ライフサイエンスコーパス: cytoplasmic

1 factor nuclear factor of activated T cells, cytoplasmic 1 (NFATc1).

2 LI2DeltaN in human keratinocytes resulted in cytoplasmic accumulation and nuclear relocalization of b

3 Accompanied with cytoplasmic accumulation of TDP-43, tau expression was e

4 n most cases of ALS is nuclear depletion and cytoplasmic accumulation of the protein TDP-43 in degene

5 However, in hypoxia, cytoplasmic accumulation of Tyr359-phosphorylated hnRNP

6 urin inhibitor-induced tubular SNAI1 protein cytoplasmic accumulation, possibly because of impaired S

7 orkhead transcription factor, leading to its cytoplasmic accumulation.

8 beta- and gamma-cytoplasmic actin are nearly indistinguishable in their

9 S or Act1) is an oxidative stress-responsive cytoplasmic adapter molecule that is an upstream regulat

10 gions in which cells extrude, it forms large cytoplasmic aggregates.

11 generative disorders are associated with the cytoplasmic aggregation of microtubule-associated protei

12 horylation and 14-3-3 protein binding of the cytoplasmic amino-terminus of iRhom2 alter its interacti

13 osphorylation to avoid toxic accumulation of cytoplasmic ammonium.

14 s and had an intermediary distribution (both cytoplasmic and cortical, but restricted to the cell api

15 rise to diverse non-membrane-bound nuclear, cytoplasmic and extracellular compartments.

16 capsid protein revealed differences in their cytoplasmic and nuclear accumulation, and data from quan

17 PCs by altering the expression of regulatory cytoplasmic and nuclear factors.

18 ntitative large-scale proteomics analysis of cytoplasmic and nuclear fractions from normal versus reg

19 ecreasing active beta-catenin levels in both cytoplasmic and nuclear fractions.

20 of the EGFR protein with effects both in its cytoplasmic and nuclear functions.

21 nsional single-cell measurements of size and cytoplasmic and nuclear morphology in high throughput, b

22 rties, we determined that this dye defect is cytoplasmic and occurs due to a highly elevated dye iont

23 ure-function analysis suggests that the NRP1 cytoplasmic and transmembrane domains are necessary and

24 romote greater antibiotic influx to increase cytoplasmic antibiotic concentration for enhanced cytoto

25 ctin cytoskeleton is a critical regulator of cytoplasmic architecture and mechanics, essential in a m

26 Membrane-bound arrays are single layered; cytoplasmic arrays are double layered.

27 hiostrepton acted synergistically to inhibit cytoplasmic AURKA activity and disrupt the nuclear AURKA

28 Supraphysiologic doses induced formation of cytoplasmic autophagic vacuoles and activation of protea

29 disabilities and psychiatric disorders.Brain cytoplasmic (BC1) RNA is a non-coding RNA that has been

30 nd migration, consistent with known roles of cytoplasmic beta-actin.

31 form of the full-length approximately 7-kDa cytoplasmic C terminus in cultured cells and purified fr

32 The GluN2B cytoplasmic C-terminal domain (CTD) represents an altern

33 ProP orthologues share an extended, cytoplasmic C-terminal domain.

34 Ca(2+)-permeable channels that can regulate cytoplasmic Ca(2+) and are needed to induce the expressi

35 s as a determinant of the competing roles of cytoplasmic Ca(2+) in autophagy regulation.

36 pped attachment to the pore and contacts the cytoplasmic Ca(2+)-binding domain from a neighbouring su

37 Cytoplasmic calcium levels and transients increased upon

38 ndings guided development of an inhibitor of cytoplasmic cap methylation whose action resulted in a s

39 , identifying elements of a pathway by which cytoplasmic cBIN1 is released into blood.

40 at has proven to be capable of following the cytoplasmic changes of iron concentration dynamics and w

41 nprotonated, as has been proposed for the BR cytoplasmic channel for protons.

