ライフサイエンスコーパス: puncta

1 rmalities (including ectropion and accessory puncta).

2 localization of the SNF1 activator Std1 into puncta.

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

4 annel (VGCC) puncta colocalized with Bassoon puncta.

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

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

7 astrocytic cells and fibers and connexin 43 puncta.

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

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

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

11 icant reduction in the size of surface GluR2 puncta.

12 autophagic vacuoles expressing RFP and EGFP puncta.

13 ulation of axon-derived material in discrete puncta.

14 , which prevents autophagy, contained no RFP puncta.

15 ors toward the recipient cell body in motile puncta.

16 er and by colocalization of Bruchpilot-short puncta.

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

18 -2/HER2 from the cell surface to cytoplasmic puncta.

19 ll dendrites to reach ectopic ribbon-protein puncta.

20 concentrated into perinuclear and peripheral puncta.

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

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

23 4Pm preferentially localized to cytoplasmic puncta.

24 increased VGAT (vesicular GABA transporter) puncta.

25 g11 is required for concentrating Atg32 into puncta.

26 n of endogenous light chain 3 (LC3)-positive puncta.

27 ith independently formed, Arp2/3-based actin puncta.

28 nd reduced the formation of ATG16L1 membrane puncta.

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

30 bi-dimensional densities obtained with SDM (puncta/100 um(2)).

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

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

33 NM2C is found in a dense, isotropic layer of puncta across the subapical domain, which transects the

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

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

36 ) all localize to discrete, regularly spaced puncta along mitochondria.

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

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

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

40 re associated with decreased peripheral Rab5 puncta and a reduced number of early endosome antigen 1

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 in-moesin (ERM) family proteins, localize to puncta and associate with the daughter cells.

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

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

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

47 (24 h) increased the number of GFP-gephyrin puncta and decreased the number of PSD95-GFP puncta.

48 2/3 pyramidal neurons could induce gephyrin puncta and dendritic spine formation via GABA type A rec

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

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

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

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

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

58 activity as measured by density of VGLUT2(+) puncta and Purkinje cell firing rate respectively, in co

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

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

61 SAGA1 localizes to multiple puncta and streaks in the pyrenoid and physically intera

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

63 tent accumulation of TDP-43 into cytoplasmic puncta and that our hit compounds can reduce this accumu

64 of IPMK increases the number of nuclear TFEB puncta and the co-localization of TFEB with Mediator and

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

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

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 es, as indicated by VGLUT2(+) immunoreactive puncta, and computational modeling demonstrated that the

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

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

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

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

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

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

77 BRD4 puncta are correlated with BRD4S but not BRD4L expressio

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

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

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

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

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

83 Puncta are separated by ~210 nm, the expected size of fi

84 a control, we demonstrated that our synaptic puncta assay is at least 10-fold more sensitive to the t

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

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

87 ound that the N723S mutant had more immobile puncta at neuronal processes compared to Mint2 wild type

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

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

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

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

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

93 activation induces the formation of CRACR2a puncta at the plasma membrane, which initially associate

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

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

96 ere we find that the endogenous LC3-positive puncta become larger in cells where autophagosome format

97 ot overlapping with gap junctions, and forms puncta before the clusters of gap junction channels appe

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

99 Y-LIKE in a subcellular complex localized to puncta both at the tip of the growing infection thread a

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

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

102 evelled levels, it forms its own cytoplasmic puncta, but these do not recruit Axin.

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

104 Indeed, Rpt subunits in the puncta can later resume their assembly into the proteaso

105 uinea pigs, counts of immunostained synaptic puncta can recover with increasing post-exposure surviva

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

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

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

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

110 These puncta colocalized with E2 and recruited newly synthesiz

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

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

113 Myo51 puncta contain multiple Myo51 molecules and walk continu

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

115 taining intensity, cell number, or forebrain puncta counts.

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

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

118 ides in either the nucleus or in cytoplasmic puncta, depending on levels of the plant hormone salicyl

119 Puncta dissociation parallelled the gating dependence of

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

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

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

123 fy the number of colocalized mature synaptic puncta for the assessment of synaptic changes in live ne

124 Our multi-labeling studies reveal that nNOS puncta form multiprotein complexes with NMDA receptors,

125 he APC IDR in colorectal cells promotes Axin puncta formation and beta-catenin degradation.

126 1 phosphorylation and led to sustained STIM1-puncta formation and Ca(2+) entry.

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

128 ondensation, and ectopic expression promotes puncta formation and target gene transcription.

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

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

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

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

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

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

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

136 hagy events represented by ATG16L1 and ATG12 puncta formation.

137 Cytoplasmic DAXX promotes p62 puncta formation.

138 7 or TBK1 knockouts blocked ATG13 and FIP200 puncta formation.

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

140 in fact express nNOS in the form of discrete puncta found at the cell membrane.

