ライフサイエンスコーパス: cytoplasm

1 ompartment that separated viral DNA from the cytoplasm.

2 ding them or failing to import them into the cytoplasm.

3 uced by reactive oxygen species (ROS) in the cytoplasm.

4 ow organelles orderly cohabit in the crowded cytoplasm.

5 NA-binding protein predominantly resident in cytoplasm.

6 and partially enveloped capsids in neuronal cytoplasm.

7 en the transfected MDM2 was localized in the cytoplasm.

8 teasomes are located in both the nucleus and cytoplasm.

9 ar vehicle for drug delivery to the neuronal cytoplasm.

10 ulum (ER) and are eventually degraded in the cytoplasm.

11 localize mRNAs to discrete locations in the cytoplasm.

12 superfluous and damaged constituents of the cytoplasm.

13 gases, and it localizes predominantly in the cytoplasm.

14 ls but also led to their accumulation in the cytoplasm.

15 on and/or processing in both the nucleus and cytoplasm.

16 decay (NMD) regulating mRNA stability in the cytoplasm.

17 This in turn facilitates mRNA export to the cytoplasm.

18 of ERK1/2, and arrests active ERK1/2 in the cytoplasm.

19 of undigested autophagosomes in the parasite cytoplasm.

20 the total content of Ca(2+) within the fibre cytoplasm.

21 ded within the nucleus and imported from the cytoplasm.

22 rotein that shuttles between the nucleus and cytoplasm.

23 (TVN), an expansion of the PVM into the host cytoplasm.

24 d to relocalize COP1 from the nucleus to the cytoplasm.

25 to, and enrichment of, the transcript in the cytoplasm.

26 sequent targeting of Ssd1 to PB sites in the cytoplasm.

27 the cells, and subsequently dissolved in the cytoplasm.

28 sor DAB2IP (DAB2-interacting protein) in the cytoplasm.

29 cGAS) and absent in melanoma 2 (AIM2) in the cytoplasm.

30 eins, which scavenge the metal ions from the cytoplasm.

31 icated that LINC00152 is found mainly in the cytoplasm.

32 ed to the cell nucleus via endosomes and the cytoplasm.

33 e sequence and exports misfolded SOD1 to the cytoplasm.

34 pt TNF initiated cell death complexes in the cytoplasm.

35 critical regulator of ion homeostasis in the cytoplasm.

36 e nucleotide pools from the mitochondria and cytoplasm.

37 some-associated Nuf disperses throughout the cytoplasm.

38 melanoma cells expressed NLRP1 mainly in the cytoplasm.

39 n microscopy as electron-dense bodies in the cytoplasm.

40 sequestration of NF-kappaB components in the cytoplasm.

41 t factors are shed as vesicles into the host cytoplasm.

42 ear export and subsequent proteolysis in the cytoplasm.

43 d partially spliced viral transcripts to the cytoplasm.

44 1 exited cortical nodes and localized in the cytoplasm.

45 R1-mediated Ca(2+) leak from the SR into the cytoplasm.

46 er RNA, which would not be translated in the cytoplasm.

47 protein gradients, thereby partitioning the cytoplasm.

48 which thereafter releases cyclin C into the cytoplasm.

49 r Rph1 translocation from the nucleus to the cytoplasm.

50 age by secreting effector molecules into the cytoplasm.

51 by microRNAs and RNA-binding proteins in the cytoplasm.

52 egions including special events occurring in cytoplasm.

53 ease in elastic modulus at the periphery and cytoplasm.

54 plate and messenger RNA (mRNA) export to the cytoplasm.

55 lasmic reticulum and to actin ruffles in the cytoplasm.

56 ly G1, when it is actively exported into the cytoplasm.

57 cessively in the nucleolus, nucleoplasm, and cytoplasm.

58 icle-rich inverted cone region, nucleus, and cytoplasm.

59 panied by the uptake of two protons from the cytoplasm.

60 bilizes the membrane nor translocates to the cytoplasm.

61 ein channels connecting the nucleus with the cytoplasm.

62 ation was heterogeneously distributed in the cytoplasm.

63 uces accumulation of gamma2 late mRNA in the cytoplasm.

64 s intravacuolar bacteria or escaped into the cytoplasm.

65 ic role in translocating the nuclease to the cytoplasm.

66 iomotin (AMOT), which sequesters YAP1 in the cytoplasm.

67 with aberrantly high levels of Ube2e1 in the cytoplasm.

