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1  accomplished by grafting only the SDRs of a xenogeneic Ab onto human Ab frameworks.
2                                         In a xenogeneic adoptive transfer model, we have compared the
3 term metabolic function of microencapsulated xenogeneic adult porcine islets (API) was assessed in a
4 ing improved regression of human cancer in a xenogeneic allograft model.
5   When rejection occurred on days 4 and 8 in xenogeneic and allogeneic recipients, 60% (57-68) and 55
6 human regulatory T cells (Tregs) to suppress xenogeneic and allogeneic responses in vitro.
7  hESC(siRNA+IB) was strongly reduced in both xenogeneic and allogeneic settings.
8 exhibit compromised rejection of allogeneic, xenogeneic and missing self bone-marrow grafts.
9                At 2 days, injection sites of xenogeneic and syngeneic cells (cardiac-derived stem cel
10 at are capable of killing a large variety of xenogeneic and syngeneic cells.
11  possibility of imaging inflammation in both xenogeneic and syngeneic tumor models, which resulted in
12 We estimated the decrease in expression of a xenogeneic antigen, Galalpha1-3Gal, which might be neede
13 ced in xenograft recipients against multiple xenogeneic antigens.
14 ursor experiments have been carried out in a xenogeneic background in order to utilize species-specif
15 licited immune response of healthy dogs to a xenogeneic BAL was blocked and BAL performance significa
16 o induce tolerance across a highly disparate xenogeneic barrier has not yet been demonstrated.
17 wo strategies to induce tolerance across the xenogeneic barrier, namely thymus transplantation and mi
18 olerance across a discordant (pig-to-baboon) xenogeneic barrier.
19 survival across the discordant pig-to-baboon xenogeneic barrier.
20 ial, but also to understanding the nature of xenogeneic barriers and mechanisms of heterochronicity,
21 nsplantation because immune responses across xenogeneic barriers are vigorous.
22 e transplant tolerance across allogeneic and xenogeneic barriers, and to support long-term thymopoies
23 ucing T cell tolerance across allogeneic and xenogeneic barriers.
24  mouse) and highly disparate (pig to rodent) xenogeneic barriers.
25 ion across allogeneic and potentially across xenogeneic barriers.
26 success of transplants across allogeneic and xenogeneic barriers.
27 nts of antigenicity in a clinically relevant xenogeneic biomaterial (i.e. BP) and further validates a
28 onstrate that anti-CD40L in combination with xenogeneic BMT can tolerize preexisting peripheral and i
29                                        Mixed xenogeneic bone marrow chimeras resulting from the trans
30         We have previously demonstrated that xenogeneic bone marrow engraftment and donor-specific to
31 on and in the facilitation of allogeneic and xenogeneic bone marrow engraftment.
32 and/or gammaDelta cell-mediated rejection of xenogeneic bone marrow.
33 increases the rapidity of PDLF attachment to xenogeneic bone replacement materials.
34 une response against the therapeutic and the xenogeneic carbohydrate galactose-alpha1-3-galactose, an
35 cellular responses that lead to rejection of xenogeneic cartilage are not well understood.
36 and may therefore contribute to rejection of xenogeneic cartilage.
37 on of KO mice with pig kidney membranes (ie, xenogeneic cell membranes expressing an abundance of alp
38 become key components for the development of xenogeneic cells and organs for human transplantation.
39 s play an important role in the rejection of xenogeneic cells and therefore represent a major obstacl
40 type; and improved survival of donor-derived xenogeneic cells at 2 and 4 wk in vivo.
41 contributes significantly to phagocytosis of xenogeneic cells by macrophages and suggest that genetic
42 y of CD47 may contribute to the rejection of xenogeneic cells by macrophages.
43  recent years, hepatic support systems using xenogeneic cells have been developed to support patients
44 nsplantation of a bioartificial adrenal with xenogeneic cells may be a treatment option for patients
45 on of coagulation pathways after exposure to xenogeneic cells or a vascularized xenograft.
46                                   The use of xenogeneic cells or tissues for tissue engineering appli
47     Even after immunization with Gal-bearing xenogeneic cells, mixed chimeras were devoid of anti-Gal
48 n the animals transplanted with syngeneic or xenogeneic cells, respectively.
