SOLID PHASE SYNTHESIS WITHOUT REPETITIVE ACIDOLYSIS von MEIENHOFER, JOHANNES, WAKI, MICHINORI, HEIMRE, EDGAR P., LAMBROS, THEODORE J., MAKOFSKE, RAYMOND C., CHANG, CHI-DEU

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Replacement of the disulfide bond in oxytocin by an amide group. Synthesis and some biological properties of [cyclo-(1-L-aspartic acid, 6-L-.alpha.,.beta.-diaminopropionic acid)]ox... von Smith, Clark W, Walter, Roderich, Moore, Stanley, Makofske, Raymond C, Meienhofer, Johannes

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A synthesis of human .beta.-endorphin in solution von Tzougraki, Chrysa, Makofske, Raymond C, Gabriel, Thomas F, Wang, Su-Sun, Kutny, Rostyslaw, Meienhofer, Johannes, Li, Choh Hao

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Synthetic domains of cystatins linked to enkephalins are novel inhibitors of brain cathepsins L/B von Marks, Neville, Berg, Martin J., Makofske, Raymond C., Danho, Waleed

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Solid phase synthesis without repetitive acidolysis. Preparation of leucyl-alanyl-glycyl-valine using 9-fluorenylmethyloxycarbonylamino acids von Meienhofer, J, Waki, M, Heimer, E P, Lambros, T J, Makofske, R C, Chang, C D

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Isolation and identification of thymosin α-1 from calf spleen using high performance liquid chromatography von DANHO, WALEED, GABRIEL, THOMAS F., MAKOFSKE, RAYMOND C.

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Synthesis of a potent enkephalin analog, Tyr-D-Thr-Gly-Phe-Δ3Pro-NH2, and some of its biological activities von TZOUGRAKI, CHRYSA, DAIRMAN, WALLACE M., MAKOFSKE, RAYMOND C., AEPPLI, LISLOT, MEIENHOFER, JOHANNES

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PREPARATIVE OXIDATIVE CONVERSION OF PROTECTED PEPTIDE Cα‐HYDRAZIDES INTO THE CORRESPONDING ACIDS BY N‐BROMOSUCCINIMIDE von MEIENHOFER, JOHANNES, DZIEDUSZYCKA, MARIA, SMULKOWSKI, MACIEJ, MAKOFSKE, RAYMOND C., DANHO, WALEED

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SYNTHESIS OF HUMAN β-ENDORPHIN IN SOLUTION USING BENZYL-TYPE SIDE CHAIN PROTECTIVE GROUPS von TZOUGRAKI, CHRYSA, MAKOFSKE, RAYMOND C., GABRIEL, THOMAS F., MICHALEWSKY, JOSEPH, MEIENHOFER, JOHANNES, LI, CHOH HAO

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PREPARATIVE OXIDATIVE CONVERSION OF PROTECTED PEPTIDE Cα-HYDRAZIDES INTO THE CORRESPONDING ACIDS BY N-BROMOSUCCINIMIDE von MEIENHOFER, JOHANNES, DZIEDUSZYCKA, MARIA, SMULKOWSKI, MACIEJ, MAKOFSKE, RAYMOND C., DANHO, WALEED

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Peptide and Peptide Mimetic Inhibitors of Antigen Presentation by HLA-DR Class II MHC Molecules. Design, Structure−Activity Relationships, and X-ray Crystal Structures von Bolin, David R, Swain, Amy L, Sarabu, Ramakanth, Berthel, Steven J, Gillespie, Paul, Huby, Nicholas J. S, Makofske, Raymond, Orzechowski, Lucja, Perrotta, Agostino, Toth, Katherine, Cooper, Joel P, Jiang, Nan, Falcioni, Fiorenza, Campbell, Robert, Cox, Donald, Gaizband, Diana, Belunis, Charles J, Vidovic, Damir, Ito, Kouichi, Crowther, Robert, Kammlott, Ursula, Zhang, Xiaolei, Palermo, Robert, Weber, David, Guenot, Jeanmarie, Nagy, Zoltan, Olson, Gary L

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Analogs of Ac-CCK-7 incorporating dipeptide mimics in place of Met28-Gly29 von Tilley, Jefferson W, Danho, Waleed, Shiuey, Shian Jan, Kulesha, Irina, Swistok, Joseph, Makofske, Raymond, Michalewsky, Joseph, Triscari, Joseph, Nelson, David

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