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1 r MSCs suggest that MSCs may not actually be immune privileged.
2 protective effects, and are considered to be immune privileged.
3 brain parenchyma, a site that is considered immune privileged.
4 cells derived from autologous iPSCs will be immune-privileged.
6 oscientists, we are taught that the brain is immune privileged and thus unlikely to be affected by th
9 neurons in the healthy brain were considered immune-privileged because they did not appear to express
10 their multipotent differentiation, and their immune-privileged behavior, reveals, at least in part, t
12 of Fas ligand (FasL) renders certain tissues immune privileged, but its expression in other tissues c
13 Neonatal porcine Sertoli cells (NPSC) are immune privileged cells showing innate phagocytic and an
15 plore the tumor-specific CTL response in the immune-privileged central nervous system using P511 mast
16 Vigorous immune responses are induced in the immune privileged CNS by injury and disease, but the mol
21 ese data refute the tenet that the cornea is immune privileged due to lack of resident lymphoreticula
23 al cells contributes to the generation of an immune-privileged environment at the maternal-fetal inte
24 d SCID mice, could survive in the relatively immune-privileged environment of dialysis membrane chamb
26 Although intraocular tumors reside in an immune-privileged environment, T cells can circumvent im
30 ta2-treated Ag-pulsed APC mimic APC from the immune privileged eye, and provide signals that generate
31 required to initiate inflammation within the immune privileged eye, as compared with nonprivileged si
32 om primary uveal melanomas that arise in the immune-privileged eye, prime and boost IFNgamma-secretin
36 ration of tumor antigens within a relatively immune privileged location present serious problems for
37 wn that it is very difficult to abrogate the immune privileged mechanism called anterior chamber-asso
40 ring maturation that could contribute to the immune-privileged nature of the CNS or potentially influ
41 rowth, played a key role in formation of the immune-privileged niche, and predicted poor prognosis in
44 AP-1 in the recruitment of leukocytes to the immune-privileged ocular tissues during acute inflammati
48 Although the inner ear has been known as an immune-privileged organ, there is emerging evidence indi
50 nfected macrophages or if ranavirus exploits immune privileged organs, such as the brain, in order to
51 s ligand (CD95L) inhibits T cell function in immune-privileged organs such as the eye and testis, yet
55 e photoreceptors and synaptic regions of the immune-privileged retina implies a role in visual transm
57 One clinical example of the function of an immune privileged site is the success of human corneal t
60 esence of parenchymal cells from the eye (an immune privileged site) express B7-2 in a manner that eq
62 Although intraocular tumors reside in an immune privileged site, some tumors are rejected nonethe
64 sult implies that the subretinal space is an immune-privileged site and a favorable site for gene tra
65 notherapy because primary tumors arise in an immune-privileged site and may express antigens to which
67 e barriers in the mammalian body, creates an immune-privileged site for postmeiotic spermatid develop
69 nt infection in the seminiferous tubules, an immune-privileged site in the testis protected by the bl
71 ent of systemic tolerance associated with an immune-privileged site suggests a mechanism involving NK
72 cades the brain has been considered to be an immune-privileged site that excludes circulating cells f
73 Although intraocular tumors reside in an immune-privileged site where immune responses are suppre
75 tudy documents that tumors growing within an immune-privileged site within the eye develop a tumor es
77 n be elicited by introducing antigen into an immune-privileged site, such as the eye, or directly int
85 f the PD-1:PD-L1 interaction in creating an "immune-privileged" site for initial viral infection and
87 ter the hypothesis that B cell follicles are immune privileged sites and suggest that strategies to a
88 rticipation in inflammatory responses within immune privileged sites such as the brain and eye is les
89 The induction of peripheral tolerance via immune privileged sites such as the eye requires splenic
92 ic infections in humans, mainly localized in immune privileged sites, such as the brain and the eye.
95 Diffuse large B-cell lymphoma arising in immune-privileged sites (eg, the central nervous system)
96 nance of tolerance, as Fas ligand can create immune-privileged sites and prevent graft rejection by i
97 if somatic stem-cell niches more broadly are immune-privileged sites by examining the haematopoietic
99 , suggesting that tumor cells originating in immune-privileged sites may have enhanced capacity for i
102 in view of the immune deviation existing in immune-privileged sites such as the brain and eye, where
103 g how EBOV disseminates into and persists in immune-privileged sites was impossible due to the absenc
104 nous lectin expressed in lymphoid organs and immune-privileged sites, induces death of human and muri
105 se the brain and testis are considered to be immune-privileged sites, the expression pattern of cdr2
106 are immune-suppressive environments, called immune-privileged sites, where multiple mechanisms coope
111 virus can persist in survivors for months in immune-privileged sites; however, viral relapse causing
112 ccommodate and even differentiate in the non-immune-privileged space beneath the kidney capsule.
113 he accessibility for routine surgery and its immune privileged state make the eye an ideal target for
116 tures of the corneal graft contribute to its immune privileged status: (a) absence of donor-derived,
118 ged self during healing and suggest that the immune-privileged status of the CNS may contribute to fa
120 t even though the retina is often considered immune-privileged, suppression of host immune-mediated c
121 long been reported to be hypoimmunogenic or 'immune privileged'; this property is thought to enable M
123 as much to the qualities of the graft as an immune-privileged tissue as to the qualities of the eye
124 tinal pigment epithelium (RPE) behaves as an immune-privileged tissue when transplanted extraocularly
126 sed on the cell surface of many tumor cells, immune-privileged tissues and activated lymphocytes.
127 er, CX3CR1(hi) patrolling monocytes serve as immune-privileged vehicles to transport MCMV via the blo
128 rast to the notion that ES-derived cells are immune-privileged, we show in this study that NK cells f
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