
| 10.14218/JCTH.2014.00035
http://scihub22266oqcxt.onion/10.14218/JCTH.2014.00035
 C4542084!4542084!26357635
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J+Clin+Transl+Hepatol 2015 ; 3 (1): 53-66 Nephropedia Template TP
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Animal Models for Fibrotic Liver Diseases: What We Have, What We Need, and What Is under Development #MMPMID26357635Delire B; St�rkel P; Leclercq IJ Clin Transl Hepatol 2015[Mar]; 3 (1): 53-66 PMID26357635show ga
Liver fibrosis is part of the wound-healing response to liver damage of various origins and represents a major health problem. Although our understanding of the pathogenesis of liver fibrosis has grown considerably over the last 20 years, effective antifibrotic therapies are still lacking. The use of animal models is crucial for determining mechanisms underlying initiation, progression, and resolution of fibrosis and for developing novel therapies. To date, no animal model can recapitulate all the hepatic and extra-hepatic features of liver disease. In this review, we will discuss the current rodent models of liver injuries. We will then focus on the available ways to target specifically particular compounds of fibrogenesis and on the new models of liver diseases like the humanized liver mouse model.�
  
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