49 ly high precursor frequency was detected for xenogeneic cellular responses in the rat anti-mouse comb
50             Furthermore, compared with fully xenogeneic chimeras (rat --> mouse), mixed xenogeneic ch
51                                        Mixed xenogeneic chimeras exhibit donor-specific humoral toler
52 y xenogeneic chimeras (rat --> mouse), mixed xenogeneic chimeras exhibit superior immunocompetence fo
53                                           In xenogeneic chimeras, T cell repertoire selection plays a
54   We have previously demonstrated that mixed xenogeneic chimerism and donor-specific T-cell tolerance
55 e ability of anti-CD40L mAb to promote mixed xenogeneic chimerism and donor-specific tolerance in B6
56         These results demonstrate that mixed xenogeneic chimerism establishes donor-specific humoral
57                          Mixed allogeneic or xenogeneic chimerism indeed tolerizes both preexisting a
58 lability of human adrenal glands, sources of xenogeneic chromaffin cells will need to be identified i
59                                              Xenogeneic CM combined with tunnel technique leads to sa
60 were treated with the tunnel technique using xenogeneic CM.
61 +, CD8+, and CD4+CD8+ T cells in a rat/mouse xenogeneic co-culture.
62                                         Both xenogeneic collagen matrices combined with FDBA were eff
63                                  Considering xenogeneic collagen matrix (CM) and enamel matrix deriva
64 e purpose of this study is to determine if a xenogeneic collagen matrix (CM) might be as effective as
65 it-mouth design with CAF procedures or CAF + xenogeneic collagen matrix (CMX).
66  of inducing tolerance in a highly disparate xenogeneic combination and may have clinical potential t
67 lity has not been demonstrated in discordant xenogeneic combinations because of the difficulty in ach
68 e induction by mixed chimerism in discordant xenogeneic combinations.
69 ity induced by TCR adenoviruses required the xenogeneic constant regions and was mediated by CD8+ T c
70 ion in a pig-to-human model also reduces the xenogeneic consumption of human platelets by the porcine
71  the effect that these modifications have on xenogeneic consumption of human platelets in the absence
72  human CD19(+) B-lineage cells purified from xenogeneic cord blood stem cell/MS-5 murine stromal cell
73   We wished to determine the extent to which xenogeneic cornea fragments placed in the eyes of normal
74                                  The fate of xenogeneic cornea implants was assessed in mice immunize
75                                              Xenogeneic corneal fragments (guinea pig) are highly res
76                                              Xenogeneic corneal fragments implanted in the anterior c
77                                 By contrast, xenogeneic corneal fragments implanted in the anterior c
78 , we wished to determine the extent to which xenogeneic corneal fragments placed intraocularly in nor
79                    Neutralization of IL-7 in xenogeneic cultures led to an increase in Ig light-chain
80 man CD19(+) cells developing in human/murine xenogeneic cultures show differential expression of the
81        Prime requirements for allogeneic, or xenogeneic, decellularized scaffolds are biocompatibilit
82                             In this model of xenogeneic DNA immunization, the presence of an hgp100 h
83 ght to improve on this strategy by combining xenogeneic DNA vaccination with an agonist anti-glucocor
84    In contrast to allogeneic donor ECDI-SPs, xenogeneic donor ECDI-SPs induced production of xenodono
85                                              Xenogeneic donor-specific tolerance can be induced by tr
86  T cells and render recipients tolerant of a xenogeneic donor.
87  porcine endogenous retroviruses (PERV) from xenogeneic donors into humans has been widely debated.
88 d by human CTL (huCTL) vs allogeneic and pig xenogeneic EC targets.
89 re of immune-competent mice to injections of xenogeneic EC-TCPS induced vigorous host immunity.
90                    Matrix-embedding protects xenogeneic ECs against immune reaction in naive mice and
91  tolerance in allogeneic and closely related xenogeneic (eg, rat-to-mouse) combinations, the ability
92 nse and the subsequent activation invoked by xenogeneic encounter.
93 c, nude rats injected intraperitoneally with xenogeneic endothelial cells (ECs) produce antibodies ag
94 redox systems may provide a means to protect xenogeneic endothelial cells from NK cell-mediated cytot
95 erated from monocytes under the influence of xenogeneic endothelial cells in the absence of exogenous
96 cells after co-culturing with allogeneic and xenogeneic endothelial cells, respectively.
97                         An in vitro model of xenogeneic engraftment was established to identify inhib
98 d hematopoietic progenitor cells within this xenogeneic environment generated mature functional T cel
99 f specific T cell receptor-Vbeta occurs in a xenogeneic environment in a predictable fashion parallel
100 rtoire selection in tolerance induction in a xenogeneic environment.
