ライフサイエンスコーパス: perinuclear

1 However, both the perinuclear accumulation and the activation of GEF-H1 we

2 ence was greatly attenuated with evidence of perinuclear accumulation in astrocytes.

3 namics by enhancing fusion and induced their perinuclear accumulation in HEK293 cells and rat primary

4 ZCL278 reduces the perinuclear accumulation of active Cdc42 in contrast to

5 ximately 0.5%) led to impaired mitophagy and perinuclear accumulation of damaged mitochondria associa

6 n of tubular membrane carriers from the TGN, perinuclear accumulation of early endosomes and impaired

7 -transfected CF airway cells showed abnormal perinuclear accumulation of GFP(+) structures.

8 nt of HeLa cells with BIG2 siRNA resulted in perinuclear accumulation of integrin beta1 and its delay

9 utants, we define the mechanisms involved in perinuclear accumulation of PKCalpha and identify the no

10 These animals developed perinuclear accumulation of ubiquitin and the E3 ubiquit

11 Abnormal perinuclear accumulation of vimentin filaments, which so

12 tion both in vitro and in vivo and maintains perinuclear accumulations of capsids, facilitating produ

13 tic diseases), was found to be important for perinuclear actin assembly.

14 ar envelope did not abolish Ca(2+)-dependent perinuclear actin assembly.

15 N) lines, which couple the nucleus to dorsal perinuclear actin cables undergoing retrograde flow.

16 ispensable for the retrograde flow of dorsal perinuclear actin cables, supporting the recently propos

17 of a subset of actin filament bundles - the perinuclear actin cap - connected to the nucleus through

18 These results establish the perinuclear actin cap and associated ACAFAs as major med

19 al model explains why LINC complexes and the perinuclear actin cap are essential in 3D migration by p

20 ll subset of actin fibers, those forming the perinuclear actin cap that wraps around the nucleus, for

21 pond rapidly to external force by remodeling perinuclear actin in a unique Ca(2+)- and INF2-dependent

22 Our data suggest that a perinuclear actin meshwork connects actin cables to nucl

23 phore A23187 recapitulated the force-induced perinuclear actin remodeling.

24 The perinuclear actin rim structure colocalized with INF2 on

25 ate a critical role for FMN2 in generating a perinuclear actin/FA system that protects the nucleus an

26 cleator FMN2 associates with and generates a perinuclear actin/focal adhesion (FA) system that is dis

27 ptin 7 knockdown lead to a disruption of the perinuclear actomyosin and persistent directional migrat

28 ic misfolded protein species that present as perinuclear aggregates known as aggresomes.

29 ear export, promoting the formation of large perinuclear aggregates of RNPs along with cellular Rab11

30 We present evidence that, as perinuclear aggresomes accumulate, they are associated w

31 trophil cytoplasmic antibodies (cytoplasmic, perinuclear and atypical perinuclear patterns).

32 Sti1-inducible foci are perinuclear and contain proteins that are bound by the a

33 P1 together with polyglutamine is shifted to perinuclear and cytoplasmic areas.

34 ull-length, canonical LANA1 by localizing to perinuclear and cytoplasmic sites.

35 es increased mitochondrial oxidant stress in perinuclear and dendritic compartments.

36 nnected network throughout the parasite with perinuclear and peripheral localizations.

37 dation intermediates being concentrated into perinuclear and peripheral puncta.

38 RC3 prevented proper trafficking of STING to perinuclear and punctated region, known to be important

39 nized smooth ER with pronounced expansion at perinuclear- and peripheral positions.

40 and autoantibodies consisting of high-titre perinuclear antineutrophil cytoplasmic antibodies (p-ANC

41 nuclear lamin A/C-mediated formation of the perinuclear apical actin cables protects the nuclear str

42 the dynamic formation of a highly organized perinuclear apicosome structure.

