Toxicity, interstrand cross-links and DNA fragmentation induced by ‘activated’ cyclophosphamide in yeast: Comparative studies on 4-hydroperoxy-cyclophosphamide, its monofunctional analogon, acrolein, phosphoramide mustard, and nor-nitrogen mustard-Reference-Cited by-同舟云学术

Toxicity, interstrand cross-links and DNA fragmentation induced by ‘activated’ cyclophosphamide in yeast: Comparative studies on 4-hydroperoxy-cyclophosphamide, its monofunctional analogon, acrolein, phosphoramide mustard, and nor-nitrogen mustard

Published:1982-03 Issue:1 Volume:39 Page:1-15
ISSN:0009-2797
Container-title:Chemico-Biological Interactions
language:en
Short-container-title:Chemico-Biological Interactions

Author:

Fleer R.,Brendel M.

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference24 articles.

1. Yeast as a model for studying DNA-alterations and biological response induced by alkylating anti-cancer drugs: effects of cyclophosphamide;Fleer,1982

2. Toxicity, interstrand cross-links and DNA fragmentation induced by ‘activated’ cyclophosphamide in yeast;Fleer;Chem.-Biol. Interact.,1981

3. Comparative study on the effects of cyclophosphamide on yeast in vitro and in the host-mediated assay: DNA damage and biological response;Ogorek;Chem.-Biol. Interact.,1981

4. Chromatin subunits from baker's yeast: isolation and partial characterization;Nelson;Proc. Natl. Acad. Sci. U.S.A.,1977

5. The problem of specificity and selectivity of alkylating cytostatics: studies on N-2-chloroethylamidooxazaphosphorines;Brock;Z. Krebsforsch.,1977

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