arginine and Genetic Predisposition

arginine has been researched along with Genetic Predisposition in 333 studies

Research

Studies (333)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	21 (6.31)	18.2507
2000's	182 (54.65)	29.6817
2010's	122 (36.64)	24.3611
2020's	8 (2.40)	2.80

Authors

Authors	Studies
Bellando-Randone, S; Fioretto, BS; Kosalka-Wegiel, J; Manetti, M; Matucci-Cerinic, M; Romano, E; Rosa, I; Sticchi, E	1
Assia Batzir, N; Bagłaj, M; Beaudet, AL; Bofferding, L; Bosanko, KB; Bouassida, S; Callewaert, B; Cannon, A; Coban Akdemir, Z; Enchautegui Colon, Y; Garnica, AD; Harr, MH; Heck, S; Hurst, ACE; Isidor, B; Jhangiani, SN; Kishor Bhagwat, P; Larson, A; Littlejohn, RO; Liu, P; Lupski, JR; Magoulas, P; Mar Fan, H; Marom, R; McLean, S; Nezarati, MM; Nugent, KM; Petersen, MB; Posey, JE; Rocha, ML; Roeder, E; Smigiel, R; Tully, I; Wangler, MF; Weisfeld-Adams, J; Wells, KO	1
Cheng, W; Jiang, H; Jiang, L; Li, W; Li, Z; Liu, J; Liu, X; Lu, K; Qi, S; Sheng, J; Shu, X; Tang, D; Wang, K; Xu, L; Yan, C; Zhan, X; Zhang, T; Zhou, C	1
Ochoa-Martínez, ÁC; Orta-García, ST; Pérez-Maldonado, IN; Varela-Silva, JA	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
Castillo-Maldonado, I; Delgadillo-Guzmán, D; Pedroza-Escobar, D; Quintanar-Escorza, MA; Sharara-Núñez, AI	1
Da Costa, RSS; Esteves, VF; Koifman, RJ; Koifman, S; Schilling, MPR; Silva, IFD	1
Banka, S; Clayton-Smith, J; Jackson, A; Lovell, S; Robinson, H; Stewart, H	1
Anaparti, V; Bernstein, CN; Bridie Clemens, E; Deutsch, AJ; El-Gabalawy, H; Ferucci, ED; Heemst, JV; Hitchon, CA; Huizinga, T; Kedzierska, K; Law, SC; Meng, X; Moustakas, AK; Papadopoulos, GK; Raychaudhuri, S; Reid, HH; Robinson, DB; Rossjohn, J; Scally, SW; Smolik, I; Sokolove, J; Thomas, R; Ting, YT; Toes, RE; van der Woude, D	1
Morris, CR; Shilo, NR	1
Atzler, D; Böger, RH; Chen, P; Chen, Y; Fassett, J; Guo, H; Hu, X; Kwak, D; Liu, X; Lu, Z; Schwedhelm, E; Wang, H; Xu, X; Yue, W; Zhang, P	1
Almendarez-Reyna, CI; Ochoa-Martínez, ÁC; Orta-García, ST; Pérez-Maldonado, IN; Ruíz-Vera, T	1
Allasia, A; Deutz, NEP; Engelen, MPKJ; Klimberg, VS	1
Atawia, RT; Bagi, Z; Bhatta, A; Caldwell, RB; Caldwell, RW; Chen, J; Fouda, AY; Lucas, R; Toque, HA; Xu, Z; Yao, L	1
Alfredsson, L; Cornillet, M; Hansson, M; Holmdahl, R; Jakobsson, PJ; Klareskog, L; Lundberg, K; Mathsson-Alm, L; Reed, E; Rönnelid, J; Serre, G; Skriner, K	1
Biczo, G; Dawson, D; Elperin, J; French, SW; Gorelick, FS; Gretler, S; Gukovskaya, AS; Gukovsky, I; Hegyi, P; Husain, SZ; Lotshaw, E; Lugea, A; Malla, SR; Mareninova, OA; Rakonczay, Z; Ruchala, P; Shalbueva, N; Vegh, ET; Wen, L; Whitelegge, J	1
Bode-Böger, SM; Brilloff, S; Heinrich, A; Hohenstein, B; Hugo, CPM; Jarzebska, N; Martens-Lobenhoffer, J; Rodionov, RN; Todorov, VT; Weiss, N	1
Chang, CW; Cohn, DE; Cosgrove, CM; Dama, P; Gillespie, JL; Goodfellow, PJ; Mutch, DG; O'Hern, MJ; Rush, CM; Selvendiran, K; Shakya, R; Smith, B; Song, JW; Stein, ME; Walker, CJ; Zingarelli, RA	1
Aleixo, AA; Coelho, LFL; da Silva, CAV; de Brito Magalhães, CL; de Fátima Silva Moraes, T; de Magalhaes, JC; de Mello Silva, B; de Oliveira Prado, AA; de Siqueira, TR; de Souza, GAP; Drumond, BP; Ferreira, GP; Ferreira, JMS; Malaquias, LCC; Pereira, ACTDC; Santos, LL	1
Ades, L; Benedict, S; Bradley, TJ; Braverman, AC; Brickner, ME; Chatfield, KC; Child, A; De Backer, J; Estrera, A; Feist, C; Holmes, KW; Iannucci, G; Lorenz, B; Mark, P; Mellor-Crummey, L; Milewicz, DM; Mitchell, AL; Morisaki, H; Morisaki, T; Morris, SA; Musolino, P; Ostergaard, JR; Pyeritz, R; Regalado, ES; Richer, J; Sallee, D; Shalhub, S; Tekin, M; Yetman, A	1
Barman-Aksözen, J; Huber, LC; Minder, E; Senn, JD	1
Battini, R; Catania, A; Chiapparini, ML; Garavaglia, B; Ghezzi, D; Nardocci, N; Pasquariello, R; Pippucci, T; Seri, M; Tiranti, V; Zorzi, G	1
Dong, Q; Liao, J; Liu, LR; Liu, SZ; Lu, DL; Ren, PW; Ren, ZJ; Yang, B; Yang, LC; Zhang, Q	1
Behjati, M; Karimian, M; Mobasseri, N; Nikzad, H; Noureddini, M	1
Barupal, DK; Chmiel, KJ; Hwang, VJ; Ishimaru, T; Jen, KY; Li, X; Mahjoub, MR; Shim, K; Stewart, BJ; Trott, JF; Weiss, RH; Zhou, JX	1
Cortés-González, V; Kheir, V; Schorderet, DF; Zenteno, JC	1
Fu, Q; Gao, H; Jiang, M; Lin, W; Lin, Y; Lu, B; Zheng, T; Zhou, S; Zhu, L	1
Camelo-Santos, J; de Paula Silveira-Lacerda, E; do Prado Barbosa, A; Guillo, LA	1
Bowe, D; Glueck, CJ; Munsif, S; Valdes, A; Wang, P	1
Lv, J; You, T; Zhou, L	1
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Barontini, M; Levin, G; Rudaz, MC; Sansó, G	1
Misra, C; Mitra, S; Panda, CK; Roychoudhury, S; Singh, RK	1
Beaulieu, JM; Burch, LH; Caron, MG; Gainetdinov, RR; Krishnan, KR; Schwartz, DA; Sotnikova, TD; Williams, RB; Zhang, X	1
Duan, LH; Guo, W; Kang, S; Li, Y; Wang, N; Zhang, JH	1
Fisher, SA; Grumley, JA; Kingsley, GH; Lad, B; Steer, S	1
Brosnan, MJ; Dominiczak, AF; Graham, D; Hamilton, CA; Hanlon, N; Lee, WK; Mathers, J; McBride, MW; McLellan, LI; Miller, WH; Polke, JM	1
Gao, J; Hu, Z; Lu, F; Luo, S; Zeng, W; Zhao, Y; Zhuo, Y	1
Heils, A; Hempelmann, A; Höfels, S; Lenzen, KP; Lohoff, FW; Lorenz, S; Sander, T; Schmitz, B	1
Bamezai, R; Malhotra, D; Reddy, BS; Relhan, V	1
Broich, P; Evert, BO; Fliessbach, K; Hans, VH; Kimonis, V; Mehta, SG; Pauls, K; Schröder, R; Thal, DR; Watts, GD	1
Fujimoto, M; Fukami, M; Hasegawa, T; Koitabashi, Y; Ogata, T; Soneda, S	1
Jeon, YT; Kang, SB; Kim, JW; Lee, HP; Park, NH; Song, YS	1
Kuzuya, N	1
Gauthier, S; Gros, P; Malo, D; Mullick, A; Tuite, A; Turcotte, K	1
Austin, MA; Edwards, KL; Williams, MA; Zhang, C	1
Boor, PP; Crusius, JB; de Jong, DJ; de Rooij, FW; Kuipers, EJ; Naber, TH; van Bodegraven, AA; van der Linde, K; Wilson, JH	1
Guo, L; Li, J; Ma, Y; Vogel, U; Wang, H; Yin, J	1
Blakemore, AI; El Nahas, AM; Khalil, MS	1
Csernus, K; Czakó, M; Erhardt, E; Kosztolányi, G; Molnár, D	1
Bresso, F; D'Amato, M; Halfvarson, J; Järnerot, G; Pettersson, S; Tysk, C	1
Heils, A; Hempelmann, A; Lenzen, KP; Lorenz, S; Sander, T	1
Abrahamsson, PA; Ahlgren, G; Gadaleanu, V; Giwercman, A; Giwercman, YL	1
Birmingham, DJ; Bottini, N; Cantor, RM; Farwell, L; Graham, DS; Grossman, JM; Hahn, BH; Hebert, LA; Jager, PL; Julkunen, H; Kere, J; Lingren, CM; Rioux, JD; Rovin, BH; Tsao, BP; Vyse, TJ; Wallace, DJ; Wu, H; Yu, CY	1
Bhattacharya, P; Sengupta, S	1
Burmester, GR; Diterich, I; Draing, C; Eckert, J; Göbel, UB; Hahn, K; Hartung, T; Hassler, D; Hermann, C; Michelsen, KS; Priem, S; Schröder, NW; Schumann, RR; von Baehr, V; Zinke, A	1
Coutlée, F; Duarte-Franco, E; Forest, P; Franco, EL; Ghosh, A; Koushik, A; Matlashewski, G; Voyer, H	1
Mitchell, BD; O'Connell, JR; Pollin, TI; Shuldiner, AR; Steinle, NI	1
Braunwald, E; DelMonte, T; Devlin, JJ; Dracopoli, NC; Hui, L; Iakoubova, OA; Kirchgessner, TG; Ranade, K; Sabatine, MS; Sacks, FM; Shaw, PM; Tsuchihashi, Z; Vishnupad, P; White, TJ	1
Auger, I; Balandraud, N; Cantagrel, A; Guis, S; Nogueira, L; Roudier, J; Sebbag, M; Serre, G; Svensson, B; Vincent, C	1
Akahoshi, M; Cheng, L; Enomoto, K; Enomoto, T; Hirota, T; Hopkin, JM; Mao, XQ; Matsuda, A; Shimizu, M; Shirakawa, T; Takahashi, N; Tamari, M; Yamasaki, A	1
Gao, J; Hu, Z; Jin, G; Liu, J; Qing, J; Shen, H; Wang, S; Wang, X; Zhai, X	1
Ambrosone, CB; Chang-Claude, J; Haase, W; Helmbold, I; Kropp, S; Popanda, O; Sautter-Bihl, ML; Schmezer, P; Tan, XL; von Fournier, D; Wenz, F	1
Capdevielle, C; Eymard, B; Gajdos, P; Garchon, HJ; Giraud, M; Jais, JP; Krumeich, S; Tranchant, C; Vandiedonck, C	1
Borg, A; Dziadziuszko, R; Jassem, E; Jassem, J; Kobierska-Gulida, G; Limon, J; Rzyman, W; Szymanowska, A	1
Butt, C; Gladman, D; Greenwood, C; Hamilton, S; Peddle, L; Rahman, P	1
Baralle, D; Bonthron, DT; Charlton, R; Cole, TR; De Vos, M; Glaser, AW; Hayward, BE; Maher, ER; Mann, JR; McKeown, CM; Picton, S; Rankin, J; Sheridan, E; Taylor, GR; Yates, JR	1
Ezquerra, M; Gaig, C; Marti, MJ; Muñoz, E; Tolosa, E; Valldeoriola, F	1
Antiñolo, G; Ayuso, C; Baiget, M; Carballo, M; Gamundi, MJ; García-Sandoval, B; Hernan, I; Martínez-Gimeno, M; Maseras, M	1
Burns, TM; Dimberg, EL; Klein, CJ; Phillips, LH; Vaught, BK	1
Kaye, DM; Yang, Z	1
DeKosky, ST; Feingold, E; Kamboh, MI; Minster, RL; Sundar, PD	1
Colditz, GA; Cox, DG; Han, J; Hunter, DJ	1
Frank, J; Merk, HF; Poblete-Gutiérrez, P; Wiederholt, T	1
Abe, LM; Carlson, KM; Carpenter, C; Hsia, YE; Marchuk, DA; Perry, AK; Person, DA; Raney, EM; Reinker, KA; Yamaga, KM	1
Ismail, T; Lee, S; Lipworth, BJ; Macgregor, DF; Mukhopadhyay, S; Palmer, CN	1
Ferreira, A; Loughlin, J; Snelling, S	1
Alpsoy, E; Bacanli, A; Sallakci, N; Yavuzer, U; Yegin, O	1
Duggan, E; Kelleher, D; McGovern, E; McManus, R; O'Dwyer, MJ; Ryan, AW; Ryan, R; Ryan, T; Thornton, J	1
Görgens, H; Hoffmann, T; Noack, B; Schackert, HK	1
Baker, M; Berger, SL; Elder, JW; Ghetti, B; Grafman, J; Hardy, J; Heflin, KA; Huey, ED; Hutton, M; Momeni, P; Pietrini, P; Spina, S; Tierney, MC; Wassermann, EM	1
Waugh, WH	1
Arici, M; Bakkaloglu, A; Berdeli, A; Besbas, N; Kutlay, S; Ozen, S; Türel, B; Yalcinkaya, F; Yilmaz, E	1
Boronow, J; Dickerson, F; Origoni, A; Stallings, C; Yolken, R	1
Latsoudis, H; Plaitakis, A; Spanaki, C	1
Bayazit, YA; Ciftci, TU; Erdal, ME; Gokdoğan, T; Kemaloglu, YK; Kokturk, O; Koybasioglu, A; Soylemez, F; Yilmaz, M	1
Alexandre, CO; Damin, AP; Damin, DC; Frazzon, AP; Hermes, V; Roehe, A; Zettler, C	1
Aasly, JO; Adler, CH; Blazquez, M; Farrer, MJ; Gibson, JM; Gwinn-Hardy, K; Haugarvoll, K; Hulihan, MM; Kachergus, J; Lynch, T; Mata, IF; Ross, OA; Stone, JT; Toft, M; White, LR	1
Dächsel, JC; Farrer, MJ; Haugarvoll, K; Hulihan, MM; Lin, CH; Ross, OA; Stone, JT; Wu, RM	1
Choi, SJ; Ji, JD; Lee, YH; Rho, YH; Song, GG	1
Böcker, U; Haas, SL; Ruether, A; Schreiber, S; Singer, MV	1
Bayet, B; Deggouj, N; Desmyter, L; Ghassibe, M; Gillerot, Y; Revencu, N; Vanwijck, R; Verellen-Dumoulin, C; Vikkula, M	1
Barkhof, F; Hooper-van Veen, T; Koper, JW; Polman, CH; Uitdehaag, BM; van Rossum, EF; van Winsen, LM	1
Ardovino, M; Bontempo, P; Cioffi, M; Cobellis, L; Colacurci, N; Iannella, I; Molinari, AM; Scaffa, C; Vietri, MT	1
Eberly, SW; Glazko, G; Goldenberg, I; Mathew, J; McNitt, S; Morray, B; Moss, AJ; Ryan, D; Zareba, W	1
Alenda, C; Andreu, M; Balaguer, F; Bessa, X; Carracedo, A; Castells, A; Castellví-Bel, S; de Cid, R; Gonzalo, V; Jover, R; Llor, X; Muñoz, J; Payá, A; Piqué, JM; Pons, E; Ruiz-Ponte, C; Xicola, RM	1
Guo, Y; Lin, D; Miao, X; Sun, T; Tan, W; Zhang, X; Zhao, D	1
Alvarez-Alvarez, M; Ciordia, R; de Pancorbo, MM; Farrer, MJ; Gómez-Busto, F; Gómez-Esteban, JC; González-Fernández, MC; Lezcano, E; Mata, IF; Rodríguez-Martínez, MB; Ross, OA; Velasco, F; Zarranz, JJ	1
Ansari, M; Hajilooi, M; Hashemi, SH; Nadi, E; Rafiei, A; Tavana, S; Zeraati, F	1
Kessels, AG; Moonen, RM; Paulussen, AD; Rubio-Gozalbo, ME; Souren, NY; Villamor, E	1
Ishida, T; Kashima, T; Makino, K; Soemantri, A	1
Fuchs, M; Hay, B; Klass, DM; Kratzer, W; Lauer, N	1
Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pöllmann, W; Rübsamen, H	1
Jiang, J; Jin, C; Shentu, X; Tang, X; Wu, R; Yao, K	1
Casali, C; Di Lorenzo, C; Di Lorenzo, G; Ghiotto, N; Grieco, GS; Guaschino, E; Nappi, G; Perrotta, A; Pierelli, F; Rengo, C; Sances, G; Santorelli, FM; Siracusano, A; Troisi, A	1
Biancone, L; Borgiani, P; Ciccacci, C; Novelli, G; Pallone, F; Perricone, C; Petruzziello, C; Romano, S	1
Adali, O; Arinç, E; Bek, S; Can Demirdöğen, B; Demirkaya, S; Sanisoğlu, Y; Türkanoğlu, A; Vural, O	1
Andreassen, T; Ekstrøm, PO; Haugen, A; Lind, H; Ryberg, D; Skaug, V; Stangeland, L; Zienolddiny, S	1
Bowen, G; Cannon-Albright, LA; Chen, W; Eliason, MJ; Florell, SR; Hansen, CB; Harris, RM; Hart, M; Leachman, SA; Porter-Gill, P; Sturm, RA; Swinyer, L	1
Cho, YD; Choi, KW; Ki, CS; Kim, JW; Lee, ST; Yeo, HT	1
Arnold, S; Brown, MA; Buchanan, D; Chenevix-Trench, G; Couch, FJ; Farrugia, DJ; Goldgar, DE; Healey, S; Henderson, BR; Lakhani, SR; Lovelock, PK; Mok, MT; Spurdle, AB; Tavtigian, SV	1
Bettecken, T; Eisensehr, I; Golic, J; Hauk, S; Holsboer, F; Illig, T; Lichtner, P; Meitinger, T; Müller-Myhsok, B; Paulus, W; Peglau, I; Pfister, H; Pütz, B; Schormair, B; Stiasny-Kolster, K; Trenkwalder, C; Uhr, M; Wichmann, HE; Winkelmann, J	1
Bermejo, JL; Gurzau, E; Hemminki, K; Koppova, K; Kumar, R; Rudnai, P; Scherer, D	1
Amorim, J; Costa, S; Lima-Ramos, V; Lopes, JM; Pacheco-Figueiredo, L; Pardal, F; Reis, RM; Silva, A	1
de Vries, RR; Feitsma, AL; Huizinga, TW; Plant, D; Thomson, W; Toes, RE; Ursum, J; van der Helm-van Mil, AH; van der Horst-Bruinsma, IE; van Rood, JJ; van Schaardenburg, D; Worthington, J	1
An, XK; Burgunder, JM; Chen, WJ; Gou, YR; Li, T; Peng, R; Wang, YC; Wu, Y; Xu, YM; Yuan, GG; Zhang, JH; Zhang, ZJ	1
Boles, RG; Dhamcharee, V	1
Bass, NJ; Choudhury, K; Curtis, D; Gurling, HM; Kosmin, M; Lawrence, J; McQuillin, A; Puri, V	1
Beppu, Y; Chuman, H; Hirose, H; Kawai, A; Masutani, M; Morioka, H; Nakatani, F; Nakayama, R; Ogino, H; Ohta, T; Sakamoto, H; Sato, Y; Sugimura, H; Toyama, Y; Yabe, H; Yoshida, T	1
Chen, CH; Chen, JY; Lai, IC; Liao, DL; Liou, YJ; Wang, LH; Wang, YC	1
Anfossi, M; Bernardi, L; Bruni, AC; Colao, R; Costanzo, A; Curcio, SA; Frangipane, F; Gallo, M; Geracitano, S; Iapaolo, D; Maletta, RG; Mirabelli, M; Puccio, G; Smirne, N; Tomaino, C	1
Lee, J; Lim, HQ; Tan, EK; Yuen, Y; Zhao, Y	1
Berg, T; Eurich, D; Halangk, J; Hellerbrand, C; Homann, N; Osterreicher, CH; Patsenker, E; Seitz, HK; Stickel, F	1
Lv, Z; Ma, X; Wang, B; Wang, J; Xie, YC; Yang, Z; Zhang, P; Zheng, C; Zhou, S	1
Margaritis, LH; Papassideri, IS; Stravopodis, DJ; Voutsinas, G; Zapheiropoulos, AZ	1
Beaudry, P; Bounneau, C; Chatelain, J; Clouscard, C; Dussaucy, M; Elsen, JM; Laplanche, JL; Launay, JM; Milan, D; Schelcher, F	1
Dahlbäck, B; He, X; Svensson, PJ; Zöller, B	1
Fonseka, S; Kasper, LH; Khan, IA; Matsuura, T	1
Hamaguchi, M; Kagami, K; Katsumi, A; Kojima, T; Okamoto, Y; Saito, H; Sugiura, I; Takamatsu, J; Yamazaki, T	1
Alahari, SK; Cizman, B; Kamoun, M; Mehra, NK; Monos, DS; Murali, R; Zerva, L; Zmijewski, CM	1
Bouchard, C; Mauriège, P	1
Grohmann, J; Koch, HG; Nowak-Göttl, U; Schneppenheim, R; Vielhaber, H	1
Corbella, J; Estape, J; Firvida, J; Fuentes, M; Galan, C; Gene, M; Gomez-Catalan, J; Huguet, E; Rodamilans, M; To-Figueras, J	1
Heikkinen, S; Kekäläinen, P; Kuopusjärvi, J; Kuusisto, J; Laakso, M; Pihlajamäki, J; Rissanen, J; Sipiläinen, R; Vanhala, M	1
Bertina, RM; Doggen, CJ; Manger Cats, V; Reitsma, PH; Rosendaal, FR; Vandenbroucke, JP	1
Buys, CH; Hayes, VM; Hofstra, RM; Hollema, H; van der Zee, AG	1
Børresen-Dale, AL; Helland, A; Johnsen, H; Langerød, A; Olsen, AO; Skovlund, E	1
Barnes, W; Bratti, MC; Brinton, LA; Carrington, M; Fraumeni, JF; Greenberg, M; Herrera, JE; Herrero, R; Hildesheim, A; Martin, M; McGowan, L; Mortel, R; Schiffman, M; Schwartz, P; Scott, DR	1
Amouyel, P; Cambien, F; Charron, P; Desnos, M; Dorent, R; Jullières, Y; Komajda, M; Nicaud, V; Peuchmaurd, M; Poirier, O; Roizès, G; Schwartz, K; Tesson, F; Tiret, L	1
Akahoshi, M; Arinobu, Y; Inoue, H; Nagano, S; Nakashima, H; Niho, Y; Niiro, H; Ogami, E; Otsuka, T; Tanaka, Y; Yamaoka, K	1
Bertorelle, R; Chieco-Bianchi, L; Del Mistro, A	1
Giannoudis, A; Graham, DA; Herrington, CS; Southern, SA	1
Baeder, S; Baur, C; Calzia, E; Eichinger, HM; Froeba, G; Georgieff, M; Marx, T; Pazhur, J; Radermacher, P	1
Keshava, C; McCanlies, EC; Sharp, DS; Sun, Y; Weston, A	1
Billiri, K; Dokianakis, DN; Koumantaki, E; Spandidos, DA	1
Baek, WK; Cha, SD; Cho, CH; Cho, JW; Lee, TS; Shin, DH; Suh, MH; Suh, SI	1
Carnevali, L; Migliora, P; Ranzani, GN; Rondo Spaudo, M; Tenti, P; Vesentini, N; Zappatore, R	1
Dokianakis, DN; Papadakis, EN; Spandidos, DA	1
Allen, TM; Collins, EJ; Dzuris, JL; Hickman, H; Hildebrand, W; Lorentzen, D; Neiffer, DL; Prilliman, K; Raphael, B; Schwartz, KJ; Sette, A; Shufflebotham, C; Urvater, JA; Watkins, DI	1
Baker, DW; Bradley, JF; Huelsman, KM; Rothberg, PG	1
Ala-Kokko, L; Göring, HH; Hakala, M; Kaitila, I; Karppinen, J; Kröger, H; Lohiniva, J; Ott, J; Paassilta, P; Palm, T; Perälä, M; Räinä, SS; Vanharanta, H	1
Barth, C; Ehren, M; Enderle, MD; Hering, S; Koch, M; Pfohl, M	1
Alonso, V; Corella, D; Folch, J; Guillén, M; Portolés, O; Sáiz, C; Sorlí, JV	1
Sabra, M; Shuldiner, AR	1
Christiani, DC; Fan, R; Liu, G; Lynch, TJ; Miller, DP; Su, L; Thurston, SW; Wain, JC; Xu, LL; Zhou, W	1
He, Z; Lin, D; Xing, D; Zhang, L	1
Cantor, RM; Dahmer, MK; Quasney, MW; Turner, D; Waterer, GW; Wunderink, RG; Zhang, Q	1
DeGraves, FJ; Feng, P; Gao, D; Huang, J; Kaltenboeck, B; Lenz, SD; Li, D; Schlapp, T	1
Chalkley, SM; Chisholm, DJ; Hettiarachchi, M; Kraegen, EW	1
Bertera, S; Chantres, MT; Dorman, JS; Gutierrez-Lopez, MD; Serrano-Rios, M; Trucco, M; Vavassori, C	1
Chang, EH; Cunningham, JM; Francis, GE; Holland, MJ; Pirollo, KF	1

Reviews

28 review(s) available for arginine 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
Pathways to pulmonary hypertension in sickle cell disease: the search for prevention and early intervention. Expert review of hematology, 2017, Volume: 10, Issue:10 Topics: Anemia, Sickle Cell; Arginine; Biomarkers; Blood Coagulation; Echocardiography; Genetic Predisposition to Disease; Hemolysis; Humans; Hypertension, Pulmonary; Hypoxia; Nitric Oxide; Oxidative Stress; Respiratory Function Tests; Risk Assessment	2017
[CME: Acute Intermittent Porphyria: When to Think of It? What Must be Checked? How to Treat?] Praxis, 2018, Volume: 107, Issue:3 Topics: Arginine; Combined Modality Therapy; Diagnosis, Differential; Female; Genetic Predisposition to Disease; Heme; Hemin; Humans; Interdisciplinary Communication; Intersectoral Collaboration; Middle Aged; Porphobilinogen; Porphyria, Acute Intermittent; Prognosis; Recurrence; Risk Factors	2018
TP53 gene Arg72Pro polymorphism and male infertility risk: A meta-analysis. Andrologia, 2018, Volume: 50, Issue:10 Topics: Arginine; Asian People; Genetic Predisposition to Disease; Humans; Infertility, Male; Male; Polymorphism, Single Nucleotide; Proline; Tumor Suppressor Protein p53	2018
Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review. BMC medical genetics, 2019, 06-17, Volume: 20, Issue:1 Topics: Arginine; Argininosuccinate Synthase; Asian People; Base Sequence; China; Citrulline; Citrullinemia; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Infant, Newborn; Language Development Disorders; Male; Mutation; Pedigree; Phenotype; Phenylalanine; RNA Splicing	2019
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 XRCC1 Arg399Gln polymorphism and risk of cancer: evidence from 297 case-control studies. PloS one, 2013, Volume: 8, Issue:10 Topics: Arginine; Asian People; Case-Control Studies; DNA-Binding Proteins; Genetic Predisposition to Disease; Humans; Neoplasms; X-ray Repair Cross Complementing Protein 1	2013
Meta-analysis of association between the TP53 Arg72Pro polymorphism and risk of endometriosis based on case-control studies. European journal of obstetrics, gynecology, and reproductive biology, 2015, Volume: 189 Topics: Arginine; Asian People; Case-Control Studies; Endometriosis; Female; Genetic Predisposition to Disease; Humans; Polymorphism, Single Nucleotide; Proline; Tumor Suppressor Protein p53; White People	2015
TP53 Arg72Pro polymorphism (rs1042522) and risk of endometriosis among Asian and Caucasian populations. European journal of obstetrics, gynecology, and reproductive biology, 2015, Volume: 189 Topics: Arginine; Asian People; Endometriosis; Female; Genetic Predisposition to Disease; Humans; Linkage Disequilibrium; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53; White People	2015
Association of LEPR Gln223Arg polymorphism with T2DM: A meta-analysis. Diabetes research and clinical practice, 2015, Volume: 109, Issue:3 Topics: Amino Acid Substitution; Arginine; Diabetes Mellitus, Type 2; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Polymorphism, Single Nucleotide; Receptors, Leptin	2015
Arg753Gln Polymorphisms in Toll-Like Receptor 2 Gene are Associated with Tuberculosis Risk: A Meta-Analysis. Medical science monitor : international medical journal of experimental and clinical research, 2015, Jul-29, Volume: 21 Topics: Arginine; Genetic Predisposition to Disease; Glycine; Humans; Polymorphism, Genetic; Toll-Like Receptor 2; Tuberculosis	2015
Review: Human guanidinoacetate n-methyl transferase (GAMT) deficiency: A treatable inborn error of metabolism. Pakistan journal of pharmaceutical sciences, 2015, Volume: 28, Issue:6 Topics: Arginine; Creatine; Dietary Proteins; Dietary Supplements; Energy Metabolism; Genetic Predisposition to Disease; Guanidinoacetate N-Methyltransferase; Humans; Language Development Disorders; Movement Disorders; Phenotype; Treatment Outcome	2015
