(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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7 January 2021

Bile salt hydrophobicity influences cholesterol recruitment from rat liver in vivo when cholesterol synthesis and lipoprotein uptake are constant

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7 January 2021

The Removal of Membrane Components from Human Erythrocytes by Glycocholate

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Topographical dissection of sheep erythrocyte membrane phospholipids by taurocholate and glycocholate

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7 January 2021

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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7 January 2021

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

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7 January 2021

The physical chemistry of cholesterol solubility in bile. Relationship to gallstone formation and dissolution in man

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7 January 2021

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

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7 January 2021

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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7 January 2021

Lipid flow in bile formation

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7 January 2021

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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7 January 2021

The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues

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7 January 2021

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7 January 2021

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

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7 January 2021

Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)

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7 January 2021

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

Affinity of phosphatidylcholine molecular species for the bovine phosphatidylcholine and phosphatidylinositol transfer proteins. Properties of the sn-1 and sn-2 acyl binding sites

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Normal serum gamma-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosis

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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

Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

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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

The human MDR3 P-glycoprotein promotes translocation of phosphatidylcholine through the plasma membrane of fibroblasts from transgenic mice

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7 January 2021

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on 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

1 reference

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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

1 reference

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7 January 2021

10.1016/S0889-8553(05)70043-1

Identifiers

DOI

1 reference

28 July 2017

1 reference