Found: 24
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Bidirectional transcription stimulates expansion and contraction of expanded (CTG)•(CAG) repeats.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. 580, doi. 10.1093/hmg/ddq501
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- Article
Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 455, doi. 10.1093/hmg/ddq492
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- Article
Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 541, doi. 10.1093/hmg/ddq499
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- Article
Absence of progeria-like disease phenotypes in knock-in mice expressing a non-farnesylated version of progerin.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 436, doi. 10.1093/hmg/ddq490
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- Article
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 628, doi. 10.1093/hmg/ddq479
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- Article
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 615
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- Article
Global patterns of genetic diversity and signals of natural selection for human ADME genes.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 528, doi. 10.1093/hmg/ddq498
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- Article
Diaphragm rescue alone prevents heart dysfunction in dystrophic mice.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 413, doi. 10.1093/hmg/ddq477
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- Article
Editorial Board.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. NP, doi. 10.1093/hmg/ddr005
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- Article
Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 510, doi. 10.1093/hmg/ddq496
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- Article
Epigenetic signatures and temporal expression of lineage-specific genes in hESCs during differentiation to hepatocytes in vitro.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 401, doi. 10.1093/hmg/ddq476
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- Article
HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 553, doi. 10.1093/hmg/ddq500
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. NP, doi. 10.1093/hmg/ddr001
- Publication type:
- Article
Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 629, doi. 10.1093/hmg/ddq480
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- Publication type:
- Article
Enhanced excitation-coupled Ca2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core disease.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 589, doi. 10.1093/hmg/ddq506
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- Article
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 482, doi. 10.1093/hmg/ddq494
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- Article
Lack of WDR36 leads to preimplantation embryonic lethality in mice and delays the formation of small subunit ribosomal RNA in human cells in vitro.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 422, doi. 10.1093/hmg/ddq478
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- Article
Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. 497, doi. 10.1093/hmg/ddq495
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- Article
PCSK6 is associated with handedness in individuals with dyslexia.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 608, doi. 10.1093/hmg/ddq475
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- Article
Cover Page.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. NP, doi. 10.1093/hmg/ddr003
- Publication type:
- Article
Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of Tuberous Sclerosis Complex.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 445, doi. 10.1093/hmg/ddq491
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- Article
ELF1 is associated with systemic lupus erythematosus in Asian populations.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 601, doi. 10.1093/hmg/ddq474
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- Article
Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. 466, doi. 10.1093/hmg/ddq493
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. NP, doi. 10.1093/hmg/ddr007
- Publication type:
- Article