(Q24313001)

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Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1

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Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1 (English)

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progressive familial intrahepatic cholestasis

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benign recurrent intrahepatic cholestasis

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5

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Coen C Paulusma

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author name string

Dineke E Folmer

1

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Vincent A van der Mark

2

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Kam S Ho-Mok

3

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Ronald P J Oude Elferink

4

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publication date

November 2009

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50

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5

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1597-605

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

FIC1 disease: a spectrum of intrahepatic cholestatic disorders

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Sequence variation in the ATP8B1 gene and intrahepatic cholestasis of pregnancy

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Intrahepatic cholestasis of pregnancy

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Fic1 is expressed at apical membranes of different epithelial cells in the digestive tract and is induced in the small intestine during postnatal development of mice.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Familial intrahepatic cholestasis 1: studies of localization and function

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

ATP8B1 requires an accessory protein for endoplasmic reticulum exit and plasma membrane lipid flippase activity

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

ATP8B1 deficiency disrupts the bile canalicular membrane bilayer structure in hepatocytes, but FXR expression and activity are maintained

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Abcg5/8 independent biliary cholesterol excretion in Atp8b1-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Activity of the bile salt export pump (ABCB11) is critically dependent on canalicular membrane cholesterol content.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Reduced hepatic expression of farnesoid X receptor in hereditary cholestasis associated to mutation in ATP8B1

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

The membrane protein ATPase class I type 8B member 1 signals through protein kinase C zeta to activate the farnesoid X receptor

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Lentiviral vectors for efficient transduction of isolated primary quiescent hepatocytes

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Electrophysiological Analysis of the Mutated Na,K-ATPase Cation Binding Pocket

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Structural organization, ion transport, and energy transduction of P-type ATPases

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

A missense mutation in FIC1 is associated with greenland familial cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

The complete inventory of the yeast Saccharomyces cerevisiae P-type transport ATPases

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Recurrent familial intrahepatic cholestasis in the Faeroe Islands. Phenotypic heterogeneity but genetic homogeneity

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Evolution of substrate specificities in the P-type ATPase superfamily.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Organization of P-type ATPases: significance of structural diversity

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

LPS-induced downregulation of MRP2 and BSEP in human liver is due to a posttranscriptional process.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Taurine supplementation induces multidrug resistance protein 2 and bile salt export pump expression in rats and prevents endotoxin-induced cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Cytokine-dependent regulation of hepatic organic anion transporter gene transactivators in mouse liver

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Geographical clustering and maintained health in individuals harbouring the mutation for Greenland familial cholestasis: A population-based study

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

21 January 2018

Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

7 January 2021

based on heuristic

inferred from DOI database lookup

Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transport

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

7 January 2021

based on heuristic

inferred from DOI database lookup

Cholestasis Familiaris Groenlandica/Byler-like disease in Greenland--a population study

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

7 January 2021

based on heuristic

inferred from DOI database lookup

Cholestasis Familiaris Groenlandica: an epidemiological, clinical and genetic study

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

7 January 2021

based on heuristic

inferred from DOI database lookup

Interleukin-6 regulates hepatic transporters during acute-phase response

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23158

7 January 2021

based on heuristic

inferred from DOI database lookup

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