Zobrazeno 1 - 3
of 3
pro vyhledávání: '"P L, Welcsh"'
Autor:
Karen M Chisholm, Sarah D Aubert, Krister P Freese, Virginia A Zakian, Mary-Claire King, Piri L Welcsh
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e30748 (2012)
Alu-mediated rearrangement of tumor suppressor genes occurs frequently during carcinogenesis. In breast cancer, this mechanism contributes to loss of the wild-type BRCA1 allele in inherited disease and to loss of heterozygosity in sporadic cancer. To
Externí odkaz:
https://doaj.org/article/123ea2d018064e7cbd047d4a35226e0f
Publikováno v:
Science (New York, N.Y.). 278(5341)
The gene responsible for autosomal dominant, fully penetrant, nonsyndromic sensorineural progressive hearing loss in a large Costa Rican kindred was previously localized to chromosome 5q31 and named DFNA1. Deafness in the family is associated with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3254e71c6f63af92dc2a34d7ab4c29e7
https://pubmed.ncbi.nlm.nih.gov/9411747
https://pubmed.ncbi.nlm.nih.gov/9411747
Autor:
E N, Levedakou, M, He, E W, Baptist, R J, Craven, W G, Cance, P L, Welcsh, A, Simmons, S L, Naylor, R J, Leach, T B, Lewis
Publikováno v:
Oncogene. 9(7)
Using polymerase chain reaction (PCR)-based methods, we have isolated cDNA clones of two new members of serine/threonine kinases, STK1 and STK2, from a cDNA library constructed from the BT-20 human breast cancer cell line. STK1 is transcribed as a 1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7f71d6494ea00f2870f87c39720e182b
https://pubmed.ncbi.nlm.nih.gov/8208544
https://pubmed.ncbi.nlm.nih.gov/8208544