Found: 14
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FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 490, doi. 10.1093/hmg/ddm326
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- Article
KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 506
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- Article
Zebrafish model of holoprosencephaly demonstrates a key role for TGIF in regulating retinoic acid metabolism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 525, doi. 10.1093/hmg/ddm328
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- Article
Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 567, doi. 10.1093/hmg/ddm331
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- Article
Strong evidence that GNB1L is associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 555, doi. 10.1093/hmg/ddm330
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- Article
Recombination rates of genes expressed in human tissues.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 577, doi. 10.1093/hmg/ddm332
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- Publication type:
- Article
Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmenti.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 639
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- Publication type:
- Article
ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 469, doi. 10.1093/hmg/ddm324
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- Publication type:
- Article
Mouse Fkbp8 activity is required to inhibit cell death and establish dorso-ventral patterning in the posterior neural tube.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 587, doi. 10.1093/hmg/ddm333
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- Article
The diabetes-linked transcription factor Pax4 is expressed in human pancreatic islets and is activated by mitogens and GLP-1.
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- Human Molecular Genetics, 2008, v. 17, n. 4, p. 478
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- Article
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 539, doi. 10.1093/hmg/ddm329
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- Article
Pink1 Parkinson mutations, the Cdc37/Hsp90 chaperones and Parkin all influence the maturation or subcellular distribution of Pink1.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 602, doi. 10.1093/hmg/ddm334
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- Publication type:
- Article
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 617
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- Publication type:
- Article
Recurrent 16p11.2 microdeletions in autism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 628
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- Publication type:
- Article