Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 5

Results: 27

GenePattern 2.0.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 500, doi. 10.1038/ng0506-500

By:

Reich, Michael;
Liefeld, Ted;
Gould, Joshua;
Lerner, Jim;
Tamayo, Pablo;
Mesirov, Jill P.

Publication type:

Article

Animal research and the search for understanding.

Published in:: 2006
Publication type:: Editorial

PTPN22 and invasive bacterial disease.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 499, doi. 10.1038/ng0506-499

By:

Chapman, Stephen J.;
Khor, Chiea C.;
Vannberg, Fredrik O.;
Maskell, Nicholas A.;
Davies, Christopher W. H.;
Hedley, Emma L.;
Segal, Shelley;
Moore, Catrin E.;
Knox, Kyle;
Day, Nicholas P.;
Gillespie, Stephen H.;
Crook, Derrick W.;
Davies, Robert J. O.;
Hill, Adrian V. S.

Publication type:

Article

Iron metabolism meets signal transduction.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 503, doi. 10.1038/ng0506-503

By:

Anderson, Gregory J.;
Frazer, David M.

Publication type:

Article

A broad band of silence.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 504, doi. 10.1038/ng0506-504

By:

Smith, Justin S.;
Costello, Joseph F.

Publication type:

Article

An adaptive path through jungle DNA.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 506, doi. 10.1038/ng0506-506

By:

de Meaux, Juliette

Publication type:

Article

mtDNA clock runs out for dopaminergic neurons.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 507, doi. 10.1038/ng0506-507

By:

Manfredi, Giovanni

Publication type:

Article

Touching base.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 509, doi. 10.1038/ng0506-509

By:

Axton, Myles;
Niemitz, Emily;
Vogan, Kyle

Publication type:

Article

Research Highlights.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 511, doi. 10.1038/ng0506-511

By:

Axton, Myles;
Bahcall, Orli;
Niemitz, Emily;
Packer, Alan;
Vogan, Kyle

Publication type:

Article

Integrating genomics against infectious disease.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 513, doi. 10.1038/ng0506-513

By:

Poland, Haley

Publication type:

Article

Corrigendum: Germline KRAS mutations cause Noonan syndrome.

Published in:

2006

By:

Schubbert, Suzanne;
Zenker, Martin;
Rowe, Sara L;
Böll, Silke;
Klein, Cornelia;
Bollag, Gideon;
van der Burgt, Ineke;
Musante, Luciana;
Kalscheuer, Vera;
Wehner, Lars-Erik;
Nguyen, Hoa;
West, Brian;
Zhang, Kam Y J;
Sistermans, Erik;
Rauch, Anita;
Niemeyer, Charlotte M;
Shannon, Kevin;
Kratz, Christian P

Publication type:

Correction Notice

Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 561, doi. 10.1038/ng1775

By:

Toydemir, Reha M.;
Rutherford, Ann;
Whitby, Frank G.;
Jorde, Lynn B.;
Carey, John C.;
Bamshad, Michael J.

Publication type:

Article

Systematic identification of human mitochondrial disease genes through integrative genomics.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 576, doi. 10.1038/ng1776

By:

Calvo, Sarah;
Mohit Jain;
Xiaohui Xie;
Sheth, Sunil A.;
Chang, Betty;
Goldberger, Olga A.;
Spinazzola, Antonella;
Zeviani, Massimo;
Carr, Steven A.;
Mootha, Vamsi K.

Publication type:

Article

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 518, doi. 10.1038/ng1778

By:

Kraytsberg, Yevgenya;
Kudryavtseva, Elena;
McKee, Ann C.;
Geula, Changiz;
Kowall, Neil W.;
Khrapko, Konstantin

Publication type:

Article

X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 528, doi. 10.1038/ng1779

By:

Musio, Antonio;
Selicorni, Angelo;
Focarelli, Maria Luisa;
Gervasini, Cristina;
Milani, Donatella;
Russo, Silvia;
Vezzoni, Paolo;
Larizza, Lidia

Publication type:

Article

Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 531, doi. 10.1038/ng1777

By:

Babitt, Jodie L.;
Huang, Franklin W.;
Wrighting, Diedra M.;
Yin Xia;
Sidis, Yisrael;
Samad, Tarek A.;
Campagna, Jason A.;
Chung, Raymond T.;
Schneyer, Alan L.;
Woolf, Clifford J.;
Andrews, Nancy C.;
Lin, Herbert Y.

Publication type:

Article

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 570, doi. 10.1038/ng1765

By:

Spinazzola, Antonella;
Viscomi, Carlo;
Fernandez-Vizarra, Erika;
Carrara, Franco;
D'Adamo, Pio;
Calvo, Sarah;
Marsano, René Massimiliano;
Donnini, Claudia;
Weiher, Hans;
Strisciuglio, Pietro;
Parini, Rossella;
Sarzi, Emmanuelle;
Chan, Alicia;
DiMauro, Salvatore;
Rötig, Agnes;
Gasparini, Paolo;
Ferrero, Iliana;
Mootha, Vamsi K.;
Tiranti, Valeria;
Zeviani, Massimo

Publication type:

Article

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 515, doi. 10.1038/ng1769

By:

Bender, Andreas;
Krishnan, Kim J.;
Morris, Christopher M.;
Taylor, Geoffrey A.;
Reeve, Amy K.;
Perry, Robert H.;
Jaros, Evelyn;
Hersheson, Joshua S.;
Betts, Joanne;
Klopstock, Thomas;
Taylor, Robert W.;
Turnbull, Douglass M.

