Electrogenic uptake of nucleosides and nucleoside-derived drugs by the human nucleoside transporter 1 (hCNT1) expressed in Xenopus laevis oocytes

FEBS Letters

Volumn 481, Issue 2, 2000, Pages 137-140

  Lostao, M Pilar ^a   Mata, Joao F ^b   Larrayoz, Ignacio M ^a   Inzillo, Simone M ^a   Casado, F Javier ^b   Pastor Anglada, Marçal ^b  

^a UNIVERSITY OF NAVARRA   (Spain)

^b UNIVERSITY OF BARCELONA   (Spain)

Author keywords

Anticancer drug; Electrophysiology; HCNT1; Nucleoside

Indexed keywords

CARRIER PROTEIN; FLUDARABINE; GEMCITABINE; NUCLEOSIDE TRANSPORTER 1; UNCLASSIFIED DRUG; URIDINE;

ANIMAL CELL; ARTICLE; DRUG PROTEIN BINDING; DRUG UPTAKE; HYPERPOLARIZATION; NONHUMAN; NUCLEOSIDE TRANSPORT; NUCLEOTIDE SEQUENCE; OOCYTE; PRIORITY JOURNAL; SODIUM CURRENT; VOLTAGE CLAMP; XENOPUS LAEVIS;

ANIMAL; ANTIMETABOLITES, ANTINEOPLASTIC; ANTINEOPLASTIC AGENTS; ANTIVIRAL AGENTS; CARRIER PROTEINS; CYTIDINE; DEOXYCYTIDINE; ELECTRIC CONDUCTIVITY; GENE EXPRESSION; HUMAN; MEMBRANE POTENTIALS; MEMBRANE PROTEINS; NUCLEOSIDE TRANSPORT PROTEINS; NUCLEOSIDES; OOCYTES; SODIUM; SUBSTRATE SPECIFICITY; SUPPORT, NON-U.S. GOV'T; URIDINE; VIDARABINE; XENOPUS LAEVIS;

XENOPUS LAEVIS;

EID: 0034666069     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(00)01983-9     Document Type: Article

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