Exon-intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated in Dubin–Johnson syndrome-Reference-Cited by-同舟云学术

Exon-intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated in Dubin–Johnson syndrome

Published:1999-09 Issue:3 Volume:117 Page:653-660
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Tsujii Hiroyuki,König Jörg,Rost Daniel,Stöckel Birgit,Leuschner Ulrich,Keppler Dietrich

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference24 articles.

1. Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with report of 12 cases;Dubin;Medicine,1954

2. Persistent nonhemolytic hyperbilirubinemia associated with lipochrome-like pigment in liver cells; report of four cases;Sprinz;Ann Intern Med,1954

3. Heme and bile pigment metabolism;Roy Chowdhury,1994

4. Absence of the canalicular isoform of the MRP gene–encoded conjugate export pump from the hepatocytes in Dubin–Johnson syndrome;Kartenbeck;Hepatology,1996

5. The canalicular conjugate export pump encoded by the cmrp/cmoat gene;Keppler,1996

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