In cardiac myoblasts, cellular redox regulates FosB and Fra-1 through multiple cis-regulatory modules

Free Radical Biology and Medicine

Volumn 51, Issue 8, 2011, Pages 1512-1521

  Jindal, Ekta ^a   Goswami, Shyamal K ^a  

^a JAWAHARLAL NEHRU UNIVERSITY   (India)

Author keywords

Apoptosis; FosB; Fra 1; Free radicals; H9c2 cardiac myoblast; Hypertrophy; Norepinephrine; ROS; SP 1

Indexed keywords

CATALASE; CCAAT ENHANCER BINDING PROTEIN; CIS ACTING ELEMENT; LUCIFERASE; NORADRENALIN; PREGNANCY SPECIFIC BETA1 GLYCOPROTEIN; REACTIVE OXYGEN METABOLITE; TRANSCRIPTION FACTOR AP 1; TRANSCRIPTION FACTOR FOSB; TRANSCRIPTION FACTOR FRA 1;

ARTICLE; CHROMATIN IMMUNOPRECIPITATION; CLONING VECTOR; CONTROLLED STUDY; GEL MOBILITY SHIFT ASSAY; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETIC REGULATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; MYOBLAST; NONHUMAN; PRIORITY JOURNAL; RAT; UPREGULATION;

ANIMALS; APOPTOSIS; CATALASE; CELL GROWTH PROCESSES; CELL LINE; GENE EXPRESSION REGULATION; GENE REGULATORY NETWORKS; METALLOPORPHYRINS; MUTAGENESIS, SITE-DIRECTED; MYOBLASTS, CARDIAC; NOREPINEPHRINE; OXIDATION-REDUCTION; PROMOTER REGIONS, GENETIC; PROTO-ONCOGENE PROTEINS C-FOS; RATS; SEQUENCE DELETION; SUPEROXIDE DISMUTASE; TRANSCRIPTIONAL ACTIVATION; TRANSGENES;

EID: 80052765361     PISSN: 08915849     EISSN: 18734596     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2011.07.008     Document Type: Article

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