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1 ansfer of activated T cells specific for the interphotoreceptor-binding protein (IRBP) 1-20 peptide.
2 ular retinaldehyde-binding protein (CRALBP), interphotoreceptor-binding protein (IRBP), and peanut ag
6 we explore the association of IRBP with the interphotoreceptor matrix (IPM) of cones vs. rods in con
7 hout the retina, particularly in the ILM and interphotoreceptor matrix (IPM) with 6-O-sulfated CS als
8 l surface into a specialized glycocalyx, the interphotoreceptor matrix (IPM), which contains hyaluron
10 st prominent 147-150-kDa band present in the interphotoreceptor matrix and is the gene product of IMP
11 mor necrosis factor-alpha (TNF-alpha) in the interphotoreceptor matrix and retinas of Irbp(-/-) mice
13 or cell death and reversed the disruption of interphotoreceptor matrix as well as the redistribution
14 ely expressed in the rods and present in the interphotoreceptor matrix at the interface between the R
15 zation of SPACRCAN protein in the developing interphotoreceptor matrix by Postnatal day 5 (P5) and in
16 in XLPRA dogs, implying that alterations in interphotoreceptor matrix composition precede retinal de
17 igen and peanut agglutinin labeling for cone interphotoreceptor matrix domains suggested that the pho
24 f RPE-J cells during phagocytosis and in the interphotoreceptor matrix of the mouse retina during the
29 duce sufficient all-trans retinol within the interphotoreceptor matrix to explain the potentiation ef
31 esized by photoreceptors is localized to the interphotoreceptor matrix where it surrounds both rods a
32 medium of retinal pigment epithelial cells, interphotoreceptor matrix, and mouse plasma, indicating
33 be involved in organization of the insoluble interphotoreceptor matrix, particularly as SPACRCAN is t
34 sociation of RPE with photoreceptors and the interphotoreceptor matrix, postnatal expansion of the RP
40 oretinitis (EAU) by active immunization with interphotoreceptor retinal binding protein or adoptive t
42 at uveitogenic T cell lines specific for the interphotoreceptor retinal-binding protein peptide, R16,
43 ient (GKO) mice with the uveitogenic protein interphotoreceptor retinoid binding protein (IRBP) and c
44 s retinol removal by the lipophilic carriers interphotoreceptor retinoid binding protein (IRBP) and s
45 he retinal autoantigens S-antigen (S-Ag) and interphotoreceptor retinoid binding protein (IRBP) can i
49 hLOP1 affected CRX transactivation, a 120-bp interphotoreceptor retinoid binding protein (IRBP) promo
54 s induced in B10RIII mice by immunization of interphotoreceptor retinoid binding protein (IRBP; pepti
56 lyze DNA sequences for part of exon 1 of the interphotoreceptor retinoid binding protein gene, includ
57 mice immunized with the retinal autoantigen interphotoreceptor retinoid binding protein in CFA and t
58 mmune uveitis, induced in B10.RIII mice with interphotoreceptor retinoid binding protein or with its
59 and cone photoreceptors driven by the human interphotoreceptor retinoid binding protein promoter was
60 severe EAU and strong cellular responses to interphotoreceptor retinoid binding protein, comparable
64 R-null (ARKO) mice were immunized with human interphotoreceptor retinoid-binding peptide (hIRPB-1-20)
66 pressing hen egg lysozyme, under the retinal interphotoreceptor retinoid-binding promoter, and a hen
67 at immunization with the uveitogenic peptide interphotoreceptor retinoid-binding protein (IRBP) 1-20
68 that the commonly used uveitogenic peptide, interphotoreceptor retinoid-binding protein (IRBP) 1-20,
69 We have previously reported that IL-17(+) interphotoreceptor retinoid-binding protein (IRBP) 161-1
70 immunization with retinal antigens, such as interphotoreceptor retinoid-binding protein (IRBP) and a
72 , immunization of naive rats with autologous interphotoreceptor retinoid-binding protein (IRBP) fails
76 from these cells and the influence that the interphotoreceptor retinoid-binding protein (IRBP) has o
77 traperitoneally [IP]) from day 0, the day of interphotoreceptor retinoid-binding protein (IRBP) immun
78 y immunization with the retinal antigen (Ag) interphotoreceptor retinoid-binding protein (IRBP) in co
79 ed DNA to express the uveitogenic retinal Ag interphotoreceptor retinoid-binding protein (IRBP) in th
89 on, B10.A mice were immunized with 50 microg interphotoreceptor retinoid-binding protein (IRBP) mixed
90 e cone cohort, as indicated by expression of interphotoreceptor retinoid-binding protein (IRBP) mRNA,
91 ion by immunization with the retinal antigen interphotoreceptor retinoid-binding protein (IRBP) or by
92 similar to those reported in mice that lack interphotoreceptor retinoid-binding protein (IRBP) or ce
93 ko mice that were or were not immunized with interphotoreceptor retinoid-binding protein (IRBP) pepti
