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1 tory on his or her response to an allogeneic tissue transplant.
2 l produce a response similar to that after a tissue transplant.
3 Immune rejection continues to threaten all tissue transplants.
4 ic subjects receiving human fetal pancreatic tissue transplants.
5 Because of limitations associated with fetal tissue transplants, a clone (1RB3AN27) of simian virus 4
9 understanding of the antigenicity of complex tissue transplants and mechanisms to promote graft accep
10 sses eGFP uniformly, and that can be used in tissue transplants and processed by in situ hybridizatio
12 he induction of immunologic tolerance of the tissue transplants because tolerance would eliminate the
14 tory response to an allogeneic or xenogeneic tissue transplant by the recipient is complex and includ
19 em cell transplants differ from conventional tissue transplants insofar as not all alloantigens are r
22 ally normal and unrelated allografted neural tissue transplanted into the brain of affected HD patien
23 tau pathology can manifest in healthy neural tissue transplanted into the brains of patients with two
24 account for the capacity of neonatal retinal tissue transplanted into the eye to alter the systemic a
25 rated using a novel approach targeting human tissues, transplanted into SCID mice, directly by in viv
28 This procedure, as well as other composite tissue transplants, offers the potential for correcting
30 erefore a target for autoimmunity disorders, tissue transplant rejection and T-cell malignancies.
32 cells are developed (e.g., stem cell-derived tissue), transplanting them in a durable device could ob
33 m (CNS), somites, and notochord by organizer tissue transplanted to the ventral side of host embryos.
35 nvelope could theoretically determine, as in tissue transplants, whether HIV-1 is "rejected" by expos
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