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Oncogene|November 17, 2005
AKT crystal structure and AKT-specific inhibitorsChandra C Kumar, Vincent Madison
Protein Engineering, Design & Selection : PEDS|March 30, 2004
Improved activity and thermostability of Candida antarctica lipase B by DNA family shufflingWen-Chen Suen, Ningyan Zhang, Li Xiao, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 9, 2002
Insights from a three-dimensional model into ligand binding to constitutive active receptorLi Xiao, Xiaoming Cui, Vincent Madison, et al.
Protein Engineering|September 12, 2003
Improving tolerance of Candida antarctica lipase B towards irreversible thermal inactivation through directed evolutionNingyan Zhang, Wen-Chen Suen, William Windsor, et al.
Bioorganic & Medicinal Chemistry Letters|March 16, 2010
Potent ketoamide inhibitors of HCV NS3 protease derived from quaternized P1 groupsSrikanth Venkatraman, Francisco Velazquez, Wanli Wu, et al.
Biochemistry|March 16, 2005
ADAM33 enzyme properties and substrate specificityJun Zou, Rumin Zhang, Feng Zhu, et al.
The Journal of Biological Chemistry|May 16, 2002
Transforming growth factor-beta 2 is a transcriptional target for Akt/protein kinase B via forkhead transcription factorAhmed A Samatar, Luquan Wang, Asra Mirza, et al.
Journal of Medicinal Chemistry|December 4, 2003
Application of the lambda-dynamics method to evaluate the relative binding free energies of inhibitors to HCV proteaseZhuyan Guo, James Durkin, Thierry Fischmann, et al.
Bioorganic & Medicinal Chemistry Letters|August 23, 2005
Synthesis and biological activity of macrocyclic inhibitors of hepatitis C virus (HCV) NS3 proteaseKevin X Chen, F George Njoroge, Andrew Prongay, et al.
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