Zobrazeno 1 - 4
of 4
pro vyhledávání: '"H A, Cocker"'
Publikováno v:
British Journal of Cancer
The MDM2 protein is known to be overexpressed in some sarcomas including rhabdomyosarcoma. However, the extent to which the MDM2 protein influences sensitivity to chemotherapeutic drugs is unclear. We have analysed this further using stable transfect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09d0ad1504daa72fb093682e305c6bd7
https://doi.org/10.1054/bjoc.2001.2145
https://doi.org/10.1054/bjoc.2001.2145
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(10)
We have established preclinical models for the development of drug resistance to vincristine (a major drug used in the treatment of pediatric rhabdomyosarcoma) using cell lines. The RD cell line has a mutant P53 phenotype and does not have detectable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9ad634f9d9e0501d00450bc38d9ea90
https://pubmed.ncbi.nlm.nih.gov/11595714
https://pubmed.ncbi.nlm.nih.gov/11595714
Publikováno v:
British Journal of Cancer
The role of multidrug resistance (MDR) and p53 functional status in the treatment of paediatric rhabdomyosarcoma is unclear. We have characterized a panel of seven human rhabdomyosarcoma cell lines for MDR and p53 phenotype. None of the cell lines ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3168c9240130740fbf4da4900f746f
https://pubmed.ncbi.nlm.nih.gov/10917549
https://pubmed.ncbi.nlm.nih.gov/10917549
Publikováno v:
East African medical journal. 68(12)
A total of 91 catalase--negative Gram-positive coccal isolates obtained from 245 clinical specimens in Lagos were characterized. Ten (11.0%) of the isolates were vancomycin resistant, they fermented glucose, sucrose, fructose, lactose, mannose, manni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4080cebde0b5e3e0c8091f7a69324208
https://pubmed.ncbi.nlm.nih.gov/1800096
https://pubmed.ncbi.nlm.nih.gov/1800096