Works matching IS 09646906 AND DT 2005 AND VI 14 AND IP 16

Results: 16

Gene expression analysis in mice with elevated glial fibrillary acidic protein and Rosenthal fibers reveals a stress response followed by glial activation and neuronal dysfunction.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2443, doi. 10.1093/hmg/ddi248

By:

Hagemann, Tracy L.;
Gaeta, Stephen A.;
Smith, Mark A.;
Johnson, Delinda A.;
Johnson, Jeffrey A.;
Messing, Albee

Publication type:

Article

Extensive polymorphisms of LILRB1 (ILT2, LIR1) and their association with HLA-DRB1 shared epitope negative rheumatoid arthritis.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2469, doi. 10.1093/hmg/ddi247

By:

Kuroki, Kimiko;
Tsuchiya, Naoyuki;
Shiroishi, Mitsunori;
Rasubala, Linda;
Yamashita, Yumi;
Matsuta, Kunio;
Fukazawa, Toru;
Kusaoi, Makio;
Murakami, Yoshinori;
Takiguchi, Masafumi;
Juji, Takeo;
Hashimoto, Hiroshi;
Kohda, Daisuke;
Maenaka, Katsumi;
Tokunaga, Katsushi

Publication type:

Article

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2399, doi. 10.1093/hmg/ddi241

By:

Myers, A.J.;
Kaleem, M.;
Marlowe, L.;
Pittman, A.M.;
Lees, A.J.;
Fung, H.C.;
Duckworth, J.;
Leung, D.;
Gibson, A.;
Morris, C.M.;
de Silva, R.;
Hardy, J.

Publication type:

Article

Differential nonsense mediated decay of mutated mRNAs in mismatch repair deficient colorectal cancers.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2435, doi. 10.1093/hmg/ddi245

By:

El-Bchiri, Jamila;
Buhard, Olivier;
Penard-Lacronique, Virginie;
Thomas, Gilles;
Hamelin, Richard;
Duval, Alex

Publication type:

Article

CHRM2 gene predisposes to alcohol dependence, drug dependence and affective disorders: results from an extended case–control structured association study.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2421, doi. 10.1093/hmg/ddi244

By:

Luo, Xingguang;
Kranzler, Henry R.;
Zuo, Lingjun;
Wang, Shuang;
Blumberg, Hilary P.;
Gelernter, Joel

Publication type:

Article

Angiotensin-converting enzyme (ACE) haplotypes and cyclosporine A (CsA) response: a model of the complex relationship between ACE quantitative trait locus and pathological phenotypes.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2357, doi. 10.1093/hmg/ddi238

By:

Catarsi, Paolo;
Ravazzolo, Roberto;
Emma, Francesco;
Fruci, Doriana;
Finos, Livio;
Frau, Andrea;
Morreale, Giacomo;
Carrea, Alba;
Ghiggeri, Gian Marco

Publication type:

Article

Tobacco smoking, estrogen receptor α gene variation and small low density lipoprotein level.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2405, doi. 10.1093/hmg/ddi242

By:

Shearman, Amanda M.;
Demissie, Serkalem;
Cupples, L. Adrienne;
Peter, Inga;
Schmid, Christopher H.;
Ordovas, Jose M.;
Mendelsohn, Michael E.;
Housman, David E.

Publication type:

Article

Different splicing defects lead to differential effects downstream of the lipid and protein phosphatase activities of PTEN.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2459, doi. 10.1093/hmg/ddi246

By:

Agrawal, Shipra;
Pilarski, Robert;
Eng, Charis

Publication type:

Article

ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2387, doi. 10.1093/hmg/ddi240

By:

Ron, Idit;
Horowitz, Mia

Publication type:

Article

Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2369, doi. 10.1093/hmg/ddi239

By:

Glynn, Dervila;
Drew, Cheney J.;
Reim, Kerstin;
Brose, Nils;
Morton, A. Jennifer

Publication type:

Article

Prediction of pathogenic mutations in mitochondrially encoded human tRNAs.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2415, doi. 10.1093/hmg/ddi243

By:

Kondrashov, Fyodor A.

Publication type:

Article

Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2349, doi. 10.1093/hmg/ddi237

By:

Lesueur, Fabienne;
Pharoah, Paul D.;
Laing, Stewart;
Ahmed, Shahana;
Jordan, Clare;
Smith, Paula L.;
Luben, Robert;
Wareham, Nicholas J.;
Easton, Douglas F.;
Dunning, Alison M.;
Ponder, Bruce A.J.

Publication type:

Article

Somatodendritic accumulation of misfolded SOD1-L126Z in motor neurons mediates degeneration: αB-crystallin modulates aggregation.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2335, doi. 10.1093/hmg/ddi236

By:

Wang, Jiou;
Xu, Guilian;
Li, Hong;
Gonzales, Victoria;
Fromholt, David;
Karch, Celeste;
Copeland, Neal G.;
Jenkins, Nancy A.;
Borchelt, David R.

Publication type:

Article

Alms1-disrupted mice recapitulate human Alström syndrome.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2323, doi. 10.1093/hmg/ddi235

By:

Collin, G.B.;
Cyr, E.;
Bronson, R.;
Marshall, J.D.;
Gifford, E.J.;
Hicks, W.;
Murray, S.A.;
Zheng, Q.Y.;
Smith, R.S.;
Nishina, P.M.;
Naggert, J.K.

Publication type:

Article

Up-regulation of the ubiquitous alternative splicing factor Tra2β causes inclusion of a germ cell-specific exon.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2289, doi. 10.1093/hmg/ddi233

By:

Venables, Julian P.;
Bourgeois, Cyril F.;
Dalgliesh, Caroline;
Kister, Liliane;
Stevenin, James;
Elliott, David J.

Publication type:

Article

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 16, p. 2305, doi. 10.1093/hmg/ddi234

By:

Tamiya, Gen;
Shinya, Minori;
Imanishi, Tadashi;
Ikuta, Tomoki;
Makino, Satoshi;
Okamoto, Koichi;
Furugaki, Koh;
Matsumoto, Toshiko;
Mano, Shuhei;
Ando, Satoshi;
Nozaki, Yasuyuki;
Yukawa, Wataru;
Nakashige, Ryo;
Yamaguchi, Daisuke;
Ishibashi, Hideo;
Yonekura, Manabu;
Nakami, Yuu;
Takayama, Seiken;
Endo, Takaho;
Saruwatari, Takuya

Publication type:

Article