ライフサイエンスコーパス: postsynaptic density

1 es at extrasynaptic sites (>0.5 mum from the postsynaptic density).

2 ctivity-dependent accumulation of tau in the postsynaptic density.

3 alpha is present in a mobile fraction of the postsynaptic density.

4 are a family of scaffolding proteins of the postsynaptic density.

5 major scaffolding protein of the excitatory postsynaptic density.

6 nclude modulation of receptor trafficking to postsynaptic density.

7 Rs) is regulated by scaffold proteins in the postsynaptic density.

8 nents of the presynaptic active zone and the postsynaptic density.

9 removal of AMPA receptors (AMPARs) from the postsynaptic density.

10 single presynaptic active zone and a single postsynaptic density.

11 stering of glutamate receptors (GLUR) at the postsynaptic density.

12 for coupling AMPAR endocytic zones with the postsynaptic density.

13 tructural protein found predominantly at the postsynaptic density.

14 re less rigidly organized than glutamatergic postsynaptic densities.

15 plasma membranes, close to, but not within, postsynaptic densities.

16 xchange factor that is localized in neuronal postsynaptic densities.

17 concentration of synaptic vesicles near the postsynaptic densities.

18 ntaining small, round vesicles and prominent postsynaptic densities.

19 regulation of mGluR1 in 5-HT(2A)R-containing postsynaptic densities.

20 d in the brain and is highly enriched within postsynaptic densities.

21 otentially compensatory expansion of AZs and postsynaptic densities.

22 ma membrane and in dendritic spines close to postsynaptic densities.

23 at received E treatment, ER-alpha within the postsynaptic density (30-60 nm from the synaptic membran

24 Postsynaptic density 93 (PSD-93) is a protein enriched a

25 Postsynaptic density-93 (PSD-93) is the most variable pa

26 synaptic cell adhesion molecule) and PSD-93 (postsynaptic density-93) are scaffold proteins that bind

27 egatively regulated dendritic spine density, postsynaptic density 95 (PSD-95) clustering, and surface

28 Postsynaptic density 95 (PSD-95) is a major synaptic sca

29 Postsynaptic density 95 (PSD-95) is a synaptic protein r

30 Postsynaptic density 95 (PSD-95), the major scaffold at

31 ation, and protein/protein interactions (eg, postsynaptic density 95 (PSD95)), may drive the predispo

32 ls concomitant with higher levels of 5-HT2CR:postsynaptic density 95 complex distinguished HI rats fr

33 amate transporter 1 and 2) and postsynaptic (postsynaptic density 95) markers, as well as dopaminergi

34 Bazooka requires its three postsynaptic density 95, discs large, zonula occludens-1

35 teracts with proteins through its three PDZ (postsynaptic density 95, discs large, zonula occludens-1

36 utamate transporter 1-positive (VGlut1+) and postsynaptic density 95-positive (PSD95+) puncta, on PV

37 n of tyrosine hydroxylase immunostaining and postsynaptic density 95-positive elements.

38 tory factor-1 (NHERF1) is a cytoplasmic PDZ (postsynaptic density 95/disc large/zona occludens) prote

39 gion specifically interacted with the NHERF1 postsynaptic density 95/disc-large/zona occludens-1 doma

40 w that the expression of GRIP1, a multi-PDZ (postsynaptic density 95/discs large/zona occludens) doma

41 nteraction modules in mammalian cells is the postsynaptic density 95/discs large/zonula occludens 1 (

42 Scaffolding proteins containing PDZ (postsynaptic density 95/discs large/zonula occludens-1)

43 Postsynaptic density 95/discs large/zonus occludens-1 (P

44 The two PDZ (postsynaptic density 95/disk large/zonula occluden 1) do

45 ulatory protein (E3KARP) both consist of two postsynaptic density 95/disks large/zona occludens-1 (PD

46 d presynaptic (Synapsin-1) and postsynaptic (postsynaptic density 95; PSD-95) staining, diffuse demye

47 an age-related increase in the ratio of both postsynaptic density-95 (PSD-95) and the GluN2A subunit