68 this recruitment by relocalizing DUX4 in the cytoplasm.

69 s associated with both the cell envelope and cytoplasm.

70 to the presence of numerous vacuoles in the cytoplasm, a decrease in collagen I production, and augm

71 y shows that the endosymbiont ingests amoeba cytoplasm, a novel form of endosymbiont-host communicati

72 until the redistribution of the mRNAs to the cytoplasm after nuclear envelope breakdown (NEBD) at pro

73 es, most RNA molecules are exported into the cytoplasm after transcription.

74 of the Carlr transcript were detected in the cytoplasm, alongside elevated expression of NF-kappaB pa

75 These muropeptides are internalized into the cytoplasm and bind to the transcriptional regulator AmpR

76 , with high enrichments present in vacuoles, cytoplasm and chloroplasts.

77 uring fertilization, sperm DNA enters oocyte cytoplasm and could potentially trigger a response.

78 hypoxia-dependent MTA1 translocation to the cytoplasm and de-repression of SGK1 transcription.

79 te that Nbeal2 is primarily localized in the cytoplasm and Dock7 on the membrane of or in alpha-granu

80 ited HMGB1 translocation from the nucleus to cytoplasm and downregulated the expression of toll-like

81 Poxviruses replicate within the cytoplasm and encode proteins for DNA and mRNA synthesis

82 and plant proteins that traffic through the cytoplasm and enter the nucleus.

83 supports filamentous actin formation in the cytoplasm and gene transcription in the nucleus.

84 Ribosomal proteins are translated in the cytoplasm and imported into the nucleus for assembly wit

85 changes in pH, which occur frequently in the cytoplasm and in secretory pathways, may induce the form

86 G-I and TRIM25 in specific areas in the cell cytoplasm and inhibits the formation of TRIM25 homocompl

87 251, showed it was dominantly located in the cytoplasm and interacted with miR-411-5p via two binding

88 ng 1 (LACC1); LACC1 is expressed in both the cytoplasm and mitochondria.

89 gests that LANA plays important roles in the cytoplasm and nuclear compartments of the cell during di

90 demonstrate that TIAM1 shuttles between the cytoplasm and nucleus antagonizing TAZ/YAP by distinct m

91 TRADD has been shown to cycle between the cytoplasm and nucleus due to its nuclear localization (N

92 Although PS-ASOs function in both the cytoplasm and nucleus, localization to different subcell

93 ting the reporter's distribution between the cytoplasm and nucleus.

94 , TFPI-2 was also distributed throughout the cytoplasm and nucleus.

95 mutant (D28A) accumulated 18S-E in both the cytoplasm and nucleus.

96 n the critical steps of viral entry into the cytoplasm and persistent viral replication in cell cultu

97 PLK-1 is enriched in the anterior cytoplasm and phosphorylates POS-1, which is both necess

98 adients and intracellular fluxes in both the cytoplasm and sarcoplasmic reticulum.

99 led into the OM after their synthesis in the cytoplasm and secretion across the inner membrane.

100 ssor role of AKT-phosphorylated FOXO1 in the cytoplasm and suggest that this function of FOXO1 can be

101 dicates that snoRNAs are also present in the cytoplasm and that snoRNAs move between the nucleus and

102 occur between viral capsid release into the cytoplasm and the expression of viral genes remain elusi

103 s allowing exchange of molecules between the cytoplasm and the extracellular milieu.

104 lation of newly synthesized H4 occurs in the cytoplasm and the function of this acetylation is typica

105 indicated that OsGRXS17 resides in both the cytoplasm and the nuclear envelope.

106 NE) presents a physical boundary between the cytoplasm and the nucleoplasm, sandwiched in between two

107 -related kinases (PIKKs) and localize to the cytoplasm and the nucleus, consistent with known subcell

108 nus truncated (DeltaC) form localized in the cytoplasm and the nucleus.

109 OsHAC4-eGFP was localized in the cytoplasm and the nucleus.

110 ing acid stress, bacteria maintain an acidic cytoplasm and the osmotic stress transcription factor Om

111 We find that hydrodynamic flows in the cytoplasm and the relative drag between the cytoskeleton

112 in subunits from the disc membranes into the cytoplasm, and a relatively higher H2O permeability of n

113 ape from the endosome, pass through the cell cytoplasm, and deliver the single-stranded DNA (ssDNA) g

114 N-terminus of RAD51, sequesters RAD51 in the cytoplasm, and impedes RAD51 binding to DNA.

115 e WT-MIP was stable dispersed throughout the cytoplasm, and it appeared to be in the membrane structu

116 e MTL protein localizes exclusively to sperm cytoplasm, and pollen RNA-sequence profiling identifies

117 prevent their accumulation, transport to the cytoplasm, and resultant disruption of protein synthesis

118 ansport dynamics in different regions of the cytoplasm, and suggest that RNA movement in both the ani

119 inant disulfide bond-requiring enzyme in the cytoplasm, and this copper-induced mechanism of disulfid

120 sequestration capacity, are exported to the cytoplasm, and undergo RAN translation.

