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R.P.J. Oude Elferink

Researcher at University of Amsterdam

Publications -  47
Citations -  6040

R.P.J. Oude Elferink is an academic researcher from University of Amsterdam. The author has contributed to research in topics: Phospholipid & Secretion. The author has an hindex of 22, co-authored 47 publications receiving 5879 citations. Previous affiliations of R.P.J. Oude Elferink include Netherlands Cancer Institute.

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Mammalian ABC Transporters in Health and Disease

TL;DR: This work focuses on three topics: ABC transporters transporting drugs (xenotoxins) and drug conjugates, and a rapidly increasing number of ABC Transporters found to play a role in lipid transport.
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Homozygous disruption of the murine MDR2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

TL;DR: It is concluded that the mdr2 P-glycoprotein has an essential role in the secretion of phosphatidylcholine into bile and hypothesize that it may be a phospholipid transport protein or phospholIPid flippase.
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Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA.

TL;DR: It is shown that cMOAT causes transport of the organic anions S-(2,4-dinitrophenyl)-glutathione, the glutathione conjugate of ethacrynic acid, and S-(PGA1)-gluten, a substrate not shown to be transported by organic anion transporters previously.
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Role of glutathione in the export of compounds from cells by the multidrug-resistance-associated protein

TL;DR: It is demonstrated that depletion of intracellular glutathione by DL-buthionine (S,R)-sulfoximine results in a complete reversal of resistance to doxorubicin, daunorubICin, vincristine, and VP-16 in lung carcinoma cells transfected with a MRP cDNA expression vector, and this results support the hypothesis that MRP functions as a glutATHione S-conjugate carrier.
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Basolateral localization and export activity of the human multidrug resistance-associated protein in polarized pig kidney cells.

TL;DR: Probenecid and sulfinpyrazone may be useful lead compounds for the development of clinical reversal agents specific for MRP-mediated drug resistance, as determined by immunocytochemistry and electron microscopy.