48 Dimeric peptide-based inhibitors of postsynaptic density-95 (PSD-95) can reduce ischemic bra

49 se hippocampal organotypic slice cultures, a postsynaptic density-95 (PSD-95) knock-out mouse line an

50 te (NMDA) neurotransmitter receptors and the postsynaptic density-95 (PSD-95) membrane-associated gua

51 entries into spines regulate the increase in postsynaptic density-95 (PSD-95) protein after brain-der

52 The coupling of the spinal postsynaptic density-95 (PSD-95) with the glutamatergic

53 ies on intracellular calcium signaling, PDZ [postsynaptic density-95 (PSD-95)/Discs large (Dlg)/zona

54 Postsynaptic density-95 (PSD95) is a 95 kDa scaffolding

55 Postsynaptic density-95 (PSD95) is a scaffolding protein

56 ressed increase in other proteins, including postsynaptic density-95 and alpha-calcium/calmodulin-dep

57 Postsynaptic density-95 is a multidomain scaffolding pro

58 Translational induction of an FMRP target, postsynaptic density-95 mRNA, required both PP2A and UPS

59 sults in increased spine density and PSD-95 (postsynaptic density-95) accumulation in membrane region

60 is provided by the scaffold protein PSD-95 (postsynaptic density-95), which is associated with alpha

61 peptide (KV1-C peptide) corresponding to the postsynaptic density-95, discs large, zonula occludens-1

62 PSD-95 (postsynaptic density-95, DLG4) orchestrates protein-prot

63 The EAAT2b cytoplasmic C terminus contains a postsynaptic density-95/Discs large/zona occludens-1 (PD

64 The PDZ (postsynaptic density-95/discs large/zona occludens-1) do

65 interaction between SAP102 and NR2B is PDZ (postsynaptic density-95/Discs large/zona occludens-1) do

66 rotein kinase and myosin domains, and a PDZ (postsynaptic density-95/Discs Large/zona occludens-1) sc

67 P-REX2 provides high-affinity binding to the postsynaptic density-95/Discs large/zona occludens-1-bin

68 The scaffolding postsynaptic density-95/disks large/zonula occludens-1 (

69 boxyl terminal (CT) of Cx43, incorporating a postsynaptic density-95/disks-large/ZO-1 (PDZ)-binding d

70 that are symmetric (in that there is little postsynaptic density), a characteristic of inhibitory sy

71 labeled endings in the DCN formed asymmetric postsynaptic densities, a feature of excitatory neurotra

72 ical slices and blocks Pyk2 translocation to postsynaptic densities, a key step required for Pyk2 act

73 GluA4 expression and phosphorylation in the postsynaptic density after morphine.

74 the major scaffolding protein at excitatory postsynaptic densities and a potent regulator of synapti

75 ve more stubby spine structures with smaller postsynaptic densities and an increase in the frequency

76 hippocampus, gamma-8 and CNIH-2 associate in postsynaptic densities and CNIH-2 protein levels are mar

77 nt tau depleted PSD-95, resulting in smaller postsynaptic densities and impaired synaptic localizatio

78 e, BC1 KO mice have enlarged spine heads and postsynaptic densities and increased synaptic levels of

79 abundance of the GluN2B subunit of NMDAR in postsynaptic densities and NMDAR-dependent long-term pot

80 ry amino acid transporter to label GABAergic postsynaptic densities and terminals, respectively.

81 allows for the concomitant remodeling of the postsynaptic density and actin spinoskeleton and for the

82 n is accompanied by PTEN localization at the postsynaptic density and anchoring within the spine.

