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Citation: D. Rund et al., EFFICIENT TRANSDUCTION OF HUMAN HEMATOPOIETIC-CELLS WITH THE HUMAN MULTIDRUG-RESISTANCE GENE-1 VIA SV40 PSEUDOVIRIONS, Human gene therapy, 9(5), 1998, pp. 649-657
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Citation: Mm. Gottesman et al., MOLECULAR DISSECTION OF THE MULTIDRUG TRANSPORTER, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 21-21
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Citation: T. Shoshani et al., ANALYSIS OF RANDOM RECOMBINATION BETWEEN HUMAN MDR1 AND MOUSE MDR1A CDNA IN A PHAMDR-DIHYDROFOLATE REDUCTASE BICISTRONIC EXPRESSION SYSTEM, Molecular pharmacology, 54(4), 1998, pp. 623-630
Citation: Cgl. Lee et Mm. Gottesman, HIV-1 PROTEASE INHIBITORS AND THE MDR1 MULTIDRUG TRANSPORTER, The Journal of clinical investigation, 101(2), 1998, pp. 287-288
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Citation: Ca. Hrycyna et al., MECHANISM OF ACTION OF HUMAN P-GLYCOPROTEIN ATPASE ACTIVITY - PHOTOCHEMICAL CLEAVAGE DURING A CATALYTIC TRANSITION-STATE USING ORTHOVANADATE REVEALS CROSS-TALK BETWEEN THE 2 ATP SITES, The Journal of biological chemistry, 273(27), 1998, pp. 16631-16634
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Citation: G. Russ et al., P-GLYCOPROTEIN PLAYS AN INSIGNIFICANT ROLE IN THE PRESENTATION OF ANTIGENIC PEPTIDES TO CD8-CELLS( T), Cancer research, 58(20), 1998, pp. 4688-4693
Citation: Dw. Shen et al., CROSS-RESISTANCE TO METHOTREXATE AND METALS IN HUMAN CISPLATIN-RESISTANT CELL-LINES RESULTS FROM A PLEIOTROPIC DEFECT IN ACCUMULATION OF THESE COMPOUNDS ASSOCIATED WITH REDUCED PLASMA-MEMBRANE BINDING-PROTEINS, Cancer research, 58(2), 1998, pp. 268-275
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Citation: P. Hafkemeyer et al., CONTRIBUTION TO SUBSTRATE-SPECIFICITY AND TRANSPORT OF NONCONSERVED RESIDUES IN TRANSMEMBRANE DOMAIN-12 OF HUMAN P-GLYCOPROTEIN, Biochemistry (Easton), 37(46), 1998, pp. 16400-16409
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Citation: Ca. Hrycyna et al., STRUCTURAL FLEXIBILITY OF THE LINKER REGION OF HUMAN P-GLYCOPROTEIN PERMITS ATP HYDROLYSIS AND DRUG TRANSPORT, Biochemistry (Easton), 37(39), 1998, pp. 13660-13673
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Citation: Ss. Chauhan et al., INVOLVEMENT OF CARBOXY-TERMINAL AMINO-ACIDS IN SECRETION OF HUMAN LYSOSOMAL PROTEASE CATHEPSIN-L, Biochemistry, 37(23), 1998, pp. 8584-8594
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Citation: M. Ramachandra et al., HUMAN P-GLYCOPROTEIN EXHIBITS REDUCED AFFINITY FOR SUBSTRATES DURING A CATALYTIC TRANSITION-STATE, Biochemistry, 37(14), 1998, pp. 5010-5019
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Citation: Cgl. Lee et al., EFFICIENT LONG-TERM COEXPRESSION OF A HAMMERHEAD RIBOZYME TARGETED TOTHE U5 REGION OF HIV-1 LTR BY LINKAGE TO THE MULTIDRUG-RESISTANCE GENE, ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 7(5), 1997, pp. 511-522
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Citation: M. Suzuki et al., RETROVIRAL COEXPRESSION OF 2 DIFFERENT TYPES OF DRUG-RESISTANCE GENESTO PROTECT NORMAL-CELLS FROM COMBINATION CHEMOTHERAPY, Clinical cancer research, 3(6), 1997, pp. 947-954
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Citation: Ca. Hrycyna et al., FUNCTIONAL-CHARACTERIZATION OF HUMAN P-GLYCOPROTEIN - EVIDENCE FOR THE NON-EQUIVALENCY OF THE 2 ATP BINDING DOMAINS, Molecular biology of the cell, 8, 1997, pp. 1107-1107
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Citation: S. Dey et al., PHOTOAFFINITY-LABELING OF HUMAN P-GLYCOPROTEIN - EVIDENCE FOR 2 NONIDENTICAL DRUG-INTERACTION SITES, Molecular biology of the cell, 8, 1997, pp. 1108-1108
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Citation: Y. Sugimoto et al., COEXPRESSION OF A MULTIDRUG-RESISTANCE GENE (MDR1) AND HERPES-SIMPLEXVIRUS THYMIDINE KINASE GENE IN A BICISTRONIC RETROVIRAL VECTOR HA-MDR-IRES-TK ALLOWS SELECTIVE KILLING OF MDR1-TRANSDUCED HUMAN TUMORS TRANSPLANTED IN NUDE-MICE, Cancer gene therapy, 4(1), 1997, pp. 51-58
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Citation: T. Ohshima et al., ALPHA-GALACTOSIDASE A DEFICIENT MICE - A MODEL OF FABRY DISEASE, Proceedings of the National Academy of Sciences of the United Statesof America, 94(6), 1997, pp. 2540-2544
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Citation: S. Dey et al., EVIDENCE FOR 2 NONIDENTICAL DRUG-INTERACTION SITES IN THE HUMAN P-GLYCOPROTEIN, Proceedings of the National Academy of Sciences of the United Statesof America, 94(20), 1997, pp. 10594-10599