ライフサイエンスコーパス: outer plexiform layer

1 s in the retina, PDGF-D is restricted to the outer plexiform layer.

2 eased and extended to the capillaries of the outer plexiform layer.

3 rod photoreceptor synaptic spherules in the outer plexiform layer.

4 ner nuclear layer and their processes in the outer plexiform layer.

5 activity is only present in processes of the outer plexiform layer.

6 alized osteonectin/SPARC specifically to the outer plexiform layer.

7 species punctate stain was restricted to the outer plexiform layer.

8 cuitry rather than feedback circuitry in the outer plexiform layer.

9 ecreted, and subsequently transported to the outer plexiform layer.

10 ies labeled mb bipolar cell dendrites in the outer plexiform layer.

11 hat extended past the cone synapses into the outer plexiform layer.

12 ission of interplexiform cell signals to the outer plexiform layer.

13 ys, and their cell bodies can be seen in the outer plexiform layer.

14 nd the formation of synaptic contacts in the outer plexiform layer.

15 noreactive processes are also present in the outer plexiform layer.

16 stricted to the inner retinal layers and the outer plexiform layer.

17 ocesses in the inner plexiform layer and the outer plexiform layer.

18 ickness, sparing the outer retina except the outer plexiform layer.

19 endrites as well as glutamate release in the outer plexiform layer.

20 inant neuronal connexin, is expressed in the outer plexiform layer.

21 otential M1 positive) in diffusely condensed outer plexiform layer.

22 ew blood vessels abnormally localized in the outer plexiform layer.

23 ciliary complex, and horizontal cells in the outer plexiform layer.

24 s well as to their processes and tips in the outer plexiform layer.

25 nd to project to different strata within the outer plexiform layer.

26 mGluR6 expression was limited to the outer plexiform layer.

27 ently coupled to form a third network in the outer plexiform layer.

28 abundant gap junctions in both the inner and outer plexiform layers.

29 GCAP2 staining within the outer segment and outer plexiform layers.

30 dial columns, reaching from the inner to the outer plexiform layers.

31 f the protein predominantly in the inner and outer plexiform layers.

32 m varicose axons arborizing in the inner and outer plexiform layers after glutamatergic synapses depo

33 form layers, whereas PKG II was found in the outer plexiform layer, amacrine cells, and somata in the

34 Ca2+ extrusion system, were expressed in the outer plexiform layer and in a subset of inner nuclear a

35 unoreactivity is present in processes of the outer plexiform layer and in certain amacrine cells and

36 s expressed within abundant processes in the outer plexiform layer and in rare neurites that extend a

37 riod, while the abnormal hyperreflectance of outer plexiform layer and inner nuclear layer on spectra

38 pump) revealed intense labelling within the outer plexiform layer and on isolated horizontal cells.

39 odeling: rods retracted their axons from the outer plexiform layer and partially degenerated, whereas

40 Cone pedicles remained in the outer plexiform layer and preserved synaptic contacts wi

41 ed in photoreceptors and in the postsynaptic outer plexiform layer and that interacts with cytoskelet

42 the distance between the outer border of the outer plexiform layer and the inner border of the ellips

43 The thickness of the outer plexiform layer and the number of photoreceptor te

44 een in the synaptic regions of the inner and outer plexiform layers and in the outer nuclear layer.

45 zed at the ganglion cell, inner nuclear, and outer plexiform layers and in the walls of the blood ves

46 e fiber, ganglion cell, inner plexiform, and outer plexiform layers and increased thickness in the in

47 lesions were limited to the photoreceptors, outer plexiform layer, and retinal pigment epithelium in

48 localized particularly to the inner retina, outer plexiform layer, and the photoreceptors during pos

49 In addition, the synaptic connections in the outer plexiform layer are defective in Oc1-null mice, an

50 or expression and synaptic structures in the outer plexiform layer are preserved, and visual response

51 neurites are segregated within the inner or outer plexiform layers are not known.

52 In humans, the inner and outer plexiform layers are sites of high resistance to t

53 Irs2 was mainly localized to the outer plexiform layer as well as to photoreceptor inner

54 BA may produce depolarizing responses in the outer plexiform layer at times when it generates hyperpo

55 Beginning 1 day after detachment, the outer plexiform layer becomes disorganized and synaptoph

56 as one substantial trunk that ascends in the outer plexiform layer below the space between the "footp

57 three major targets of histamine are in the outer plexiform layer, but the retinopetal axons contain

58 In the outer plexiform layer, CB1 was located in and/or on cone

59 itic branching pattern and field size in the outer plexiform layer, cell body size, and layering with

60 a, the horizontal cells, stratify within the outer plexiform layer, extending dendritic terminals tha

61 The inner and outer plexiform layers formed the sites of highest resis

62 ntral photoreceptor axons, which changed the outer plexiform layer from a thin sheet of synaptic pedi

63 ter nuclear layer, in their processes in the outer plexiform layer in retinal explants, and in their

64 ation of significantly thicker GCL, IPL, and outer plexiform layer in the central retinal area (i.e.,

65 localized to the outer nuclear layer and the outer plexiform layer in the CNGB3(-/-) retina.

66 tion in the photoreceptor inner segments and outer plexiform layer in the WT controls with EAU; but s

67 ere were apparent fluid-filled spaces in the outer plexiform layer in three of these maculas, suggest

68 hisis cavities spanned the inner nuclear and outer plexiform layers in all retinas.

69 lar cell structures in the inner nuclear and outer plexiform layers in paraneoplastic vitelliform ret

70 er and as punctate staining in the inner and outer plexiform layers in the salamander retina.

71 (IR) was restricted to a narrow band in the outer plexiform layer, in which it appeared as bright do

72 e delayed temporal expression of KCC2 in the outer plexiform layer indicates that GABAergic function

73 receptor synaptic markers was reduced in the outer plexiform layer, indicating loss of photoreceptor

74 Xbp1 splicing in the retinal ganglia cells, outer plexiform layer, inner nuclear layer, and outer nu

75 mbrane irregularity (18%), outer nuclear and outer plexiform layer irregularity (8%), and inner nucle

76 found that Gbeta5S expression in the retinal outer plexiform layer is eliminated, as is the ERG b-wav

77 This suggests that the organization of the outer plexiform layer is more complex than classically t

78 extending from the inner nuclear layer (INL)/outer plexiform layer junction to involve the full-thick

79 In the outer plexiform layer, KCC2 was detected as soon as this

80 egeneration of photoreceptor synapses in the outer plexiform layer, leading to a progressive function

81 l or flat contacts with cone pedicles in the outer plexiform layer, leading to their identification a

82 nner plexiform layer, disorganization of the outer plexiform layer, loss of regularity of the outer n

83 macular inner nuclear layer (mINL), macular outer plexiform layer (mOPL), macular outer nuclear laye

84 eginning at the ganglion cell layer (n = 1), outer plexiform layer (n = 4), outer nuclear layer (n =

85 inner plexiform layer neurites, and varicose outer plexiform layer neurites all bear spines, that som

86 In the outer plexiform layer, numerous plaques colocalized with

87 r segments are reduced by 50% in length; the outer plexiform layer of mutant animals is disrupted spe

88 aucomatous retinas, but was increased in the outer plexiform layer of only the memantine-treated glau

89 s localized mostly in the inner segments and outer plexiform layer of photoreceptor cells in both lig

90 Y DHP, L-type channels were localized in the outer plexiform layer of retinal sections and in presyna

91 REEP6 was localized to the inner segment and outer plexiform layer of rod photoreceptors.

92 ated elaborate, axonal arborization into the outer plexiform layer of the host retina.

93 use retina and were found to interact in the outer plexiform layer of the retina containing the photo

94 ssay the organization of cells making up the outer plexiform layer of the retina in the absence of Ds

95 at the HRG4-RRG4 protein is localized in the outer plexiform layer of the retina in the synaptic term

96 calized to the photoreceptor synapses in the outer plexiform layer of the retina.

97 rtners, Gbeta5 and R9AP, were reduced in the outer plexiform layer of the RGS11(-/-) and RGS7(Delta/D

98 ing of pre- and postsynaptic elements in the outer plexiform layer of this species.

