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Modulation of paclitaxel resistance by annexin IV in human cancer cell linesCloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.33,3′,4,4′,5-Pentachlorobiphenyl Inhibits Drug Efflux Through P-Glycoprotein in KB-3 Cells Expressing Mutant Human P-GlycoproteinAromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: comparisons with 2,3,7,8-tetrachlorodibenzo-p-dioxinFunctional analysis of chimeric genes obtained by exchanging homologous domains of the mouse mdr1 and mdr2 genesMultidrug resistance in Leishmania donovani is conferred by amplification of a gene homologous to the mammalian mdr1 geneFunctional study of the novel multidrug resistance gene HA117 and its comparison to multidrug resistance gene 1Functional expression of murine multidrug resistance in Xenopus laevis oocytes.Isolation and characterization of Drosophila multidrug resistance gene homologs.Docking applied to the prediction of the affinity of compounds to P-glycoproteinQuantitative analysis of MDR1 (multidrug resistance) gene expression in human tumors by polymerase chain reactionMolecular basis of preferential resistance to colchicine in multidrug-resistant human cells conferred by Gly-185----Val-185 substitution in P-glycoprotein.The amplified H circle of methotrexate-resistant leishmania tarentolae contains a novel P-glycoprotein geneA general genetic approach in Escherichia coli for determining the mechanism(s) of action of tumoricidal agents: application to DMP 840, a tumoricidal agent.Overexpression of the cystic fibrosis transmembrane conductance regulator in NIH 3T3 cells lowers membrane potential and intracellular pH and confers a multidrug resistance phenotype.Clinical implications of the stress responseEpidermal growth factor regulates the in vitro sensitivity of human ovarian carcinoma cells to cisplatin.Imaging recognition of inhibition of multidrug resistance in human breast cancer xenografts using 99mTc-labeled sestamibi and tetrofosmin.Sucralose, a synthetic organochlorine sweetener: overview of biological issuesImaging recognition of multidrug resistance in human breast tumors using 99mTc-labeled monocationic agents and a high-resolution stationary SPECT system.Very important pharmacogene summary: ABCB1 (MDR1, P-glycoprotein)Expression of Streptomyces peucetius genes for doxorubicin resistance and aklavinone 11-hydroxylase in Streptomyces galilaeus ATCC 31133 and production of a hybrid aclacinomycin.Mediation of cimetidine secretion by P-glycoprotein and a novel H(+)-coupled mechanism in cultured renal epithelial monolayers of LLC-PK1 cells.Control of Mycosphaerella graminicola on wheat seedlings by medical drugs known to modulate the activity of ATP-binding cassette transportersMDR1 gene expression in primary colorectal carcinomas.Overexpression of P-glycoprotein and glutathione S-transferase-pi in resistant non-small cell lung carcinomas of smokers.The multidrug resistance (mdr1) gene product functions as an ATP channelExpression of the multidrug resistance-associated protein (MRP) gene in colorectal carcinomas.Cancer cell progression and chemoimmunotherapy--dual effects in the induction of resistance to therapyAn improved method of encapsulation of doxorubicin in liposomes: pharmacological, toxicological and therapeutic evaluationP-glycoprotein is expressed and causes resistance to chemotherapy in EBV-positive T-cell lymphoproliferative diseasesA