101  characteristics that allow persistence in a xenogeneic environment.
102 d receptor in innate cellular recognition of xenogeneic epitopes.
103       Although a vigorous immune response to xenogeneic extracellular matrix biomaterials is expected
104 l biological scaffolds made of allogeneic or xenogeneic extracellular matrix derived from non-autolog
105 ival 3 weeks after injection of syngeneic or xenogeneic ferumoxides-labeled stem cells (cardiac-deriv
106 r tumorigenesis, we selectively targeted the xenogeneic form of survivin, a survival protein overexpr
107 ty was induced by DNA immunization against a xenogeneic form of TRP-2, but not against the syngeneic
108 induced by DEC205 targeting of the Ag in its xenogeneic form to maturing DCs.
109 an embryonic stem (hES) cells in defined and xenogeneic-free conditions will contribute substantially
110 ents a key step toward the fully defined and xenogeneic-free culture of hES cells.
111                  C57BL/6 mice immunized with xenogeneic full-length hgp100 DNA were protected against
112 om autoimmune destruction and allogeneic and xenogeneic graft rejection.
113 s, and can instill long-lived allogeneic and xenogeneic graft tolerance.
114 t, in a preclinical humanized mouse model of xenogeneic graft-versus-host disease (GVHD), sGARP preve
115 onstrate that IL-15 but not IL-2 exacerbates xenogeneic graft-versus-host disease (X-GVHD) in severe
116 a-treated Treg in a humanized mouse model of xenogeneic graft-versus-host disease confirmed IFN-alpha
117 e induction of IFNgamma-secreting Tregs in a xenogeneic graft-versus-host disease model and in adopti
118  T cells and complete rescue from hyperacute xenogeneic graft-versus-host disease modeling early and
119 ls mediated tumor rejection without inducing xenogeneic graft-versus-host disease, thus resulting in
120 generated Tregs that consistently suppressed xenogeneic graft-vs-host disease in immunodeficient mice
121 munosuppression by human Tregs in a model of xenogeneic graft-vs.-host disease induced by the transfe
122 d could influence the findings; for example, xenogeneic grafts may not recognize host inhibitory sign
123 nd residual host immune function against the xenogeneic grafts results in defective development and m
124 to enhance the recruitment of host huTreg to xenogeneic grafts to regulate cell-mediated xenograft re
125 hway and promotes survival of allogeneic and xenogeneic grafts.
126 hat were capable of rejecting allogeneic and xenogeneic grafts.
127       Here, we report a novel, optimized NHP xenogeneic GVHD (xeno-GVHD) small animal model that reca
128 s expressing an irrelevant CAR at preventing xenogeneic GVHD caused by HLA-A2+ T cells.
129 R gene also conferred resistance to DEX in a xenogeneic GVHD model in sublethally irradiated NOD-scid
130                                   In a human xenogeneic GVHD model, human IL-21-secreting cells were
131 d prolonged time to fatal GVHD in an in vivo xenogeneic GVHD model.
132 iate into effectors able to mediate a potent xenogeneic GVHD.
133    Murine complement is capable of resisting xenogeneic hematopoietic engraftment through an antibody
134 A1CMAH knockout pigs were compared for their xenogeneic hepatic consumption of human platelets.
135 osuppression allows long-term functioning of xenogeneic hepatocyte retransplants and suggests that he
136 tocytes might address this problem; however, xenogeneic hepatocytes are thought to be functionally in
137                 Following a single infusion, xenogeneic hepatocytes functioned for more than 80 days
138                          The extent to which xenogeneic hepatocytes metabolize and excrete human orga
139                    Transplants consisting of xenogeneic hepatocytes might overcome these problems, an
140 e-specific autoimmunity was seen only when a xenogeneic homolog of PAP was used as the immunogen.
141 generated by blastocyst complementation in a xenogeneic host.
142 s, and, as a result, are rapidly rejected in xenogeneic hosts.
143 ry considerably in their transmissibility to xenogeneic hosts.
144 hibiting allogeneic pig T cell responses and xenogeneic human anti-pig T cell responses in vitro.
145 4IgG4 on allogeneic pig T cell responses and xenogeneic human anti-pig T cell responses.
146 and the effects of costimulatory blockade on xenogeneic human anti-porcine T cell responses are also
147       Finally, CTLA4IgG4 prevented secondary xenogeneic human anti-porcine T cell responses.
148 ither tumor Valpha or Vbeta regions fused to xenogeneic human constant regions.
