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

By:

Sittler, Annie

Publication type:

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

By:

Roberds, Steven L.

Publication type:

Article

Genetic polymorphisms of biotransformation enzymes in patients with Hodgkin's and non-Hodgkin's lymphomas.

Published in:

Human Molecular Genetics, 2001, v. 10, n. 12, p. 1265

By:

armanová, Jana

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

By:

Wolf, Stephan

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

By:

Ikeda, Akihiro

Publication type:

Article

Evidence for BLM and Topoisomerase III α interaction in genomic stability.

Published in:

Human Molecular Genetics, 2001, v. 10, n. 12, p. 1287

By:

Hu, Peng

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

By:

Petersén, Åsa;
Larsen, Kristin E.;
Behr, Gerald G.;
Romero, Norma;
Przedborski, Serge;
Brundin, Patrik;
Sulzer, David

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

By:

Bastepe, M.

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

By:

Iwata, Tomoko

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

By:

Holzinger, Andreas

Publication type:

Article