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Mutation of residue 33 of human equilibrative nucleoside transporters 1 and 2 alters sensitivity to inhibition of transport by dilazep and dipyridamole.

Immunohistochemical variation of human equilibrative nucleoside transporter 1 protein in primary breast cancers.

Functional and molecular characterization of nucleobase transport by recombinant human and rat equilibrative nucleoside transporters 1 and 2. Chimeric constructs reveal a role for the ENT2 helix 5-6 region in nucleobase translocation.

An ancient prevertebrate Na+-nucleoside cotransporter (hfCNT) from the Pacific hagfish (Eptatretus stouti).

Use of a small reporter molecule to determine cell-surface proteins by capillary electrophoresis and laser-induced fluorescence: use of 5-SAENTA-x8f for quantitation of the human equilibrative nucleoside transporter 1 protein.

Differential expression of human equilibrative nucleoside transporter 1 (hENT1) protein in the Reed-Sternberg cells of Hodgkin's disease.

Molecular biology and regulation of nucleoside and nucleobase transporter proteins in eukaryotes and prokaryotes.

Comparison of the interaction of uridine, cytidine, and other pyrimidine nucleoside analogues with recombinant human equilibrative nucleoside transporter 2 (hENT2) produced in Saccharomyces cerevisiae.

The role of membrane transporters in cellular resistance to anticancer nucleoside drugs.

Control of glutamatergic neurotransmission in the rat spinal dorsal horn by the nucleoside transporter ENT1.

Hydrodynamic and spectroscopic studies of substrate binding to human recombinant deoxycytidine kinase.

Functional characterization of a H+/nucleoside co-transporter (CaCNT) from Candida albicans, a fungal member of the concentrative nucleoside transporter (CNT) family of membrane proteins.

The equilibrative nucleoside transporter family, SLC29.

Immunohistochemical variation of human equilibrative nucleoside transporter 1 protein in primary breast cancers.

Spectroscopic studies of DNA and ATP binding to human polynucleotide kinase: evidence for a ternary complex.

Nucleoside anticancer drugs: the role of nucleoside transporters in resistance to cancer chemotherapy.

Uridine Binding Motifs of Human Concentrative Nucleoside Transporters 1 and 3 Produced in Saccharomyces cerevisiae.

Transport of physiological nucleosides and anti-viral and anti-neoplastic nucleoside drugs by recombinant Escherichia coli nucleoside-H(+) cotransporter (NupC) produced in Xenopus laevis oocytes.

Uridine recognition motifs of human equilibrative nucleoside transporters 1 and 2 produced in Saccharomyces cerevisiae.

Interactions of nucleoside analogs, caffeine, and nicotine with human concentrative nucleoside transporters 1 and 2 stably produced in a transport-defective human cell line.

Electrophysiological characterization of a recombinant human Na+-coupled nucleoside transporter (hCNT1) produced in Xenopus oocytes.

Functional redundancy of two nucleoside transporters of the ENT family (CeENT1, CeENT2) required for development of Caenorhabditis elegans.

Quantitative analysis of nucleoside transporter and metabolism gene expression in chronic lymphocytic leukemia (CLL): identification of fludarabine-sensitive and -insensitive populations.

Role of human nucleoside transporters in the cellular uptake of two inhibitors of IMP dehydrogenase, tiazofurin and benzamide riboside.

Characterization of binding of folates and antifolates to brush-border membrane vesicles isolated from human kidney.

Analysis of human equilibrative nucleoside transporter 1 (hENT1) protein in non-Hodgkin's lymphoma by immunohistochemistry.

Allelic isoforms of the H+/nucleoside co-transporter (CaCNT) from Candida albicans reveal separate high- and low-affinity transport systems for nucleosides.

Biophysical characterization of human XRCC1 and its binding to damaged and undamaged DNA.

Residue 33 of human equilibrative nucleoside transporter 2 is a functionally important component of both the dipyridamole and nucleoside binding sites.

Identification and mutational analysis of amino acid residues involved in dipyridamole interactions with human and Caenorhabditis elegans equilibrative nucleoside transporters.

Functional characterization of novel human and mouse equilibrative nucleoside transporters (hENT3 and mENT3) located in intracellular membranes.

The molecular architecture of the mammalian DNA repair enzyme, polynucleotide kinase.

Identification and functional characterization of variants in human concentrative nucleoside transporter 3, hCNT3 (SLC28A3), arising from single nucleotide polymorphisms in coding regions of the hCNT3 gene.

The broadly selective human Na+/nucleoside cotransporter (hCNT3) exhibits novel cation-coupled nucleoside transport characteristics.

Cytosine arabinoside affects multiple cellular factors and induces drug resistance in human lymphoid cells.

Uridine binding and transportability determinants of human concentrative nucleoside transporters.

Polarized distribution of nucleoside transporters in rat brain endothelial and choroid plexus epithelial cells.

Polarized distribution of nucleoside transporters in rat brain endothelial and choroid plexus epithelial cells.

The role of human nucleoside transporters in cellular uptake of 4'-thio-{beta}-D-arabinofuranosylcytosine and {beta}-D-arabinosylcytosine.

Association of DNA repair and steroid metabolism gene polymorphisms with clinical late toxicity in patients treated with conformal radiotherapy for prostate cancer.

Nucleoside transporters: from scavengers to novel therapeutic targets.

Characterization of uridine permease, Fui1p, of saccharomyces cerevisiae: The transport mechanism and permeant-binding profile.

Distribution and Functional Characterization of Equilibrative Nucleoside Transporter-4, a Novel Cardiac Adenosine Transporter Activated at Acidic pH.

Nucleoside transport and its significance for anticancer drug resistance.



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