ライフサイエンスコーパス: cytoplasm

1 required for lanthanide incorporation to the cytoplasm.

2 lecular exchange between the nucleus and the cytoplasm.

3 ctly delivers the antigenic peptide into the cytoplasm.

4 d NRP1 predominantly interact throughout the cytoplasm.

5 T), and export of assembling subunits to the cytoplasm.

6 dense metaphase spindle and the surrounding cytoplasm.

7 ry step that precedes late maturation in the cytoplasm.

8 oating and delivery of the RNA genome to the cytoplasm.

9 n rhodopsins, in HeRs the N termini face the cytoplasm.

10 lumen within the tracheal terminal cell (TC) cytoplasm.

11 pelling their nucleoid-based genome into the cytoplasm.

12 the contracting network and the surrounding cytoplasm.

13 of gene expression between their nucleus and cytoplasm.

14 hly dynamic structures that coalesced in the cytoplasm.

15 llular epithelium into a giant multinucleate cytoplasm.

16 d predominantly to either the nucleus or the cytoplasm.

17 tivates the receptor for COPI binding in the cytoplasm.

18 obably owing to phage mRNA localizing to the cytoplasm.

19 scriptionally active core particles into the cytoplasm.

20 D/B-type retroviruses, which assemble in the cytoplasm.

21 cruits multiple regulatory proteins from the cytoplasm.

22 the nucleus and subsequent transport to the cytoplasm.

23 omolecular transport between the nucleus and cytoplasm.

24 a significantly higher mass density than the cytoplasm.

25 eckles and is frequently translocated to the cytoplasm.

26 appearance with foamy granular eosinophilic cytoplasm.

27 quality control mechanism that occurs in the cytoplasm.

28 n both a diffuse and punctate pattern in the cytoplasm.

29 teins directly into the eukaryotic host cell cytoplasm.

30 ral classes of RNAs, from the nucleus to the cytoplasm.

31 mes within a few hours and replicates in the cytoplasm.

32 verse regulatory programs within the crowded cytoplasm.

33 or direct delivery of proteins into the cell cytoplasm.

34 ike hydrogel which could further escape into cytoplasm.

35 ning domain (PAG1(TM-)) and localized to the cytoplasm.

36 T was overexpressed and redistributed to the cytoplasm.

37 as correlated to the depletion of tau in the cytoplasm.

38 n of organelles long-distance throughout the cytoplasm.

39 aqueous AfrLEA6 raises the viscosity of the cytoplasm.

40 absence of host plant, FgANK1 resides in the cytoplasm.

41 port of vitamin B12 to the mitochondrion and cytoplasm.

42 calization that shuttles between nucleus and cytoplasm.

43 d of photolytically uncaged H(+) ions across cytoplasm.

44 inal region of AKAP8L binds to mTORC1 in the cytoplasm.

45 mpact the relative stability of RBP16 in the cytoplasm.

46 ich viruses can control the nucleus from the cytoplasm.

47 re localized in the nucleus, centrosome, and cytoplasm.

48 vely, were selectively enriched in wild type cytoplasm.

49 nd bacteria, propelling microbes through the cytoplasm.

50 umans, where it localizes to the nucleus and cytoplasm.

51 a, complemented by aerobic glycolysis in the cytoplasm.

52 mble into structures in both the nucleus and cytoplasm.

53 cation of the TRAF2 complex from CD40 to the cytoplasm.

54 rm 1 was predominantly expressed in the cell cytoplasm.

55 ively translocated from the nucleus into the cytoplasm.

56 ration and stress granule recruitment in the cytoplasm.

57 ehow crosses the bacterial envelope into the cytoplasm.

58 envelope, which connects the nucleus to the cytoplasm.

59 on and delivery of RNA from exo-HAV into the cytoplasm.

60 re and helped KEAP1 to sequester NRF2 in the cytoplasm.

61 ever, MTCH2xx was found predominantly in the cytoplasm.

62 accumulated as mobile punctate bodies in the cytoplasm.

63 ediates diverse trafficking processes in the cytoplasm.

64 nstimulated ECs, YAP localized mainly in the cytoplasm.

65 s through a particular trajectory within the cytoplasm.

66 PLGA NPs containing short PNA probes in the cytoplasm.

67 ociated with the hexameric subcomplex in the cytoplasm.

68 brane with its RING finger domain facing the cytoplasm.

