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Amrita V. Kamath

Department of Metabolism and Pharmacokinetics

Bristol-Myers Squibb Pharmaceutical Research Institute

Princeton

NJ 08543

USA

[email]@bms.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, NJ 08543, USA. 2005

References

  1. P-glycoprotein plays a role in the oral absorption of BMS-387032, a potent cyclin-dependent kinase 2 inhibitor, in rats. Kamath, A.V., Chong, S., Chang, M., Marathe, P.H. Cancer Chemother. Pharmacol. (2005) [Pubmed]
  2. Effect of fruit juices on the oral bioavailability of fexofenadine in rats. Kamath, A.V., Yao, M., Zhang, Y., Chong, S. J. Pharm. Sci (2005) [Pubmed]
  3. Multiple pathways are involved in the oral absorption of BMS-262084, a tryptase inhibitor, in rats: role of paracellular transport, binding to trypsin, and P-glycoprotein efflux. Kamath, A.V., Morrison, R.A., Harper, T.W., Lan, S.J., Marino, A.M., Chong, S. J. Pharm. Sci (2005) [Pubmed]
  4. Preclinical pharmacokinetics and oral bioavailability of BMS-310705, a novel epothilone B analog. Kamath, A.V., Chang, M., Lee, F.Y., Zhang, Y., Marathe, P.H. Cancer Chemother. Pharmacol. (2005) [Pubmed]
 
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