Structural Determinants of P-Glycoprotein-Mediated Transport of Glucocorticoids

Author： Yates Charles R.   Chang Cheng   Kearbey Jeffrey D.   Yasuda Kazuto   Schuetz Erin G.   Miller Duane D.   Dalton James T.   Swaan Peter W.  

Publisher： Springer Publishing Company

ISSN： 0724-8741

Source： Pharmaceutical Research, Vol.20, Iss.11, 2003-11, pp. : 1794-1803

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

The possible clinical impact of risperidone on P‐glycoprotein‐mediated transport of tacrolimus: A case report and in vitro study

By  

Biopharmaceutics And Drug Disposition, Vol. 39, Iss. 1, 2018-01 ,pp. : 30-37

John Wiley & Sons Inc

Access to resources Recommend Favorite

Verapamil metabolites: potential P-glycoprotein-mediated multidrug resistance reversal agents

By Woodland Cindy   Koren Gideon   Wainer Irving W   Batist Gerry   Ito Shinya  

Canadian Journal of Physiology and Pharmacology, Vol. 81, Iss. 8, 2003-08 ,pp. : 800-805

NRC Research Press

Access to resources Recommend Favorite

Combating P-glycoprotein-Mediated Multidrug Resistance Using Therapeutic Nanoparticles

By  

Current Pharmaceutical Design, Vol. 19, Iss. 37, 2013-11 ,pp. : 6655-6666

Bentham Science Publishers

Access to resources Recommend Favorite

SB203580, a specific inhibitor of p38-MAPK pathway, is a new reversal agent of P-glycoprotein-mediated multidrug resistance

By Baranck M.   Bohacova V.   Kvackajova J.   Hudecova S.   Krizanova O.   Breier A.  

European Journal of Pharmaceutical Sciences, Vol. 14, Iss. 1, 2001-08 ,pp. : 29-36

Elsevier

Access to resources Recommend Favorite

JWA Sensitizes P-Glycoprotein-Mediated Drug-Resistant Choriocarcinoma Cells to Etoposide VIA JNK and Mitochondrial-Associated Signal Pathway

By Zhang Yan   Zhou Jinhong   Xu Wenxia   Li Aiping   Zhou Jianwei   Xu Shan  

Journal of Toxicology and Environmental Health, Vol. 72, Iss. 11-12, 2009-01 ,pp. : 774-781

Taylor & Francis Ltd

Access to resources Recommend Favorite