Spontaneous cholecysto- and hepatolithiasis inMdr2?/? mice: A model for low phospholipid-associated cholelithiasis
Author:
Publisher
Wiley
Subject
Hepatology
Reference55 articles.
1. Homozygous disruption of the murine MDR2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease
2. Regulation of biliary lipid secretion by mdr2 P-glycoprotein in the mouse.
3. The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood
4. Protective role of biliary cholesterol and phospholipid lamellae against bile acid-induced cell damage
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