Loss of hif-1 promotes resistance to the exogenous mitochondrial stressor ethidium bromide in Caenorhabditis elegans

BMC Cell Biology

Volumn 17, Issue 1, 2016, Pages

  Kamal, Muntasir ^a,b   D'Amora, Dayana R ^a   Kubiseski, Terrance J ^a  

^a YORK UNIVERSITY   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

C. elegans; DJ 1; Hypoxia inducible factor; Mitochondria; P38 MAPK

Indexed keywords

ETHIDIUM BROMIDE; HYPOXIA INDUCIBLE FACTOR 1; MITOGEN ACTIVATED PROTEIN KINASE P38; REACTIVE OXYGEN METABOLITE; ALDEHYDE DEHYDROGENASE; CAENORHABDITIS ELEGANS PROTEIN; DJR-1.1 PROTEIN, C ELEGANS; ETHIDIUM; HIF-1 PROTEIN, C ELEGANS; TRANSCRIPTION FACTOR;

ADULT; ANIMAL EXPERIMENT; ARTICLE; CAENORHABDITIS ELEGANS; CELL FUNCTION; CELL STRESS; CELL SURVIVAL; CONTROLLED STUDY; DJR 1.1 GENE; GENE; HIF 1 GENE; LOSS OF FUNCTION MUTATION; MITOCHONDRION; NONHUMAN; SIGNAL TRANSDUCTION; ANIMAL; DRUG EFFECTS; GENETICS; METABOLISM; MUTATION;

ALDEHYDE OXIDOREDUCTASES; ANIMALS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; ETHIDIUM; HYPOXIA-INDUCIBLE FACTOR 1; MITOCHONDRIA; MUTATION; REACTIVE OXYGEN SPECIES; TRANSCRIPTION FACTORS;

EID: 84987678216     PISSN: None     EISSN: 14712121     Source Type: Journal    
DOI: 10.1186/s12860-016-0112-x     Document Type: Article

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