Works matching IS 09646906 AND DT 2014 AND VI 23 AND IP 24
Results: 30
Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6659, doi. 10.1093/hmg/ddu374
- By:
- Publication type:
- Article
De novo CNVs in bipolar affective disorder and schizophrenia.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6677, doi. 10.1093/hmg/ddu379
- By:
- Publication type:
- Article
TCF7L2 is a master regulator of insulin production and processing.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6419, doi. 10.1093/hmg/ddu359
- By:
- Publication type:
- Article
Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6495, doi. 10.1093/hmg/ddu369
- By:
- Publication type:
- Article
Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6481, doi. 10.1093/hmg/ddu368
- By:
- Publication type:
- Article
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6607, doi. 10.1093/hmg/ddu361
- By:
- Publication type:
- Article
Oxaloacetate activates brain mitochondrial biogenesis, enhances the insulin pathway, reduces inflammation and stimulates neurogenesis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6528, doi. 10.1093/hmg/ddu371
- By:
- Publication type:
- Article
A calcineurin- and NFAT-dependent pathway is involved in α-synuclein-induced degeneration of midbrain dopaminergic neurons.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6567, doi. 10.1093/hmg/ddu377
- By:
- Publication type:
- Article
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6616, doi. 10.1093/hmg/ddu363
- By:
- Publication type:
- Article
Selective demethylation and altered gene expression are associated with ICF syndrome in human-induced pluripotent stem cells and mesenchymal stem cells.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6448, doi. 10.1093/hmg/ddu365
- By:
- Publication type:
- Article
Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6432
- By:
- Publication type:
- Article
Deficiency of Patched 1-induced Gli1 signal transduction results in astrogenesis in Swedish mutated APP transgenic mice.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6512
- By:
- Publication type:
- Article
Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6634, doi. 10.1093/hmg/ddu364
- By:
- Publication type:
- Article
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6684, doi. 10.1093/hmg/ddu386
- By:
- Publication type:
- Article
Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6668, doi. 10.1093/hmg/ddu375
- By:
- Publication type:
- Article
Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6458, doi. 10.1093/hmg/ddu366
- By:
- Publication type:
- Article
Polycomb group complexes are recruited to reactivated FMR1 alleles in Fragile X syndrome in response to FMR1 transcription.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6575, doi. 10.1093/hmg/ddu378
- By:
- Publication type:
- Article
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6695, doi. 10.1093/hmg/ddu496
- By:
- Publication type:
- Article
Competing targets of microRNA-608 affect anxiety and hypertension.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6694, doi. 10.1093/hmg/ddu495
- By:
- Publication type:
- Article
ZBTB42 mutation defines a novel lethal congenital contracture syndrome (LCCS6).
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6584, doi. 10.1093/hmg/ddu384
- By:
- Publication type:
- Article
The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6441, doi. 10.1093/hmg/ddu362
- By:
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. NP, doi. 10.1093/hmg/ddu592
- Publication type:
- Article
Epigallocatechin-3-gallate and tetracycline differently affect ataxin-3 fibrillogenesis and reduce toxicity in spinocerebellar ataxia type 3 model.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6542, doi. 10.1093/hmg/ddu373
- By:
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. NP, doi. 10.1093/hmg/ddu590
- Publication type:
- Article
Exploiting the interaction between Grp94 and aggregated myocilin to treat glaucoma.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6470, doi. 10.1093/hmg/ddu367
- By:
- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. NP, doi. 10.1093/hmg/ddu591
- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. NP, doi. 10.1093/hmg/ddu593
- Publication type:
- Article
The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6594, doi. 10.1093/hmg/ddu385
- By:
- Publication type:
- Article
SUCLG2 identified as both a determinator of CSF Aβ1–42 levels and an attenuator of cognitive decline in Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6644
- By:
- Publication type:
- Article
New BRAF knockin mice provide a pathogenetic mechanism of developmental defects and a therapeutic approach in cardio-facio-cutaneous syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6553, doi. 10.1093/hmg/ddu376
- By:
- Publication type:
- Article