Meta analysis on the association between FcgammaRIIa-R/H131 polymorphisms and systemic lupus erythematosus. Molecular biology reports, 2009, Volume: 36, Issue:5 Topics: Arginine; Ethnicity; Genetic Predisposition to Disease; Histidine; Humans; Lupus Erythematosus, Systemic; Lupus Nephritis; Odds Ratio; Polymorphism, Single Nucleotide; Publication Bias; Receptors, IgG; Regression Analysis	2009
Asthma management: reinventing the wheel in sickle cell disease. American journal of hematology, 2009, Volume: 84, Issue:4 Topics: Acute Disease; Adult; Anemia, Sickle Cell; Anti-Asthmatic Agents; Arginase; Arginine; Asthma; Black or African American; Chest Pain; Child; Child, Preschool; Combined Modality Therapy; Comorbidity; Erythrocytes, Abnormal; Genetic Predisposition to Disease; Humans; Hypertension, Pulmonary; Hypoxia; Long QT Syndrome; Nitric Oxide; Oxidative Stress; Oxygen Inhalation Therapy; Prevalence; United States	2009
The Arg194Trp polymorphism in the X-ray repair cross-complementing group 1 gene as a potential risk factor of oral cancer: a meta-analysis. The Tohoku journal of experimental medicine, 2009, Volume: 219, Issue:1 Topics: Arginine; Asia; Carcinoma, Squamous Cell; DNA-Binding Proteins; Europe; Gene Frequency; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Mouth Neoplasms; Odds Ratio; Polymorphism, Single Nucleotide; Tryptophan; X-ray Repair Cross Complementing Protein 1	2009
Genetic background of tolerance breakdown in rheumatoid arthritis. Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology, 2010, Volume: 33, Issue:2 Topics: Animals; Arginine; Arthritis, Rheumatoid; Autoantibodies; Autoimmunity; Citrulline; Genetic Predisposition to Disease; Genome-Wide Association Study; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Hydrolases; Immune Tolerance; Lymphocytes; Mice; Multifactorial Inheritance; Peptides; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Protein-Arginine Deiminase Type 4; Protein-Arginine Deiminases; Receptors, Immunologic	2010
ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis. PloS one, 2010, Oct-27, Volume: 5, Issue:10 Topics: Alcohol Dehydrogenase; Alcohol Drinking; Arginine; Asia; Carcinoma, Squamous Cell; Case-Control Studies; Epistasis, Genetic; Esophageal Neoplasms; Genetic Predisposition to Disease; Histidine; Humans; Incidence; Polymorphism, Genetic	2010
Citrullinated peptide and its relevance to rheumatoid arthritis: an update. International journal of rheumatic diseases, 2010, Volume: 13, Issue:4 Topics: Arginine; Arthritis, Rheumatoid; Autoantibodies; Biomarkers; Citrulline; Epitopes; Genetic Predisposition to Disease; Humans; Peptides; Peptides, Cyclic; Predictive Value of Tests; Prognosis; Risk Assessment; Risk Factors	2010
Complement factor B polymorphism 32W protects against age-related macular degeneration. Molecular vision, 2011, Apr-20, Volume: 17 Topics: Aged; Aged, 80 and over; Arginine; Case-Control Studies; Complement Activation; Complement Factor B; Complement Factor H; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; High-Temperature Requirement A Serine Peptidase 1; Humans; Linkage Disequilibrium; Macular Degeneration; Male; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Retina; Risk Factors; Serine Endopeptidases; Smoking; Tryptophan	2011
Meta-analysis shows significant association of the TP53 Arg72Pro with ovarian cancer risk. Molecular biology reports, 2012, Volume: 39, Issue:4 Topics: Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Homozygote; Humans; Ovarian Neoplasms; Polymorphism, Single Nucleotide; Proline; Publication Bias; Risk Factors; Tumor Suppressor Protein p53	2012
[The role of hereditary and environmental factors in autoimmune thyroid diseases]. Orvosi hetilap, 2012, Jul-01, Volume: 153, Issue:26 Topics: Arginine; Autoantibodies; Gene-Environment Interaction; Genetic Predisposition to Disease; Graves Disease; Hashimoto Disease; HLA-DRB1 Chains; Humans; Hyperthyroidism; Hypothyroidism; Iodide Peroxidase; Major Histocompatibility Complex; Polymorphism, Genetic; Receptors, Thyrotropin; Thyroglobulin; Thyroid Gland; Thyroiditis, Autoimmune	2012
Meta-analysis of the association between P53 codon 72 polymorphisms and gastric cancer. Journal of surgical oncology, 2013, Volume: 107, Issue:4 Topics: Arginine; Asian People; Codon; Genetic Predisposition to Disease; Genotype; Humans; Odds Ratio; Polymorphism, Single Nucleotide; Proline; Risk Factors; Stomach Neoplasms; Tumor Suppressor Protein p53; White People	2013
X-ray repair cross-complementing group 1 (XRCC1) genetic polymorphisms and cervical cancer risk: a huge systematic review and meta-analysis. PloS one, 2012, Volume: 7, Issue:9 Topics: Arginine; Asian People; DNA Damage; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamine; Humans; Odds Ratio; Polymorphism, Genetic; Risk; Risk Factors; Tryptophan; Uterine Cervical Neoplasms; X-ray Repair Cross Complementing Protein 1	2012
Citrullinated proteins in rheumatoid arthritis. Frontiers in bioscience : a journal and virtual library, 2005, Jan-01, Volume: 10 Topics: Arginine; Arthritis, Rheumatoid; Autoimmunity; Citrulline; Genetic Predisposition to Disease; Humans; Hydrolases; Models, Biological; Peptides; Protein Processing, Post-Translational; Protein-Arginine Deiminase Type 4; Protein-Arginine Deiminases; Synovial Membrane	2005
Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1). Arthritis and rheumatism, 2004, Dec-15, Volume: 51, Issue:6 Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome	2004
[Beta3-adrenergic receptor gene polymorphism in diabetes]. Nihon rinsho. Japanese journal of clinical medicine, 2005, Volume: 63 Suppl 2 Topics: Adipocytes; Amino Acid Substitution; Arginine; Diabetes Mellitus; Genetic Predisposition to Disease; Humans; Lipid Metabolism; Mutation, Missense; Racial Groups; Receptors, Adrenergic, beta-3; Tryptophan	2005
Endothelial dysfunction and impaired L-arginine transport in hypertension and genetically predisposed normotensive subjects. Trends in cardiovascular medicine, 2006, Volume: 16, Issue:4 Topics: Arginine; Biological Transport; Endothelium, Vascular; Genetic Predisposition to Disease; Humans; Hypertension; Risk Factors; Vasodilation	2006
Gorillas with spondyloarthropathies express an MHC class I molecule with only limited sequence similarity to HLA-B27 that binds peptides with arginine at P2. Journal of immunology (Baltimore, Md. : 1950), 2001, Mar-01, Volume: 166, Issue:5 Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Arginine; Arthritis; Cells, Cultured; Female; Genetic Predisposition to Disease; Gorilla gorilla; Histocompatibility Antigens Class I; HLA-B27 Antigen; Humans; Male; Molecular Sequence Data; Oligopeptides; Protein Binding; Sequence Homology, Amino Acid; Spondylitis	2001

Trials

3 trial(s) available for arginine 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
The R230C variant of the ATP binding cassette protein A1 (ABCA1) gene is associated with a decreased response to glyburide therapy in patients with type 2 diabetes mellitus. Metabolism: clinical and experimental, 2013, Volume: 62, Issue:5 Topics: Adult; Aged; Amino Acid Substitution; Arginine; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters; Cysteine; Diabetes Mellitus, Type 2; Dose-Response Relationship, Drug; Drug Resistance; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glyburide; Humans; Hypoglycemic Agents; Male; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Single-Blind Method; Young Adult	2013
Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group. Journal of molecular and cellular cardiology, 1999, Volume: 31, Issue:5 Topics: Adult; Alleles; Arginine; Cardiomyopathy, Dilated; Evaluation Studies as Topic; Female; Genetic Code; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glycine; Humans; Male; Middle Aged; Polymorphism, Genetic; Receptors, Adrenergic, beta-1	1999

Other Studies

303 other study(ies) available for arginine and Genetic Predisposition

Article	Year
A candidate gene study reveals association between a variant of the SRp55 splicing factor gene and systemic sclerosis. Clinical and experimental rheumatology, 2022, Volume: 40, Issue:10 Topics: Arginine; Autoantibodies; Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Lung Diseases, Interstitial; Phosphoproteins; Polymorphism, Single Nucleotide; RNA Splicing Factors; RNA, Messenger; Scleroderma, Systemic; Serine; Serine-Arginine Splicing Factors	2022
Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Human mutation, 2020, Volume: 41, Issue:3 Topics: Abnormalities, Multiple; Actins; Adult; Amino Acid Substitution; Arginine; Colon; DNA Mutational Analysis; Exome Sequencing; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Intestinal Pseudo-Obstruction; Male; Molecular Diagnostic Techniques; Mutation; Phenotype; Urinary Bladder; Young Adult	2020
Cryo-EM structure of C9ORF72-SMCR8-WDR41 reveals the role as a GAP for Rab8a and Rab11a. Proceedings of the National Academy of Sciences of the United States of America, 2020, 05-05, Volume: 117, Issue:18 Topics: Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Arginine; Autophagy; Autophagy-Related Proteins; C9orf72 Protein; Carrier Proteins; Cryoelectron Microscopy; Filamins; Frontotemporal Dementia; Genetic Predisposition to Disease; GTPase-Activating Proteins; Humans; Multiprotein Complexes; rab GTP-Binding Proteins; Sequence Alignment	2020
Influence of Human Paraoxonase-1 Polymorphism (Q192R) on Serum Levels of Clinical Biomarkers Indicatives of Cardiovascular Diseases Risk in Mexican Women. Biochemical genetics, 2020, Volume: 58, Issue:5 Topics: Adult; Arginine; Aryldialkylphosphatase; Biomarkers; Cardiovascular Diseases; Cross-Sectional Studies; Fatty Acid-Binding Proteins; Female; Genetic Predisposition to Disease; Heart Disease Risk Factors; Humans; Male; Mexico; MicroRNAs; Polymorphism, Genetic; Sex Factors	2020
Leptin G-2548A and Leptin Receptor Q223R Gene Polymorphisms are Differently Associated with Oxidative Process in Mexican Mestizo and Indigenous with Obesity. Endocrine, metabolic & immune disorders drug targets, 2021, Volume: 21, Issue:8 Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Cross-Sectional Studies; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Indigenous Peoples; Leptin; Lipid Peroxidation; Male; Mexico; Middle Aged; Obesity; Overweight; Oxidative Stress; Polymorphism, Single Nucleotide; Receptors, Leptin; Young Adult	2021
Gene-Environment Interaction between Arg72Pro SNP and Selected Environmental Exposures among Brazilian Women Diagnosed with Benign Breast Disease. Asian Pacific journal of cancer prevention : APJCP, 2020, Dec-01, Volume: 21, Issue:12 Topics: Arginine; Brazil; Breast Neoplasms; Cross-Sectional Studies; Environmental Exposure; Female; Follow-Up Studies; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Polymorphism, Single Nucleotide; Prognosis; Risk Factors; Tumor Suppressor Protein p53	2020
Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotype. American journal of medical genetics. Part A, 2021, Volume: 185, Issue:10 Topics: Adolescent; Arginine; Child; Child, Preschool; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Hypertrichosis; Intellectual Disability; Megalencephaly; Musculoskeletal Abnormalities; Mutation, Missense; Phenotype; Potassium Channels, Sodium-Activated	2021
Molecular basis for increased susceptibility of Indigenous North Americans to seropositive rheumatoid arthritis. Annals of the rheumatic diseases, 2017, Volume: 76, Issue:11 Topics: Alaska; Alaskan Natives; Alleles; Arginine; Arthritis, Rheumatoid; Autoantibodies; Canada; Case-Control Studies; CD4-Positive T-Lymphocytes; Citrulline; Female; Flow Cytometry; Genetic Predisposition to Disease; Genotype; HLA-DRB1 Chains; Humans; Indians, North American; Male; Peptides, Cyclic; Polymorphism, Genetic; Risk Factors; Vimentin	2017
Cardiomyocyte dimethylarginine dimethylaminohydrolase-1 (DDAH1) plays an important role in attenuating ventricular hypertrophy and dysfunction. Basic research in cardiology, 2017, 08-17, Volume: 112, Issue:5 Topics: Amidohydrolases; Animals; Arginine; Atrial Natriuretic Factor; Disease Models, Animal; Fibrosis; Genetic Predisposition to Disease; Hypertrophy, Left Ventricular; Male; Mice, Knockout; Myocytes, Cardiac; Nitric Oxide; Phenotype; Signal Transduction; Tyrosine; Ventricular Dysfunction, Left; Ventricular Function, Left; Ventricular Remodeling	2017
Influence on serum asymmetric dimethylarginine (ADMA) concentrations of human paraoxonase 1 polymorphism (Q192R) and exposure to polycyclic aromatic hydrocarbons (PAHs) in Mexican women, a gene-environment interaction. Chemosphere, 2017, Volume: 186 Topics: Adult; Alleles; Arginine; Aryldialkylphosphatase; Biomarkers; Cardiovascular Diseases; Creatinine; Environmental Exposure; Environmental Pollutants; Female; Gene Frequency; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Mexico; Polycyclic Aromatic Hydrocarbons; Polymorphism, Genetic; Pyrenes; Risk Factors	2017
Major surgery diminishes systemic arginine availability and suppresses nitric oxide response to feeding in patients with early stage breast cancer. Clinical nutrition (Edinburgh, Scotland), 2018, Volume: 37, Issue:5 Topics: Adult; Arginine; Breast Neoplasms; Citrulline; Female; Genetic Predisposition to Disease; Glutamine; Humans; Mastectomy; Metabolic Clearance Rate; Middle Aged; Nitric Oxide; Postoperative Complications; Postprandial Period	2018
Obesity-induced vascular dysfunction and arterial stiffening requires endothelial cell arginase 1. Cardiovascular research, 2017, Nov-01, Volume: 113, Issue:13 Topics: Animals; Arginase; Arginine; Blood Glucose; Blood Pressure; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Diet, High-Fat; Dietary Sucrose; Endothelium, Vascular; Enzyme Inhibitors; Fibrosis; Genetic Predisposition to Disease; Insulin; Male; Metabolic Syndrome; Mice, Inbred C57BL; Mice, Knockout; Nitric Oxide; Obesity; Ornithine; Oxidative Stress; Phenotype; Signal Transduction; Vascular Diseases; Vascular Stiffness; Vasodilation	2017
Anticitrullinated protein/peptide antibody multiplexing defines an extended group of ACPA-positive rheumatoid arthritis patients with distinct genetic and environmental determinants. Annals of the rheumatic diseases, 2018, Volume: 77, Issue:2 Topics: Adolescent; Adult; Aged; Alleles; Anti-Citrullinated Protein Antibodies; Arginine; Arthritis, Rheumatoid; Case-Control Studies; Female; Genetic Predisposition to Disease; Genotype; HLA-DRB1 Chains; Humans; Male; Middle Aged; Protein Array Analysis; Sensitivity and Specificity; Smoking; Young Adult	2018
Mitochondrial Dysfunction, Through Impaired Autophagy, Leads to Endoplasmic Reticulum Stress, Deregulated Lipid Metabolism, and Pancreatitis in Animal Models. Gastroenterology, 2018, Volume: 154, Issue:3 Topics: Acute Disease; Animals; Arginine; Autophagy; Bile Acids and Salts; Calcium Signaling; Ceruletide; Choline Deficiency; Cyclophilins; Disease Models, Animal; Endoplasmic Reticulum Stress; Ethionine; Genetic Predisposition to Disease; Humans; Lipid Metabolism; Membrane Potential, Mitochondrial; Mice, Inbred C57BL; Mice, Knockout; Mitochondria; Mitochondrial Proton-Translocating ATPases; Pancreas; Pancreatitis; Peptidyl-Prolyl Isomerase F; Phenotype; Rats; Time Factors; Trehalose	2018
ADMA reduction does not protect mice with streptozotocin-induced diabetes mellitus from development of diabetic nephropathy. Atherosclerosis. Supplements, 2017, Volume: 30 Topics: Albuminuria; Amidohydrolases; Animals; Arginine; Cell Proliferation; Creatinine; Diabetes Mellitus, Experimental; Diabetic Nephropathies; Disease Progression; Down-Regulation; Genetic Predisposition to Disease; Glomerular Mesangium; Glomerulonephritis; Hydrolysis; Kidney; Male; Mice, Inbred C57BL; Mice, Transgenic; Phenotype; Streptozocin	2017
MAX Mutations in Endometrial Cancer: Clinicopathologic Associations and Recurrent MAX p.His28Arg Functional Characterization. Journal of the National Cancer Institute, 2018, 05-01, Volume: 110, Issue:5 Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Animals; Animals, Outbred Strains; Arginine; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Carcinoma, Endometrioid; Cells, Cultured; Codon, Nonsense; Endometrial Neoplasms; Female; Genetic Association Studies; Genetic Predisposition to Disease; HEK293 Cells; Histidine; Humans; Mice; Mice, Nude; Middle Aged; Neoplasm Invasiveness; Neovascularization, Pathologic	2018
High prevalence of dengue antibodies and the arginine variant of the FcγRIIa polymorphism in asymptomatic individuals in a population of Minas Gerais State, Southeast Brazil. Immunogenetics, 2018, Volume: 70, Issue:6 Topics: Adult; Arginine; Brazil; Cell Adhesion Molecules; Dengue; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Lectins, C-Type; Male; Middle Aged; Polymorphism, Single Nucleotide; Prevalence; Receptors, Calcitriol; Receptors, Cell Surface; Receptors, IgG; Tumor Necrosis Factor-alpha	2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. Genetics in medicine : official journal of the American College of Medical Genetics, 2018, Volume: 20, Issue:10 Topics: Actins; Adolescent; Adult; Aortic Aneurysm, Thoracic; Arginine; Child; Child, Preschool; Ductus Arteriosus, Patent; Eye Diseases, Hereditary; Genetic Predisposition to Disease; Genetic Testing; Humans; Infant; Medical Records; Muscle, Smooth; Mydriasis; Young Adult	2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome. Neurogenetics, 2018, Volume: 19, Issue:3 Topics: Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Cells, Cultured; Child; Child, Preschool; Consanguinity; Cysteine; Female; Follow-Up Studies; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation, Missense; Neuroaxonal Dystrophies; Pedigree; Proteins; Siblings; Spastic Paraplegia, Hereditary	2018
Arg399Gln substitution in XRCC1 as a prognostic and predictive biomarker for prostate cancer: Evidence from 8662 subjects and a structural analysis. The journal of gene medicine, 2018, Volume: 20, Issue:10-11 Topics: Alleles; Amino Acid Substitution; Arginine; Case-Control Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Iran; Male; Meta-Analysis as Topic; Odds Ratio; Polymorphism, Single Nucleotide; Prognosis; Prostatic Neoplasms; Risk Factors; X-ray Repair Cross Complementing Protein 1	2018
Arginine reprogramming in ADPKD results in arginine-dependent cystogenesis. American journal of physiology. Renal physiology, 2018, 12-01, Volume: 315, Issue:6 Topics: Animals; Arginine; Argininosuccinate Synthase; Cell Proliferation; Cells, Cultured; Disease Models, Animal; Energy Metabolism; Female; Genetic Predisposition to Disease; Humans; Kidney; Male; Metabolomics; Mice, Knockout; Phenotype; Polycystic Kidney, Autosomal Dominant; Receptors, Cell Surface; Signal Transduction; TRPP Cation Channels	2018
Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies. Human mutation, 2019, Volume: 40, Issue:6 Topics: Amyloidosis, Familial; Arginine; Corneal Dystrophies, Hereditary; Databases, Genetic; Extracellular Matrix Proteins; Female; Genetic Predisposition to Disease; Humans; Male; Mutation; Pedigree; Phenotype; Transforming Growth Factor beta; Web Browser	2019
Arginine homozygosity in codon 72 of p53 correlates with failure to imatinib response in chronic myeloid leukemia. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2013, Volume: 67, Issue:2 Topics: Adult; Alleles; Antineoplastic Agents; Arginine; Benzamides; Codon; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Male; Piperazines; Polymorphism, Genetic; Proline; Pyrimidines; Tumor Suppressor Protein p53	2013
The endothelial nitric oxide synthase T-786c mutation, a treatable etiology of Prinzmetal's angina. Translational research : the journal of laboratory and clinical medicine, 2013, Volume: 162, Issue:1 Topics: Angina Pectoris, Variant; Arginine; Calcium Channel Blockers; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation; Nitrates; Nitric Oxide Synthase Type III; Surveys and Questionnaires	2013
Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. Epilepsia, 2013, Volume: 54, Issue:7 Topics: Adolescent; Animals; Arginine; Cell Line; Child; Child, Preschool; Epilepsy; Ether-A-Go-Go Potassium Channels; Exome; Female; Genetic Predisposition to Disease; Guanine Nucleotide Exchange Factors; Humans; Infant; Male; Membrane Potentials; Mutation; Oocytes; Patch-Clamp Techniques; Protein Serine-Threonine Kinases; rhoA GTP-Binding Protein; Sequence Analysis, DNA; Transduction, Genetic; Transfection; Xenopus laevis	2013
