Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 1
Results: 22
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. NP, doi. 10.1093/hmg/ddq505
- Publication type:
- Article
DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 40, doi. 10.1093/hmg/ddq430
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- Publication type:
- Article
Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 64, doi. 10.1093/hmg/ddq432
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- Publication type:
- Article
The β1 subunit of the Na,K-ATPase pump interacts with megalencephalic leucoencephalopathy with subcortical cysts protein 1 (MLC1) in brain astrocytes: new insights into MLC pathogenesis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 90, doi. 10.1093/hmg/ddq435
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- Publication type:
- Article
Rapid and transient recruitment of DNMT1 to DNA double-strand breaks is mediated by its interaction with multiple components of the DNA damage response machinery.
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- Human Molecular Genetics, 2011, v. 20, n. 1, p. 126, doi. 10.1093/hmg/ddq451
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- Article
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 202, doi. 10.1093/hmg/ddq454
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- Publication type:
- Article
Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 186, doi. 10.1093/hmg/ddq417
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. NP, doi. 10.1093/hmg/ddq503
- Publication type:
- Article
The KRAB-containing zinc-finger transcriptional regulator ZBRK1 activates SCA2 gene transcription through direct interaction with its gene product, ataxin-2.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 104, doi. 10.1093/hmg/ddq436
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- Publication type:
- Article
Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 176, doi. 10.1093/hmg/ddq456
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. NP, doi. 10.1093/hmg/ddq502
- Publication type:
- Article
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 1, doi. 10.1093/hmg/ddq427
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- Publication type:
- Article
Naturally occurring germline and tumor-associated mutations within the ATP-binding motifs of PTEN lead to oxidative damage of DNA associated with decreased nuclear p53.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 80, doi. 10.1093/hmg/ddq434
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- Publication type:
- Article
Identification of genes specific to mouse primordial germ cells through dynamic global gene expression.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 115, doi. 10.1093/hmg/ddq450
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- Publication type:
- Article
Drosophila FMRP regulates microtubule network formation and axonal transport of mitochondria.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 51, doi. 10.1093/hmg/ddq431
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- Publication type:
- Article
The Machado–Joseph disease-associated mutant form of ataxin-3 regulates parkin ubiquitination and stability.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 141, doi. 10.1093/hmg/ddq452
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. NP, doi. 10.1093/hmg/ddq504
- Publication type:
- Article
The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis–ichthyosis–deafness syndrome.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 28, doi. 10.1093/hmg/ddq429
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- Publication type:
- Article
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensation.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 155, doi. 10.1093/hmg/ddq453
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- Publication type:
- Article
Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutant.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 16, doi. 10.1093/hmg/ddq428
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- Publication type:
- Article
Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profile.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 193, doi. 10.1093/hmg/ddq449
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- Publication type:
- Article
Protein kinase A regulates caspase-1 via Ets-1 in bone stromal cell-derived lesions: a link between cyclic AMP and pro-inflammatory pathways in osteoblast progenitors.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 165, doi. 10.1093/hmg/ddq455
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- Publication type:
- Article