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Benjamin F. Cravatt

The Skaggs Institute for Chemical Biology and the Departments of Cell Biology

The Scripps Research Institute

10550 North Torrey Pines Road

La Jolla

USA

[email]@scripps.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • The Skaggs Institute for Chemical Biology and the Departments of Cell Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, USA. 2000 - 2008

References

  1. Activity-based protein profiling: from enzyme chemistry to proteomic chemistry. Cravatt, B.F., Wright, A.T., Kozarich, J.W. Annu. Rev. Biochem. (2008) [Pubmed]
  2. The biological impact of mass-spectrometry-based proteomics. Cravatt, B.F., Simon, G.M., Yates, J.R. Nature (2007) [Pubmed]
  3. Functional disassociation of the central and peripheral fatty acid amide signaling systems. Cravatt, B.F., Saghatelian, A., Hawkins, E.G., Clement, A.B., Bracey, M.H., Lichtman, A.H. Proc. Natl. Acad. Sci. U.S.A. (2004) [Pubmed]
  4. The endogenous cannabinoid system and its role in nociceptive behavior. Cravatt, B.F., Lichtman, A.H. J. Neurobiol. (2004) [Pubmed]
  5. Fatty acid amide hydrolase: an emerging therapeutic target in the endocannabinoid system. Cravatt, B.F., Lichtman, A.H. Curr. Opin. Chem. Biol (2003) [Pubmed]
  6. The enzymatic inactivation of the fatty acid amide class of signaling lipids. Cravatt, B.F., Lichtman, A.H. Chem. Phys. Lipids (2002) [Pubmed]
  7. Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase. Cravatt, B.F., Demarest, K., Patricelli, M.P., Bracey, M.H., Giang, D.K., Martin, B.R., Lichtman, A.H. Proc. Natl. Acad. Sci. U.S.A. (2001) [Pubmed]
  8. Chemical strategies for the global analysis of protein function. Cravatt, B.F., Sorensen, E.J. Curr. Opin. Chem. Biol (2000) [Pubmed]
 
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