The mechanism of biliary lipid secretion and its defects (Q33591423)

28 July 2017

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title

The mechanism of biliary lipid secretion and its defects (English)

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28 July 2017

Elferink RP

1

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28 July 2017

Groen AK

series ordinal

2

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28 July 2017

publication date

1 March 1999

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Gastroenterology Clinics of North America

28 July 2017

published in

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28 July 2017

volume

28

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28 July 2017

issue

1

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28 July 2017

page(s)

59-74, vi

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Histologic pathology of the liver in progressive familial intrahepatic cholestasis

28 July 2017

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Byler-like familial cholestasis in an extended kindred

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Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity

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A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

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Studies on the origin of biliary phospholipid. Effect of dehydrocholic acid and cholic acid infusions on hepatic and biliary phospholipids

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In vitro evidence that phospholipid secretion into bile may be coordinated intracellularly by the combined actions of bile salts and the specific phosphatidylcholine transfer protein of liver

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Lipid flow in bile formation

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Retrograde intrabiliary injection of amphipathic materials causes phospholipid secretion into bile. Taurocholate causes phosphatidylcholine secretion, 3-[(3-cholamidopropyl)dimethylammonio]-propane-1-sulphonate (CHAPS) causes mixed phospholipid secr

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Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

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7 January 2021

A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency

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7 January 2021

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7 January 2021

Regulation of biliary lipid secretion by mdr2 P-glycoprotein in the mouse

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7 January 2021

Protective role of biliary cholesterol and phospholipid lamellae against bile acid-induced cell damage

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7 January 2021

Hepatoprotection by hydrophilic bile salts

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7 January 2021

Phosphatidylcholine translocase: a physiological role for the mdr2 gene

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7 January 2021

Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs

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7 January 2021

P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs

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7 January 2021

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7 January 2021

Hepatocyte-specific expression of the human MDR3 P-glycoprotein gene restores the biliary phosphatidylcholine excretion absent in Mdr2 (-/-) mice

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7 January 2021

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7 January 2021

Identification of a Locus for Progressive Familial Intrahepatic Cholestasis PFIC2on Chromosome 2q24

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7 January 2021

Bile acid profiles in siblings with progressive intrahepatic cholestasis: absence of biliary chenodeoxycholate

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7 January 2021

MDR1 P-glycoprotein is a lipid translocase of broad specificity, while MDR3 P-glycoprotein specifically translocates phosphatidylcholine

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7 January 2021

The role of bile salt composition in liver pathology of mdr2 (-/-) mice: differences between males and females

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7 January 2021

Effects of Ursodeoxycholate and cholate feeding on liver disease in FVB mice with a disrupted mdr2 P-glycoprotein gene.

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7 January 2021

Cell type-dependent effect of phospholipid and cholesterol on bile salt cytotoxicity

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7 January 2021

Clinical and biochemical findings in progressive familial intrahepatic cholestasis

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7 January 2021

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Identifiers

DOI

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28 July 2017

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