XRCC1 Arg194Trp and Arg399Gln polymorphisms are significantly associated with shorter survival in acute myeloid leukemia. Leukemia & lymphoma, 2014, Volume: 55, Issue:2 Topics: Acute Disease; Adult; Aged; Amino Acid Substitution; Arginine; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leukemia, Myeloid; Male; Middle Aged; Polymorphism, Genetic; Risk Factors; Survival Analysis; Tryptophan; X-ray Repair Cross Complementing Protein 1	2014
P53 (Pro72Arg) polymorphism associated with the risk of oral squamous cell carcinoma in gutka, niswar and manpuri addicted patients of Pakistan. Oral oncology, 2013, Volume: 49, Issue:8 Topics: Areca; Arginine; Base Sequence; Carcinoma, Squamous Cell; Cocarcinogenesis; DNA Primers; Genes, p53; Genetic Predisposition to Disease; Humans; Mouth Neoplasms; Pakistan; Polymerase Chain Reaction; Polymorphism, Genetic; Proline	2013
Effect of metabolic abnormalities on endothelial dysfunction in normotensive offspring of subject with hypertension. International angiology : a journal of the International Union of Angiology, 2013, Volume: 32, Issue:4 Topics: Adiponectin; Adult; Arginine; Biomarkers; Brachial Artery; Case-Control Studies; Disease Progression; Female; Genetic Predisposition to Disease; Heredity; Humans; Hyperemia; Hyperinsulinism; Hypertension; Insulin; Insulin Resistance; Linear Models; Male; Multivariate Analysis; Pedigree; Phenotype; Risk Factors; Ultrasonography; Vasodilation	2013
Dissecting the genetic predisposition to albuminuria and endothelial dysfunction in a genetic rat model. Journal of hypertension, 2013, Volume: 31, Issue:11 Topics: Acetylcholine; Albuminuria; Animals; Aorta; Arginine; Endothelium, Vascular; Genetic Predisposition to Disease; Indomethacin; Male; Nitric Oxide; Quantitative Trait Loci; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Superoxides; Vascular Diseases	2013
DNA repair gene polymorphisms and risk of head and neck cancer in the Tunisian population. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2014, Volume: 43, Issue:3 Topics: Adenine; Adolescent; Adult; Aged; Aged, 80 and over; Alcohol Drinking; Arginine; Case-Control Studies; DNA Helicases; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Glutamine; Guanine; Head and Neck Neoplasms; Humans; Lysine; Male; Middle Aged; Occupational Exposure; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Smoking; X-ray Repair Cross Complementing Protein 1; Xeroderma Pigmentosum Group D Protein; Young Adult	2014
Clinical relevance and functional consequences of the TNFRSF1A multiple sclerosis locus. Neurology, 2013, Nov-26, Volume: 81, Issue:22 Topics: Animals; Arginine; Chemokine CXCL10; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Genotype; Glutamine; HEK293 Cells; Humans; Immunologic Factors; Longitudinal Studies; Male; Monocytes; Multiple Sclerosis; Mutation; Phorbol Esters; Receptors, Tumor Necrosis Factor, Type I; RNA Isoforms; Signal Transduction; Tumor Necrosis Factor-alpha	2013
The codon 399 Arg/Gln XRCC1 polymorphism is associated with lung cancer in Indians. Asian Pacific journal of cancer prevention : APJCP, 2013, Volume: 14, Issue:9 Topics: Adenocarcinoma; Arginine; Carcinoma, Non-Small-Cell Lung; Carcinoma, Squamous Cell; Case-Control Studies; Codon; DNA; DNA-Binding Proteins; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; India; Lung Neoplasms; Male; Middle Aged; Neoplasm Staging; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Prognosis; Risk Factors; Survival Rate; X-ray Repair Cross Complementing Protein 1	2013
Synergistic effect of LEP and LEPR gene polymorphism on body mass index in a Chinese population. Obesity research & clinical practice, 2013, Volume: 7, Issue:6 Topics: Adult; Alleles; Arginine; Asian People; Asparagine; Body Mass Index; China; Female; Genetic Predisposition to Disease; Genotype; Humans; Leptin; Logistic Models; Lysine; Male; Obesity; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Polymorphism, Single-Stranded Conformational; Prevalence; Receptors, Leptin; Risk Factors; Waist-Hip Ratio	2013
Phenotypic variability and risk of malignancy in SDHC-linked paragangliomas: lessons from three unrelated cases with an identical germline mutation (p.Arg133). The Journal of clinical endocrinology and metabolism, 2014, Volume: 99, Issue:3* Topics: Arginine; Female; Genetic Heterogeneity; Genetic Predisposition to Disease; Germ-Line Mutation; Glomus Jugulare Tumor; Head and Neck Neoplasms; Heart Neoplasms; Humans; Loss of Heterozygosity; Lumbar Vertebrae; Male; Membrane Proteins; Middle Aged; Paraganglioma; Phenotype; Risk Factors; Spinal Neoplasms	2014
Dental caries and enamelin haplotype. Journal of dental research, 2014, Volume: 93, Issue:4 Topics: Amino Acid Substitution; Arginine; Child; Dental Caries; Dental Caries Susceptibility; DMF Index; Exons; Extracellular Matrix Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Haplotypes; Humans; Introns; Isoleucine; Linkage Disequilibrium; Male; Mutation, Missense; Polymorphism, Single Nucleotide; Proteins; Threonine; Young Adult	2014
Arg972 insulin receptor substrate-1 polymorphism and risk and severity of Alzheimer's disease. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2014, Volume: 21, Issue:7 Topics: Age Factors; Aged; Aged, 80 and over; Alzheimer Disease; Arginine; China; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin Receptor Substrate Proteins; Male; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Retrospective Studies	2014
[Study of codon 72 of p53 gene as a risk-factor in cervical cancer in Senegal]. Bulletin du cancer, 2014, Volume: 101, Issue:9 Topics: Adult; Age Distribution; Aged; Aged, 80 and over; Alleles; Arginine; Case-Control Studies; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Polymorphism, Genetic; Risk Factors; Senegal; Uterine Cervical Neoplasms	2014
A common polymorphism in extracellular superoxide dismutase affects cardiopulmonary disease risk by altering protein distribution. Circulation. Cardiovascular genetics, 2014, Volume: 7, Issue:5 Topics: Animals; Antioxidants; Arginine; Bronchoalveolar Lavage Fluid; Genetic Predisposition to Disease; Genotype; Glycine; Heparin; Humans; Hypertension, Pulmonary; Lung; Mice; Mice, Inbred C57BL; Mice, Transgenic; Polymorphism, Single Nucleotide; Risk Factors; Sepharose; Sequence Analysis, DNA; Superoxide Dismutase	2014
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia. Alzheimer's & dementia : the journal of the Alzheimer's Association, 2014, Volume: 10, Issue:6 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arginine; Brain; Cohort Studies; Creutzfeldt-Jakob Syndrome; Exons; Female; Frontotemporal Dementia; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Genotype; Histidine; Humans; Male; Membrane Glycoproteins; Middle Aged; Phenotype; Receptors, Immunologic; Risk Factors	2014
Chaperone therapy for homocystinuria: the rescue of CBS mutations by heme arginate. Journal of inherited metabolic disease, 2015, Volume: 38, Issue:2 Topics: Animals; Arginine; Catalytic Domain; CHO Cells; Cricetulus; Cystathionine beta-Synthase; Female; Fibroblasts; Genetic Predisposition to Disease; Heme; Homocystinuria; Homozygote; Humans; Models, Molecular; Molecular Chaperones; Mutation; Phenotype; Protein Conformation; Protein Folding; Proteostasis Deficiencies; Structure-Activity Relationship; Substrate Specificity; Transfection	2015
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study. Parkinsonism & related disorders, 2015, Volume: 21, Issue:3 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Cross-Sectional Studies; DNA Mutational Analysis; Essential Tremor; Female; Genetic Predisposition to Disease; Genotype; Germany; Histidine; Humans; International Cooperation; Italy; Male; Membrane Glycoproteins; Middle Aged; North America; Receptors, Immunologic; Risk Factors; Spain; Taiwan; Young Adult	2015
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human molecular genetics, 2015, Oct-01, Volume: 24, Issue:19 Topics: Adenosine Triphosphate; Amino Acid Substitution; Arginine; Australasia; Binding Sites; Genetic Association Studies; Genetic Predisposition to Disease; Glutamine; Humans; Models, Molecular; Multiple Sclerosis; Receptors, Purinergic P2X7; White People	2015
A robust distribution-free test for genetic association studies of quantitative traits. Statistical applications in genetics and molecular biology, 2015, Volume: 14, Issue:5 Topics: Arginine; Case-Control Studies; Computer Simulation; Data Interpretation, Statistical; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Models, Genetic; Models, Statistical; Monte Carlo Method; Phenotype; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Transaminases	2015
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia. Neuromuscular disorders : NMD, 2016, Volume: 26, Issue:1 Topics: Anesthetics; Arginine; B-Lymphocytes; Caffeine; Cell Line, Transformed; Cresols; Family Health; Female; Fungicides, Industrial; Genetic Predisposition to Disease; Germany; Halothane; Humans; Male; Malignant Hyperthermia; Muscle Contraction; Muscle, Skeletal; Phosphodiesterase Inhibitors; Polymorphism, Single Nucleotide; Ryanodine Receptor Calcium Release Channel; Tryptophan	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
[Association of the Arg399Gln polymorphisms of the XRCC1 gene with breast cancer risk in Kyrgiz women]. Voprosy onkologii, 2015, Volume: 61, Issue:6 Topics: Adult; Aged; Alleles; Arginine; Breast Neoplasms; DNA-Binding Proteins; DNA, Neoplasm; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Heterozygote; Humans; Kyrgyzstan; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Risk Assessment; Risk Factors; X-ray Repair Cross Complementing Protein 1	2015
The His131Arg substitution in the FCGR2A gene (rs1801274) is not associated with the severity of influenza A(H1N1)pdm09 infection. BMC research notes, 2016, Jun-07, Volume: 9 Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Child; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Host-Pathogen Interactions; Humans; Influenza A Virus, H1N1 Subtype; Influenza, Human; Logistic Models; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, IgG; Severity of Illness Index; Young Adult	2016
Association of rs1137101 polymorphism in LEPR and susceptibility to knee osteoarthritis in a Northwest Chinese Han population. BMC musculoskeletal disorders, 2016, 07-25, Volume: 17 Topics: Aged; Amplified Fragment Length Polymorphism Analysis; Arginine; Asian People; Biomarkers; Case-Control Studies; Ethnicity; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Middle Aged; Osteoarthritis, Knee; Polymorphism, Single Nucleotide; Receptors, Leptin; Sequence Analysis, DNA; Sex Factors	2016
PADI4 has genetic susceptibility to gastric carcinoma and upregulates CXCR2, KRT14 and TNF-α expression levels. Oncotarget, 2016, Sep-20, Volume: 7, Issue:38 Topics: Apoptosis; Arginine; Carcinogenesis; Carcinoma; Cell Line, Tumor; Cell Proliferation; Citrulline; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Genotyping Techniques; Humans; Keratin-14; Neovascularization, Pathologic; Polymorphism, Single Nucleotide; Protein-Arginine Deiminase Type 4; Protein-Arginine Deiminases; Receptors, Interleukin-8B; RNA Interference; RNA, Small Interfering; Signal Transduction; Stomach Neoplasms; Tumor Necrosis Factor-alpha; Up-Regulation	2016
Olfactory Dysfunction in Parkinson's Disease Patients with the LRRK2 G2385R Variant. Neuroscience bulletin, 2016, Volume: 32, Issue:6 Topics: Aged; Aged, 80 and over; Arginine; Female; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Olfaction Disorders; Parkinson Disease; Polymorphism, Single Nucleotide; Sensory Thresholds	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 COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population. Genetics and molecular research : GMR, 2016, Dec-19, Volume: 15, Issue:4 Topics: Adult; Arginine; Asian People; Case-Control Studies; Collagen Type IX; Female; Genetic Predisposition to Disease; Glutamine; Humans; Intervertebral Disc Degeneration; Intervertebral Disc Displacement; Male; Middle Aged; Mutation	2016
Mutation in a highly conserved glycine residue in strand 5B of plasminogen activator inhibitor 1 causes polymerisation. Thrombosis and haemostasis, 2017, 05-03, Volume: 117, Issue:5 Topics: Aged; Amino Acid Substitution; Animals; Arginine; Chlorocebus aethiops; Conserved Sequence; COS Cells; Cytosine; DNA Mutational Analysis; Exons; Female; Genetic Predisposition to Disease; Glycine; Guanine; Hemorrhage; Hemostasis; Homozygote; Humans; Models, Molecular; Molecular Weight; Mutation; Phenotype; Plasminogen Activator Inhibitor 1; Polymerization; Protein Conformation; Structure-Activity Relationship; Transfection	2017
Differential coupling of Arg- and Gly389 polymorphic forms of the beta1-adrenergic receptor leads to pathogenic cardiac gene regulatory programs. Physiological genomics, 2008, Sep-17, Volume: 35, Issue:1 Topics: Animals; Arginine; Gene Regulatory Networks; Genetic Predisposition to Disease; Glycine; Humans; Mice; Mice, Transgenic; Myocardium; Polymorphism, Genetic; Receptors, Adrenergic, beta-1	2008
Ethnicity determines association of p53Arg72Pro alleles with cervical cancer in China. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP), 2008, Volume: 17, Issue:5 Topics: Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Arginine; Base Sequence; Carcinoma; Case-Control Studies; China; Female; Genes, p53; Genetic Linkage; Genetic Predisposition to Disease; Humans; Middle Aged; Molecular Sequence Data; Polymorphism, Single Nucleotide; Proline; Uterine Cervical Neoplasms	2008
Association between lysyl oxidase polymorphisms and oral submucous fibrosis in older male areca chewers. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2009, Volume: 38, Issue:1 Topics: Adenine; Age Factors; Alleles; Amino Acid Sequence; Areca; Arginine; Genetic Predisposition to Disease; Genotype; Glutamine; Guanine; Heterozygote; Humans; Male; Middle Aged; Oral Submucous Fibrosis; Polymorphism, Single Nucleotide; Precancerous Conditions; Protein-Lysine 6-Oxidase; Risk Factors	2009
P2RX7 Gln460Arg polymorphism is associated with depression among diabetic patients. Progress in neuro-psychopharmacology & biological psychiatry, 2008, Dec-12, Volume: 32, Issue:8 Topics: Arginine; Brain-Derived Neurotrophic Factor; Depression; Diabetes Complications; Diabetes Mellitus; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Multivariate Analysis; Polymorphism, Genetic; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Serotonin Plasma Membrane Transport Proteins; Tryptophan Hydroxylase	2008
p53 codon 72 proline/arginine polymorphism and autoimmune thyroid diseases. Journal of clinical laboratory analysis, 2008, Volume: 22, Issue:5 Topics: Adolescent; Adult; Aged; Arginine; Codon; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genotype; Hashimoto Disease; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Thyroiditis, Autoimmune; Tumor Suppressor Protein p53	2008
Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients. Parkinsonism & related disorders, 2009, Volume: 15, Issue:4 Topics: Adult; Age Factors; Aged; Aged, 80 and over; Arginine; Cysteine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glycine; Humans; Italy; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Population Groups; Protein Serine-Threonine Kinases; Serine; Tomography, Emission-Computed, Single-Photon	2009
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism. Parkinsonism & related disorders, 2009, Volume: 15, Issue:6 Topics: Adult; Arginine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Histidine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinsonian Disorders; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases	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
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction. Journal of the neurological sciences, 2009, Jan-15, Volume: 276, Issue:1-2 Topics: Adult; Amyotrophic Lateral Sclerosis; Arginine; Cytochromes c; DNA Mutational Analysis; Family Health; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mitochondria, Muscle; Mitochondrial Diseases; Mutation; Superoxide Dismutase; Superoxide Dismutase-1	2009
Leptin receptor Gln223Arg polymorphism and breast cancer risk in Nigerian women: a case control study. BMC cancer, 2008, Nov-18, Volume: 8 Topics: Arginine; Breast Neoplasms; Carcinoma, Ductal, Breast; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Nigeria; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Postmenopause; Premenopause; Receptors, Leptin; Risk Factors; Signal Transduction	2008
Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases. Neurology, 2008, Nov-25, Volume: 71, Issue:22 Topics: Adult; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Arginine; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Glatiramer Acetate; Glutamine; HLA-D Antigens; Humans; Immunosuppressive Agents; Male; Middle Aged; Mitoxantrone; Multiple Sclerosis; Mutation; Natalizumab; Penetrance; Peptides; Phenotype; Receptors, Tumor Necrosis Factor, Type I; Sequence Analysis, DNA; Young Adult	2008
Relation between human vasopressin 1a gene variance, fat intake, and diabetes. The American journal of clinical nutrition, 2009, Volume: 89, Issue:1 Topics: Alleles; Animals; Arginine; Blood Glucose; Body Mass Index; Cohort Studies; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Dietary Fats; Female; Genetic Predisposition to Disease; Genetic Variation; Humans; Hypertriglyceridemia; Male; Mice; Mice, Knockout; Middle Aged; Obesity; Polymorphism, Single Nucleotide; Prevalence; Prospective Studies; Receptors, Vasopressin; Triglycerides	2009
A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy. Epilepsy research, 2009, Volume: 83, Issue:2-3 Topics: Adolescent; Adult; Arginine; Child; Child, Preschool; DNA Mutational Analysis; Electroencephalography; Epilepsy, Frontal Lobe; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histidine; Humans; Infant; Male; Mutation, Missense; Receptors, Nicotinic; Young Adult	2009
TP53 codon 72 polymorphism in adult soft tissue sarcomas. Genetics and molecular research : GMR, 2008, Volume: 7, Issue:4 Topics: Adult; Aged; Aged, 80 and over; Arginine; Codon; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Sarcoma; Tumor Suppressor Protein p53; Young Adult	2008
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis. Neurology, 2009, May-05, Volume: 72, Issue:18 Topics: Adolescent; Amino Acid Sequence; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Inheritance Patterns; Ion Channel Gating; Membrane Potentials; Muscle Contraction; Muscle, Skeletal; Mutation; NAV1.4 Voltage-Gated Sodium Channel; Paralysis, Hyperkalemic Periodic; Protein Structure, Tertiary; Sodium Channels; Young Adult	2009
Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis. PLoS genetics, 2009, Volume: 5, Issue:1 Topics: Age of Onset; Alleles; Animals; Arginine; Atherosclerosis; Female; Genetic Predisposition to Disease; Genotype; Humans; Linkage Disequilibrium; Lod Score; Male; Mice; Mice, Transgenic; Middle Aged; Neuropeptide Y; Polymorphism, Genetic; Receptors, Neuropeptide Y	2009
Disseminated and rapidly fatal tuberculosis in mice bearing a defective allele at IFN regulatory factor 8. Journal of immunology (Baltimore, Md. : 1950), 2009, Mar-01, Volume: 182, Issue:5 Topics: Alleles; Amino Acid Substitution; Animals; Arginine; Cysteine; Female; Genetic Predisposition to Disease; Interferon Regulatory Factors; Interferons; Liver; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred DBA; Mutation; Mycobacterium tuberculosis; Spleen; Tuberculosis, Pulmonary; Virulence	2009
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society, 2009, May-15, Volume: 24, Issue:7 Topics: Aged; Arginine; DNA Mutational Analysis; Exons; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Japan; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Meta-Analysis as Topic; Middle Aged; Models, Statistical; Molecular Sequence Data; Mutation; Parkinson Disease; Protein Serine-Threonine Kinases; Risk Factors	2009
