Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 13
Results: 22
Cover Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. NP, doi. 10.1093/hmg/ddp224
- Publication type:
- Article
Involvement of SMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2483, doi. 10.1093/hmg/ddp166
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- Publication type:
- Article
Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2317, doi. 10.1093/hmg/ddp164
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. NP, doi. 10.1093/hmg/ddp225
- Publication type:
- Article
Ectopic expression of CGG containing mRNA is neurotoxic in mammals.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2443, doi. 10.1093/hmg/ddp182
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- Publication type:
- Article
Systems biology of autosomal dominant polycystic kidney disease (ADPKD): computational identification of gene expression pathways and integrated regulatory networks.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2328, doi. 10.1093/hmg/ddp165
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- Publication type:
- Article
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2495, doi. 10.1093/hmg/ddp169
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- Publication type:
- Article
Decreased TCF7L2 protein levels in type 2 diabetes mellitus correlate with downregulation of GIP- and GLP-1 receptors and impaired beta-cell function.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2388, doi. 10.1093/hmg/ddp178
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. NP, doi. 10.1093/hmg/ddp223
- Publication type:
- Article
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARγ pathway as a therapeutic target in Friedreich’s ataxia.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2452, doi. 10.1093/hmg/ddp183
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- Publication type:
- Article
Activating the synthesis of progerin, the mutant prelamin A in Hutchinson–Gilford progeria syndrome, with antisense oligonucleotides.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2462, doi. 10.1093/hmg/ddp184
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- Publication type:
- Article
Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2431, doi. 10.1093/hmg/ddp181
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- Publication type:
- Article
A hypomorphic allele of Tsc2 highlights the role of TSC1/TSC2 in signaling to AKT and models mild human TSC2 alleles.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2378, doi. 10.1093/hmg/ddp176
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. NP, doi. 10.1093/hmg/ddp228
- Publication type:
- Article
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2414, doi. 10.1093/hmg/ddp180
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- Publication type:
- Article
A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2370, doi. 10.1093/hmg/ddp170
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- Publication type:
- Article
Formin1 disruption confers oligodactylism and alters Bmp signaling.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2472, doi. 10.1093/hmg/ddp185
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- Publication type:
- Article
Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinism.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2400, doi. 10.1093/hmg/ddp179
- By:
- Publication type:
- Article
TRIM32 is an E3 ubiquitin ligase for dysbindin.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2344, doi. 10.1093/hmg/ddp167
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- Publication type:
- Article
Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2518, doi. 10.1093/hmg/ddp177
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- Publication type:
- Article
Functional polymorphisms, altered gene expression and genetic association link NRH:quinone oxidoreductase 2 to breast cancer with wild-type p53.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2502, doi. 10.1093/hmg/ddp171
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- Publication type:
- Article
Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2359, doi. 10.1093/hmg/ddp168
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- Publication type:
- Article