Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 15
Results: 15
Major basic protein-1 promotes fibrosis of dystrophic muscle and attenuates the cellular immune response in muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2280, doi. 10.1093/hmg/ddn129
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- Article
Neurological deficits and glycosphingolipid accumulation in saposin B deficient mice.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2345, doi. 10.1093/hmg/ddn135
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- Article
Evidence that the gene encoding insulin degrading enzyme influences human lifespan.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2370, doi. 10.1093/hmg/ddn137
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- Article
Novel variants in human Aquaporin-4 reduce cellular water permeability.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2379, doi. 10.1093/hmg/ddn138
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- Article
Variants in the estrogen receptor alpha gene and its mRNA contribute to risk for schizophrenia.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2293, doi. 10.1093/hmg/ddn130
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- Article
Epidermal expression of the truncated prelamin A causing Hutchinson–Gilford progeria syndrome: effects on keratinocytes, hair and skin.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2357, doi. 10.1093/hmg/ddn136
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- Article
Iron-dependent regulation of frataxin expression: implications for treatment of Friedreich ataxia.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2265
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- Article
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2405, doi. 10.1093/hmg/ddn140
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- Article
Nf1+/− mice have increased neointima formation via hyperactivation of a Gleevec sensitive molecular pathway.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2336, doi. 10.1093/hmg/ddn134
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- Article
Activated caspase-6 and caspase-6-cleaved fragments of huntingtin specifically colocalize in the nucleus.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2390, doi. 10.1093/hmg/ddn139
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- Article
Sphingosine kinase 1/S1P receptor signaling axis controls glial proliferation in mice with Sandhoff disease.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2257, doi. 10.1093/hmg/ddn126
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- Article
Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2310, doi. 10.1093/hmg/ddn131
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- Article
Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2274
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- Article
Progressive loss of mitochondrial DNA in thymidine kinase 2-deficient mice.
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- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2329, doi. 10.1093/hmg/ddn133
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- Article
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2320, doi. 10.1093/hmg/ddn132
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- Article