69 aining autophagosomes were absent within the cytoplasm.

70 urface, whereas the kinase is exposed to the cytoplasm.

71 and secretion of GRA effectors into the host cytoplasm.

72 the movement of TFEB and TFE3 back into the cytoplasm.

73 meres are short, and TLC1 accumulates in the cytoplasm.

74 ndrial intermembrane space proteins into the cytoplasm.

75 of nanometers in size, crowd the eukaryotic cytoplasm.

76 segregates the genome of Eukaryota from the cytoplasm.

77 sarily stable in the context of the cellular cytoplasm, a reducing environment.

78 ity assays, we demonstrate that two parallel cytoplasm-accessible networks of conserved hydrophilic r

79 In the cytoplasm, acetylation of a number of cytoskeletal prote

80 ties and the release of nuclear DNA into the cytoplasm, activating the cGAS-STING pathway.

81 e release of the chaperones in the bacterial cytoplasm after the dissociation from their exported pro

82 dual papillar cells assemble a multinucleate cytoplasm, allowing passage of proteins of at least 62 k

83 sited eggs begin development with an immense cytoplasm and a single overwhelmed nucleus.

84 hnRNPA2B1 was quantitatively exported to the cytoplasm and at least a fraction of hnRNPA2B1 colocaliz

85 MTV) and C-type HIV-1, which assemble in the cytoplasm and at the plasma membrane, respectively.

86 g localized CSF-2 primarily to decidual cell cytoplasm and cytotrophoblast cell membranes.

87 am-negative bacteria, PG is assembled in the cytoplasm and exported into the periplasm where it under

88 dney cancer, SPOP largely accumulates in the cytoplasm and fails to promote degradation of AR located

89 sulting in the mislocalization of FUS in the cytoplasm and formation of stress granule-like inclusion

90 These truncated isoforms accumulated in the cytoplasm and formed insoluble inclusions that sequester

91 cation of Ro60, since Ro60 is reduced in the cytoplasm and increased in nucleoli when Y RNAs are abse

92 rast, the Raf kinase domain extends into the cytoplasm and its assembly is away from the crowded memb

93 toxic drugs by promoting p53 accumulation in cytoplasm and loss from mitochondrial and nuclear compar

94 ecies that delineates the extent of the cell cytoplasm and lowers the detection threshold of z-scan P

95 umulation of nonfunctional M proteins in the cytoplasm and nuclei of NiV-infected cells and thus prov

96 hat Ppt1 regulates Hsp82 distribution in the cytoplasm and nucleus by dephosphorylating the S485 resi

97 of an average-sized protein in the mammalian cytoplasm and nucleus is spatially heterogeneous at the

98 e spectral dataset to demarcate spectra from cytoplasm and nucleus, and test the feasibility of ident

99 st to the transient activity observed in the cytoplasm and nucleus.

100 otic cells, including in the nucleus, in the cytoplasm and on membranes.

101 l cells, owing to the higher uptake into the cytoplasm and perhaps importantly lower efflux of HgII b

102 ith and stabilizes the telomerase RNA in the cytoplasm and promotes its nuclear re-import.

103 ntracellular networks, which span the entire cytoplasm and provide mechanical strength to the cell.

104 the formation of a protein seal between the cytoplasm and the channel.

105 he electric potential difference between the cytoplasm and the extracellular medium.

106 ar environment and the cytoplasm or from the cytoplasm and the intracellular matrix of the organelles

107 ly secreted HCV RNA derives equally from the cytoplasm and the replication compartments.

108 c proteins to sense its presence in the cell cytoplasm and trigger an immune response by the host cel

109 ealed amiodarone-treated cells with enlarged cytoplasm and very thin regions corresponding to collaps

110 ng [BCALM]) transcripts are localized in the cytoplasm and, as expected, CRISPR/Cas9 knockout of AC09

111 ss of turgor, subsequent accumulation in the cytoplasm, and elevated levels in nucleoli of germlings.

112 and then NE rupture to release DNA into the cytoplasm, and finally plasma membrane rupture and disch

113 sis and processing, ribosome export into the cytoplasm, and global protein synthesis.

114 onal buffering of transcript activity in the cytoplasm, and has recently been implicated in neurodege

115 cretion, depleting insulin vesicles from the cytoplasm, and impairing GSIS.

