Elevations of hepatic quinone reductase, glutathione, and α- and μ- class glutathione S-transferase isoforms in mice with chronic hepatitis: A compensatory response to injury

Archives of Biochemistry and Biophysics

Volumn 331, Issue 1, 1996, Pages 104-116

  Fernandes, Christabel L ^a   Dong, Jia Hui ^a   Roebuck, Bill D ^b   Chisari, Francis V ^c   Montali, Julie A ^d   Schmidt Jr , Donald E ^d   Prochaska, Hans J ^a  

^a MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^b DARTMOUTH MEDICAL SCHOOL   (United States)

^c SCRIPPS RESEARCH INSTITUTE   (United States)

^d Terrapin Technologies Inc   (United States)

Author keywords

apoptosis; cancer; carcinogen; chemoprevention; drug metabolism; enzyme regulation; inflammation; liver; oxidative stress

Indexed keywords

ALANINE AMINOTRANSFERASE; GLUTATHIONE; GLUTATHIONE TRANSFERASE; HEPATITIS B SURFACE ANTIGEN; LIVER ENZYME; MALONALDEHYDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE (PHOSPHATE) DEHYDROGENASE (QUINONE);

AGE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CHRONIC HEPATITIS; CONTROLLED STUDY; DETOXIFICATION; DNA STRAND BREAKAGE; ENZYME ACTIVITY; ENZYME SUBUNIT; HEPATITIS B VIRUS; LIVER NECROSIS; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; TRANSGENIC MOUSE;

EID: 0030200449     PISSN: 00039861     EISSN: None     Source Type: Journal    
DOI: 10.1006/abbi.1996.0288     Document Type: Article

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