Found: 11
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Haplotypes spanning SPEC2, PDZ-GEF2 and ACSL6 genes are associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3329, doi. 10.1093/hmg/ddl409
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- Article
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3324, doi. 10.1093/hmg/ddl408
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- Article
DISC1–NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3313, doi. 10.1093/hmg/ddl407
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- Article
A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3306, doi. 10.1093/hmg/ddl406
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- Article
Sesn1 is a novel gene for left–right asymmetry and mediating nodal signaling.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3369, doi. 10.1093/hmg/ddl413
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- Article
Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3361, doi. 10.1093/hmg/ddl412
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- Article
Identification of susceptibility loci for cervical carcinoma by genome scan of affected sib-pairs.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3351, doi. 10.1093/hmg/ddl411
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- Article
The N-terminal domain of the Aurora-A Phe-31 variant encodes an E3 ubiquitin ligase and mediates ubiquitination of IκBα.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3343, doi. 10.1093/hmg/ddl410
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- Article
Analysis of Nsdhl-deficient embryos reveals a role for Hedgehog signaling in early placental development.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3293, doi. 10.1093/hmg/ddl405
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- Article
Kinesin-2 mediates physical and functional interactions between polycystin-2 and fibrocystin.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3280, doi. 10.1093/hmg/ddl404
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- Article
A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3273, doi. 10.1093/hmg/ddl403
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- Publication type:
- Article