BILE ACID TRANSPORT
- 1 March 1999
- journal article
- review article
- Published by Elsevier in Gastroenterology Clinics of North America
- Vol. 28 (1) , 27-58
- https://doi.org/10.1016/s0889-8553(05)70042-x
Abstract
No abstract availableKeywords
This publication has 135 references indexed in Scilit:
- Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1Nature Genetics, 1997
- 7 alpha-dehydroxylating bacteria enhance deoxycholic acid input and cholesterol saturation of bile in patients with gallstonesPublished by Elsevier ,1996
- Selective surgical management of progressive familial intrahepatic cholestasis (Byler's disease)Journal of Pediatric Surgery, 1995
- Identification of the bile acid binding proteins in human serum by photoaffinity labelingBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1995
- A new cause of progressive intrahepatic cholestasis: 3β-Hydroxy-C27-steroid dehydrogenase/isomerase deficiencyThe Journal of Pediatrics, 1994
- Normal serum γ-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosisThe Journal of Pediatrics, 1987
- Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 casesThe Journal of Pediatrics, 1987
- Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmurThe Journal of Pediatrics, 1975
- Hereditary lymphedema and obstructive jaundiceThe Journal of Pediatrics, 1971
- Byler's disease: Fatal familial intrahepatic cholestasis in an Amish kindredThe Journal of Pediatrics, 1965