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Pharmacology|May 1, 2015
Cytoprotection of human endothelial cells from oxidant stress with CDDO derivatives: network analysis of genes responsible for cytoprotectionJames A Bynum, Ashish Rastogi, Salomon A Stavchansky, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|August 20, 2021
A unique cause of coronary obstruction after transcatheter aortic valve replacementChih-Wei Chang, Subeer Kanwar Wadia, Ashish Rastogi, et al.
Biopharmaceutics & Drug Disposition|June 23, 2009
Pharmacokinetics of caffeic acid phenethyl ester and its catechol-ring fluorinated derivative following intravenous administration to ratsXinyu Wang, Jihai Pang, Jacqueline A Maffucci, et al.
Journal of Pharmaceutical Sciences|September 17, 2011
Biowaiver monographs for immediate-release solid oral dosage forms: stavudineArthur L L Silva, Rodrigo Cristofoletti, Silvia Storpirtis, et al.
Journal of Pharmaceutical Sciences|March 5, 2011
Biowaiver monographs for immediate release solid oral dosage forms: levofloxacinMarcelle O Koeppe, Rodrigo Cristofoletti, Eduardo F Fernandes, et al.
Journal of Pharmaceutical Sciences|March 5, 2011
Biowaiver monographs for immediate release solid oral dosage forms: metronidazoleCamila F Rediguieri, Valentina Porta, Diana S G Nunes, et al.
Clinical Therapeutics|January 4, 2011
Challenges and opportunities in establishing scientific and regulatory standards for determining therapeutic equivalence of modified-release products: Workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
The AAPS Journal|May 5, 2010
Challenges and opportunities in establishing scientific and regulatory standards for assuring therapeutic equivalence of modified release products: workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|March 30, 2010
Challenges and opportunities in establishing scientific and regulatory standards for assuring therapeutic equivalence of modified-release products: workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
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