43 arned that Vasa interacted with mRNAs in the perinuclear area and at the spindle in an Importin-depen

44 of Atg16L1-positive recycling endosomes to a perinuclear area and for delivery of Atg16L1- and LC3-po

45 mostly cytoplasmic protein localizing in the perinuclear area and forms highly stable dimers/oligomer

46 opy of YC-36 showed drug distribution in the perinuclear area and plasma membrane.

47 translocation of ASC from the nucleus to the perinuclear area during inflammasome activation.

48 remains under the control of IKKalpha in the perinuclear area following translocation of the ASC/IKKa

49 ant accumulation of these TG6 mutants in the perinuclear area led to activation of the unfolded prote

50 nsport of PIP2 rich organelles from the cell perinuclear area to the edge, along actin fibers.

51 ear depletion, increased accumulation in the perinuclear area, insolubility and loss of enzymatic fun

52 protein mainly localized to the nucleus and perinuclear area, whereas five TG6 mutations showed nucl

53 ork in Miro1(-/-) MEFs was restricted to the perinuclear area, with few mitochondria present at the c

54 conjugate was distributed in cytoplasmic and perinuclear areas during the first 1 h of incubation and

55 ally, the ratio of ATP to ADP was highest at perinuclear areas of dense mitochondria and gradually de

56 is suppressed by vesicular recycling through perinuclear areas with high PTP1B activity.

57 constraints imposed by chromosome length and perinuclear attachment determine the amount of SCI that

58 Rab8A colocalizes with GLUT4 in perinuclear but not submembrane regions visualized by co

59 er sustained oscillations of the nuclear and perinuclear Ca(2+) concentration (Ca(2+) spiking), which

60 in the rough ER/perinuclear region promotes perinuclear Ca(2+) signaling and predisposes to ryanodin

61 cardiac calsequestrin (CSQ2) trafficking on perinuclear Ca(2+) signaling, we manipulated the subcell

62 not induced and that both Nod factor-induced perinuclear calcium spiking and calcium influx at the ro

63 tent with this, microtubules extend from the perinuclear centrosome to the plasma membrane and allow

64 nd relocalizes the transcription factor to a perinuclear cluster of mitochondria.

65 in turn, alter p38 and ERK1/2 signaling from perinuclear, clustered signaling endosomes.

66 gradation upon internalization, did not form perinuclear clusters with PICK1, and PICK1 did not affec

67 unofluorescence images indicated a potential perinuclear co-localization between IGFBP-1 and CSNK-2be

68 endent way and displayed detectable spots of perinuclear co-localization with Rac1 and RhoGDI.

69 in the case of overexpressed Cav1-GFP, this perinuclear compartment consists of cytoplasmic inclusio

70 trafficking, including its accumulation in a perinuclear compartment previously identified as the Gol

71 ains, and correlated with movement between a perinuclear compartment, adhesions, and the plasma membr

72 nduced CFTR movement into an aggresome-like, perinuclear compartment.

73 e 2-mediated Ca(2+) waves from CSQ2-enriched perinuclear compartments and myocyte hypotrophy.

74 o aberrant localization of HIF-1alpha to the perinuclear compartments and surprisingly stimulates nuc

75 nificant delay in transferrin trafficking to perinuclear compartments, demonstrating an integral role

76 anslocates from the endoplasmic reticulum to perinuclear compartments.

77 vitro but was necessary for the genesis of a perinuclear-concentrated network of keratin filaments, n

78 mal cadherin-catenin complex assembly in the perinuclear cytoplasm and subsequent localization to the

79 cells, we observed their colocalization in a perinuclear cytoplasmic compartment that was associated

80 . gingivalis-NDK transfected GECs revealed a perinuclear/cytoplasmic localization of NDK.

81 e cellular distribution of PER2 is primarily perinuclear/cytoplasmic.

82 3 regulates vascular endothelial cell shape, perinuclear cytoskeletal architecture, and important asp

83 discriminant of mechanical properties in the perinuclear cytoskeleton (pnCSK) of various stem cell ty

84 -MyoVa-CT collapses the GTPase into enlarged perinuclear depots.

