Relative mutagenicity and teratogenicity of cyclophosphamide and two of its structural analogs
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
Reference24 articles.
1. Some studies of the active intermediates formed in the microsomal metabolism of cyclophosphamide and isophosphamide
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1. Structure-activity relationship in the induction of chromosomal aberrations and spindle disturbances in Chinese hamster epithelial liver cells by regioisomeric phenanthrene quinones;Cell Biology and Toxicology;1997
2. Mutagenic damage to mammalian cells by therapeutic alkylating agents;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1996-08
3. Cytogenetic mechanisms in the selective toxicity of cyclophosphamide analogs and metabolites towards avian embryonic B lymphocytes in vivo;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1992-07
4. Application of an epithelial liver cell line, metabolically competent, for mutation studies of promutagens;Mutation Research/Environmental Mutagenesis and Related Subjects;1992-02
5. Co-administration of ascorbic acid with cydophosphamide (CPA) to pregnant mice inhibits the clastogenic activity of CPA in preimplantation murine blastocysts;Mutagenesis;1989
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