ライフサイエンスコーパス: puncta

1 antigen 1 (LANA-1; ORF73) and LANA-1 nuclear puncta.

2 and recruitment to the Atg12-5-16L1-positive puncta.

3 puncta within the colonies but fewer VGluT-1 puncta.

4 icant reduction in the size of surface GluR2 puncta.

5 autophagic vacuoles expressing RFP and EGFP puncta.

6 ulation of axon-derived material in discrete puncta.

7 , which prevents autophagy, contained no RFP puncta.

8 ors toward the recipient cell body in motile puncta.

9 er and by colocalization of Bruchpilot-short puncta.

10 of newly formed spines acquired PSD-95-eGFP puncta.

11 -2/HER2 from the cell surface to cytoplasmic puncta.

12 ll dendrites to reach ectopic ribbon-protein puncta.

13 concentrated into perinuclear and peripheral puncta.

14 puncta and decreased the number of PSD95-GFP puncta.

15 distribution of VGluT2-immunoreactive (-ir) puncta.

16 4Pm preferentially localized to cytoplasmic puncta.

17 increased VGAT (vesicular GABA transporter) puncta.

18 I molecules accumulate in large perinuclear puncta.

19 distributed to the cortex and intracellular puncta.

20 ontrol medium, increased the density of VGAT puncta.

21 LC3-II accumulation and formation of GFP-LC3 puncta.

22 oth proteins localize to positionally stable puncta.

23 ns are required for their concentration into puncta.

24 jority of OSR1, like WNK1, is on cytoplasmic puncta.

25 Ssd1 to localize prominently to cytoplasmic puncta.

26 localization of the SNF1 activator Std1 into puncta.

27 uced autophagic vacuoles (AVs) and less LC3B puncta.

28 annel (VGCC) puncta colocalized with Bassoon puncta.

29 Sorting 35) in the cytoplasm as fast-moving puncta.

30 es reveal local Ca(2+) influx at STIM1-Orai1 puncta.

31 astrocytic cells and fibers and connexin 43 puncta.

32 on from the TGN to cytoplasmic endosome-like puncta.

33 ast, individual gephyrin-immunoreactive (IR) puncta, a postsynaptic scaffolding protein at inhibitory

34 n spine density and PSD-95-positive synaptic puncta, a reduction of persistent spines, and impaired l

35 red for Myo51's localizations to cytoplasmic puncta, actin cables, and the contractile ring.

36 lved in formation of the mechanical adhesive puncta adherentia junctions of synapses.

37 sulted in a markedly increased number of EdU puncta, allowing efficient quantification of HIV-1 rever

38 . elegans CAMSAP protein PTRN-1 localizes to puncta along neuronal processes, stabilizes MT foci, and

39 In endothelial cells, some ARHGAP18 puncta also colocalized to Weibel-Palade bodies on the m

40 induce rapid compaction of DNA strands into puncta, although with different characteristics.

41 LC3-II/LC3-I ratio increased as did GFP-LC3 puncta and acidic vesicles; p62 levels decreased in a ly

42 Piccolo puncta sandwiched Bassoon puncta and aligned in a Piccolo-Bassoon-Piccolo structur

43 e, is normally cytosolic but concentrates in puncta and at sites of polarized growth during intense o

44 a and Rab14 colocalize in both intracellular puncta and at the plasma membrane and that Rab14 express

45 at the WIP sites reduces Dvl accumulation in puncta and attenuates beta-catenin signaling, whereas it

46 (24 h) increased the number of GFP-gephyrin puncta and decreased the number of PSD95-GFP puncta.

47 2/3 pyramidal neurons could induce gephyrin puncta and dendritic spine formation via GABA type A rec

48 creased and decreased the number of gephyrin puncta and dendritic spines, respectively.

49 uman tumors, as assessed by induction of LC3 puncta and diminished p62.

50 STIM1 does not form sustained puncta and does not colocalize with Orai1 either under b

51 ncluding formation of multiple aberrant Atg8 puncta and drastically impaired autophagosome biogenesis

52 showed the accumulation of LC3-GFP positive puncta and dystrophic neurites.

