ライフサイエンスコーパス: endocytosis

1 nfected cells (exo-HAV) by clathrin-mediated endocytosis.

2 dependence of these effects on TFR1-mediated endocytosis.

3 the upregulation of protein degradation and endocytosis.

4 ling glycoprotein clustering, signaling, and endocytosis.

5 ulated in ESCs, with a resulting decrease in endocytosis.

6 but not beta-arrestin recruitment or PAR(2) endocytosis.

7 lular functions, including cell motility and endocytosis.

8 ch the Nef dimer bridges SERINC5 to AP-2 for endocytosis.

9 proaches to better characterize HSV entry by endocytosis.

10 hibition, suggesting selective targeting for endocytosis.

11 pneumoniae is internalized via EGFR-mediated endocytosis.

12 the plasma membrane and are internalized by endocytosis.

13 olvement in AP-2 adaptor phosphorylation and endocytosis.

14 rieves Flower to bulk endosomes, terminating endocytosis.

15 BCR clusters by classical clathrin-mediated endocytosis.

16 s of tamalin played critical roles in mGluR1 endocytosis.

17 doublecortin, a potent facilitator of NF186 endocytosis.

18 C2 signaling independently of their roles in endocytosis.

19 affecting phagocytosis or clathrin-mediated endocytosis.

20 artner and substrate of CK1delta/epsilon for endocytosis.

21 specifically and originates from fluid-phase endocytosis.

22 role in generating membrane curvature during endocytosis.

23 E-cadherin clustering and dynamin-dependent endocytosis.

24 activity and the increased Na(+) accelerated endocytosis.

25 actin/dynamin-binding protein implicated in endocytosis.

26 m of cytosolic Na(+) in accelerating vesicle endocytosis.

27 erge on DAT to facilitate PKC-stimulated DAT endocytosis.

28 assemble branched actin networks that drive endocytosis.

29 lar processes including circadian rhythm and endocytosis.

30 n concerning the sites of bulk secretion and endocytosis.

31 et-derived growth factor receptor-alpha cell endocytosis.

32 ia clathrin-independent, lipid raft-mediated endocytosis.

33 sicular trafficking, including secretion and endocytosis.

34 s also display a dynamin-dependent ultrafast endocytosis.

35 R/14-3-3 interaction occurred after receptor endocytosis.

36 osophila homolog of CHD7 and CHD8, regulates endocytosis.

37 in the generation of membrane curvature and endocytosis.

38 d increased Rab5-GTP levels, consistent with endocytosis.

39 ted to expression of PLCG2 and activation of endocytosis.

40 inated control of plasma membrane growth and endocytosis.

41 nd adaptor protein complex 2 (AP2)-dependent endocytosis.

42 ous studies found that Ark/Prk play roles in endocytosis.

43 inal domain increases its ubiquitination and endocytosis.

44 ent transporters and protect them from rapid endocytosis.

45 trafficked into cells via membrane repairing endocytosis.

46 zide prevented SNA uptake, suggesting active endocytosis.

47 but not beta-arrestin recruitment or PAR(2) endocytosis.

48 iched at the cell surface including sites of endocytosis.

49 2 in its C-terminal domain, facilitating its endocytosis.

50 which initiates exclusive substrate-induced endocytosis.

51 taken up by CNS cells via receptor-mediated endocytosis.

52 known to be key factors in clathrin-mediated endocytosis.

53 ceptor-mediated uptake of the bound virus by endocytosis(1), it is the HA that mediates fusion of the

54 c G-protein signalling and promotes receptor endocytosis(1).

55 ton has been implicated in clathrin-mediated endocytosis, a clear requirement for actomyosin in clath

56 nce of metabolites along the BBB, as well as endocytosis across the BBB.

57 nd other cellular characteristics, including endocytosis activity, viability and expression of cell-s

58 stimulation induces activity-dependent bulk endocytosis (ADBE) to recapture large quantities of SV c

59 of harmful substances involve phagocytosis, endocytosis, adhesion, and signaling.