99 synaptic layers of the retina, the inner and outer plexiform layers, of all six species examined.

100 but its highest levels were detected in the outer plexiform layer on the tips of horizontal cell den

101 er segment (OS) and outer nuclear layer plus outer plexiform layer (ONL+) thicknesses fell below the

102 thicknesses of the outer nuclear layer plus outer plexiform layer (ONL+), outer segment (OS), and re

103 ent (OS) layer, the outer nuclear layer plus outer plexiform layer (ONL+), the retinal pigment epithe

104 thicker ganglion cell layer (P = 0.003) and outer plexiform layer (OPL) (P < 0.001) compared with co

105 apex pointing toward the inner limit of the outer plexiform layer (OPL) adjacent to the margin betwe

106 esent in cone, but not rod, terminals in the outer plexiform layer (OPL) and in many synaptic termina

107 showed VGLUT1-IR by P8, when they invade the outer plexiform layer (OPL) and initiate synaptogenesis.

108 e in these areas included: subsidence of the outer plexiform layer (OPL) and inner nuclear layer (INL

109 1-immunoreactive fibers were present in the outer plexiform layer (OPL) and inner plexiform layer (I

110 mbrane; the beta(2) subunit localized to the outer plexiform layer (OPL) and inner plexiform layer (I

111 branches of HC axons fail to stratify in the outer plexiform layer (OPL) and invade the outer nuclear

112 uctural and optical property features of the outer plexiform layer (OPL) and the complex formed by th

113 Their stratification in the outer plexiform layer (OPL) and the IPL was not affected

114 immunoreactivity support localization in the outer plexiform layer (OPL) as cone pedicles, HCs and BC

115 lesion above (type 1) or below (type 2) the outer plexiform layer (OPL) at 6 tertiary referral cente

116 with correlating confirmed expansion of the outer plexiform layer (OPL) by optical coherence tomogra

117 receptor terminals are ensheathed within the outer plexiform layer (OPL) by the processes of one type

118 ing HCs by puffing kainic acid (KA) into the outer plexiform layer (OPL) caused a positive voltage sh

119 ner retinal layers limited externally by the outer plexiform layer (OPL) in 15 eyes (93.7%).

120 xtend well beyond the normal boundary of the outer plexiform layer (OPL) into the outer nuclear layer

121 tonin receptors mediating this action in the outer plexiform layer (OPL) is not clear.

122 aging at the inner plexiform layer (IPL) and outer plexiform layer (OPL) of living rat retinal slices

123 NKCC1) is localized primarily throughout the outer plexiform layer (OPL) of the distal retina, a syna

124 tion in the number of synaptic triads in the outer plexiform layer (OPL) of the Gbeta5-/- mice, which

125 signal confined to the inner portion of the outer plexiform layer (OPL) on PD-OCT.

126 al Dendrites (ORDs) either ramify within the outer plexiform layer (OPL) or the inner nuclear layer,

127 n retina, which are restricted to either the outer plexiform layer (OPL) or the inner plexiform layer

128 Eyes of these mice had a thinner outer plexiform layer (OPL) than eyes of control animals

129 r degeneration with severe disruption of the outer plexiform layer (OPL) that decreases at older ages

130 ions where rods failed to differentiate, the outer plexiform layer (OPL) was disrupted.

131 ation of the inner plexiform layer (IPL) and outer plexiform layer (OPL) was identified at each age,

132 ner and outermost regions of the INL, in the outer plexiform layer (OPL), and in the inner segments o

133 layer + inner plexiform and nuclear layers), outer plexiform layer (OPL), and outer retinal complex (

134 triad ribbon synapses established within the outer plexiform layer (OPL), initiating retinal visual p

135 NF-H-immunopositive fibers were found in the outer plexiform layer (OPL), inner plexiform layer (IPL)

136 Their processes extend toward the outer plexiform layer (OPL), receiving synaptic inputs f

137 r cell body, near the distal boundary of the outer plexiform layer (OPL), suggesting that apical syna

138 photoreceptor cells extend terminals to the outer plexiform layer (OPL), where they form characteris

139 The retina expresses several laminins in the outer plexiform layer (OPL), where they may provide an e

140 to the signalling of horizontal cells in the outer plexiform layer (OPL).

