The amino terminus of the human C5a receptor is required for high affinity C5a binding and for receptor activation by C5a but not C5a analogs von DEMARTINO, J. A, VAN RIPER, G, SICILIANO, S. J, MOLINEAUX, C. J, KONTEATIS, Z. D, ROSEN, H, SPRINGER, M. S

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Development of C5a receptor antagonists. Differential loss of functional responses von Konteatis, ZD, Siciliano, SJ, Van Riper, G, Molineaux, CJ, Pandya, S, Fischer, P, Rosen, H, Mumford, RA, Springer, MS

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d-Amino acid and alanine scans of the bioactive portion of porcine motilin von Peeters, Theo L., Macielag, Mark J., Depoortere, Inge, Konteatis, Zenon D., Florance, James R., Lessor, Ralph A., Galdes, Alphonse

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Arginine 206 of the C5a Receptor Is Critical for Ligand Recognition and Receptor Activation by C-terminal Hexapeptide Analogs (∗) von DeMartino, Julie A., Konteatis, Zenon D., Siciliano, Salvatore J., Van Riper, Gail, Underwood, Dennis J., Fischer, Paul A., Springer, Martin S.

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Synthesis and in vitro evaluation of [Leu 13]porcine motilin fragments von Macielag, Mark J., Peeters, Theo L., Konteatis, Zenon D., Florance, James R., Depoortere, Inge, Lessor, Ralph A., Bare, Lance A., Cheng, Yea-Shun, Galdes, Alphonse

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Capillary zone electrophoresis studies of motilin peptides: Effects of charge, hydrophobicity, secondary structure and length von Florance, James R., Konteatis, Zenon D., Macielag, Mark J., Lessor, Ralph A., Galdes, Alphonse

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Development of C5a receptor antagonist. Differential loss of functional responses von Konteatis, Z D, Siciliano, S J, Van Riper, G, Molineaux, C J, Pandya, S, Fischer, P, Rosen, H, Mumford, R A, Springer, MS

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SYNTHESIS AND INVITRO EVALUATION OF [LEU13]PORCINE MOTILIN FRAGMENTS von MACIELAG, MJ, PEETERS, TL, KONTEATIS, ZD, FLORANCE, DEPOORTERE, LESSOR, RA, BARE, LA, CHENG, YS, GALDES, A

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Capillary zone electrophoresis studies of motilin peptides : effects of charge, hydrogphobicity, secondary structure and length von FLORANCE, J. R, KONTEATIS, Z. D, MACIELAG, M. J, LESSOR, R. A, GALDES, A

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2,4- OR 4,6-DIAMINOPYRIMIDINE COMPOUNDS AS IDH2 MUTANTS INHIBITORS FOR THE TREATMENT OF CANCER IDH2 24- 46 von POPOVICI-MULLER, Janeta J, TRAVINS, Jeremy J, KONTEATIS, Zenon, D. ZD

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Discovery of a novel class of non-ATP site DFG-out state p38 inhibitors utilizing computationally assisted virtual fragment-based drug design (vFBDD) von Moffett, Kristofer, Konteatis, Zenon, Nguyen, Duyan, Shetty, Rupa, Ludington, Jennifer, Fujimoto, Ted, Lee, Kyoung-Jin, Chai, Xiaomei, Namboodiri, Haridasan, Karpusas, Michael, Dorsey, Bruce, Guarnieri, Frank, Bukhtiyarova, Marina, Springman, Eric, Michelotti, Enrique

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Discovery and investigation of a novel class of thiophene-derived antagonists of the human glucagon receptor von Duffy, Joseph L., Kirk, Brian A., Konteatis, Zenon, Campbell, Elizabeth L., Liang, Rui, Brady, Edward J., Candelore, Mari Rios, Ding, Victor D.H., Jiang, Guoqiang, Liu, Frank, Qureshi, Sajjad A., Saperstein, Richard, Szalkowski, Deborah, Tong, Sharon, Tota, Lauri M., Xie, Dan, Yang, Xiaodong, Zafian, Peter, Zheng, Song, Chapman, Kevin T., Zhang, Bei B., Tata, James R.

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Mimicry of Erythropoietin by a Nonpeptide Molecule von Qureshi, Sajjad A., Kim, Ronald M., Konteatis, Zenon, Biazzo, Dawn E., Motamedi, Haideh, Rodrigues, Robert, Boice, Judith A., Calaycay, Jimmy R., Bednarek, Maria A., Griffin, Patrick, Gao, Ying-Duo, Chapman, Kevin, Mark, David F.

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