Works matching IS 09646906 AND DT 2005 AND VI 14 AND IP 9
Results: 12
Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1109, doi. 10.1093/hmg/ddi123
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- Article
The Parkinson's disease-associated DJ-1 protein is a transcriptional co-activator that protects against neuronal apoptosis.
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- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1231, doi. 10.1093/hmg/ddi134
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- Article
Sox9 is sufficient for functional testis development producing fertile male mice in the absence of Sry.
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- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1221, doi. 10.1093/hmg/ddi133
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- Article
Ethnic- and gender-specific association of the nicotinic acetylcholine receptor α4 subunit gene (CHRNA4) with nicotine dependence.
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- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1211, doi. 10.1093/hmg/ddi132
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- Article
RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin.
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- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1183, doi. 10.1093/hmg/ddi129
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- Article
A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1199, doi. 10.1093/hmg/ddi131
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- Article
The role of histone acetylation in SMN gene expression.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1171, doi. 10.1093/hmg/ddi130
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- Article
Evidence for effect of mutant PCSK9 on apolipoprotein B secretion as the cause of unusually severe dominant hypercholesterolaemia.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1161, doi. 10.1093/hmg/ddi128
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- Article
Activating mutations of the tyrosine kinase receptor FGFR3 are associated with benign skin tumors in mice and humans.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1153, doi. 10.1093/hmg/ddi127
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- Article
Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophy.
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- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1139, doi. 10.1093/hmg/ddi126
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- Article
Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1127, doi. 10.1093/hmg/ddi125
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- Article
Inferring gene transcriptional modulatory relations: a genetical genomics approach.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 9, p. 1119, doi. 10.1093/hmg/ddi124
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- Publication type:
- Article