116 e specific metal or multiple metals from the cytoplasm, and it is not known whether the CTD takes an

117 ce of differing biological materials such as cytoplasm, and lipids in the skin.

118 forces and flow of the extracellular fluid, cytoplasm, and nucleoplasm.

119 to serum starvation, eIF6 accumulates in the cytoplasm, and this altered localization depends on phos

120 to apoptosis, accumulate beta-catenin in the cytoplasm, and translocate NF-kappa-B to the nucleus.

121 globin (Hb), transport it into the bacterial cytoplasm, and ultimately release iron from the porphyri

122 dent of lipid accumulation, stemmed from the cytoplasm, and was mitigated by OCA.

123 llae, with the presence of macrophages whose cytoplasm appeared clear and granular.

124 Cobalamin derivatives entering the cytoplasm are converted by CblC to a common cob(II)alami

125 Multiple nuclei sharing a common cytoplasm are found in diverse tissues, organisms, and d

126 and MTs outwards, while other components of cytoplasm are static.

127 ere detected by fluorescent microscopy in EC cytoplasm (associated with endoplasmic reticulum and Gol

128 y axonemal dyneins that are assembled in the cytoplasm before deployment to cilia.

129 has an ATP-binding domain exposed to the MC cytoplasm, but the role of ATP in regulating Pro-sigma(K

130 smic P(i) can be gradually imported into the cytoplasm by ATP-powered transport, however, the proton

131 germ cells (PGCs) jettison mitochondria and cytoplasm by forming a large lobe that is cannibalized b

132 umber of intracellular "cargos" navigate the cytoplasm by hitchhiking on motor-driven "carrier" organ

133 resentative types were packed into simulated cytoplasm by our framework, and numerical verification p

134 growth through deSUMOylation of BZR1 in the cytoplasm by promoting the accumulation of the BZR1 targ

135 ts can cause a toxic gain of function in the cytoplasm by repressing the translation of mRNA at polyr

136 oaded carboxymycobactin is imported into the cytoplasm by the ATP binding cassette (ABC) transporter

137 import nearly their entire proteome from the cytoplasm by translocating precursor proteins through th

138 oncentrated in liquid-like organelles in the cytoplasm called DynAPs (Dynein Axonemal Particles).

139 systems for fatty acid synthesis, one in the cytoplasm (catalyzed by fatty acid synthase, FASN) and o

140 tive splicing (AS) transitions, while in the cytoplasm, CELF1 regulates mRNA stability and translatio

141 etected a higher abundance of PUN RNA in the cytoplasm compared to wild-type-infected cells.

142 or new models in which all components of the cytoplasm comprise a mechanically integrated aster gel t

143 Samples of isolated cytoplasm, devoid of active processing, of the same cell

144 leoplasm maintains a lower mass density than cytoplasm during cell cycle progression by scaling its v

145 ess granules by coacervating with RNA in the cytoplasm during stress and may be involved in these pat

146 of the morphology of vital organelles in the cytoplasm, during all phases of the cell life cycle (fro

147 ause transporting nutrients via a contiguous cytoplasm enables continued exploitation of remaining re

148 e find that binding to tensed F-actin in the cytoplasm excludes the cancer-associated transcriptional

149 The antagonist binds to a cytoplasm-facing pocket formed by S1-S4 and the TRP heli

150 luding those structurally constrained in the cytoplasm-facing state and either apo, bound to sodium i

151 a cycle of fast exodus of nuclear YAP to the cytoplasm followed by fast reentry to the nucleus ("loca

152 of active histone marks and localize to the cytoplasm following daughter nuclei formation and cytoki

153 can effectively recruit RAF kinase from the cytoplasm for activation at the membrane.

154 ited to the cortex, which may pressurize the cytoplasm for blebbing.

155 e nucleus and mRNAs undergo transport to the cytoplasm for the purpose of producing proteins.

156 This is initiated following transcytosis of cytoplasm from cancer cells into fibroblasts, leading to

157 lize as a mechanism to protect the bacterial cytoplasm from excessive nitrite toxicity during anaerob

158 How bulk cytoplasm generates forces to separate post-anaphase mic

159 Inside the cytoplasm, H2A reorganizes bacterial chromosomal DNA and

160 ile influence of the CBC can extend into the cytoplasm, here we review the roles of the CBC in the nu

161 Invaginations in the glial cell cytoplasm house the neurites, an association reminiscent

162 ow that UBE3A predominantly localizes to the cytoplasm in both wild type and isoform-null cells.