85 The tgDISC1 rat displayed mainly perinuclear DISC1 aggregates in neurons.

86 ular localization of altered ELOVL5 showed a perinuclear distribution with a signal increase in the G

87 in human skeletal muscle, where it showed a perinuclear distribution.

88 We determined the crystal structure of the perinuclear domain of human LAP1.

89 localized AAA+ ATPases, through a conserved, perinuclear domain.

90 In addition, strongly positive perinuclear dots were observed in 30 of 36 specimens (83

91 nits in HeLa cells recapitulates the loss of perinuclear dynein in ASUN-small interfering RNA cells.

92 tion sequence blocks its capacity to restore perinuclear dynein in both cultured human cells lacking

93 hat ASUN down-regulation causes reduction of perinuclear dynein in prophase of mitosis.

94 is required in Drosophila spermatocytes for perinuclear dynein localization and nucleus-centrosome c

95 his paper, we reveal the passage of LDs from perinuclear endoplasmic reticulum association to entry i

96 islocalization of R-opsin and S-opsin to the perinuclear endoplasmic reticulum.

97 r mechanisms underlying Ca(2+) regulation by perinuclear endoplasmic/sarcoplasmic reticulum (ER/SR) c

98 endosomes (PEs), c-Met needs to traffic to a perinuclear endosome (PNE) to sustain Rac1 signalling, t

99 so causes mislocalization of Lck to Rab11(+) perinuclear endosomes.

100 We found that perinuclear enriched CSQ2-DsRed, but not normally distri

101 We present a model in which ASUN promotes perinuclear enrichment of dynein at G2/M that facilitate

102 l symmetry between the cortical ER (cER) and perinuclear ER (pnER).

103 ression in HEK293T cells localizes it to the perinuclear ER region and it trans-rescues the ankB muta

104 sociated with lipid droplet formation in the perinuclear ER, is responsible for the initial rapid exi

105 e-bound organelles and highlight research on perinuclear factories induced by the nucleocytoplasmic l

106 Although RILP localizes in a perinuclear fashion, cRILP moves to the cell periphery.

107 membranes and is internalized to hydrophobic perinuclear features, the nuclear membrane and inside th

108 calization of both proteins in a meshwork of perinuclear filamentous structures.

109 Also, no perinuclear fluorescence was detected in cells expressin

110 n germline P granules and in cytoplasmic and perinuclear foci in somatic cells.

111 cation of Gbetagamma to the Golgi stimulated perinuclear Golgi PI4P depletion and nuclear PKD activat

112 a indicate that Gbetagamma regulation of the perinuclear Golgi PI4P pathway and a separate pathway at

113 hosphate (PI4P) and binds GABARAPs, from the perinuclear Golgi region to autophagosomes to generate P

114 , these cisternae are stitched together as a perinuclear Golgi ribbon, which is required for the esta

115 enin trafficking, leading to accumulation at perinuclear Golgi structures.

116 wn facilitates the spatial relocalization of perinuclear H3K9me3-positive heterochromatin, thus promo

117 and transcriptional upregulation through the perinuclear hydrolysis of phosphatidylinositol 4,5-bipho

118 ype HMGCLL1 exhibits a punctate as well as a perinuclear immunostaining pattern, indicating myristoyl

119 expression increases and becomes nuclear or perinuclear in advanced PCa.

120 frequently concentrated to the aggresome, a perinuclear inclusion body, and subsequently removed by

121 The progression of perinuclear inclusions being accompanied by cell-cycle a

122 Electron microscopy reveals that perinuclear inclusions disrupt the nuclear envelope.

123 , medium spiny neurons (MSNs) that exhibited perinuclear inclusions expressed cell-cycle markers typi

124 2, were required for the generation of these perinuclear initiated Ca(2+) waves.

125 The perinuclear insulin-like growth factor 1 receptor pool c

126 or 1 receptor signaling complexes present in perinuclear invaginations of the plasma membrane.