Cancer. Puzzling patterns of predisposition. Science (New York, N.Y.), 2009, Apr-10, Volume: 324, Issue:5924 Topics: Amino Acid Substitution; Arginine; Brain Neoplasms; Citric Acid Cycle; Dinucleoside Phosphates; Fumarate Hydratase; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Glioblastoma; Glutamates; Humans; Hydroxylation; Hypoxia-Inducible Factor 1; Isocitrate Dehydrogenase; Mutation; NADP; Oncogenes; Succinate Dehydrogenase	2009
Getting a charge out of periodic paralysis? Neurology, 2009, May-05, Volume: 72, Issue:18 Topics: Arginine; Calcium Channels; Calcium Channels, L-Type; DNA Mutational Analysis; Genetic Predisposition to Disease; Genetic Testing; Humans; Hypokalemic Periodic Paralysis; Ion Channel Gating; Membrane Potentials; Muscle, Skeletal; Mutation; NAV1.4 Voltage-Gated Sodium Channel; Sodium Channels	2009
The polymorphism of DNA repair gene ERCC2/XPD Arg156Arg and susceptibility to breast cancer in a Chinese population. Biochemical genetics, 2009, Volume: 47, Issue:7-8 Topics: Adult; Age of Onset; Alleles; Arginine; Asian People; Breast Neoplasms; Case-Control Studies; DNA Repair; Female; Genetic Markers; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Polymorphism, Genetic; Xeroderma Pigmentosum Group D Protein	2009
[The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy]. Yi chuan = Hereditas, 2009, Volume: 31, Issue:5 Topics: Adult; Amino Acid Sequence; Animals; Arginine; Cardiac Myosins; Cardiomyopathy, Hypertrophic, Familial; Cattle; Dogs; Female; Genetic Predisposition to Disease; Glycine; Humans; Male; Mice; Mutation, Missense; Myosin Heavy Chains; Rats; Sequence Alignment; Swine	2009
Association between genetic polymorphism of XRCC1 Arg194Trp and risk of schizophrenia. Psychiatry research, 2009, Sep-30, Volume: 169, Issue:2 Topics: Arginine; Case-Control Studies; Chi-Square Distribution; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Polymorphism, Single Nucleotide; Risk Factors; Schizophrenia; Tryptophan; X-ray Repair Cross Complementing Protein 1	2009
Analysis of the LRRK2 Gly2385Arg variant in Alzheimer's disease in Taiwan. Parkinsonism & related disorders, 2010, Volume: 16, Issue:1 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arginine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Taiwan	2010
The unfolding of the prion protein sheds light on the mechanisms of prion susceptibility and species barrier. Biochemistry, 2009, Sep-15, Volume: 48, Issue:36 Topics: Animals; Arginine; Cricetinae; Genetic Predisposition to Disease; Glutamine; Mice; Mutagenesis, Site-Directed; Prion Diseases; Prion Proteins; Prions; Protein Denaturation; Protein Folding; Species Specificity; Thermodynamics; Tryptophan	2009
Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers. Journal of cancer research and clinical oncology, 2010, Volume: 136, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Biomarkers, Tumor; Case-Control Studies; Colorectal Neoplasms; Esophageal Neoplasms; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Head and Neck Neoplasms; Humans; Incidence; Isoleucine; Japan; Lung Neoplasms; Male; Methionine; Middle Aged; Neoplasms; Polymorphism, Single Nucleotide; Proline; Protein Tyrosine Phosphatase, Non-Receptor Type 13; Receptor-Like Protein Tyrosine Phosphatases, Class 3; Risk Factors	2010
LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China. Movement disorders : official journal of the Movement Disorder Society, 2009, Oct-15, Volume: 24, Issue:13 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Asian People; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Proline; Protein Serine-Threonine Kinases; Young Adult	2009
Polymorphisms of XRCC1 gene and risk of gastric cardiac adenocarcinoma. Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus, 2009, Volume: 22, Issue:5 Topics: Adenine; Adenocarcinoma; Adult; Aged; Arginine; Cardia; Case-Control Studies; Codon; Cytosine; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; Histidine; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Smoking; Stomach Neoplasms; Thymine; Tryptophan; X-ray Repair Cross Complementing Protein 1	2009
Association of Gly972Arg polymorphism of IRS1 gene with type 2 diabetes mellitus in lean participants of a national health survey in Mexico: a candidate gene study. Metabolism: clinical and experimental, 2010, Volume: 59, Issue:1 Topics: Aged; Arginine; Body Mass Index; Diabetes Mellitus, Type 2; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Health Surveys; Humans; Insulin Receptor Substrate Proteins; Logistic Models; Mexico; Middle Aged; Polymorphism, Single Nucleotide	2010
Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation. Anesthesia and analgesia, 2009, Volume: 109, Issue:4 Topics: Amino Acid Substitution; Anesthetics, Inhalation; Arginine; Carnitine O-Palmitoyltransferase; Child, Preschool; Cysteine; Female; Genetic Predisposition to Disease; Halothane; Heterozygote; Humans; Malignant Hyperthermia; Metabolism, Inborn Errors; Mutation; Neuromuscular Depolarizing Agents; Risk Factors; Succinylcholine; Syndrome	2009
The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population. Parkinsonism & related disorders, 2010, Volume: 16, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Korea; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinson Disease; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Risk Factors; Young Adult	2010
Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2010, Volume: 14, Issue:4 Topics: Arginine; Choline O-Acetyltransferase; Electric Stimulation; Electroencephalography; Enzyme Inhibitors; Female; Genetic Predisposition to Disease; Genetic Testing; Glycine; Histidine; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Male; Muscle, Skeletal; Mutation; Myasthenic Syndromes, Congenital; Receptor Protein-Tyrosine Kinases; Receptors, Cholinergic	2010
Leptin G-2548A and leptin receptor Q223R gene polymorphisms are not associated with obesity in Romanian subjects. Biochemical and biophysical research communications, 2010, Jan-01, Volume: 391, Issue:1 Topics: Adult; Arginine; Body Mass Index; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Leptin; Male; Middle Aged; Obesity; Polymorphism, Single Nucleotide; Receptors, Leptin; Romania; White People	2010
Dynamics of the interaction of human IgG subtype immune complexes with cells expressing R and H allelic forms of a low-affinity Fc gamma receptor CD32A. Journal of immunology (Baltimore, Md. : 1950), 2009, Dec-15, Volume: 183, Issue:12 Topics: Alleles; Animals; Antigen-Antibody Complex; Arginine; Autoimmune Diseases; Bacterial Infections; Binding, Competitive; Cell Line; Cell Membrane; CHO Cells; Cricetinae; Cricetulus; Dimerization; Genetic Predisposition to Disease; Histidine; Humans; Immunoglobulin G; Ligands; Polymorphism, Genetic; Protein Binding; Receptors, IgG; Recombinant Fusion Proteins	2009
Genetic polymorphisms of DNA repair gene XRCC1 and risk of uterine leiomyoma. Molecular and cellular biochemistry, 2010, Volume: 338, Issue:1-2 Topics: Adult; Aged; Arginine; Asian People; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Leiomyoma; Middle Aged; Odds Ratio; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; X-ray Repair Cross Complementing Protein 1	2010
Pathogenic cysteine mutations affect progranulin function and production of mature granulins. Journal of neurochemistry, 2010, Volume: 112, Issue:5 Topics: Animals; Arginine; Axons; Brain; Cell Enlargement; Cell Line, Transformed; Cysteine; Dithiothreitol; Embryo, Mammalian; Enzyme-Linked Immunosorbent Assay; Family Health; Frontotemporal Dementia; Gene Expression Regulation; Genetic Predisposition to Disease; Green Fluorescent Proteins; Humans; Intercellular Signaling Peptides and Proteins; Motor Neurons; Mutation; Neurites; Pancreatic Elastase; Progranulins; Rats; Rats, Wistar; RNA, Messenger; Transfection; Tyrosine	2010
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion. Neuromuscular disorders : NMD, 2010, Volume: 20, Issue:3 Topics: Adenosine Triphosphate; Arginine; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Muscle; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Mutagenesis, Site-Directed; Mutation; Thymidine Kinase; Tryptophan	2010
A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease. Circulation research, 2010, Apr-02, Volume: 106, Issue:6 Topics: Aged; Amidohydrolases; Arginine; Asian People; Binding Sites; Biomarkers; Case-Control Studies; Cells, Cultured; Chi-Square Distribution; China; Coronary Artery Disease; DNA Mutational Analysis; DNA-Binding Proteins; Female; Gene Expression Regulation, Enzymologic; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutagenesis, Insertional; Odds Ratio; Phenotype; Polymorphism, Genetic; Promoter Regions, Genetic; Risk Assessment; Risk Factors; Sequence Deletion; Stroke; Thrombosis; Transcription Factor MTF-1; Transcription Factors; Transcriptional Activation; Transfection	2010
Association of TP53 codon 72 polymorphism with cervical cancer risk in Chinese women. Cancer genetics and cytogenetics, 2010, Volume: 197, Issue:2 Topics: Adult; Arginine; Case-Control Studies; Chi-Square Distribution; China; Codon; Cohort Studies; Female; Genetic Predisposition to Disease; Humans; Middle Aged; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms	2010
Study of association of IRS-1 and IRS-2 genes polymorphisms with clinical and metabolic features in women with polycystic ovary syndrome. Is there an impact? Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 2010, Volume: 26, Issue:9 Topics: Adult; Amino Acid Substitution; Arginine; Aspartic Acid; Case-Control Studies; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Glycine; Greece; Humans; Insulin Receptor Substrate Proteins; Polycystic Ovary Syndrome; Polymorphism, Genetic; Young Adult	2010
Down but not out: candidate gene-based studies still have value in a world dominated by whole genome approaches. Circulation research, 2010, Apr-02, Volume: 106, Issue:6 Topics: Amidohydrolases; Arginine; Asian People; Biomarkers; China; Coronary Artery Disease; Evidence-Based Medicine; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Phenotype; Polymorphism, Genetic; Promoter Regions, Genetic; Risk Factors; Stroke; Thrombosis	2010
Association of P53 codon 72 polymorphism and ameloblastoma. Oral diseases, 2010, Volume: 16, Issue:7 Topics: Alleles; Ameloblastoma; Arginine; Codon; Cytosine; Double-Blind Method; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Guanine; Homozygote; Humans; Male; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proline; Sex Factors; Thailand; Tumor Suppressor Protein p53	2010
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy. Circulation, 2010, May-25, Volume: 121, Issue:20 Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Cardiomyopathies; Cardiomyopathy, Dilated; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Humans; Myocardium; Pedigree; Pregnancy; Pregnancy Complications; Puerperal Disorders; Troponin C	2010
The T1405N carbamoyl phosphate synthetase polymorphism does not affect plasma arginine concentrations in preterm infants. PloS one, 2010, May-25, Volume: 5, Issue:5 Topics: Amino Acid Substitution; Arginine; Carbamoyl-Phosphate Synthase (Ammonia); Female; Genetic Predisposition to Disease; Health; Humans; Infant, Newborn; Infant, Premature; Male; Polymorphism, Single Nucleotide; Pregnancy; Premature Birth; Urea	2010
Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2011, Volume: 24, Issue:2 Topics: Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Gestational Age; Glucuronosyltransferase; Glycine; Humans; Hyperbilirubinemia, Neonatal; Infant, Newborn; Male; Polymorphism, Single Nucleotide; Turkey	2011
The carriage of the type 1 diabetes-associated R262W variant of human LNK correlates with increased proliferation of peripheral blood monocytes in diabetic patients. Pediatric diabetes, 2011, Volume: 12, Issue:2 Topics: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Amino Acid Substitution; Arginine; Blood Cell Count; Case-Control Studies; Cell Proliferation; Child; Cross-Sectional Studies; Diabetes Mellitus, Type 1; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Intracellular Signaling Peptides and Proteins; Male; Monocytes; Polymorphism, Single Nucleotide; Proteins; Tryptophan; Up-Regulation; Young Adult	2011
Association of polymorphism of DNA repair gene XRCC1 with sporadic late-onset Alzheimer's disease and age of onset in elderly Han Chinese. Journal of the neurological sciences, 2010, Aug-15, Volume: 295, Issue:1-2 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Apolipoproteins E; Arginine; Asian People; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Humans; Male; Mental Status Schedule; Polymorphism, Genetic; Tryptophan; X-ray Repair Cross Complementing Protein 1	2010
XRCC1, but not APE1 and hOGG1 gene polymorphisms is a risk factor for pterygium. Molecular vision, 2010, Jun-04, Volume: 16 Topics: Aged; Aged, 80 and over; Alleles; Arginine; DNA Glycosylases; DNA-(Apurinic or Apyrimidinic Site) Lyase; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Pterygium; X-ray Repair Cross Complementing Protein 1	2010
LRRK2 Gly2385Arg polymorphism, cigarette smoking, and risk of sporadic Parkinson's disease: a case-control study in Japan. Journal of the neurological sciences, 2010, Oct-15, Volume: 297, Issue:1-2 Topics: Aged; Arginine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glycine; Humans; Japan; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinson Disease; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Retrospective Studies; Risk Factors; Smoking; Surveys and Questionnaires	2010
Shared molecular amino acid signature in the HLA-DR peptide binding pocket predisposes to both autoimmune diabetes and thyroiditis. Proceedings of the National Academy of Sciences of the United States of America, 2010, Sep-28, Volume: 107, Issue:39 Topics: Amino Acid Motifs; Arginine; Binding Sites; Diabetes Mellitus, Type 1; Female; Genetic Predisposition to Disease; HLA-DR Antigens; Humans; Male; Protein Binding; Protein Conformation; Sequence Analysis, Protein; Thyroiditis, Autoimmune	2010
Substitution (γ335Trp→Arg) in fibrinogen Fremantle causes diminished γ chain expression and increased sialic acid content. Thrombosis and haemostasis, 2010, Volume: 104, Issue:6 Topics: Adult; Amino Acid Substitution; Arginine; Blood Coagulation; Blood Coagulation Disorders, Inherited; Female; Fibrinogen; Fibrinogens, Abnormal; Genetic Predisposition to Disease; Heredity; Humans; Middle Aged; Mutation; N-Acetylneuraminic Acid; Pedigree; Phenotype; Protein Conformation; Structure-Activity Relationship; Tryptophan	2010
Membranoproliferative pattern of glomerular injury associated with complement component 9 deficiency due to Arg95Stop mutation. Clinical and experimental nephrology, 2011, Volume: 15, Issue:1 Topics: Adult; Arginine; Complement C9; DNA Mutational Analysis; Genetic Predisposition to Disease; Glomerulonephritis; Humans; Japan; Kidney Failure, Chronic; Male; Middle Aged; Mutation	2011
Latex allergy and filaggrin null mutations. Journal of dentistry, 2011, Volume: 39, Issue:2 Topics: Aerosols; Allergens; Arginine; Dental Assistants; Dentists; Dermatitis, Allergic Contact; Female; Filaggrin Proteins; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Hypersensitivity, Immediate; Intermediate Filament Proteins; Latex Hypersensitivity; Male; Mutation; Occupational Diseases; Occupational Exposure; Protein Precursors; Sequence Deletion	2011
Transgenic overexpression of Anks6(p.R823W) causes polycystic kidney disease in rats. The American journal of pathology, 2010, Volume: 177, Issue:6 Topics: Amino Acid Substitution; Animals; Arginine; Gene Expression; Genetic Predisposition to Disease; Male; Mutant Proteins; Nuclear Proteins; Polycystic Kidney Diseases; Polymorphism, Single Nucleotide; Rats; Rats, Sprague-Dawley; Rats, Transgenic; Tryptophan; Up-Regulation	2010
Role of TP53 Arg72Pro polymorphism in urinary bladder cancer predisposition and predictive impact of proline related genotype in advanced tumors in an ethnic Kashmiri population. Cancer genetics and cytogenetics, 2010, Volume: 203, Issue:2 Topics: Adult; Arginine; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Proline; Risk Factors; Smoking; Tumor Suppressor Protein p53; Urinary Bladder Neoplasms	2010
Genetic predisposition of white matter infarction with protein S deficiency and R355C mutation. Neurology, 2010, Dec-14, Volume: 75, Issue:24 Topics: Adolescent; Adult; Aged; Arginine; Brain; Cerebral Infarction; Child; Cysteine; Female; Genetic Predisposition to Disease; Haplotypes; Hong Kong; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Molecular Sequence Annotation; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Protein S; Protein S Deficiency; Risk Factors; Young Adult	2010
Neonatal cholestasis: an uncommon presentation of hyperargininemia. Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3 Topics: Amino Acids, Essential; Arginase; Arginine; Biomarkers; Child; Child Development; Child, Preschool; Cholestasis; Diet, Protein-Restricted; Disease Progression; End Stage Liver Disease; Female; Genetic Predisposition to Disease; Humans; Hyperargininemia; Hypertension, Portal; Infant; Infant, Newborn; Liver Cirrhosis, Biliary; Liver Transplantation; Neonatal Screening; Phenotype; Treatment Outcome	2010
The association of dimethylarginine dimethylaminohydrolase 1 gene polymorphism with type 2 diabetes: a cohort study. Cardiovascular diabetology, 2011, Feb-09, Volume: 10 Topics: Aged; Amidohydrolases; Analysis of Variance; Arginine; Biomarkers; Blood Glucose; Cardiovascular Diseases; Case-Control Studies; Chi-Square Distribution; Chromatography, High Pressure Liquid; Cohort Studies; Coronary Angiography; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Humans; Insulin; Insulin Resistance; Kaplan-Meier Estimate; Linear Models; Linkage Disequilibrium; Logistic Models; Male; Middle Aged; Odds Ratio; Phenotype; Polymorphism, Genetic; Proportional Hazards Models; Prospective Studies; Risk Assessment; Risk Factors; Taiwan	2011
Arg753Gln polymorphism of the human Toll-like receptor 2 gene from infection to disease in pediatric tuberculosis. Human immunology, 2011, Volume: 72, Issue:5 Topics: Adolescent; Arginine; Child; Child, Preschool; Disease Progression; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Mutation; Polymorphism, Genetic; Toll-Like Receptor 2; Tuberculosis, Pulmonary; Turkey	2011
Taking pain out of NGF: a "painless" NGF mutant, linked to hereditary sensory autonomic neuropathy type V, with full neurotrophic activity. PloS one, 2011, Feb-28, Volume: 6, Issue:2 Topics: Amino Acid Substitution; Animals; Arginine; BALB 3T3 Cells; Cells, Cultured; Chick Embryo; Genetic Predisposition to Disease; Hereditary Sensory and Autonomic Neuropathies; Humans; Male; Mice; Mutant Proteins; Nerve Growth Factors; Pain; Pain Perception; PC12 Cells; Rats; Receptor, Nerve Growth Factor; Sensory Receptor Cells; Tryptophan	2011
Survival bias and drug interaction can attenuate cross-sectional case-control comparisons of genes with health outcomes. An example of the kinesin-like protein 6 (KIF6) Trp719Arg polymorphism and coronary heart disease. BMC medical genetics, 2011, Mar-24, Volume: 12 Topics: Arginine; Canada; Case-Control Studies; Comparative Genomic Hybridization; Computer Simulation; Coronary Disease; Cross-Sectional Studies; Drug Interactions; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Kinesins; Logistic Models; Myocardial Infarction; Odds Ratio; Polymorphism, Single Nucleotide; Prospective Studies; Research Design; Risk Assessment; Risk Factors; Selection Bias; Survival Analysis; Treatment Outcome; Tryptophan	2011
Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease. Molecular biology reports, 2011, Volume: 38, Issue:8 Topics: Alleles; Arginine; Aryldialkylphosphatase; Case-Control Studies; Coronary Artery Disease; Coronary Stenosis; Demography; Diabetes Complications; Female; Genetic Predisposition to Disease; Humans; Iran; Lipids; Male; Middle Aged; Odds Ratio; Risk Factors	2011
Association of TRB3 Q84R polymorphism with polycystic ovary syndrome in Chinese women. Reproductive biology and endocrinology : RB&E, 2011, Apr-14, Volume: 9 Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Asian People; Blood Glucose; Case-Control Studies; Cell Cycle Proteins; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Obesity; Polycystic Ovary Syndrome; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Repressor Proteins; Young Adult	2011
Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Volume: 36, Issue:8 Topics: Adult; Arginine; Carrier Proteins; Cerebral Cortex; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Glutamic Acid; Humans; Intracellular Signaling Peptides and Proteins; Lysine; Male; Polymorphism, Genetic; Schizophrenia; Young Adult	2011
The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2012, Volume: 25, Issue:4 Topics: Abortion, Habitual; Abortion, Spontaneous; Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Glycine; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Pregnancy; Receptor, IGF Type 2; Young Adult	2012
Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease. Molecular biology reports, 2012, Volume: 39, Issue:3 Topics: Alleles; Arginine; Aryldialkylphosphatase; Coronary Artery Disease; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; INDEL Mutation; Iran; Linear Models; Male; Middle Aged; Odds Ratio; Peptidyl-Dipeptidase A; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Risk Factors	2012
Relationship between polymorphisms in the 5' leader cistron, positions 16 and 27 of the adrenergic β2 receptor gene and asthma in a Han population from southwest China. Respirology (Carlton, Vic.), 2011, Volume: 16, Issue:8 Topics: Adrenergic beta-2 Receptor Agonists; Albuterol; Arginine; Asian People; Asthma; Bronchodilator Agents; Case-Control Studies; China; Female; Forced Expiratory Volume; Gene Expression Regulation; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Haplotypes; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Adrenergic, beta-2	2011
Arg16Gly β2-adrenergic receptor gene polymorphism in Japanese patients with aspirin-exacerbated respiratory disease. International archives of allergy and immunology, 2011, Volume: 156, Issue:4 Topics: Adult; Aged; Alleles; Amino Acid Substitution; Arginine; Asian People; Asthma, Aspirin-Induced; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Japan; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Adrenergic, beta-2	2011
Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history. The British journal of psychiatry : the journal of mental science, 2011, Volume: 199, Issue:3 Topics: Adult; Arginine; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Exotropia; Female; Frameshift Mutation; Genetic Predisposition to Disease; Homeodomain Proteins; Humans; Lactoylglutathione Lyase; Lysine; Polymerase Chain Reaction; Schizophrenia; Transcription Factors	2011
Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q. PloS one, 2011, Volume: 6, Issue:10 Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Cell Line, Transformed; Clone Cells; Conserved Sequence; Genetic Predisposition to Disease; Humans; Inflammatory Bowel Diseases; Interleukin-23; Leukocytes, Mononuclear; Lymphocyte Count; Models, Biological; Molecular Sequence Data; Phosphorylation; Polymorphism, Single Nucleotide; Receptors, Interleukin; Species Specificity; STAT Transcription Factors; T-Lymphocytes; Tissue Donors	2011
TP53 codon 72 polymorphisms in favorable histology Wilms tumors. Pediatric blood & cancer, 2012, Volume: 59, Issue:2 Topics: Alleles; Arginine; Bone Neoplasms; Child; Child, Preschool; Codon; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Humans; Infant; Male; Neoplasm Recurrence, Local; Neoplasm Staging; Polymorphism, Single Nucleotide; Proline; Retrospective Studies; Risk Factors; Tumor Suppressor Protein p53; Wilms Tumor	2012
Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2012, Volume: 41, Issue:4 Topics: Adult; Areca; Arginine; Arylamine N-Acetyltransferase; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Heterozygote; Homozygote; Humans; India; Lysine; Male; Methionine; Multifactor Dimensionality Reduction; Oral Submucous Fibrosis; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tobacco, Smokeless; Tryptophan; X-ray Repair Cross Complementing Protein 1	2012
Genetic polymorphism of Fcγ-receptors IIa, IIIa and IIIb in South Indian patients with generalized aggressive periodontitis. Journal of oral science, 2011, Volume: 53, Issue:4 Topics: Adult; Aggressive Periodontitis; Amino Acid Substitution; Analysis of Variance; Arginine; Case-Control Studies; Chi-Square Distribution; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; GPI-Linked Proteins; Histidine; Humans; India; Isoantigens; Male; Mouth Mucosa; Odds Ratio; Periodontal Index; Phenylalanine; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Receptors, IgG; Risk Factors; Valine; White People; Young Adult	2011
Codon 72 and G13964C intron 6 polymorphisms of TP53 in relation to development and progression of breast cancer in India. Asian Pacific journal of cancer prevention : APJCP, 2011, Volume: 12, Issue:8 Topics: Alleles; Arginine; Breast Neoplasms; Case-Control Studies; Codon; Disease Progression; Female; Gene Frequency; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; India; Introns; Middle Aged; Neoplasm Staging; Obesity; Polymorphism, Genetic; Tumor Suppressor Protein p53	2011
Association of K832R and R952K SNPs of Wilson's disease gene with Alzheimer's disease. Journal of Alzheimer's disease : JAD, 2012, Volume: 29, Issue:4 Topics: Adenosine Triphosphatases; Aged; Aged, 80 and over; Alzheimer Disease; Arginine; Cation Transport Proteins; Copper-Transporting ATPases; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Linkage Disequilibrium; Logistic Models; Lysine; Male; Middle Aged; Polymorphism, Single Nucleotide	2012
Association between autoantibodies to the Arginine variant of the Zinc transporter 8 (ZnT8) and stimulated C-peptide levels in Danish children and adolescents with newly diagnosed type 1 diabetes. Pediatric diabetes, 2012, Volume: 13, Issue:6 Topics: Adolescent; Age Factors; Amino Acid Substitution; Arginine; Autoantibodies; C-Peptide; Cation Transport Proteins; Child; Child, Preschool; Denmark; Diabetes Mellitus, Type 1; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Infant; Male; Mutant Proteins; Up-Regulation; Zinc Transporter 8	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
Allelic variants of XRCC1 and XRCC3 repair genes and susceptibility of oral cancer in Brazilian patients. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2013, Volume: 42, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Alleles; Arginine; Carcinoma, Squamous Cell; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Humans; Lymphatic Metastasis; Male; Methionine; Middle Aged; Mouth Neoplasms; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tryptophan; X-ray Repair Cross Complementing Protein 1; Young Adult	2013
Schizophrenia shows a unique metabolomics signature in plasma. Translational psychiatry, 2012, Aug-14, Volume: 2 Topics: Adult; Aged; Analysis of Variance; Antipsychotic Agents; Arginine; Biomarkers; Case-Control Studies; Female; Genetic Markers; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamine; Humans; Least-Squares Analysis; Logistic Models; Male; Mass Spectrometry; Metabolomics; Middle Aged; Schizophrenia	2012
Role of p53 codon 72 polymorphism in chromosomal aberrations and mitotic index in patients with chronic hepatitis B. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 2012, Volume: 45, Issue:11 Topics: Adult; Arginine; Case-Control Studies; Chromosome Aberrations; Codon; Female; Genetic Predisposition to Disease; Genotype; Hepatitis B, Chronic; Humans; Male; Mitotic Index; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53	2012
Feto-placental nitric oxide, asymmetric dimethylarginine and vascular endothelial growth factor (VEGF) levels and VEGF gene polymorphisms in severe preeclampsia. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2013, Volume: 26, Issue:3 Topics: Adolescent; Adult; Arginine; Case-Control Studies; Female; Fetal Blood; Genetic Predisposition to Disease; Humans; Infant, Newborn; Nitric Oxide; Pilot Projects; Placenta; Placental Circulation; Polymorphism, Single Nucleotide; Pre-Eclampsia; Pregnancy; Severity of Illness Index; Umbilical Veins; Vascular Endothelial Growth Factor A; Young Adult	2013
XRCC1 gene polymorphisms and risk of ameloblastoma. Archives of oral biology, 2013, Volume: 58, Issue:6 Topics: Adenine; Adult; Ameloblastoma; Arginine; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Guanine; Haplotypes; Histidine; Humans; Male; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Sequence Analysis, DNA; Thailand; Thymine; Tryptophan; X-ray Repair Cross Complementing Protein 1	2013
Association of MDM2 and p53 polymorphisms with the advancement of cervical carcinoma. DNA and cell biology, 2013, Volume: 32, Issue:1 Topics: Adult; Aged; Alleles; Arginine; Codon; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Odds Ratio; Papillomavirus Infections; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Proto-Oncogene Proteins c-mdm2; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms; Young Adult	2013
Polymorphism Arg72Pro of p53 confers susceptibility to squamous cell carcinoma of lungs in a North Indian population. DNA and cell biology, 2013, Volume: 32, Issue:2 Topics: Aged; Amino Acid Substitution; Arginine; Asian People; Carcinoma, Squamous Cell; Case-Control Studies; Female; Genes, p53; Genetic Predisposition to Disease; Genetics, Population; Genotype; Humans; India; Lung Neoplasms; Male; Middle Aged; Polymorphism, Single Nucleotide; Proline	2013
The Arg allele in position 192 of PON1 is associated with carotid atherosclerosis in subjects with elevated HDLs. Atherosclerosis, 2002, Volume: 164, Issue:2 Topics: Adult; Alleles; Analysis of Variance; Arginine; Aryldialkylphosphatase; Base Sequence; Carotid Artery Diseases; Cholesterol, HDL; Cohort Studies; Confidence Intervals; Esterases; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Middle Aged; Molecular Sequence Data; Odds Ratio; Polymerase Chain Reaction; Polymorphism, Genetic; Probability; Risk Assessment; Sampling Studies; Sensitivity and Specificity; Severity of Illness Index; Ultrasonography, Doppler	2002
Major differences in antigen-processing correlate with a single Arg71<-->Lys substitution in HLA-DR molecules predisposing to rheumatoid arthritis and with their selective interactions with 70-kDa heat shock protein chaperones. Journal of immunology (Baltimore, Md. : 1950), 2002, Sep-15, Volume: 169, Issue:6 Topics: Amino Acid Substitution; Animals; Antigen Presentation; Arginine; Arthritis, Rheumatoid; Clone Cells; Epitopes, T-Lymphocyte; Escherichia coli Proteins; Genetic Predisposition to Disease; HLA-DR Antigens; HSP70 Heat-Shock Proteins; Humans; Hybridomas; Leukemia P388; Lysine; Mice; Protein Subunits; Receptors, Cholinergic; Recombinant Proteins; T-Lymphocytes; Transfection; Tumor Cells, Cultured	2002
[Polymorphism in codon 72 of the p53 gene and cervico-uterine cancer risk in Mexico]. Ginecologia y obstetricia de Mexico, 2002, Volume: 70 Topics: Adult; Arginine; Case-Control Studies; Codon; DNA Mutational Analysis; DNA-Binding Proteins; Exons; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Mexico; Oncogene Proteins, Viral; Papillomaviridae; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Repressor Proteins; Risk Factors; Substrate Specificity; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms	2002
RNASEL Arg462Gln variant is implicated in up to 13% of prostate cancer cases. Nature genetics, 2002, Volume: 32, Issue:4 Topics: Aged; Amino Acid Substitution; Arginine; Case-Control Studies; DNA Mutational Analysis; Endoribonucleases; Gene Deletion; Gene Dosage; Genetic Predisposition to Disease; Germ-Line Mutation; Heterozygote; Homozygote; Humans; Male; Middle Aged; Pedigree; Point Mutation; Prostate-Specific Antigen; Prostatic Neoplasms	2002
The transcobalamin codon 259 polymorphism influences the risk of human spontaneous abortion. Human reproduction (Oxford, England), 2002, Volume: 17, Issue:12 Topics: Abortion, Spontaneous; Alleles; Arginine; Codon; Female; Gene Frequency; Genetic Predisposition to Disease; Gestational Age; Homozygote; Humans; Polymorphism, Genetic; Pregnancy; Proline; Transcobalamins	2002
Lack of association between Alzheimer's disease and Gln-Arg 192 Q/R polymorphism of the PON-1 gene in an Italian population. Dementia and geriatric cognitive disorders, 2003, Volume: 15, Issue:2 Topics: Aged; Alzheimer Disease; Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Case-Control Studies; Esterases; Female; Genetic Predisposition to Disease; Glycine; Humans; Italy; Male; Polymorphism, Genetic	2003
Endothelium-dependent relaxation in pulmonary arteries of L-NAME-treated Wistar and stroke-prone spontaneously hypertensive rats. Journal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi, 2002, Volume: 38, Issue:4-5 Topics: Animals; Arginine; Blood Pressure; Body Weight; Cardiovascular Agents; Endothelium, Vascular; Enzyme Inhibitors; Genetic Predisposition to Disease; Hypertension; Indomethacin; Male; NG-Nitroarginine Methyl Ester; Nitric Oxide Donors; Nitroarginine; Nitroprusside; Pulmonary Artery; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Rats, Wistar; Stroke; Vasodilation	2002
PAX4 mutation (R121W) as a prodiabetic variant in Okinawans. Biochemical and biophysical research communications, 2003, Mar-07, Volume: 302, Issue:2 Topics: Aged; Amino Acid Substitution; Arginine; Diabetes Mellitus; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Homeodomain Proteins; Humans; Japan; Male; Mutation; Paired Box Transcription Factors; Transcription Factors; Tryptophan	2003
The Gly972-->Arg IRS-1 variant is associated with type 1 diabetes in continental Italy. Diabetes, 2003, Volume: 52, Issue:3 Topics: Adolescent; Adult; Arginine; Case-Control Studies; Child; Child, Preschool; Diabetes Mellitus, Type 1; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heterozygote; HLA Antigens; HLA-DQ Antigens; HLA-DQ beta-Chains; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Infant; Insulin Receptor Substrate Proteins; Italy; Male; Phosphoproteins; Polymerase Chain Reaction	2003
Association between human paraoxonase gene polymorphism and chronic symptoms in pesticide-exposed workers. Journal of occupational and environmental medicine, 2003, Volume: 45, Issue:2 Topics: Adult; Agriculture; Arginine; Aryldialkylphosphatase; Chronic Disease; Cross-Sectional Studies; Esterases; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Occupational Exposure; Pesticides; Polymorphism, Genetic	2003
The transcobalamin codon 259 polymorphism should be designated 776C>G, not 775G>C. Blood, 2003, May-01, Volume: 101, Issue:9 Topics: Adult; Aged; Arginine; Codon; Deoxyribonucleases, Type II Site-Specific; Genetic Predisposition to Disease; Humans; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Terminology as Topic; Transcobalamins; Vitamin B 12 Deficiency	2003
The p53 codon 72 genotypes in HPV infection and cervical disease. European journal of obstetrics, gynecology, and reproductive biology, 2003, Jul-01, Volume: 109, Issue:1 Topics: Alleles; Arginine; Codon; DNA, Viral; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53; Uterine Cervical Diseases; Vaginal Smears	2003
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
Beta 1-adrenergic receptor polymorphisms confer differential function and predisposition to heart failure. Nature medicine, 2003, Volume: 9, Issue:10 Topics: Adrenergic beta-Antagonists; Animals; Arginine; Cardiac Output, Low; Echocardiography; Genetic Predisposition to Disease; Glycine; Humans; Mice; Mice, Transgenic; Myocardial Contraction; Phenotype; Polymorphism, Genetic; Receptors, Adrenergic, beta-1	2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease. Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:9 Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Analysis; Electrophysiology; Family Health; Female; Genetic Predisposition to Disease; Glycine; Histidine; Humans; Male; Microscopy, Electron; Mutation; Nerve Tissue Proteins; Neural Conduction; Pedigree; Peripheral Nerves; Sequence Analysis, DNA; Tryptophan	2003
Characterization of a pseudoachondroplasia-associated mutation (His587-->Arg) in the C-terminal, collagen-binding domain of cartilage oligomeric matrix protein (COMP). The Biochemical journal, 2004, Jan-15, Volume: 377, Issue:Pt 2 Topics: Arginine; Binding Sites; Cartilage Oligomeric Matrix Protein; Cell Line; Collagen; Extracellular Matrix Proteins; Genetic Predisposition to Disease; Glycoproteins; Histidine; Humans; Matrilin Proteins; Mutation; Osteochondrodysplasias; Protein Conformation; Protein Structure, Tertiary	2004
Susceptibility to pre-eclampsia in Finnish women is associated with R485K polymorphism in the factor V gene, not with Leiden mutation. European journal of human genetics : EJHG, 2004, Volume: 12, Issue:3 Topics: Arginine; Factor V; Female; Finland; Genetic Predisposition to Disease; Humans; Lysine; Mutation; Polymorphism, Genetic; Pre-Eclampsia; Pregnancy	2004
Polymorphism R92Q of the tumour necrosis factor receptor 1 gene is associated with myocardial infarction and carotid intima-media thickness--the ECTIM, AXA, EVA and GENIC Studies. European journal of human genetics : EJHG, 2004, Volume: 12, Issue:3 Topics: Adult; Aged; Antigens, CD; Arginine; Arteriosclerosis; Brain Infarction; Carotid Arteries; Cross-Sectional Studies; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamine; Humans; Introns; Male; Middle Aged; Mutation; Myocardial Infarction; Odds Ratio; Polymorphism, Genetic; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Tunica Intima; Tunica Media; Ultrasonography	2004
Prognostic value of TP53 codon 72 polymorphism in advanced gastric adenocarcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research, 2004, Jan-01, Volume: 10, Issue:1 Pt 1 Topics: Adenocarcinoma; Adult; Age Distribution; Aged; Aged, 80 and over; Arginine; Codon; DNA, Neoplasm; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Neoplasm Staging; Polymerase Chain Reaction; Polymorphism, Genetic; Prognosis; Risk Factors; Stomach Neoplasms; Survival Rate	2004
The Arg753GLn polymorphism of the human toll-like receptor 2 gene in tuberculosis disease. The European respiratory journal, 2004, Volume: 23, Issue:2 Topics: Adult; Alleles; Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Immune Tolerance; Immunogenetics; Male; Membrane Glycoproteins; Middle Aged; Mycobacterium tuberculosis; Phenotype; Polymorphism, Single Nucleotide; Receptors, Cell Surface; Retrospective Studies; Toll-Like Receptor 2; Toll-Like Receptors; Tuberculosis, Lymph Node; Tuberculosis, Pleural; Tuberculosis, Pulmonary; Turkey	2004
The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults. Archives of neurology, 2004, Volume: 61, Issue:3 Topics: Adult; Arginine; Aryldialkylphosphatase; Case-Control Studies; Confidence Intervals; Demography; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Logistic Models; Male; Odds Ratio; Open Reading Frames; Polymerase Chain Reaction; Polymorphism, Genetic; Promoter Regions, Genetic; Risk; Sequence Analysis, DNA; Stroke	2004
Arginine at position 74 of the HLA-DR beta1 chain is associated with Graves' disease. Genes and immunity, 2004, Volume: 5, Issue:3 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Arginine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Graves Disease; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Male; Middle Aged; Polymerase Chain Reaction; White People	2004
Gene-environment interactions between the smoking habit and polymorphisms in the DNA repair genes, APE1 Asp148Glu and XRCC1 Arg399Gln, in Japanese lung cancer risk. Carcinogenesis, 2004, Volume: 25, Issue:8 Topics: Adult; Aged; Alleles; Arginine; Aspartic Acid; Codon; DNA Repair; DNA-(Apurinic or Apyrimidinic Site) Lyase; DNA-Binding Proteins; Environment; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Risk; Risk Factors; Smoking; X-ray Repair Cross Complementing Protein 1	2004
A comparison study of gastric cancer risk in patients with duodenal and gastric ulcer: roles of gastric mucosal histology and p53 codon 72 polymorphism. Digestive diseases and sciences, 2004, Volume: 49, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Codon; Duodenal Ulcer; Gastric Mucosa; Gastritis; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Risk Factors; Stomach Neoplasms; Stomach Ulcer	2004
