Works matching IS 10614036 AND DT 2005 AND VI 37 AND IP 8

Results: 29

WayStation to HUGOBase.

Published in:: 2005
Publication type:: Editorial

Pharmacogenetics goes 3D.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 794, doi. 10.1038/ng0805-794

By:

McLeod, Howard L.;
Marsh, Sharon

Publication type:

Article

Reply to "Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor".

Published in:

2005

By:

Cerrato, Flavia;
Sparago, Angela;
Farina, Lucia;
Ferrero, Giovanni Battista;
Silengo, Margherita Cirillo;
Riccio, Andrea

Publication type:

Letter

Are we making progress in the debate over racial and ethnic categories in biomedical research?

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 789, doi. 10.1038/ng0805-789

By:

Wolf, Susan M

Publication type:

Article

Evo-devo for the general reader.

Published in:

2005

By:

Wilkins, Adam S

Publication type:

Book Review

Unraveling TACIt functions.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 793, doi. 10.1038/ng0805-793

By:

Martin, Flavius;
Dixit, Vishva M.

Publication type:

Article

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor.

Published in:

2005

By:

Prawitt, Dirk;
Enklaar, Thorsten;
Gärtner-Rupprecht, Barbara;
Spangenberg, Christian;
Lausch, Ekkehart;
Reutzel, Dirk;
Fees, Stephan;
Korzon, Maria;
Brozek, Izabela;
Limon, Janusz;
Housman, David E;
Pelletier, Jerry;
Zabel, Bernhard

Publication type:

Letter

Splicing on the brain.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 796, doi. 10.1038/ng0805-796

By:

Blencowe, Benjamin J

Publication type:

Article

Touching base.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 799, doi. 10.1038/ng0805-799

By:

Axton, Myles;
Packer, Alan;
Vogan, Kyle

Publication type:

Article

Research Highlights.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 801, doi. 10.1038/ng0805-801

By:

K.V.

Publication type:

Article

Corrigendum: Table of contents.

Published in:: 2005
Publication type:: Correction Notice

Corrigendum: An adaptive radiation model for the origin of new gene functions.

Published in:

2005

By:

Francino, M. P.

Publication type:

Correction Notice

Distinct epigenetic changes in the stromal cells of breast cancers.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 899, doi. 10.1038/ng1596

By:

Min Hu;
Jun Yao;
Li Cai;
Bachman, Kurt E.;
van den Brûle, Frédéric;
Velculescu, Victor;
Polyak, Kornelia

Publication type:

Article

Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 889, doi. 10.1038/ng1597

By:

Spitz, François;
Herkenne, Carole;
Morris, Michael A.;
Duboule, Denis

Publication type:

Article

Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 853, doi. 10.1038/ng1598

By:

Weber, Michael;
Davies, Jonathan J.;
Wittig, David;
Oakeley, Edward J.;
Haase, Michael;
Lam, Wan L.;
Schübeler, Dirk

Publication type:

Article

Complement factor 5 is a quantitative trait gene that modifies liver fibrogenesis in mice and humans.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 835, doi. 10.1038/ng1599

By:

Hillebrandt, Sonja;
Wasmuth, Hermann E.;
Weiskirchen, Ralf;
Hellerbrand, Claus;
Keppeler, Hildegard;
Werth, Alexa;
Schirin-Sokhan, Ramin;
Wilkens, Gabriele;
Geier, Andreas;
Lorenzen, Johann;
Köhl, Jörg;
Gressner, Axel M.;
Matern, Siegfried;
Lammert, Frank

Publication type:

Article

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 820, doi. 10.1038/ng1600

By:

Salzer, U.;
Chapel, H. M.;
Webster, A. D. B.;
Pan-Hammarström, Q.;
Schmitt-Graeff, A.;
Schlesier, M.;
Peter, H. H.;
Rockstroh, J. K.;
Schneider, P.;
Schäffer, A. A.;
Hammarström, L.;
Grimbacher, B.

Publication type:

Article

TACI is mutant in common variable immunodeficiency and IgA deficiency.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 829, doi. 10.1038/ng1601

By:

Castigli, Emanuela;
Wilson, Stephen A.;
Garibyan, Lilit;
Rachid, Rima;
Bonilla, Francisco;
Schneider, Lynda;
Geha, Raif S.