42 Opening of the cytoplasmic channel to cations in GtCCR2 requires the As

43 ; the cytoplasmic Cu(+) sensor CueR controls cytoplasmic chaperones and plasma membrane transporters,

44 Here we show that cytoplasmic chromatin activates the innate immunity cyto

45 In this study, we focus on the LPS-induced cytoplasmic circRNA, mcircRasGEF1B, and combine targeted

46 activated chloride channel (CaCC), regulates cytoplasmic Cl(-) homeostasis and promotes plasma membra

47 ncovers a critical function of CaCC-mediated cytoplasmic Cl(-) homeostasis in controlling the organiz

48 Cytoplasmic Cl(-) level is dynamically regulated by Cl(-

49 This newly defined role of cytoplasmic Cl(-) may shed light on the mechanisms of in

50 However, whether cytoplasmic Cl(-) plays additional roles in animal devel

51 strate RNA to nuage, a distinct membraneless cytoplasmic compartment, which surrounds the nucleus of

52 NAs and small noncoding RNAs, but also their cytoplasmic compartmentalization during spermiogenesis.

53 miRNAs appear to control cytoplasmic compartmentalization of mRNAs based on 3' UT

54 hway that involves sequestration of selected cytoplasmic components by multilayered vesicles called a

55 Partitioning of cell organelles and cytoplasmic components determines the fate of daughter c

56 trides have been made toward elucidating the cytoplasmic components of MAPK signaling, the key downst

57 adian regulation of membrane conductance and cytoplasmic conductivity that depends on the cycling of

58 lular mitochondrial modifications that alter cytoplasmic conductivity, and these changes are benchmar

59 operatively enable the efficient severing of cytoplasmic connections between dividing daughter cells.

60 ns mainly support exchange of lipids but not cytoplasmic content between cells, resembling hemifusion

61 as the passive outcome of the difference in cytoplasmic content of egg and sperm; however, active pr

62 The ability to establish cytoplasmic continuity between the proximal and distal e

63 levels appear independently controlled; the cytoplasmic Cu(+) sensor CueR controls cytoplasmic chape

64 omponents, CCR4 and CAF1, which are the main cytoplasmic deadenylases in eukaryotic cells.

65 preventing its nuclear export that leads to cytoplasmic degradation of the deacetylase.

66 the mouse, the protein had a broad punctate cytoplasmic distribution in the vestibular hair cells, w

67 f Class I retrotransposons and activation of cytoplasmic DNA viral sensors.

68 vital to productive infection of this large cytoplasmic DNA virus.

69 he VEGF164-binding site of NRP1 and the NRP1 cytoplasmic domain (NCD), but not the known NCD interact

70 on reminiscent to the PRC but located in the cytoplasmic domain and possibly stabilized by D38.

71 is report, we investigated the role of CD103 cytoplasmic domain and the focal adhesion-associated pro

72 In addition, the adam13 cytoplasmic domain is cleaved by gamma secretase, transl

73 In contrast, Pcdh15a lacking the entire cytoplasmic domain is not functional.

74 blasts through the signaling function of the cytoplasmic domain of ICAM-1.

75 of key regulatory residues within the large cytoplasmic domain of KCC2 in neurons.

76 , coupled with the contrasting intracellular cytoplasmic domain of LAG3 as compared with other IRs, h

77 when V1 is released from Vo, the N-terminal cytoplasmic domain of subunit a (aNT) changes conformati

78 of the Galpha13 protein from binding to the cytoplasmic domain of the beta3 integrin prevents outsid

79 M2 distal cytoplasmic domain sequences were still required for opt

80 y we showed that salt bridges located at the cytoplasmic domain subunit interfaces (CD-Is) of eukaryo

81 erized, 12-amino acid region within the NRP1 cytoplasmic domain that mediates HH signal promotion.

82 e domain, serine rich region and a conserved cytoplasmic domain.

83 d by two transmembrane segments and a single cytoplasmic domain.

