Works matching IS 09646906 AND DT 2014 AND VI 23 AND IP 3
Results: 26
Contents Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu015
- Publication type:
- Article
Tsc1 deficiency-mediated mTOR hyperactivation in vascular endothelial cells causes angiogenesis defects and embryonic lethality.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 693, doi. 10.1093/hmg/ddt456
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- Article
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 749, doi. 10.1093/hmg/ddt460
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- Article
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 820, doi. 10.1093/hmg/ddt464
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- Article
Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 590, doi. 10.1093/hmg/ddt447
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- Article
Reversibility of neuropathology in Tay–Sachs-related diseases.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 730
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu017
- Publication type:
- Article
The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 563, doi. 10.1093/hmg/ddt445
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- Article
Abnormal Ras signaling in Costello syndrome (CS) negatively regulates enamel formation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 682, doi. 10.1093/hmg/ddt455
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu016
- Publication type:
- Article
Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 782, doi. 10.1093/hmg/ddt461
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- Publication type:
- Article
Genetic comorbidities in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 831
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- Publication type:
- Article
Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 637, doi. 10.1093/hmg/ddt450
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- Publication type:
- Article
NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 706, doi. 10.1093/hmg/ddt457
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- Publication type:
- Article
Altered CpG methylation in sporadic Alzheimer's disease is associated with APP and MAPT dysregulation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 648, doi. 10.1093/hmg/ddt451
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- Publication type:
- Article
Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 618, doi. 10.1093/hmg/ddt449
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- Publication type:
- Article
Dynamic changes in DNA methylation and hydroxymethylation when hES cells undergo differentiation toward a neuronal lineage.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 657, doi. 10.1093/hmg/ddt453
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- Publication type:
- Article
Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 810, doi. 10.1093/hmg/ddt463
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- Publication type:
- Article
Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 767, doi. 10.1093/hmg/ddt467
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- Publication type:
- Article
Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 602, doi. 10.1093/hmg/ddt448
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- Publication type:
- Article
Widespread spinal cord transduction by intrathecal injection of rAAV delivers efficacious RNAi therapy for amyotrophic lateral sclerosis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 668, doi. 10.1093/hmg/ddt454
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- Publication type:
- Article
Human chromosome 21 orthologous region on mouse chromosome 17 is a major determinant of Down syndrome-related developmental cognitive deficits.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 578, doi. 10.1093/hmg/ddt446
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- Publication type:
- Article
p53 increases caspase-6 expression and activation in muscle tissue expressing mutant huntingtin.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 717, doi. 10.1093/hmg/ddt458
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- Publication type:
- Article
DJ-1 modulates aggregation and pathogenesis in models of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 755, doi. 10.1093/hmg/ddt466
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu018
- Publication type:
- Article
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 796, doi. 10.1093/hmg/ddt462
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- Publication type:
- Article