149                                    We used a xenogeneic human cord blood stem cell/murine stromal cel
150 ostimulatory pathways block the rejection of xenogeneic human embryonic-stem-cell-derived pancreatic
151  equivalents or normoglycemic rats with 5000 xenogeneic human islet equivalents.
152         Finally, huTreg partially suppressed xenogeneic human NK cell adhesion, NK cytotoxicity and d
153 fficient zygote genome editing technologies, xenogeneic human pluripotent stem cells may also open ne
154  We conclude that porcine Kupffer cells bind xenogeneic human RBC by recognition of a carbohydrate ep
155                                        Using xenogeneic (human) cells in immunosuppressed animals wit
156 is a murine T cell clone that recognizes the xenogeneic (human) class I MHC HLA-A2.1 molecule (A2) an
157 f primary GalT-KO skin grafts led to an anti-xenogeneic humoral response with no evidence for sensiti
158 ve-type CD4 cells (CD4/CD45RA ) and in vitro xenogeneic hyporesponsiveness were observed.
159      Porcine thymic tissue is able to induce xenogeneic hyporesponsiveness.
160 endothelial-mediated activation of allo- and xenogeneic immune cells.
161  not appear to differ in the nature of their xenogeneic immune response to the administered rabbit se
162  and exhibited similar levels of anti-rabbit xenogeneic immune response, the NZW mice had significant
163                                              Xenogeneic immunization with orthologous Ags induces can
164 ion between pig cell microchimerism and true xenogeneic infection.
165 occurred, and no evidence of transmission of xenogeneic infections was found.
166 tested this hypothesis in a human-into-mouse xenogeneic islet transplant model and validated the conc
167                            In a rat-to-mouse xenogeneic islet transplant model, we show that rat ECDI
168 nal requirements for tolerance induction for xenogeneic islet transplantation using donor ECDI-SPs.
169 trategy for tolerance induction for clinical xenogeneic islet transplantation.
170                                              Xenogeneic islets are susceptible to complement-mediated
171                                              Xenogeneic islets implanted in nonimmunosuppressed rats
172 nologic challenges facing transplantation of xenogeneic islets, and the concerns regarding transmissi
173 mechanisms of post-transplant proteinuria in xenogeneic kidney transplantation and a potential strate
174 d the early development of proteinuria after xenogeneic kidney transplantation in baboons.
175 s combinations, its role in the rejection of xenogeneic marrow engraftment is unknown.
176 is to investigate the effect of filling with xenogeneic material the postextractive sockets of two su
177 results suggest that indirect recognition of xenogeneic MHC antigen plays a predominant role in graft
178 cells elicit a vigorous response to allo- or xenogeneic MHC class I molecules.
179          At present, it is not clear whether xenogeneic MHC molecules are recognized by T cells direc
180 survival of T cells positively selected by a xenogeneic MHC, as well as incomplete intrathymic deleti
181 ed decreased signal intensity not only for a xenogeneic mismatch in species but, surprisingly, also f
182                           Human anti-porcine xenogeneic MLRs were blocked by CTLA4IgG4, but only mini
183 vitro, as well as engraftment potential in a xenogeneic model after partial myeloablation.
184 ited antileukemic activity in vivo against a xenogeneic model of disseminated AML.
185 t efficiency have been explored in a primate xenogeneic model of in utero hematopoietic stem cell tra
186 the induction of tolerance in the discordant xenogeneic model of pig-to-rodent thymic transplantation
187 ferent cellular mechanisms in allogeneic and xenogeneic model systems.
188                                       In the xenogeneic model, we quantified islet transplant exosome
189 profile of human HSC engraftment in a living xenogeneic model.
190 r differentiation of the human cells in this xenogeneic model.
191                               Moreover, in a xenogeneic mouse model of breast carcinoma, in vivo trea
192 ablished from EBV-infected B-cell lines in a xenogeneic mouse model of PTLD.
193 on in the presence of immunosuppression in a xenogeneic mouse model.
194 f HER2/neu-positive human breast tumors in a xenogeneic mouse model.
195                                              Xenogeneic mouse models are broadly used to study human
196                                          Two xenogeneic mouse models bearing intracranial human GBMs
197 his study reports the establishment of fully xenogeneic mouse-->rat multilineage chimeras and evaluat
198                                        Fully xenogeneic multilineage bone marrow chimerism was produc
199 sus-leukemia (GVL) effects in allogeneic and xenogeneic murine GVHD models.