84 Isoforms of PCDH15 differ in their cytoplasmic domains (CD1, CD2, and CD3), but share the e

85 t conformation by integrin transmembrane and cytoplasmic domains must be overcome by cellular energy

86 cAMP binding rotates cytoplasmic domains to favor opening of the inner helica

87 ial roles for the receptor transmembrane and cytoplasmic domains, as well as for the TARP extracellul

88 We now report that cytoplasmic DPPA3 is partially cleaved by the ubiquitin-

89 rotubules are polarity sorted in the axon by cytoplasmic dynein but that additional factors are also

90 In contrast, cytoplasmic dynein efficiently navigates both axons and

91 Cytoplasmic dynein is an enormous minus end-directed mic

92 litates the localization of Mcp5 and that of cytoplasmic dynein on the membrane.

93 sitioning, are mediated by the motor protein cytoplasmic dynein, which produces force on the microtub

94 Cytoplasmic dynein-1 binds dynactin and cargo adaptor pr

95 In human cells, cytoplasmic dynein-1 is essential for long-distance tran

96 DYNC1H1 encodes the heavy chain of cytoplasmic dynein-1, a 1.4-MDa motor complex that traff

97 gical and genetic manipulation, we show that cytoplasmic dynein-1, which localizes to the junction be

98 sitive to BFA treatment, indicating that the cytoplasmic effector follows an alternative route for de

99 The cytoplasmic effector Pi04314, expressed as a monomeric r

100 Here we demonstrate that the cytoplasmic effector PsAvh23 produced by the soybean pat

101 us sites for delivery of both apoplastic and cytoplasmic effectors during infection, following distin

102 methylation not only affects the function of cytoplasmic EGFR, but also that of nuclear EGFR.

103 ner pore formed by the criss-crossing of the cytoplasmic ends of the S6 segments (the S6 bundle cross

104 changes in mitochondrial positioning affect cytoplasmic energy distribution and cell migration, an e

105 cation, gene expression, capsid assembly and cytoplasmic envelopment, and transcellular transmission

106 eus, it paradoxically increases and prolongs cytoplasmic ERK activity.

107 great interest to study the contribution of cytoplasmic Esrp1 in maintenance of epithelial cell func

108 rate that the production of both nuclear and cytoplasmic Esrp1 isoforms through alternative splicing

109 ntegrates nuclear and previously unsuspected cytoplasmic events of centriole amplification, providing

110 ncrease in K(+) selectivity at low pH on the cytoplasmic face, for instance, appeared to be associate

111 echanism of G protein activation mediated by cytoplasmic factors.

112 Many crowns were associated with long cytoplasmic fibrils, likely to be exported progeny RNA.

113 edly, we found that vRNA-vRNA association in cytoplasmic foci was independent of MT.

114 y the synthesis of viral DNA within discrete cytoplasmic foci.

115 nfection, accompanied by intense labeling of cytoplasmic foci.

116 nd RIG-I and foreign circRNA co-aggregate in cytoplasmic foci.

117 Mechanistically, a cytoplasmic form of CCN3 interacted with the AR N-termin

118 CLIP), in which chromatin, nucleoplasmic and cytoplasmic fractions are prepared from UV-crosslinked c

119 with gastrin and separated into nuclear and cytoplasmic fractions.

120 Platelets are anucleate cytoplasmic fragments that lack genomic DNA, but continu

121 it both specific and overlapping nuclear and cytoplasmic functions, have different expression levels

122 Patient-derived MNs show typical cytoplasmic FUS pathology, hypoexcitability, as well as

123 and water sites and a helix controlling the cytoplasmic gate of KdpA is linked to the phosphorylatio

124 entiation was accompanied by upregulation of cytoplasmic gelsolin (cGSN), an abundant actin-severing

125 e differentiation and maturation through the cytoplasmic gelsolin signaling pathway, providing new dr

126 Eo-MDSC exhibit eosinophilic cytoplasmic granules and express CD11b, the eosinophil m

127 in development and is localized in distinct cytoplasmic granules where its target mRNA can be detect

128 h preceding the induction of cell cycle- and cytoplasmic growth-associated genes.

129 ves that significantly reduced the amount of cytoplasmic HBV DNA were discovered.

