Anti-recombinogenic and convertible co-mutagenic effects of (E)-5-(2-bromovinyl)-2′-deoxyuridine (BVDU) and other 5-substituted pyrimidine nucleoside analogs in S. cerevisiae MPI

Author:

Fahrig Rudolf

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology

Reference28 articles.

1. Antiherpes drags: Promises and pitfalls;De Clercq;Eur. J. Clin. Microbiol.,1984

2. Synthesis and antiviral properties of 5-vinylpyrimidine nucleoside analogs;De Clercq;Pharmacol. Ther.,1984

3. Incorporation of (E)-5-(2-125iodovinyl)-2′-deoxyuridine and 5-125iodo-2′-de-oxyuridine into DNA of non-infected and herpes simplex type 1 virus-infected primary rabbit-kidney cell cultures;Descamps;Arch. Int. Physiol. Biochim.,1981

4. Genotoxic properties of (E)-5-(2-bromovinyl)-2′-deoxyuridine (BVDU), Fundam;Oshiro;Appl. Toxicol.,1992

5. Potent antiviral 5-(2-bromovinyl)uracil nucleosides are inactive at inducing gene mutations in Salmonelly ty-phimurium and V79 Chinese hamster cells and unscheduled DNA synthesis in primary rat hepatocytes;Marquardt;Carcinogenesis,1985

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