(Q33715915)

28 July 2017

1 reference

title

Genetic basis of progressive familial intrahepatic cholestasis (English)

1 reference

progressive familial intrahepatic cholestasis

28 July 2017

main subject

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author name string

Jacquemin E

series ordinal

1

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28 July 2017

Hadchouel M

series ordinal

2

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28 July 2017

publication date

1 August 1999

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28 July 2017

published in

Journal of Hepatology

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28 July 2017

volume

31

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28 July 2017

issue

2

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28 July 2017

page(s)

377-381

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

28 July 2017

1 reference

7 January 2021

Byler's disease: fatal intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Progressive familial cholestatic cirrhosis and bile acid metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Clinical and biochemical findings in progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Bile acid profiles in siblings with progressive intrahepatic cholestasis: absence of biliary chenodeoxycholate

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Molecular pathogenesis of cholestasis.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Histologic pathology of the liver in progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Progressive idiopathic cholestasis presenting with profuse watery diarrhoea and recurrent infections (Byler's disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Byler-like familial cholestasis in an extended kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Progressive familial intrahepatic cholestasis among the Arab population in Israel

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Diagnostic Value of Serum γ-Glutamyl Transpeptidase Activity in Liver Diseases in Children

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

The human MDR3 P-glycoprotein promotes translocation of phosphatidylcholine through the plasma membrane of fibroblasts from transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Phosphatidylcholine translocase: a physiological role for the mdr2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Hepatocyte-specific expression of the human MDR3 P-glycoprotein gene restores the biliary phosphatidylcholine excretion absent in Mdr2 (-/-) mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Effects of Ursodeoxycholate and cholate feeding on liver disease in FVB mice with a disrupted mdr2 P-glycoprotein gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Partial external diversion of bile for the treatment of intractable pruritus associated with intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

Orthotopic liver transplantation for Byler disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2899%2980240-2

7 January 2021

10.1016/S0168-8278(99)80240-2

Identifiers

DOI

1 reference

28 July 2017

1 reference