Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 18
Results: 22
Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3407, doi. 10.1093/hmg/ddp281
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- Article
Loss of positive allosteric interactions between neuronal nitric oxide synthase and phosphofructokinase contributes to defects in glycolysis and increased fatigability in muscular dystrophy.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3439, doi. 10.1093/hmg/ddp288
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. NP, doi. 10.1093/hmg/ddp348
- Publication type:
- Article
The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3452, doi. 10.1093/hmg/ddp289
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- Article
Common body mass index-associated variants confer risk of extreme obesity.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3502
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- Article
Association of variants in the PCSK1 gene with obesity in the EPIC-Norfolk study.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3496, doi. 10.1093/hmg/ddp280
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- Article
Direct and indirect roles of RECQL4 in modulating base excision repair capacity.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3470, doi. 10.1093/hmg/ddp291
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- Publication type:
- Article
Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3462, doi. 10.1093/hmg/ddp290
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- Article
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3516, doi. 10.1093/hmg/ddp296
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- Article
Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3525, doi. 10.1093/hmg/ddp295
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. NP, doi. 10.1093/hmg/ddp351
- Publication type:
- Article
Loss of Bloom syndrome protein destabilizes human gene cluster architecture.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3417, doi. 10.1093/hmg/ddp282
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- Article
Common variants in KCNQ1 are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3508, doi. 10.1093/hmg/ddp294
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. NP, doi. 10.1093/hmg/ddp350
- Publication type:
- Article
Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3365, doi. 10.1093/hmg/ddp276
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- Article
Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3397, doi. 10.1093/hmg/ddp279
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- Article
Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3384, doi. 10.1093/hmg/ddp278
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- Publication type:
- Article
Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals.
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- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3375, doi. 10.1093/hmg/ddp277
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- Publication type:
- Article
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3484, doi. 10.1093/hmg/ddp297
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- Article
Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3353, doi. 10.1093/hmg/ddp275
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. NP, doi. 10.1093/hmg/ddp349
- Publication type:
- Article
A cell-autonomous role for WT1 in regulating Sry in vivo.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3429, doi. 10.1093/hmg/ddp283
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- Article