Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 24
Results: 11
ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein β-subunit.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3569, doi. 10.1093/hmg/ddl433
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- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3592, doi. 10.1093/hmg/ddl435
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- Article
Mutant huntingtin inhibits clathrin-independent endocytosis and causes accumulation of cholesterol in vitro and in vivo.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3578, doi. 10.1093/hmg/ddl434
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- Article
Increased SK3 expression in DM1 lens cells leads to impaired growth through a greater calcium-induced fragility.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3559, doi. 10.1093/hmg/ddl432
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- Article
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3544, doi. 10.1093/hmg/ddl431
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- Article
Unexpected mosaicism of R201H-GNAS1 mutant-bearing cells in the testes underlie macro-orchidism without sexual precocity in McCune–Albright syndrome.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3538, doi. 10.1093/hmg/ddl430
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- Article
Haplotype-specific expression of exon 10 at the human MAPT locus.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3529, doi. 10.1093/hmg/ddl429
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- Article
Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3520, doi. 10.1093/hmg/ddl428
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- Article
Intragenic deletion of Tgif causes defectsin brain development.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3508, doi. 10.1093/hmg/ddl427
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- Article
Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations.
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- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3498, doi. 10.1093/hmg/ddl426
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- Article
Itch genetically interacts with Notch1 in a mouse autoimmune disease model.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3485, doi. 10.1093/hmg/ddl425
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- Article