Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases.

Hussain, S P

Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases. [electronic resource] - Proceedings of the National Academy of Sciences of the United States of America Nov 2000 - 12770-5 p. digital

Publication Type: Journal Article

0027-8424

10.1073/pnas.220416097 doi


Aldehydes--pharmacology
Animals
Cell Line
Copper--metabolism
Free Radicals
Genes, MHC Class I
HLA Antigens--genetics
Hemochromatosis--genetics
Hemochromatosis Protein
Hepatolenticular Degeneration--genetics
Histocompatibility Antigens Class I--genetics
Humans
Iron--metabolism
Liver--metabolism
Membrane Proteins
Mutagenesis--drug effects
Mutation
Nitric Oxide Synthase--biosynthesis
Nitric Oxide Synthase Type II
Rabbits
Tumor Suppressor Protein p53--genetics