Works matching IS 09646906 AND DT 2001 AND VI 10 AND IP 17
Results: 15
Molecular scanning of the human sorbin and SH3-domain-containing-1 ( SORBS1) gene: positive association of the T228A polymorphism with obesity and type 2 diabetes.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1753, doi. 10.1093/hmg/10.17.1753
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- Article
Domain homologues of dopamine β -hydroxylase and ferric reductase: roles for iron metabolism in neurodegenerative disorders?
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1853, doi. 10.1093/hmg/10.17.1853
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- Article
Identification of an endogenous RNA transcribed from the antisense strand of the HFE gene.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1859, doi. 10.1093/hmg/10.17.1859
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- Article
Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1785, doi. 10.1093/hmg/10.17.1785
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- Article
The mutational spectrum of human malignant autosomal recessive osteopetrosis.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1767, doi. 10.1093/hmg/10.17.1767
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- Article
Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1721, doi. 10.1093/hmg/10.17.1721
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- Article
Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1729, doi. 10.1093/hmg/10.17.1729
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- Article
Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1819, doi. 10.1093/hmg/10.17.1819
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- Article
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1775, doi. 10.1093/hmg/10.17.1775
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- Article
α -synuclein gene haplotypes are associated with Parkinson’s disease.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1847, doi. 10.1093/hmg/10.17.1847
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- Article
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1761, doi. 10.1093/hmg/10.17.1761
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- Article
Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington’s disease.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1829, doi. 10.1093/hmg/10.17.1829
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- Article
Insights into psoriasis and other inflammatory diseases from large-scale gene expression studies.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1793, doi. 10.1093/hmg/10.17.1793
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- Article
Fumarylacetoacetate, the metabolite accumulating in hereditary tyrosinemia, activates the ERK pathway and induces mitotic abnormalities and genomic instability.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1741, doi. 10.1093/hmg/10.17.1741
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- Article
The huntingtin interacting protein HIP1 is a clathrin and α -adaptin-binding protein involved in receptor-mediated endocytosis.
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- Human Molecular Genetics, 2001, v. 10, n. 17, p. 1807, doi. 10.1093/hmg/10.17.1807
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- Article