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.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2443, doi. 10.1093/hmg/ddi248
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- Article
Extensive polymorphisms of LILRB1 (ILT2, LIR1) and their association with HLA-DRB1 shared epitope negative rheumatoid arthritis.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2469, doi. 10.1093/hmg/ddi247
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- Article
Different splicing defects lead to differential effects downstream of the lipid and protein phosphatase activities of PTEN.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2459, doi. 10.1093/hmg/ddi246
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- Article
Differential nonsense mediated decay of mutated mRNAs in mismatch repair deficient colorectal cancers.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2435, doi. 10.1093/hmg/ddi245
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- Article
CHRM2 gene predisposes to alcohol dependence, drug dependence and affective disorders: results from an extended case–control structured association study.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2421, doi. 10.1093/hmg/ddi244
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- Article
Prediction of pathogenic mutations in mitochondrially encoded human tRNAs.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2415, doi. 10.1093/hmg/ddi243
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- Article
Tobacco smoking, estrogen receptor α gene variation and small low density lipoprotein level.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2405, doi. 10.1093/hmg/ddi242
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- Article
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2399, doi. 10.1093/hmg/ddi241
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- Article
ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2387, doi. 10.1093/hmg/ddi240
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- Article
Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2369, doi. 10.1093/hmg/ddi239
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- 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.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2357, doi. 10.1093/hmg/ddi238
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- Article
Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2349, doi. 10.1093/hmg/ddi237
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- Article
Somatodendritic accumulation of misfolded SOD1-L126Z in motor neurons mediates degeneration: αB-crystallin modulates aggregation.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2335, doi. 10.1093/hmg/ddi236
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- Article
Alms1-disrupted mice recapitulate human Alström syndrome.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2323, doi. 10.1093/hmg/ddi235
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- Article
Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2305, doi. 10.1093/hmg/ddi234
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- Article
Up-regulation of the ubiquitous alternative splicing factor Tra2β causes inclusion of a germ cell-specific exon.
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- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2289, doi. 10.1093/hmg/ddi233
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- Article