Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 3
Results: 24
Re-investigation and RNA sequencing-based identification of genes with placenta-specific imprinted expression.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 548, doi. 10.1093/hmg/ddr488
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- Article
GATA2 negatively regulates PTEN by preventing nuclear translocation of androgen receptor and by androgen-independent suppression of PTEN transcription in breast cancer.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 569, doi. 10.1093/hmg/ddr491
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Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 711, doi. 10.1093/hmg/ddr489
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- Article
Cover Page.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. NP, doi. 10.1093/hmg/dds008
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- Article
Whirlin interacts with espin and modulates its actin-regulatory function: an insight into the mechanism of Usher syndrome type II.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 692, doi. 10.1093/hmg/ddr503
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- Article
The tumor suppressor CDC73 interacts with the ring finger proteins RNF20 and RNF40 and is required for the maintenance of histone 2B monoubiquitination.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 559, doi. 10.1093/hmg/ddr490
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Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 623, doi. 10.1093/hmg/ddr496
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- Article
MicroRNA-mediated dysregulation of neural developmental genes in HPRT deficiency: clues for Lesch–Nyhan disease?
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 609, doi. 10.1093/hmg/ddr495
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- Article
Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 647, doi. 10.1093/hmg/ddr498
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- Article
α-Synuclein accumulates in huntingtin inclusions but forms independent filaments and its deficiency attenuates early phenotype in a mouse model of Huntington's disease.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 495, doi. 10.1093/hmg/ddr507
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- Article
Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 536, doi. 10.1093/hmg/ddr487
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- Article
Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 526, doi. 10.1093/hmg/ddr482
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- Article
An aggregation sensing reporter identifies leflunomide and teriflunomide as polyglutamine aggregate inhibitors.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 664, doi. 10.1093/hmg/ddr500
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- Article
Characterization of inclusion bodies with cytoprotective properties formed by seipinopathy-linked mutant seipin.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 635, doi. 10.1093/hmg/ddr497
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- Article
Specific alterations of carbohydrate metabolism are associated with hepatocarcinogenesis in mitochondrially impaired mice.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 656, doi. 10.1093/hmg/ddr499
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 3, p. NP, doi. 10.1093/hmg/dds009
- Publication type:
- Article
α-Synuclein levels modulate Huntington's disease in mice.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 485, doi. 10.1093/hmg/ddr477
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 3, p. NP, doi. 10.1093/hmg/dds007
- Publication type:
- Article
Lack of Pur-alpha alters postnatal brain development and causes megalencephaly.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 473, doi. 10.1093/hmg/ddr476
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- Article
Inhibition of GSK3β improves hippocampus-dependent learning and rescues neurogenesis in a mouse model of fragile X syndrome.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 681, doi. 10.1093/hmg/ddr501
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- Article
Loss of ceramide synthase 3 causes lethal skin barrier disruption.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 586, doi. 10.1093/hmg/ddr494
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 3, p. NP, doi. 10.1093/hmg/dds010
- Publication type:
- Article
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 577, doi. 10.1093/hmg/ddr493
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- Article
Leucine-rich repeat kinase 2 regulates autophagy through a calcium-dependent pathway involving NAADP.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 511, doi. 10.1093/hmg/ddr481
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- Article