163 gh nuclear pores and uncoating occurs in the cytoplasm in coordination with reverse transcription or

164 GFP:EXO70A2 was localized to the nucleus and cytoplasm in developing pollen grains and later to the a

165 te the directional formation of LDs into the cytoplasm in eukaryotic cells.

166 We show that DAAM2 localizes to the cytoplasm in podocytes and in kidney sections.

167 teadily translocates from the nucleus to the cytoplasm in response to increasing CDK activity and con

168 rane-associated state and relocalizes to the cytoplasm in response to mechanical stimuli, allowing Gr

169 ze "cell-projection pumping" (CPP), in which cytoplasm in retracting cell projections partially equil

170 Spatial reorganization of cytoplasm in zygotic cells is critically important for e

171 a, we measured the growth of both nuclei and cytoplasm independently, over many days, without loss of

172 transcript subpopulations in the nucleus and cytoplasm indicate post-transcriptional processes enable

173 and involves a transient visit to the glial cytoplasm, indicating that phagocytic glia act as obliga

174 did not prevent Gag-gRNA interactions in the cytoplasm, indicating that the two ZFs display redundant

175 cells whereas p22(CBX7) was localized to the cytoplasm, induced by serum starvation in both human and

176 that can phase-separate from nucleoplasm and cytoplasm into distinct liquid-droplet structures.

177 suppressed the translocation of p65 from the cytoplasm into the nucleus after incubation with saliva.

178 by the transport of these proteins from the cytoplasm into the nucleus.

179 This mixture of organelles and cytoplasm is bound by a plasma membrane that is itself s

180 hat phage genome translocation to the host's cytoplasm is defective.

181 drial membrane, whose necked aperture to the cytoplasm is gated by a 12-fold symmetric, 35-nm diamete

182 e ubiquitous entry gate to within the cells' cytoplasm is macropinocytosis.

183 zed(4,5), delivery of exosome cargo into the cytoplasm is poorly understood(3).

184 ipopolysaccharide transfection into the host cytoplasm is sufficient to trigger active cathepsin accu

185 seudorabies virus (PRV) in the infected cell cytoplasm is thought to involve the late-acting cellular

186 (i.e., nucleus, lysosomes, mitochondria, and cytoplasm) is extremely advantageous in the search for a

187 ODA subunits, localizes specifically to the cytoplasm, is enriched in DynAPs, and is required for th

188 nd virion assembly occur at sites within the cytoplasm known as factories.

189 mittivity of the inner core (composed of the cytoplasm, lipid droplets, and nucleus) decreased by 21.

190 runcated METTL3 methyltransferase domain and cytoplasm-localized fusions with a modified METTL3:METTL

191 In hESCs, cytoplasm-localized hFAST binds to the WD40 domain of th

192 igh levels of U1 snRNA binding compared with cytoplasm-localized messenger RNAs.

193 band to separate the parasite from host cell cytoplasm, making it as an intracellular but extracytopl

194 ding of electrical activity, after which the cytoplasm may be extracted for single cell RNA-Seq ("Pat

195 restore normality as the ratio of nuclei to cytoplasm (N/C) increases.

196 al communication between the nucleus and the cytoplasm, now doubles as the gatekeeper of cellular ide

197 ystematically quantify the mass densities of cytoplasm, nucleoplasm, and nucleoli of human cell lines

198 GL3 volume fraction (proportion of podocyte cytoplasm occupied by GL3) increased with age up to abou

199 to which different nuclei within the shared cytoplasm of a myofiber may display transcriptional dive

200 function as intercellular pores linking the cytoplasm of adjacent cells.

201 proteins that in ALS can mislocalize to the cytoplasm of affected motor neuron cells, often forming

202 is f. sp. hordei PCS1, which is found in the cytoplasm of cells of healthy plants, translocates upon

203 ependent degradative pathway that clears the cytoplasm of dysfunctional organelles.

204 We expressed His-tagged hGH variants in the cytoplasm of genetically modified Rosetta-gami B DE3 Esc

205 gher fraction of lncRNAs is localized in the cytoplasm of hESCs than in mESCs.

206 uses acquire their membrane envelopes in the cytoplasm of infected cells via a molecular mechanism th

207 s this by generating inclusion bodies in the cytoplasm of infected cells.

