The P38α and P38δ map kinases may be gene therapy targets in the future treatment of severe burns

Shock

Volumn 34, Issue 2, 2010, Pages 176-182

  Wang, Shuyun ^a   Huang, Qiaobing ^a   Guo, Xiaohua ^a   Brunk, Ulf T ^b   Han, Jiahuai ^c   Zhao, Keseng ^a   Zhao, Ming ^a  

^a SOUTHERN MEDICAL UNIVERSITY   (China)

^b LINKÖPING UNIVERSITY   (Sweden)

^c SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Burn injuries; cytoskeleton; MAP kinase; Rho kinase; vascular permeability

Indexed keywords

4 (4 FLUOROPHENYL) 2 (4 METHYLSULFINYLPHENYL) 5 (4 PYRIDYL)IMIDAZOLE; ACTIN; ADENOVIRUS VECTOR; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE 13; MITOGEN ACTIVATED PROTEIN KINASE 14; PHALLOIDIN; PROTEIN ZO1; ENZYME INHIBITOR; IMIDAZOLE DERIVATIVE; PROTEIN KINASE C; PYRIDINE DERIVATIVE;

ADENOVIRUS; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BLOOD VESSEL PERMEABILITY; BURN; CONTROLLED STUDY; CYTOSKELETON; DISEASE SEVERITY; FLUORESCENCE; GENE REARRANGEMENT; GENE TARGETING; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; IN VIVO STUDY; LABELING INDEX; MALE; NONHUMAN; RAT; SERUM; SIGNAL TRANSDUCTION; STRESS FIBER; SURVIVAL RATE; TIGHT JUNCTION; VIRAL GENE DELIVERY SYSTEM; ANIMAL; BLOOD; CAPILLARY PERMEABILITY; CELL CULTURE; DRUG ANTAGONISM; DRUG EFFECT; GENE THERAPY; METABOLISM; METHODOLOGY;

ACTINS; ANIMALS; BURNS; CAPILLARY PERMEABILITY; CELLS, CULTURED; ENZYME INHIBITORS; GENE THERAPY; HUMANS; IMIDAZOLES; MAP KINASE SIGNALING SYSTEM; MITOGEN-ACTIVATED PROTEIN KINASE 13; MITOGEN-ACTIVATED PROTEIN KINASE 14; PROTEIN KINASE C; PYRIDINES; TIGHT JUNCTIONS;

EID: 77954985921     PISSN: 10732322     EISSN: None     Source Type: Journal    
DOI: 10.1097/SHK.0b013e3181cff88c     Document Type: Article

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