53 ACE inhibition, result in the loss of axonal puncta and in the accumulation of unprocessed proforms i

54 ers with gephyrin and GABA(A) Rs in synaptic puncta and is recruited to postsynaptic specializations

55 ble levels along the Z-disk, in a pattern of puncta and linear segments consistent with the STIM1 loc

56 tin modulates the turnover of NET3C at these puncta and microtubules regulate the exchange of VAP27 a

57 f NS1, Scribble, and Dlg1 within perinuclear puncta and mislocalization of plasma membrane-associated

58 r glutamate transporter 1-positive [VGlut1+] puncta and postsynaptic density protein 95-positive [PSD

59 d deficiency of GABA perisomatic bouton-like puncta and processes in the KF nucleus; (ii) blockade of

60 found that the number of Atg12/16L1-positive puncta and recruitment of the Atg12-5-16L1 complex to Wi

61 Tat increased numbers of LC3 puncta and resulted in the formation of abnormal autopha

62 ncentrated into puncta can be liberated from puncta and subsequently degraded.

63 lso caused the accumulation of Atg5-positive puncta and the formation of multilamellar structures.

64 increased both the number and size of PSD-95 puncta and the frequency and amplitude of miniature EPSC

65 cells revealed that both localize to nuclear puncta and the shorter isoform displays higher nuclear l

66 le of autonomously localizing to subcellular puncta and to the plasma membrane.

67 lbino RPE cells have fewer small connexin 43 puncta, and a larger fraction of phosphorylated connexin

68 uctions in Oct1 nuclear periphery-associated puncta, and a reduced association with lamin B1.

69 ed protein 1 light chain 3 (LC3)-II, GFP-LC3 puncta, and autophagy flux.

70 and muNS resulted in disruption of normal SG puncta, and in cells lacking G3BP1, MRV replication was

71 by increased LC3-II levels, formation of LC3 puncta, and increased LC3 turnover.

72 Optn was recruited to Atg12-5-16L1-positive puncta, and interacted with Atg5 and also with Atg12-5 c

73 a-target cell conjugation, transfer of viral puncta, and posttransfer.

74 outons were defined as PV/GAD65 dual-labeled puncta, and PVBC inputs were defined as a PVBC bouton th

75 These cytoplasmic puncta appear to be part of larger membranes of endocyti

76 As furrows ingress, cytoplasmic Rab8 puncta are depleted and Rab8 accumulates at the plasma m

77 In buffer-treated control roots, LYK3:GFP puncta are dynamic.

78 At both stages, PSD-95 puncta are enriched in the most lateral neuropil corresp

79 esponding to distal dendrites while gephyrin puncta are enriched on neuronal somata and in the medial

80 urthermore, the distributions of gephyrin-IR puncta are heterogeneous and appear as clusters along th

81 f the Atg12-5-16L1 complex to Wipi2-positive puncta are reduced in Optn-deficient cells.

82 lation with compatible S. meliloti, LYK3:GFP puncta are relatively stable.

83 induced a significant loss of SV2 and PSD-95 puncta as well as dendritic spines.

84 nd unlike WT p55, they fail to form distinct puncta associated with mtDNA nucleoids.

85 gy, we show that cadherin-10 forms nanoscale puncta at excitatory and inhibitory synapses, maintains

86 wild type (Bd21-3) and had dense fluorescent puncta at or near the plasma membrane.

87 accompanied by the formation of new F-actin puncta at sites of synaptic growth.

88 ary phase, given its accumulation as dynamic puncta at the cortex of such cells.

89 Z-line protein, colocalizes with F-actin in puncta at the cytoplasmic face of nuclei before sarcomer

90 in puncta increasing to match that of PSD-95 puncta at the larval stage.

