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W Priebe

Showing results (51-60 of 81) with videos related to

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Biochemistry|May 2, 2001
Hypersensitization of tumor cells to glycolytic inhibitorsH Liu, Y P Hu, N Savaraj, et al.
European Journal of Biochemistry|March 15, 2001
P-glycoprotein preferentially effluxes anthracyclines containing free basic versus charged amineF Frézard, E Pereira-Maia, P Quidu, et al.
The Journal of Antibiotics|May 1, 1985
Sugar-ring analogs of daunorubicin: 3'-epidaunorubicin, 3'-hydroxy-3',5'-diepidaunorubicin and 3',6'-dihydroxy-3',5'-diepidaunorubicinT M Cheung, D Horton, W Priebe, et al.
Current Medicinal Chemistry|February 15, 2001
Analysis of the effects of daunorubicin and WP631 on transcriptionJ Portugal, B Martín, A Vaquero, et al.
Biochemical Pharmacology|December 8, 2000
Rho(0) tumor cells: a model for studying whether mitochondria are targets for rhodamine 123, doxorubicin, and other drugsY Hu, C T Moraes, N Savaraj, et al.
Biochimica Et Biophysica Acta|July 9, 1999
Correlation between the kinetics of anthracycline uptake and the resistance factor in cancer cells expressing the multidrug resistance protein or the P-glycoproteinC Marbeuf-Gueye, D Ettori, W Priebe, et al.
Molecular Pharmacology|May 1, 1996
Cell cycle-dependent cytotoxicity, G2/M phase arrest, and disruption of p34cdc2/cyclin B1 activity induced by doxorubicin in synchronized P388 cellsY H Ling, A K el-Naggar, W Priebe, et al.
International Journal of Cancer|July 1, 1994
Hydroxyrubicin, a deaminated derivative of doxorubicin, inhibits mammalian DNA topoisomerase II and partially circumvents multidrug resistanceE Solary, Y H Ling, R Perez-Soler, et al.
Biochemical and Biophysical Research Communications|July 2, 1998
Doxorubicin- and daunorubicin-glutathione conjugates, but not unconjugated drugs, competitively inhibit leukotriene C4 transport mediated by MRP/GS-X pumpW Priebe, M Krawczyk, M T Kuo, et al.
European Journal of Medicinal Chemistry|August 13, 2019
Curcumin as tyrosine kinase inhibitor in cancer treatmentA Golonko, H Lewandowska, R Świsłocka, et al.
Pageof 9

Showing results (51-60 of 81) with videos related to

Sort By:
Pageof 9
Biochemistry|May 2, 2001
Hypersensitization of tumor cells to glycolytic inhibitorsH Liu, Y P Hu, N Savaraj, et al.
European Journal of Biochemistry|March 15, 2001
P-glycoprotein preferentially effluxes anthracyclines containing free basic versus charged amineF Frézard, E Pereira-Maia, P Quidu, et al.
The Journal of Antibiotics|May 1, 1985
Sugar-ring analogs of daunorubicin: 3'-epidaunorubicin, 3'-hydroxy-3',5'-diepidaunorubicin and 3',6'-dihydroxy-3',5'-diepidaunorubicinT M Cheung, D Horton, W Priebe, et al.
Current Medicinal Chemistry|February 15, 2001
Analysis of the effects of daunorubicin and WP631 on transcriptionJ Portugal, B Martín, A Vaquero, et al.
Biochemical Pharmacology|December 8, 2000
Rho(0) tumor cells: a model for studying whether mitochondria are targets for rhodamine 123, doxorubicin, and other drugsY Hu, C T Moraes, N Savaraj, et al.
Biochimica Et Biophysica Acta|July 9, 1999
Correlation between the kinetics of anthracycline uptake and the resistance factor in cancer cells expressing the multidrug resistance protein or the P-glycoproteinC Marbeuf-Gueye, D Ettori, W Priebe, et al.
Molecular Pharmacology|May 1, 1996
Cell cycle-dependent cytotoxicity, G2/M phase arrest, and disruption of p34cdc2/cyclin B1 activity induced by doxorubicin in synchronized P388 cellsY H Ling, A K el-Naggar, W Priebe, et al.
International Journal of Cancer|July 1, 1994
Hydroxyrubicin, a deaminated derivative of doxorubicin, inhibits mammalian DNA topoisomerase II and partially circumvents multidrug resistanceE Solary, Y H Ling, R Perez-Soler, et al.
Biochemical and Biophysical Research Communications|July 2, 1998
Doxorubicin- and daunorubicin-glutathione conjugates, but not unconjugated drugs, competitively inhibit leukotriene C4 transport mediated by MRP/GS-X pumpW Priebe, M Krawczyk, M T Kuo, et al.
European Journal of Medicinal Chemistry|August 13, 2019
Curcumin as tyrosine kinase inhibitor in cancer treatmentA Golonko, H Lewandowska, R Świsłocka, et al.
Pageof 9