83 iary subunits, SynDIG4 is de-enriched at the postsynaptic density and colocalizes with extrasynaptic

84 flow-cytometry analysis, down-regulation of postsynaptic density and dendrite spine morphology regul

85 kinases (MAGUKs) are major components of the postsynaptic density and play important roles in synapti

86 actin is presumed to anchor receptors in the postsynaptic density and play numerous roles regulating

87 geted mass spectrometry was used to quantify postsynaptic density and voltage-gated calcium channel p

88 They were often found in the postsynaptic density and were closely associated with sy

89 PrP(C) is enriched in postsynaptic densities, and Abeta-PrP(C) interaction lea

90 , synaptic vesicles, spines, spine apparati, postsynaptic densities, and mitochondria) are rendered a

91 ptic terminals, labelling both dendrites and postsynaptic densities, and simultaneously labelling a r

92 dly, SynCAM 1 can form ensembles proximal to postsynaptic densities, and synapses containing these en

93 illed cells, ultrastructural analysis of the postsynaptic density, and electrophysiological recording

94 ed, including the subsynaptic reticulum, the postsynaptic density, and the glutamate receptor cluster

95 ors receptors and signaling molecules to the postsynaptic density-and are regulated by the phosphoryl

96 acellular scaffold proteins that make up the postsynaptic density are largely unknown in vivo.

97 central synapses, the presynaptic bouton and postsynaptic density are structurally correlated.

98 number of release sites, active zone length, postsynaptic density area and number of vesicles in the

99 resynaptic AZ number per bouton area and the postsynaptic density area are both increased in dnlg2 mu

100 d spines had larger synapses, as measured by postsynaptic density area, than single-labeled and unlab

101 ynapses in M1 were larger than in S1 (median postsynaptic density areas of 0.064 mum(2) vs 0.042 mum(

102 res of neurons, such as dendritic spines and postsynaptic density areas, in addition to its distribut

103 marked, NMDA receptor-dependent increase in postsynaptic densities associated with activated (phosph

104 vity alone, robustly increased the number of postsynaptic densities associated with activated (phosph

105 lices to 1 nM E2 increases the percentage of postsynaptic densities associated with high levels of im

106 97, and SAP102 are central organizers of the postsynaptic density at excitatory synapses on pyramidal

107 one of the main scaffolding proteins of the postsynaptic density at GABAergic synapses, to monitor t

108 de novo mutations in genes belonging to the postsynaptic density at glutamatergic synapses, particul

109 rotein that anchors multiple elements of the postsynaptic density at the synapse.

110 s are adjacent synaptic regions that share a postsynaptic density, but nascent zones lack the presyna

111 ), a K63-specific deubiquitinase enriched in postsynaptic densities, cleaves K63-chains from PSD-95.

112 d P=3.44 x 10(-6)), a member of the neuronal postsynaptic density complex.

113 actin organization through interaction with postsynaptic density components.

114 old proteins, suggesting that maintenance of postsynaptic density composition is TNFalpha dependent.

115 ribution of GluN2B-immunolabeling within the postsynaptic density did not change after BZ withdrawal.

116 including reduced mGlu5 association with the postsynaptic density, enhanced constitutive mGlu5 signal

117 id expansion of the synaptic active zone and postsynaptic density, enhanced dendritic spine plasticit

118 lcin, the clathrin adaptor molecule AP2, the postsynaptic density enriched protein PSD-95 and NMDARs.

119 calization of mGluR5 to both synaptosome and postsynaptic density-enriched fractions in the hippocamp

120 In the young implanted cats, postsynaptic densities exhibited normal size, shape, and

121 Notably, members of the postsynaptic density family of proteins that are critica

122 nt manner to facilitate its translocation to postsynaptic densities for synaptic tagging and maintena

123 subunits (GluA1/2/3/4) in homogenates and in postsynaptic density fractions from spinal cord dorsal h

124 is to identify changes in the composition of postsynaptic densities from GluN2B(-/-) mouse primary ne

125 We isolated the postsynaptic density from human neocortex (hPSD) and ide

126 Moreover, we show that the postsynaptic density further enhances receptor trapping,

127 e Extinction group, there was an increase in postsynaptic density GluR1, PSD95, and actin proteins; w

128 Within the postsynaptic density, however, AMPA receptors coassemble

129 ding immunogold revealed AIDA-1 label within postsynaptic densities in both hippocampus and cortex.