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

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

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

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

145 ependent mode of TAX1BP1 recruitment to NBR1 puncta, highlighting that TAX1BP1 recruitment and cluste

146 we show that TgDrpC localizes to cytoplasmic puncta; however, in dividing parasites, TgDrpC redistrib

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 hat synthesizes nitric oxide (NO), occurs as puncta in apparently all neurons in the central nucleus

150 light chain 3 (LC3) form II (LC3-II) and LC3 puncta in Atg5-competent BMMs but not in Atg5-deficient

151 -1 forms filaments in vitro and localizes as puncta in cells along the plasma membrane.

152 multimeric assemblies, MORC-1 forms nuclear puncta in cells and can also form phase-separated drople

153 e point mutations eliminate the formation of puncta in cells and have been shown previously to elimin

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

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

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

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

158 I levels and increased accumulation of green puncta in GFP-LC3 Tg hearts.

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

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

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

162 itro and is localized within distinct motile puncta in L. japonicus root hairs and in Nicotiana benth

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

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

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

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

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

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

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

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

171 (SDM), to estimate the number of fluorescent puncta in the CA1 area of the hippocampus.

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

173 unit of NF-kappaB is rerouted to perinuclear puncta in the cytoplasm, which are synonymous with viral

174 reductase activity; and PvOCT4 localizes as puncta in the cytoplasm.

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

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

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

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 orescence recovery signal is concentrated to puncta in the spatial Fourier domain, with substantial i

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

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 onstrated colocalization of mGlu5 with GluD1 punctas in the hippocampus.

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

186 3-II and SQSTM1 and also potentiated GFP-LC3 puncta index in GFP-LC3-transfected hippocampal neural s

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

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

189 hagocytosis), quantification of LC3-positive puncta is considered as a gold-standard assay for assess

190 rightness of different neurites and synaptic puncta is heterogeneous due to the variation of antibody

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

192 anslocation of the ULK complex to autophagic puncta, is repressed during mitosis, even when mTORC1 is

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

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

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

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

197 ity of perisomatic excitatory and inhibitory puncta, longer axonal initial segments (AISs), and highe

198 ab5, and new microtubule growth initiated at puncta marked with fz, dsh, Axin, and Rab5.

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

200 Synaptic puncta move all over the hair cell membrane during recov

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

202 NA movement involves nuclear and cytoplasmic puncta not surrounded by investing membranes.

203 nimals revealed alterations in autophagosome puncta number reflecting those phenotypes seen in vitro.

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

205 and-induced monoubiquitination and endosomal puncta of BIK1 exhibit spatial and temporal dynamics tha

206 EP1 and GCalpha are expressed in cytoplasmic puncta of both male and female gametocytes.

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

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

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

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

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

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 omatic region but not on the PV+ perisomatic puncta on pyramidal neurons.

220 ound a decrease in the density of inhibitory puncta on their perisomatic region but not on the PV+ pe

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

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

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

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

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

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

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

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

229 derived from the patients show reduced WIPI2 puncta, reduced LC3 lipidation and reduced autophagic fl

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

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

232 Piccolo puncta sandwiched Bassoon puncta and aligned in a Piccol

233 These puncta showed no statistically significant spatial bias,

234 eir chaperones are sequestered into multiple puncta specifically during early-stage Rpt ring assembly

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

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

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

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

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

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

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

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

243 iation and form discrete and dynamic nuclear puncta that are characteristic of biomolecular hubs cons

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

245 mation of alpha-synuclein/ubiquitin-positive puncta that are degraded by autophagy.

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

247 Pcdh-gammaC4 forms puncta that are frequently apposed to glutamatergic and

248 11-Atg32 interactions concentrate Atg32 into puncta that are thought to represent sites of mitophagy

249 ted in distribution of this protein as large puncta that co-localized with IVC markers, including fru

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

251 emonstrated that nuclear TFEB forms distinct puncta that colocalize with the Mediator complex and wit

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

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

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

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

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

257 g region (LIR) to traffic into ATG8-positive puncta that often initiate from three-way ER tubule junc

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

259 , in human cancer cells, BRD4S forms nuclear puncta that possess liquid-like properties and that colo

260 resistant version, which localized to active puncta that promote lysosomal-mediated stimulator of int

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

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

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 cell wall with trapping within intracellular puncta; this deletion was accompanied by reduced virulen

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

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

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

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

270 in how mRNA molecules can be passed from one puncta to another, forming a relay that directs mRNAs to

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

272 fundus images, we observed radially arranged puncta typical of RLBP1/CRALBP-associated disease.

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

274 We created A-IDP puncta using these simple principles, which are capable

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

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

277 napses per OHCs, defined as postsynaptic SK2 puncta, was reduced in aged OHCs of all strains apart fr

278 Capsid puncta were also observed at the PM.

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

280 Finally, Cx37 puncta were associated with the entire surface of both m

281 These puncta were juxtaposed to immunolabeled presynaptic effe

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

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

287 g signals of endogenous Kv2.1, Nir2, and VAP puncta were spatially correlated in cultured neurons.

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

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

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

291 sion led to an increased density of synaptic puncta, while isoform 2 ameliorated the calcium signalli

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

293 de a robust engineered platform for creating puncta with new, phase-separation-mediated control of bi

294 gulatory role, DDX3 localized to cytoplasmic puncta with SG marker PABP1 in CRPC.

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

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

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

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.