Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 9
Results: 22
A major recombination hotspot in the XqYq pseudoautosomal region gives new insight into processing of human gene conversion events.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2029, doi. 10.1093/hmg/dds019
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- Article
Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptor.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 1989, doi. 10.1093/hmg/dds012
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- Article
Disrupted in Schizophrenia 1 forms pathological aggresomes that disrupt its function in intracellular transport.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2017, doi. 10.1093/hmg/dds018
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- Article
Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2068, doi. 10.1093/hmg/dds024
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- Article
TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2124, doi. 10.1093/hmg/dds028
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- Article
Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2132, doi. 10.1093/hmg/dds029
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. NP-a, doi. 10.1093/hmg/dds120
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. NP, doi. 10.1093/hmg/dds119
- Publication type:
- Article
LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 1931, doi. 10.1093/hmg/dds003
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- Article
The DNA translocase activity of FANCM protects stalled replication forks.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2005, doi. 10.1093/hmg/dds013
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- Publication type:
- Article
Rescue from excitotoxicity and axonal degeneration accompanied by age-dependent behavioral and neuroanatomical alterations in caspase-6-deficient mice.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 1954, doi. 10.1093/hmg/dds005
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- Article
Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 1968, doi. 10.1093/hmg/dds006
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- Publication type:
- Article
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 1945, doi. 10.1093/hmg/dds004
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- Publication type:
- Article
Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 1979, doi. 10.1093/hmg/dds011
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- Article
Transcriptional analysis of pluripotency reveals the Hippo pathway as a barrier to reprogramming.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2054, doi. 10.1093/hmg/dds023
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- Publication type:
- Article
Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2102, doi. 10.1093/hmg/dds020
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- Publication type:
- Article
The effects of EBV transformation on gene expression levels and methylation profiles.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2142, doi. 10.1093/hmg/dds027
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- Publication type:
- Article
IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2076, doi. 10.1093/hmg/dds025
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. NP-b, doi. 10.1093/hmg/dds121
- Publication type:
- Article
The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2111, doi. 10.1093/hmg/dds021
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- Publication type:
- Article
Periconceptional maternal micronutrient supplementation is associated with widespread gender related changes in the epigenome: a study of a unique resource in the Gambia.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2086, doi. 10.1093/hmg/dds026
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- Article
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
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- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2039, doi. 10.1093/hmg/dds022
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- Article