Showing results (1-10 of 127) with videos related to
Sort By:
Pageof 13
Radiation Research|August 28, 2009
Radiofrequency radiation and gene/protein expression: a reviewJ P McNamee, V ChauhanRadiation Research|November 22, 2005
Evaluating DNA damage in rodent brain after acute 60 Hz magnetic-field exposureJ P McNamee, P V Bellier, V Chauhan, et al.Radiation Research|April 4, 2006
Gene expression analysis of a human lymphoblastoma cell line exposed in vitro to an intermittent 1.9 GHz pulse-modulated radiofrequency fieldV Chauhan, A Mariampillai, P V Bellier, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 1, 1996
Cytochrome P4503A is the major source of N-vinylprotoporphyrin IX formation after administration of 3-[2-(2,4,6-trimethylphenyl)thioethyl]-4-methylsydnone to untreated and dexamethasone-pretreated ratsJ P McNamee, G S MarksMutation Research. Genetic Toxicology and Environmental Mutagenesis|July 28, 2015
Use of a standardized JaCVAM in vivo rat comet assay protocol to assess the genotoxicity of three coded test compounds; ampicillin trihydrate, 1,2-dimethylhydrazine dihydrochloride, and N-nitrosodimethylamineJ P McNamee, P V BellierRadiation Research|January 12, 2007
Evaluating the biological effects of intermittent 1.9 GHz pulse-modulated radiofrequency fields in a series of human-derived cell linesV Chauhan, A Mariampillai, B C Kutzner, et al.International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|January 21, 2006
Response to pulsed dose rate and low dose rate irradiation with and without mild hyperthermia using human breast carcinoma cell linesM Niedbala, J P McNamee, G P RaaphorstRadiation Research|June 29, 2006
Microarray gene expression profiling of a human glioblastoma cell line exposed in vitro to a 1.9 GHz pulse-modulated radiofrequency fieldS S Qutob, V Chauhan, P V Bellier, et al.Biochemical Pharmacology|May 17, 1995
Inactivation of chick embryo hepatic cytochrome P450 1A, 2H and 3A following in ovo administration of 3,5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-ethylpyridine and 3-[2-(2,4,6-trimethylphenyl)thioethyl]-4-methylsydnoneJ P McNamee, S M Kimmett, G S MarksCanadian Journal of Physiology and Pharmacology|April 1, 1994
Mechanism-based inactivation of hepatic cytochrome P450 2C6 and P450 3A1 following in vivo administration of 3,5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-ethylpyridine to rats: differences from previously observed in vitro resultsS M Kimmett, J P McNamee, G S MarksPageof 13