[引用][C] In vitro and in vivo modulation by rhizoxin of non-P-glycoprotein-mediated vindesine resistance

有岡仁 - 1997 - ci.nii.ac.jp
CiNii 博士論文 - In vitro and in vivo modulation by rhizoxin of non-P-glycoprotein-mediated
vindesine resistance CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 論文・データをさがす …

In vitro and in vivo modulation by rhizoxin of non-P-glycoprotein-mediated vindesine resistance

H Arioka, K Nishio, Y Heike, S Abe, N Saijo - Journal of cancer research …, 1997 - Springer
Rhizoxin is an antineoplastic drug that inhibits tubulin polymerization. In this study, we
demonstrated that rhizoxin was approximately twice as active in vitro against a human small …

Vinflunine (20′, 20′-difluoro-3′, 4′-dihydrovinorelbine), a novel Vinca alkaloid, which participates in P-glycoprotein (Pgp)-mediated multidrug resistance in vivo …

C Etievant, JM Barret, A Kruczynski, D Perrin… - Investigational new …, 1998 - Springer
Vinflunine (VFL) is a novel derivative of vinorelbine (NVB, Navelbine®), which has shown
markedly superior antitumor activity to NVB, in various experimental animal models. To …

[引用][C] 629 Acquired irofulven-resistance is mediated by a novel and drug-specific resistance mechanism associated with overexpression of ABCA12

F Koeppel, JP Annereau, A Escargueil… - EJC Supplements, 2004 - infona.pl
629 Acquired irofulven-resistance is mediated by a novel and drug-specific resistance
mechanism associated with overexpression of ABCA12 × Close The Infona portal uses …

Studying gene induction of glycopeptide resistance using gene swapping

HJ Hong - Antibiotic Resistance Protocols: Second Edition, 2010 - Springer
Gene swapping is a simple but effective genetic tool for characterizing the functioning of a
gene, where the gene in question is known to fulfil a distinctive biological role in the cell …

Effect of a new triazinoaminopiperidine derivative [S9788] on the binding of vinceistine to and 1-acid glycoprotein: implication in multidrug resistance phenomena

AR Mahran S, W Barry G, L Catherine - 1997 - pesquisa.bvsalud.org
Multidrug resistance [MDR] was circumvented by a large number of compounds including
verapamil and a newly synthesized triazinoaminopiperidine derivative S9788 [Servier 9788] …

[图书][B] Reversal of multidrug resistance and evaluation of anticancer drugs employing in vivo hollow fiber tests

Q Mi - 2001 - search.proquest.com
Novel tropane alkaloids obtained from extracts of Erythroxylum pervillei Baillon and
Erythroxylum rotundifolium Lanan (Erythroxylaceae) by means of bioassay-directed fraction …

[PDF][PDF] Characterisation of the effector ligand recognised by VanS, a key protein triggering resistance to vancomycin

MJ Kwun, G Novotna, AR Hesketh, L Hill, HJ Hong - smbb.mx
Ming Jung Kwun1, Gabriela Novotna1, Andrew R. Hesketh1, 2, Lionel Hill3, and Hee-Jeon
Hong1 1Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, UK …

Binding of Cellular Protein from Venturia nashicola Isolates to Carbendazim: Its Relationship with Sensitivity to N-Phenylcarbamates, N-Phenylformamidoximes, and …

H Ishii, S Iwasaki, Z Sato, I Inoue - 1990 - ACS Publications
Most of the highly benzimidazole-resistant isolates of Venturia nashicola (the scab fungus of
Japanese pear) show increased sensitivity to the N-phenylcarbamate compound MDPC and …

Pervilleine A, a novel tropane alkaloid that reverses the multidrug-resistance phenotype

Q Mi, B Cui, GL Silva, D Lantvit, E Lim, H Chai, M You… - Cancer Research, 2001 - AACR
P-Glycoprotein-mediated drug efflux can yield a multidrug-resistance (MDR) phenotype that
is associated with a poor response to cancer chemotherapy. Pervilleine A, a novel tropane …