Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 16
Results: 11
SUT-1 enables tau-induced neurotoxicity in C. elegans.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1959, doi. 10.1093/hmg/ddm143
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- Publication type:
- Article
Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1951, doi. 10.1093/hmg/ddm142
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- Publication type:
- Article
Disease-associated mutations affect GPR56 protein trafficking and cell surface expression.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1972, doi. 10.1093/hmg/ddm144
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- Publication type:
- Article
Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1940, doi. 10.1093/hmg/ddm141
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- Publication type:
- Article
GNAS transcripts in skeletal progenitors: evidence for random asymmetric allelic expression of Gsα.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1921, doi. 10.1093/hmg/ddm139
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- Publication type:
- Article
Non-disjunction of chromosome 13.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 2004, doi. 10.1093/hmg/ddm148
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- Publication type:
- Article
Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1986, doi. 10.1093/hmg/ddm146
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- Publication type:
- Article
In vitro assays fail to predict in vivo effects of regulatory polymorphisms.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1931, doi. 10.1093/hmg/ddm140
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- Publication type:
- Article
MPP1 links the Usher protein network and the Crumbs protein complex in the retina.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1993, doi. 10.1093/hmg/ddm147
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- Publication type:
- Article
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1905, doi. 10.1093/hmg/ddm138
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- Publication type:
- Article
Mechanism of action of a sulphonylurea receptor SUR1 mutation (F132L) that causes DEND syndrome.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 2011, doi. 10.1093/hmg/ddm149
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- Publication type:
- Article