130 R and mGluR1 were found to be coexpressed in postsynaptic densities in dorsal horn neurons.

131 o measure protein organization within single postsynaptic densities in rat hippocampal neurons.

132 tric disorders, has a regulatory role in the postsynaptic density in association with the NMDA-type g

133 esponses and GluA1 levels in the hippocampal postsynaptic density in wild-type and GluA1-S845A mutant

134 rgest CNVs (>500 kb) in genes present in the postsynaptic density, in genomic regions implicated via

135 T131-phosphorylated NDE1 is present at the postsynaptic density, in proximal axons, within the nucl

136 ssing PSD-95, a major scaffolding protein of postsynaptic density involved in synapse formation, syna

137 Proper localization of SAP102 at the postsynaptic density is essential to these functions.

138 95, a principal scaffolding component of the postsynaptic density, is targeted to synapses by palmito

139 rate at which they unbind from and exit the postsynaptic density (Koff).

140 Cross sectional area, postsynaptic density length and curvature, and mitochond

141 ar only later in life, together with reduced postsynaptic density levels.

142 plasticity by orchestrating the assembly of postsynaptic density macromolecular signalling complex.

143 sity GluR1, PSD95, and actin proteins; while postsynaptic density mGluR5 protein decreased and there

144 proteins are major scaffold proteins of the postsynaptic density; mutations in the human SHANK3 gene

145 , Extinction training reversed the decreased postsynaptic density NMDAR1 protein in the Home and Box

146 In the postsynaptic density, O-GlcNAcylation on multiple protei

147 e A (PKA), PKC, and calcineurin (CaN) to the postsynaptic densities of neurons, but its role in inhib

148 ty was not influenced by Nogo-A, the size of postsynaptic densities of PF-PC synapses was negatively

149 oltage-sensitive calcium ion channels at the postsynaptic density of a dendritic spine is investigate

150 nderlies the maturation of adhesions and the postsynaptic density of dendritic spines.

151 intense synaptic activity drives tau to the postsynaptic density of excitatory synapses and that Abe

152 Protein expression in the postsynaptic density of excitatory synapses is tightly r

153 e we demonstrate that OGT is enriched in the postsynaptic density of excitatory synapses.

154 P-binding protein Arf6 that localizes to the postsynaptic density of excitatory synapses.

155 ultidomain scaffold protein localized to the postsynaptic density of excitatory synapses.

156 In the postsynaptic density of glutamatergic synapses, the disc

157 the content of the beta3 integrin subunit in postsynaptic density of the accumbens core at 24 h after

158 ations of PSD-95, Homer1b/c, and Narp in the postsynaptic density of the core, whereas no proteins me

159 eas no proteins measured were altered in the postsynaptic density of the shell in either extinguished

160 1-S845 and GluA1 levels in their hippocampal postsynaptic density on the third day of acquisition, wh

161 cluster size in DBA mice, without changes in postsynaptic density or active zone.

162 mmunocytochemistry, electron microscopy, and postsynaptic density preparation that LRP1 is located po

163 dentate hilus, and significant increases in postsynaptic density protein (PSD-95) were found along d

164 ifs with their interacting proteins, such as postsynaptic density protein (PSD95), Drosophila disc la

165 Previously, we reported that postsynaptic density protein 95 (PSD-95) acts as a stop

166 s were measured in the nucleus accumbens for postsynaptic density protein 95 (PSD-95) and SAP90/PSD-9

167 hat SR interacts with the synaptic proteins, postsynaptic density protein 95 (PSD-95) and stargazin,

168 ate (NMDA) receptor and its interaction with postsynaptic density protein 95 (PSD-95) at the synapse

169 mals and cultured slices, and an increase in postsynaptic density protein 95 (PSD-95) by overexpressi

170 Postsynaptic density protein 95 (PSD-95) is essential fo

171 72, whereas the synaptic scaffolding protein postsynaptic density protein 95 (PSD-95) stabilizes the

172 troporation of DsRedExpress- and eGFP-tagged postsynaptic density protein 95 (PSD-95) to investigate

173 Postsynaptic density protein 95 (PSD-95), a member of th

174 egradation of the synaptic scaffold protein, postsynaptic density protein 95 (PSD-95), a process that

175 ces and assessing the expression of synaptic postsynaptic density protein 95 (PSD-95).

