Found: 26
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Arap3 is dysregulated in a mouse model of hypotrichosis–lymphedema–telangiectasia and regulates lymphatic vascular development.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1286, doi. 10.1093/hmg/ddt518
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- Article
Connexin defects underlie arrhythmogenic right ventricular cardiomyopathy in a novel mouse model.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1134, doi. 10.1093/hmg/ddt508
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- Article
Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1271, doi. 10.1093/hmg/ddt517
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- Article
Editorial Board.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. NP, doi. 10.1093/hmg/ddu062
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- Article
Statin-induced changes in gene expression in EBV-transformed and native B-cells.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1202, doi. 10.1093/hmg/ddt512
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- Article
Restoration of muscle strength in dystrophic muscle by angiotensin-1-7 through inhibition of TGF-β signalling.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1237
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- Article
NF1 is a critical regulator of muscle development and metabolism.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1250, doi. 10.1093/hmg/ddt515
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- Article
Coregulation and modulation of NFκB-related genes in celiac disease: uncovered aspects of gut mucosal inflammation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1298, doi. 10.1093/hmg/ddt520
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. NP, doi. 10.1093/hmg/ddu063
- Publication type:
- Article
Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1211, doi. 10.1093/hmg/ddt513
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- Article
ACAD9, a complex I assembly factor with a moonlighting function in fatty acid oxidation deficiencies.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1311, doi. 10.1093/hmg/ddt521
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. NP, doi. 10.1093/hmg/ddu060
- Publication type:
- Article
Cross-sectional and longitudinal changes in DNA methylation with age: an epigenome-wide analysis revealing over 60 novel age-associated CpG sites.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1186, doi. 10.1093/hmg/ddt531
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- Publication type:
- Article
Presenilin influences glycogen synthase kinase-3 β (GSK-3β) for kinesin-1 and dynein function during axonal transport.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1121, doi. 10.1093/hmg/ddt505
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- Publication type:
- Article
Inactivation of the Carney complex gene 1 (PRKAR1A) alters spatiotemporal regulation of cAMP and cAMP-dependent protein kinase: a study using genetically encoded FRET-based reporters.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1163, doi. 10.1093/hmg/ddt510
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- Publication type:
- Article
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve degeneration at old age.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1320, doi. 10.1093/hmg/ddt522
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- Publication type:
- Article
Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1151, doi. 10.1093/hmg/ddt509
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- Publication type:
- Article
A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1175, doi. 10.1093/hmg/ddt511
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- Publication type:
- Article
Lipid-enriched diet rescues lethality and slows down progression in a murine model of VCP-associated disease.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1333, doi. 10.1093/hmg/ddt523
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- Publication type:
- Article
Genome-wide association study identifies multiple loci associated with bladder cancer risk.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1387, doi. 10.1093/hmg/ddt519
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- Publication type:
- Article
Sex-biased methylome and transcriptome in human prefrontal cortex.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1260, doi. 10.1093/hmg/ddt516
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- Article
Human APOE genotype affects intraneuronal Aβ1–42 accumulation in a lentiviral gene transfer model.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1365, doi. 10.1093/hmg/ddt525
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- Article
Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1345, doi. 10.1093/hmg/ddt524
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- Article
Transcriptional activation of TFEB/ZKSCAN3 target genes underlies enhanced autophagy in spinobulbar muscular atrophy.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1376, doi. 10.1093/hmg/ddt527
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. NP, doi. 10.1093/hmg/ddu061
- Publication type:
- Article
DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1224, doi. 10.1093/hmg/ddt553
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- Publication type:
- Article