Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 12
Results: 22
The eczema risk variant on chromosome 11q13 (rs7927894) in the population-based ALSPAC cohort: a novel susceptibility factor for asthma and hay fever.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2443, doi. 10.1093/hmg/ddr117
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- Article
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2482, doi. 10.1093/hmg/ddr123
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- Article
Mutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stability.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2322, doi. 10.1093/hmg/ddr125
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- Article
Cover Page.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. NP, doi. 10.1093/hmg/ddr183
- Publication type:
- Article
Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2394, doi. 10.1093/hmg/ddr146
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- Article
Editorial Board.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. NP, doi. 10.1093/hmg/ddr184
- Publication type:
- Article
Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2308, doi. 10.1093/hmg/ddr124
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- Article
Mimicking a SURF1 allele reveals uncoupling of cytochrome c oxidase assembly from translational regulation in yeast.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2379, doi. 10.1093/hmg/ddr145
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- Article
Gene copy number reduction in the azoospermia factor c (AZFc) region and its effect on total motile sperm count.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2457, doi. 10.1093/hmg/ddr119
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- Article
Common genetic variants associated with open-angle glaucoma.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2464, doi. 10.1093/hmg/ddr120
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- Article
Expression of tumor-promoting Cyr61 is regulated by hTRA2-β1 and acidosis.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2356, doi. 10.1093/hmg/ddr128
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- Article
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2297, doi. 10.1093/hmg/ddr122
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- Article
Mitogen- and stress-activated protein kinase 1-induced neuroprotection in Huntington's disease: role on chromatin remodeling at the PGC-1-alpha promoter.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2422, doi. 10.1093/hmg/ddr148
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- Article
Genome-wide meta-analysis for severe diabetic retinopathy.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2472, doi. 10.1093/hmg/ddr121
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- Publication type:
- Article
Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2Dy-w mice, a model for congenital muscular dystrophy type 1A.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2333, doi. 10.1093/hmg/ddr126
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- Article
An autosomal locus that controls chromosome-wide replication timing and mono-allelic expression.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2366, doi. 10.1093/hmg/ddr138
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- Article
Improved risk prediction for Crohn's disease with a multi-locus approach.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2435
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 12, p. NP, doi. 10.1093/hmg/ddr186
- Publication type:
- Article
The MYH9/APOL1 region and chronic kidney disease in European-Americans.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2450, doi. 10.1093/hmg/ddr118
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- Article
ApoE isoform-specific regulation of regeneration in the peripheral nervous system.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2406, doi. 10.1093/hmg/ddr147
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- Article
Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis.
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- Human Molecular Genetics, 2011, v. 20, n. 12, p. 2344, doi. 10.1093/hmg/ddr127
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 12, p. NP, doi. 10.1093/hmg/ddr182
- Publication type:
- Article