Works matching IS 09646906 AND DT 2001 AND VI 10 AND IP 12
Results: 10
Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1307, doi. 10.1093/hmg/10.12.1307
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- Article
BACE knockout mice are healthy despite lacking the primary β -secretase activity in brain: implications for Alzheimer's disease therapeutics.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1317, doi. 10.1093/hmg/10.12.1317
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- Article
Genetic polymorphisms of biotransformation enzymes in patients with Hodgkin's and non-Hodgkin's lymphomas.
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- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1265
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- Publication type:
- Article
B-cell neoplasia associated gene with multiple splicing ( BCMS): the candidate B-CLL gene on 13q14 comprises more than 560 kb covering all critical regions.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1275, doi. 10.1093/hmg/10.12.1275
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- Publication type:
- Article
Neural tube defects and neuroepithelial cell death in Tulp3 knockout mice.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1325, doi. 10.1093/hmg/10.12.1325
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- Article
Evidence for BLM and Topoisomerase III α interaction in genomic stability.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1287
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- Publication type:
- Article
Expanded CAG repeats in exon 1 of the Huntington's disease gene stimulate dopamine-mediated striatal neuron autophagy and degeneration.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1243, doi. 10.1093/hmg/10.12.1243
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- Publication type:
- Article
Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1 locus.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1231, doi. 10.1093/hmg/10.12.1231
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- Publication type:
- Article
Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1255, doi. 10.1093/hmg/10.12.1255
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- Publication type:
- Article
Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 12, p. 1299, doi. 10.1093/hmg/10.12.1299
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- Publication type:
- Article