Circumvention of P-glycoprotein-mediated drug resistance in human leukaemic cells by non-immunosuppressive cyclosporin D analogue, SDZ PSC 833-Reference-Cited by-同舟云学术

Circumvention of P-glycoprotein-mediated drug resistance in human leukaemic cells by non-immunosuppressive cyclosporin D analogue, SDZ PSC 833

Published:1995-06 Issue:2 Volume:90 Page:375-383
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

JIANG XU-RONG,KELSEY STEPHEN M.,Wn YU-LING,NEWLAND ADRIAN C.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1995.tb05162.x/fullpdf

Reference22 articles.

1. Most drugs that reverse multidrug resistance also inhibit photo-affinity labeling of P-glycoprotein by a vinblastine analogue;Akiyama;Molecular Pharmacology,1988

2. A kinetic and clonal analysis of heterogeneity in K562 cells;Alder;Journal of Cell Physiology,1984

3. The biochemistry of P-glycoprotein-mediated multidrug resistance;Edincott;Annual Reviews in Biochemistry,1989

4. Identification of the multidrug-resistance-related P-glycoprotein as a cyclosporin-binding protein;Foxwell;Molecular Pharmacology,1989

5. SDZ PSC 833, a non-immunosuppressive cyclosporin analog, is a very potent multidrug-resistance modifier;Gaveriaux;Journal of Cell Pharmacology,1991

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