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32P-postlabeling test for structurally diverse DNA adducts
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32P-postlabeling analysis of nonradioactive aromatic carcinogen-DNA adducts
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32P-postlabeling methods for DNA adduct detection: Overview and critical evaluation
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A comparison between different types of covalent DNA modifications (I-compounds, persistent carcinogen adducts and 5-methylcytosine) in regenerating rat liver
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Randerath,K., Lu,L.-J.W. and Li,D. (1988) A comparison between different types of covalent DNA modifications (I-compounds, persistent carcinogen adducts and 5-methylcytosine) in regenerating rat liver. Carcinogenesis, 9, 1843-1848.
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Age-related DNA modifications (I-compounds): Modulation by physiological and pathological processes
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Randerath,K., Li,D. and Randerath,E. (1990) Age-related DNA modifications (I-compounds): modulation by physiological and pathological processes. Mutat. Res., 238, 245-253.
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Biomarkers of aging: Correlation of DNA I-compound levels with median lifespan of calorically restricted and ad libitum fed rats and mice
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Randerath,K., Zhou,G.-D., Hart,R.W., Turturro,A. and Randerath,E. (1993) Biomarkers of aging: correlation of DNA I-compound levels with median lifespan of calorically restricted and ad libitum fed rats and mice. Mutat. Res., 295, 247-263.
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0027264363
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Enhancement of age-related increases in DNA I-compound levels by calorie restriction: Comparison of male B-N and F-344 rats
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Randerath,K., Hart,R.W., Zhou,G.-D., Reddy,R., Danna,T.F. and Randerath,E. (1993) Enhancement of age-related increases in DNA I-compound levels by calorie restriction: comparison of male B-N and F-344 rats. Mutat. Res., 295. 31-46.
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0025603018
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Persistent reduction of I-compound levels in liver DNA from male Fischer rats fed choline-devoid diet and in DNA of resulting neoplasms
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Li,D., Xu,D., Chandar,B., Lombardi,B. and Randerath,K. (1990) Persistent reduction of I-compound levels in liver DNA from male Fischer rats fed choline-devoid diet and in DNA of resulting neoplasms. Cancer Res., 50, 7577-7580.
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0025280930
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Lack of I-compounds in DNA from a spectrum of Morris hepatomas
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Randerath,K., Randerath,E. and Danna,T.F. (1990) Lack of I-compounds in DNA from a spectrum of Morris hepatomas. Carcinogenesis, 11, 1041-1044.
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Specific reduction of I-compound levels in DNA from spontaneous hepatomas of 22-24 month old male C3H mice
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Li,D., Chen,S., Becker,F.F. and Randerath,K. (1991) Specific reduction of I-compound levels in DNA from spontaneous hepatomas of 22-24 month old male C3H mice. Carcinogenesis, 12, 2389-2391.
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Li, D.1
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0028924809
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Intensification and depletion of specific bulky renal DNA adducts (I-compounds) following exposure of male F344 rats to the renal carcinogen ferric nitrilotriacetate (Fe-NTA)
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Randerath,E., Watson,W.P., Zhou,G.-D., Chang,J. and Randerath,K. (1995) Intensification and depletion of specific bulky renal DNA adducts (I-compounds) following exposure of male F344 rats to the renal carcinogen ferric nitrilotriacetate (Fe-NTA). Mutat. Res., 341, 265-279.
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15
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0027048407
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Crcadian rhythm of covalent modifications in liver DNA
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Nath,R.G., Vulimiri,S.V. and Randerath,K. (1992) Crcadian rhythm of covalent modifications in liver DNA. Biochem. Biophys. Res. Commun., 189, 545-550.
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Biochem. Biophys. Res. Commun.
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Nath, R.G.1
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0030468435
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Organ-specific oxidative DNA damage associated with normal birth in rats
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Corrigendum, Carcinogenesis, 18, 859-866, 1997
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Randerath,E., Zhou,G.-D. and Randerath,K. (1996) Organ-specific oxidative DNA damage associated with normal birth in rats. Carcinogenesis, 17, 2563-2570 [Corrigendum, Carcinogenesis, 18, 859-866, 1997].
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32P-postlabeling in DNA modified by oxidative damage in vitro. Comparison with rat lung I-compounds
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32P-postlabeling in DNA modified by oxidative damage in vitro. Comparison with rat lung I-compounds. Mutat. Res., 250, 135-144.
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18
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32P-postlabeling of DNA adducts induced by a Fenton-type oxygen radical-generating system
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32P-postlabeling of DNA adducts induced by a Fenton-type oxygen radical-generating system. Carcinogenesis, 13, 1127-1135.
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19
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0030069695
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Structural origins of bulky oxidative DNA adducts (type II I-compounds) as deduced by oxidation of oligonucleotides of known sequence
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Randerath,K., Randerath,E., Smith,C.V. and Chang,J. (1996) Structural origins of bulky oxidative DNA adducts (type II I-compounds) as deduced by oxidation of oligonucleotides of known sequence. Chem. Res. Toxicol., 9, 247-254.
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0025101246
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32P-postlabeled monophosphate 7,12-dimethyl-benz[a]anthracene-DNA adducts
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32P-postlabeled monophosphate 7,12-dimethyl-benz[a]anthracene-DNA adducts, Carcinogenesis, 11, 159-164.
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0032520718
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Inhibition of CYP1A1 activities by the PAH fluoranthene
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Willett,K.L., Randerath,K., Zhou,G.-D. and Safe,S.H. (1998) Inhibition of CYP1A1 activities by the PAH fluoranthene. Biochem. Pharmacol., 55, 831-839.
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Commentary. Lipid peroxidation as a potential endogenous source for the formation of exocyclic DNA adducts
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Chung,F.-L., Chen,H.-Y.C. and Nath,R.G. (1996) Commentary. Lipid peroxidation as a potential endogenous source for the formation of exocyclic DNA adducts. Carcinogenesis, 17, 2105-2111.
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0025326795
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Association between diet and age-related DNA modifications (I-compounds) in rat liver and kidney
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Li,D. and Randerath,K. (1990) Association between diet and age-related DNA modifications (I-compounds) in rat liver and kidney. Cancer Res., 50, 3991-3996.
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Li, D.1
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Modulation of DNA modification (I-compound) levels in rat liver and kidney by dietary carbohydrate, protein, fat, vitamin, and mineral content
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Li,D. and Randerath,K. (1992) Modulation of DNA modification (I-compound) levels in rat liver and kidney by dietary carbohydrate, protein, fat, vitamin, and mineral content. Mutat. Res., 275, 47-56.
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Mutat. Res.
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0027274901
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Effects of polychlorinated dibenzofurans on I-compounds in hepatic DNA of female Sprague-Dawley rats. Structure dependence and mechanistic considerations
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Randerath,E., Randerath,K., Reddy,R., Narasimhan,T.R., Wang,X. and Safe,S. (1993) Effects of polychlorinated dibenzofurans on I-compounds in hepatic DNA of female Sprague-Dawley rats. Structure dependence and mechanistic considerations. Chem. Biol. Interact., 88, 175-190.
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Chem. Biol. Interact.
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