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1  space, and underneath the kidney capsule of histoincompatible BALB/c mice.
2  approach with respect to transplantation of histoincompatible bone marrow, we undertook a clinical t
3 oreover, VV-US2 and lysates from VV-infected histoincompatible cells elicit T(CD8)(+) specific for a
4 ty barriers or whether embryonic exposure to histoincompatible cells induces allotolerance.
5                                              Histoincompatible chimeras that lost detectable chimeris
6                                              Histoincompatible chimeras were unstable, with chimerism
7  of ALS and donor BMC infusion in a strongly histoincompatible class I and II MHC-disparate DBA/2-to-
8  P511 cells (CD-1, allogeneic; BALB/c, minor histoincompatible; DBA/2, syngeneic) received tumor cell
9 human HSCs rejected human skin grafts from a histoincompatible donor, indicating the development of a
10 d mononuclear cells (PBMCs) co-cultured with histoincompatible DSCCs was significantly lower than wit
11                           The co-presence of histoincompatible fetal and maternal cells is a characte
12 ty and promote prolonged graft acceptance in histoincompatible hosts in the absence of immunosuppress
13 splants from one individual to an irradiated histoincompatible individual of the same species are rej
14                                     In fully histoincompatible LEW-->BB transplants, in which rejecti
15  oral tolerance abrogates rejection of minor histoincompatible lung transplants, its ability to preve
16 parameters of acute inflammation in a highly histoincompatible model of rat lung allograft rejection
17 eters of acute inflammation seen in a highly histoincompatible model of rat lung AR.
18 hed successfully with a crossmatch-negative, histoincompatible organ.
19 or the first time, longterm patency of fully histoincompatible orthotopic tracheal allografts in noni
20 ly higher growth rates and survivorship than histoincompatible pairings.
21 g acute allograft rejection (AR) in a highly histoincompatible rat lung transplant model, BN-->LEW, a
22 R and parameters of inflammation in a highly histoincompatible rat lung transplant model.
23 longs cardiac allograft survival in a highly histoincompatible rat model.
24 ost disease (GVHD) after in vivo transfer to histoincompatible recipients.
25 detect chimerism in both histocompatible and histoincompatible settings.
26  and it blunts the alloimmunogenicity of the histoincompatible stroma and endothelium.
27                                  Infusion of histoincompatible T cells resulted in a significant rise
28  histocompatible T cells, whereas mice given histoincompatible T cells showed inappropriate up-regula
29 h syngeneic (histocompatible) or allogeneic (histoincompatible) T lymphocytes.
30  Thus, the potency of the T cell response to histoincompatible tissue is likely due to many small T c
31     The robustness of the T cell response to histoincompatible tissue is not understood.
32    We have previously reported that delaying histoincompatible transplantation after total body irrad
33 e GVHD mortality in normal hosts after major histoincompatible transplantation.
34 bretinal space supports immune deviation for histoincompatible tumor cells and soluble protein antige

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