127 ered and failed to regain its characteristic perinuclear, lace-like morphology.

128 ormation (PGL-1 and PGL-3) and promote their perinuclear localization (GLH-1 and GLH-4) [9] and inves

129 HCMV-induced, amino acid depletion-resistant perinuclear localization and activation of mTORC1 occurs

130 This bias for perinuclear localization increased during embryogenesis

131 This was particularly evident by the perinuclear localization of aggregates and redistributio

132 cells, concomitant with a disruption in the perinuclear localization of LMP1.

133 Rab7 and negatively regulates rab7-dependent perinuclear localization of lysosomes.

134 t the molecular motor dynein is required for perinuclear localization of mTORC1 in both uninfected an

135 To investigate the role of nesprin-3 in the perinuclear localization of plectin, we generated nespri

136 We associated perinuclear localization of the activated NOTCH4 intrace

137 Perinuclear localization of the uninduced gene depended

138 piRNA production, transposon silencing, and perinuclear localization of Vasa.

139 ZDHHCs 3, 7, and 15, which showed a defined perinuclear localization pattern, suggesting that the lo

140 ocalization of XIST, depletion of Cot-1 RNA, perinuclear localization, and ubiquitination of H2A occu

141 ocation and assembly of 5-LO and LTC(4) S at perinuclear locations and lipid bodies.

142 al3(+) endosomes occurs most frequently from perinuclear locations.

143 assive accumulation in the lumen of enlarged perinuclear, lysosomal-associated membrane protein 1 (LA

144 promotes rather than inhibits rab7-dependent perinuclear lysosome clustering, with these effects of m

145 ized with upregulated Rab7 in LampI-positive perinuclear lysosome compartments.

146 shown earlier to displace phagosomes toward perinuclear lysosomes.

147 riminate between stem cell types by coupling perinuclear mechanical properties to nuclear shape.

148 exin A2 and p11 and show increased fusion of perinuclear membrane vesicles.

149 bilizes association of this complex with the perinuclear membrane.

150 sted of expanded endoplasmic reticulum (ER), perinuclear mitochondria, and a higher abundance of stre

151 FYN and NOX4 colocalized in perinuclear mitochondria, ER, and nuclear fractions in C

152 TCO1), complex I activity, and the number of perinuclear mitochondria.

153 ed by pathological erythroid precursors with perinuclear mitochondrial iron deposition in bone marrow

154 lcium entry through L-type channels elevates perinuclear mitochondrial oxidant stress in SNc dopamine

155 nogen activator system (uPAS) to relocate to perinuclear mitochondrial regions.

156 g, EGFR accumulates in a subset of LBPA-rich perinuclear multivesicular bodies (MVBs) distinct from t

157 causes redistribution of alpha2 integrin to perinuclear multivesicular bodies, alpha2-MVBs.

158 oplasmic P granules at the nuclear pores and perinuclear Mutator foci contribute to target mRNA surve

159 4 is necessary for the formation of a stable perinuclear network of keratin filaments (with type II p

160 MSP300 (nesprin) and rigidity provided by a perinuclear network of microtubules stabilized by Shot (

161 horing device organizing and stabilizing the perinuclear network of vimentin filaments.

162 Virus-induced Asyn localized to perinuclear, neuronal regions expressing viral envelope

163 Our previous work recognized perinuclear Nox-4 as a key contributor to EOMA growth.

164 gulated, resulting in an increased number of perinuclear nuage-like granules where Piwi proteins loca

165 ers are processed into primary piRNAs in the perinuclear nuage.

166 ne (Aub) and Argonaute-3 (Ago3), localize to perinuclear "nuage" granules and use guide piRNAs to tar

167 The fraction of cells with diffuse, perinuclear or intranuclear mHTT changed in parallel wit

168 We did not observe the perinuclear or perinucleolar replicative labeling patter

169 olution of our approach are 1) conversion of perinuclear organelle clustering into a two-dimensional

170 ining proteins, namely endophilin B2, in the perinuclear organization of intermediate filaments.