176 Additionally, we found higher postsynaptic density protein 95 (PSD95) and lower glutam

177 Postsynaptic density protein 95 (PSD95) and synapse-asso

178 in, but did not affect palmitate turnover on postsynaptic density protein 95 (PSD95) or N-Ras.

179 synapse-associated protein 102 (SAP102) and postsynaptic density protein 95 (PSD95).

180 iates with a different synaptic PDZ protein, postsynaptic density protein 95 (PSD95).

181 cal imaging of neurons expressing DsRed2 and postsynaptic density protein 95 fused to green fluoresce

182 We observed decreased levels of postsynaptic density protein 95 in Opa1(+/-) mutant mice

183 on of GluN2A and GluN2B subunits, as well as postsynaptic density protein 95 in the rat hippocampus.

184 active, expanded allele (EX-Xa) have reduced postsynaptic density protein 95 protein expression, redu

185 found that the postsynaptic scaffold PSD-95 (postsynaptic density protein 95) undergoes K63 polyubiqu

186 that promotes the clustering of the PSD-95 (postsynaptic density protein 95).

187 ate a role for synaptic proteins synapsin-1, postsynaptic density protein 95, and glutamate receptor

188 s in spine density and levels of synapsin-1, postsynaptic density protein 95, and glutamate receptor

189 and levels of synaptic proteins synapsin-1, postsynaptic density protein 95, and glutamate receptor

190 av-1 and membrane/lipid raft localization of postsynaptic density protein 95, NMDA receptor, and trop

191 which targets the synaptic scaffold protein, postsynaptic density protein 95, to enhance downstream s

192 Synapse-associated protein 90/postsynaptic density protein 95-associated protein 3 (SA

193 impairments in synapse-associated protein 90/postsynaptic density protein 95-associated protein 3 (SA

194 transporter 1-positive [VGlut1+] puncta and postsynaptic density protein 95-positive [PSD95+] puncta

195 Selective disruption of interactions with postsynaptic density protein 95/disks large/zonula occlu

196 ynapse-associated protein of 97 kilodaltons; postsynaptic density protein of 93 kilodaltons; synapse-

197 ct matches that of the prototypical scaffold postsynaptic density protein of 95 kDa (PSD-95) identify

198 Of the many GPCR-interacting proteins, postsynaptic density protein of 95 kilodaltons, disc lar

199 membrane-associated guanylate-like kinases [postsynaptic density protein of 95 kilodaltons; synapse-

200 At this time, levels of GluN2A, GluN2B and postsynaptic density protein PSD-95 were all increased.

201 We used this method to label the postsynaptic density protein PSD-95 with mVenus without

202 Moreover, the association of the postsynaptic density protein PSD-95 with TrkB is critica

203 MRP) regulates expression of the scaffolding postsynaptic density protein PSD95, but the mode of cont

204 The postsynaptic density protein, PSD-95, is highly enriched

205 Postsynaptic density protein-95 (PSD-95) is a central el

206 Postsynaptic density protein-95 (PSD-95) localizes AMPA-

207 Specifically, postsynaptic density protein-95 (PSD-95) was absolutely

208 in postsynaptic structures can interact with postsynaptic density protein-95 (PSD-95), a key scaffold

209 complex of the synaptic scaffolding protein postsynaptic density protein-95 (PSD-95), neuronal nitri

210 re immunopositive for glutamate receptor and postsynaptic density proteins (viz., GluR1, GluR4, NR1,

211 of Ptchd1-interacting proteins that include postsynaptic density proteins and the retromer complex,

212 or subtypes are differentially stabilized by postsynaptic density proteins in or out of the postsynap

213 ine self-administration, and measurements of postsynaptic density proteins in the core and shell subc

214 he synapse and interacts with multiple known postsynaptic density proteins including the scaffolding

215 s on live neurons were labeled with sQDs and postsynaptic density proteins were visualized with super

216 Assays of postsynaptic density proteins, spine morphology, and syn

217 naling cascades that converge onto GABAergic postsynaptic density proteins, we performed MS analysis

218 renia with the exception of a small group of postsynaptic density proteins, whose co-expression incre

219 rites and directly trigger the clustering of postsynaptic density proteins.