new aspect on glutathione-associated biological function of MRP/GS-X pump and its gene expression.P-glycoprotein structure and evolutionary homologies.Results of a phase III, double-blind, placebo-controlled trial of megestrol acetate modulation of P-glycoprotein-mediated drug resistance in the first-line management of small-cell lung carcinoma.The multidrug resistance phenotype confers immunological resistance.Anti-tumour activities of a new benzo[c]phenanthridine agent, 2,3-(methylenedioxy)-5-methyl-7-hydroxy-8-methoxybenzo[c]phena nthridini um hydrogensulphate dihydrate (NK109), against several drug-resistant human tumour cell lines.Thiomer-coated liposomes harbor permeation enhancing and efflux pump inhibitory properties.Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl-thiazoles analogues as potent and orally bioavailable anticancer agentsA possible role for a mammalian facilitative hexose transporter in the development of resistance to drugsIncreased expression and DNA-binding activity of transcription factor Sp1 in doxorubicin-resistant HL-60 leukemia cells
P2860
Q24644209-C52BAD35-6F14-419F-B511-0A8C8BC3EF49Q24674982-B20267CD-87FB-4931-81A5-6465B34DCB5FQ24796511-D9E49F4B-5677-470F-9122-588045E9644EQ28321853-170D8F43-5428-48E9-B337-AECFF504B691Q28589032-0733FD19-BFA2-471E-8F43-62281A793DE2Q31162495-0F39AB79-E809-4159-BB77-DDE61CBB9D22Q33636104-7F7FF2CC-536F-4114-B17A-F60022BFA745Q33642250-723C3BCD-B9A7-4C40-AB0C-280129C3793DQ33668301-4B21271A-2CAA-4F42-B167-347CCD66104CQ33757813-F734F4E1-555B-4770-B2F1-A86C8FF43921Q33796247-98C44E60-A88E-4E7F-867D-0225B223E459Q33800929-9AE1F2E0-E807-434C-B4C6-B3C88BF9AFE1Q33919185-8C3725CC-B596-4CD0-AF1A-049CA0C36465Q33940540-A1177551-97B9-494F-BB3F-CEDCB16D2F76Q34047158-D5E7397A-F47A-4AA2-ACD5-C1AE137C9F73Q34192112-0A217D67-CCC5-4F05-B947-BB404BD62F14Q34263559-A68F452D-9481-4854-9028-9852777958ACQ34450507-D62085BF-0A2E-4F84-BB29-97DCCC8A5275Q34657381-02F4F99B-770C-481D-9840-102D1FD68744Q34711648-23C068C0-7EE0-43A5-A7E5-BA5B80713E98Q34994901-D3CBC4BC-3A4B-4938-961C-7449DF892C39Q35116565-EADD498E-3927-4E27-8385-1EF1535339D5Q35873933-4A9842BA-91A4-40FE-AA7E-BEAB08189858Q35946793-24BC9258-05CA-4C2F-86DB-79D80F4876FAQ35977393-F35A74A8-6A8B-4FE3-8BF5-E57F600E8B0CQ35993861-0355DFFD-195B-443C-9368-6D632BA7A1D3Q36045380-E70AF2EE-7D50-4F8A-8BB8-E78A58FFACB8Q36115974-26A58185-0969-4591-AE84-7B370737AB5FQ36135064-3C4F7AC8-F406-4F2E-977B-637233CBB028Q36135564-26345435-CFCD-4E3B-BD15-671F53C09FD8Q36201459-446C42AB-8287-47FC-B7B1-D520B3A6F05BQ36254826-26F1FA0D-B076-4333-AB90-BD5E9F4AD6FEQ36254844-19799A65-0697-4D70-926B-ADC550F3D7FBQ36291680-0735C7F4-355F-4C8B-83F7-581EBCD941F4Q36366884-EA43455A-0405-44D7-84CF-F960EF993FF6Q36431000-E43CB81B-A4AD-4D93-87DC-AB30930293D5Q36575250-3512C0A7-B82A-4A88-A42D-9826B01D17CEQ36584907-6DC2A977-9110-4D65-B47D-23C4B29CF125Q36724025-168AB056-0AAE-48AA-8E7E-47E514FE50AFQ36729898-6AA25AE5-2FD7-414A-8567-68857D687C25
P2860
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
The multidrug transporter, a double-edged sword.
@en
The multidrug transporter, a double-edged sword.
@nl
type
label
The multidrug transporter, a double-edged sword.
@en
The multidrug transporter, a double-edged sword.
@nl
prefLabel
The multidrug transporter, a double-edged sword.
@en
The multidrug transporter, a double-edged sword.
@nl
P1476
The multidrug transporter, a double-edged sword.
@en
P2093
Gottesman MM
P304
12163-12166
P407
P577
1988-09-01T00:00:00Z