Nucleoside anticancer drugs: the role of nucleoside transporters in resistance to cancer chemotherapy.
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Polyplex Nanogel formulations for drug delivery of cytotoxic nucleoside analogs.Marine nucleosides: structure, bioactivity, synthesis and biosynthesisReduced Ribavirin Antiviral Efficacy via Nucleoside Transporter-Mediated Drug ResistanceCrystal structure of a concentrative nucleoside transporter from Vibrio cholerae at 2.4 ÅStructural basis of nucleoside and nucleoside drug selectivity by concentrative nucleoside transportersUpdate on the management of pancreatic cancer: surgery is not enoughCharacterization of the rat Na+/nucleoside cotransporter 2 and transport of nucleoside-derived drugs using electrophysiological methodsEquilibrative nucleoside transporters-A review.Deoxycytidine kinase modulates the impact of the ABC transporter ABCG2 on clofarabine cytotoxicity.A novel in vitro assay to assess phosphorylation of 3'-[(18)F]fluoro-3'-deoxythymidine.Cellular influx, efflux, and anabolism of 3-carboranyl thymidine analogs: potential boron delivery agents for neutron capture therapyEquilibrative nucleoside transporter 1 genotype, cytidine deaminase activity and age predict gemcitabine plasma clearance in patients with solid tumours.Cation coupling properties of human concentrative nucleoside transporters hCNT1, hCNT2 and hCNT3.Efficient microwave-assisted solid phase coupling of nucleosides, small library generation and mild conditions for release of nucleoside derivativesClinical pharmacology and pharmacogenetics of gemcitabine.Prognostic value of human equilibrative nucleoside transporter1 in pancreatic cancer receiving gemcitabin-based chemotherapy: a meta-analysis.Pharmacodynamics of cytarabine induced leucopenia: a retrospective cohort studyNovel strategy with gemcitabine for advanced pancreatic cancer.Stearoyl gemcitabine nanoparticles overcome resistance related to the over-expression of ribonucleotide reductase subunit M1.A conformationally mobile cysteine residue (Cys-561) modulates Na+ and H+ activation of human CNT3Synthesis and in vitro evaluation of novel lipophilic monophosphorylated gemcitabine derivatives and their nanoparticles.Different modes of transport for 3H-thymidine, 3H-FLT, and 3H-FMAU in proliferating and nonproliferating human tumor cells.Using genome-wide CRISPR library screening with library resistant DCK to find new sources of Ara-C drug resistance in AMLStratification of nucleoside analog chemotherapy using 1-(2'-deoxy-2'-18F-fluoro-β-D-arabinofuranosyl)cytosine and 1-(2'-deoxy-2'-18F-fluoro-β-L-arabinofuranosyl)-5-methylcytosine PET.Application of artificial neural network to investigate the effects of 5-fluorouracil on ribonucleotides and deoxyribonucleotides in HepG2 cells.Synthesis and anti-HIV activities of bis-(cycloSaligenyl) pronucleotides derivatives of 3'-fluoro-3'-deoxythymidine and 3'-azido-3'-deoxythymidine.Retroviral Replicating Vectors Deliver Cytosine Deaminase Leading to Targeted 5-Fluorouracil-Mediated Cytotoxicity in Multiple Human Cancer Types.Mechanisms and insights into drug resistance in cancerRenal nucleoside transporters: physiological and clinical implications.Ex vivo chemosensitivity testing and gene expression profiling predict response towards adjuvant gemcitabine treatment in pancreatic cancerOvercoming S-phase checkpoint-mediated resistance: sequence-dependent synergy of gemcitabine and 7-ethyl-10-hydroxycamptothecin (SN-38) in human carcinoma cell linesPhysiology of nucleoside transporters: back to the future. . . .Conserved glutamate residues Glu-343 and Glu-519 provide mechanistic insights into cation/nucleoside cotransport by human concentrative nucleoside transporter hCNT3Antifreeze protein-induced selective crystallization of a new thermodynamically and kinetically less preferred molecular crystal.The MUC4 mucin mediates gemcitabine resistance of human pancreatic cancer cells via the Concentrative Nucleoside Transporter family.Human nucleoside transporters: biomarkers for response to nucleoside drugs.Vasohibin 2 reduces chemosensitivity to gemcitabine in pancreatic cancer cells via Jun proto-oncogene dependent transactivation of ribonucleotide reductase regulatory subunit M2.Fluorinase: a tool for the synthesis of ¹⁸F-labeled sugars and nucleosides for PET.Translocation of nucleoside analogs across the plasma membrane in hematologic malignancies.Emerging transporters of clinical importance: an update from the International Transporter Consortium.
P2860
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P2860
Nucleoside anticancer drugs: the role of nucleoside transporters in resistance to cancer chemotherapy.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@ast
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@en
type
label
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@ast
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@en
prefLabel
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@ast
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@en
P2093
P2860
P356
P1433
P1476
Nucleoside anticancer drugs: t ...... stance to cancer chemotherapy.
@en
P2093
Carol E Cass
James D Young
John Mackey
Michael B Sawyer
Sambasivarao Damaraju
Vijaya L Damaraju
P2860
P2888
P304
P356
10.1038/SJ.ONC.1206952
P407
P577
2003-10-01T00:00:00Z