A defect in nrf2 signaling constitutes a mechanism for cellular stress hypersensitivity in a genetic rat model of type 2 diabetes

American Journal of Physiology - Endocrinology and Metabolism

Volumn 301, Issue 6, 2011, Pages

  Bitar, Milad S ^a   Al Mulla, Fahd ^a  

^a KUWAIT UNIVERSITY   (Kuwait)

Author keywords

Glycogen synthetase kinase 3 ; NF E2 related factor 2

Indexed keywords

GLYCOGEN SYNTHASE KINASE 3BETA; HYDROGEN PEROXIDE; MESSENGER RNA; OLIGOMYCIN; PROTEIN KINASE FYN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE; SUPEROXIDE; TERT BUTYLHYDROQUINONE; TRANSCRIPTION FACTOR NRF2;

ANIMAL CELL; ANIMAL CELL CULTURE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIOXIDANT ACTIVITY; ARTICLE; CELL DEATH; CELL LEVEL; CELL NUCLEUS; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME INHIBITION; FEMALE; FIBROBLAST CULTURE; GENE EXPRESSION; MITOCHONDRION; NON INSULIN DEPENDENT DIABETES MELLITUS; NONHUMAN; OXIDATION REDUCTION REACTION; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN DEFECT; PROTEIN STABILITY; PROTEIN TRANSPORT; RAT; SKIN FIBROBLAST; TRANSCRIPTION INITIATION;

EID: 82355183968     PISSN: 01931849     EISSN: 15221555     Source Type: Journal    
DOI: 10.1152/ajpendo.00047.2011     Document Type: Article

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