91 usions localized as transient MotA-dependent puncta at the membrane when induced at subinhibitory lev

92 demonstrate that NET3C and VAP27 localize to puncta at the PM and that NET3C and VAP27 form homodimer

93 CYAM accumulated slowly into puncta based on vacuolar H(+)-ATPase activity and disper

94 ytosol to mitochondria and other cytoplasmic puncta before returning to their pre-stressed localizati

95 es in a punctate pattern, with >95% of these puncta being indistinguishable from the plasma membrane

96 R-1 is found in uniformly-distributed, small puncta both throughout the cytoplasm and the nucleus, on

97 phospho-defective STIM1-Y361F mutant formed puncta but failed to recruit Orai1, thereby preventing.

98 wo proteins are colocalised in intracellular puncta, but in the posterior PSM, where DeltaC is at a l

99 ditions, nephrons expressed few EGFP and RFP puncta, but ischemia-reperfusion injury (IRI) led to dyn

100 gp120 IIIB decreased the number of PSD95-GFP puncta by 37 +/- 4%.

101 y is low the slGFP that is concentrated into puncta can be liberated from puncta and subsequently deg

102 umber of amacrine cells and localized HR2 to puncta closely associated with synaptic ribbons inside c

103 orn mice and adult human skin, we report LC3 puncta coincident with misshaped nuclei within the granu

104 of putative podosome precursors: actin-rich puncta coinciding with matrix degradation sites and cont

105 e in rotavirus-infected cells and that STIM1 puncta colocalize with the PM-localized Orai1 SOCE calci

106 /Q-type voltage-gated calcium channel (VGCC) puncta colocalized with Bassoon puncta.

107 These puncta colocalized with E2 and recruited newly synthesiz

108 EV PBM relocalized Scribble into cytoplasmic puncta concentrated in perinuclear regions and also prot

109 eling resulted in divergence of labeled LamB puncta, consistent with a spatial pattern of OM growth i

110 NLL1 as well as DYNLL2 localised to cilia in puncta, consistent with IFT particles, and physically in

111 The majority of bright vGAT puncta contacting the NL3-overexpressing neurons have no

112 Myo51 puncta contain multiple Myo51 molecules and walk continu

113 synthesized viral RNAs localize to cytosolic puncta containing the nucleoprotein (N) of the virus.

114 This suggests that the Vipp1 puncta could be involved in protein assembly.

115 eductions of beta-catenin and alphaN-catenin puncta densities and 35% reduction in EphB2 puncta densi

116 tein 95 protein expression, reduced synaptic puncta density and reduced neurite length.

117 However, Bassoon puncta density and signal intensity were significantly a

118 -major variant ratios predicted lower PSD95+ puncta density on PV interneurons.

119 f GABA and exhibited an increase in gephyrin puncta density, suggesting increased postsynaptic GABAA

120 puncta densities and 35% reduction in EphB2 puncta density.

121 However, the cAMP-induced STIM1 puncta did not co-cluster with Orai1, and there was no a

122 Puncta dissociation parallelled the gating dependence of

123 distributed throughout the cell in numerous puncta distinct from glycosomes and other organelles.

124 ges from uniform nano-, meso- and microscale puncta (distinct protein droplets) to multilayered ortho

125 een cytochrome oxidase density and VGluT2-ir puncta distribution.

126 izes to the nuclear envelope, with prominent puncta evident near karyomere-karyomere interfaces corre

127 A minor portion of ClaH puncta exhibited bidirectional movement, likely along mi

128 The puncta exhibited changes in fluorescence intensity with

129 1 phosphorylation and led to sustained STIM1-puncta formation and Ca(2+) entry.

