(Q28264570)

1

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M J van Eijk

2

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L Pawlikowska

3

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J A DeYoung

4

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J A Juijn

5

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M Liao

6

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L W Klomp

7

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N Lomri

8

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R Berger

9

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B F Scharschmidt

10

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A S Knisely

11

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R H Houwen

12

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N B Freimer

https://scigraph.springernature.com/pub.10.1038/ng0398-219

13

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language of work or name

English

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publication date

March 1998

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published in

Nature Genetics

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volume

18

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page(s)

219-24

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issue

3

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exact match

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cites work

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Phosphatidylcholine translocase: a physiological role for the mdr2 gene

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MDR1 P-glycoprotein is a lipid translocase of broad specificity, while MDR3 P-glycoprotein specifically translocates phosphatidylcholine

20 April 2017

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Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

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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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Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis

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Byler's disease: fatal intrahepatic cholestasis

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

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

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Benign recurrent intrahepatic cholestasis: altered bile acid metabolism

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

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

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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

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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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7 January 2021

A subfamily of P-type ATPases with aminophospholipid transporting activity

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P-type ATPases of eukaryotes and bacteria: sequence analyses and construction of phylogenetic trees

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Organization of P-type ATPases: significance of structural diversity

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Structural organization, ion transport, and energy transduction of P-type ATPases

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

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7 January 2021

Back and forth: the regulation and function of transbilayer phospholipid movement in eukaryotic cells

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Production and characterization of a mutant cell line defective in aminophospholipid translocase

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Byler-like familial cholestasis in an extended kindred

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Familial cholestasis with elevated sweat electrolyte concentations

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A new bacteriophage P1-derived vector for the propagation of large human DNA fragments

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DOP-vector PCR: a method for rapid isolation and sequencing of insert termini from PAC clones

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A simple method for displaying the hydropathic character of a protein

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