Exon-intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated in Dubin-Johnson syndrome (Q28143088)

2

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D Rost

3

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B Stöckel

4

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U Leuschner

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D Keppler

Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases

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language of work or name

English

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publication date

September 1999

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published in

Gastroenterology

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volume

117

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issue

3

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page(s)

653-60

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cites work

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Persistent non-hemolytic hyperbilirubinemia associated with lipochrome-like pigment in liver cells: report of four cases

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Expression of the MRP gene-encoded conjugate export pump in liver and its selective absence from the canalicular membrane in transport-deficient mutant hepatocytes

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Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene

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cDNA cloning of the hepatocyte canalicular isoform of the multidrug resistance protein, cMrp, reveals a novel conjugate export pump deficient in hyperbilirubinemic mutant rats

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A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome

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Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome

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Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA

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Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

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ATP-dependent transport of bilirubin glucuronides by the multidrug resistance protein MRP1 and its hepatocyte canalicular isoform MRP2

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The Sister of P-glycoprotein Represents the Canalicular Bile Salt Export Pump of Mammalian Liver

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Analysis of the intron-exon organization of the human multidrug-resistance protein gene (MRP) and alternative splicing of its mRNA

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Binary specification of nonsense codons by splicing and cytoplasmic translation

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A splice mutation in the human canalicular multispecific organic anion transporter gene causes Dubin-Johnson syndrome

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Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome

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