130 akes multiple interactions that support Dnm1 puncta formation and may be essential after this step, s

131 ted calcium entry (SOCE) by decreasing STIM1 puncta formation near the plasma membrane upon calcium d

132 Reversible Std1 puncta formation occurs under non-stressful, ambient con

133 S-glutathionylation and calcium-independent puncta formation of the ER calcium sensor STIM1 underlie

134 ) as a biosensor to assess STIM1 activation (puncta formation) by rotavirus infection and NSP4 expres

135 TIM1 to the plasma membrane, and STIM1/Orai1 puncta formation, and may cause the channel to be in the

136 ics describing IP3-receptor, DTS-plasmalemma puncta formation, SOCE via assembly of STIM1 and Orai1,

137 substantively different from those for Orai1 puncta formation, suggesting that ion selectivity and ga

138 stromal interaction molecule 1 (STIM1)/ORAI1 puncta formation, which is correlated with cytoskeleton

139 in neonatal cardiomyocytes resulted in STIM1 puncta formation, which was inhibited in a dose-dependen

140 hagy events represented by ATG16L1 and ATG12 puncta formation.

141 onversion; reduced ATG14L, ATG12, and WIPI-1 puncta formation; and significantly decreased Vps34 acti

142 that RyR are co-localized with STIM1 in the puncta formed after store depletion.

143 Measurements of puncta from infrared and OCT images were obtained along

144 Orai1 channels gated by CAD, and small Orai1 puncta gated by STIM1, exhibit repetitive fluctuations i

145 into extracellular matrix (ECM) as discrete puncta has been documented in various tissue and cell bi

146 rom punctoplasty, with patients with smaller puncta having greater symptomatic improvement.

147 Consistent with this, synaptic puncta immunopositive for VGLUT1 decreased in area after

148 e investigated the distribution of VGluT2-ir puncta in all layers of macaque monkey primary visual co

149 -1 forms filaments in vitro and localizes as puncta in cells along the plasma membrane.

150 Pontin protein is enriched in cytosolic puncta in ciliated cells in zebrafish embryos.

151 P4 in HEK293 cells increased synapsin or SV2 puncta in contacting axons of cocultured neurons, sugges

152 he density of alpha-synuclein immunoreactive puncta in dendritic processes of cultured neurons.

153 s exhibited distinct caspase-1 and caspase-8 puncta in diseasedPtpn6(spin)neutrophils.

154 ous Rab7 led to the appearance of large TrkA puncta in enlarged Rab5-early endosomes within the cytop

155 hat WNK1 and OSR1 co-localize on cytoplasmic puncta in HeLa and other cell types.

156 ss of PSD95-positive excitatory postsynaptic puncta in hippocampal area CA1 compared with sham-immuni

157 many aspects, the distribution of VGluT2-ir puncta in human was qualitatively similar to that of the

158 ed injury and increased the levels of LC3(+) puncta in injured tissue of Nod2(-/-) mice.

159 tracer also colocalized with GAD-67-positive puncta in labeled fibers, which in some cases made close

160 distribution in layers 1 and 6, and very few puncta in layers 5 and 4B.

161 s to determine the distribution of VGluT2-ir puncta in macaque and human visual cortex.

162 ity and colocalizes with extrasynaptic GluA1 puncta in primary dissociated neuron culture.

163 The absence of puncta in resting cells was required to prevent spontane

164 majority of WNK1 is localized on cytoplasmic puncta in resting cells.

165 ule (STIM) 2, but not STIM1, was arranged in puncta in resting shTRPC2 cells but not in control cells

166 ed fluorescence and accumulation of pure red puncta in skeletal muscle, which were completely amelior

167 ein light chain 3 form 2 (LC3-II) or GFP-LC3 puncta in the absence and presence of the lysosome inhib

168 abeled ribosomes are detected as fluorescent puncta in the axons and synaptic terminals of specific n

169 The NPY puncta in the axons of hippocampal and hypothalamic neur

170 sing this approach, we observed distinct EdU puncta in the cytoplasm of infected cells within 12 h po

171 V40 mobilizes a pool of Grp170 into discrete puncta in the ER called foci.

172 gers B12 and B14 to reorganize into discrete puncta in the ER membrane called foci, structures postul

173 cant increase in synaptophysin immunolabeled puncta in the hippocampal subregion, CA1, in APPSWE /PS1

174 A subset (about 50%) of the GlyRalpha4 puncta in the inner plexiform layer, however, was found

175 uronal NOS (nNOS) was localized primarily in puncta in the inner plexiform layer, in amacrine cells,

176 ificantly improves the resolution of protein puncta in the lateral plane to allow accurate and fast c

177 ation of Arc, and decreased numbers of GluR1 puncta in the neuronal processes.

