Possible role of the glucuronide conjugate in the biochemical mechanism op binding of the carcinogen N-hydroxy-2-acetylaminofluorene to rat-liver deoxyribonucleic acid in vivo
- 31 October 1969
- journal article
- Published by Elsevier in Chemico-Biological Interactions
- Vol. 1 (1), 19-26
- https://doi.org/10.1016/0009-2797(69)90016-7
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Reaction of the glucuronide of the carcinogen N-hydroxy-2-acetylaminofluorene with nucleic acidsBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1969
- The Metabolic Activation of Carcinogenic Aromatic Amines and Amides1Published by S. Karger AG ,1969
- Isolation of deoxyribonucleic acid and ribosomal ribonucleic acid from rat liverBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1968
- Difference in binding of 2-acetylaminofluorene to rat liver deoxyribonucleic acid and ribosomal ribonucleic acid in vivoBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1968
- Biosynthesis and Studies of the Alkaline Sensitivity of the NO-Glucuronide of the Carcinogen N-2-Fluorenylacethydroxamic Acid*Biochemistry, 1967
- Dehydroxylation and deacetylation of N-hydroxy-N-2-fluorenylacetamide by rat liver and brain homogenatesBiochimica et Biophysica Acta (BBA) - General Subjects, 1965
- On the interaction of N-2-fluorenylhydroxylamine with nucleic acids in, vitroBiochemical and Biophysical Research Communications, 1965