Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 8
Results: 24
MeCP2 involvement in the regulation of neuronal α-tubulin production.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1415, doi. 10.1093/hmg/ddp048
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. NP, doi. 10.1093/hmg/ddp142
- Publication type:
- Article
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1405, doi. 10.1093/hmg/ddp047
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- Article
Large replication study and meta-analyses of DVWA as an osteoarthritis susceptibility locus in European and Asian populations.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1518, doi. 10.1093/hmg/ddp053
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- Article
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1524, doi. 10.1093/hmg/ddp059
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- Article
Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1543, doi. 10.1093/hmg/ddp050
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- Article
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1439, doi. 10.1093/hmg/ddp054
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- Publication type:
- Article
Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden.
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- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1489
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- Publication type:
- Article
Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1377, doi. 10.1093/hmg/ddp042
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- Publication type:
- Article
Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy.
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- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1471, doi. 10.1093/hmg/ddp058
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- Publication type:
- Article
Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1424, doi. 10.1093/hmg/ddp049
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- Publication type:
- Article
Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1504, doi. 10.1093/hmg/ddp051
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- Publication type:
- Article
Notch signaling contributes to the pathogenesis of human osteosarcomas.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1464, doi. 10.1093/hmg/ddp057
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. NP, doi. 10.1093/hmg/ddp140
- Publication type:
- Article
Deletion of eIF2beta suppresses testicular cancer incidence and causes recessive lethality in agouti-yellow mice.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1395, doi. 10.1093/hmg/ddp045
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. NP, doi. 10.1093/hmg/ddp141
- Publication type:
- Article
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1510, doi. 10.1093/hmg/ddp052
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- Publication type:
- Article
Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1544, doi. 10.1093/hmg/ddp056
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. NP, doi. 10.1093/hmg/ddp139
- Publication type:
- Article
ADH single nucleotide polymorphism associations with alcohol metabolism in vivo.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1533, doi. 10.1093/hmg/ddp060
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- Publication type:
- Article
Gigaxonin controls vimentin organization through a tubulin chaperone-independent pathway.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1384, doi. 10.1093/hmg/ddp044
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- Publication type:
- Article
No evidence for activation of the unfolded protein response in neuronopathic models of Gaucher disease.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1482, doi. 10.1093/hmg/ddp061
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- Publication type:
- Article
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1497
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- Publication type:
- Article
Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1449, doi. 10.1093/hmg/ddp055
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- Publication type:
- Article