Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2523, doi. 10.1093/hmg/9.17.2523
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2000 AND VI 9 AND IP 17
Results: 11
1
2
Interaction between the G1057D variant of IRS-2 and overweight in the pathogenesis of type 2 diabetes.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2517, doi. 10.1093/hmg/9.17.2517
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- Publication type:
- Article
3
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2553, doi. 10.1093/hmg/9.17.2553
- By:
- Publication type:
- Article
4
Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for Duchenne muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2507, doi. 10.1093/hmg/9.17.2507
- By:
- Publication type:
- Article
5
Pleiotropic effects of the melanocortin 1 receptor ( MC1R) gene on human pigmentation.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2531, doi. 10.1093/hmg/9.17.2531
- By:
- Publication type:
- Article
6
Intramuscular injection of a plasmid vector expressing human apolipoprotein E limits progression of xanthoma and aortic atheroma in apoE-deficient mice.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2545, doi. 10.1093/hmg/9.17.2545
- By:
- Publication type:
- Article
7
Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2491, doi. 10.1093/hmg/9.17.2491
- By:
- Publication type:
- Article
8
Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2539, doi. 10.1093/hmg/9.17.2539
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- Publication type:
- Article
9
Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2563, doi. 10.1093/hmg/9.17.2563
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- Publication type:
- Article
10
The neuronal apoptosis inhibitory protein suppresses neuronal differentiation and apoptosis in PC12 cells.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2479, doi. 10.1093/hmg/9.17.2479
- By:
- Publication type:
- Article
11
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2471, doi. 10.1093/hmg/9.17.2471
- By:
- Publication type:
- Article