Found: 19
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- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. NP, doi. 10.1093/hmg/ddp547
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. NP, doi. 10.1093/hmg/ddp544
- Publication type:
- Article
The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 342, doi. 10.1093/hmg/ddp500
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- Publication type:
- Article
Fibroblast phenotype in male carriers of FMR1 premutation alleles.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 299, doi. 10.1093/hmg/ddp497
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- Publication type:
- Article
Proteotoxic stress increases nuclear localization of ataxin-3.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 235, doi. 10.1093/hmg/ddp482
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- Publication type:
- Article
Replication of the five novel loci for uric acid concentrations and potential mediating mechanisms.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 387, doi. 10.1093/hmg/ddp489
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- Publication type:
- Article
Sporadic ALS has compartment-specific aberrant exon splicing and altered cell–matrix adhesion biology.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 313, doi. 10.1093/hmg/ddp498
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- Publication type:
- Article
Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 262, doi. 10.1093/hmg/ddp490
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- Publication type:
- Article
The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 250, doi. 10.1093/hmg/ddp484
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- Publication type:
- Article
Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 223, doi. 10.1093/hmg/ddp481
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- Publication type:
- Article
Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 374, doi. 10.1093/hmg/ddp503
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- Publication type:
- Article
Frataxin interacts with Isu1 through a conserved tryptophan in its β-sheet.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 276, doi. 10.1093/hmg/ddp495
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- Publication type:
- Article
PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 217, doi. 10.1093/hmg/ddp480
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- Publication type:
- Article
Nesprin 1 is critical for nuclear positioning and anchorage.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 329, doi. 10.1093/hmg/ddp499
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. NP, doi. 10.1093/hmg/ddp546
- Publication type:
- Article
Phosphorylation of parkin by Parkinson disease-linked kinase PINK1 activates parkin E3 ligase function and NF-κB signaling.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 352, doi. 10.1093/hmg/ddp501
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. NP, doi. 10.1093/hmg/ddp545
- Publication type:
- Article
Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryos.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 364, doi. 10.1093/hmg/ddp502
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- Publication type:
- Article
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 287
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- Publication type:
- Article