Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 23
Results: 25
Common fragile sites are characterized by histone hypoacetylation.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4501, doi. 10.1093/hmg/ddp410
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- Article
Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4677, doi. 10.1093/hmg/ddp428
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- Article
Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4576, doi. 10.1093/hmg/ddp425
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- Article
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4650, doi. 10.1093/hmg/ddp413
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- Article
Pharmacological activation of PPARβ/δ stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4640, doi. 10.1093/hmg/ddp431
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- Article
The ocular albinism type 1 (OA1) G-protein-coupled receptor functions with MART-1 at early stages of melanogenesis to control melanosome identity and composition.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4530, doi. 10.1093/hmg/ddp415
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Contents Page.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. NP, doi. 10.1093/hmg/ddp485
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- Article
Ku70 regulates Bax-mediated pathogenesis in laminin-α2-deficient human muscle cells and mouse models of congenital muscular dystrophy.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4467, doi. 10.1093/hmg/ddp399
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- Article
Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4552, doi. 10.1093/hmg/ddp421
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- Article
Editorial Board.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. NP, doi. 10.1093/hmg/ddp487
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- Article
A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4565, doi. 10.1093/hmg/ddp422
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- Article
Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4662, doi. 10.1093/hmg/ddp423
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- Article
GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4629, doi. 10.1093/hmg/ddp430
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- Publication type:
- Article
X11β rescues memory and long-term potentiation deficits in Alzheimer's disease APPswe Tg2576 mice.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4492, doi. 10.1093/hmg/ddp408
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- Article
Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4669, doi. 10.1093/hmg/ddp424
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- Publication type:
- Article
An increased frequency of the 5A allele in the promoter region of the MMP3 gene is associated with abdominal aortic aneurysms.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4688, doi. 10.1093/hmg/ddp439
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- Article
Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4615, doi. 10.1093/hmg/ddp429
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- Article
Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4478, doi. 10.1093/hmg/ddp407
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- Publication type:
- Article
Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4603, doi. 10.1093/hmg/ddp427
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- Article
Functional analysis of 5-lipoxygenase promoter repeat variants.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4521, doi. 10.1093/hmg/ddp414
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- Article
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4590, doi. 10.1093/hmg/ddp426
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- Article
Pathogenic NAP57 mutations decrease ribonucleoprotein assembly in dyskeratosis congenita.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4546, doi. 10.1093/hmg/ddp416
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Subscription Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 23, p. NP, doi. 10.1093/hmg/ddp488
- Publication type:
- Article
An allergy-associated polymorphism in a novel regulatory element enhances IL13 expression.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4513, doi. 10.1093/hmg/ddp411
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 23, p. NP, doi. 10.1093/hmg/ddp486
- Publication type:
- Article