141 r, with scattered compact projections to the outer plexiform layer (OPL).

142 f the inner plexiform layer (IPL) and to the outer plexiform layer (OPL).

143 le-occupying region into the neuropil of the outer plexiform layer (OPL).

144 were in the optic fiber layer (OFL) and the outer plexiform layer (OPL).

145 is upon the organization and assembly of the outer plexiform layer (OPL).

146 mbrane (ELM), outer nuclear layer (ONL), and outer plexiform layer (OPL).

147 ATs) form a third independent network in the outer plexiform layer (OPL).

148 ayer, the inner nuclear layer (INL), and the outer plexiform layer (OPL).

149 sin, rhodopsin, and a synaptic marker in the outer plexiform layer (OPL; dystrophin).

150 ually dependent synaptic transmission in the outer plexiform layer or to some other early, pre-visual

151 aptic terminals is reduced in regions of the outer plexiform layer over drusen, synaptic proteins are

152 nsity-dependent cellular interactions in the outer plexiform layer overcome this variability to ensur

153 glion cell layer, inner nuclear layer, inner/outer plexiform layers, photoreceptor inner segments, an

154 course of idiopathic ERM, deformation of the outer plexiform layer progresses and is associated with

155 F receptor-LI was present in photoreceptors, outer plexiform layer, retinal ganglion cell axons, and

156 inner nuclear layer (T6 and N6 sectors), and outer plexiform layer (S6 sector), as well as the overal

157 ning from the retinal ganglion cell layer to outer plexiform layer (standardized beta = 0.657 to 0.77

158 ner plexiform layer appears earlier than the outer plexiform layer, synaptic proteins, and ribbons ar

159 6 was found to label synaptic ribbons in the outer plexiform layer that partially enclosed the alpha-

160 yer plus inner plexiform layer, the INL plus outer plexiform layer (the combined thickness of these l

161 in the ganglion cell layer as well as in the outer plexiform layer, the inner nuclear layer, and the

162 e nuclei of ganglion and amacrine cells, the outer plexiform layer, the nerve fiber layer, and the ax

163 ith bipolar cell markers and preservation of outer plexiform layer thickness.

164 on can be obtained by measuring the areas of outer plexiform layer thinning (adjusted R(2) = 0.93), e

165 d well beyond their normal strata within the outer plexiform layer to innervate the outer nuclear lay

166 etina, whereas expression was delayed in the outer plexiform layer until P7 but reached its adult lev

167 Staining for mGluR1alpha in the outer plexiform layer was seen in numerous punctate stru

168 a single row of photoreceptor cells, and the outer plexiform layer was thin and disorganized.

169 nals, and stratification of terminals in the outer plexiform layer were comparable among coneless, co

170 ent of RCBM thickening in capillaries of the outer plexiform layer were determined in all groups.

171 channel complement, and the extension of the outer plexiform layer were diminished.

172 The synapses in the outer plexiform layer were extensively degenerated and r

173 t loss of ganglion cells and thinning of the outer plexiform layer were first seen in 7- to 8-month-o

174 Microscopically, the inner nuclear layer and outer plexiform layer were the most affected retinal str

175 Changes in the outer nuclear and outer plexiform layers were analyzed, using immunohistoc

176 aptic layers of the retina and the inner and outer plexiform layers, were both moderately stained for

177 ness of the combined outer nuclear layer and outer plexiform layer when we compared MSNON or MSON eye

178 erplexiform cells that send processes to the outer plexiform layer where dopamine is released in a li

179 ses also crossed the INL and ramified in the outer plexiform layer where they formed a sparse meshwor

180 min-1 and TULP1 colocalized primarily to the outer plexiform layer, where photoreceptor terminals syn

181 The outer plexiform layer, which contains the photoreceptor

182 el with which to study synaptogenesis at the outer plexiform layer within regions that lack different