Works matching IS 09646906 AND DT 2001 AND VI 10 AND IP 6
Results: 22
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 573, doi. 10.1093/hmg/10.6.573
- By:
- Publication type:
- Article
Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith–Lemli–Opitz syndrome.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 555, doi. 10.1093/hmg/10.6.555
- By:
- Publication type:
- Article
WBSCR14, a gene mapping to the Williams–Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 617, doi. 10.1093/hmg/10.6.617
- By:
- Publication type:
- Article
PTEN inhibits insulin-stimulated MEK/MAPK activation and cell growth by blocking IRS-1 phosphorylation and IRS-1/Grb-2/Sos complex formation in a breast cancer model.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 605, doi. 10.1093/hmg/10.6.605
- By:
- Publication type:
- Article
Primary non-random X inactivation associated with disruption of Xist promoter regulation.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 581, doi. 10.1093/hmg/10.6.581
- By:
- Publication type:
- Article
Rats made congenic for Oia3 on chromosome 10 become susceptible to squalene-induced arthritis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 565, doi. 10.1093/hmg/10.6.565
- By:
- Publication type:
- Article
Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith-Lemli-Opitz syndrome.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 555, doi. 10.1093/hmg/10.6.555
- By:
- Publication type:
- Article
Mutation rates at two human Y-chromosomal microsatellite loci using small pool PCR techniques.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 629, doi. 10.1093/hmg/10.6.629
- By:
- Publication type:
- Article
Prediction of deleterious human alleles.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 591, doi. 10.1093/hmg/10.6.591
- By:
- Publication type:
- Article
Association of acetylated histones with paternally expressed genes in the Prader–Willi deletion region.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 645, doi. 10.1093/hmg/10.6.645
- By:
- Publication type:
- Article
PTEN coordinates G1 arrest by down-regulating cyclin D1 via its protein phosphatase activity and up-regulating p27 via its lipid phosphatase activity in a breast cancer model.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 599, doi. 10.1093/hmg/10.6.599
- By:
- Publication type:
- Article
Mutations in the regulatory domain of cystathionine β–synthase can functionally suppress patient-derived mutations in cis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 635, doi. 10.1093/hmg/10.6.635
- By:
- Publication type:
- Article
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 573, doi. 10.1093/hmg/10.6.573
- By:
- Publication type:
- Article
Prediction of deleterious human alleles.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 591, doi. 10.1093/hmg/10.6.591
- By:
- Publication type:
- Article
WBSCR14, a gene mapping to the Williams-Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 617, doi. 10.1093/hmg/10.6.617
- By:
- Publication type:
- Article
Primary non-random X inactivation associated with disruption of Xist promoter regulation.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 581, doi. 10.1093/hmg/10.6.581
- By:
- Publication type:
- Article
Mutations in the regulatory domain of cystathionine β-synthase can functionally suppress patient-derived mutations in cis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 635, doi. 10.1093/hmg/10.6.635
- By:
- Publication type:
- Article
Mutation rates at two human Y-chromosomal microsatellite loci using small pool PCR techniques.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 629, doi. 10.1093/hmg/10.6.629
- By:
- Publication type:
- Article
Rats made congenic for Oia3 on chromosome 10 become susceptible to squalene-induced arthritis.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 565, doi. 10.1093/hmg/10.6.565
- By:
- Publication type:
- Article
PTEN inhibits insulin-stimulated MEK/MAPK activation and cell growth by blocking IRS-1 phosphorylation and IRS-1/Grb-2/Sos complex formation in a breast cancer model.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 605, doi. 10.1093/hmg/10.6.605
- By:
- Publication type:
- Article
PTEN coordinates G[sub 1] arrest by down-regulating cyclin D1 via its protein phosphatase activity and up-regulating p27 via its lipid phosphatase activity in a breast cancer model.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 599, doi. 10.1093/hmg/10.6.599
- By:
- Publication type:
- Article
Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 6, p. 645, doi. 10.1093/hmg/10.6.645
- By:
- Publication type:
- Article