208 any viruses replicate almost entirely in the cytoplasm of infected cells; however, how these pathogen

209 tracellular bacterial replication within the cytoplasm of infected macrophages.

210 , P < .01) specific NIR FI in the nuclei and cytoplasm of islets cells than in non-treated control mi

211 sive assay of global molecular events in the cytoplasm of living animals.

212 d actin networks, its mechanical role in the cytoplasm of living cells remains unknown.

213 clei, which are known to induce cGAS, in the cytoplasm of neurons derived from human HD embryonic ste

214 eriments show that replacement of the entire cytoplasm of oocytes from a sensitive mouse strain overc

215 m and is at most half-bound to Ca(2+) in the cytoplasm of resting cells.

216 as rapidly internalized and delivered to the cytoplasm of target myeloid cells and leukemic cells.

217 Replication takes place predominantly in the cytoplasm of the cell and involves complex interactions

218 es were unevenly distributed in the nucleus, cytoplasm of the cell body, and axon.

219 ON (CLE) peptide effectors secreted into the cytoplasm of the initial feeding cell could have an effe

220 pids, nutrients, and metabolites between the cytoplasm of the parasite and the cytoplasm of the RBC.

221 etween the cytoplasm of the parasite and the cytoplasm of the RBC.

222 xample of the incompatibility of the reduced cytoplasms of microbes with the oxic world in which they

223 s from the extracellular environment and the cytoplasm or from the cytoplasm and the intracellular ma

224 ic manner to control its localization to the cytoplasm or mitochondrial exterior or interior.

225 l dyneins into the axoneme directly from the cytoplasm, possibly by localizing translation.

226 ontain hundreds of myonuclei within a shared cytoplasm, presenting unique challenges for regulating g

227 9AC (400 um) applied to the cytoplasm produced a non-significant increase in spark f

228 Lnc13 translocation from the nucleus to the cytoplasm promoting the interaction of STAT1 mRNA with (

229 olgi intermediate compartment (ERGIC) in the cytoplasm (Raote et al., 2018).

230 ilia in which the axoneme resides within the cytoplasm rather than within the ciliary compartment, ar

231 ore reflect what the pathogen 'feels' in its cytoplasm, rather than the nutrient concentration in hos

232 rly dense organelle surrounded by less dense cytoplasm, recent studies have begun to report the oppos

233 to inflammation enables accumulation in the cytoplasm; reduced nuclear MSH3 increases EMAST and DNA

234 determine if the abundance of message in the cytoplasm relative to the nucleus is altered in Fmr1 kno

235 Long-range movement of organelles within the cytoplasm relies on coupling to microtubule motors, a pr

236 any of antiviral detection mechanisms in the cytoplasm remains relatively uncharacterized.

237 entially to these structures within a shared cytoplasm remains unclear.

238 -derived cholesterol from lysosomes into the cytoplasm requires NPC1 protein; NPC1L1 mediates uptake

239 The export of mRNA from nucleus to cytoplasm requires the conserved and essential transcrip

240 also report that entry of gRNA into the host cytoplasm requires the F-plasmid-encoded coupling protei

241 rphology with abundant granular eosinophilic cytoplasm, resembling mitochondria-rich apocrine-like ca

242 1-TC infection, had green or red foci in the cytoplasm, respectively, that colocalized with VP3 and d

243 kely 'hijacked' by cytoplasmic Malat1 to the cytoplasm, resulting in the depletion of nuclear TDP-43

244 ious subcellular localizations including the cytoplasm, SDVs and vacuoles.

245 Papillar cytoplasm sharing does not employ canonical mechanisms s

246 Cytoplasm sharing invariably involves plasma membrane br

247 In contrast, we discovered cytoplasm sharing without membrane breaching in highly r

248 face between the stiff brush border and soft cytoplasm suggesting a mechanical buffering function to

249 s deletion (Delta27bp MSH3) localizes to the cytoplasm, suggesting that NLS1 function in Delta27bp MS

250 development, requiring extension of a narrow cytoplasm surrounding a lumen exerting osmotic pressure

251 In contrast, in meiosis II, cytoplasm that contains upregulated factors including Pr

252 cin112 (Onc112) suggest that on reaching the cytoplasm, the peptide occupies its binding site prior t

253 bition limiting interaction with CYK4 in the cytoplasm, these results suggest that a spatial gradient

254 Once in the cytoplasm, they have a broad (1000-fold) range of deaden

255 ursors acquire translation competence in the cytoplasm through stepwise release of bound assembly fac

256 trol esx-1 gene expression in the M. marinum cytoplasm through the conserved WhiB6 transcription fact

257 nd nontranslating RNAs are well mixed in the cytoplasm; thus, Gag biogenesis occurs throughout the cy

258 ate transcription, but their function in the cytoplasm to control nongenomic actions is also crucial.