Publication type:

Article

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 556, doi. 10.1038/ng1770

By:

Service, Susan;
DeYoung, Joseph;
Karayiorgou, Maria;
Roos, J. Louw;
Pretorious, Herman;
Bedoya, Gabriel;
Ospina, Jorge;
Ruiz-Linares, Andres;
Macedo, António;
Palha, Joana Almeida;
Heutink, Peter;
Aulchenko, Yurii;
Oostra, Ben;
van Duijn, Cornelia;
Jarvelin, Marjo-Riitta;
Varilo, Teppo;
Peddle, Lynette;
Rahman, Proton;
Piras, Giovanna;
Monne, Maria

Publication type:

Article

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 521, doi. 10.1038/ng1771

By:

Stoetzel, Corinne;
Laurier, Virginie;
Davis, Erica E.;
Muller, Jean;
Rix, Suzanne;
Badano, José L;
Leitch, Carmen C.;
Salem, Nabiha;
Chouery, Eliane;
Corbani, Sandra;
Jalk, Nadine;
Vicaire, Serge;
Sarda, Pierre;
Hamel, Christian;
Lacombe, Didier;
Holder, Muriel;
Odent, Sylvie;
Holder, Susan;
Brooks, Alice S.;
Elcioglu, Nursel H.

Publication type:

Article

A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 566, doi. 10.1038/ng1773

By:

Ropero, Santiago;
Fraga, Mario F.;
Ballestar, Esteban;
Hamelin, Richard;
Yamamoto, Hiroyuki;
Boix-Chornet, Manuel;
Caballero, Rosalia;
Alaminos, Miguel;
Setien, Fernando;
Paz, Maria F.;
Herranz, Michel;
Palacios, Jose;
Arango, Diego;
Orntoft, Torben F.;
Aaltonen, Lauri A.;
Schwartz Jr, Simó;
Esteller, Manel

Publication type:

Article

Ablation of PDK1 in pancreatic β cells induces diabetes as a result of loss of β cell mass.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 589, doi. 10.1038/ng1774

By:

Hashimoto, Naoko;
Kido, Yoshiaki;
Uchida, Tohru;
Asahara, Shun-ichiro;
Shigeyama, Yutaka;
Matsuda, Tomokazu;
Takeda, Akihiko;
Tsuchihashi, Daisuke;
Nishizawa, Akihiko;
Ogawa, Wataru;
Fujimoto, Yoshito;
Okamura, Hitoshi;
Arden, Karen C.;
Herrera, Pedro L.;
Noda, Tetsuo;
Kasuga, Masato

Publication type:

Article

Epigenetic remodeling in colorectal cancer results in coordinate gene suppression across an entire chromosome band.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 540, doi. 10.1038/ng1781

By:

Frigola, Jordi;
Song, Jenny;
Stirzaker, Clare;
Hinshelwood, Rebecca A.;
Peinado, Miguel A.;
Clark, Susan J.

Publication type:

Article

A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 550, doi. 10.1038/ng1782

By:

Graham, Robert R.;
Kozyrev, Sergey V.;
Baechler, Emily C.;
Reddy, M. V. Prasad Linga;
Plenge, Robert M.;
Bauer, Jason W.;
Ortmann, Ward A.;
Koeuth, Thearith;
Escribano, Ma Francisca González;
Pons-Estel, Bernardo;
Petri, Michelle;
Daly, Mark;
Gregersen, Peter K.;
Martín, Javier;
Altshuler, David;
Behrens, Timothy W.;
Alarcón-Riquelme, Marta E.

Publication type:

Article

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 525, doi. 10.1038/ng1783

By:

Shore, Eileen M.;
Meiqi Xu;
Feldman, George J;
Fenstermacher, David A.;
Brown, Matthew A.;
Kaplan, Frederick S.

Publication type:

Article

A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 594, doi. 10.1038/ng1784

By:

Clark, Richard M.;
Wagler, Tina Nussbaum;
Quijada, Pablo;
Doebley, John

Publication type:

Article

Total insulin and IGF-I resistance in pancreatic β cells causes overt diabetes.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 583, doi. 10.1038/ng1787

By:

Ueki, Kohjiro;
Okada, Terumasa;
Hu, Jiang;
Liew, Chong Wee;
Assmann, Anke;
Dahlgren, Gabriella M;
Peters, Jennifer L;
Shackman, Jonathan G;
Zhang, Min;
Artner, Isabella;
Satin, Leslie S;
Stein, Roland;
Holzenberger, Martin;
Kennedy, Robert T;
Kahn, C Ronald;
Kulkarni, Rohit N

Publication type:

Article