171 ockdown using RNA interference disturbed the perinuclear organization of vimentin.

172 PGL-1 is required to localize FBF-2 to perinuclear P granules and for efficient binding of FBF-

173 ts with the NF-kappaB ortholog Relish inside perinuclear particles and delivers active Relish to PARP

174 n pattern: Although beta-catenin exhibited a perinuclear pattern in undifferentiated wild-type cells,

175 odies (cytoplasmic, perinuclear and atypical perinuclear patterns).

176 ted from cell surface GPCRs to activation of perinuclear PLCepsilon is not clear.

177 We conclude that perinuclear PLCepsilon, scaffolded to mAKAP in cardiac m

178 b (Ras homology enriched in brain)-GTP, to a perinuclear position that corresponds to the viral cytop

179 fter activation and endosomal transport to a perinuclear position.

180 hsp-16.2 promoter was sufficient to mediate perinuclear positioning under basal level conditions of

181 hery; (2) PM invagination and formation of a perinuclear pre-DMS; (3) expansion through membrane deli

182 om the normal dispersed pattern to a stacked perinuclear presence.

183 n homogenate, resulting in a coarse granular perinuclear PrP(TSE) staining pattern.

184 n, complex I specifically was sequestered in perinuclear PTEN-induced putative kinase 1 (PINK1) and P

185 calization of NS1, Scribble, and Dlg1 within perinuclear puncta and mislocalization of plasma membran

186 ted collagen I molecules accumulate in large perinuclear puncta.

187 ly intersects the TfR and pIgR pathways at a perinuclear Rab11-negative compartment termed common rec

188 K-2beta interactions were also predominantly perinuclear rather than nuclear as indicated by mTOR and

189 ulin-stimulated mobilization of GLUT4 from a perinuclear recycling endosome/TGN compartment.

190 Moreover, E5-expressing cells exhibit a perinuclear redistribution of annexin A2 and p11 and sho

191 ral genome replication and recapitulated the perinuclear redistribution of NS5A seen in the S225A mut

192 tion to the nuclear envelope, there exists a perinuclear region (PNR or perinucleus) with unknown com

193 Absence of sarcomeres in the perinuclear region and abnormal invaginations of nuclei

194 y, pDox nanoparticles are transported to the perinuclear region and cleaved into Dox, thereby avoidin

195 MCECs), Borg5 associates with septins in the perinuclear region and colocalizes with actomyosin fiber

196 Osm extended CLN3 distribution away from the perinuclear region and enhanced the lysosomal localizati

197 ), leads to the collapse of lysosomes to the perinuclear region and inhibition of PMR.

198 BP-1 and CSNK-2beta interactions were in the perinuclear region and mTOR and CSNK-2beta interactions

199 xpressed in skeletal muscle, enriched in the perinuclear region and the triad, and found in intracell

200 1 is localized in the nucleus, cytoplasm, or perinuclear region but is transiently redistributed to c

201 t KCNQ1 and KCNE1 are both translated in the perinuclear region but traffic by different routes, inde

202 ile population of endosomes moved toward the perinuclear region in directed bursts of microtubule-bas

203 vealed that the BMV 1a and 2a colocalized to perinuclear region in human cells.

204 lues within the nucleus in LoVo-R and in the perinuclear region in LoVo-S cells.

205 Herein, the concept of the perinuclear region is advanced as a formal, identifiable

206 ancreas, S100PBP is expressed in the nuclear/perinuclear region of both exocrine and endocrine compar

207 ions were found to rapidly accumulate in the perinuclear region of cells within 2h, 37+/-19% and 47+/

208 RHBDD2 is distinctly abundant in the perinuclear region of cells, and it localizes to their G

209 that the majority of rAAV accumulates in the perinuclear region of cells, presumably unable to traffi

210 sn) does not inhibit ExoS trafficking to the perinuclear region of intoxicated cells.

