FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte (Q24291838)

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

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scholarly article

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

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ATPase phospholipid transporting 8B1

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GOA release 2020-03-11

author name string

E F Eppens

1

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S W van Mil

2

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J M de Vree

3

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K S Mok

4

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J A Juijn

5

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R P Oude Elferink

6

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R Berger

7

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R H Houwen

8

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L W Klomp

9

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language of work or name

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publication date

October 2001

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Journal of Hepatology

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35

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4

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436-43

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The secretory function of the liver: new aspects of hepatobiliary transport

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

7 January 2021

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Molecular pathogenesis of cholestasis.

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7 January 2021

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Hepatobiliary secretion of organic compounds; molecular mechanisms of membrane transport

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

7 January 2021

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Hepatobiliary transport

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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Chronic cholestatic diseases

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Genetic basis of progressive familial intrahepatic cholestasis

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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inferred from DOI database lookup

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Byler's disease: fatal intrahepatic cholestasis

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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THE SYNDROME OF BENIGN RECURRENT CHOLESTASIS

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Benign recurrent intrahepatic cholestasis: a long-term follow-up study of two patients

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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Autosomal‐recessive inheritance of benign recurrent intrahepatic cholestasis

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

7 January 2021

based on heuristic

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

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Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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A missense mutation in FIC1 is associated with greenland familial cholestasis

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Cloning, expression, and chromosomal mapping of a human ATPase II gene, member of the third subfamily of P-type ATPases and orthologous to the presumed bovine and murine aminophospholipid translocase

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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Organization of P-type ATPases: significance of structural diversity

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

7 January 2021

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A subfamily of P-type ATPases with aminophospholipid transporting activity

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Loss of Drs2p does not abolish transfer of fluorescence-labeled phospholipids across the plasma membrane of Saccharomyces cerevisiae

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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Structural and functional polarity of canalicular and basolateral plasma membrane vesicles isolated in high yield from rat liver

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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Zonal down-regulation and redistribution of the multidrug resistance protein 2 during bile duct ligation in rat liver

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Enterohepatic circulation in the rat.

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https://api.crossref.org/works/10.1016%2FS0168-8278%2801%2900158-1

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

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Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

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7 January 2021

based on heuristic

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Biliary diversion by use of the appendix (cholecystoappendicostomy) in progressive familial intrahepatic cholestasis

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based on heuristic

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Rat cholangiocytes absorb bile acids at their apical domain via the ileal sodium-dependent bile acid transporter

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based on heuristic

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Functional expression of the apical Na+-dependent bile acid transporter in large but not small rat cholangiocytes

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7 January 2021

based on heuristic

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Cracking the genetic code for benign recurrent and progressive familial intrahepatic cholestasis

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based on heuristic

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Identifiers

10.1016/S0168-8278(01)00158-1

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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