Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 21
Results: 23
Large common deletions associate with mortality at old age.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4290, doi. 10.1093/hmg/ddr340
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- Article
‘Progress’ renders detrimental an ancient mitochondrial DNA genetic variant.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4224, doi. 10.1093/hmg/ddr350
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr467
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- Article
LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4209, doi. 10.1093/hmg/ddr348
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- Article
Defhc1.1, a homologue of the juvenile myoclonic gene EFHC1, modulates architecture and basal activity of the neuromuscular junction in Drosophila.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4248, doi. 10.1093/hmg/ddr352
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- Article
Increased PKA signaling disrupts recognition memory and spatial memory: role in Huntington's disease.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4232, doi. 10.1093/hmg/ddr351
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- Article
Differential effects of the Huntington's disease CAG mutation in striatum and cerebellum are quantitative not qualitative.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4258, doi. 10.1093/hmg/ddr355
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- Article
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4268, doi. 10.1093/hmg/ddr303
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- Article
A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4282, doi. 10.1093/hmg/ddr342
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- Article
Positional identification of variants of Adamts16 linked to inherited hypertension.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4297, doi. 10.1093/hmg/ddr286
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- Article
MeCP2 Rett mutations affect large scale chromatin organization.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4187, doi. 10.1093/hmg/ddr346
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr465
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr466
- Publication type:
- Article
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4132
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- Article
Pyrimethamine inhibits adult polycystic kidney disease by modulating STAT signaling pathways.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4143, doi. 10.1093/hmg/ddr338
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- Article
The in vivo contribution of motor neuron TrkB receptors to mutant SOD1 motor neuron disease.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4116, doi. 10.1093/hmg/ddr335
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- Publication type:
- Article
Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4102, doi. 10.1093/hmg/ddr334
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- Article
Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4196, doi. 10.1093/hmg/ddr347
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- Article
A variant OSR1 allele which disturbs OSR1 mRNA expression in renal progenitor cells is associated with reduction of newborn kidney size and function.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4167, doi. 10.1093/hmg/ddr341
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr464
- Publication type:
- Article
Increased hedgehog signaling in postnatal kidney results in aberrant activation of nephron developmental programs.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4155, doi. 10.1093/hmg/ddr339
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- Publication type:
- Article
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4175, doi. 10.1093/hmg/ddr344
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- Article
Specific correction of a splice defect in brain by nutritional supplementation.
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- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4093, doi. 10.1093/hmg/ddr333
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- Article