Works matching IS 09646906 AND DT 2002 AND VI 11 AND IP 15

Results: 10

PTEN blocks insulin-mediated ETS-2 phosphorylation through MAP kinase, independently of the phosphoinositide 3-kinase pathway.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1687, doi. 10.1093/hmg/11.15.1687

By:

Weng, Liang-Ping;
Brown, Jessica L.;
Baker, Kim M.;
Ostrowski, Michael C.;
Eng, Charis

Publication type:

Article

A common protein interaction domain links two recently identified epilepsy genes.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1757, doi. 10.1093/hmg/11.15.1757

By:

Scheel, Hartmut;
Tomiuk, Stefan;
Hofmann, Kay

Publication type:

Article

Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1775, doi. 10.1093/hmg/11.15.1775

By:

Inoue, Koichi;
Matsuda, Koichi;
Itoh, Makoto;
Kawaguchi, Hiroshi;
Tomoike, Hitonobu;
Aoyagi, Teruhiko;
Nagai, Ryozo;
Hori, Masatsugu;
Nakamura, Yusuke;
Tanaka, Toshihiro

Publication type:

Article

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1743, doi. 10.1093/hmg/11.15.1743

By:

Nakabayashi, Kazuhiko;
Bentley, Louise;
Hitchins, Megan P.;
Mitsuya, Kohzoh;
Meguro, Makiko;
Minagawa, Sachi;
Bamforth, John S.;
Stanier, Philip;
Preece, Michael;
Weksberg, Rosanna;
Oshimura, Mitsuo;
Moore, Gudrun E.;
Scherer, Stephen W.

Publication type:

Article

Pioglitazone improves the phenotype and molecular defects of a targeted Pkd1 mutant.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1731, doi. 10.1093/hmg/11.15.1731

By:

Muto, Satoru;
Aiba, Atsu;
Saito, Yuichirou;
Nakao, Kazuki;
Nakamura, Kenji;
Tomita, Kyoichi;
Kitamura, Tadaichi;
Kurabayashi, Masahiko;
Nagai, Ryozo;
Higashihara, Eiji;
Harris, Peter C.;
Katsuki, Motoya;
Horie, Shigeo

Publication type:

Article

EDA targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby EDA-A1 transgenic mice.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1763, doi. 10.1093/hmg/11.15.1763

By:

Cui, Chang-Yi;
Durmowicz, Meredith;
Tanaka, Tetsuya S.;
Hartung, Andrew J.;
Tezuka, Tadashi;
Hashimoto, Ken;
Ko, Minoru S.H.;
Srivastava, Anand K.;
Schlessinger, David

Publication type:

Article

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11– q13 duplications.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1707, doi. 10.1093/hmg/11.15.1707

By:

Herzing, Laura B.K.;
Cook, Jr, Edwin H.;
Ledbetter, David H.

Publication type:

Article

The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1697, doi. 10.1093/hmg/11.15.1697

By:

Santucci-Darmanin, Sabine;
Neyton, Sophie;
Lespinasse, Françoise;
Saunières, Anne;
Gaudray, Patrick;
Paquis-Flucklinger, Véronique

Publication type:

Article

Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1719, doi. 10.1093/hmg/11.15.1719

By:

Roberts, Michael L.;
Wells, Dominic J.;
Graham, Ian R.;
Fabb, Stewart A.;
Hill, Vanessa J.;
Duisit, Ghislaine;
Yuasa, Katsutoshi;
Takeda, Shin'ichi;
Cosset, François-Loïc;
Dickson, George

Publication type:

Article

SMN, the spinal muscular atrophy protein, forms a pre-import snRNP complex with snurportin1 and importin β.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 15, p. 1785, doi. 10.1093/hmg/11.15.1785

By:

Narayanan, Usha;
Ospina, Jason K.;
Frey, Mark R.;
Hebert, Michael D.;
Matera, A. Gregory

Publication type:

Article