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Arco Y. Jeng

Novartis Institute for Biomedical Research

Novartis Pharmaceuticals Corporation

Building 435

Room 2191

USA

[email]@*.novartis.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Novartis Institute for Biomedical Research, Novartis Pharmaceuticals Corporation, Building 435, Room 2191, USA. 2003
  • Metabolic and Cardiovascular Diseases Research, Novartis Institute for Biomedical Research, Summit, NJ 07901, USA. 2002
  • Novartis Institute for Biomedical Research, Summit, New Jersey 07901, USA. 1999
  • Research Department, Novartis Pharmaceuticals Corp., Summit, New Jersey 07901, USA. 1997

References

  1. Utility of endothelin-converting enzyme inhibitors for the treatment of cardiovascular diseases. Jeng, A.Y. Curr. Opin. Investig. Drugs (2003) [Pubmed]
  2. Nonpeptidic endothelin-converting enzyme inhibitors and their potential therapeutic applications. Jeng, A.Y., Mulder, P., Kwan, A.L., Battistini, B. Can. J. Physiol. Pharmacol. (2002) [Pubmed]
  3. CGS 34226, a thiol-based dual inhibitor of endothelin converting enzyme-1 and neutral endopeptidase 24.11. Jeng, A.Y., Savage, P., Beil, M.E., Bruseo, C.W., Hoyer, D., Fink, C.A., Trapani, A.J. Clin. Sci. (2002) [Pubmed]
  4. Enhanced expression of matrix metalloproteinase-3, -12, and -13 mRNAs in the aortas of apolipoprotein E-deficient mice with advanced atherosclerosis. Jeng, A.Y., Chou, M., Sawyer, W.K., Caplan, S.L., Von Linden-Reed, J., Jeune, M., Prescott, M.F. Ann. N. Y. Acad. Sci. (1999) [Pubmed]
  5. Suppression of substance P biosynthesis in sensory neurons of dorsal root ganglion by prodrug esters of potent peptidylglycine alpha-amidating monooxygenase inhibitors. Jeng, A.Y., Fujimoto, R.A., Chou, M., Tan, J., Erion, M.D. J. Biol. Chem. (1997) [Pubmed]
 
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