Wiessler M - Search Results

1

Characterization of DNA adducts formed by aristolochic acids in the target organ (forestomach) of rats by 32P-postlabelling analysis using different chromatographic procedures.

Stiborová M, Fernando RC, Schmeiser HH, Frei E, Pfau W, Wiessler M. Stiborová M, et al. Among authors: wiessler m. Carcinogenesis. 1994 Jun;15(6):1187-92. doi: 10.1093/carcin/15.6.1187. Carcinogenesis. 1994. PMID: 8020154

2

Carcinogenic aristolochic acids upon activation by DT-diaphorase form adducts found in DNA of patients with Chinese herbs nephropathy.

Stiborová M, Frei E, Sopko B, Wiessler M, Schmeiser HH. Stiborová M, et al. Among authors: wiessler m. Carcinogenesis. 2002 Apr;23(4):617-25. doi: 10.1093/carcin/23.4.617. Carcinogenesis. 2002. PMID: 11960915

3

Human cytosolic enzymes involved in the metabolic activation of carcinogenic aristolochic acid: evidence for reductive activation by human NAD(P)H:quinone oxidoreductase.

Stiborová M, Frei E, Sopko B, Sopková K, Marková V, Lanková M, Kumstýrová T, Wiessler M, Schmeiser HH. Stiborová M, et al. Among authors: wiessler m. Carcinogenesis. 2003 Oct;24(10):1695-703. doi: 10.1093/carcin/bgg119. Epub 2003 Jul 17. Carcinogenesis. 2003. PMID: 12869422

4

Human hepatic and renal microsomes, cytochromes P450 1A1/2, NADPH:cytochrome P450 reductase and prostaglandin H synthase mediate the formation of aristolochic acid-DNA adducts found in patients with urothelial cancer.

Stiborová M, Frei E, Hodek P, Wiessler M, Schmeiser HH. Stiborová M, et al. Among authors: wiessler m. Int J Cancer. 2005 Jan 10;113(2):189-97. doi: 10.1002/ijc.20564. Int J Cancer. 2005. PMID: 15386410

5

Identification and mutagenicity of metabolites of aristolochic acid formed by rat liver.

Schmeiser HH, Pool BL, Wiessler M. Schmeiser HH, et al. Among authors: wiessler m. Carcinogenesis. 1986 Jan;7(1):59-63. doi: 10.1093/carcin/7.1.59. Carcinogenesis. 1986. PMID: 3510750

6

Benzenediazonium ion derived from Sudan I forms an 8-(phenylazo)guanine adduct in DNA.

Stiborová M, Asfaw B, Frei E, Schmeiser HH, Wiessler M. Stiborová M, et al. Among authors: wiessler m. Chem Res Toxicol. 1995 Jun;8(4):489-98. doi: 10.1021/tx00046a002. Chem Res Toxicol. 1995. PMID: 7548728

7

Translesional synthesis on DNA templates containing site-specifically placed deoxyadenosine and deoxyguanosine adducts formed by the plant carcinogen aristolochic acid.

Broschard TH, Wiessler M, von der Lieth CW, Schmeiser HH. Broschard TH, et al. Among authors: wiessler m. Carcinogenesis. 1994 Oct;15(10):2331-40. doi: 10.1093/carcin/15.10.2331. Carcinogenesis. 1994. PMID: 7955074

8

Formation and persistence of specific purine DNA adducts by 32P-postlabelling in target and non-target organs of rats treated with aristolochic acid I.

Fernando RC, Schmeiser HH, Scherf HR, Wiessler M. Fernando RC, et al. Among authors: wiessler m. IARC Sci Publ. 1993;(124):167-71. IARC Sci Publ. 1993. PMID: 8225480

9

Effect of diallyl sulfide on aristolochic acid-induced forestomach carcinogenesis in rats.

Hadjiolov D, Fernando RC, Schmeiser HH, Wiessler M, Hadjiolov N, Pirajnov G. Hadjiolov D, et al. Among authors: wiessler m. Carcinogenesis. 1993 Mar;14(3):407-10. doi: 10.1093/carcin/14.3.407. Carcinogenesis. 1993. PMID: 8453716

10

Comparison of DNA adduct formation by aristolochic acids in various in vitro activation systems by 32P-post-labelling: evidence for reductive activation by peroxidases.

Schmeiser HH, Frei E, Wiessler M, Stiborova M. Schmeiser HH, et al. Among authors: wiessler m. Carcinogenesis. 1997 May;18(5):1055-62. doi: 10.1093/carcin/18.5.1055. Carcinogenesis. 1997. PMID: 9163696

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