Works matching IS 09646906 AND DT 2004 AND VI 13 AND IP 11

Results: 10

A series of maturity onset diabetes of the young, type 2 (MODY2) mouse models generated by a large-scale ENU mutagenesis program.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1147, doi. 10.1093/hmg/ddh133

By:

Inoue, Maki;
Sakuraba, Yoshiyuki;
Motegi, Hiromi;
Kubota, Naoto;
Toki, Hideaki;
Matsui, Junko;
Toyoda, Yukiyasu;
Miwa, Ichitomo;
Terauchi, Yasuo;
Kadowaki, Takashi;
Shigeyama, Yutaka;
Kasuga, Masato;
Adachi, Takashi;
Fujimoto, Naomi;
Matsumoto, Rie;
Tsuchihashi, Keiko;
Kagami, Tomoko;
Inoue, Ayako;
Kaneda, Hideki;
Ishijima, Junko

Publication type:

Article

Data mining and multiparameter analysis of lung surfactant protein genes in bronchopulmonary dysplasia.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1095, doi. 10.1093/hmg/ddh132

By:

Rova, Meri;
Haataja, Ritva;
Marttila, Riitta;
Ollikainen, Vesa;
Tammela, Outi;
Hallman, Mikko

Publication type:

Article

Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1183, doi. 10.1093/hmg/ddh131

By:

Minamiyama, Makoto;
Katsuno, Masahisa;
Adachi, Hiroaki;
Waza, Masahiro;
Sang, Chen;
Kobayashi, Yasushi;
Tanaka, Fumiaki;
Doyu, Manabu;
Inukai, Akira;
Sobue, Gen

Publication type:

Article

Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1117, doi. 10.1093/hmg/ddh130

By:

Chan, Elayne M.;
Ackerley, Cameron A.;
Lohi, Hannes;
Ianzano, Leonarda;
Cortez, Miguel A.;
Shannon, Patrick;
Scherer, Stephen W.;
Minassian, Berge A.

Publication type:

Article

Transgenic rescue of neurogenic atrophy in the nmd mouse reveals a role for Ighmbp2 in dilated cardiomyopathy.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1105, doi. 10.1093/hmg/ddh129

By:

Maddatu, Terry P.;
Garvey, Sean M.;
Schroeder, David G.;
Hampton, Thomas G.;
Cox, Gregory A.

Publication type:

Article

Reversal of mutant myocilin non-secretion and cell killing: implications for glaucoma.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1193, doi. 10.1093/hmg/ddh128

By:

Liu, Yuhui;
Vollrath, Douglas

Publication type:

Article

Molecular evolution of microcephalin, a gene determining human brain size.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1131, doi. 10.1093/hmg/ddh127

By:

Wang, Yin-qiu;
Su, Bing

Publication type:

Article

Reconstructing the evolutionary history of microcephalin, a gene controlling human brain size.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1139, doi. 10.1093/hmg/ddh126

By:

Evans, Patrick D.;
Anderson, Jeffrey R.;
Vallender, Eric J.;
Choi, Sun Shim;
Lahn, Bruce T.

Publication type:

Article

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1171, doi. 10.1093/hmg/ddh124

By:

Uda, Manuela;
Ottolenghi, Chris;
Crisponi, Laura;
Garcia, Jose Elias;
Deiana, Manila;
Kimber, Wendy;
Forabosco, Antonino;
Cao, Antonio;
Schlessinger, David;
Pilia, Giuseppe

Publication type:

Article

Disruption of the WFS1 gene in mice causes progressive β-cell loss and impaired stimulus–secretion coupling in insulin secretion.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 11, p. 1159, doi. 10.1093/hmg/ddh125

By:

Ishihara, Hisamitsu;
Takeda, Satoshi;
Tamura, Akira;
Takahashi, Rui;
Yamaguchi, Suguru;
Takei, Daisuke;
Yamada, Takahiro;
Inoue, Hiroshi;
Soga, Hiroyuki;
Katagiri, Hideki;
Tanizawa, Yukio;
Oka, Yoshitomo

Publication type:

Article