259 eport that an enzyme acting in the bacterial cytoplasm to degrade lipids also acts as an effector pro

260 icrotubules effectively fluidize the mitotic cytoplasm to equalize mesoscale mobility across a densel

261 that dynamic actin cross-linking enables the cytoplasm to flow at long timescales.

262 agy plays important roles in removing excess cytoplasm to promote myelin compaction and development o

263 acts as an effector protein in the host cell cytoplasm to suppress inflammation.

264 ffic other unrelated small peptides from the cytoplasm to the apoplast of host cells via a previously

265 achinery to redirect these peptides from the cytoplasm to the apoplast of plant cells.

266 retracting cell projections normally returns cytoplasm to the cell body.

267 ation of signal-containing proteins from the cytoplasm to the nucleus.

268 lkappa and shifted its localization from the cytoplasm to the nucleus.

269 import protein that shuttles cargo from the cytoplasm to the nucleus.

270 plex, shuttles excessive l-cysteine from the cytoplasm to the periplasm, thereby maintaining redox ho

271 proach, where FGFR ICD is recruited from the cytoplasm to the plasma membrane by light, followed by i

272 (SERCA) transports two Ca(2+) ions from the cytoplasm to the reticulum lumen at the expense of ATP h

273 osecond timescale, revealing a novel passive cytoplasm-to-lumen proton flow beside the well-known inv

274 To surpass this challenge, we developed a cytoplasm-to-membrane translocation approach, where FGFR

275 I interactions induced impairment of nuclear/cytoplasm transport, chromatin remodeling and nuclear la

276 action and releases the transcripts into the cytoplasm, triggering a pulse of negative limb gene prot

277 circadian clock, which are released into the cytoplasm upon rewarming allowing synthesis of specific

278 rs bacterial proteins directly into the host cytoplasm using a Dot/Icm type IV secretion system (T4SS

279 organelles that encapsulate enzymes from the cytoplasm using an icosahedral protein shell that resemb

280 Morphological alterations included cytoplasm vacuolization and partial loss of epidermal st

281 ar import, before relocalization back to the cytoplasm via a nuclear re-export step.

282 g extracellular environmental signals to the cytoplasm via inner-membrane sigma regulators.

283 Rate-limiting diffusion across cytoplasm was demonstrated by osmotically induced change

284 , long believed to happen exclusively in the cytoplasm, was recently proposed to also occur in the nu

285 ndria to that of a protein translated in the cytoplasm, we showed that aminoglycosides can paradoxica

286 nuclei to reduce transport distances to the cytoplasm were of less importance, and these fibers exhi

287 This lipase must be delivered into the host cytoplasm where it preferentially uses fatty acids assoc

288 the nucleus and subsequently exported to the cytoplasm where they serve as essential adaptor molecule

289 new cell, viral cores are released into the cytoplasm where they undergo a process termed "uncoating

290 onstitutively localized to the cardiomyocyte cytoplasm, where it promotes cardiac hypertrophy.

291 n, transporting its components back into the cytoplasm, where they can be used for subsequent rounds

292 ct TgSPY-MYC(3) localizes to the nucleus and cytoplasm, whereas catalytic mutants often displayed red

293 paB is rerouted to perinuclear puncta in the cytoplasm, which are synonymous with viral inclusion bod

294 embly of enveloped particles in the neuronal cytoplasm, which explains why HSV virions do not enter a

295 th LINE-1 ribonucleoprotein complexes in the cytoplasm, which is essential for restriction.

296 genomic RNA was diffusely distributed in the cytoplasm with genomic RNA also in perinuclear vesicle-l

297 which are granular, membraneless regions of cytoplasm with liquid organelle-like properties.

298 n turn generates the directional movement of cytoplasm within the whole egg.

299 ; thus, Gag biogenesis occurs throughout the cytoplasm without being constrained to particular subcel

300 Despite replicating in the cytoplasm, ZIKV and Dengue virus (DENV) polymerases, NS5