121 ization of RNA5SP141 from the nucleus to the cytoplasm, and virus-induced shutoff of host protein syn

122 f-channels that access the periplasm and the cytoplasm are exposed to the same pH, these data are con

123 type 1 (HIV-1) RNAs serve dual roles in the cytoplasm as mRNAs encoding the Gag and Gag-Pol capsid p

124 nslocated ERAD-M substrates are moved to the cytoplasm as part of the normal ERAD pathway, where they

125 majority of proteins are synthesized in the cytoplasm as preproteins and then imported into the orga

126 mislocalization of all but one mutant in the cytoplasm, as well as nuclear localization.

127 ocalized and specifically accumulated in the cytoplasm at the cell edges and cell-cell contacts.

128 RhoGAP Deleted in liver cancer (DLC1) in the cytoplasm at the cell front.

129 accompanied by highly activated RHOA in the cytoplasm at the cell rear and its fluctuating activity

130 NS5A sequesters NAP1L1 in the cytoplasm, blocking its nuclear translocation.

131 eus, Ssd1 fails to associate with PBs in the cytoplasm but rather is targeted to cytosolic insoluble

132 ing virion-mediated genome delivery into the cytoplasm, but not in any virion-assigned step, such as

133 ntain five topoisomerases in the nucleus and cytoplasm, but which one is the major topoisomerase for

134 nd that snoRNAs move between the nucleus and cytoplasm by a mechanism that is regulated by lipotoxic

135 y divergent proteins in the Escherichia coli cytoplasm by in-cell NMR.

136 es replicate on membranous structures in the cytoplasm called replication complexes (RCs).

137 Targeting mRNAs to distinct regions of the cytoplasm contributes to protein localization by providi

138 om the trans-Golgi network to the peripheral cytoplasm, contributing to lipidation of the autophagy p

139 mitted by (64)Cu from the cell surface (CS), cytoplasm (Cy), or nucleus (N) of a single cell; monolay

140 ction include release of the capsid into the cytoplasm, docking of the capsid at a nuclear pore, and

141 -3-3 protein Rad24 that sequesters it in the cytoplasm during cell division.

142 bly, PSPC1 relocates from the nucleus to the cytoplasm during differentiation, coinciding with enhanc

143 When PpMS is targeted to the cytoplasm employing a heterologous nuclear export signal

144 the translocation of nuclear La/SSB into the cytoplasm, enhanced the protein synthesis of LAMB1 by ac

145 ob1 and how the late factor's removal in the cytoplasm ensures the structural integrity of the maturi

146 , RNA viruses that replicate strictly in the cytoplasm, express a protein variant that localizes to n

147 ns-envelope syringe, the injectisome, with a cytoplasm-facing translocase channel.

148 ow that, because of HIs between the MTs, the cytoplasm-filled astral MTs behave like a porous medium,

149 r dsRNA from endocytic compartments into the cytoplasm for immune activation.

150 n aggregates and damaged organelles from the cytoplasm for recycling.

151 ism, whereby cells autodigest parts of their cytoplasm for removal or turnover.

152 he cell nucleus before being exported to the cytoplasm for translation.

153 that Ccp lacks enough activity to shield the cytoplasm from exogenous H2O2 However, it receives elect

154 E), a double membrane barrier separating the cytoplasm from the nucleoplasm.

155 We conclude that the cellular cytoplasm has a remarkable capacity for self-organizatio

156 gs suggest that intron-retained mRNAs in the cytoplasm have previously uncharacterized functions and/

157 ryotes, nascent subunits are exported to the cytoplasm in a functionally inactive state.

158 s indicates that SCM:GFP is localized to the cytoplasm in a non cell type dependent manner instead of

159 o vacuoles and then subsequently, within the cytoplasm in a rapid and Shu1-dependent manner.

160 Vinculin is present in the cytoplasm in an autoinhibited conformation in which its

161 gly to R2TP, with one mutant retained in the cytoplasm in an R2TP-dependent manner.

