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1 ty were transferred in mice receiving a K(d) skin transplant.
2 istinct from male-specific minor Ags, and 3) skin transplant.
3 d graft survival in recipients of allogeneic skin transplant.
4 transfusion and anti-CD154 and given an allo-skin transplant.
5 ly mount a Th1 or Th2 response to allogeneic skin transplants.
6 ssays), as well as in live mice and on human skin transplants.
7 cantly less effective in older recipients of skin transplants.
8 H3a+H3b were used for orthotopic corneal and skin transplants.
9 -mismatched rhesus pairs with two sequential skin transplants.
10 sensitized to each other with two sequential skin transplants.
11                                           In skin transplants, allograft survival was enhanced with A
12 uman B cells as well as in murine allogeneic skin transplant and alloantigen-induced T cell expansion
13 ne model of complete mismatch full-thickness skin transplant by grafting dorsal skin from BALB/c mice
14 ly lower in fasted mice receiving allogeneic skin transplants compared with fed mice (P = 0.0009 and
15  rats were challenged with Wistar-Furth (WF) skin transplants, followed 7 days later by transplantati
16                                              Skin transplanted from transgenic B6.A2 to B6 mice was r
17                       C57BL/6J mice received skin transplants from BALB/c donors with: a) no treatmen
18 animals were sensitized using two sequential skin transplants from maximally major histocompatibility
19 cipient chimeric dogs (n=4) were tolerant to skin transplants from their marrow donors but rejected s
20 Splenocytes from mice treated with CsA after skin transplants had no response to third-party alloanti
21 s imply that cutaneous gene delivery through skin transplants may add a new option to treat drug abus
22 corneal-grafted mice, only CD8+ T cells from skin-transplanted mice mounted a cytotoxic response.
23  NK cells in Rag(-/-) mice using a stringent skin transplant model and found that NK cells at a resti
24                                   The murine skin transplant model has been used for decades as a sen
25 come these constraints we developed a murine skin transplant model in humanized mice and used it to t
26                                         In a skin transplant model in which rejection was mediated by
27                   We now demonstrate using a skin transplant model that alloantibody indirectly induc
28            Using a highly immunogenic murine skin transplant model that resists transplantation toler
29         In the present study, we showed in a skin transplant model that the skin allografts contain a
30           Here, employing a well-established skin transplant model with a single major histocompatibi
31 studied class I determinant recognition in a skin transplant model with beta-galactosidase (beta-gal)
32                                         In a skin transplant model, blocking both CD28/CD40L and the
33  the rat and dog and is efficacious in a rat skin transplant model, indicating that S1P3 receptor ago
34                                         In a skin transplant model, the addition of IL-2 synergizes w
35                     Using a highly stringent skin transplant model, the GelMA/anti-IL-6 IMB almost do
36 exhausted CD8(+) T cells in a male-to-female skin transplant model.
37 D8 T cells, we used a fully mismatched mouse skin transplant model.
38 on of allografts using an immunogenic murine skin transplant model.
39 ctivation using a BALB/c to C57BL/6 heart or skin transplant model.
40  of allograft response biomarkers in a mouse skin transplant model.
41  histocompatibility complex (MHC)-mismatched skin transplant model.
42 d lung transplant models, and in a humanized skin transplant model.
43 f intercellular adhesion molecule-1 in human skin transplanted on severe compromised immunodeficient
44 ammatory changes in human psoriatic lesional skin transplanted onto immunodeficient mice.
45                                        Human skin transplanted onto NSG mice develops an inflammatory
46 ophils in a transmigration model using human skin transplanted onto SCID mice.
47  human angiogenesis was established in human skin transplanted onto severe combined immunodeficient (
48 luate the immunologic response to allogeneic skin transplanted onto this region of lymphatic isolatio
49  bearing either a ovalbumin-transgenic mouse skin transplant or OVA-B16F10 tumor could be traced by f
50                                       In the skin transplant paradigm, combining an NK cell-specific
51 ferred CD27low NK cells into Rag1-/-T-bet-/- skin transplant recipients and found that the CD27low NK
52 response was generated against H4 peptide in skin transplant recipients.
53 nhanced the rapidity of cardiac allograft or skin transplant rejection in mice.
54 27high NK cells in a model of Tcell-mediated skin transplant rejection under costimulatory blockade c
55 onor haptoglobin enhanced the onset of acute skin transplant rejection, whereas haptoglobin-deficient
56 he influence of host and donor microbiota on skin transplant rejection.
57 ty complex class II alloantigens to suppress skin transplant rejection.
58 ve antibody plays a lesser role in mediating skin transplant rejection.
59                                    Syngeneic skin transplants served as controls.
60 ceiving Tregs display stable long-term human skin transplant survival along with a reduction in the C
61               Cutaneous gene therapy through skin transplants that elicit drug elimination may offer
62                              Nonvascularized skin transplants triggered vigorous direct and indirect
63                             First, psoriatic skin transplants were injected with either 1alpha,25-dih
64 smatched vascularized cardiac transplants or skin transplants were performed using BALB/c (H-2d), C57
65 neic primarily vascularized and conventional skin transplants were rejected at the same pace.
66  effected consistent rejection of HA-bearing skin transplants, whereas a significantly greater number