(Q77078719)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

0 references

1 reference

title

FIC1: another bile salt carrier within the enterohepatic circulation? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

author name string

B Stieger

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

publication date

1 October 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

published in

Journal of Hepatology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

page(s)

522-524

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

Characterizing mechanisms of hepatic bile acid transport utilizing isolated membrane vesicles

2 December 2019

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Genetic basis of progressive familial intrahepatic cholestasis

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Genetic defects in hepatocanalicular transport.

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A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

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Mechanisms of biliary lipid secretion and their role in lipid homeostasis

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

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7 January 2021

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

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7 January 2021

A subfamily of P-type ATPases with aminophospholipid transporting activity

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Molecular cloning and sequence of two novel P-type adenosinetriphosphatases from Plasmodium falciparum.

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

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2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans

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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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7 January 2021

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

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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

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

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7 January 2021

6alpha-hydroxylation of taurochenodeoxycholic acid and lithocholic acid by CYP3A4 in human liver microsomes

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7 January 2021

Byler's disease: fatal intrahepatic cholestasis

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7 January 2021

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

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7 January 2021

Drug- and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver

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7 January 2021

Characterization of the mouse bile salt export pump overexpressed in the baculovirus system

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7 January 2021

Molecular cloning and characterization of the murine bile salt export pump

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7 January 2021

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

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7 January 2021

Selective surgical management of progressive familial intrahepatic cholestasis (Byler's disease).

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7 January 2021

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

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7 January 2021

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7 January 2021

Byler-like familial cholestasis in an extended kindred

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7 January 2021

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

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7 January 2021

Targeted inactivation of sister of P-glycoprotein gene (spgp) in mice results in nonprogressive but persistent intrahepatic cholestasis

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7 January 2021

10.1016/S0168-8278(01)00182-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11682038%20AND%20SRC:MED&resulttype=core&format=json

2 December 2019

1 reference