211 based GSTs) are also over-represented in the perinuclear region of mammalian cells, possibly for nucl

212 aled redistribution of activated Pyk2 to the perinuclear region of stressed pyramidal neurons.

213 from ER+ breast tumors, HDAC6 localizes to a perinuclear region of the cell, undergoing transport to

214 served rapid transport of peroxisomes to the perinuclear region of the cell.

215 1 hour by HepG2 cells and accumulated in the perinuclear region of the hepatocyte.

216 transcription is completed in the nucleus or perinuclear region of the infected cell, where it is dep

217 he cytoplasm and completed in the nucleus or perinuclear region of the infected cell.

218 ke all known MSUD proteins, localizes in the perinuclear region of the meiotic cell.

219 rst time that CSQ2 retention in the rough ER/perinuclear region promotes perinuclear Ca(2+) signaling

220 This interaction was colocalized in the perinuclear region that could be dissociated by CDDP in

221 tructures and are found to accumulate in the perinuclear region with increasing incubation time.

222 d induce transient actin accumulation in the perinuclear region within approximately 2 min.

223 lysosomes appeared to be concentrated in the perinuclear region, and autophagy flux was impaired.

224 nal motion in the cortex with respect to the perinuclear region, and suggests that the tracking routi

225 cular and tubular membranes localized to the perinuclear region, collectively known as the endocytic

226 tion of vinculin from focal adhesions to the perinuclear region, formation of cortical actin-rich lar

227 creased organelle proximity primarily in the perinuclear region, rapamycin increased organelle contac

228 ed stimulation of ARP2/3 concentrated in the perinuclear region, resulting in defective cell adhesion

229 Additionally, they all localize in the perinuclear region, suggesting that it is a center of MS

230 -dependent movement of effector kinases to a perinuclear region, thereby creating connections to uniq

231 mal compartments unidirectionally toward the perinuclear region, where most acidification events for

232 nt acted to prevent loss of virions from the perinuclear region, which correlated with increased cell

233 aberrant increase in ribosome-free ER in the perinuclear region, without inducing ER stress response.

234 calized in the cytoplasm and the cytoplasmic perinuclear region.

235 d GEF-H1 and microtubule accumulation in the perinuclear region.

236 ption occurred both within nuclei and in the perinuclear region.

237 were mislocalized to the inner segments and perinuclear region.

238 eas non-proteasomal processing occurs in the perinuclear region.

239 ocalized to both the plasma membrane and the perinuclear region.

240 with an apparent higher concentration in the perinuclear region.

241 alpha2B-AR and arrested the receptor in the perinuclear region.

242 redistribute from the cell periphery to the perinuclear region.

243 e), the mutation in NS5A was restricted to a perinuclear region.

244 ivity by immunohistochemistry accumulated in perinuclear regions and rimmed vacuoles in IBM muscle, l

245 more actively propagating Ca(2+) waves from perinuclear regions than did CSQ2-WT.

246 Ubiquitinated pAKT translocates to perinuclear regions, where it is released into the cytop

247 dynamics are required for RRV trafficking to perinuclear regions.

248 , we show that oncogenic RAS and BRAF induce perinuclear relocalization of several RAS pathway protei

249 crease in promoter accessibility and exhibit perinuclear repositioning of the locus from a silent to

250 in a 10-fold reduction in replication and a perinuclear restricted distribution of NS5A, whereas the

251 ks fuse laterally to form the characteristic perinuclear ribbon structure.

252 ol myristate acetate and ionophore A23187, a perinuclear ring pattern was observed for 5LO.

253 conserved in two related proteins, spermatid perinuclear RNA-binding protein (SPNR) and zinc-finger R

254 DsRed, which specifically accumulates in the perinuclear rough ER.

255 Together, they form a flexible perinuclear shield that protects myonuclei from intrinsi

256 Notably, these perinuclear signaling complexes (PSC) are present in tum

257 silicacomes from the blood vessel lumen to a perinuclear site within cancer cells.