130 HDAC6 is a cytoplasmic histone deacetylase regulating multiple pro-

131 emistry (IHC) showed increased expression of cytoplasmic HMGB1 in dengue-extracted tissues when compa

132 rmoxia, miR-574-3p, acting as a decoy, binds cytoplasmic hnRNP L and prevents its binding to the CARE

133 Surprisingly, Ssb1, a cytoplasmic Hsp70 that binds ribosome-associated nascent

134 In human specimens, levels of cytoplasmic HuR were increased in colonic epithelial cel

135 and nestin, we show that the distribution of cytoplasmic IFs results from a continuous turnover based

136 2R-MIP was diminished and almost exclusively cytoplasmic in the HeLa cells; whereas the WT-MIP was st

137 he ER in wild-type plants but accumulated as cytoplasmic inclusions in get1, get3, or get4 mutants.

138 alpha-Synuclein (alphaS) forms round cytoplasmic inclusions in Parkinson's disease (PD) and d

139 The mutant protein forms cytoplasmic inclusions when expressed in Drosophila, the

140 ggregates in oligodendrocytes, forming glial cytoplasmic inclusions.

141 zannae (iES), infected by Cardinium inducing cytoplasmic incompatibility (CI), and its sibling specie

142 hia parameters including, bacterial density, cytoplasmic incompatibility, or resistance to infection

143 The most common reproductive manipulation is cytoplasmic incompatibility, which results in embryonic

144 Loss of SET1B or its unique cytoplasmic-interacting protein, BOD1, leads to up-regul

145 formation, it almost exclusively focused on cytoplasmic interactions among receptors and other chemo

146 These cytoplasmic introns were found to be highly conserved an

147 Cs, MKL1 was constitutively nuclear and MKL2 cytoplasmic, irrespective of mitogens or cAMP.

148 plice variants encoding distinct nuclear and cytoplasmic isoforms of fusilli, the D.

149 Truncation experiments revealed that the cytoplasmic juxtamembrane domain is necessary for maxima

150 conductivity that depends on the cycling of cytoplasmic K(+) levels.

151 Mass spectrometry analysis demonstrated that cytoplasmic LANA isoforms were full length, containing t

152 Cytoplasmic lipid droplets (LDs) of neutral lipids (tria

153 o have different proportions of nucleoid and cytoplasmic localization by altering their length and/or

154 e activity, L290P/V mutations enhance ERK3's cytoplasmic localization by increasing the interaction w

155 alization sequence was altered, resulting in cytoplasmic localization of PELP1 (PELP1-cyto).

156 In preliminary clinical studies, cytoplasmic localization of PELP1 was seen in 36% of wom

157 Cytoplasmic localization of proline, glutamic acid, leuc

158 Overexpressed C3G shows predominant cytoplasmic localization, but endogenous C3G is a compon

159 apping experiments identified histidine-rich cytoplasmic loops within the ZIP6/ZIP10 heteromer as a n

160 ily in the carboxyl terminus but also in the cytoplasmic loops, and subsequent binding of arrestins.

161 e cellular pool of nutrients by sequestering cytoplasmic material for degradation.

162 f intercellular connectivity is to transport cytoplasmic materials from 'nurse' cells to oocytes, a c

163 The bacterial cytoplasmic membrane is composed of roughly equal propor

164 enerate holes in the cell wall through which cytoplasmic membrane material protrudes and is released

165 Through these openings, cytoplasmic membrane material protrudes into the extrace

166 ation of a galactoside and a H(+) across the cytoplasmic membrane of Escherichia coli (galactoside/H(

167 nic pathway for protein secretion across the cytoplasmic membrane or insertion of integral membrane p

168 led cytochrome bd 1 ubiquinol oxidase in the cytoplasmic membrane show that CpcA-PEB and CpcA-PCB are

169 are unclear, as these cells possess a single cytoplasmic membrane that is surrounded by a thick cell

170 , predicted to export the protein beyond the cytoplasmic membrane, resulted in loss of functional tra

171 les that originate from invaginations of the cytoplasmic membrane.

172 organisms as they affect the function of the cytoplasmic membrane.

