FIC1: another bile salt carrier within the enterohepatic circulation?
- 31 October 2001
- journal article
- editorial
- Published by Elsevier in Journal of Hepatology
- Vol. 35 (4), 522-524
- https://doi.org/10.1016/s0168-8278(01)00182-9
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyteJournal of Hepatology, 2001
- Mechanisms of Biliary Lipid Secretion and Their Role in Lipid HomeostasisSeminars in Liver Disease, 2000
- Genetic Defects in Hepatocanalicular TransportSeminars in Liver Disease, 2000
- Genetic basis of progressive familial intrahepatic cholestasisJournal of Hepatology, 1999
- BILE ACID TRANSPORTGastroenterology Clinics of North America, 1999
- A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisNature Genetics, 1998
- Molecular Pathogenesis of CholestasisNew England Journal of Medicine, 1998
- A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasisNature Genetics, 1998
- A Subfamily of P-Type ATPases with Aminophospholipid Transporting ActivityScience, 1996
- [33] Characterizing mechanisms of hepatic bile acid transport utilizing isolated membrane vesiclesMethods in Enzymology, 1990