Nature Genetics

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A deletion in the bovine myostatin gene causes the double–muscled phenotype in cattle
Nature Genetics - Tập 17 Số 1 - Trang 71-74 - 1997
Luc Grobet, L. J. Royo, Dominique Poncelet, Dimitri Pirottin, Benoît Brouwers, Juliette Riquet, Andreina Schoeberlein, S. Dunner, François Ménissier, Julio Massabanda, Ruedi Fries, R. Hanset, Michel Georges
Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation
Nature Genetics - Tập 23 Số 1 - Trang 62-66 - 1999
Paul A. Wade, Anne Gégonne, Peter Lloyd Jones, Esteban Ballestar, Fabien Aubry, Alan P. Wolffe
The nucleolar remodeling complex NoRC mediates heterochromatin formation and silencing of ribosomal gene transcription
Nature Genetics - Tập 32 Số 3 - Trang 393-396 - 2002
Raffaella Santoro, Junwei Li, Ingrid Grummt
Gene-expression profile of the ageing brain in mice
Nature Genetics - Tập 25 Số 3 - Trang 294-297 - 2000
Cheol‐Koo Lee, Richard Weindruch, Tomas A. Prolla
Comparing genomic expression patterns across species identifies shared transcriptional profile in aging
Nature Genetics - Tập 36 Số 2 - Trang 197-204 - 2004
Steven A. McCarroll, Coleen T. Murphy, Sige Zou, Scott D. Pletcher, Chen-Shan Chin, Yuh Nung Jan, Cynthia Kenyon, Cornelia I. Bargmann, Hao Li
Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass
Nature Genetics - Tập 26 Số 1 - Trang 97-102 - 2000
Airu S. Chen, Donald J. Marsh, Myrna E. Trumbauer, Easter G. Frazier, Xiao-Ming Guan, Hong Yu, Charles Rosenblum, Aurawan Vongs, Yue Feng, Lequn Cao, Joseph M. Metzger, Alison M. Strack, Ramon E. Camacho, T.N. Mellin, Christian Nunes da Silva, William Min, Jill K. Fisher, Shobhna Gopal-Truter, D. Euan MacIntyre, Howard Y. Chen, Lex H.T. Van der Ploeg
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
Nature Genetics - Tập 36 Số 4 - Trang 377-381 - 2004
Giles Watts, Jill Wymer, Margaret J. Kovach, Sarju Mehta, Steven Mumm, Daniel Darvish, Alan Pestronk, Michael P. Whyte, Virginia Kimonis
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling
Nature Genetics - Tập 46 Số 5 - Trang 503-509 - 2014
Gillian Rice, Yoandris del Toro Duany, Emma Jenkinson, Gabriella Forte, Beverley Anderson, Giada Ariaudo, Brigitte Bader‐Meunier, Eileen Baildam, Roberta Battini, Michael W. Beresford, Manuela Casarano, Mondher Chouchane, Rolando Cimaz, Abigail E. Collins, Nuno Cordeiro, Russell C. Dale, Joyce Davidson, Liesbeth De Waele, Isabelle Desguerre, Laurence Faivre, Elisa Fazzi, Bertrand Isidor, Lieven Lagae, Andrew Latchman, Pierre Lebon, Chumei Li, John H. Livingston, Charles Marques Lourenço, Maria Margherita Mancardi, Gregory J. Pazour, Iain B. McInnes, Manoj P. Menezes, Cyril Mignot, James O’Sullivan, Simona Orcesi, Paolo Picco, Enrica Riva, Robert A. Robinson, Diana Rodriguez, E. Salvatici, Christiaan Scott, Marta Szybowska, John Tolmie, Adeline Vanderver, Catherine Vanhulle, José Pedro Vieira, Kate Webb, Robyn Whitney, Simon G. Williams, Lynne A. Wolfe, Sameer M. Zuberi, Sun Hur, Yanick J. Crow
MDA5 and autoimmune disease
Nature Genetics - Tập 46 Số 5 - Trang 418-419 - 2014
Jonathan J. Miner, Michael Diamond
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis
Nature Genetics - Tập 43 Số 4 - Trang 306-308 - 2011
Bertrand Isidor, Pierre Lindenbaum, Olivier Pichon, Stéphane Bézieau, Christian Dina, Sébastien Jacquemont, Dominique Martin–Coignard, Christel Thauvin‐Robinet, Martine Le Merrer, Jean‐Louis Mandel, Albert David, Laurence Faivre, Valérie Cormier‐Daire, Richard Redon, Cédric Le Caignec
Tổng số: 687   
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