Works matching IS 09646906 AND DT 2002 AND VI 11 AND IP 15
Results: 10
PTEN blocks insulin-mediated ETS-2 phosphorylation through MAP kinase, independently of the phosphoinositide 3-kinase pathway.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1687, doi. 10.1093/hmg/11.15.1687
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- Article
A common protein interaction domain links two recently identified epilepsy genes.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1757, doi. 10.1093/hmg/11.15.1757
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- Article
Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1775, doi. 10.1093/hmg/11.15.1775
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- Article
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1743, doi. 10.1093/hmg/11.15.1743
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- Article
Pioglitazone improves the phenotype and molecular defects of a targeted Pkd1 mutant.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1731, doi. 10.1093/hmg/11.15.1731
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- Article
EDA targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby EDA-A1 transgenic mice.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1763, doi. 10.1093/hmg/11.15.1763
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- Article
SMN, the spinal muscular atrophy protein, forms a pre-import snRNP complex with snurportin1 and importin β.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1785, doi. 10.1093/hmg/11.15.1785
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- Article
The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1697, doi. 10.1093/hmg/11.15.1697
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- Article
Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11– q13 duplications.
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- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1707, doi. 10.1093/hmg/11.15.1707
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- Article
Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 15, p. 1719, doi. 10.1093/hmg/11.15.1719
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- Article