(Q43128402)

English

ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural history

scientific article published in May 2010

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scholarly article

1 reference

Europe PubMed Central

14 November 2017

ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural history (English)

1 reference

Europe PubMed Central

14 November 2017

progressive familial intrahepatic cholestasis

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Emmanuel Jacquemin

8

object named as

Emmanuel Jacquemin

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Europe PubMed Central

14 November 2017

author name string

Anne Davit-Spraul

1

1 reference

Europe PubMed Central

14 November 2017

Monique Fabre

2

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Europe PubMed Central

14 November 2017

Sophie Branchereau

3

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Europe PubMed Central

14 November 2017

Christiane Baussan

4

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Europe PubMed Central

14 November 2017

Emmanuel Gonzales

5

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Europe PubMed Central

14 November 2017

Bruno Stieger

6

1 reference

Europe PubMed Central

14 November 2017

Olivier Bernard

7

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Europe PubMed Central

14 November 2017

language of work or name

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publication date

1 May 2010

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Europe PubMed Central

14 November 2017

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Europe PubMed Central

14 November 2017

51

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Europe PubMed Central

14 November 2017

5

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Europe PubMed Central

14 November 2017

1645-1655

1 reference

Europe PubMed Central

14 November 2017

Progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

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.23539

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Histologic pathology of the liver in progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Clinical and biochemical findings in progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

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.23539

21 January 2018

ATP8B1 is essential for maintaining normal hearing

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Allograft steatohepatitis in progressive familial intrahepatic cholestasis type 1 after living donor liver transplantation.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Rifampin relieves pruritus in children with cholestatic liver disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Evaluation of in silico splice tools for decision-making in molecular diagnosis.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Functional expression of the canalicular bile salt export pump of human liver

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicing

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Partial external biliary diversion in children with progressive familial intrahepatic cholestasis and Alagille disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

21 January 2018

FIC1 and BSEP defects in Taiwanese patients with chronic intrahepatic cholestasis with low γ-glutamyltranspeptidase levels

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

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.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations and polymorphisms in the bile salt export pump and the multidrug resistance protein 3 associated with drug-induced liver injury

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Normal serum gamma-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Safety of living-related liver transplantation for progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Treatment of progressive familial intrahepatic cholestasis: liver transplantation or partial external biliary diversion

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Preoperative observations and short-term outcome after partial external biliary diversion in 13 patients with progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

4-phenylbutyrate enhances the cell surface expression and the transport capacity of wild-type and mutated bile salt export pumps

1 reference

https://api.crossref.org/works/10.1002%2FHEP.23539

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HEP.23539

1 reference

Europe PubMed Central

14 November 2017

1 reference

Europe PubMed Central

14 November 2017

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