Found: 15
Select item for more details and to access through your institution.
Functional substitution for TAFII250 by a retroposed homolog that is expressed in human spermatogenesis.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2341, doi. 10.1093/hmg/11.19.2341
- By:
- Publication type:
- Article
Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2233, doi. 10.1093/hmg/11.19.2233
- By:
- Publication type:
- Article
Poly(ADP-ribose) polymerase 2 localizes to mammalian active centromeres and interacts with PARP-1, Cenpa, Cenpb and Bub3, but not Cenpc.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2319, doi. 10.1093/hmg/11.19.2319
- By:
- Publication type:
- Article
Mutations of the GREAT gene cause cryptorchidism.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2309, doi. 10.1093/hmg/11.19.2309
- By:
- Publication type:
- Article
Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2289, doi. 10.1093/hmg/11.19.2289
- By:
- Publication type:
- Article
Nucleocytoplasmic transfer of the NF2 tumor suppressor protein merlin is regulated by exon 2 and a CRM1-dependent nuclear export signal in exon 15.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2269, doi. 10.1093/hmg/11.19.2269
- By:
- Publication type:
- Article
Evaluating test statistics to select interesting genes in microarray experiments† This paper is part of the Microarray Report Special Series. See Orr, H.J. (2002) Hum. Mol. Genet., 11: 1909–1910.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2223, doi. 10.1093/hmg/11.19.2223
- By:
- Publication type:
- Article
PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2243, doi. 10.1093/hmg/11.19.2243
- By:
- Publication type:
- Article
Estimating the statistical significance of gene expression changes observed with oligonucleotide arrays† This paper is part of the Microarray Report Special Series. See Orr, H.J. (2002) Hum. Mol. Genet., 11: 1909–1910.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2207, doi. 10.1093/hmg/11.19.2207
- By:
- Publication type:
- Article
ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2331, doi. 10.1093/hmg/11.19.2331
- By:
- Publication type:
- Article
Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2297, doi. 10.1093/hmg/11.19.2297
- By:
- Publication type:
- Article
Modulation of polyglutamine-induced cell death by genes identified by expression profiling.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2279, doi. 10.1093/hmg/11.19.2279
- By:
- Publication type:
- Article
Multiple susceptibility loci for multiple sclerosis.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2251
- By:
- Publication type:
- Article
Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2257, doi. 10.1093/hmg/11.19.2257
- By:
- Publication type:
- Article
Validation in mesenchymal progenitor cells of a mutation-independent ex vivo approach to gene therapy for osteogenesis imperfecta.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 19, p. 2201, doi. 10.1093/hmg/11.19.2201
- By:
- Publication type:
- Article