95 tinal soluble proteins such as S-antigen and interphotoreceptor retinoid-binding protein (IRBP) play
96 is not clear what role, if any, the abundant interphotoreceptor retinoid-binding protein (IRBP) presu
97 er system coupled to either the rhodopsin or interphotoreceptor retinoid-binding protein (IRBP) promo
100 s rats, peptide 273-283 (TWEGSGVLPCV) of rat interphotoreceptor retinoid-binding protein (IRBP) serve
101 lls from mice given a uveitogenic regimen of interphotoreceptor retinoid-binding protein (IRBP) were
102 tor matrix is believed to be mediated by the interphotoreceptor retinoid-binding protein (IRBP), a pr
103 elop EAU in response to the retinal antigen, interphotoreceptor retinoid-binding protein (IRBP), and
104 lines containing different promoters (murine interphotoreceptor retinoid-binding protein (IRBP), huma
105 r the Aire-dependent tissue-specific antigen interphotoreceptor retinoid-binding protein (IRBP), in t
106 tis induced in mice with the retinal antigen interphotoreceptor retinoid-binding protein (IRBP), is c
107 lipopolysaccharide (LPS) or S-antigen and to interphotoreceptor retinoid-binding protein (IRBP), myel
108 ory T cells specific to retinal autoantigen, interphotoreceptor retinoid-binding protein (IRBP), relo
111 IL-17(+) T cells were present in CD4 and CD8 interphotoreceptor retinoid-binding protein (IRBP)-speci
112 r human uveitis induced with the uveitogenic interphotoreceptor retinoid-binding protein (IRBP).
113 Susceptible C57BL/6 mice were immunized with interphotoreceptor retinoid-binding protein (IRBP).
114 retinitis after active immunization with the interphotoreceptor retinoid-binding protein (IRBP).
115 s induced in B10.A mice by immunization with interphotoreceptor retinoid-binding protein (IRBP).
116 and wild-type (WT) mice by immunization with interphotoreceptor retinoid-binding protein (IRBP).
117 f thymic expression of a single eye antigen, interphotoreceptor retinoid-binding protein (IRBP).
118 ufficiency of a uveitogenic retinal antigen, interphotoreceptor retinoid-binding protein (IRBP).
119 mice immunized with an uveitogenic peptide, interphotoreceptor retinoid-binding protein (IRBP)1-20,
121 10-RIII mice before the adoptive transfer of interphotoreceptor retinoid-binding protein (IRBP; an oc
122 ated the effect of intracameral injection of interphotoreceptor retinoid-binding protein (IRPB) pepti
124 with a uveitogenic regimen of the retinal Ag interphotoreceptor retinoid-binding protein could be pro
125 e abundance of mRNA encoding actin, G3PDH or interphotoreceptor retinoid-binding protein did not chan
126 in mice by immunization with the retinal Ag interphotoreceptor retinoid-binding protein in CFA is dr
127 , or TLR9 were immunized with the retinal Ag interphotoreceptor retinoid-binding protein in CFA, and
128 ptively transferred into mice immunized with interphotoreceptor retinoid-binding protein in complete
129 n B10.RIII mice by subcutaneous injection of interphotoreceptor retinoid-binding protein peptide 161-
130 eitis induced by immunization with the human interphotoreceptor retinoid-binding protein peptides 1-2
131 have observed that the adoptive transfer of interphotoreceptor retinoid-binding protein residues 117
132 ophasic disease induced by immunization with interphotoreceptor retinoid-binding protein residues 117
134 mice immunized with a uveitogenic regimen of interphotoreceptor retinoid-binding protein were treated
135 other photoreceptor cell-specific proteins (interphotoreceptor retinoid-binding protein, beta-phosph
136 genic peptide, IRBP161-180, derived from the interphotoreceptor retinoid-binding protein, or by adopt
137 a uveitogenic regimen of the retinal antigen interphotoreceptor retinoid-binding protein, treated wit
138 mice immunized with the uveitogenic peptide interphotoreceptor retinoid-binding protein, while enhan
139 cells had little effect on the activation of interphotoreceptor retinoid-binding protein-specific alp
140 leading to decreased activation of IL-17(+) interphotoreceptor retinoid-binding protein-specific T c
143 Importantly, IL-10-Tg mice that received interphotoreceptor retinoid-binding protein-specific uve
152 -), or CD4-STAT3KO mice by immunization with interphotoreceptor retinoid-binding protein/complete Fre
153 6) mice were immunized with the uveitogenic, interphotoreceptor retinoid-binding protein1-20 peptide
154 sion profiles of heme oxygenase-1 (HO-1) and interphotoreceptor retinol binding protein (IRBP) were d
156 (SV) 40 T antigen under control of the human interphotoreceptor retinol-binding protein (IRBP) promot
157 Rats with EAU induced by immunization with interphotoreceptor retinol-binding protein 1177-1191 pep
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