173 ains the so-called common region (CR) at the cytoplasmic/membrane interface still has the ability to

174 F-actin imaging revealed a cytoplasmic meshwork that might restrict transport in a

175 ir proteins to segregate away from DNA, with cytoplasmic mis-localization sustained for many hours as

176 ase in secreted MMP-9 and an accumulation of cytoplasmic MMP-2 over time, but no significant MMP-3 or

177 umor cell contact allows for the transfer of cytoplasmic molecules from macrophages to tumor cells co

178 We find that cytoplasmic motility constitutes a combination of direct

179 orders orchestrated by changes in DNA and/or cytoplasmic mRNA.

180 ittle methylation or demethylation occurs in cytoplasmic mRNA.

181 ansfer energy metabolites to neurons through cytoplasmic "myelinic" channels and monocarboxylate tran

182 s present in skeletal muscle and has a large cytoplasmic N-terminal domain and smaller C-terminal por

183 nd cell volumes decrease with the nuclear-to-cytoplasmic (N/C) volume ratio reaching a maximum at the

184 te-aspartate shuttle, which is important for cytoplasmic NAD(+) regeneration that sustains rapid gluc

185 nd low-molecular-weight isoform of cyclin E (cytoplasmic)-negative) is a reliable prognostic biomarke

186 Knockdown of cytoplasmic nucleoside kinases reduced mtDNA levels in A

187 ing (SHAPE-MaP) to probe PAN in its nuclear, cytoplasmic or viral environments or following cell/viri

188 The endoplasmic reticulum, the cytoplasmic organelle that matures a massive amount of n

189 Mitochondria are essential cytoplasmic organelles that generate energy (ATP) by oxi

190 ttenuated glucose consumption, Bcl-xL blocks cytoplasmic p53 from triggering intrinsic apoptosis.

191 inds and suppresses over half of nuclear and cytoplasmic p53 under normal conditions, independent of

192 oncogene signaling, glucose metabolism, and cytoplasmic p53, which may potentially be exploited for

193 d mitochondrial translocation of nuclear and cytoplasmic p53.

194 Interestingly, cytoplasmic particles became associated with keratin fil

195 have different expression levels and nuclear-cytoplasmic partitioning.

196 ead-to-tail" dimer upon binding ATP; and the cytoplasmic pathway, found closed off in other ATP-bindi

197 liferation-associated 1 like 1) binds to the cytoplasmic PDZ-ligand motif of aquaporin-2 and accelera

198 dynamics, imaged in Colo357 spheroids using cytoplasmic pH as a read-out, indicated that lactate ani

199 This hypothesis was tested by imaging cytoplasmic pH in spheroidal tissue growths of connexin4

200 Whereas cytoplasmic pH is strongly dependent on glucose abundanc

201 betaS) is essentially fibril-resistant under cytoplasmic physiological conditions.

202 protein level and shortens the half-life of cytoplasmic Plk3 in a ubiquitin-proteasome-dependent man

203 cleus in spatially organizing actin flow and cytoplasmic polarity.

204 ipt each terminating ribosome returns to the cytoplasmic pool before initiating anew on a different t

205 expansion is largely driven by regulation of cytoplasmic pressure.

206 precursors from components required for the cytoplasmic processing steps.

207 l expansion, and an accelerated severance of cytoplasmic projections between the cumulus cells outsid

208 we show that Beclin 1 is a prenatal primary cytoplasmic protein but rapidly relocated into the nucle

209 s as an example, we study the influence of a cytoplasmic protein domain on the clustering behaviour.

210 mbrane segment produce loose clusters, while cytoplasmic protein interactions mediate a tightly packe

211 can be applied to different membrane protein-cytoplasmic protein pairs.

212 IQCJ-SCHIP1 is a cytoplasmic protein present in axon initial segments and

213 tners and localizes to both intranuclear and cytoplasmic protein quality control (PQC) aggregates und

214 SHP2 is an ubiquitously expressed cytoplasmic protein tyrosine phosphatase.

215 function of the polyQ tracts in many normal cytoplasmic proteins is unclear.

216 nzyme that glycosylates numerous nuclear and cytoplasmic proteins on serine and threonine.

