Nrf2-dependent activation of the antioxidant responsive element by tert-butylhydroquinone is independent of oxidative stress in IMR-32 human neuroblastoma cells

Biochemical and Biophysical Research Communications

Volumn 280, Issue 1, 2001, Pages 286-292

  Lee, Jong Min ^a   Moehlenkamp, Jeffrey D ^c   Hanson, Janean M ^c   Johnson, Jeffrey A ^a,b  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CIS ACTING ELEMENT; GENE PRODUCT; MALEIC ACID DIETHYL ESTER; OXIDOREDUCTASE; PALINDROMIC DNA; PROTEIN C JUN; QUINONE OXIDOREDUCTASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; TERT BUTYLHYDROQUINONE; TRANSCRIPTION FACTOR NRF2; UNCLASSIFIED DRUG;

ANTIOXIDANT RESPONSIVE ELEMENT; ARTICLE; CONTROLLED STUDY; DETOXIFICATION; DOSE RESPONSE; GENE ACTIVATION; GENE OVEREXPRESSION; GENE TRANSLOCATION; HUMAN; HUMAN CELL; NEUROBLASTOMA; NEUROBLASTOMA CELL; OXIDATIVE STRESS; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION;

EID: 0034805627     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2000.4106     Document Type: Article

References (26)

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