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1 (DTT) showed that the majority of remaining lymphocytotoxicity against GalT-KO swine was mediated by
3 Screening was done by complement-dependent lymphocytotoxicity and antihuman globulin augmentation t
5 onsiveness was demonstrated by cell-mediated lymphocytotoxicity and mixed lymphocyte response, and su
6 xed lymphocyte reaction (MLR), cell-mediated lymphocytotoxicity, and cytokine profile of unresponsive
7 fractoriness in longitudinal panels from 170 lymphocytotoxicity assay (LCA)(-) and 20 LCA(+) TRAP par
8 sms to sensitize appropriate target cells in lymphocytotoxicity assays and found that the MTF is deri
9 g 29 patients, FCXM and complement-dependent lymphocytotoxicity assays were performed 10+/-2 and 28+/
10 ytotoxic cross-matches (complement-dependent lymphocytotoxicity assays) were stratified on the basis
11 on of the four methods, complement-dependent lymphocytotoxicity (CDC) and C1q-, C4d-, and IgG-Luminex
12 than was obtainable by complement-dependent lymphocytotoxicity (CDC) assays has resulted in a new pa
14 lymphocyte cultures (MLC) and cell-mediated lymphocytotoxicity (CML) culture systems analogous to th
19 lity was determined at study entry only by a lymphocytotoxicity screening assay (s-LCA) against a pan
20 lysis is a more useful clinical parameter of lymphocytotoxicity testing than simple reporting of % PR
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