217 ndings reveal information encoded within the cytoplasmic proteins required for their unconventional s

218 the nucleus and in so doing protects it from cytoplasmic proteins that cause PTEN degradation.

219 The proteasome is a nuclear-cytoplasmic proteolytic complex involved in nearly all r

220 erties may thus limit the composition of the cytoplasmic proteome.

221 l changes between periplasmic, membrane, and cytoplasmic regions.

222 e Cat L inhibitor Z-FY-CHO led to nuclear-to-cytoplasmic relocalization of Cat L, decreased binding o

223 To investigate the potential role of MT1-MMP cytoplasmic residue Thr(567) phosphorylation in regulati

224 In contrast, cytoplasmic-restricted CASZ1 staining or low nuclear CAS

225 d to be mediated through phosphorylation and cytoplasmic retention of YAP and reduced expression of d

226 sugar modifications can become localized to cytoplasmic ribonucleoprotein granules such as stress gr

227 PSI (+)] shows the appearance of fluorescent cytoplasmic rings when the prion domain is fused with GF

228 Our technique highlights AO-labeled cytoplasmic RNA as an important early marker of cellular

229 he 5'-to-3'-exoribonuclease component of the cytoplasmic RNA decay machinery.

230 omic RNA within incoming virus particles via cytoplasmic RNA sensors to produce type I interferon (IF

231 whereas the lumenal loop and the N-terminal cytoplasmic segment are necessary for the functional int

232 subsequent YAP Ser-127 phosphorylation, YAP cytoplasmic sequestration, and reduction in YAP target g

233 ergistic effect on hD4R levels is noted when cytoplasmic serine (Ser) and threonine (Thr) residues ar

234 s 176-192) that contributes to CASZ1 nuclear-cytoplasmic shuttling in a chromosomal maintenance 1-dep

235 Thus, nuclear-cytoplasmic shuttling of ICAP1 influences both integrin

236 g the pore blocker toxin maurocalcine on the cytoplasmic side of RyR.

237 sembles next to the mother SPB (mSPB) on the cytoplasmic side of the nuclear envelope (NE).

238 nhibiting Ca(2+)-binding site located on the cytoplasmic side of the RyR channel.

239 motifs that mediate functions by binding to cytoplasmic signaling and scaffolding molecules.

240 SIRT2 is a cytoplasmic sirtuin that plays a role in various cellula

241 HMPV IBs were shown to be cytoplasmic sites of active transcription and replicatio

242 nuclear residence of genes to the disparate, cytoplasmic sites of protein synthesis.

243 cilitated by a dileucine motif housed in the cytoplasmic Slack C terminus that binds AP-2.

244 lecules despite the apparent lack of an open cytoplasmic sleeve, forcing the reassessment of the mech

245 A poorly understood adaptive pathway links cytoplasmic slicing of target RNA by the PIWI protein MI

246 inner membrane export apparatus, and a large cytoplasmic sorting platform.

247 f Pseudomonas aeruginosa catalyzes the first cytoplasmic step in recycling of muropeptides, cell-wall

248 a B12-processing enzyme involved in an early cytoplasmic step in the cofactor-trafficking pathway.

249 ty acid saturation levels, and reductions in cytoplasmic storage granules.

250 together, drive endomembrane trafficking and cytoplasmic streaming in the plant cells.

251 significant degradation in cell membrane and cytoplasmic structures, compared to expression of cataly

252 localized to the periphery of virus-encoded cytoplasmic structures, termed virus factories (VFs), wh

253 addition to their canonical function at the cytoplasmic surface of the plasma membrane (PM), where t

254 tion creates high-contrast, 3D images of the cytoplasmic surface of the plasma membrane but is more c

255 ring metaphase and early anaphase and to the cytoplasmic surface of the SPBs during late anaphase.

