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1 ntribution of the bone marrow component in a composite tissue allograft.
2 80% of her face was replaced with a tailored composite tissue allograft.
3 rance in the recipients of the rat hind limb composite tissue allografts.
4 nce could be generated in miniature swine to composite tissue allografts across a major histocompatib
5 tolerance to the musculoskeletal elements of composite tissue allografts across an MHC barrier in min
6 himerism induces donor-specific tolerance to composite tissue allografts across major histocompatibil
8 herapy has been found to effectively prevent composite tissue allograft (CTA) rejection with minimal
10 ole of host thymus in tolerance induction in composite tissue allografts (CTA) across major histocomp
15 ne A (CsA) to induce tolerance for hind limb composite tissue allograft in rats without chronic immun
16 fforts have been made to induce tolerance to composite tissue allografts in adult recipients, thus fa
17 t that the vascularized bone marrow within a composite tissue allograft is not the component that cau
18 large volume of vascularized bone marrow in composite tissue allografts may be a risk factor for PTL
19 nimals and humans and suggests that although composite tissue allografts may have a significant skin
21 n be significantly delayed in a large-animal composite tissue allograft model including skin using on
22 ation, we developed a large-animal extremity composite tissue allograft model to assess the antirejec
24 complex craniofacial defects, application of composite tissue allografts opens unique one-stage recon
26 of donor-specific tolerance in rat hind-limb composite tissue allografts using a alphabeta-TCR/CsA pr
29 lantation and immunosuppressive regimen, the composite tissue allograft with vascularized bone marrow
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