Works matching IS 09646906 AND DT 2014 AND VI 23 AND IP 17
Results: 27
Formin 1 and Filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4663
- By:
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. NP, doi. 10.1093/hmg/ddu404
- Publication type:
- Article
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4693, doi. 10.1093/hmg/ddu158
- By:
- Publication type:
- Article
No large-effect low-frequency coding variation found for myocardial infarction.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4721, doi. 10.1093/hmg/ddu175
- By:
- Publication type:
- Article
Multi-ethnic fine-mapping of 14 central adiposity loci.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4738
- By:
- Publication type:
- Article
Progressive axonal transport and synaptic protein changes correlate with behavioral and neuropathological abnormalities in the heterozygous Q175 KI mouse model of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4510, doi. 10.1093/hmg/ddu166
- By:
- Publication type:
- Article
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4729
- By:
- Publication type:
- Article
Defining the therapeutic window in a severe animal model of spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4559, doi. 10.1093/hmg/ddu169
- By:
- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. NP, doi. 10.1093/hmg/ddu405
- Publication type:
- Article
Developmental transcriptome analysis of human erythropoiesis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4528, doi. 10.1093/hmg/ddu167
- By:
- Publication type:
- Article
Overexpression of LARGE suppresses muscle regeneration via down-regulation of insulin-like growth factor 1 and aggravates muscular dystrophy in mice.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4543, doi. 10.1093/hmg/ddu168
- By:
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. NP, doi. 10.1093/hmg/ddu402
- Publication type:
- Article
TGFBI (βIG-H3) is a diabetes-risk gene based on mouse and human genetic studies.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4597, doi. 10.1093/hmg/ddu173
- By:
- Publication type:
- Article
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4479, doi. 10.1093/hmg/ddu160
- By:
- Publication type:
- Article
Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4674, doi. 10.1093/hmg/ddu187
- By:
- Publication type:
- Article
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4703, doi. 10.1093/hmg/ddu172
- By:
- Publication type:
- Article
Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4621, doi. 10.1093/hmg/ddu178
- By:
- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. NP, doi. 10.1093/hmg/ddu403
- Publication type:
- Article
Glia are critical for the neuropathology of complex I deficiency in Drosophila.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4686, doi. 10.1093/hmg/ddu188
- By:
- Publication type:
- Article
The novel Parkinson's disease linked mutation G51D attenuates in vitro aggregation and membrane binding of α-synuclein, and enhances its secretion and nuclear localization in cells.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4491, doi. 10.1093/hmg/ddu165
- By:
- Publication type:
- Article
Identification of a splicing variant that regulates type 2 diabetes risk factor CDKAL1 level by a coding-independent mechanism in human.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4639, doi. 10.1093/hmg/ddu184
- By:
- Publication type:
- Article
Competing targets of microRNA-608 affect anxiety and hypertension.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4569, doi. 10.1093/hmg/ddu170
- By:
- Publication type:
- Article
Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4651, doi. 10.1093/hmg/ddu185
- By:
- Publication type:
- Article
Prion protein facilitates synaptic vesicle release by enhancing release probability.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4581, doi. 10.1093/hmg/ddu171
- By:
- Publication type:
- Article
Abnormal visual gain control in a Parkinson's disease model.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4465, doi. 10.1093/hmg/ddu159
- By:
- Publication type:
- Article
Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4710
- By:
- Publication type:
- Article
Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4612, doi. 10.1093/hmg/ddu176
- By:
- Publication type:
- Article