseases; Phenotype	2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts. International journal of cancer, 2007, Dec-15, Volume: 121, Issue:12 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
Impact of FXIII-A Val34Leu polymorphism on coronary artery disease in Croatian patients. Molecular biology reports, 2009, Volume: 36, Issue:1 Topics: Aged; Chi-Square Distribution; Coronary Artery Disease; Coronary Thrombosis; Croatia; Factor XIII; Female; Genetic Predisposition to Disease; Humans; Leucine; Logistic Models; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Risk Factors; Statistics, Nonparametric; Valine	2009
Isolation of nucleotide binding site-leucine rich repeat and kinase resistance gene analogues from sugarcane (Saccharum spp.). Pest management science, 2008, Volume: 64, Issue:1 Topics: Amino Acid Sequence; Binding Sites; Cloning, Molecular; Fungi; Genes, Plant; Genetic Predisposition to Disease; Hybridization, Genetic; Leucine; Molecular Sequence Data; Nucleotides; Phosphotransferases; Phylogeny; Plant Diseases; Plant Proteins; Plant Viruses; Saccharum	2008
Distribution of neuropeptide Y Leu7Pro polymorphism in patients with type 1 diabetes and diabetic nephropathy among Swedish and American populations. European journal of endocrinology, 2007, Volume: 157, Issue:5 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
Parkin polymorphisms in progressive supranuclear palsy. Journal of the neurological sciences, 2008, May-15, Volume: 268, Issue:1-2 Topics: Aged; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Leucine; Male; Polymorphism, Genetic; Supranuclear Palsy, Progressive; tau Proteins; Ubiquitin-Protein Ligases; Valine	2008
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. Movement disorders : official journal of the Movement Disorder Society, 2008, Feb-15, Volume: 23, Issue:3 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
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. Public health nutrition, 2008, Volume: 11, Issue:11 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
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders. Archives of neurology, 2008, Volume: 65, Issue:3 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
Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's disease. Cellular and molecular neurobiology, 2008, Volume: 28, Issue:7 Topics: Adenosine Triphosphatases; Amino Acid Substitution; DNA Damage; DNA Mutational Analysis; DNA, Mitochondrial; Genetic Predisposition to Disease; Genetic Testing; Humans; Huntington Disease; Leucine; Lysine; Mitochondrial Diseases; Mutation; RNA, Transfer	2008
Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families. Acta neurologica Scandinavica, 2008, Volume: 118, Issue:5 Topics: Adolescent; Adult; Amino Acid Substitution; Charcot-Marie-Tooth Disease; Child; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Humans; Italy; Leucine; Male; Middle Aged; Mutation; Myelin P0 Protein; Neural Conduction; Pedigree; Peripheral Nerves; Phenotype; Polymorphism, Genetic; Serine; Severity of Illness Index; Young Adult	2008
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Molecular vision, 2008, May-08, Volume: 14 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Aryl Hydrocarbon Hydroxylases; Asian People; Case-Control Studies; Cell Line; Child; Cytochrome P-450 CYP1B1; Cytochrome P-450 Enzyme System; Ethnicity; Gene Frequency; Genetic Predisposition to Disease; Geography; Glaucoma, Open-Angle; Haplotypes; Humans; India; Leucine; Linkage Disequilibrium; Middle Aged; Pigment Epithelium of Eye; Polymorphism, Single Nucleotide; Reactive Oxygen Species; Software; Valine	2008
Association of a polymorphism of the transforming growth factor-beta1 gene with genetic susceptibility to osteoporosis in postmenopausal Japanese women. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 1998, Volume: 13, Issue:10 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
Evidence for a role of the N terminus and leucine-rich repeat region of the Mi gene product in regulation of localized cell death. The Plant cell, 2000, Volume: 12, Issue:8 Topics: Amino Acid Sequence; Animals; Aphids; Cell Death; DNA-Binding Proteins; Genes, Lethal; Genes, Plant; Genetic Predisposition to Disease; Host-Parasite Interactions; Leucine; Microphthalmia-Associated Transcription Factor; Models, Biological; Molecular Sequence Data; Nicotiana; Plant Diseases; Plant Leaves; Plant Roots; Plants, Genetically Modified; Plants, Toxic; Recombinant Fusion Proteins; Repetitive Sequences, Amino Acid; Rhizobium; RNA, Messenger; RNA, Plant; Sequence Alignment; Signal Transduction; Solanum lycopersicum; Transcription Factors; Tylenchoidea	2000
Association of a Leu(10)-->Pro polymorphism of the transforming growth factor-beta1 with genetic susceptibility to osteoporosis and spinal osteoarthritis. Mechanisms of ageing and development, 2000, Jul-31, Volume: 116, Issue:2-3 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
Is the P25L a "real" VHL mutation? Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology, 2001, Volume: 6, Issue:1 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
A polymorphism in the 5' untranslated region and a Met229-->Leu variant in exon 5 of the human UCP1 gene are associated with susceptibility to type II diabetes mellitus. Diabetologia, 2001, Volume: 44, Issue:3 Topics: 5' Untranslated Regions; Aged; Alleles; Amino Acid Substitution; Asian People; Carrier Proteins; Diabetes Mellitus, Type 2; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Ion Channels; Japan; Leucine; Male; Membrane Proteins; Methionine; Middle Aged; Mitochondria; Mitochondrial Proteins; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Reference Values; Uncoupling Protein 1	2001
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature, 2001, May-31, Volume: 411, Issue:6837 Topics: Alleles; Carrier Proteins; Chromosomes, Human, Pair 16; Cloning, Molecular; Colitis, Ulcerative; Crohn Disease; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Intracellular Signaling Peptides and Proteins; Leucine; NF-kappa B; Nod2 Signaling Adaptor Protein; Polymorphism, Single Nucleotide; Proteins; Repetitive Sequences, Amino Acid; Signal Transduction	2001
Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease. Journal of medical genetics, 2002, Volume: 39, Issue:2 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