Sfoglia per Rivista  NATURE GENETICS

Opzioni
Vai a: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Mostrati risultati da 1 a 5 di 5
Titolo Data di pubblicazione Autore(i) File
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps 1-gen-2016 Iotchkova, Valentina; Huang, Jie; Morris, John A; Jain, Deepti; Barbieri, Caterina; Walter, Klaudia; Min, Josine L; Chen, Lu; Astle, William; Cocca, Massimilian; Deelen, Patrick; Elding, Heather; Farmaki, Aliki Eleni; Franklin, Christopher S; Franberg, Mattias; Gaunt, Tom R; Hofman, Albert; Jiang, Tao; Kleber, Marcus E; Lachance, Genevieve; Luan, Jian'An; Malerba, Giovanni; Matchan, Angela; Mead, Daniel; Memari, Yasin; Ntalla, Ioanna; Panoutsopoulou, Kalliope; Pazoki, Raha; Perry, John R. B; Rivadeneira, Fernando; Sabater Lleal, Maria; Sennblad, Bengt; Shin, So Youn; Southam, Lorraine; Traglia, Michela; van Dijk, Freerk; van Leeuwen, Elisabeth M; Zaza, Gianluigi; Zhang, Weihua; Amin, Najaf; Butterworth, Adam; Chambers, John C; Dedoussis, George; Dehghan, Abbas; Franco, Oscar H; Franke, Lude; Frontini, Mattia; Gambaro, Giovanni; Gasparini, Paolo; Hamsten, Anders; Issacs, Aaron; Kooner, Jaspal S; Kooperberg, Charles; Langenberg, Claudia; Marz, Winfried; Scott, Robert A; Swertz, Morris A; Toniolo, Daniela; Uitterlinden, Andre G; van Duijn, Cornelia M; Watkins, Hugh; Zeggini, Eleftheria; Maurano, Mathew T; Timpson, Nicholas J; Reiner, Alexander P; Auer, Paul L; Soranzo, Nicole
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy. 1-gen-2023 Kiryluk, K; Sanchez-Rodriguez, E; Zhou, Xj; Zanoni, F; Liu, L; Mladkova, N; Khan, A; Marasa, M; Zhang, Jy; Balderes, O; Sanna-Cherchi, S; Bomback, As; Canetta, Pa; Appel, Gb; Radhakrishnan, J; Trimarchi, H; Sprangers, B; Cattran, Dc; Reich, H; Pei, Y; Ravani, P; Galesic, K; Maixnerova, D; Tesar, V; Stengel, B; Metzger, M; Canaud, G; Maillard, N; Berthoux, F; Berthelot, L; Pillebout, E; Monteiro, R; Nelson, R; Wyatt, Rj; Smoyer, W; Mahan, J; Samhar, Aa; Hidalgo, G; Quiroga, A; Weng, P; Sreedharan, R; Selewski, D; Davis, K; Kallash, M; Vasylyeva, Tl; Rheault, M; Chishti, A; Ranch, D; Wenderfer, Se; Samsonov, D; Claes, Dj; Akchurin, O; Goumenos, D; Stangou, M; Nagy, J; Kovacs, T; Fiaccadori, E; Amoroso, A; Barlassina, C; Cusi, D; Del Vecchio, L; Battaglia, Gg; Bodria, M; Boer, E; Bono, L; Boscutti, G; Caridi, G; Lugani, F; Ghiggeri, G; Coppo, R; Peruzzi, L; Esposito, V; Esposito, C; Feriozzi, S; Polci, R; Frasca, G; Galliani, M; Garozzo, M; Mitrotti, A; Gesualdo, L; Granata, S; Zaza, G; Londrino, F; Magistroni, R; Pisani, I; Magnano, A; Marcantoni, C; Messa, P; Mignani, R; Pani, A; Ponticelli, C; Roccatello, D; Salvadori, M; Salvi, E; Santoro, D; Gembillo, G; Savoldi, S; Spotti, D; Zamboli, P; Izzi, C; Alberici, F; Delbarba, E; Florczak, M; Krata, N; Mucha, K; Pączek, L; Niemczyk, S; Moszczuk, B; Pańczyk-Tomaszewska, M; Mizerska-Wasiak, M; Perkowska-Ptasińska, A; Bączkowska, T; Durlik, M; Pawlaczyk, K; Sikora, P; Zaniew, M; Kaminska, D; Krajewska, M; Kuzmiuk-Glembin, I; Heleniak, Z; Bullo-Piontecka, B; Liberek, T; Dębska-Slizien, A; Hryszko, T; Materna-Kiryluk, A; Miklaszewska, M; Szczepańska, M; Dyga, K; Machura, E; Siniewicz-Luzeńczyk, K; Pawlak-Bratkowska, M; Tkaczyk, M; Runowski, D; Kwella, N; Drożdż, D; Habura, I; Kronenberg, F; Prikhodina, L; van Heel, D; Fontaine, B; Cotsapas, C; Wijmenga, C; Franke, A; Annese, V; Gregersen, Pk; Parameswaran, S; Weirauch, M; Kottyan, L; Harley, Jb; Suzuki, H; Narita, I; Goto, S; Lee, H; Kim, Dk; Kim, Ys; Park, Jh; Cho, B; Choi, M; Van Wijk, A; Huerta, A; Ars, E; Ballarin, J; Lundberg, S; Vogt, B; Mani, Ly; Caliskan, Y; Barratt, J; Abeygunaratne, T; Kalra, Pa; Gale, Dp; Panzer, U; Rauen, T; Floege, J; Schlosser, P; Ekici, Ab; Eckardt, Ku; Chen, N; Xie, J; Lifton, Rp; Loos, Rjf; Kenny, Ee; Ionita-Laza, I; Köttgen, A; Julian, Ba; Novak, J; Scolari, F; Zhang, H; Gharavi, Ag.
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. 1-gen-2005 Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw
Multiple common variants for celiac disease influencing immune gene expression 1-gen-2010 Dubois, Pc; Trynka, G; Franke, L; Hunt, Ka; Romanos, J; Curtotti, A; Zhernakova, A; Heap, Ga; Adány, R; Aromaa, A; Bardella, Mt; van den Berg, Lh; Bockett, Na; de la Concha, Eg; Dema, B; Fehrmann, Rs; Fernández-Arquero, M; Fiatal, S; Grandone, E; Green, Pm; Groen, Hj; Gwilliam, R; Houwen, Rh; Hunt, Se; Kaukinen, K; Kelleher, D; Korponay-Szabo, I; Kurppa, K; Macmathuna, P; Mäki, M; Mazzilli, Mc; Mccann, Ot; Mearin, Ml; Mein, Ca; Mirza, Mm; Mistry, V; Mora, B; Morley, Ki; Mulder, Cj; Murray, Ja; Núñez, C; Oosterom, E; Ophoff, Ra; Polanco, I; Peltonen, L; Platteel, M; Rybak, A; Salomaa, V; Schweizer, Jj; Sperandeo, Mp; Tack, Gj; Turner, G; Veldink, Jh; Verbeek, Wh; Weersma, Rk; Wolters, Vm; Urcelay, E; Cukrowska, B; Greco, L; Neuhausen, Sl; Mcmanus, R; Barisani, D; Deloukas, P; Barrett, Jc; Saavalainen, P; Wijmenga, C; van Heel, Da
Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. 1-gen-2000 Seri, M; Cusano, R; Gangarossa, S; Caridi, G; Bordo, D; LO NIGRO, C; Ghiggeri, Gm; Ravazzolo, R; Savino, M; DEL VECCHIO, M; D'Apolito, M; Iolascon, Achille; Zelante, Ll; Savoia, A; Balduini, Cl; Noris, P; Magrini, U; Belletti, S; Heath, Ke; Babcock, M; Glucksman, Mj; Aliprandis, E; Bizzaro, N; Desnick, Rj; Martignetti, J. A.
Mostrati risultati da 1 a 5 di 5
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile