ライフサイエンスコーパス: interphotoreceptor

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 was a significant reduction of sVLDLR in the interphotoreceptor matrix (IPM) in the laser-induced CNV

6 The interphotoreceptor matrix (IPM) is a specialized extrace

7 The interphotoreceptor matrix (IPM) is a specialized extrace

8 we explore the association of IRBP with the interphotoreceptor matrix (IPM) of cones vs. rods in con

9 hout the retina, particularly in the ILM and interphotoreceptor matrix (IPM) with 6-O-sulfated CS als

10 l surface into a specialized glycocalyx, the interphotoreceptor matrix (IPM), which contains hyaluron

11 unded by an extracellular matrix, called the interphotoreceptor matrix (IPM).

12 s the major soluble protein component of the interphotoreceptor matrix (IPM).

13 d surrounded by an extracellular matrix, the interphotoreceptor matrix (IPM).

14 st prominent 147-150-kDa band present in the interphotoreceptor matrix and is the gene product of IMP

15 mor necrosis factor-alpha (TNF-alpha) in the interphotoreceptor matrix and retinas of Irbp(-/-) mice

16 We show that PEDF extractions from the interphotoreceptor matrix are more efficient with increa

17 or cell death and reversed the disruption of interphotoreceptor matrix as well as the redistribution

18 ely expressed in the rods and present in the interphotoreceptor matrix at the interface between the R

19 zation of SPACRCAN protein in the developing interphotoreceptor matrix by Postnatal day 5 (P5) and in

20 in XLPRA dogs, implying that alterations in interphotoreceptor matrix composition precede retinal de

21 igen and peanut agglutinin labeling for cone interphotoreceptor matrix domains suggested that the pho

22 Removal of soluble materials in the interphotoreceptor matrix facilitated detection of RPGR

23 presenting migration of RPE cell clusters or interphotoreceptor matrix from the RB are potential biom

24 Rapid transport of retinoids across the interphotoreceptor matrix is a critical part of the visu

25 The interphotoreceptor matrix is a unique extracellular comp

26 lar increase in bFGF immunoreactivity in the interphotoreceptor matrix is also apparent.

27 The transport of retinoids in the interphotoreceptor matrix is believed to be mediated by

28 50-kDa glycoprotein present in the insoluble interphotoreceptor matrix of the human retina.

29 f RPE-J cells during phagocytosis and in the interphotoreceptor matrix of the mouse retina during the

30 ycan that is present in the pineal gland and interphotoreceptor matrix of the retina.

31 The "pooling" of PEDF within the interphotoreceptor matrix places this molecule in a prim

32 Interphotoreceptor matrix proteoglycan 1 and 2 (IMPG1 an

33 Biallelic mutations in interphotoreceptor matrix proteoglycan 2 (IMPG2) in huma

34 aptosome-associated protein 25 (SNAP25), and interphotoreceptor matrix proteoglycan 2 (IMPG2), rapidl

35 n that has been previously documented in the interphotoreceptor matrix surrounding cones.

36 Interphotoreceptor matrix surrounding the connecting cil

37 duce sufficient all-trans retinol within the interphotoreceptor matrix to explain the potentiation ef

38 Accumulation of shed OSs in the interphotoreceptor matrix was observed by transmission e

39 esized by photoreceptors is localized to the interphotoreceptor matrix where it surrounds both rods a

40 medium of retinal pigment epithelial cells, interphotoreceptor matrix, and mouse plasma, indicating

41 be involved in organization of the insoluble interphotoreceptor matrix, particularly as SPACRCAN is t

42 sociation of RPE with photoreceptors and the interphotoreceptor matrix, postnatal expansion of the RP

43 The protein is restricted to the interphotoreceptor matrix, with lesser amounts in the pi

44 ds peanut agglutinin and is localized to the interphotoreceptor matrix.

45 ular scaffold, which comprises the insoluble interphotoreceptor matrix.

46 is molecule is an important component of the interphotoreceptor matrix.

47 disc morphogenesis, which accumulate in the interphotoreceptor matrix.

48 ity in cells located in the proximity of the interphotoreceptor matrix.

49 oretinitis (EAU) by active immunization with interphotoreceptor retinal binding protein or adoptive t

50 In this study, we show that an interphotoreceptor retinal-binding protein peptide consi

51 at uveitogenic T cell lines specific for the interphotoreceptor retinal-binding protein peptide, R16,

52 ient (GKO) mice with the uveitogenic protein interphotoreceptor retinoid binding protein (IRBP) and c

53 s retinol removal by the lipophilic carriers interphotoreceptor retinoid binding protein (IRBP) and s

54 he retinal autoantigens S-antigen (S-Ag) and interphotoreceptor retinoid binding protein (IRBP) can i

55 Interphotoreceptor retinoid binding protein (IRBP) is a

56 Interphotoreceptor retinoid binding protein (IRBP) is th

57 B10.RIII mice were immunized with human interphotoreceptor retinoid binding protein (IRBP) pepti

58 hLOP1 affected CRX transactivation, a 120-bp interphotoreceptor retinoid binding protein (IRBP) promo

59 Interphotoreceptor retinoid binding protein (IRBP), a pu

60 ediated disease induced by immunization with interphotoreceptor retinoid binding protein (IRBP).

61 EAU induced with the uveitogenic retinal Ag interphotoreceptor retinoid binding protein (IRBP).

62 n 1 of the single-copy nuclear gene known as interphotoreceptor retinoid binding protein (IRBP).

63 s induced in B10RIII mice by immunization of interphotoreceptor retinoid binding protein (IRBP; pepti

64 Given that the interphotoreceptor retinoid binding protein gene is a si

65 lyze DNA sequences for part of exon 1 of the interphotoreceptor retinoid binding protein gene, includ

66 mice immunized with the retinal autoantigen interphotoreceptor retinoid binding protein in CFA and t

67 mmune uveitis, induced in B10.RIII mice with interphotoreceptor retinoid binding protein or with its

68 and cone photoreceptors driven by the human interphotoreceptor retinoid binding protein promoter was

69 severe EAU and strong cellular responses to interphotoreceptor retinoid binding protein, comparable

70 in mice by immunization with the retinal Ag interphotoreceptor retinoid binding protein.

71 genes, including the opsins and the gene for interphotoreceptor retinoid binding protein.

72 zation with retinal proteins such as S-Ag or interphotoreceptor retinoid binding protein.

73 R-null (ARKO) mice were immunized with human interphotoreceptor retinoid-binding peptide (hIRPB-1-20)

74 Lewis rats were immunized with bovine interphotoreceptor retinoid-binding peptide (IRBP) to de

75 pressing hen egg lysozyme, under the retinal interphotoreceptor retinoid-binding promoter, and a hen

76 at immunization with the uveitogenic peptide interphotoreceptor retinoid-binding protein (IRBP) 1-20

77 that the commonly used uveitogenic peptide, interphotoreceptor retinoid-binding protein (IRBP) 1-20,

78 We have previously reported that IL-17(+) interphotoreceptor retinoid-binding protein (IRBP) 161-1

79 immunization with retinal antigens, such as interphotoreceptor retinoid-binding protein (IRBP) and a

80 Interphotoreceptor retinoid-binding protein (IRBP) appea

81 , immunization of naive rats with autologous interphotoreceptor retinoid-binding protein (IRBP) fails

82 Cones are critically dependent on interphotoreceptor retinoid-binding protein (IRBP) for r

83 Interphotoreceptor retinoid-binding protein (IRBP) has b

84 Interphotoreceptor retinoid-binding protein (IRBP) has b

85 from these cells and the influence that the interphotoreceptor retinoid-binding protein (IRBP) has o

86 traperitoneally [IP]) from day 0, the day of interphotoreceptor retinoid-binding protein (IRBP) immun

87 y immunization with the retinal antigen (Ag) interphotoreceptor retinoid-binding protein (IRBP) in co

88 ed DNA to express the uveitogenic retinal Ag interphotoreceptor retinoid-binding protein (IRBP) in th

89 Interphotoreceptor retinoid-binding protein (IRBP) is a

90 Interphotoreceptor retinoid-binding protein (IRBP) is a

91 Interphotoreceptor retinoid-binding protein (IRBP) is a

92 The interphotoreceptor retinoid-binding protein (IRBP) is a

93 Interphotoreceptor retinoid-binding protein (IRBP) is a

94 Interphotoreceptor retinoid-binding protein (IRBP) is an

95 It has been proposed that the interphotoreceptor retinoid-binding protein (IRBP) is es

96 Because interphotoreceptor retinoid-binding protein (IRBP) is ex

97 Interphotoreceptor retinoid-binding protein (IRBP) is pr

98 Interphotoreceptor retinoid-binding protein (IRBP) is th

99 on, B10.A mice were immunized with 50 microg interphotoreceptor retinoid-binding protein (IRBP) mixed

100 e cone cohort, as indicated by expression of interphotoreceptor retinoid-binding protein (IRBP) mRNA,

101 ion by immunization with the retinal antigen interphotoreceptor retinoid-binding protein (IRBP) or by

102 e uveitis (EAU) induced by immunization with interphotoreceptor retinoid-binding protein (IRBP) or by

103 similar to those reported in mice that lack interphotoreceptor retinoid-binding protein (IRBP) or ce

104 ko mice that were or were not immunized with interphotoreceptor retinoid-binding protein (IRBP) pepti

105 RACs were isolated and cocultured with interphotoreceptor retinoid-binding protein (IRBP) pepti

106 tinal soluble proteins such as S-antigen and interphotoreceptor retinoid-binding protein (IRBP) play

107 is not clear what role, if any, the abundant interphotoreceptor retinoid-binding protein (IRBP) presu

108 er system coupled to either the rhodopsin or interphotoreceptor retinoid-binding protein (IRBP) promo

109 Interphotoreceptor retinoid-binding protein (IRBP) secre

110 Interphotoreceptor retinoid-binding protein (IRBP) secre

111 s rats, peptide 273-283 (TWEGSGVLPCV) of rat interphotoreceptor retinoid-binding protein (IRBP) serve

112 lls from mice given a uveitogenic regimen of interphotoreceptor retinoid-binding protein (IRBP) were

113 (DCs) with an increased ability to activate interphotoreceptor retinoid-binding protein (IRBP)(1-20)

114 tor matrix is believed to be mediated by the interphotoreceptor retinoid-binding protein (IRBP), a pr

115 elop EAU in response to the retinal antigen, interphotoreceptor retinoid-binding protein (IRBP), and

116 lines containing different promoters (murine interphotoreceptor retinoid-binding protein (IRBP), huma

117 r the Aire-dependent tissue-specific antigen interphotoreceptor retinoid-binding protein (IRBP), in t

118 tis induced in mice with the retinal antigen interphotoreceptor retinoid-binding protein (IRBP), is c

119 lipopolysaccharide (LPS) or S-antigen and to interphotoreceptor retinoid-binding protein (IRBP), myel

120 ory T cells specific to retinal autoantigen, interphotoreceptor retinoid-binding protein (IRBP), relo

121 Interphotoreceptor retinoid-binding protein (IRBP), whic

122 We show that in vitro activation of interphotoreceptor retinoid-binding protein (IRBP)-speci

123 IL-17(+) T cells were present in CD4 and CD8 interphotoreceptor retinoid-binding protein (IRBP)-speci

124 r human uveitis induced with the uveitogenic interphotoreceptor retinoid-binding protein (IRBP).

125 Susceptible C57BL/6 mice were immunized with interphotoreceptor retinoid-binding protein (IRBP).

126 retinitis after active immunization with the interphotoreceptor retinoid-binding protein (IRBP).

127 s induced in B10.A mice by immunization with interphotoreceptor retinoid-binding protein (IRBP).

128 s due to T cell reactivity to Aire-regulated interphotoreceptor retinoid-binding protein (IRBP).

129 and wild-type (WT) mice by immunization with interphotoreceptor retinoid-binding protein (IRBP).

130 f thymic expression of a single eye antigen, interphotoreceptor retinoid-binding protein (IRBP).

131 ufficiency of a uveitogenic retinal antigen, interphotoreceptor retinoid-binding protein (IRBP).

132 mice immunized with an uveitogenic peptide, interphotoreceptor retinoid-binding protein (IRBP)1-20,

133 CD4 T cells prepared from naive or interphotoreceptor retinoid-binding protein (IRBP)1-20-i

134 vertebrate and invertebrate vision hinges on interphotoreceptor retinoid-binding protein (IRBP, also

135 10-RIII mice before the adoptive transfer of interphotoreceptor retinoid-binding protein (IRBP; an oc

136 ated the effect of intracameral injection of interphotoreceptor retinoid-binding protein (IRPB) pepti

137 Among visual cycle proteins, interphotoreceptor retinoid-binding protein and stimulat

138 with a uveitogenic regimen of the retinal Ag interphotoreceptor retinoid-binding protein could be pro

139 e abundance of mRNA encoding actin, G3PDH or interphotoreceptor retinoid-binding protein did not chan

140 n two strains of wild-type mice by modifying interphotoreceptor retinoid-binding protein dose and pep

141 in mice by immunization with the retinal Ag interphotoreceptor retinoid-binding protein in CFA is dr

142 , or TLR9 were immunized with the retinal Ag interphotoreceptor retinoid-binding protein in CFA, and

143 ptively transferred into mice immunized with interphotoreceptor retinoid-binding protein in complete

144 arget-6 (ESAT-6) or the retinal autoantigen, interphotoreceptor retinoid-binding protein peptide (pIR

145 n B10.RIII mice by subcutaneous injection of interphotoreceptor retinoid-binding protein peptide 161-

146 eitis induced by immunization with the human interphotoreceptor retinoid-binding protein peptides 1-2

147 have observed that the adoptive transfer of interphotoreceptor retinoid-binding protein residues 117

148 ophasic disease induced by immunization with interphotoreceptor retinoid-binding protein residues 117

149 Subsequent adaptive responses to interphotoreceptor retinoid-binding protein showed evide

150 mice immunized with a uveitogenic regimen of interphotoreceptor retinoid-binding protein were treated

151 other photoreceptor cell-specific proteins (interphotoreceptor retinoid-binding protein, beta-phosph

152 genic peptide, IRBP161-180, derived from the interphotoreceptor retinoid-binding protein, or by adopt

153 a uveitogenic regimen of the retinal antigen interphotoreceptor retinoid-binding protein, treated wit

154 mice immunized with the uveitogenic peptide interphotoreceptor retinoid-binding protein, while enhan

155 cells had little effect on the activation of interphotoreceptor retinoid-binding protein-specific alp

156 leading to decreased activation of IL-17(+) interphotoreceptor retinoid-binding protein-specific T c

157 Our results showed that CD8 interphotoreceptor retinoid-binding protein-specific T c

158 Interphotoreceptor retinoid-binding protein-specific T c

159 miR-223-3p was significantly up-regulated in interphotoreceptor retinoid-binding protein-specific T(h

160 Importantly, IL-10-Tg mice that received interphotoreceptor retinoid-binding protein-specific uve

161 Adoptive transfer of activated interphotoreceptor retinoid-binding protein-specific uve

162 eceptor-specific promoters for rhodopsin and interphotoreceptor retinoid-binding protein.

163 mune uveitis, B10.A mice were immunized with interphotoreceptor retinoid-binding protein.

164 llular responses after immunization with the interphotoreceptor retinoid-binding protein.

165 with a uveitogenic regimen of the retinal Ag interphotoreceptor retinoid-binding protein.

166 ith a uveitogenic regimen of the retinal Ag, interphotoreceptor retinoid-binding protein.

167 EAU and had unaltered adaptive responses to interphotoreceptor retinoid-binding protein.

168 r matrix (IPM) a 124-kDa glycoprotein termed interphotoreceptor retinoid-binding protein.

169 -), or CD4-STAT3KO mice by immunization with interphotoreceptor retinoid-binding protein/complete Fre

170 6) mice were immunized with the uveitogenic, interphotoreceptor retinoid-binding protein1-20 peptide

171 sion profiles of heme oxygenase-1 (HO-1) and interphotoreceptor retinol binding protein (IRBP) were d

172 nalysis of retinal heme oxygenase (HO)-1 and interphotoreceptor retinol binding protein (IRBP).

173 (SV) 40 T antigen under control of the human interphotoreceptor retinol-binding protein (IRBP) promot

174 Rats with EAU induced by immunization with interphotoreceptor retinol-binding protein 1177-1191 pep

175 Both the vesicular profiles in the interphotoreceptor space and the inner segment plasma me