Conformations of adducts formed between the genotoxic benzo[a]pyrene-7,8-dione and 2'-deoxycytidine.
Jeon SH, Jin B, Kim SK, Lee HM.
J Biomol Struct Dyn · research support, non-u.s. gov't; journal article · DOI 10.1080/07391102.2014.989407 PUBLIKATIONSREGISTRET
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Publikationer i urvalet
11 träffarInterception of benzo[a]pyrene-7,8-dione by UDP glucuronosyltransferases (UGTs) in human lung cells.
Zhang L, Huang M, Blair IA, Penning TM.
Chem Res Toxicol · research support, non-u.s. gov't; research-article; journal article; research support, n.i.h., extramural · DOI 10.1021/tx400268qIdentification of stable benzo[a]pyrene-7,8-dione-DNA adducts in human lung cells.
Huang M, Blair IA, Penning TM.
Chem Res Toxicol · research support, non-u.s. gov't; research-article; journal article; research support, n.i.h., extramural · DOI 10.1021/tx300476mThe role of base excision repair genes OGG1, APN1 and APN2 in benzo[a]pyrene-7,8-dione induced p53 mutagenesis.
Abedin Z, Louis-Juste M, Stangl M, Field J.
Mutat Res · research-article; journal article; research support, n.i.h., extramural · DOI 10.1016/j.mrgentox.2012.10.003Detoxication of benzo[a]pyrene-7,8-dione by sulfotransferases (SULTs) in human lung cells.
Zhang L, Huang M, Blair IA, Penning TM.
J Biol Chem · research-article; journal article; research support, n.i.h., extramural · DOI 10.1074/jbc.m112.386052Metabolism and distribution of benzo[a]pyrene-7,8-dione (B[a]P-7,8-dione) in human lung cells by liquid chromatography tandem mass spectrometry: detection of an adenine B[a]P-7,8-dione adduct.
Huang M, Liu X, Basu SS, Zhang L, Kushman ME, Harvey RG, Blair IA, Penning TM.
Chem Res Toxicol · research-article; journal article; research support, n.i.h., extramural · DOI 10.1021/tx200463sConformational analysis of genotoxic benzo[a]pyrene- 7,8-dione-duplex DNA adducts using a molecular dynamics method.
Jin B, Lee HM, Kim S.
J Biomol Struct Dyn · research support, non-u.s. gov't; journal article · DOI 10.1080/07391102.2010.10507330Aryl hydrocarbon receptor facilitates DNA strand breaks and 8-oxo-2'-deoxyguanosine formation by the aldo-keto reductase product benzo[a]pyrene-7,8-dione.
Park JH, Mangal D, Frey AJ, Harvey RG, Blair IA, Penning TM.
J Biol Chem · research-article; journal article; research support, n.i.h., extramural · DOI 10.1074/jbc.m109.042143Conformations of adducts formed between the genotoxic benzo[a]pyrene-7,8-dione and nucleosides studied by density functional theory.
Lee HM, Chae YH, Kwon C, Kim SK.
Biophys Chem · research support, non-u.s. gov't; journal article · DOI 10.1016/j.bpc.2006.07.015Identification and characterization of novel stable deoxyguanosine and deoxyadenosine adducts of benzo[a]pyrene-7,8-quinone from reactions at physiological pH.
Balu N, Padgett WT, Lambert GR, Swank AE, Richard AM, Nesnow S.
Chem Res Toxicol · research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/tx034207sReactivity of benzo[a]pyrene-7,8-dione with DNA. Evidence for the formation of deoxyguanosine adducts.
Shou M, Harvey RG, Penning TM.
Carcinogenesis · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; journal article · DOI 10.1093/carcin/14.3.475