200  T-cell function is severely impaired in the xenogeneic murine microenvironment.
201 further genetic modification of the pig, and xenogeneic NK cell recognition and activation may be inh
202 irus (EBV)-driven human B-cell lymphoma in a xenogeneic NOD/SCID/IL2rg(null) mouse model.
203 of JAM-C in homing of human B cells, using a xenogeneic nonobese diabetic/severe combined immunodefic
204 of T cells (and T cell subsets) after either xenogeneic or allogeneic activation in vitro or in vivo.
205  issue because the ability to implant either xenogeneic or allogeneic cells would greatly enhance the
206 ornea upon grafting to LSC-deficient mice in xenogeneic or syngeneic transplantation models.
207 tiple rounds of stimulation with allogeneic, xenogeneic, or antigen-pulsed autologous antigen-present
208  Immunization of mice with plasmids encoding xenogeneic orthologues of tumor differentiation antigens
209       Expression of HLA-G on PAECs protected xenogeneic PAECs against human polyclonal NK cell-mediat
210 one Ceropithecus aethiops) were treated with xenogeneic pancreatic islets (Macaca mulatta).
211 uch as eptifibatide, interfere directly with xenogeneic PBPC-platelet interactions and may further am
212 bile acids in patient serum increases during xenogeneic perfusion for unknown reasons.
213                                              Xenogeneic peripheral blood chimerism was assessed after
214 methods for induction of immune tolerance to xenogeneic pig antigens.
215  prolong allogeneic islet graft survival and xenogeneic pig islet graft survival in diabetic NOD mice
216 prolongs allogeneic islet graft survival and xenogeneic pig islet graft survival in diabetic NOD mice
217                             Highly disparate xenogeneic pig skin graft tolerance and efficient repopu
218                             Highly disparate xenogeneic pig skin graft tolerance can be achieved by g
219 een with either allogeneic (rat-into-rat) or xenogeneic (pig-into-rat) transplants over 28 days, comp
220            A maternal immune response to the xenogeneic placental antigen was shown by the presence o
221 d ASGR1 expression as well as ASGR1-mediated xenogeneic platelet phagocytosis in vitro and ex vivo on
222 tiated cell lines are capable of recognizing xenogeneic porcine aortic endothelial cells in a calcium
223 rge-animal model raises the possibility that xenogeneic porcine islet tissue will also survive in hum
224 is potent enough to prevent the rejection of xenogeneic porcine islets in a large-animal model.
225 CD4 T cells are specifically tolerant of the xenogeneic porcine thymus donor and the recipient, but a
226 ll-depleted, thymectomized mice grafted with xenogeneic porcine thymus tissue.
227                              However, in the xenogeneic rat-to-mouse combination, additional anti-Thy
228 he hypothesis that porcine sialoadhesin is a xenogeneic receptor that mediates porcine macrophage bin
229 poietic cell engraftment in highly disparate xenogeneic recipients remains unclear.
230 swine-specific tolerance in widely disparate xenogeneic recipients, this study aimed to achieve long-
231 sed regimen was not effective for preventing xenogeneic rejection.
232 l ignorance and experience largely mitigated xenogeneic rejection.
233 ever, the immunogenicity of cells expressing xenogeneic reporter constructs limits their survival and
234 egs may be required to suppress the stronger xenogeneic response.
235  CD4 T cells and the indirect pathway in the xenogeneic response.
236               Both discordant and concordant xenogeneic responses are dominated by humoral immunity.
237 uTreg) suppress CD4+ T cell-mediated antipig xenogeneic responses in vitro and might therefore be use
238 fference between human T cell allogeneic and xenogeneic responses in vivo.
239                                              Xenogeneic responses were unique in the continued expres
240 ccommodation has been widely investigated in xenogeneic responses.
241 repared from monocytes ex vivo without using xenogeneic serum and may be used for immunotherapy.
242       As a consequence, thymopoiesis in this xenogeneic setting began by weeks 4-6, peaked at mo 3, a
243 derstanding the biochemistry of H-NS and how xenogeneic silencing affects bacterial evolution.
244 standing of the mechanisms and importance of xenogeneic silencing and counter-silencing in the succes
245                                              Xenogeneic silencing of horizontally-acquired genes by H
246                                Most notably, xenogeneic silencing proteins bind incoming DNA that has
247 ession of foreign DNA in a process known as 'xenogeneic silencing.' Counter-silencing by a variety of
248 kin did not lead to accelerated rejection of xenogeneic skin.