220 or genes encoding members of mouse and human postsynaptic density proteomes (odds ratio 4.56, P = 5.0

221 major scaffolding protein in the excitatory postsynaptic density (PSD) and a potent regulator of syn

222 ucing IKK kinase complex is localized at the postsynaptic density (PSD) and activated under basal con

223 eatment, GluR1 subunits are increased at the postsynaptic density (PSD) and at extrasynaptic sites, w

224 conditioned inhibition groups, the ratio of postsynaptic density (PSD) area to docked vesicles at sy

225 term depression (LTD), and a thinning of the postsynaptic density (PSD) at hippocampal synapses.

226 n SGNs to drive differentiation of the large postsynaptic density (PSD) characteristic of the ribbon

227 The postsynaptic density (PSD) contains a collection of scaf

228 ositioning of glutamate receptors within the postsynaptic density (PSD) determine excitatory synaptic

229 show that an exocytic domain adjacent to the postsynaptic density (PSD) enables fusion of large, AMPA

230 in (GAP) found in high concentrations in the postsynaptic density (PSD) fraction from the mammalian f

231 .2 L-type Ca(2+) channel mRNA and protein in postsynaptic density (PSD) fractions of the hippocampus,

232 Accumulation of PSD-95 to the postsynaptic density (PSD) is known to lead to synaptic

233 ty of synapses, immunolabeled for either the postsynaptic density (PSD) marker PSD95 or the presynapt

234 SK2-containing channels are expressed in the postsynaptic density (PSD) of dendritic spines on mouse

235 organize an extensive protein complex at the postsynaptic density (PSD) of excitatory glutamatergic s

236 synaptic scaffolding protein enriched in the postsynaptic density (PSD) of excitatory synapses.

237 SynGAP, a protein abundant at the postsynaptic density (PSD) of glutamatergic neurons, is

238 ses overall synapse proteome complexity, the postsynaptic density (PSD) proteome of zebrafish has low

239 However, CaMKII actions away from the postsynaptic density (PSD) remain poorly understood, in

240 ensin is an abundant scaffold protein in the postsynaptic density (PSD) that forms a high-affinity co

241 that PSD-95, a major scaffold protein of the postsynaptic density (PSD) that promotes synaptic streng

242 Together, there was an increase in postsynaptic density (PSD) thickness and an upregulation

243 finement in the synapse, and trapping at the postsynaptic density (PSD) through reversible interactio

244 g, and receptor molecules concentrate at the postsynaptic density (PSD) to regulate synaptic strength

245 ribution patterns of the two isoforms at the postsynaptic density (PSD) under basal and excitatory co

246 In contrast, the postsynaptic density (PSD) was independently remodeled,

247 K-801 binding and NMDA receptor complexes in postsynaptic density (PSD) were in fact increased in sch

248 nd GEFs have been shown to be present at the postsynaptic density (PSD) within excitatory glutamaterg

249 in transiently decreased GluA1 levels at the postsynaptic density (PSD), but did not affect extrasyna

250 sion by establishing the architecture of the postsynaptic density (PSD), but the small size of the sy

251 MAGUKs), which are essential proteins in the postsynaptic density (PSD), cluster and anchor glutamate

252 At the postsynaptic density (PSD), extracellular Abetao bound t

253 nucleotide exchange factor localized to the postsynaptic density (PSD), modulates dendritic spine mo

254 fic reduction of dendritic spine density and postsynaptic density (PSD)-95 and spinophilin-positive c

255 The postsynaptic density (PSD)-95 family of membrane-associa

256 Their C termini are predicted to bind postsynaptic density (PSD)-95/Discs Large/ZO-1 (PDZ) dom

257 with yoked-saline controls, 42 proteins in a postsynaptic density (PSD)-enriched subfraction of the N

258 Kalirin-7 (Kal7), a postsynaptic density (PSD)-localized Rho-guanine nucleot

259 presence of an endocytic zone (EZ) near the postsynaptic density (PSD).

