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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
3      Xenopus rods and cones secrete into the interphotoreceptor matrix (IPM) a 124-kDa glycoprotein t
4                                          The interphotoreceptor matrix (IPM) contains an array of pro
5                                          The interphotoreceptor matrix (IPM) is a specialized extrace
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
9 s the major soluble protein component of the interphotoreceptor matrix (IPM).
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
12       We show that PEDF extractions from the interphotoreceptor matrix are more efficient with increa
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
18          Removal of soluble materials in the interphotoreceptor matrix facilitated detection of RPGR
19      Rapid transport of retinoids across the interphotoreceptor matrix is a critical part of the visu
20                                          The interphotoreceptor matrix is a unique extracellular comp
21 lar increase in bFGF immunoreactivity in the interphotoreceptor matrix is also apparent.
22            The transport of retinoids in the interphotoreceptor matrix is believed to be mediated by
23 50-kDa glycoprotein present in the insoluble interphotoreceptor matrix of the human retina.
24 f RPE-J cells during phagocytosis and in the interphotoreceptor matrix of the mouse retina during the
25 ycan that is present in the pineal gland and interphotoreceptor matrix of the retina.
26             The "pooling" of PEDF within the interphotoreceptor matrix places this molecule in a prim
27 n that has been previously documented in the interphotoreceptor matrix surrounding cones.
28                                              Interphotoreceptor matrix surrounding the connecting cil
29 duce sufficient all-trans retinol within the interphotoreceptor matrix to explain the potentiation ef
30              Accumulation of shed OSs in the interphotoreceptor matrix was observed by transmission e
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
35             The protein is restricted to the interphotoreceptor matrix, with lesser amounts in the pi
36 ds peanut agglutinin and is localized to the interphotoreceptor matrix.
37 ular scaffold, which comprises the insoluble interphotoreceptor matrix.
38 is molecule is an important component of the interphotoreceptor matrix.
39 ity in cells located in the proximity of the interphotoreceptor matrix.
40 oretinitis (EAU) by active immunization with interphotoreceptor retinal binding protein or adoptive t
41               In this study, we show that an interphotoreceptor retinal-binding protein peptide consi
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
46                                              Interphotoreceptor retinoid binding protein (IRBP) is a
47                                              Interphotoreceptor retinoid binding protein (IRBP) is th
48      B10.RIII mice were immunized with human interphotoreceptor retinoid binding protein (IRBP) pepti
49 hLOP1 affected CRX transactivation, a 120-bp interphotoreceptor retinoid binding protein (IRBP) promo
50                                              Interphotoreceptor retinoid binding protein (IRBP), a pu
51 ediated disease induced by immunization with interphotoreceptor retinoid binding protein (IRBP).
52  EAU induced with the uveitogenic retinal Ag interphotoreceptor retinoid binding protein (IRBP).
53 n 1 of the single-copy nuclear gene known as interphotoreceptor retinoid binding protein (IRBP).
54 s induced in B10RIII mice by immunization of interphotoreceptor retinoid binding protein (IRBP; pepti
55                               Given that the interphotoreceptor retinoid binding protein gene is a si
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
61  in mice by immunization with the retinal Ag interphotoreceptor retinoid binding protein.
62 genes, including the opsins and the gene for interphotoreceptor retinoid binding protein.
63 zation with retinal proteins such as S-Ag or interphotoreceptor retinoid binding protein.
64 R-null (ARKO) mice were immunized with human interphotoreceptor retinoid-binding peptide (hIRPB-1-20)
65        Lewis rats were immunized with bovine interphotoreceptor retinoid-binding peptide (IRBP) to de
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
71                                              Interphotoreceptor retinoid-binding protein (IRBP) appea
72 , immunization of naive rats with autologous interphotoreceptor retinoid-binding protein (IRBP) fails
73            Cones are critically dependent on interphotoreceptor retinoid-binding protein (IRBP) for r
74                                              Interphotoreceptor retinoid-binding protein (IRBP) has b
75                                              Interphotoreceptor retinoid-binding protein (IRBP) has b
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
80                                              Interphotoreceptor retinoid-binding protein (IRBP) is a
81                                              Interphotoreceptor retinoid-binding protein (IRBP) is a
82                                              Interphotoreceptor retinoid-binding protein (IRBP) is a
83                                          The interphotoreceptor retinoid-binding protein (IRBP) is a
84                                              Interphotoreceptor retinoid-binding protein (IRBP) is an
85                It has been proposed that the interphotoreceptor retinoid-binding protein (IRBP) is es
86                                      Because interphotoreceptor retinoid-binding protein (IRBP) is ex
87                                              Interphotoreceptor retinoid-binding protein (IRBP) is pr
88                                              Interphotoreceptor retinoid-binding protein (IRBP) is 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
94       RACs were isolated and cocultured 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
98                                              Interphotoreceptor retinoid-binding protein (IRBP) secre
99                                              Interphotoreceptor retinoid-binding protein (IRBP) secre
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
109                                              Interphotoreceptor retinoid-binding protein (IRBP), whic
110          We show that in vitro activation of interphotoreceptor retinoid-binding protein (IRBP)-speci
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,
120           CD4 T cells prepared from naive or interphotoreceptor retinoid-binding protein (IRBP)1-20-i
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
123                 Among visual cycle proteins, interphotoreceptor retinoid-binding protein and stimulat
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
133             Subsequent adaptive responses to interphotoreceptor retinoid-binding protein showed evide
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
141                  Our results showed that CD8 interphotoreceptor retinoid-binding protein-specific T c
142                                              Interphotoreceptor retinoid-binding protein-specific T c
143     Importantly, IL-10-Tg mice that received interphotoreceptor retinoid-binding protein-specific uve
144               Adoptive transfer of activated interphotoreceptor retinoid-binding protein-specific uve
145 eceptor-specific promoters for rhodopsin and interphotoreceptor retinoid-binding protein.
146 mune uveitis, B10.A mice were immunized with interphotoreceptor retinoid-binding protein.
147 llular responses after immunization with the interphotoreceptor retinoid-binding protein.
148 with a uveitogenic regimen of the retinal Ag interphotoreceptor retinoid-binding protein.
149 ith a uveitogenic regimen of the retinal Ag, interphotoreceptor retinoid-binding protein.
150  EAU and had unaltered adaptive responses to interphotoreceptor retinoid-binding protein.
151 r matrix (IPM) a 124-kDa glycoprotein termed interphotoreceptor retinoid-binding protein.
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
155 nalysis of retinal heme oxygenase (HO)-1 and interphotoreceptor retinol binding protein (IRBP).
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
158           Both the vesicular profiles in the interphotoreceptor space and the inner segment plasma me

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