162 the nucleus in G2 phase and released to the cytoplasm in anaphase, where it accumulates at the bud n

163 rapid translocation of 5-LOX from nucleus to cytoplasm in both ECs and VSMCs, potentially facilitatin

164 ed with alanines, primarily localizes to the cytoplasm in budding cells.

165 cells to probe the capacity of the cellular cytoplasm in dealing with foreign material and to develo

166 on, we determined that LANA localizes to the cytoplasm in different cell types undergoing the lytic c

167 extracellular space (>100 mM) and within the cytoplasm in eukaryotes (10 approximately 20 mM).

168 in proliferating cells, RNF8 operates in the cytoplasm in neurons to suppress synapse differentiation

169 e nuclear, shuttle with messenger RNA to the cytoplasm in pluripotent P19 cells, but not in different

170 o initiate a pro-inflammatory pathway in the cytoplasm in senescence and cancer.

171 se that degrades proteins in the nucleus and cytoplasm, in homolog juxtaposition and crossing over.

172 ir DDR functions, yet both are also found in cytoplasm, including on neuronal synaptic vesicles.

173 hat virus particles are transported from the cytoplasm into the most proximal segments of axons.

174 relaxation by pumping calcium ions from the cytoplasm into the sarcoplasmic reticulum.

175 7A, which mediates copper transport from the cytoplasm into the secretory pathway, as well as copper

176 We propose that Mn export from the cytoplasm into the thylakoid lumen is crucial to prevent

177 ort of molecules between the nucleus and the cytoplasm is facilitated by highly selective and efficie

178 The ability of lysosomes to move within the cytoplasm is important for many cellular functions.

179 es relevant to epithelial morphogenesis, the cytoplasm is predominantly viscous, whereas the cellular

180 Within P. polycephalum, cytoplasm is shuttled in a peristaltic wave driven by cr

181 t least some U12-type splicing occurs in the cytoplasm is still unclear.

182 cellular components between the nucleus and cytoplasm is the defining feature of eukaryotic life.

183 The possible activity of BAP1 in the cytoplasm is unknown.

184 The cytoplasm is usually a DNA-free zone, but during fertili

185 ng of macromolecules between the nucleus and cytoplasm, is tightly regulated by nuclear pore complexe

186 nslocation to specialized regions within the cytoplasm, leading to tegumentation, secondary envelopme

187 genetic material via introduction into donor cytoplasm may offer a source of oocytes for infertility

188 In both the nucleus and the cytoplasm, mRNAs harboring 8 repeats moved faster than t

189 uantification of fine details in cell shape, cytoplasm, nucleus, lipid bodies and cytoskeletal struct

190 revealed that MIWI2 protein localized to the cytoplasm of a discrete population of multiciliated airw

191 ulfide bond-folded proteins in the bacterial cytoplasm of an Escherichia coli reporter strain.

192 l DNA viruses, replicate entirely within the cytoplasm of animal cells, raising questions regarding t

193 stemmed from the accumulation of DNA in the cytoplasm of AT and Artemis-deficient cells.

194 lticellular bacterial communities within the cytoplasm of bladder epithelial cells.

195 zed expression of aquaporin-2 protein in the cytoplasm of CD cells.

196 opic whispering gallery mode lasers into the cytoplasm of cells and to use their characteristic, size

197 py, ephrinA1, known to markedly collapse the cytoplasm of cells expressing the EphA2 receptor, to inv

198 rticle core can be directly delivered to the cytoplasm of cells upon US-mediated rupture of the carri

199 ing to monitor levels of testosterone in the cytoplasm of cells with a promising application value in

200 MDFIC associated with GR in the cytoplasm of cells, and treatment with glucocorticoids r

201 ytoskeleton, they physically interact in the cytoplasm of chondrocytes, and loss of FlnA enhances Fln

202 in the accumulation of DNA fragments in the cytoplasm of cornifying lingual keratinocytes and co-del

203 orly understood manner and aggregates in the cytoplasm of degenerating neurons in Parkinson's disease

204 and expressed it as a soluble protein in the cytoplasm of E. coli.

205 nslational diffusion coefficients (D) in the cytoplasm of Escherichia coli, Lactococcus lactis and Ha

206 procollagen I molecules were present in the cytoplasm of fibroblasts exposed to nicotine-free fluids

207 P300 translocates from the nucleus into the cytoplasm of hepatocytes.

208 nfection, the presence of foreign DNA in the cytoplasm of host cells can initiate type I IFN signalin

209 ication of 20 metabolites recovered from the cytoplasm of individual HeLa cells.

