Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 4

Results: 13

The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 625, doi. 10.1093/hmg/ddi478

By:

Gillingwater, Thomas H.;
Wishart, Thomas M.;
Chen, Philip E.;
Haley, Jane E.;
Robertson, Kevin;
MacDonald, Stephen H.-F.;
Middleton, Susan;
Wawrowski, Kolja;
Shipston, Michael J.;
Melmed, Shlomo;
Wyllie, David J.A.;
Skehel, Paul A.;
Coleman, Michael P.;
Ribchester, Richard R.

Publication type:

Article

Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REGγ as a therapeutic target.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 665, doi. 10.1093/hmg/ddi488

By:

Bett, John S.;
Goellner, Geoffrey M.;
Woodman, Ben;
Pratt, Gregory;
Rechsteiner, Martin;
Bates, Gillian P.

Publication type:

Article

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 653, doi. 10.1093/hmg/ddi480

By:

Boguslavsky, Revekka L.;
Stewart, Colin L.;
Worman, Howard J.

Publication type:

Article

Histone acetylation dependent allelic expression imbalance of BAPX1 in patients with the oculo-auriculo-vertebral spectrum.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 581, doi. 10.1093/hmg/ddi474

By:

Fischer, Sven;
Lüdecke, Hermann-Josef;
Wieczorek, Dagmar;
Böhringer, Stefan;
Gillessen-Kaesbach, Gabriele;
Horsthemke, Bernhard

Publication type:

Article

Deletion of the triplet repeat encoding polyglutamine within the mouse Huntington's disease gene results in subtle behavioral/motor phenotypes in vivo and elevated levels of ATP with cellular senescence in vitro.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 607, doi. 10.1093/hmg/ddi477

By:

Clabough, Erin B.D.;
Zeitlin, Scott O.

Publication type:

Article

Genetic analysis of BRCA1 ubiquitin ligase activity and its relationship to breast cancer susceptibility.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 599, doi. 10.1093/hmg/ddi476

By:

Morris, Joanna R.;
Pangon, Laurent;
Boutell, Chris;
Katagiri, Toyomasa;
Keep, Nicholas H.;
Solomon, Ellen

Publication type:

Article

Stochastic imprinting in the progeny of Dnmt3L−/− females.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 589, doi. 10.1093/hmg/ddi475

By:

Arnaud, Philippe;
Hata, Kenichiro;
Kaneda, Masahiro;
Li, En;
Sasaki, Hiroyuki;
Feil, Robert;
Kelsey, Gavin

Publication type:

Article

Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 637, doi. 10.1093/hmg/ddi479

By:

Melcon, Gisela;
Kozlov, Serguei;
Cutler, Dedra A.;
Sullivan, Terry;
Hernandez, Lidia;
Zhao, Po;
Mitchell, Stephanie;
Nader, Gustavo;
Bakay, Marina;
Rottman, Jeff N.;
Hoffman, Eric P.;
Stewart, Colin L.

Publication type:

Article

Multi-level regulation of myotubularin-related protein-2 phosphatase activity by myotubularin-related protein-13/set-binding factor-2.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 569, doi. 10.1093/hmg/ddi473

By:

Berger, Philipp;
Berger, Imre;
Schaffitzel, Christiane;
Tersar, Kristian;
Volkmer, Benjamin;
Suter, Ueli

Publication type:

Article

Proteolytic cleavage of polyglutamine-expanded ataxin-3 is critical for aggregation and sequestration of non-expanded ataxin-3.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 555, doi. 10.1093/hmg/ddi472

By:

Haacke, Annette;
Broadley, Sarah A.;
Boteva, Raina;
Tzvetkov, Nikolay;
Hartl, F. Ulrich;
Breuer, Peter

Publication type:

Article

Transgenic Drosophila models of Noonan syndrome causing PTPN11 gain-of-function mutations.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 543, doi. 10.1093/hmg/ddi471

By:

Oishi, Kimihiko;
Gaengel, Konstantin;
Krishnamoorthy, Srinivasan;
Kamiya, Kenichi;
Kim, In-Kyong;
Ying, Huiwen;
Weber, Ursula;
Perkins, Lizabeth A.;
Tartaglia, Marco;
Mlodzik, Marek;
Pick, Leslie;
Gelb, Bruce D.

Publication type:

Article

Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 531, doi. 10.1093/hmg/ddi470

By:

Nenci, Arianna;
Huth, Marion;
Funteh, Alfred;
Schmidt-Supprian, Marc;
Bloch, Wilhelm;
Metzger, Daniel;
Chambon, Pierre;
Rajewsky, Klaus;
Krieg, Thomas;
Haase, Ingo;
Pasparakis, Manolis

Publication type:

Article

Single nucleotide polymorphisms in the human interleukin-1B gene affect transcription according to haplotype context.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 4, p. 519, doi. 10.1093/hmg/ddi469

By:

Chen, Hongmin;
Wilkins, Leon M.;
Aziz, Nazneen;
Cannings, Christopher;
Wyllie, David H.;
Bingle, Colin;
Rogus, John;
Beck, James D.;
Offenbacher, Steven;
Cork, Michael J.;
Rafie-Kolpin, Maryam;
Hsieh, Chung-Ming;
Kornman, Kenneth S.;
Duff, Gordon W.

Publication type:

Article