Found: 14
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Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1127, doi. 10.1093/hmg/ddn002
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- Article
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1137, doi. 10.1093/hmg/ddn003
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- Article
MeCP2-dependent repression of an imprinted miR-184 released by depolarization.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1192, doi. 10.1093/hmg/ddn011
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- Article
Dysregulation of miRNA 181b in the temporal cortex in schizophrenia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1156, doi. 10.1093/hmg/ddn005
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- Article
Polymorphisms in thrombospondin genes and myocardial infarction: a case–control study and a meta-analysis of available evidence.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1120, doi. 10.1093/hmg/ddn001
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- Article
Polycystin-2 is regulated by endoplasmic reticulum-associated degradation.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1109, doi. 10.1093/hmg/ddm383
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- Publication type:
- Article
An Actn3 knockout mouse provides mechanistic insights into the association between α-actinin-3 deficiency and human athletic performance.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1076, doi. 10.1093/hmg/ddm380
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- Article
Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1169, doi. 10.1093/hmg/ddn006
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- Publication type:
- Article
Atypical Mowat–Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1175, doi. 10.1093/hmg/ddn007
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- Article
Wild-type PABPN1 is anti-apoptotic and reduces toxicity of the oculopharyngeal muscular dystrophy mutation.
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- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1097, doi. 10.1093/hmg/ddm382
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- Publication type:
- Article
Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1063, doi. 10.1093/hmg/ddm379
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- Article
Genetic and epigenetic mechanisms combine to control MMP1 expression and its association with preterm premature rupture of membranes.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1087, doi. 10.1093/hmg/ddm381
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- Publication type:
- Article
Two different forms of palindrome resolution in the human genome: deletion or translocation.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1184, doi. 10.1093/hmg/ddn008
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- Publication type:
- Article
Genetic variation in the CRP promoter: association with systemic lupus erythematosus.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1147, doi. 10.1093/hmg/ddn004
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- Publication type:
- Article