Mice and men: Are they bile-ologically different?

Hepatology

Volumn 33, Issue 6, 2001, Pages 1551-1553

  Arrese, Marco ^a   Ananthanarayanan, Meenakshisundaram ^a  

^a UNIVERSITY OF CHILE   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

BILE SALT; CHOLESTEROL; GLYCOPROTEIN P; SISTER OF P GLYCOPROTEIN; UNCLASSIFIED DRUG;

BILE SECRETION; CHOLESTASIS; GENE LOCUS; GENE MUTATION; HUMAN; MEMBRANE TRANSPORT; MOUSE; NOTE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS; PROTEIN TRANSPORT; SPECIES DIFFERENCE;

EID: 0034982495     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1053/jhep.2001.0331551     Document Type: Article

References (10)

1. Hepatic transport of bile salts
2. Hepatic canalicular membrane 4. Bile acid across the hepatocyte canalicular membrane
3. Hepatocellular transport of bile acids. Evidence for distinct subeellular localizations of electrogenic and ATP-dependent taurocholate transport in rat hepatocytes
4. Enhanced secretion of glycocholic acid in a specially adapted cell line is associated with overexpression of apparently novel ATP-binding cassette proteins
5. The sister of P-glycoprotein represents the canalicular bile salt export pump of mammalian liver
6. Identification of a sister gene to P-glycoprotein
7. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis
8. The continuing importance of bile acids in liver and intestinal disease
9. Mechanisms of biliary lipid secretion and their role in lipid homeostasis
10. Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters