Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis (Q28139039)

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2 November 2019

title

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

1 reference

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progressive familial intrahepatic cholestasis

2 November 2019

main subject

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author

Etienne Sokal

5

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2 November 2019

Richard J. Thompson

14

1 reference

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2 November 2019

Michael Müller

15

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2 November 2019

author name string

P L Jansen

1

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2 November 2019

S S Strautnieks

2

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2 November 2019

E Jacquemin

3

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2 November 2019

M Hadchouel

4

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2 November 2019

G J Hooiveld

6

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2 November 2019

J H Koning

7

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2 November 2019

A De Jager-Krikken

8

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2 November 2019

F Kuipers

9

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2 November 2019

F Stellaard

10

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2 November 2019

C M Bijleveld

11

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2 November 2019

A Gouw

12

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H Van Goor

13

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2 November 2019

language of work or name

English

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publication date

1 December 1999

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2 November 2019

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2 November 2019

volume

117

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2 November 2019

issue

6

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2 November 2019

page(s)

1370-1379

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2 November 2019

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

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

7 January 2021

1 reference

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Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

7 January 2021

1 reference

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Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

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

7 January 2021

1 reference

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Locus heterogeneity in progressive familial intrahepatic cholestasis

7 January 2021

1 reference

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Linkage studies of cholestasis familiaris groenlandica/Byler-like disease with polymorphic protein and blood group markers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Progressive familial intrahepatic cholestasis (Byler's disease) in Arab children.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24

7 January 2021

1 reference

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

The sister of P-glycoprotein represents the canalicular bile salt export pump of mammalian liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Up-regulation of the multidrug resistance genes, Mrp1 and Mdr1b, and down-regulation of the organic anion transporter, Mrp2, and the bile salt transporter, Spgp, in endotoxemic rat liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Measurement of bile acid kinetics in human serum using stable isotope labeled chenodeoxycholic acid and capillary gas chromatography electron impact mass spectrometry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

Benign recurrent intrahepatic cholestasis: altered bile acid metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970287-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0016-5085(99)70287-8

2 references

Consolidated OpenCitations Corpus – April 2017

829756

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579978%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

829756

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

829756