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Citation: Cm. Kam et al., MAMMALIAN TISSUE TRYPSIN-LIKE ENZYMES - SUBSTRATE-SPECIFICITY AND INHIBITORY POTENCY OF SUBSTITUTED ISOCOUMARIN MECHANISM-BASED INHIBITORS,BENZAMIDINE DERIVATIVES, AND ARGININE FLUOROALKYL KETONE TRANSITION-STATE INHIBITORS, Archives of biochemistry and biophysics, 316(2), 1995, pp. 808-814
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Citation: Mr. Player et al., 1,3-OXAZINO[4,5-B]INDOLE-2,4-(1H,9H)-DIONES AND ETHYLPYRROLO-[2,3-D]-1,3-OXAZIN-2,4-(1H,7H)-DIONES AS SERINE-PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 4(7), 1994, pp. 949-954
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Citation: Sl. Woodard et al., IDENTIFICATION OF AN ESSENTIAL CHYMASE COMPONENT OF THE PERFORIN SYSTEM OF LYSIS, The FASEB journal, 8(4), 1994, pp. 10000206-10000206
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Citation: Cm. Kam et al., MECHANISM-BASED ISOCOUMARIN INHIBITORS FOR BLOOD-COAGULATION SERINE PROTEASES - EFFECT OF THE 7-SUBSTITUENT IN AMINO-4-CHLORO-3-(ISOTHIOUREIDOALKOXY)ISOCOUMARINS ON INHIBITORY AND ANTICOAGULANT POTENCY, Journal of medicinal chemistry, 37(9), 1994, pp. 1298-1306
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Citation: B. Boduszek et al., DIPEPTIDE PHOSPHONATES AS INHIBITORS OF DIPEPTIDYL PEPTIDASE-IV, Journal of medicinal chemistry, 37(23), 1994, pp. 3969-3976
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Citation: Sl. Woodard et al., CHYMASE-DIRECTED SERINE-PROTEASE INHIBITOR THAT REACTS WITH A SINGLE 30-KDA GRANZYME AND BLOCKS NK-MEDIATED CYTOTOXICITY, The Journal of immunology, 153(11), 1994, pp. 5016-5025
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Citation: Mg. Silva et al., HUMAN-LYMPHOCYTES PRETREATED WITH NEW, PEPTIDE-BASED IRREVERSIBLE SERINE-PROTEASE INHIBITORS HAVE DEPRESSED NK ACTIVITY, Experimental hematology, 21(8), 1993, pp. 1042-1042
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Citation: Zz. Li et al., PEPTIDE ALPHA-KETO ESTER, ALPHA-KETO AMIDE, AND ALPHA-KETO ACID INHIBITORS OF CALPAINS AND OTHER CYSTEINE PROTEASES, Journal of medicinal chemistry, 36(22), 1993, pp. 3472-3480
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SAYERS TJ
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Citation: Mj. Smyth et al., MET-ASE - CLONING AND DISTINCT CHROMOSOMAL LOCATION OF A SERINE-PROTEASE PREFERENTIALLY EXPRESSED IN HUMAN NATURAL-KILLER-CELLS, The Journal of immunology, 151(11), 1993, pp. 6195-6205
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POWERS JC
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MEYER EF
Citation: Ma. Hernandez et al., EFFECT OF THE 7-AMINO SUBSTITUENT ON THE INHIBITORY POTENCY OF MECHANISM-BASED ISOCOUMARIN INHIBITORS FOR PORCINE PANCREATIC AND HUMAN NEUTROPHIL ELASTASES - A 1.85-A X-RAY STRUCTURE OF THE COMPLEX BETWEEN PORCINE PANCREATIC ELASTASE AND LPHENYLALANYL)AMINO]-4-CHLORO-3-METHOXYISOCOUMARIN, Journal of medicinal chemistry, 35(6), 1992, pp. 1121-1129