Zobrazeno 1 - 10
of 16
pro vyhledávání: '"D S, Gerhard"'
Publikováno v:
Cancer research. 61(13)
Two polymorphisms in the newly cloned prostate cancer susceptibility gene, HPC2/ELAC2, are suspected to be associated with an increased risk of developing the disease. These missense variants result in a serine (S) to leucine (L) substitution at amin
Publikováno v:
Genes, chromosomescancer. 27(4)
We previously showed loss of heterozygosity at 6p to be a common genetic alteration in cervical cancer and cervical intraepithelial neoplasia. To characterize this critical area of deletion in chromosome 6, we evaluated 107 invasive cervical cancers,
Publikováno v:
Genes, chromosomescancer. 22(1)
We have shown previously that a significant number of invasive cervical cancers (ICC) have nonrandom chromosomal losses in 3p, 6p, 11q, 2q, 6q, and 19q, thereby suggesting that genes involved in the suppression of tumor development or progression are
Publikováno v:
Oncogene. 13(12)
The best characterized factor in the development of cervical cancer is the integration, of human papillomavirus into cervical cell chromosomes. In addition to HPV integration, the neoplastic process probably requires the activation of cellular protoo
Publikováno v:
American journal of human genetics. 59(6)
Progress of a full-genome scan for predisposition loci for affective disorder in the Old Order Amish is reported. LOD-score results have been previously published for 51 loci on chromosomes 1 and 11, collectively. The present report contains results
Publikováno v:
Blood. 88(2)
Translocations involving the IgH locus at chromosomal locus 14q32.3 are a common event in many B-cell malignancies. The translocations, which generally occur into JH and switch regions, are mediated by errors in the two developmentally regulated, lym
Autor:
R A, Bascom, J, García-Heras, C L, Hsieh, D S, Gerhard, C, Jones, U, Francke, H F, Willard, D H, Ledbetter, R R, McInnes
Publikováno v:
American journal of human genetics. 51(5)
Rom-1 is a retinal integral membrane protein that, together with the product of the human retinal degeneration slow gene (RDS), defines a photoreceptor-specific protein family. The gene for rom-1 (HGM symbol: ROM1) has been assigned to human chromoso
Publikováno v:
Cancer research. 50(20)
Multiple endocrine neoplasia type 1 is an autosomal dominant condition characterized by the development of parathyroid hyperplasia, pituitary adenomas, and pancreatic islet cell tumors. Recently the gene for multiple endocrine neoplasia type 1 was ma
Publikováno v:
Psychiatric Genetics. 2:S7A
Publikováno v:
Journal of Virology. 39:920-934
During serial passages of an avian leukosis virus (the transformation-defective, src deletion mutant of Bratislava 77 avian sarcoma virus, designated tdB77) in chicken embryo fibroblasts, viruses which transformed chicken embryo fibroblasts in vitro