Found: 19
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Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2113, doi. 10.1093/hmg/ddw069
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- Article
Integrated analyses of gene expression and genetic association studies in a founder population.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2104, doi. 10.1093/hmg/ddw061
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- Article
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2093, doi. 10.1093/hmg/ddw058
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- Article
Testing the role of predicted gene knockouts in human anthropometric trait variation.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2082, doi. 10.1093/hmg/ddw055
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- Article
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2070, doi. 10.1093/hmg/ddw048
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- Article
Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2045, doi. 10.1093/hmg/ddw078
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- Article
The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2060, doi. 10.1093/hmg/ddw079
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- Article
ARL3 regulates trafficking of prenylated phototransduction proteins to the rod outer segment.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2031, doi. 10.1093/hmg/ddw077
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- Article
DNA methylation profiling in human Huntington's disease brain.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2013, doi. 10.1093/hmg/ddw076
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- Article
Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2005, doi. 10.1093/hmg/ddw075
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- Article
mGlu<sub>5</sub> positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndrome.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1990, doi. 10.1093/hmg/ddw074
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- Article
A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1979, doi. 10.1093/hmg/ddw073
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- Article
Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1965, doi. 10.1093/hmg/ddw068
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- Article
Drosophila clueless is involved in Parkin-dependent mitophagy by promoting VCP-mediated Marf degradation.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1946, doi. 10.1093/hmg/ddw067
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- Article
BRCA2 minor transcript lacking exons 4-7 supports viability in mice and may account for survival of humans with a pathogenic biallelic mutation.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1934, doi. 10.1093/hmg/ddw066
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- Article
Loss of carbonic anhydrase XII function in individuals with elevated sweat chloride concentration and pulmonary airway disease.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1923, doi. 10.1093/hmg/ddw065
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- Article
Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1912, doi. 10.1093/hmg/ddw064
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- Article
Defective membrane fusion and repair in Anoctamin5-deficient muscular dystrophy.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1900, doi. 10.1093/hmg/ddw063
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- Article
Pharmacokinetics, pharmacodynamics, and efficacy of a small-molecule SMN2 splicing modifier in mouse models of spinal muscular atrophy.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 1885, doi. 10.1093/hmg/ddw062
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- Article