Susceptibility to primary sclerosing cholangitis is associated with polymorphisms of intercellular adhesion molecule-1. Journal of hepatology, 2004, Volume: 40, Issue:3 Topics: Alleles; Arginine; Case-Control Studies; Cholangitis, Sclerosing; Cohort Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glycine; Haplotypes; HLA Antigens; Homozygote; Humans; Intercellular Adhesion Molecule-1; Lysine; Polymorphism, Genetic; Primed In Situ Labeling	2004
Disorder-associated mutations lead to functional inactivation of neuroligins. Human molecular genetics, 2004, Jul-15, Volume: 13, Issue:14 Topics: Animals; Arginine; Aspartic Acid; Autistic Disorder; Carrier Proteins; Cell Adhesion Molecules, Neuronal; Chlorocebus aethiops; COS Cells; Genetic Predisposition to Disease; Hippocampus; Humans; Intellectual Disability; Membrane Proteins; Mutation, Missense; Nerve Tissue Proteins; Neurons; Point Mutation; Protein Transport	2004
Analysis of polymorphisms at the tumor suppressor gene p53 (TP53) in contributing to the risk for schizophrenia and its associated neurocognitive deficits. Neuroscience letters, 2004, Jun-03, Volume: 363, Issue:1 Topics: Adult; Alleles; Arginine; Chi-Square Distribution; Cognition Disorders; DNA Transposable Elements; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Polymorphism, Genetic; Proline; Risk; Schizophrenia; Tumor Suppressor Protein p53	2004
Association of p53 genetic polymorphism (Arg72Pro) with estrogen receptor positive breast cancer risk in Japanese women. Cancer letters, 2004, Jul-16, Volume: 210, Issue:2 Topics: Adult; Aged; Arginine; Breast Neoplasms; Case-Control Studies; Codon; DNA Mutational Analysis; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Japan; Menopause; Middle Aged; Polymorphism, Genetic; Proline; Receptors, Estrogen; Risk Factors	2004
Pulmonary arterial hypertension: future directions: report of a National Heart, Lung and Blood Institute/Office of Rare Diseases workshop. Circulation, 2004, Jun-22, Volume: 109, Issue:24 Topics: Adult; Animals; Arginine; Bone Morphogenetic Protein Receptors, Type II; Enzyme Inhibitors; Female; Forecasting; Genetic Predisposition to Disease; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypertension, Pulmonary; Male; Models, Biological; Pancreatic Elastase; Platelet Aggregation Inhibitors; Potassium Channels; Protein Serine-Threonine Kinases; Rats; Research; Signal Transduction	2004
Functional variants within the secreted frizzled-related protein 3 gene are associated with hip osteoarthritis in females. Proceedings of the National Academy of Sciences of the United States of America, 2004, Jun-29, Volume: 101, Issue:26 Topics: Arginine; Cartilage; Chromosomes, Human, Pair 2; Cohort Studies; Exons; Female; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Microsatellite Repeats; Mutation, Missense; Odds Ratio; Osteoarthritis, Hip; Polymorphism, Single Nucleotide; Proteins; Sex Characteristics	2004
Association of p53 arginine polymorphism with skin cancer. International journal of dermatology, 2004, Volume: 43, Issue:7 Topics: Arginine; Brazil; Cell Transformation, Neoplastic; Epidermodysplasia Verruciformis; Genetic Predisposition to Disease; Humans; Papillomavirus Infections; Polymorphism, Genetic; Prevalence; Risk Factors; Skin Neoplasms; Tumor Suppressor Protein p53	2004
Neuronal accumulation of abnormal prion protein in sheep carrying a scrapie-resistant genotype (PrPARR/ARR). The Journal of general virology, 2004, Volume: 85, Issue:Pt 9 Topics: Alanine; Alleles; Animals; Arginine; Brain; Genetic Predisposition to Disease; Genotype; Germany; Homozygote; Immunoblotting; Immunohistochemistry; Neurons; PrP 27-30 Protein; PrPSc Proteins; Scrapie; Sheep	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
Arginine and glutamine availability and macrophage functions in the obese insulin-resistant Zucker rat. Journal of cellular physiology, 2005, Volume: 202, Issue:1 Topics: Animals; Arginine; Cells, Cultured; Disease Models, Animal; Dose-Response Relationship, Drug; Down-Regulation; Genetic Predisposition to Disease; Glutamine; Immune System; Immunity, Innate; Infections; Insulin Resistance; Lipopolysaccharides; Macrophages; Male; Nitric Oxide; Obesity; Rats; Rats, Zucker; Signal Transduction; Tumor Necrosis Factor-alpha	2005
Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsy. Journal of paediatrics and child health, 2004, Volume: 40, Issue:11 Topics: Arginine; Autopsy; Child; Cysteine; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Genetic Predisposition to Disease; Humans; Infant, Newborn; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Male; Molecular Diagnostic Techniques; Mutation, Missense; Neonatal Screening; Pedigree; Potassium Channels, Voltage-Gated	2004
[A twin study of association of beta3AR Trp64Arg polymorphisms with insulin sensitivity]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 2004, Volume: 36, Issue:5 Topics: Arginine; Diseases in Twins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin; Insulin Resistance; Polymorphism, Genetic; Receptors, Adrenergic, beta-3; Tryptophan; Twins, Dizygotic	2004
Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy. European journal of heart failure, 2004, Volume: 6, Issue:7 Topics: Adolescent; Adult; Aged; Arginine; Blood Pressure; Cardiomyopathy, Dilated; Child; Female; Finland; Follow-Up Studies; Genetic Predisposition to Disease; Glutamine; Heart Failure; Humans; Hypertrophy, Left Ventricular; Male; Middle Aged; Mutation; Myosin Heavy Chains; Pedigree; Phenotype; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sarcomeres; Stroke Volume; Tropomyosin; Troponin C; Troponin I; Troponin T; Tryptophan; Ventricular Myosins	2004
Impaired L-arginine transport and endothelial function in hypertensive and genetically predisposed normotensive subjects. Circulation, 2004, Dec-14, Volume: 110, Issue:24 Topics: Acetylcholine; Adolescent; Adult; Arginine; Biological Transport; Cationic Amino Acid Transporter 1; Cell Membrane; Endothelium, Vascular; Forearm; Genetic Predisposition to Disease; Humans; Hypertension; In Vitro Techniques; Male; Nitric Oxide; Nitric Oxide Donors; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Nitroprusside; RNA, Messenger; Vasodilation	2004
Met proto-oncogene juxtamembrane rare variations in mouse and humans: differential effects of Arg and Cys alleles on mouse lung tumorigenesis. Oncogene, 2005, Feb-03, Volume: 24, Issue:6 Topics: Adenocarcinoma; Alleles; Amino Acid Sequence; Animals; Arginine; Carcinoma, Non-Small-Cell Lung; Cell Transformation, Neoplastic; Cysteine; Disease Models, Animal; DNA Mutational Analysis; Genetic Linkage; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Lung Neoplasms; Mice; Mice, Inbred Strains; Molecular Sequence Data; Multifactorial Inheritance; Proto-Oncogene Mas; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-met; Receptors, Growth Factor; Receptors, Thrombin; Reverse Transcriptase Polymerase Chain Reaction	2005
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
Association of specific genotype and haplotype of p53 gene with cervical cancer in India. Journal of clinical pathology, 2005, Volume: 58, Issue:1 Topics: Adult; Arginine; Carcinoma, Squamous Cell; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Middle Aged; Neoplasm Staging; Papillomaviridae; Polymorphism, Genetic; Uterine Cervical Neoplasms	2005
Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron, 2005, Jan-06, Volume: 45, Issue:1 Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Bipolar Disorder; Brain; Depressive Disorder, Major; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Histidine; Humans; Male; Mice; Middle Aged; Molecular Sequence Data; Mutation; PC12 Cells; Polymorphism, Single Nucleotide; Rats; Serotonin; Tryptophan Hydroxylase	2005
[Association of p53 gene polymorphism with susceptibility to ovarian cancer]. Zhonghua fu chan ke za zhi, 2004, Volume: 39, Issue:11 Topics: Adult; Arginine; Asian People; China; Codon; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Neoplasm Staging; Ovarian Neoplasms; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Risk Factors	2004
Association of R602W in a protein tyrosine phosphatase gene with a high risk of rheumatoid arthritis in a British population: evidence for an early onset/disease severity effect. Arthritis and rheumatism, 2005, Volume: 52, Issue:1 Topics: Adult; Age of Onset; Arginine; Arthritis, Rheumatoid; England; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Protein Tyrosine Phosphatases; Severity of Illness Index; Tryptophan; White People	2005
Reduction of Gstm1 expression in the stroke-prone spontaneously hypertension rat contributes to increased oxidative stress. Hypertension (Dallas, Tex. : 1979), 2005, Volume: 45, Issue:4 Topics: Amino Acid Sequence; Animals; Aorta; Arginine; Blotting, Western; Computer Systems; Genetic Predisposition to Disease; Glutathione Transferase; Histidine; Hypertension; Immunohistochemistry; Kidney; Molecular Sequence Data; Oxidative Stress; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Stroke; Superoxides	2005
[p53 gene codon 72 polymorphism and susceptibility to keloid in Chinese population]. Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery, 2005, Volume: 19, Issue:1 Topics: Alleles; Arginine; Asian People; China; Codon; Exons; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Keloid; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53	2005
Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy. Epilepsy research, 2005, Volume: 63, Issue:2-3 Topics: Alleles; Arginine; Case-Control Studies; Chi-Square Distribution; Cysteine; DNA Mutational Analysis; Epilepsy, Generalized; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Mutation, Missense; Polymorphism, Genetic; Potassium Channels, Inwardly Rectifying	2005
TLR2 Arg677Trp polymorphism in leprosy: revisited. Human genetics, 2005, Volume: 116, Issue:5 Topics: Arginine; Base Sequence; Case-Control Studies; Genetic Predisposition to Disease; Genetic Variation; Humans; Leprosy, Lepromatous; Membrane Glycoproteins; Molecular Sequence Data; Polymorphism, Genetic; Promoter Regions, Genetic; Receptors, Cell Surface; Toll-Like Receptor 2; Toll-Like Receptors; Tryptophan	2005
Mutant valosin-containing protein causes a novel type of frontotemporal dementia. Annals of neurology, 2005, Volume: 57, Issue:3 Topics: Adenosine Triphosphatases; Amyloid beta-Protein Precursor; Arginine; Blotting, Western; Brain; Cell Cycle Proteins; Cysteine; Dementia; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glial Fibrillary Acidic Protein; Humans; Immunohistochemistry; Middle Aged; Mutation, Missense; Staining and Labeling; tau Proteins; Ubiquitin; Valosin Containing Protein	2005
Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signaling. Endocrine journal, 2005, Volume: 52, Issue:1 Topics: Adolescent; Alanine; Arginine; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Child; Child, Preschool; Congenital Abnormalities; Dioxins; Gene Frequency; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Lysine; Male; Penis; Polymorphism, Genetic; Proline; Receptors, Aryl Hydrocarbon; Repressor Proteins; Signal Transduction	2005
DNA repair gene XRCC1 Arg399Gln polymorphism is associated with increased risk of uterine leiomyoma. Human reproduction (Oxford, England), 2005, Volume: 20, Issue:6 Topics: Adult; Arginine; Asian People; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamine; Heterozygote; Humans; Korea; Leiomyoma; Middle Aged; Polymorphism, Genetic; Uterine Neoplasms; X-ray Repair Cross Complementing Protein 1	2005
A mutation in the Icsbp1 gene causes susceptibility to infection and a chronic myeloid leukemia-like syndrome in BXH-2 mice. The Journal of experimental medicine, 2005, Mar-21, Volume: 201, Issue:6 Topics: Amino Acid Substitution; Animals; Arginine; Chromosomes, Mammalian; Cysteine; Genetic Predisposition to Disease; Immunologic Deficiency Syndromes; Interferon Regulatory Factors; Interferon-gamma; Interleukin-12; Leukemia, Myeloid; Mice; Mutagenesis, Insertional; Mycobacterium bovis; Point Mutation; Quantitative Trait Loci; Repressor Proteins; Retroviridae; RNA, Messenger; Spleen; Tuberculosis; Virus Replication	2005
Trp64Arg polymorphism of the beta3-adrenergic receptor gene, pre-pregnancy obesity and risk of pre-eclampsia. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2005, Volume: 17, Issue:1 Topics: Adult; Arginine; Body Mass Index; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Heterozygote; Humans; Logistic Models; Obesity; Odds Ratio; Polymorphism, Genetic; Pre-Eclampsia; Pregnancy; Receptors, Adrenergic, beta-3; Tryptophan	2005
A functional interleukin-10 mutation in Dutch patients with Crohn's disease. 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:5 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Crohn Disease; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glycine; Humans; Interleukin-10; Intracellular Signaling Peptides and Proteins; Male; Middle Aged; Netherlands; Nod2 Signaling Adaptor Protein; Point Mutation; Restriction Mapping	2005
The DNA repair gene ERCC2/XPD polymorphism Arg 156Arg (A22541C) and risk of lung cancer in a Chinese population. Cancer letters, 2005, Jun-08, Volume: 223, Issue:2 Topics: Adenocarcinoma; Adult; Aged; Arginine; Carcinoma, Non-Small-Cell Lung; Case-Control Studies; China; DNA Helicases; DNA Repair; DNA-Binding Proteins; Ethnicity; Female; Genetic Predisposition to Disease; Humans; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Risk Factors; Sex Factors; Smoking; Transcription Factors; Xeroderma Pigmentosum Group D Protein	2005
Transforming growth factor-beta1 SNPs: genetic and phenotypic correlations in progressive kidney insufficiency. Nephron. Experimental nephrology, 2005, Volume: 101, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Arginine; Case-Control Studies; Cytosine; Disease Progression; Female; Fibrosis; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glomerulosclerosis, Focal Segmental; Haplotypes; Homozygote; Humans; Immunohistochemistry; Kidney; Kidney Failure, Chronic; Male; Middle Aged; Phenotype; Polymorphism, Single Nucleotide; Proline; Severity of Illness Index; Staining and Labeling; Thymine; Transforming Growth Factor beta; Transforming Growth Factor beta1	2005
The frequency of Trp64Arg polymorphism of the beta3-adrenergic receptor gene in healthy and obese Hungarian children and its association with cardiovascular risk factors. European journal of clinical nutrition, 2005, Volume: 59, Issue:8 Topics: Alleles; Arginine; Blood Glucose; Cardiovascular Diseases; Case-Control Studies; Child; DNA Fragmentation; Female; Genetic Predisposition to Disease; Glucose Tolerance Test; Humans; Hungary; Hypertension; Insulin; Male; Obesity; Polymerase Chain Reaction; Polymorphism, Genetic; Proteins; Receptors, Adrenergic, beta-3; Tryptophan	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
Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy. Epilepsy research, 2005, Volume: 65, Issue:1-2 Topics: Arginine; Case-Control Studies; Chi-Square Distribution; DNA Mutational Analysis; Epilepsy, Generalized; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Histidine; Humans; Male; Polymorphism, Genetic; Receptors, GABA-A; Retrospective Studies	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
Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease. Arthritis and rheumatism, 2005, Volume: 52, Issue:8 Topics: Arginine; Autoimmune Diseases; Cohort Studies; Gene Frequency; Genetic Predisposition to Disease; Humans; Lupus Erythematosus, Systemic; Polymorphism, Genetic; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Protein Tyrosine Phosphatases; Thyroid Diseases; Tryptophan; White People	2005
Lack of evidence that proline homozygosity at codon 72 of p53 and rare arginine allele at codon 31 of p21, jointly mediate cervical cancer susceptibility among Indian women. Gynecologic oncology, 2005, Volume: 99, Issue:1 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Arginine; Cell Cycle Proteins; Codon; Cyclin-Dependent Kinase Inhibitor p21; DNA, Neoplasm; DNA, Viral; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; India; Middle Aged; Papillomaviridae; Papillomavirus Infections; Polymorphism, Restriction Fragment Length; Proline; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms	2005
Heterozygous Arg753Gln polymorphism of human TLR-2 impairs immune activation by Borrelia burgdorferi and protects from late stage Lyme disease. Journal of immunology (Baltimore, Md. : 1950), 2005, Aug-15, Volume: 175, Issue:4 Topics: Adult; Alleles; Animals; Arginine; Borrelia burgdorferi; Cell Line; Cells, Cultured; Cytokines; Genetic Carrier Screening; Genetic Predisposition to Disease; Glutamine; Humans; Incidence; Lyme Disease; Mice; Mice, Inbred C57BL; Mice, Knockout; Middle Aged; Polymorphism, Single Nucleotide; Toll-Like Receptor 2	2005
The p53 codon 72 polymorphism and risk of high-grade cervical intraepithelial neoplasia. Cancer detection and prevention, 2005, Volume: 29, Issue:4 Topics: Adult; Arginine; Canada; Case-Control Studies; Codon; DNA, Neoplasm; Female; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Odds Ratio; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Proline; Risk Factors; Sequence Analysis, DNA; Tumor Suppressor Protein p53; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms	2005
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
Evaluation of the paraoxonases as candidate genes for stroke: Gln192Arg polymorphism in the paraoxonase 1 gene is associated with increased risk of stroke. Stroke, 2005, Volume: 36, Issue:11 Topics: Arginine; Aryldialkylphosphatase; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Genotype; Glutamine; Heterozygote; Homozygote; Humans; Lipoproteins, LDL; Male; Multivariate Analysis; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Pravastatin; Risk; Risk Factors; Stroke	2005
Influence of HLA-DR genes on the production of rheumatoid arthritis-specific autoantibodies to citrullinated fibrinogen. Arthritis and rheumatism, 2005, Volume: 52, Issue:11 Topics: Alleles; Amino Acid Sequence; Arginine; Arthritis, Rheumatoid; Autoantibodies; Cell Proliferation; Cells, Cultured; Female; Genetic Predisposition to Disease; HLA-DR Antigens; Humans; Leukocytes, Mononuclear; Male; Middle Aged; Molecular Sequence Data; Peptides, Cyclic; T-Lymphocytes	2005
Lack of association between the IL13 variant Arg110Gln and susceptibility to cedar pollinosis in a Japanese population. International archives of allergy and immunology, 2006, Volume: 139, Issue:1 Topics: Arginine; Cryptomeria; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamic Acid; Humans; Interleukin-13; Japan; Pollen; Rhinitis, Allergic, Seasonal	2006
Polymorphisms of ADPRT Val762Ala and XRCC1 Arg399Glu and risk of breast cancer in Chinese women: a case control analysis. Oncology reports, 2006, Volume: 15, Issue:1 Topics: Adult; Alanine; Amino Acid Substitution; Arginine; Asian People; Breast Neoplasms; Case-Control Studies; China; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Middle Aged; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Polymorphism, Genetic; Risk; Valine; X-ray Repair Cross Complementing Protein 1	2006
Association between TP53 and p21 genetic polymorphisms and acute side effects of radiotherapy in breast cancer patients. Breast cancer research and treatment, 2006, Volume: 97, Issue:3 Topics: Arginine; Body Mass Index; Breast Neoplasms; Cyclin-Dependent Kinase Inhibitor p21; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Linkage Disequilibrium; Middle Aged; Polymorphism, Genetic; Proline; Proportional Hazards Models; Radiodermatitis; Radiotherapy; Retrospective Studies; Serine; Tumor Suppressor Protein p53	2006
Association of the PTPN22R620W polymorphism with autoimmune myasthenia gravis. Annals of neurology, 2006, Volume: 59, Issue:2* Topics: Adult; Aged; Alleles; Arginine; Confidence Intervals; Connectin; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Muscle Proteins; Myasthenia Gravis; Odds Ratio; Polymorphism, Genetic; Protein Kinases; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Protein Tyrosine Phosphatases; Tryptophan	2006
Increased risk of non-small cell lung cancer and frequency of somatic TP53 gene mutations in Pro72 carriers of TP53 Arg72Pro polymorphism. Lung cancer (Amsterdam, Netherlands), 2006, Volume: 52, Issue:1 Topics: Adenocarcinoma; Arginine; Carcinoma, Large Cell; Carcinoma, Non-Small-Cell Lung; Carcinoma, Squamous Cell; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Lung Neoplasms; Male; Middle Aged; Mutation; Polymorphism, Genetic; Proline; Risk Factors; Tumor Suppressor Protein p53	2006
