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Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. NP, doi. 10.1093/hmg/ddr254
- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. NP, doi. 10.1093/hmg/ddr256
- Publication type:
- Article
Identification of DNA methylation markers for lineage commitment of in vitro hepatogenesis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2722, doi. 10.1093/hmg/ddr171
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- Publication type:
- Article
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2879, doi. 10.1093/hmg/ddr190
- By:
- Publication type:
- Article
The liver receptor homolog-1 (LRH-1) is expressed in human islets and protects β-cells against stress-induced apoptosis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2823
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- Publication type:
- Article
Disrupted-in-Schizophrenia-1 (Disc1) is necessary for migration of the pyramidal neurons during mouse hippocampal development.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2834, doi. 10.1093/hmg/ddr194
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- Publication type:
- Article
Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2869, doi. 10.1093/hmg/ddr189
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. NP, doi. 10.1093/hmg/ddr260
- Publication type:
- Article
A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2861, doi. 10.1093/hmg/ddr169
- By:
- Publication type:
- Article
Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2783, doi. 10.1093/hmg/ddr177
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- Publication type:
- Article
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2897, doi. 10.1093/hmg/ddr192
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- Publication type:
- Article
Huntingtin affinity for partners is not changed by polyglutamine length: aggregation itself triggers aberrant interactions.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2795, doi. 10.1093/hmg/ddr178
- By:
- Publication type:
- Article
A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2734, doi. 10.1093/hmg/ddr172
- By:
- Publication type:
- Article
HD CAG-correlated gene expression changes support a simple dominant gain of function.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2846, doi. 10.1093/hmg/ddr195
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. NP, doi. 10.1093/hmg/ddr258
- Publication type:
- Article
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2745, doi. 10.1093/hmg/ddr173
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- Publication type:
- Article
A gender-specific association of CNV at 6p21.3 with NPC susceptibility†.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2889, doi. 10.1093/hmg/ddr191
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- Publication type:
- Article
Silencing of frataxin gene expression triggers p53-dependent apoptosis in human neuron-like cells.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2807, doi. 10.1093/hmg/ddr187
- By:
- Publication type:
- Article
Intracerebroventricular enzyme infusion corrects central nervous system pathology and dysfunction in a mouse model of metachromatic leukodystrophy.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2760, doi. 10.1093/hmg/ddr175
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- Publication type:
- Article
Tissue-specific demethylation in CpG-poor promoters during cellular differentiation.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2710, doi. 10.1093/hmg/ddr170
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- Publication type:
- Article
Neurofibromin (Nf1) is required for skeletal muscle development.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2697, doi. 10.1093/hmg/ddr149
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- Publication type:
- Article
Transgenic mice expressing caspase-6-derived N-terminal fragments of mutant huntingtin develop neurologic abnormalities with predominant cytoplasmic inclusion pathology composed largely of a smaller proteolytic derivative.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2770, doi. 10.1093/hmg/ddr176
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- Publication type:
- Article