Publication type:

Article

Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 809, doi. 10.1038/ng1602

By:

Cam, Hugh P.;
Sugiyama, Tomoyasu;
Ee Sin Chen;
Xi Chen;
FitzGerald, Peter C.;
Grewal, Shiv I. S.

Publication type:

Article

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 803, doi. 10.1038/ng1603

By:

Aubin, Isabelle;
Adams, Carolyn P.;
Opsahl, Sibylle;
Septier, Dominique;
Bishop, Colin E.;
Auge, Nathalie;
Salvayre, Robert;
Negre-Salvayre, Anne;
Goldberg, Michel;
Guénet, Jean-Louis;
Poirier, Christophe

Publication type:

Article

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 863, doi. 10.1038/ng1604

By:

Meyre, David;
Bouatia-Naji, Nabila;
Tounian, Agnès;
Samson, Chantal;
Lecoeur, Cécile;
Vatin, Vincent;
Ghoussaini, Maya;
Wachter, Christophe;
Hercberg, Serge;
Charpentier, Guillaume;
Patsch, Wolfgang;
Pattou, François;
Charles, Marie-Aline;
Tounian, Patrick;
Clément, Karine;
Jouret, Béatrice;
Weill, Jacques;
Maddux, Betty A.;
Goldfine, Ira D.;
Walley, Andrew

Publication type:

Article

Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 883, doi. 10.1038/ng1605

By:

Ko, Michael A.;
Rosario, Carla O.;
Hudson, John W.;
Kulkarni, Sarang;
Pollett, Aaron;
Dennis, James W.;
Swallow, Carol J.

Publication type:

Article

Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 873, doi. 10.1038/ng1606

By:

Zsurka, Gábor;
Kraytsberg, Yevgenia;
Kudina, Tatiana;
Kornblum, Cornelia;
Elger, Christian E.;
Khrapko, Konstantin;
Kunz, Wolfram S.

Publication type:

Article

Demonstrating stratification in a European American population.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 868, doi. 10.1038/ng1607

By:

Campbell, Catarina D.;
Ogburn, Elizabeth L.;
Lunetta, Kathryn L.;
Lyon, Helen N.;
Freedman, Matthew L.;
Groop, Leif C.;
Altshuler, David;
Ardlie, Kristin G.;
Hirschhorn, Joel N.

Publication type:

Article

A stress-sensitive reporter predicts longevity in isogenic populations of Caenorhabditis elegans.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 894, doi. 10.1038/ng1608

By:

Rea, Shane L;
Wu, Deqing;
Cypser, James R.;
Vaupel, James W.;
Johnson, Thomas E.

Publication type:

Article

Nova regulates brain-specific splicing to shape the synapse.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 844, doi. 10.1038/ng1610

By:

Ule, Jernej;
Ule, Aljaž;
Spencer, Joanna;
Williams, Alan;
Jing-Shan Hu;
Cline, Melissa;
Hui Wang;
Clark, Tyson;
Fraser, Claire;
Ruggiu, Matteo;
Zeeberg, Barry R.;
Kane, David;
Weinstein, John N.;
Blume, John;
Darnell, Robert B.

Publication type:

Article

Short double-stranded RNA induces transcriptional gene silencing in human cancer cells in the absence of DNA methylation.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 906, doi. 10.1038/ng1611

By:

Ting, Angela H.;
Schuebel, Kornel E.;
Herman, James G.;
Baylin, Stephen B.

Publication type:

Article

Karyotypic abnormalities create discordance of germline genotype and cancer cell phenotypes.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 878, doi. 10.1038/ng1612

By:

Qing Cheng;
Wenjian Yang;
Raimondi, Susana C.;
Ching-Hon Pui;
Relling, Mary V.;
Evans, William E.

Publication type:

Article

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 806, doi. 10.1038/ng1609

By:

Skibinski, Gaia;
Parkinson, Nicholas J.;
Brown, Jeremy M.;
Chakrabarti, Lisa;
Lloyd, Sarah L.;
Hummerich, Holger;
Nielsen, Jørgen E.;
Hodges, John R.;
Spillantini, Maria Grazia;
Thusgaard, Tove;
Brandner, Sebastian;
Brun, Arne;
Rossor, Martin N.;
Gade, Anders;
Johannsen, Peter;
Sørensen, Sven Asger;
Gydesen, Susanne;
Fisher, Elizabeth MC;
Collinge, John

Publication type:

Article