Dermal wound healing is subject to redox control

Molecular Therapy

Volumn 13, Issue 1, 2006, Pages 211-220

  Roy, Sashwati ^a   Khanna, Savita ^a   Nallu, Kishore ^a   Hunt, Thomas K ^b   Sen, Chandan K ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Hydrogen peroxide; Oxygen; Redox signaling; Trauma

Indexed keywords

ADENOVIRUS VECTOR; BETA GALACTOSIDASE; CATALASE; FOCAL ADHESION KINASE; HYDROGEN PEROXIDE; OXYGEN; PLACEBO; PROTEIN P47; REACTIVE OXYGEN METABOLITE; SODIUM CHLORIDE; TYROSINE; VASCULOTROPIN;

ANGIOGENESIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DOSE RESPONSE; DRUG MECHANISM; ENZYME PHOSPHORYLATION; HUMAN; HUMAN CELL; MALE; MOUSE; NONHUMAN; OXIDATION REDUCTION STATE; PROGNOSIS; PROTEIN EXPRESSION; SKIN DEFECT; VIRAL GENE DELIVERY SYSTEM; WOUND HEALING;

ADENOVIRIDAE; ANIMALS; CATALASE; CELL LINE; CHEMOKINE CCL2; ENDOTHELIAL CELLS; FOCAL ADHESION KINASE 1; HUMANS; HYDROGEN PEROXIDE; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NADPH OXIDASE; NEOVASCULARIZATION, PHYSIOLOGIC; OXIDATION-REDUCTION; PHOSPHORYLATION; SKIN; TYROSINE; WOUND HEALING;

ADENOVIRIDAE; ANIMALIA;

EID: 28844474578     PISSN: 15250016     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ymthe.2005.07.684     Document Type: Article

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