260 tic spines, where it was associated with the postsynaptic density (PSD).

261 on is SHANK3, which encodes a protein in the postsynaptic density (PSD).

262 kinases (MAGUKs) that are components of the postsynaptic density (PSD).

263 d in the brain where they are present in the postsynaptic density (PSD).

264 e abundance of receptors concentrated at the postsynaptic density (PSD).

265 tic vesicle zone (SVZ), active zone (AZ) and postsynaptic density (PSD).

266 s of genes, especially those involved in the postsynaptic density (PSD).

267 The kinase is a major component of the postsynaptic density (PSD); however, it is also containe

268 neck) and the "distal" half (containing the postsynaptic density [PSD]), whereas after delayed fixat

269 uter and inner stratifying dendrites express postsynaptic density (PSD95) immunoreactive puncta sugge

270 Postsynaptic densities (PSDs) are membrane semi-enclosed

271 However, the number of postsynaptic densities (PSDs) does not fully recover and

272 protein (GAP) that is a major constituent of postsynaptic densities (PSDs) from mammalian forebrain.

273 n kinase II (CaMKII) is a major component of postsynaptic densities (PSDs) involved in synaptic regul

274 ependent modifications in the composition of postsynaptic densities (PSDs) isolated from rat primary

275 rphology and distribution of proteins within postsynaptic densities (PSDs) isolated from rats before

276 l surface-expression of EphA7 essentially in postsynaptic densities (PSDs) of dendritic spines and sh

277 in and metalloproteinase that resides in the postsynaptic densities (PSDs) of excitatory synapses, ha

278 alysis of membranes associated with isolated postsynaptic densities (PSDs) suggests the PSD-associate

279 arger volume and harbor significantly larger postsynaptic densities (PSDs) than those contacted by vG

280 PSD95 and SAP97 conformation in vitro and in postsynaptic densities (PSDs) using FRET and EM, and exa

281 the plasma membrane and is found at neuronal postsynaptic densities (PSDs), but the role of MyoVa in

282 ndrites in each individual neuron, except at postsynaptic densities (PSDs), where it is typically hig

283 se sites of rods are apposed by one to three postsynaptic densities (PSDs).

284 ial localization and clustering of iGluRs at postsynaptic densities (PSDs).

285 urrent study investigated the expression and postsynaptic density redistribution of glutamate recepto

286 igin-1 (NL1), which is located at excitatory postsynaptic densities, regulates activity-dependent syn

287 l vesicle numbers, SNARE protein levels, and postsynaptic densities remained unaffected.

288 Homer1, a gene encoding a postsynaptic density scaffolding protein, was selected f

289 ton-associated scaffold protein (ARC) of the postsynaptic density, sets previously implicated by geno

290 y 86%; bouton volume by 105%) rather than to postsynaptic density shape.

291 No correlation was found between the postsynaptic density size and the estimated spine R(neck

292 us synapses in layers 2-3 of LPFC had larger postsynaptic density surface areas and a higher proporti

293 2-C) to be cleaved and translocated from the postsynaptic density to nuclei.

294 5) and dopamine receptor 1 (DRD1) within the postsynaptic density to regulate DRD1 trafficking.

295 mination of the majority of spines; however, postsynaptic densities were preserved on dendritic shaft

296 length, spine diameter, and the area of the postsynaptic density were measured from the 3D reconstru

297 e II (CaMKII) forms a major component of the postsynaptic density where its functions in synaptic pla

298 nes and colocalized with constituents of the postsynaptic density, whereas SNAP-25 was restricted to

299 these genes: 1) they localized to the human postsynaptic density, which is crucial for neuronal func

300 mity to synaptic contacts (<0.5 mum from the postsynaptic density), while 27% were distributed along