Myofibroblasts revert to an inactive phenotype during regression of liver fibrosis

Proceedings of the National Academy of Sciences of the United States of America

Volumn 109, Issue 24, 2012, Pages 9448-9453

  Kisseleva, Tatiana ^a   Cong, Min ^a   Paik, YongHan ^a,b   Scholten, David ^a,c   Jiang, Chunyan ^a   Benner, Chris ^d   Iwaisako, Keiko ^a   Moore Morris, Thomas ^e   Scott, Brian ^a   Tsukamoto, Hidekazu ^f   Evans, Sylvia M ^e   Dillmann, Wolfgang ^a   Glass, Christopher K ^d   Brenner, David A ^a  

^a UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^b Sungkyunkwan University School of Medicine   (South Korea)

^c UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; CARBON TETRACHLORIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL SURVIVAL; CONTROLLED STUDY; DOWN REGULATION; FIBROGENESIS; GENE; GENE CONTROL; HSPA1A GENE; HSPA1B GENE; LIVER FIBROSIS; MOUSE; MYOFIBROBLAST; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; STELLATE CELL; UPREGULATION;

ADOPTIVE TRANSFER; ANIMALS; COLLAGEN TYPE I; LIVER CIRRHOSIS; MICE; MYOFIBROBLASTS; PHENOTYPE; TAMOXIFEN;

EID: 84862195154     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1201840109     Document Type: Article

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