A flippase-independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells (Q24316145)

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English	A flippase-independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells	scientific article

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scholarly article

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A flippase-independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells (English)

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ATPase phospholipid transporting 8B1

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GOA release 2020-03-11

regulation of microvillus assembly

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GOA release 2020-03-11

intrahepatic cholestasis

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based on heuristic

inferred from title

3

object named as

Viola Oorschot

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Judith Klumperman

5

object named as

Judith Klumperman

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author name string

Patricia M Verhulst

1

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Lieke M van der Velden

2

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Ernst E van Faassen

4

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Roderick H J Houwen

6

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Thomas G Pomorski

7

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Joost C M Holthuis

8

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Leo W J Klomp

9

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language of work or name

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publication date

June 2010

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51

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6

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2049-60

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Characterization of mutations in ATP8B1 associated with hereditary cholestasis

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

PERSPECTIVES IN PEDIATRIC PATHOLOGY: Progressive Familial Intrahepatic Cholestasis: A Personal Perspective

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

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.23586

21 January 2018

Familial intrahepatic cholestasis 1: studies of localization and function

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https://api.crossref.org/works/10.1002%2FHEP.23586

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.

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

ATP8B1 is essential for maintaining normal hearing

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

The type 4 subfamily of P-type ATPases, putative aminophospholipid translocases with a role in human disease

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Role of C. elegans TAT-1 protein in maintaining plasma membrane phosphatidylserine asymmetry.

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Flippases and vesicle-mediated protein transport

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

On the origin of lipid asymmetry: the flip side of ion transport

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Phospholipid translocation and miltefosine potency require both L. donovani miltefosine transporter and the new protein LdRos3 in Leishmania parasites.

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Tracking down lipid flippases and their biological functions.

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

The Arabidopsis P4-ATPase ALA3 localizes to the golgi and requires a beta-subunit to function in lipid translocation and secretory vesicle formation.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Roles for the Drs2p-Cdc50p complex in protein transport and phosphatidylserine asymmetry of the yeast plasma membrane

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Drs2p-related P-type ATPases Dnf1p and Dnf2p are required for phospholipid translocation across the yeast plasma membrane and serve a role in endocytosis

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

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

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

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

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Protein-mediated inward translocation of phospholipids occurs in both the apical and basolateral plasma membrane domains of epithelial cells.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.

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https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Transcriptional modulation of genes encoding structural characteristics of differentiating enterocytes during development of a polarized epithelium in vitro

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

A Chinese hamster ovary cell mutant defective in the non-endocytic uptake of fluorescent analogs of phosphatidylserine: isolation using a cytosol acidification protocol

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

Cinnamycin (Ro 09-0198) promotes cell binding and toxicity by inducing transbilayer lipid movement

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

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Organization, chemistry, and assembly of the cytoskeletal apparatus of the intestinal brush border

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

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Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

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.23586

21 January 2018

DRS1 to DRS7, novel genes required for ribosome assembly and function in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

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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.23586

21 January 2018

Defects in structural integrity of ergosterol and the Cdc50p-Drs2p putative phospholipid translocase cause accumulation of endocytic membranes, onto which actin patches are assembled in yeast

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

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A pump-independent function of the Na,K-ATPase is required for epithelial junction function and tracheal tube-size control

1 reference

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21 January 2018

Structure of the ankyrin-binding domain of alpha-Na,K-ATPase

1 reference

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A role for myosin-1A in the localization of a brush border disaccharidase

1 reference

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MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.

1 reference

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21 January 2018

Benign recurrent intrahepatic "obstructive" jaundice

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23586

7 January 2021

based on heuristic

inferred from DOI database lookup

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.23586

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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.23586

7 January 2021

based on heuristic

inferred from DOI database lookup

mRNA localization in polarized intestinal epithelial cells

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7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1002/HEP.23586

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