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E Randerath

Showing results (31-40 of 103) with videos related to

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Biochemical and Biophysical Research Communications|April 15, 1993
Flavor constituents in cola drinks induce hepatic DNA adducts in adult and fetal miceK Randerath, K L Putman, E Randerath
Carcinogenesis|April 1, 1997
Organ-specific oxidative DNA damage associated with normal birth in ratsE Randerath, G D Zhou, K Randerath
Biochemical and Biophysical Research Communications|November 30, 1981
Rat liver mitochondrial lysine tRNA (anticodon U*UU) contains a rudimentary D-arm and 2 hypermodified nucleotides in its anticodon loopE Randerath, H P Agrawal, K Randerath
Nucleic Acids Research|November 1, 1976
A double-labeling procedure for sequence analysis of picomole amounts of nonradioactive RNA fragmentsR C Gupta, E Randerath, K Randerath
Biochemical Pharmacology|March 7, 1997
Effects of cytochrome P450 inducers on tamoxifen genotoxicity in female mice in vivoB Moorthy, P Sriram, E Randerath, et al.
Mutation Research|November 4, 1996
Monophosphate 32P-postlabeling assay of DNA adducts from 1,2:3,4-diepoxybutane, the most genotoxic metabolite of 1,3-butadiene: in vitro methodological studies and in vivo dosimetryN Mabon, B Moorthy, E Randerath, et al.
IARC Scientific Publications|January 1, 1993
I-compounds--endogenous DNA markers of nutritional status, ageing, tumour promotion and carcinogenesisK Randerath, D Li, B Moorthy, et al.
Experimental Gerontology|September 1, 1992
Exogenous and endogenous DNA modifications as monitored by 32P-postlabeling: relationships to cancer and agingK Randerath, D Li, R Nath, et al.
Chemico-Biological Interactions|November 16, 1992
Oat lipids-induced covalent DNA modifications (I-compounds) in female Sprague-Dawley rats, as determined by 32P-postlabelingD Li, S Chen, E Randerath, et al.
Carcinogenesis|November 1, 1995
Evidence from 32P-postlabeling and the use of pentachlorophenol for a novel metabolic activation pathway of diethylstilbestrol and its dimethyl ether in mouse live: likely alpha-hydroxylation of ethyl group(s) followed by sulfate conjugationB Moorthy, J Liehr, E Randerath, et al.
Pageof 11

Showing results (31-40 of 103) with videos related to

Sort By:
Pageof 11
Biochemical and Biophysical Research Communications|April 15, 1993
Flavor constituents in cola drinks induce hepatic DNA adducts in adult and fetal miceK Randerath, K L Putman, E Randerath
Carcinogenesis|April 1, 1997
Organ-specific oxidative DNA damage associated with normal birth in ratsE Randerath, G D Zhou, K Randerath
Biochemical and Biophysical Research Communications|November 30, 1981
Rat liver mitochondrial lysine tRNA (anticodon U*UU) contains a rudimentary D-arm and 2 hypermodified nucleotides in its anticodon loopE Randerath, H P Agrawal, K Randerath
Nucleic Acids Research|November 1, 1976
A double-labeling procedure for sequence analysis of picomole amounts of nonradioactive RNA fragmentsR C Gupta, E Randerath, K Randerath
Biochemical Pharmacology|March 7, 1997
Effects of cytochrome P450 inducers on tamoxifen genotoxicity in female mice in vivoB Moorthy, P Sriram, E Randerath, et al.
Mutation Research|November 4, 1996
Monophosphate 32P-postlabeling assay of DNA adducts from 1,2:3,4-diepoxybutane, the most genotoxic metabolite of 1,3-butadiene: in vitro methodological studies and in vivo dosimetryN Mabon, B Moorthy, E Randerath, et al.
IARC Scientific Publications|January 1, 1993
I-compounds--endogenous DNA markers of nutritional status, ageing, tumour promotion and carcinogenesisK Randerath, D Li, B Moorthy, et al.
Experimental Gerontology|September 1, 1992
Exogenous and endogenous DNA modifications as monitored by 32P-postlabeling: relationships to cancer and agingK Randerath, D Li, R Nath, et al.
Chemico-Biological Interactions|November 16, 1992
Oat lipids-induced covalent DNA modifications (I-compounds) in female Sprague-Dawley rats, as determined by 32P-postlabelingD Li, S Chen, E Randerath, et al.
Carcinogenesis|November 1, 1995
Evidence from 32P-postlabeling and the use of pentachlorophenol for a novel metabolic activation pathway of diethylstilbestrol and its dimethyl ether in mouse live: likely alpha-hydroxylation of ethyl group(s) followed by sulfate conjugationB Moorthy, J Liehr, E Randerath, et al.
Pageof 11