249 opoietic engraftment across highly disparate xenogeneic species barriers poses a major obstacle to ex
250 ing T cell tolerance across highly disparate xenogeneic species barriers.
251 ant in the rejection of solid organs in some xenogeneic species combinations, its role in the rejecti
252 orcine donor responses in a highly disparate xenogeneic species.
253      This could present major limitations to xenogeneic stem cell transplantation as an approach to t
254  use of homologous stem cells, allogeneic or xenogeneic stem cells have been studied extensively in e
255 ated inflammatory reaction to allogeneic and xenogeneic stem cells may elicit a spectrum of effects,
256 response that is exaggerated with the use of xenogeneic stem cells.
257 ming comparing activation with allogeneic or xenogeneic stimulators.
258 fluence T cell repertoire in response to the xenogeneic stimulus.
259 n leukocyte antigen (HLA) antibodies against xenogeneic swine leukocyte antigen (SLA) antigens.
260 well as the nature of Th unresponsiveness to xenogeneic (swine) antigens induced by Ts.
261                                      Using a xenogeneic system, here we define the bioenergetic chang
262                                      In this xenogeneic system, human mesenchymal stem cells engrafte
263                                 However, the xenogeneic T cell precursor frequency was found to be ma
264 litates metastasis in both the syngeneic and xenogeneic (T and B lymphocyte deficient) systems.
265 ted with an increased spontaneous killing of xenogeneic target cells.
266 2-Dd, might display public specificities for xenogeneic target structures.
267 tudies suggest that mouse NK cells recognize xenogeneic targets in a strain-specific manner, implicat
268 autologous fibroblasts and rVVenv-expressing xenogeneic targets similarly, suggesting a lack of genet
269 ive selection is mediated exclusively by the xenogeneic thymic MHC.
270  Our results support the interpretation that xenogeneic thymic transplantation is a feasible strategy
271 normal mice usually remain healthy following xenogeneic thymic transplantation, thymus-grafted congen
272                           Transplantation of xenogeneic thymus tissue allows xenograft tolerance indu
273                                              Xenogeneic thymus transplantation is an effective approa
274                              The survival of xenogeneic tissue in the absence of immunosuppression in
275                Mice were implanted s.c. with xenogeneic tissue, syngeneic tissue, or SIS, and the gra
276 ra-abdominal testis supports the survival of xenogeneic tissue.
277                                      Because xenogeneic tissues are subject to vigorous immune reject
278                                              Xenogeneic tissues induce vigorous T cell immunity, refl
279 haracterize further the cellular response to xenogeneic tissues, we used the intracellular fluorescen
280                CD4 T-cell reconstitution and xenogeneic tolerance is achieved in T cell-depleted, thy
281 econstitute mouse CD4+ T cells and to induce xenogeneic tolerance to donor pig skin grafts.
282 LIV in the mediastinum, suggesting that full xenogeneic tolerance was not achieved in euthymic mice.
283 t before syngeneic, suboptimal syngeneic, or xenogeneic transplant exhibited superior function compar
284 ma and ascites formation in an athymic mouse xenogeneic transplant model of ovarian cancer.
285 rent research efforts in both allogeneic and xenogeneic transplantation are presented and discussed.
286 ed from the islets of the pancreas can cross xenogeneic transplantation immune barriers, induce tissu
287                               In conclusion, xenogeneic transplantation of human PBSCs into NOD/SCID
288 lls, tissues, and organs after allogeneic or xenogeneic transplantation.
289  and 3) models of syngeneic, allogeneic, and xenogeneic transplantation.
290 t preservation in syngeneic, allogeneic, and xenogeneic transplantation.
291  of T cell-mediated immune responses against xenogeneic transplants.
292                            The expression of xenogeneic TRIM5alpha proteins can restrict infection in
293                  The results showed that the xenogeneic tumors can grow and metastasize.
294                           The eradication of xenogeneic tumors in a murine environment shows that the
295                                 Rejection of xenogeneic tumors was also T-cell dependent as demonstra
296 peutic efficacy in mice with RL cell-derived xenogeneic tumors.
297 luenza virus type 1 (Sendai virus [SV]) as a xenogeneic vector to deliver the G glycoprotein of RSV.
298                               Differences in xenogeneic versus allogeneic activation profiles exist t
299 linical efficacy of synthetic, allogeneic or xenogeneic vessels has been limited by thrombosis, rejec
300 llogeneic BALB/c or phylogenetically related xenogeneic WF rat stimulator cells while having undetect

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