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1 to prolong allograft survival in a model of skin transplantation.
2 with an emphasis on cell-based therapies and skin transplantation.
3 ited number of lymphatic capillaries through skin transplantation.
4 ent inflammatory process in a mouse model of skin transplantation.
5 CD154 antibody following allogeneic islet or skin transplantation.
6 with thromboembolism risk) in the context of skin transplantation 2 years before the angiography stud
7 ntation with LN excision (n = 6), allogeneic skin transplantation alone (n = 6), or syngeneic skin tr
8 ishing mixed chimerism was tested in vivo by skin transplantation and in vitro by mixed leukocyte rea
10 F rats were presensitized to ACI antigens by skin transplantation and received heterotopic osteomyocu
11 These T cells proliferated modestly after skin transplantation and underwent relatively weak funct
13 of WF spleen cells (2x10[7]) at the time of skin transplantation (day -7) abrogated <24-hr rejection
14 stinct antigenic hierarchy between heart and skin transplantation: H60-specific CD8(+) T cells were t
15 ases allograft survival in a murine model of skin transplantation in fully mismatched strain combinat
18 espite this difference in outcome, heart and skin transplantation induced antidonor T cell responses
26 used a mouse model of MHC-class I mismatched skin transplantation to investigate the contribution of
28 compounds, and a murine model of allogeneic skin transplantation was adopted to assess the in vivo e
29 lantation, C57BL/6 mice underwent allogeneic skin transplantation with LN excision (n = 6), allogenei
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