178 postinfection and subsequent accumulation of puncta in the nucleus, which remained stable through 5 d

179 ranches and post-synaptic density protein 95 puncta in the peri-infarct cortex 6 weeks after treatmen

180 al axon collateral branches with presynaptic puncta in the spinal cord and enhanced recovery of forel

181 +) depletion triggered accumulation of STIM1 puncta in the subplasmalemmal ER where they co-clustered

182 densities in layer 4C, patches of VGluT2-ir puncta in the supragranular layer (2/3), lower but clear

183 in vitro data, MEC-10, but not MEC-6, formed puncta in TRN neurites that colocalize with MEC-4 when M

184 on induced formation of fluorescent membrane puncta in WT but not in TRPC4(-/-) cells, indicating tha

185 onstrated colocalization of mGlu5 with GluD1 punctas in the hippocampus.

186 y colocalized within two distinct classes of puncta, including relatively dim puncta that were locate

187 postnatal development, the number of Bassoon puncta increased as the size of the synapses increased.

188 The density of VGAT puncta increased with development, first within the vent

189 gephyrin puncta, with the number of gephyrin puncta increasing to match that of PSD-95 puncta at the

190 3-II and SQSTM1 and also potentiated GFP-LC3 puncta index in GFP-LC3-transfected hippocampal neural s

191 ed inflammasomes and increased light chain 3 puncta indicative of autophagosomes in glomeruli from do

192 well as increased VGlut2- and PSD95-positive puncta, indicative of increased excitatory synapses.

193 nd find that the localization of both within puncta is highly stable.

194 We suggest that GORK clustering in puncta is related to its gating and conductance, and ref

195 Moreover, the density of paxillin puncta is significantly lower in hippocampal growth cone

196 o colocalizes with the iGluRs at the PSDs in puncta juxtaposing the active zones.

197 se-reared animals had larger VGlut1-positive puncta, larger profiles in electron micrographs, and mor

198 tch enabling recruitment of Orai1 into STIM1 puncta leading to SOCE.

199 In contrast, puncta levels of VGlut1 and PSD95 proteins were higher i

200 ing calcineurin activity impairs STIM1/ORAI1 puncta-like formation and cytoskeleton organization.

201 protein light chain 3 (LC3) and p62, GFP-LC3 puncta, monodansylcadaverine (MDC) staining, and transmi

202 y constant from postnatal day 0 to 54 at 2.3 puncta/mum(2) , while the synapse size increased 3.3-fol

203 aberrant accumulations of PAR-6 cytoplasmic puncta near the centrosome along with early endosomes.

204 Significantly, similar to synaptic puncta, neuronal processes also exhibit medial-lateral t

205 large nuclear aggregates, with only smaller puncta observed in the cytoplasm.

206 increases in bronchial epithelial cells with puncta of both total ubiquitin and K63-ubiquitin, centra

207 s accumulate as unprocessed proforms, axonal puncta of CRD-NRG1 and NRG3 are comprised of processed p

208 well as accumulation of pure red fluorescent puncta of damaged mitochondria targeted for mitophagy.

209 In the spindle, fluorescent puncta of GFP-Kif15 move toward the equatorial region at

210 on of autophagy as a significant increase in puncta of LC3(+) autophagosomes, endogenous levels of LC

211 tezomib alone resulted in an accumulation of puncta of ubiquitinated proteins that was further enhanc

212 24 h) caused an Mdm2-dependent loss of NMDAR puncta on a timescale similar to adaption of NMDAR funct

213 ondria, enhancing the retention time of Drp1 puncta on mitochondria during the fission process.

214 Active myosin II accumulates in puncta on mitochondria in an actin- and INF2-dependent m

215 re important for the number and size of Drp1 puncta on mitochondria.