258 aused redistribution of OATP1B1 and HMGCR to perinuclear sites.

259 GFP)-MyoVa colocalizes with mCherry-Rab8A in perinuclear small puncta, whereas GFP-MyoVa-CT collapses

260 of GABA-A receptors were distributed in the perinuclear space and along the processes of GFAP(+) cel

261 n at early stages, and focal swelling of the perinuclear space at late stages.

262 the C terminus of ORF67 that resides in the perinuclear space does not impair the functions of ORF67

263 he retention of progeny nucleocapsids in the perinuclear space during egress.

264 Distortions of the perinuclear space observed in unc-84 mutant muscle nucle

265 and MKL2, respectively) are enriched in the perinuclear space of epicardial cells during development

266 ysis revealed vesicle-like structures in the perinuclear space of intestinal and germ cell nuclei, si

267 hat progeny nucleocapsids were retained in a perinuclear space surrounded by inner and outer nuclear

268 i were morphologically abnormal with a wider perinuclear space than normal myonuclei.

269 imod causes accumulation of TLR4 and TLR9 in perinuclear space, consistent with endoplasmic reticulum

270 ormation, nuclear export by budding into the perinuclear space, tegument formation, and envelopment t

271 rved N-terminal domain that extends into the perinuclear space.

272 2A (PP2A) to the sarcoplasmic reticulum and perinuclear space.

273 ies on direct binding of KASH and SUN in the perinuclear space.

274 Skeletal muscle GLUT4 was trapped at perinuclear spaces, most pronounced in patients with CIM

275 However, no perinuclear spherule-like structures were detected in hu

276 The wild-type LHbeta subunit exhibited a perinuclear staining corresponding to the ER/nuclear env

277 mal tissues and particularly strong dot-like perinuclear staining in the lining epithelial cells, sug

278 ltaT and LHbetaL119A displayed no detectable perinuclear staining; only peripheral ER puncta were obs

279 y processed but retained in the aggresome, a perinuclear structure, where misfolded proteins aggregat

280 se recruitment domain (ASC) micrometer-sized perinuclear structures (specks).

281 These perinuclear structures colocalize with the trans-Golgi n

282 ositol 4-phosphate (PI4P) is identified as a perinuclear substrate in the Golgi apparatus for mAKAP-s

283 ng oocyte activation and being stored in the perinuclear theca, the sperm compartment whose content i

284 enome associates with dynein and induces its perinuclear trafficking has remained unclear.

285 c recycling compartment (ERC) is a series of perinuclear tubular and vesicular membranes that regulat

286 overexpression causes localization of APP in perinuclear tubular structures, an increase of lipid raf

287 mentous forms in the cytoplasm to aggregated perinuclear tubules that form a cage-like structure arou

288 , whereas FIP1B, FIP1C, and FIP3 localize to perinuclear tubules.

289 tructures revealed aberrant formation of the perinuclear tubules.

290 ive fusion and membrane biogenesis to form a perinuclear tubuloreticular structure enabling mixing of

291 These perinuclear vesicles displayed positivity for histone in

292 lin-associated glycoprotein (MAG) in LAMP1(+)perinuclear vesicles that fail to migrate to the nascent

293 absence of the vitamin, TTP is localized to perinuclear vesicles that harbor CD71, transferrin, and

294 lower epidermis, and an increased number of perinuclear vesicles.

295 e in the densely packed nucleocapsids inside perinuclear viral inclusions and in the dispersed rod-li

296 port of ebolavirus (EBOV) nucleocapsids from perinuclear viral inclusions, where they are formed, to

297 ds bud at the inner nuclear membrane forming perinuclear viral particles that subsequently fuse with

298 ds bud at the inner nuclear membrane to form perinuclear virions that subsequently fuse with the oute

299 This redistribution from cytosolic to perinuclear was clearly compromised in both CLP- and FLA

300 a homolog of the human pathogen KSHV, led to perinuclear wrapping by acetylated MT bundles and identi