Zobrazeno 1 - 10
of 26
pro vyhledávání: '"D. W. Yandell"'
Publikováno v:
Molecular and Cellular Biology. 14:4373-4379
A major question in carcinogenesis is, How can a normal cell accumulate multiple mutations in different genes on different chromosomes, when the mutation rate of each gene is in the range of 10(-8) to 10(-5) per cell division? We hypothesize that man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c45c6a485f1f7aca57118c38c3072fd3
https://doi.org/10.1128/mcb.14.7.4373
https://doi.org/10.1128/mcb.14.7.4373
Autor:
Klaus Kruse, Qian Huang, Gernot H. G. Sinnecker, Olaf Hiort, H. J. Wolfe, D. W. Yandell, A. Sadeghi-Nejad
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 77:262-266
Recent studies indicate that mutations in the androgen receptor gene are associated with androgen insensitivity syndromes, a heterogeneous group of related disorders involving defective sexual differentiation in karyotypic males. In this report, we a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0993d187dda990cef2b456bcab2360
https://doi.org/10.1210/jcem.77.1.8325950
https://doi.org/10.1210/jcem.77.1.8325950
Publikováno v:
Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih. 14(4)
Aberrations of chromosome 9 p21-22 are involved in the genesis of many forms of cancer. The gene p16 and p15 have been assigned to this region. Both p16 and p15 are an inhibitor of cyclin D-cdk4,cyclin D-cdk6 complex and have been implicated in a wid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::678194b3e51a2fb15f73cf6a5e348856
https://pubmed.ncbi.nlm.nih.gov/12894891
https://pubmed.ncbi.nlm.nih.gov/12894891
Publikováno v:
Zhonghua zhong liu za zhi [Chinese journal of oncology]. 21(1)
To study the status of several tumor suppressor genes in primary retinoblastoma.Single stranded conformation polymorphism (SSCP) analysis associated with direct DNA sequencing was used to identify point mutations in the coding sequence of Rb, p53, p1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e79623370d6313d4f536bc1a30d5f5a
https://pubmed.ncbi.nlm.nih.gov/11776785
https://pubmed.ncbi.nlm.nih.gov/11776785
Autor:
D. W. Yandell, Cosimi Ab, Sanjay Saini, W. N. Katkov, John A. Powelson, Judith A. Ferry, Chuan Li, Ira J. Spiro
Publikováno v:
New England Journal of Medicine. 329:27-29
Non-Hodgkin's lymphoma after organ transplantation is a recognized complication of immunosuppressive therapy. A number of cases of post-transplantation lymphoma arising in allografted tissue have been described1. In addition, leukemia and lymphoma ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1df7413bd0a8d3e3e45abc3f8cc6fc38
https://doi.org/10.1056/nejm199307013290105
https://doi.org/10.1056/nejm199307013290105
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 15(3)
To investigate the possible cause and molecular mechanism of low penetrance in hereditary retinoblastoma kindred.The DNAs from tumor or blood of affected and unaffected individuals in hereditary retinoblastoma families showing low penetrance were scr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd1ddc9946c5a8afddb029080fb03d02
https://pubmed.ncbi.nlm.nih.gov/9621119
https://pubmed.ncbi.nlm.nih.gov/9621119
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 15(2)
To develop a diagnostic test for direct identification of disease-causing mutation in the patients with retinoblastoma and correct prediction of carrier- status in unaffected adults and newborns in the RB kindred.Southern blot hybridized by Rb cDNA a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea2eeee4865b948b61764285a9f41345
https://pubmed.ncbi.nlm.nih.gov/9531640
https://pubmed.ncbi.nlm.nih.gov/9531640
Autor:
D W, Yandell, C, Poremba
Publikováno v:
Medical and pediatric oncology. Supplement. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::938d29e0a77436b04ae0af4ac2ab36b6
https://pubmed.ncbi.nlm.nih.gov/8643044
https://pubmed.ncbi.nlm.nih.gov/8643044
Publikováno v:
Human pathology. 26(4)
Mutations of the p53 gene are common in human ovarian carcinomas; however, their role in the early development of ovarian cancer is unclear. Twelve ovarian borderline tumors (BTs; eight of them p53 immunopositive) and 10 stage I carcinomas (four of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8783b3c5c5dddde8dc798b58d4c6ed12
https://pubmed.ncbi.nlm.nih.gov/7705816
https://pubmed.ncbi.nlm.nih.gov/7705816
Publikováno v:
Oncology research. 7(7-8)
Expression of mutant p53 detected by immunohistochemistry has been described in human malignant melanoma, but there are few reports of molecular analyses. To investigate the genetic basis for p53 expression in malignant melanoma, we examined 58 prima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9a56cf5b9c015854f5437af92b37a69d
https://pubmed.ncbi.nlm.nih.gov/8747596
https://pubmed.ncbi.nlm.nih.gov/8747596