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

Results: 10

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
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
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
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
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
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
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