Analysis of the structure and expression pattern of MRP7 (ABCC10), a new member of the MRP subfamily (Q28141973)

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M G Belinsky

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H Zeng

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A Tosolini

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J R Testa

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G D Kruh

Biochemistry of multidrug resistance mediated by the multidrug transporter

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language of work or name

English

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publication date

26 January 2001

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published in

Cancer Letters

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volume

162

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issue

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page(s)

181-91

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cites work

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

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

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Overexpression of the gene encoding the multidrug resistance-associated protein results in increased ATP-dependent glutathione S-conjugate transport.

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ATP-dependent 17 beta-estradiol 17-(beta-D-glucuronide) transport by multidrug resistance protein (MRP). Inhibition by cholestatic steroids

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Functional Analysis of a Canalicular Multispecific Organic Anion Transporter Cloned from Rat Liver

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Functional expression of the rat liver canalicular isoform of the multidrug resistance-associated protein

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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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The human multidrug resistance-associated protein MRP is a plasma membrane drug-efflux pump

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Enhanced transport of anticancer agents and leukotriene C4 by the human canalicular multispecific organic anion transporter (cMOAT/MRP2)

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Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database

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The anthracycline resistance-associated (ara) gene, a novel gene associated with multidrug resistance in a human leukaemia cell line

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Characterization of MOAT-C and MOAT-D, new members of the MRP/cMOAT subfamily of transporter proteins

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MOAT-E (ARA) is a full-length MRP/cMOAT subfamily transporter expressed in kidney and liver

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Isolation of a novel human canalicular multispecific organic anion transporter, cMOAT2/MRP3, and its expression in cisplatin-resistant cancer cells with decreased ATP-dependent drug transport

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cDNA Cloning of a Short Type of Multidrug Resistance Protein Homologue,SMRP,from a Human Lung Cancer Cell Line

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cDNA cloning and inducible expression of human multidrug resistance associated protein 3 (MRP3)

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Characterization of the transport properties of cloned rat multidrug resistance-associated protein 3 (MRP3).

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ATP-dependent transport of bile salts by rat multidrug resistance-associated protein 3 (Mrp3)

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The multidrug resistance protein 5 functions as an ATP-dependent export pump for cyclic nucleotides

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Transport function and hepatocellular localization of mrp6 in rat liver

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MRP3, an organic anion transporter able to transport anti-cancer drugs

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Analysis of the MRP4 drug resistance profile in transfected NIH3T3 cells

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MRP4: A previously unidentified factor in resistance to nucleoside-based antiviral drugs

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pABC11 (also known as MOAT-C and MRP5), a member of the ABC family of proteins, has anion transporter activity but does not confer multidrug resistance when overexpressed in human embryonic kidney 293 cells

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Multidrug-resistance protein 5 is a multispecific organic anion transporter able to transport nucleotide analogs

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Prediction of transmembrane segments in proteins utilising multiple sequence alignments

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Chromosomal localization of a gene, GF1, encoding a novel zinc finger protein reveals a new syntenic region between man and rodents

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Membrane topology of the multidrug resistance protein (MRP). A study of glycosylation-site mutants reveals an extracytosolic NH2 terminus.

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Mapping of the glutamate-cysteine ligase catalytic subunit gene (GLCLC) to human chromosome 6p12 and mouse chromosome 9D-E and of the regulatory subunit gene (GLCLR) to human chromosome 1p21-p22 and mouse chromosome 3H1-3

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Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21

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Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12

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

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Pseudoxanthoma elasticum: mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter

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Mutations in ABCC6 cause pseudoxanthoma elasticum

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Identifiers

DOI

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Fatcat ID

release_vsoikfysajelpclrpsag2zxss4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vsoikfysajelpclrpsag2zxss4

24 November 2022