216 cortactin, which is present in F-actin-rich puncta on MT1-MMP-positive endosomes and regulates corta

217 Mean density of VGlut1+/PSD95+ puncta on PV+ neurons predicted the activity-dependent e

218 Mean density of VGlut1+/PSD95+ puncta on PV+ neurons was 18% lower in schizophrenia, a

219 RPTPsigma and HSPGs colocalize in puncta on sensory neurons in culture, whereas CSPGs occu

220 nd postsynaptic density 95-positive (PSD95+) puncta, on PV interneurons was lower in postpubertal rel

221 long the ventral PM in discrete vesicle-like puncta or in large (2-10 mum) tubuloreticular plaques.

222 At the embryonic stage, we found that PSD-95 puncta outnumber gephyrin puncta, with the number of gep

223 BATS puncta overlap with Atg16 and LC3, and partially with DF

224 ppocampal slices, fluorescently tagged GLT-1 puncta overlapped with fluorescently tagged mitochondria

225 ynaptic density protein 95-positive [PSD95+] puncta) per surface area of parvalbumin-positive (PV+) o

226 ys after IRI, whereas the high levels of RFP puncta persisted, indicating autophagy initiation at day

227 n of these particles into sharply delimited "puncta" positioned upon raised membrane subdomains.

228 is perturbed, and Alix accumulates in large puncta positive for cortactin.

229 hereas the density of PV-immunoreactive (IR) puncta (presumed PVBC boutons) increases during adolesce

230 to the strongly posteriorly-enriched GFP-Dvl puncta previously reported in zebrafish.

231 reduced spine density and increased synaptic puncta, providing quantitative measures of risk for deve

232 Newly synthesized LamB appeared in discrete puncta, rather than evenly distributed over the cell sur

233 Importantly, the density of Bassoon puncta remained relatively constant from postnatal day 0

234 At the poles, puncta remained relatively stationary through several ro

235 hagy and caused accumulation of p62-positive puncta reminiscent of the p62 pathology observed in C9AL

236 Y-Venus, the distribution of the fluorescent puncta replicated the cell type-specific distribution of

237 The number of EGFP puncta returned to control levels at 3 days after IRI, w

238 Piccolo puncta sandwiched Bassoon puncta and aligned in a Piccol

239 These puncta showed no statistically significant spatial bias,

240 ding diminishes the formation of cytoplasmic puncta, shows partially impaired regulation of transport

241 ors preceded presynaptic increases in GAD-65 puncta size.

242 postsynaptic density (PSD95) immunoreactive puncta suggesting that they receive synaptic input from

243 liferation decreased in cells containing RFP puncta, suggesting that autophagic cells are less likely

244 umulation of LC3 reporter RFP+ GFP+ (yellow) puncta, suggesting that HIV-1 infection triggers autopha

245 nd an increase in the density of presynaptic puncta, suggesting that reduced arborization is accompan

246 cell-target cell contact, formation of viral puncta-target cell conjugation, transfer of viral puncta

247 ion in vitro forms smaller and fewer nuclear puncta than phosphorylated HP1alpha.

248 for the formation of cytoplasmic proteasome puncta that accumulate when autophagosome formation is b

249 he SCAR/WAVE complex, locates to vesicles or puncta that appear upon applied pressure.

250 eptide cargo form DIMM-dependent fluorescent puncta that are coassociated by super-resolution microsc

251 g shows dynamic properties of localized PFKL puncta that are enriched at the plasma membrane.

252 mp1 protein localizes in periodically spaced puncta that are in register with the taenidial spacing.

253 We found that WHAMM forms puncta that colocalize and comigrate with the autophagy

254 We observed highly motile internal puncta that colocalized with E2 protein, which may repre

255 agged GluN1 subunits resulted in fluorescent puncta that colocalized with synaptic markers.

256 rsely, in the absence of Ubr1, slGFP and the puncta that contain slGFP are relatively stable.

257 cortex, where it is organized into nanoscale puncta that influence the size of their associated PSDs.

