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1     Graft take was poor in wounds containing xenogenic ADM and moderately good in those containing al
2 ull-thickness skin defects, but healing with xenogenic ADM was poor.
3             Contraction of wounds containing xenogenic ADM was significantly greater than that of wou
4 nd 30 days after surgery in wounds receiving xenogenic ADM, allogenic ADM, and thin STSGs.
5                                              Xenogenic and allogenic ADMs were produced by treating p
6                   A major hurdle for current xenogenic-based and other approaches aimed at engineerin
7 spontaneous metastasis models (syngeneic and xenogenic) because they incorporate microenvironmental i
8 This study found that the addition of PRP to xenogenic bone grafts demonstrated a low regenerative po
9 uence of platelet-rich plasma (PRP) added to xenogenic bone grafts on bone histomorphometric paramete
10           The availability of bovine derived xenogenic bone substitutes has made it possible to avoid
11                   Intraoral autologous bone, xenogenic bone, and DFDBA appear to interfere with norma
12 in 8 patients after implantation with either xenogenic bovine bone (n=5 sites), demineralized freeze-
13                                              Xenogenic bovine bone and DFDBA did not contribute to bo
14  and to study the impact of the beads and/or xenogenic cells on retinal integrity.
15 ought into contact with foreign organisms or xenogenic cells.
16 urrent techniques are hampered by the use of xenogenic components that limits their clinical applicat
17 k to impair their capability to engraft in a xenogenic context, we evaluated the possibility to use g
18 ired APC function derived from autologous or xenogenic feeder cells.
19                                         In a xenogenic GVHD mouse model, fucosylated Tregs showed pro
20                  We found that lv-expressing xenogenic human gp100 could induce potent CD8 responses
21 eic murine tumor cell line, Sa1, or with the xenogenic human tumor, MDA435.
22 he goal of using genetic manipulation of the xenogenic immune response to increase the availability o
23                               We developed a xenogenic mouse lung-perfusion model.
24 tance and anti-PTLD activity in vivo using a xenogenic mouse model, suggesting that the proposed stra
25 ey could strongly suppress tumor growth in a xenogenic mouse model.
26  hNSG mice reliably and predictably reject a xenogenic mouse skin graft by a human T cell mediated me
27                       Acellular materials of xenogenic origin are used worldwide as xenografts, and p
28 ntation enables organ-specific enrichment of xenogenic pluripotent stem cell (PSC) derivatives.
29 obliterative bronchiolitis might occur after xenogenic pulmonary transplantation.
30 n prevent hyperacute rejection in discordant xenogenic recipients, their physiologic role in the homo
31 ing that these antibodies were elicited as a xenogenic response to the protein.
32 tablished medulloblastomas in an orthotopic, xenogenic severe combined immunodeficiency model.
33 mented in operations that involve processing xenogenic tissue for human use.
34   The prompt and vigorous immune response to xenogenic tissue remains a significant barrier to clinic
35 n immune response against the vector and its xenogenic transgene product, hFIX.
36                                           In xenogenic transplants, hTERT-expressing BMSSCs (BMSSC-Ts

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