210 oach, we observed distinct EdU puncta in the cytoplasm of infected cells within 12 h postinfection an

211 oportions of empty (DNA-less) capsids in the cytoplasm of infected cells, suggesting that UL21 may pl

212 relationship between Rab11A and vRNA in the cytoplasm of infected cells.

213 utant superoxide dismutase 1 (SOD1) into the cytoplasm of invertebrate neurons rapidly suppresses the

214 nd MIWI stabilization sequesters RNF8 in the cytoplasm of late spermatids.

215 (NPs) with the capacity to accumulate in the cytoplasm of leukaemia cells for several days and releas

216 sma membrane, in the nucleoplasm, and in the cytoplasm of living cells.

217 ased on the stable expression of BirA in the cytoplasm of maize plants and on engineering of Ustilago

218 iRNA delivered intranasally was found in the cytoplasm of neurons and glial cells of the prefrontal c

219 of their native promoters, localized in the cytoplasm of pollen grains, pollen tubes, and also root

220 ization of TnBVANK1 and Alix proteins in the cytoplasm of polyclonal S2 cells.

221 he NME proteins co-localize with IRF6 in the cytoplasm of primary palatal epithelial cells in vivo, a

222 AR N-terminal domain to sequester AR in the cytoplasm of prostate cancer cells, thereby reducing AR

223 ulation of SNAI1 protein was detected within cytoplasm of proximal tubules localized, for some of the

224 d flavivirus-like particles were detected in cytoplasm of spinal neurons, and spinal cord samples wer

225 get nucleic acids (DNA, tRNA or rRNA) in the cytoplasm of susceptible bacteria, usually closely relat

226 components including the apical membrane and cytoplasm of the cell at the tissue scale level as well

227 the ability of NS5A to spread throughout the cytoplasm of the cell.

228 the C terminus of pHLIP gets exposed to the cytoplasm of the target cell, providing a means to trans

229 ed ssDNA present in the neuron and astrocyte cytoplasm of TREX1 mutated stem cell-derived organoids.

230 l effect gene, is present in the nucleus and cytoplasm of zygotes and has been associated with protec

231 TB4 interacted with either smoothened at the cytoplasm or GLI2 at the nucleus in LX-2.

232 rounds and sequesters random portions of the cytoplasm or selectively targets individual intracellula

233 evolved to replicate exclusively within the cytoplasm or vacuole of a eukaryotic cell.

234 e II (MII) oocytes into enucleated donor MII cytoplasm (PBNT).

235 wing a positive staining of their nucleus or cytoplasm per 1 high-power field 200x (grades 0-3).

236 In the cytoplasm, PERs, CRYs, and CK1delta were distributed int

237 cal microscopy, was dispersed throughout the cytoplasm prior to activation.

238 ranular, eosinophilic, and mitochondria-rich cytoplasm, prominent nucleoli, and markers of hepatocyte

239 oncentration of MEX-5/PLK-1 in the posterior cytoplasm provides a permissive environment for the rete

240 most oskar mRNA to localise in the posterior cytoplasm rather than cortically.

241 accumulated in large numbers in the neuronal cytoplasm rather than reaching cell surfaces as wild-typ

242 have recently demonstrated that the nuclear/cytoplasm ratio (NCR), rather than cell size, is a key p

243 ells are characterized by a large nucleus-to-cytoplasm ratio.

244 T1 in PCs caused them to expand their apical cytoplasm, rearrange mitochondrial/lysosome trafficking,

245 ydrolysis leads to substrate delivery to the cytoplasm, release of the SBP, and resetting of the syst

246 ecisely how cellular DNA gains access to the cytoplasm remains to be determined.

247 o be distinctly located in the periplasm and cytoplasm respectively.

248 ester specific organelles/substrates or bulk cytoplasm, respectively, inside autophagosomes as cargo

249 er isoforms, which are located mainly in the cytoplasm, Ser5-001 is localized primarily to the plasma

250 translocation of HuR from the nucleus to the cytoplasm, specifically promoting stabilization of a new

251 and R2TP bind unassembled U5 proteins in the cytoplasm, stabilize them, and promote the formation of

252 rtions of empty capsids were observed in the cytoplasm, suggesting a role for UL21 in preventing thei

253 mitochondrial proteins were enriched in the cytoplasm, suggesting that the accumulation of mitochond

254 he nucleus and is rapidly transported to the cytoplasm, suggesting the existence of myosin XI-driven

255 Ribeye between other ribbons via the cell's cytoplasm takes several hours.

256 s to deliver cytotoxic Yop proteins into the cytoplasm that prevent phagocytosis and generation of pr

257 the nucleus, their site of synthesis, to the cytoplasm, their site of function for protein synthesis.

