Zobrazeno 1 - 10
of 38
pro vyhledávání: '"R C, Smart"'
Publikováno v:
Oncogene. 25:1272-1276
The CCAAT/enhancer binding protein beta (C/EBP beta) is implicated in the regulation of many different molecular and physiological processes. Mice with a germline deletion of C/EBP beta (C/EBP beta(-/-)) display phenotypes in a multitude of cell type
Autor:
R C, SMART
Publikováno v:
The Dental record. 66(12)
Autor:
R C, Smart, H S, Oh
Publikováno v:
The Journal of investigative dermatology. 111(1)
Publikováno v:
Molecular carcinogenesis. 20(1)
Mirex is a potent tumor promoter in 7,1 2-dimethylbenz[a]anthracene (DMBA)-initiated female CD-1 mouse skin. Like 12-O-tetradecanoylphorbol-13-acetate (TPA), mirex promotes papillomas that have a Ha-ras mutation; however, unlike TPA promotion, mirex
Publikováno v:
The Journal of arthroplasty. 11(4)
To define the precision (reproducibility) of measurement of periprosthetic bone mineral density and bone mineral content, dual-energy x-ray absorptiometry scans were obtained on 45 randomly selected patients who had had a unilateral total hip arthrop
Publikováno v:
Cancer research. 55(14)
TG.AC transgenic mice harbor a v-Ha-ras transgene and retain two normal c-Ha-ras alleles and are susceptible to skin tumor formation by 12-O-tetradecanoylphorbol-13-acetate (TPA). To determine whether normal c-Ha-ras antagonizes the oncogenic potenti
Publikováno v:
Carcinogenesis. 15(1)
Mirex, an organochlorine pesticide and non-genotoxic rodent hepatocarcinogen, is also a potent non-phorbol ester-type promoter of mouse skin tumors. Mirex, unlike most other skin tumor promoters, is not a significant epidermal hyperplasiogen even at
Autor:
S J, Boyd, R C, Smart
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 34(9)
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 33(11)
Publikováno v:
Cancer research. 52(3)
The hepatocarcinogenic organochlorine pesticide, mirex, was examined as a tumor promoter in the mouse skin initiation-promotion model. Female CD-1 mice were initiated with 200 nmol 7,12-dimethylbenz[a] anthracene and topically promoted three times we