Association of functional variants of PTPN22 and tp53 in psoriatic arthritis: a case-control study. Arthritis research & therapy, 2006, Volume: 8, Issue:1 Topics: Adult; Arginine; Arthritis, Psoriatic; Case-Control Studies; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Male; Newfoundland and Labrador; Ontario; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Protein Tyrosine Phosphatases; Risk; Tryptophan; Tumor Suppressor Protein p53; White People	2006
PMS2 mutations in childhood cancer. Journal of the National Cancer Institute, 2006, Mar-01, Volume: 98, Issue:5 Topics: Adenosine Triphosphatases; Adolescent; Arginine; Astrocytoma; Cafe-au-Lait Spots; Child; Colonic Polyps; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Female; Founder Effect; Genetic Predisposition to Disease; Glioma; Humans; Leukemia, T-Cell; Lymphoma, B-Cell; Lymphoma, T-Cell; Male; Mismatch Repair Endonuclease PMS2; Mutation; Neoplasms; Neoplasms, Second Primary; Pakistan; Precursor Cell Lymphoblastic Leukemia-Lymphoma; United Kingdom	2006
LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance. Archives of neurology, 2006, Volume: 63, Issue:3 Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Arginine; Child; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Pedigree; Protein Serine-Threonine Kinases; Serine; Spain	2006
Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population. BMC medical genetics, 2006, Apr-05, Volume: 7 Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; DNA Mutational Analysis; Exons; Eye Proteins; Female; Genetic Predisposition to Disease; Humans; Male; Microtubule-Associated Proteins; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Retinitis Pigmentosa; Sequence Deletion; Spain	2006
Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful neuropathy. Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:5 Topics: Acute Disease; Amino Acid Substitution; Arginine; Disease Progression; DNA Mutational Analysis; Genetic Predisposition to Disease; Genetic Testing; Hereditary Sensory and Motor Neuropathy; Humans; Inheritance Patterns; Male; Middle Aged; Myelin P0 Protein; Neuralgia; Peripheral Nerves; Peripheral Nervous System Diseases; Point Mutation; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating; Time Factors; Tryptophan	2006
Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Neurobiology of aging, 2007, Volume: 28, Issue:6 Topics: Adaptor Proteins, Signal Transducing; Aged; Alzheimer Disease; Apolipoprotein E4; Arginine; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters; Autophagy-Related Proteins; Carrier Proteins; Cell Cycle Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Linkage Disequilibrium; Logistic Models; Lysine; Male; Polymorphism, Genetic; Sex Characteristics	2007
The p53 codon 72 polymorphism, sunburns, and risk of skin cancer in US Caucasian women. Molecular carcinogenesis, 2006, Volume: 45, Issue:9 Topics: Adult; Alleles; Arginine; Codon; Female; Genetic Predisposition to Disease; Hair Color; Humans; Middle Aged; Polymorphism, Genetic; Risk; Skin Neoplasms; Sunburn; Tumor Suppressor Protein p53; White People	2006
[Laboratory tests and therapeutic strategies for the porphyrias]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2006, Volume: 57, Issue:6 Topics: Algorithms; Arginine; Critical Care; Diagnosis, Differential; Dose-Response Relationship, Drug; Drug Administration Schedule; Genetic Predisposition to Disease; Heme; Humans; Photosensitivity Disorders; Porphyria Cutanea Tarda; Porphyrias	2006
Precocious osteoarthritis in a family with recurrent COL2A1 mutation. The Journal of rheumatology, 2006, Volume: 33, Issue:6 Topics: Arginine; Collagen Type II; Cysteine; Family Health; Female; Genetic Predisposition to Disease; Genetic Testing; Humans; Male; Microsatellite Repeats; Mutation, Missense; Osteoarthritis, Hip; Osteoarthritis, Knee; Osteochondrodysplasias; Pedigree; Polymerase Chain Reaction; Radiography	2006
Arginine-16 beta2 adrenoceptor genotype predisposes to exacerbations in young asthmatics taking regular salmeterol. Thorax, 2006, Volume: 61, Issue:11 Topics: Adolescent; Adrenergic beta-Agonists; Albuterol; Arginine; Asthma; Child; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Receptors, Adrenergic, beta-2; Salmeterol Xinafoate; Scotland	2006
Allelic expression analysis suggests that cis-acting polymorphism of FRZB expression does not contribute to osteoarthritis susceptibility. Osteoarthritis and cartilage, 2007, Volume: 15, Issue:1 Topics: Aged; Aged, 80 and over; Allelic Imbalance; Arginine; Cartilage, Articular; Chondrocytes; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Osteoarthritis; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Proteins; RNA, Messenger	2007
Toll-like receptor 2 Arg753Gln gene polymorphism in Turkish patients with Behçet's disease. Clinical and experimental dermatology, 2006, Volume: 31, Issue:5 Topics: Adult; Arginine; Behcet Syndrome; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Toll-Like Receptor 2; Turkey	2006
Gene polymorphism and requirement for vasopressor infusion after cardiac surgery. The Annals of thoracic surgery, 2006, Volume: 82, Issue:3 Topics: Adaptor Proteins, Signal Transducing; Aged; Alleles; Amidohydrolases; Arginine; Cardiac Surgical Procedures; Casein Kinase II; Cohort Studies; Comorbidity; Elective Surgical Procedures; Epinephrine; Female; Genetic Predisposition to Disease; Genotype; Histocompatibility Antigens Class II; Humans; Inflammation; Lymphotoxin-alpha; Major Histocompatibility Complex; Male; Middle Aged; Norepinephrine; Polymorphism, Single Nucleotide; Postoperative Complications; Tumor Necrosis Factor-alpha; Vascular Resistance; Vasoconstrictor Agents; Vasodilation	2006
CARD15 gene variants in aggressive periodontitis. Journal of clinical periodontology, 2006, Volume: 33, Issue:11 Topics: Adult; Arginine; Base Sequence; Case-Control Studies; Cytosine; Disease Susceptibility; DNA Transposable Elements; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Glycine; Guanine; Humans; Male; Middle Aged; Mutation; Nod2 Signaling Adaptor Protein; Periodontitis; Thymine; Tryptophan	2006
Characteristics of frontotemporal dementia patients with a Progranulin mutation. Annals of neurology, 2006, Volume: 60, Issue:3 Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Arginine; Chromosomes, Human, Pair 17; Dementia; Deoxyglucose; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Intercellular Signaling Peptides and Proteins; Male; Microtubule-Associated Proteins; Middle Aged; Mutation; Neuropsychological Tests; Positron-Emission Tomography; tau Proteins	2006
Apolipoprotein E gene and macular degeneration. Ophthalmology, 2006, Volume: 113, Issue:10 Topics: Apolipoproteins E; Arginine; Genetic Predisposition to Disease; Genotype; Humans; Macular Degeneration; Risk Factors	2006
Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease. The Journal of rheumatology, 2006, Volume: 33, Issue:12 Topics: Amyloidosis; Arginine; Environment; Familial Mediterranean Fever; Genetic Predisposition to Disease; Glutamine; Humans; Phenotype; Point Mutation; Polymorphism, Restriction Fragment Length; Toll-Like Receptor 2	2006
The lymphotoxin Cys13Arg polymorphism and cognitive functioning in individuals with schizophrenia. Schizophrenia research, 2007, Volume: 89, Issue:1-3 Topics: Adult; Antibodies, Viral; Arginine; Bipolar Disorder; Cognition Disorders; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Herpesvirus 1, Human; Humans; Intelligence; Lymphotoxin-alpha; Male; Middle Aged; Neuropsychological Tests; Polymorphism, Genetic; Schizophrenia	2007
LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP. Neurology, 2006, Oct-24, Volume: 67, Issue:8 Topics: Age of Onset; Aged; Aged, 80 and over; Arginine; Cohort Studies; Dementia; Disease Progression; Female; Genetic Predisposition to Disease; Greece; Histidine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Pedigree; Protein Serine-Threonine Kinases; Supranuclear Palsy, Progressive	2006
Insulin receptor substrate gene polymorphism is associated with obstructive sleep apnea syndrome in men. The Laryngoscope, 2006, Volume: 116, Issue:11 Topics: Adult; Arginine; Female; Genetic Predisposition to Disease; Glycine; Humans; Insulin Receptor Substrate Proteins; Insulin Resistance; Male; Middle Aged; Phosphoproteins; Polymorphism, Genetic; Sex Factors; Sleep Apnea, Obstructive	2006
Evidence for an association of TP53 codon 72 polymorphism with breast cancer risk. Cancer detection and prevention, 2006, Volume: 30, Issue:6 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Arginine; Brazil; Breast Neoplasms; Carcinoma, Ductal; Carcinoma, Lobular; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Proline; Risk Factors	2006
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society, 2007, Feb-15, Volume: 22, Issue:3 Topics: Aged; Aged, 80 and over; Arginine; Case-Control Studies; Female; Genetic Predisposition to Disease; Glutamine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Mutation; Parkinson Disease; Protein Serine-Threonine Kinases	2007
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia. Parkinsonism & related disorders, 2007, Volume: 13, Issue:2 Topics: Aged; Arginine; Asian People; Female; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinson Disease; Protein Serine-Threonine Kinases; Risk Factors	2007
The association between hyperuricemia and the Trp64Arg polymorphism of the beta-3 adrenergic receptor. Rheumatology international, 2007, Volume: 27, Issue:9 Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Arginine; DNA Mutational Analysis; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Hyperuricemia; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Receptors, Adrenergic, beta-3; Sex Factors; Tryptophan	2007
Functional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease. Scandinavian journal of immunology, 2007, Volume: 65, Issue:2 Topics: Alanine; Amino Acid Substitution; Arginine; Case-Control Studies; Crohn Disease; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Histidine; Humans; Male; Polymorphism, Single Nucleotide; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Tyrosine	2007
Orofacial clefting: update on the role of genetics. B-ENT, 2006, Volume: 2 Suppl 4 Topics: Arginine; Cleft Lip; Cleft Palate; Cohort Studies; Environment; Exons; Genes, Dominant; Genetic Predisposition to Disease; Genotype; Humans; Interferon Regulatory Factors; Leg; Lip; Mutation; Phenotype; Polymorphism, Single Nucleotide; Syndrome	2006
Glucocorticoid receptor gene polymorphisms associated with more aggressive disease phenotype in MS. Journal of neuroimmunology, 2007, Volume: 186, Issue:1-2 Topics: Adult; Arginine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Multiple Sclerosis; Odds Ratio; Phenotype; Polymorphism, Genetic; Receptors, Glucocorticoid	2007
Arg72Pro p53 polymorphism in Italian women: no association with endometriosis. Fertility and sterility, 2007, Volume: 88, Issue:5 Topics: Adolescent; Adult; Arginine; Endometriosis; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Italy; Middle Aged; Polymorphism, Genetic; Proline	2007
Polymorphisms in the paraoxonase and endothelial nitric oxide synthase genes and the risk of early-onset myocardial infarction. The American journal of cardiology, 2007, Apr-15, Volume: 99, Issue:8 Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Arginine; Aryldialkylphosphatase; Aspartic Acid; Cohort Studies; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Male; Middle Aged; Myocardial Infarction; Nitric Oxide Synthase Type III; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors	2007
Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer. Carcinogenesis, 2007, Volume: 28, Issue:8 Topics: ADP-Ribosylation Factors; Amino Acid Substitution; Arginine; Base Sequence; Case-Control Studies; Colorectal Neoplasms; Cysteine; Genetic Predisposition to Disease; Genetic Variation; Humans; Incidence; Middle Aged; Molecular Sequence Data; Risk Factors; Spain	2007
Platelet 12-lipoxygenase Arg261Gln polymorphism: functional characterization and association with risk of esophageal squamous cell carcinoma in combination with COX-2 polymorphisms. Pharmacogenetics and genomics, 2007, Volume: 17, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Arachidonate 12-Lipoxygenase; Arginine; Base Sequence; Blood Platelets; Carcinoma, Squamous Cell; Case-Control Studies; Cyclooxygenase 2; DNA Mutational Analysis; Esophageal Neoplasms; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Male; Membrane Proteins; Middle Aged; Molecular Sequence Data; Polymorphism, Single Nucleotide; Risk	2007
Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain. Parkinsonism & related disorders, 2007, Volume: 13, Issue:8 Topics: Adult; Aged; Arginine; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinsonian Disorders; Protein Serine-Threonine Kinases; Serine; Spain	2007
E-selectin S128R polymorphism leads to severe asthma. Iranian journal of allergy, asthma, and immunology, 2007, Volume: 6, Issue:2 Topics: Adolescent; Adult; Arginine; Asthma; Case-Control Studies; E-Selectin; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Middle Aged; Polymorphism, Restriction Fragment Length; Respiratory Function Tests; Serine	2007
Carbamoyl phosphate synthetase polymorphisms as a risk factor for necrotizing enterocolitis. Pediatric research, 2007, Volume: 62, Issue:2 Topics: Arginine; Carbamoyl-Phosphate Synthase (Ammonia); Case-Control Studies; Enterocolitis, Necrotizing; Female; Gene Frequency; Genetic Predisposition to Disease; Gestational Age; Humans; Incidence; Infant, Newborn; Infant, Premature; Male; Odds Ratio; Polymorphism, Single Nucleotide; Retrospective Studies; Risk Assessment; Risk Factors; Severity of Illness Index	2007
TP53 codon 72 polymorphism in 12 populations of insular Southeast Asia and Oceania. Journal of human genetics, 2007, Volume: 52, Issue:8 Topics: Amino Acid Substitution; Arginine; Asia, Southeastern; Codon; Gene Frequency; Genetic Predisposition to Disease; Humans; Neoplasms; Oceania; Polymorphism, Genetic; Population; Proline; Tumor Suppressor Protein p53	2007
Arg64 variant of the beta3-adrenergic receptor is associated with gallstone formation. The American journal of gastroenterology, 2007, Volume: 102, Issue:11 Topics: Arginine; Body Mass Index; Cross-Sectional Studies; DNA Mutational Analysis; Female; Gallstones; Gene Frequency; Genetic Predisposition to Disease; Genotype; Germany; Humans; Logistic Models; Male; Middle Aged; Mutation, Missense; Polymorphism, Genetic; Receptors, Adrenergic, beta-3; Tryptophan	2007
Association analysis of gamma2 subunit of gamma-aminobutyric acid (GABA) type A receptor and voltage-gated sodium channel type II alpha-polypeptide gene mutation in southern Chinese children with febrile seizures. Journal of child neurology, 2007, Volume: 22, Issue:6 Topics: Arginine; Chi-Square Distribution; Child; Child, Preschool; China; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Infant; Lysine; Male; Methionine; Mutation; NAV1.2 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Polymorphism, Single Nucleotide; Receptors, GABA-A; Seizures, Febrile; Sodium Channels; Tryptophan	2007
Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation. Arthritis and rheumatism, 2007, Volume: 56, Issue:8 Topics: Adult; Arginine; Diagnosis, Differential; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Heterozygote; Humans; Hypergammaglobulinemia; Male; Middle Aged; Multiple Sclerosis; Mutation; Pedigree; Prospective Studies; Receptors, Tumor Necrosis Factor, Type I	2007
Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients. Molecular vision, 2007, Jul-24, Volume: 13 Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Asian People; Base Sequence; Child; Cysteine; DNA Mutational Analysis; Ectopia Lentis; Female; Fibrillin-1; Fibrillins; Genetic Predisposition to Disease; Humans; Male; Marfan Syndrome; Microfilament Proteins; Molecular Sequence Data; Mutation; Pedigree	2007
The wolframin His611Arg polymorphism influences medication overuse headache. Neuroscience letters, 2007, Sep-13, Volume: 424, Issue:3 Topics: Adult; Arginine; Case-Control Studies; DNA Mutational Analysis; Drug-Related Side Effects and Adverse Reactions; Female; Genetic Predisposition to Disease; Headache; Histidine; Humans; Male; Membrane Proteins; Middle Aged; Multivariate Analysis; Polymorphism, Genetic	2007
Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population. Gastroenterology, 2007, Volume: 133, Issue:3 Topics: Adolescent; Adult; Arginine; Case-Control Studies; Crohn Disease; Female; Genetic Predisposition to Disease; Glycine; Humans; Italy; Male; Phenotype; Polymorphism, Single Nucleotide; Receptors, Interleukin	2007
Paraoxonase/arylesterase ratio, PON1 192Q/R polymorphism and PON1 status are associated with increased risk of ischemic stroke. Clinical biochemistry, 2008, Volume: 41, Issue:1-2 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Carboxylic Ester Hydrolases; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Hypoxia-Ischemia, Brain; Male; Middle Aged; Polymorphism, Genetic; Risk; Stroke	2008
Frequency of TP53 mutations in relation to Arg72Pro genotypes in non small cell lung cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2007, Volume: 16, Issue:10 Topics: Aged; Alleles; Arginine; Carcinoma, Non-Small-Cell Lung; Cell Transformation, Neoplastic; Codon; DNA Mutational Analysis; Female; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Lung Neoplasms; Male; Middle Aged; Norway; Polymorphism, Single Nucleotide; Proline; Smoking; Tumor Suppressor Protein p53	2007
Multiple primary melanomas in a CDKN2A mutation carrier exposed to ionizing radiation. Archives of dermatology, 2007, Volume: 143, Issue:11 Topics: 5' Untranslated Regions; Adult; Arginine; Cysteine; Environmental Exposure; Female; Genes, p16; Genetic Predisposition to Disease; Hair Color; Heterozygote; Humans; Melanoma; Mutation; Neoplasms, Multiple Primary; Neoplasms, Radiation-Induced; Nuclear Weapons; Receptor, Melanocortin, Type 1; Skin Neoplasms	2007
Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations. Journal of the neurological sciences, 2008, Apr-15, Volume: 267, Issue:1-2 Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Apoptosis Regulatory Proteins; Arginine; Brain; Codon, Nonsense; DNA Mutational Analysis; Female; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemangioma, Cavernous, Central Nervous System; Humans; Inheritance Patterns; Korea; Magnetic Resonance Imaging; Male; Membrane Proteins; Proto-Oncogene Proteins; Seizures; Spinal Cord	2008
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants? Breast cancer research : BCR, 2007, Volume: 9, Issue:6 Topics: Alanine; Arginine; Biomarkers, Tumor; Breast Neoplasms; Centrosome; DNA, Complementary; Factor Analysis, Statistical; Female; Genes, BRCA1; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Humans; Immunohistochemistry; Keratins; Mutation, Missense; Nucleic Acid Amplification Techniques; Plasmids; Polymorphism, Single Nucleotide; Predictive Value of Tests; Receptors, Estrogen; Risk Assessment; Risk Factors; Sequence Analysis, DNA; Valine	2007
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. Movement disorders : official journal of the Movement Disorder Society, 2008, Feb-15, Volume: 23, Issue:3 Topics: Adult; Aged; Arginine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Nitric Oxide Synthase Type I; Polymorphism, Single Nucleotide; Restless Legs Syndrome	2008
MC1R variants associated susceptibility to basal cell carcinoma of skin: interaction with host factors and XRCC3 polymorphism. International journal of cancer, 2008, Apr-15, Volume: 122, Issue:8 Topics: Adult; Aged; Arginine; Carcinoma, Basal Cell; Case-Control Studies; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Hungary; Male; Methionine; Middle Aged; Polymorphism, Genetic; Receptor, Melanocortin, Type 1; Risk Factors; Romania; Sequence Analysis, DNA; Skin Neoplasms; Slovakia; Threonine	2008
TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas. Cancer genetics and cytogenetics, 2008, Jan-01, Volume: 180, Issue:1 Topics: Adult; Arginine; Brain Neoplasms; Case-Control Studies; Codon; Combined Modality Therapy; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Glioma; Humans; Male; Middle Aged; Polymorphism, Genetic; Proline; Retrospective Studies; Survival Rate; Treatment Outcome	2008
Protective effect of noninherited maternal HLA-DR antigens on rheumatoid arthritis development. Proceedings of the National Academy of Sciences of the United States of America, 2007, Dec-11, Volume: 104, Issue:50 Topics: Alanine; Alleles; Arginine; Arthritis, Rheumatoid; Aspartic Acid; Child; Cohort Studies; Epitopes; Fathers; Female; Genetic Predisposition to Disease; Glutamic Acid; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Male; Mothers; Pregnancy; Prospective Studies	2007
LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China. European journal of neurology, 2008, Volume: 15, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Arginine; Asian People; Chi-Square Distribution; China; Female; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinson Disease; Polymorphism, Genetic; Protein Serine-Threonine Kinases; Risk Factors	2008
FGFR mutations and plagiocephaly. The Journal of craniofacial surgery, 2008, Volume: 19, Issue:1 Topics: Acrocephalosyndactylia; Arginine; Craniofacial Dysostosis; Craniosynostoses; Electrophoresis; Exons; Genetic Predisposition to Disease; Genetic Variation; Humans; Infant; Mutation; Plagiocephaly, Nonsynostotic; Proline; Receptor, Fibroblast Growth Factor, Type 1; Receptor, Fibroblast Growth Factor, Type 2; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor	2008
Case-control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipolar-affective disorders. Molecular psychiatry, 2009, Volume: 14, Issue:6 Topics: Amino Acid Substitution; Arginine; Bipolar Disorder; Case-Control Studies; Chromosomes, Human, Pair 12; Depressive Disorder; Gene Frequency; Genes, Dominant; Genetic Predisposition to Disease; Glutamine; Haplotypes; Heterozygote; Homozygote; Humans; Linkage Disequilibrium; Microsatellite Repeats; Receptors, Purinergic P2; Receptors, Purinergic P2X7	2009
Association of a missense single nucleotide polymorphism, Cys1367Arg of the WRN gene, with the risk of bone and soft tissue sarcomas in Japan. Cancer science, 2008, Volume: 99, Issue:2 Topics: Adult; Alleles; Arginine; Base Sequence; Bone Neoplasms; Case-Control Studies; Cysteine; Exodeoxyribonucleases; Female; Genetic Predisposition to Disease; Genotype; Humans; Japan; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense; Polymorphism, Single Nucleotide; RecQ Helicases; Sarcoma; Werner Syndrome Helicase	2008
Association of missense variants of the PRKC, apoptosis, WT1, regulator (PAWR) gene with schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry, 2008, Apr-01, Volume: 32, Issue:3 Topics: 5' Untranslated Regions; Adult; Apoptosis Regulatory Proteins; Arginine; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Methionine; Middle Aged; Mutation, Missense; Polymorphism, Genetic; Proline; Schizophrenia; Sex Factors; Taiwan	2008
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia. Neurobiology of aging, 2009, Volume: 30, Issue:11 Topics: Adult; Arginine; Cysteine; DNA Mutational Analysis; Family Health; Female; Fluorodeoxyglucose F18; Frontotemporal Dementia; Genetic Predisposition to Disease; Humans; Intercellular Signaling Peptides and Proteins; Male; Microtubule-Associated Proteins; Middle Aged; Mutation; Presenilin-1; Progranulins; Radionuclide Imaging	2009
Essential tremor and the common LRRK2 G2385R variant. Parkinsonism & related disorders, 2008, Volume: 14, Issue:7 Topics: Adult; Aged; Arginine; Cohort Studies; Confidence Intervals; DNA Mutational Analysis; Essential Tremor; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Odds Ratio; Protein Serine-Threonine Kinases	2008
Evaluation of the transforming growth factor beta1 codon 25 (Arg-->Pro) polymorphism in alcoholic liver disease. Cytokine, 2008, Volume: 42, Issue:1 Topics: Adult; Alcohol Drinking; Arginine; Codon; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Liver Cirrhosis, Alcoholic; Liver Diseases, Alcoholic; Liver Transplantation; Male; Middle Aged; Multivariate Analysis; Polymorphism, Genetic; Proline; Transforming Growth Factor beta1	2008
Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease. Journal of the neurological sciences, 2008, Jul-15, Volume: 270, Issue:1-2 Topics: Aged; Alzheimer Disease; Apolipoprotein E4; Arginine; Chi-Square Distribution; China; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamine; Humans; Male; Polymorphism, Genetic; tau Proteins; Tumor Necrosis Factor-alpha	2008
A PCR-based integrated protocol for the structural analysis of the 13th exon of the human beta-myosin heavy chain gene (MYH7): development of a diagnostic tool for HCM disease. Experimental and molecular pathology, 2008, Volume: 84, Issue:3 Topics: Arginine; Cardiac Myosins; Cardiomyopathy, Hypertrophic; Exons; Female; Genetic Predisposition to Disease; Humans; Male; Myosin Heavy Chains; Polymerase Chain Reaction	2008
Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie. The Journal of general virology, 1995, Volume: 76 ( Pt 8) Topics: Animals; Arginine; Base Sequence; Codon; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Male; Molecular Sequence Data; Nematode Infections; Polymerase Chain Reaction; Polymorphism, Genetic; PrPC Proteins; Scrapie; Sequence Analysis, DNA; Sheep	1995
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. The Journal of clinical investigation, 1994, Volume: 94, Issue:6 Topics: Arginine; Base Sequence; Drug Resistance; Enzyme Activation; Factor V; Female; Genetic Predisposition to Disease; Glutamine; Heterozygote; Homozygote; Humans; Male; Molecular Sequence Data; Point Mutation; Protein C; Risk Factors; Survival Analysis; Sweden; Thrombophlebitis	1994
Production of nitric oxide (NO) is not essential for protection against acute Toxoplasma gondii infection in IRF-1-/- mice. Journal of immunology (Baltimore, Md. : 1950), 1996, Jan-15, Volume: 156, Issue:2 Topics: Animals; Arginine; CD4-Positive T-Lymphocytes; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Immunologic Factors; Interferon Regulatory Factor-1; Interferon-gamma; Interleukin-10; Interleukin-12; Lymphocyte Activation; Lymphocyte Depletion; Mice; Mice, Inbred C57BL; Mice, Knockout; Nitric Oxide; Nitric Oxide Synthase; omega-N-Methylarginine; Phosphoproteins; T-Lymphocyte Subsets; Toxoplasma; Toxoplasmosis, Animal; Transforming Growth Factor beta	1996
Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474. Blood, 1996, Jun-01, Volume: 87, Issue:11 Topics: Androgen-Binding Protein; Animals; Arginine; Base Sequence; Binding Sites; Cattle; Cell Line, Transformed; Chlorocebus aethiops; CHO Cells; Consanguinity; Cricetinae; Cysteine; DNA, Complementary; Female; Genetic Predisposition to Disease; Genetic Vectors; Humans; Laminin; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Protein S; Protein S Deficiency; Rabbits; Rats; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Thrombosis	1996
Arginine at positions 13 or 70-71 in pocket 4 of HLA-DRB1 alleles is associated with susceptibility to tuberculoid leprosy. The Journal of experimental medicine, 1996, Mar-01, Volume: 183, Issue:3 Topics: Alleles; Amino Acid Sequence; Arginine; Chi-Square Distribution; Crystallography, X-Ray; Genes, MHC Class II; Genetic Predisposition to Disease; Histocompatibility Testing; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Leprosy, Tuberculoid; Macromolecular Substances; Models, Molecular; Molecular Sequence Data; Polymerase Chain Reaction; Protein Conformation; Reference Values; Risk Factors	1996
Trp64Arg mutation in beta 3-adrenoceptor gene of doubtful significance for obesity and insulin resistance. Lancet (London, England), 1996, Sep-14, Volume: 348, Issue:9029 Topics: Animals; Arginine; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Heterozygote; Humans; Insulin Resistance; Mutation; Obesity; Receptors, Adrenergic, beta; Receptors, Adrenergic, beta-3; Tryptophan	1996
Arginine506 to glutamin mutation in the factor V gene in infancy and childhood: evidence of fibrinolytic impairment. European journal of pediatrics, 1997, Volume: 156, Issue:3 Topics: Adolescent; Arginine; Child; Child, Preschool; DNA Mutational Analysis; Factor V; Female; Fibrin Fibrinogen Degradation Products; Fibrinolysis; Genetic Carrier Screening; Genetic Predisposition to Disease; Glutamine; Homozygote; Humans; Infant; Infant, Newborn; Male; Oligopeptides; Protein C; Thrombin; Thrombophlebitis	1997
Glutathione-S-Transferase M1 and codon 72 p53 polymorphisms in a northwestern Mediterranean population and their relation to lung cancer susceptibility. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 1996, Volume: 5, Issue:5 Topics: Adenocarcinoma; Adult; Age Factors; Aged; Aged, 80 and over; Alleles; Amino Acid Sequence; Arginine; Carcinoma; Carcinoma, Small Cell; Codon; Female; Gene Deletion; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Proline; Risk Factors; Smoking; Spain	1996
The Trp64Arg polymorphism of the beta 3-Adrenergic receptor gene. Lack of association with NIDDM and features of insulin resistance syndrome. Diabetes care, 1997, Volume: 20, Issue:8 Topics: Adult; Alleles; Arginine; Diabetes Mellitus, Type 2; DNA; DNA Primers; Exons; Female; Finland; Gene Frequency; Genetic Predisposition to Disease; Humans; Insulin Resistance; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Receptors, Adrenergic, beta; Receptors, Adrenergic, beta-3; Syndrome; Tryptophan	1997
A genetic propensity to high factor VII is not associated with the risk of myocardial infarction in men. Thrombosis and haemostasis, 1998, Volume: 80, Issue:2 Topics: Adult; Aged; Antigens; Arginine; Case-Control Studies; Factor VII; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Middle Aged; Myocardial Infarction; Polymorphism, Genetic; Risk Factors	1998
Homozygous arginine-72 in wild type p53 and risk of cervical cancer. Lancet (London, England), 1998, Nov-28, Volume: 352, Issue:9142 Topics: Alleles; Arginine; Cell Transformation, Neoplastic; Female; Genetic Predisposition to Disease; Homozygote; Humans; Neoplasm Staging; Papillomaviridae; Papillomavirus Infections; Proline; Risk Factors; Tumor Suppressor Protein p53; Tumor Virus Infections; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms	1998
p53 polymorphism and risk of cervical cancer. Nature, 1998, Dec-10, Volume: 396, Issue:6711 Topics: Alleles; Arginine; Breast Neoplasms; DNA-Binding Proteins; Female; Gene Frequency; Genes, p53; Genetic Predisposition to Disease; Humans; Oncogene Proteins, Viral; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Repressor Proteins; Risk Factors; Tumor Suppressor Protein p53; Tumor Virus Infections; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms	1998
p53 polymorphism and risk of cervical cancer. Nature, 1998, Dec-10, Volume: 396, Issue:6711 Topics: Arginine; DNA-Binding Proteins; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Oncogene Proteins, Viral; Papillomaviridae; Polymorphism, Genetic; Repressor Proteins; Risk Factors; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms	1998
The combination of polymorphisms within interferon-gamma receptor 1 and receptor 2 associated with the risk of systemic lupus erythematosus. FEBS letters, 1999, Jun-18, Volume: 453, Issue:1-2 Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamine; Humans; Interferon gamma Receptor; Lupus Erythematosus, Systemic; Male; Methionine; Middle Aged; Molecular Sequence Data; Odds Ratio; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Receptors, Interferon; Reverse Transcriptase Polymerase Chain Reaction; Valine	1999
Papillomavirus and p53 codon 72 polymorphism. International journal of cancer, 1999, Aug-12, Volume: 82, Issue:4 Topics: Arginine; Case-Control Studies; Cell Division; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Tumor Virus Infections; Uterine Cervical Neoplasms	1999
p53 codon 72 ARG/PRO polymorphism is not related to HPV type or lesion grade in low- and high-grade squamous intra-epithelial lesions and invasive squamous carcinoma of the cervix. International journal of cancer, 1999, Sep-24, Volume: 83, Issue:1 Topics: Arginine; Carcinoma, Squamous Cell; Condylomata Acuminata; Female; Genes, p53; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Oncogene Proteins, Viral; Papillomaviridae; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Risk Factors; Uterine Cervical Dysplasia; Uterine Cervical Neoplasms	1999
Xenon does not trigger malignant hyperthermia in susceptible swine. Anesthesiology, 1999, Volume: 91, Issue:4 Topics: Amino Acid Substitution; Anesthesia, General; Anesthetics, Inhalation; Animals; Arginine; Blood Pressure; Cardiac Output; Cysteine; Genetic Predisposition to Disease; Halothane; Heart Rate; Homozygote; Malignant Hyperthermia; Mutation; Ryanodine Receptor Calcium Release Channel; Swine; Xenon	1999
DNA sequence variants of p53: cancer and aging. American journal of human genetics, 1999, Volume: 65, Issue:6 Topics: Aged; Aged, 80 and over; Aging; Arginine; Codon; Genes, p53; Genetic Predisposition to Disease; Genetic Variation; Genotype; Haplotypes; Humans; Middle Aged; Neoplasms; Odds Ratio; Polymorphism, Genetic; Proline	1999
P53 codon 72 polymorphism as a risk factor in the development of HPV-associated non-melanoma skin cancers in immunocompetent hosts. International journal of molecular medicine, 2000, Volume: 5, Issue:4 Topics: Arginine; Carcinoma, Basal Cell; Carcinoma, Squamous Cell; Codon; DNA Primers; DNA, Viral; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Middle Aged; Papillomaviridae; Papillomavirus Infections; Polymerase Chain Reaction; Polymorphism, Genetic; Risk Factors; Skin Neoplasms; Tumor Virus Infections	2000
p53 codon 72 polymorphism and risk of cervical carcinoma in Korean women. Journal of Korean medical science, 2000, Volume: 15, Issue:1 Topics: Alleles; Arginine; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Humans; Papillomaviridae; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Risk Factors; Tumor Suppressor Protein p53; Uterine Cervical Neoplasms	2000
p53 codon 72 polymorphism does not affect the risk of cervical cancer in patients from northern Italy. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2000, Volume: 9, Issue:4 Topics: Adult; Aged; Arginine; Case-Control Studies; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Humans; Italy; Middle Aged; Odds Ratio; Papillomaviridae; Papillomavirus Infections; Polymorphism, Genetic; Retrospective Studies; Risk Assessment; Tumor Virus Infections; Uterine Cervical Neoplasms	2000
p53 codon 72 polymorphism as a risk factor in the development of breast cancer. Molecular cell biology research communications : MCBRC, 2000, Volume: 3, Issue:6 Topics: Adult; Alleles; Amino Acid Substitution; Arginine; Breast Neoplasms; Codon; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Middle Aged; Neoplasm Staging; Polymorphism, Genetic; Proline; Receptors, Estrogen; Receptors, Progesterone; Tumor Suppressor Protein p53	2000
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
Identification of a novel common genetic risk factor for lumbar disk disease. JAMA, 2001, Apr-11, Volume: 285, Issue:14 Topics: Adult; Aged; Alleles; Arginine; Case-Control Studies; Collagen; Collagen Type IX; DNA Mutational Analysis; Electrophoresis; Finland; Genetic Predisposition to Disease; Humans; Intervertebral Disc Displacement; Lumbar Vertebrae; Magnetic Resonance Imaging; Middle Aged; Point Mutation; Polymerase Chain Reaction; Risk Factors; Tomography, X-Ray Computed; Tryptophan	2001
Paraoxonase 1 192 Gln/Arg gene polymorphism and cerebrovascular disease: interaction with type 2 diabetes. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association, 2001, Volume: 109, Issue:3 Topics: Aged; Alleles; Arginine; Aryldialkylphosphatase; Cerebrovascular Disorders; Diabetes Mellitus, Type 2; Esterases; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Smoking	2001
Gender specific associations of the Trp64Arg mutation in the beta3-adrenergic receptor gene with obesity-related phenotypes in a Mediterranean population: interaction with a common lipoprotein lipase gene variation. Journal of internal medicine, 2001, Volume: 250, Issue:4 Topics: Adolescent; Adult; Aged; Alleles; Arginine; Body Mass Index; Body Weight; DNA Mutational Analysis; Female; Genetic Carrier Screening; Genetic Predisposition to Disease; Genetic Variation; Humans; Lipoprotein Lipase; Male; Middle Aged; Obesity; Phenotype; Receptors, Adrenergic, beta-3; Sex Factors; Spain; Tryptophan	2001
Trp64Arg beta3-adrenoceptor: when does a candidate gene become a disease-susceptibility gene? Obesity research, 2001, Volume: 9, Issue:12 Topics: Arginine; Body Mass Index; Genetic Predisposition to Disease; Genetic Variation; Humans; Prospective Studies; Receptors, Adrenergic, beta-3; Tryptophan	2001
Differential association of the codon 72 p53 and GSTM1 polymorphisms on histological subtype of non-small cell lung carcinoma. Cancer research, 2001, Dec-15, Volume: 61, Issue:24 Topics: Adenocarcinoma; Aged; Alleles; Arginine; Carcinoma, Squamous Cell; Case-Control Studies; Codon; Female; Genes, p53; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Logistic Models; Lung Neoplasms; Male; Middle Aged; Polymorphism, Genetic; Proline	2001
[p53 gene codon 72 polymorphism and susceptibility to esophageal squamous cell carcinoma in a Chinese population]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2002, Volume: 19, Issue:1 Topics: Alleles; Arginine; Asian People; Carcinoma, Squamous Cell; Codon; Confidence Intervals; Esophageal Neoplasms; Genetic Predisposition to Disease; Genotype; Humans; Odds Ratio; Polymorphism, Genetic; Proline; Tumor Suppressor Protein p53	2002
Intracellular adhesion molecule Gly241Arg polymorphism has no impact on ARDS or septic shock in community-acquired pneumonia. Chest, 2002, Volume: 121, Issue:3 Suppl Topics: Arginine; Community-Acquired Infections; Genetic Predisposition to Disease; Glycine; Humans; Intercellular Adhesion Molecule-1; Phenotype; Pneumonia; Point Mutation; Polymorphism, Genetic; Prospective Studies; Respiratory Distress Syndrome; Shock, Septic	2002
The quantity of nitric oxide released by macrophages regulates Chlamydia-induced disease. Proceedings of the National Academy of Sciences of the United States of America, 2002, Mar-19, Volume: 99, Issue:6 Topics: Animals; Arginase; Arginine; Catalysis; Chlamydia; Chlamydia Infections; Genetic Predisposition to Disease; Macrophages; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type II; Phenotype; RNA, Messenger	2002
Long-term high-fat feeding leads to severe insulin resistance but not diabetes in Wistar rats. American journal of physiology. Endocrinology and metabolism, 2002, Volume: 282, Issue:6 Topics: Acyl Coenzyme A; Aging; Animals; Arginine; Blood Glucose; Body Composition; Diabetes Mellitus; Dietary Fats; Fasting; Genetic Predisposition to Disease; Glucose Clamp Technique; Glucose Intolerance; Glucose Tolerance Test; Glycogen; Insulin; Insulin Resistance; Liver; Male; Muscle, Skeletal; Rats; Rats, Wistar; Time Factors; Triglycerides; Weight Gain	2002
Susceptibility to type 1 (insulin-dependent) diabetes mellitus in Spanish patients correlates quantitatively with expression of HLA-DQ alpha Arg 52 and HLA-DQ beta non-Asp 57 alleles. Diabetologia, 1992, Volume: 35, Issue:6 Topics: Alleles; Arginine; Aspartic Acid; Base Sequence; Cells, Cultured; Diabetes Mellitus, Type 1; Disease Susceptibility; Gene Frequency; Genetic Predisposition to Disease; Genotype; HLA-DQ alpha-Chains; HLA-DQ Antigens; HLA-DQ beta-Chains; Homozygote; Humans; Lymphocytes; Molecular Sequence Data; Oligodeoxyribonucleotides; Oligonucleotide Probes; Polymerase Chain Reaction; Reference Values; Risk Factors; Spain	1992
Aberrant DNA topoisomerase II activity, radioresistance and inherited susceptibility to cancer. British journal of cancer, 1991, Volume: 63, Issue:1 Topics: Amsacrine; Ataxia Telangiectasia; Cell Line; Cell Nucleus; Cell Transformation, Neoplastic; Cytarabine; Cytoplasm; DNA Repair; DNA Topoisomerases, Type II; DNA, Circular; DNA, Superhelical; Female; Fibroblasts; Gene Expression; Genetic Predisposition to Disease; Humans; Male; Neoplasms; Oncogenes; Radiation Tolerance; Teniposide; Topoisomerase II Inhibitors	1991