256 ions of transmembrane helices 6 and 7 at the cytoplasmic surface using site-directed spin labeling an

257 cts with a soluble transducer protein on its cytoplasmic surface, and its binding affinity is modulat

258 h interactions with host cell machinery, the cytoplasmic tail (CT) of F is a likely interactive domai

259 chimeric form in which its transmembrane and cytoplasmic tail (TMCT) domains were replaced with those

260 ermining talin binding to the beta3-integrin cytoplasmic tail and inducing a kink in the transmembran

261 The beta1 cytoplasmic tail has two NPxY motifs that mediate functi

262 onstrated proteoforms of ADAM8 that lack the cytoplasmic tail in the supernatant.

263 al regulation of the Thr(567) in the MT1-MMP cytoplasmic tail may function as a regulatory mechanism

264 ion of the DXXLL-motif sequence DISLL in the cytoplasmic tail of BACE1.

265 tinin competes with talin for binding to the cytoplasmic tail of beta3-integrin, whereas it cooperate

266 Proteins binding to the cytoplasmic tail of L-selectin regulate L-selectin funct

267 ith the first luminal loop of Glut4, and the cytoplasmic tail of sortilin binds to retromer.

268 Mutations in the distal cytoplasmic tail region of M2, and in particular a tyros

269 nomodulatory fusion proteins (IFPs) with the cytoplasmic tail replaced by the signaling domain of the

270 ur results show how Pxn binding to the CD103 cytoplasmic tail triggers alphaEbeta7 integrin outside-i

271 in the membrane-proximal region of the GluA2 cytoplasmic tail, and suggest a distinct model for the r

272 tes Pro(1146) for Ser in the integrin alphaM cytoplasmic tail.

273 and p120-binding domains within the cadherin cytoplasmic tail.

274 In contrast, PyMT increases the cytoplasmic Taz level.

275 To address that question, sequential cytoplasmic TbetaRI truncations and point mutations iden

276 omal protein, RACK1, and that an increase in cytoplasmic TDP-43 represses global protein synthesis, a

277 jects throughout the airway wall with marked cytoplasmic to nuclear shift in COPD (P < 0.01).

278 vely exports phospholipid complexes from the cytoplasmic to the exocytoplasmic leaflet of membranes.

279 e an assembly pathway regulated by GAPVD1, a cytoplasmic trafficking factor.

280 Cell, Roh-Johnson et al. (2017) reveal that cytoplasmic transfer from macrophages to melanoma cells

281 HIV genomic DNA within infected cells during cytoplasmic transit, nuclear import, and mRNA synthesis.

282 increases Akt phosphorylation, which induces cytoplasmic translocation of FoxO1 and suppression of No

283 tion because of hypoxia-triggered nucleus-to-cytoplasmic translocation of MTA1.

284 pathways, including RNA splicing and nuclear-cytoplasmic transport have been increasingly linked both

285 Taken together, our data suggest that cytoplasmic transport of influenza vRNA may include a Ra

286 In the cells, two cytoplasmic tRNA species, tRNAAspGUC and tRNAHisGUG, ser

287 Previously, we have shown that mature cytoplasmic tRNAs are cleaved during stress response to

288 d cells lacking all ATG8 proteins accumulate cytoplasmic UB aggregates, which are resolved following

289 ines RNF8 and UBC13 as components of a novel cytoplasmic ubiquitin-signaling network that suppresses

290 SNAI1 cytoplasmic up-regulation was particularly evident in bi

291 opathy biopsy specimens suggested that SNAI1 cytoplasmic up-regulation was preceded by a transient in

292 These studies indicated that 13 induces cytoplasmic vacuolization that is lysosomal in nature.

293 Moreover, MLKL phosphorylation, cytoplasmic vacuolization, and cytolysis were observed i

294 ential for cell survival, surprisingly has a cytoplasmic variant.

295 The relative cytoplasmic versus nuclear fluorescence of the KTR const

296 e a means to unravel the significance of the cytoplasmic versus the secreted form of mutant SOD1 in t

297 Clathrin accumulated in the cytoplasmic virus assembly compartment (vAC) of infected

298 The authors find that large cytoplasmic volume affects spindle pole morphology, chro

299 We were able to generate oocytes with cytoplasmic volumes reduced by 86% and observed changes

300 Finally, we found that cytoplasmic YAP positively regulated the activity of the