258 Hh and Ptc were present in puncta that moved along the basal cytonemes and formed c

259 ules, with increased numbers of RFP and EGFP puncta that peaked at 1 day after IRI.

260 These studies showed that GORK assembles in puncta that reversibly dissociated as a function of the

261 doplasmic reticulum (ER) store, organizes as puncta that trigger store-operated Ca(2+) entry (SOCE) v

262 classes of puncta, including relatively dim puncta that were located at active zones and may reflect

263 ectopically expressed Nrbf2 formed cytosolic puncta that were positive for isolation membrane markers

264 ndocytic collar"); and small, rapidly moving puncta that were seen trafficking long distances in near

265 pithelium, obscurins localize in cytoplasmic puncta, the cell membrane, and the nucleus.

266 tant for retaining the enzyme in cytoplasmic puncta, thereby inhibiting activity at the plasma membra

267 -stranded DNA binding protein I3 in multiple puncta throughout the interior of factories, which were

268 sion of Mybphl in the atria, and in discrete puncta throughout the right ventricular wall and septum,

269 rons, NHE6 was found to localize to discrete puncta throughout the soma and neurites, with noticeable

270 Vti1a in mammalian cells caused LC3-positive puncta to accumulate and blocks autophagic flux.

271 ellular junction components from the lateral puncta to the cell termini.

272 ecrease in the number of presynaptic Bassoon puncta, together with a reduction of PSD-95 levels at de

273 ells did not increase LC3-II or LC3-positive puncta under hyperosmotic conditions.

274 dition a greater number of perisomatic GAD67 puncta was observed suggesting a potential increase in p

275 lthough the arrangement of Orai1 channels in puncta was substantially unstructured, a portion of chan

276 Capsid puncta were also observed at the PM.

277 Dvl puncta were also observed, but only upon elevated overex

278 campal neurons, most of the postsynaptic NPY puncta were clustered opposite synapsin-containing varic

279 In the autophagic myopathy subjects, puncta were coarser and tended to coalesce into linear s

280 VGAT immunofluorescent puncta were first seen sparsely in NL at E9.

281 NPY puncta were found in the dendrites and axons of hippocam

282 activation, spines that were endowed with SP puncta were much more likely to expand than SP(-) spines

283 Postsynaptic SynCAM 1 surface puncta were not static but became enlarged after a long-

284 ble perinuclear staining; only peripheral ER puncta were observed.

285 mma2 subunit clusters and presynaptic GAD-65 puncta were observed.

286 In the mouse retina, Cx50-immunoreactive puncta were predominantly localized on large axon termin

287 Importantly, CA3 synaptic puncta were similar between WT and C3 KO mice at P30.

288 istributed to discrete membrane subdomains ("puncta"), where they form asymmetric contacts between ne

289 izes with mCherry-Rab8A in perinuclear small puncta, whereas GFP-MyoVa-CT collapses the GTPase into e

290 there was a sparse distribution of VGluT2-ir puncta, whereas in macaque, there was a dense distributi

291 tidase from the apical membrane to subapical puncta, whereas multidrug resistance protein 2 distribut

292 opy and colocalization of ubiquitin-positive puncta with lysosomal-associated membrane proteins 1 and

293 ted in 70% fewer and less intense N-cadherin puncta with similar reductions of beta-catenin and alpha

294 manner, and caused the association of DFCP1 puncta with the autophagosomes.

295 found that PSD-95 puncta outnumber gephyrin puncta, with the number of gephyrin puncta increasing to

296 e-lapse imaging reveals that alpha-actinin-1 puncta within actomyosin bundles move more quickly than

297 f NMJs revealed that the majority of Bassoon puncta within an NMJ were attached to the presynaptic me

298 tion of thrombospondin-1 or thrombospondin-5 puncta within cell-derived ECM is controlled by a novel,

299 ght induces Vipp1 coalescence into localised puncta within minutes, with net relocation of Vipp1 to t

300 aled large numbers of synaptophysin-positive puncta within the colonies but fewer VGluT-1 puncta.