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 7 di 7
Titolo Data di pubblicazione Autore(i) File
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes 1-gen-2004 Guo, Dh; Li, My; Zhang, Y; Yang, P; Eckenrode, S; Hopkins, D; Zheng, Wp; Purohit, S; Podolsky, Rh; Muir, A; Wang, Jz; Dong, Z; Brusko, T; Atkinson, M; Pozzilli, P; Zeidler, A; Raffel, Lj; Jacob, Co; Park, Y; Serrano-Rios, M; Larrad, Mtm; Zhang, Zx; Garchon, Hj; Bach, Jf; Rotter, Ji; She, Jx; Wang, Cy
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes (vol 36, pg 837, 2004) 1-gen-2004 Guo, D; Li, M; Zhang, Y; Yang, P; Eckenrode, S; Hopkins, D; Zheng, W; Purohit, S; Podolsky, Rh; Muir, A; Wang, J; Dong, Z; Brusko, T; Atkinson, M; Pozzilli, P; Zeidler, A; Raffel, Lj; Jacob, Co; Park, Y; Serrano-Rios, M; Larrad, Mtm; Zhang, Z; Garchon, Hj; Bach, Jf; Rotter, Ji; She, Jx; Wang, Cy
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele 1-gen-1997 Bennett, St; Wilson, Aj; Esposito, L; Bouzekri, N; Undlien, De; Cucca, F; Nistico, L; Buzzetti, R; Bosi, E; Pociot, F; Nerup, J; Cambonthomsen, A; Pugliese, A; Shield, Jph; Mckinney, Pa; Bain, Sc; Polychronakos, C; Todd, Ja; Pozzilli, P; Visalli, N; Baroni, M; Fioriti, E; Mesturino, C; Signore, A; Cavallo, M; Lucentini, L; Matteoli, M; Crino, A; Teodonio, C; Amoretti, R; Tombesi, A; Ruggeri, M; Pisano, L; Suraci, C; Pennafina, M; Boscherini, B; Stoduto, S; Fonte, M; Mancabitti, M; Multari, G; Suppa, M; Demattia, G; Faldetta, Mc; Laurenti, O; Marietti, G; Pitocco, D; Ferrazzoli, F; Bizzarri, C; Ghirlanda, G
Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer 1-gen-2012 Martin Peifer, Lynnette Fernández-Cuesta; Sos, Martin L; George, Julie; Seidel, Danila; Kasper, Lawryn H; Plenker, Dennis; Leenders, Frauke; Sun, Ruping; Zander, Thomas; Menon, Roopika; Koker, Mirjam; Dahmen, Ilona; Müller, Christian; Cerbo8, Vincenzo Di; Schildhaus, Hans-Ulrich; Altmüller, Janine; Baessmann, Ingelore; Becker, Christian; Wilde, Bram de; Vandesompele, Jo; Böhm, Diana; Ansén, Sascha; Gabler, Franziska; Wilkening, Ines; Heynck, Stefanie; Heuckmann, Johannes M; Lu, Xin; Cibulskis, Kristian; Banerji, Shantanu; Getz, Gad; Park, Kwon-Sik; Rauh, Daniel; Grütter, Christian; Fischer, Matthias; Pasqualucci, Laura; Wright, Gavin; Wainer, Zoe; Russe, Prudence; Petersen, Iver; Chen, Yuan; Stoelben, Erich; Ludwig, Corinna; Schnabe, Philipp; Hoffmann, Hans; Muley, Thomas; Brockmann, Michael; Engel-Riede, Walburga; Muscarella, Lucia A; V. M., Fazio; Groen, Harry; Timens, Wim; Sietsma, Hannie; Thunnissen, Erik; Smit, Egbert; Heideman, Daniëlle AM; Snijders, Peter JF; Cappuzzo, Federico; Ligorio, Claudia; Damiani, Stefania; Field, John; Solberg, Steinar; Brustugun, Odd Terje; Lund-Iversen, Marius; Sänger, Jörg; Clement, Joachim H; Soltermann, Alex; Moch, Holger; Weder, Walter; Solomon, Benjamin; Soria, Jean-Charles; Validire, Pierre; Besse, Benjamin; Brambilla, Elisabeth; Brambilla, Christian; Lantuejoul, Sylvie; Lorimier, Philippe; Schneider, Peter M; Hallek, Michael; Pao, William; Meyerson, Matthew; Sage, Julien; Shendure, Jay; Schneider, Robert; Büttner, Reinhard; Wolf, Jürgen; Nürnberg10, Peter; Perner, Sven; Heukamp, Lukas C; Brindle, Paul K; Haas, Stefan; Thomas, Roman K; Fazio, VITO MICHELE
Interaction of reelin signaling and Lis1 in brain development 1-gen-2003 Assadi, Ah; Zhang, Gc; Beffert, U; Mcneil, Rs; Renfro, Al; Niu, S; Quattrocchi, C; Antalffy, Ba; Sheldon, M; Armstrong, Dd; Wynshaw-Boris, A; Herz, J; D'Arcangelo, G; Clark, Gd
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. 1-gen-2012 Heinzen, El; Swoboda, Kj; Hitomi, Y; Gurrieri, Fiorella; Tiziano, Francesco Danilo; Nicole, S; Fontaine, B; De Vries, B; Walley, Nm; Heavin, S; Panagiotakaki, E; Koelewijn, S; Kamphorst, J; Geilenkirchen, M; Pelzer, N; Laan, L; Haan, J; Ferrari, Mirella; Van Den Maagdenberg, A; Fiori, S; Abiusi, E; Di Pietro, Lorena; Sweney, Mt; Newcomb, Tm; Viollet, L; Huff, C; Jorde, Lb; Reyna, Sp; Murphy, Kj; Shianna, Kv; Gumbs, Ce; Little, L; Silver, K; Ptáček, Lj; Haan, J; Herke, S Gk; Whitelaw, Cm; Webb, D; Lynch, Bj; Uldall, P; King, Md; Scheffer, Ie; Neri, Giovanni; Arzimanoglou, A; Sisodiya, Sm; Mikati, Ma; Goldstein, Db
PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY CRITICAL REGION ON CHROMOSOME-7Q36 RID A-1081-2010 1-gen-1993 Gurrieri, F; Trask, Bj; Vandenengh, G; Krauss, Cm; Schinzel, A; Pettenati, Mj; Schindler, D; Dietzband, J; Vergnaud, G; Scherer, Sw; Tsui, Lc; Muenke, M
Mostrati risultati da 1 a 7 di 7
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