258 ent 6beta-stranded form that diffuses in the cytoplasm to an active 4beta-stranded form bound to the

259 us and shuttles, at least in neurons, to the cytoplasm to form TDP-43 RNA granules.

260 zation from MAN2A1 and translocated from the cytoplasm to Golgi in cancer cell lines.

261 reported ability to relocalize Sis1 from the cytoplasm to nucleus.

262 ranscription coactivators shuttling from the cytoplasm to the nucleus.

263 nd this activated Pak1 translocates from the cytoplasm to the nucleus.

264 at leads to NF-kappaB translocation from the cytoplasm to the nucleus.

265 al cells and GSK-3beta mobilization from the cytoplasm to the nucleus.

266 rine/arginine-rich splicing factors from the cytoplasm to the nucleus.

267 d DNABII proteins transit from the bacterial cytoplasm to the periplasm via an inner-membrane pore co

268 s function to translocate the virus from the cytoplasm to the plasma membrane leading to virion buddi

269 strategy, we found that macrophages transfer cytoplasm to tumor cells in zebrafish and mouse models.

270 We further found that macrophages transfer cytoplasm to tumor cells upon cell contact in vitro.

271 applies to molecular encounters in the cell cytoplasm, to animals looking for food or mates in natur

272 KPNA4 mediates the cytoplasm-to-nucleus translocation of transcription fact

273 ly site, Atg24 in cargo engulfment, Atg26 in cytoplasm-to-vacuole targeting, and Ssd1, Did4, and othe

274 in-1-dependent pri-miR-34a is present in the cytoplasm together with a small isoform of Drosha, imply

275 lead to the accumulation of self-DNA in the cytoplasm, triggering a STING-mediated innate immune res

276 elivery of virulence effectors into the cell cytoplasm via a type III secretion system (T3SS).

277 recognizes viral or mitochondrial DNA in the cytoplasm via activation of the recently discovered cycl

278 endocytosis of the complex, iron enters the cytoplasm via DMT1 in the endosomal membrane.

279 The cytoplasm was measured to be approximately 10(3)-fold as

280 cytotic pathway gaining direct access to the cytoplasm, we have studied iron NP uptake under this per

281 Immunoreactivity in the nucleus and cytoplasm were graded by estimating the percentage of pr

282 lasma membrane but still associated with the cytoplasm were released after oxytocin-mediated contract

283 nto adipocytes and accumulated lipids in the cytoplasm when cultured with butyric acid, a principal s

284 translation of viral mRNAs in the host cell cytoplasm where cellular transcripts are competing for t

285 em and an N-terminus fragment remains in the cytoplasm where it associates with early and re-cycling

286 rticles were selectively disassembled in the cytoplasm where they released miRNA.

287 ed not only in the cell wall but also in the cytoplasm, where they are coupled to other monolignols a

288 Piezo1 localizes to the plasma membrane and cytoplasm, whereas in dense regions in which cells extru

289 ly assemble enveloped virus particles in the cytoplasm, which blocks anterograde transport of envelop

290 sids and enveloped particles in the neuronal cytoplasm, which can explain the reduced anterograde tra

291 a four-helix bundle subdomain located in the cytoplasm, which functions as the osmosensing core throu

292 eduction increases the crowded nature of the cytoplasm, which is expected to affect protein stability

293 s of the lamellipodial actin diffuses in the cytoplasm with nearly uniform density, whereas the rest

294 ng molecules from early endosomes in a dense cytoplasm with single-molecule resolution.

295 coupling intercompartmental transport in the cytoplasm with stabilization of the active form in the n

296 to as hemichannels, may open and connect the cytoplasm with the extracellular fluid.

297 however, IRF6 is found predominantly in the cytoplasm, with its import into the nucleus tightly regu

298 ribed in the cell nucleus be exported to the cytoplasm without being spliced.

299 can directly deliver gene and proteins into cytoplasm without microbubbles, which enables controlled

300 and that vRNA may be transported through the cytoplasm without Rab11A RE in the absence of intact MT.