Hydrodynamic gene delivery of interleukin-22 protects the mouse liver from concanavalin A-, carbon tetrachloride-, and Fas ligand-induced injury via activation of STAT3.

Cellular & molecular immunology

Volumn 1, Issue 1, 2004, Pages 43-49

  Pan, Hongna ^a   Hong, Feng ^a   Radaeva, Svetlana ^a   Gao, Bin ^a  

^a NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BCL2L1 PROTEIN, MOUSE; CARBON TETRACHLORIDE; CONCANAVALIN A; FAS LIGAND; FASL PROTEIN, MOUSE; FASLG PROTEIN, HUMAN; INTERLEUKIN 22; INTERLEUKIN DERIVATIVE; INTERLEUKIN-22; MCL1 PROTEIN; MEMBRANE PROTEIN; PROTEIN BCL 2; PROTEIN BCL X; STAT3 PROTEIN; TUMOR NECROSIS FACTOR; TUMOR PROTEIN;

ANIMAL; ARTICLE; C57BL MOUSE; GENE TRANSFER; GENETICS; HUMAN; LIVER; METABOLISM; MOUSE; PATHOLOGY; PHYSIOLOGY; TOXIC HEPATITIS;

ANIMALS; BCL-X PROTEIN; CARBON TETRACHLORIDE; CONCANAVALIN A; FAS LIGAND PROTEIN; GENE TRANSFER TECHNIQUES; HEPATITIS, TOXIC; HUMANS; INTERLEUKINS; LIVER; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED C57BL; NEOPLASM PROTEINS; PROTO-ONCOGENE PROTEINS C-BCL-2; STAT3 TRANSCRIPTION FACTOR; TUMOR NECROSIS FACTORS;

EID: 2342458559     PISSN: 16727681     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)