60 diabetes (T2D) and obesity, undergoes rapid endocytosis after stimulation by endogenous and therapeu

61 y, not as preformed complexes, and implicate endocytosis along axons as a mechanism of clearance.

62 M did not elicit p38 MAPK phosphorylation or endocytosis, although these processes occurred with Pam(

63 internalization signal for clathrin-mediated endocytosis and a determinant of NF-kappaB activation.

64 re, CAP-stimulated membrane repair increases endocytosis and accelerates the uptake of gold nanoparti

65 rasites, including Trypanosoma brucei brucei Endocytosis and acidification of high-density lipoprotei

66 results indicate that EMCN modulates VEGFR2 endocytosis and activity and point to EMCN as a potentia

67 ing pathways have been discovered, ultrafast endocytosis and activity-dependent bulk endocytosis, in

68 arrestin-Rsp5-complexes to control selective endocytosis and adapt nutrient acquisition.

69 ssion in the mouse leads to an impairment of endocytosis and an enlarged endosomal compartment in neu

70 egulator that binds phosphoinositides during endocytosis and at invadopodia.

71 In various biological processes such as endocytosis and caveolae formation, the cell membrane is

72 e (BMP2K) has been potentially implicated in endocytosis and cell differentiation but its molecular f

73 m presenting cells to NK cells through trans-endocytosis and contribute to the phosphorylation of rib

74 Recent work demonstrated that IRT1 endocytosis and degradation are controlled by IRT1 non-i

75 evel of HLA-DR was not a result of increased endocytosis and degradation but was a result of a reduct

76 Wnt treatment markedly increased the endocytosis and degradation in lysosomes of BSA.

77 cover a novel enhancer of ligand-induced MOR endocytosis and determine its effects on analgesia, tole

78 docytic proteins, which differs from regular endocytosis and does not involve other known selective a

79 ated by background signal-dependent receptor endocytosis and down-regulation.

80 In endocytosis and early endosome development, net VPS34CII

81 ies, drive virus entry via receptor-mediated endocytosis and endosomal membrane fusion.

82 DOPr endocytosis and endosomal signaling by protein kinase C

83 mbrane trafficking, including, mechanisms of endocytosis and exocytosis, although the exact role of a

84 (+) accelerated both slow and rapid forms of endocytosis and facilitated endocytosis overshoot, but d

85 Moreover, luteolin stimulates endocytosis and improves the expression of the endocytic

86 cross-links EGFR physically triggering EGFR endocytosis and incorporation onto ILVs and so Sym004 se

87 al in cells lacking the WDD owing to delayed endocytosis and inefficient early trafficking of IL10/IL

88 opic Notch signalling by increasing receptor endocytosis and inhibiting Sanpodo trafficking towards a

89 eover we identify multiple genes involved in endocytosis and intracellular membrane trafficking that

90 of eukaryotic cells during clathrin-mediated endocytosis and intracellular trafficking.

91 INPP4A is dispensable for clathrin-mediated endocytosis and is undetectable in endocytic clathrin-co

92 Following endocytosis and its internalization into endolysosomes,

93 cells and normal cells by caveolin-dependent endocytosis and macropinocytosis, respectively.

94 through interactions with components of the endocytosis and nucleocytoplasmic transport pathways, re

95 ilament networks pivotal for cell migration, endocytosis and pathogen infection.

96 mplications for biological processes such as endocytosis and physical phenomena like phase separation

97 , which is required for BCR-mediated antigen endocytosis and postendocytic sorting to lysosomes, resp

98 lar protein leak, tubular protein uptake via endocytosis and PT water reabsorption.

99 In yeast, the endocytosis and QC of most plasma membrane (PM) proteins

100 proteins with exocyst protein Sec15 and with endocytosis and recycling regulators Rab5, Rab7, and Rab

101 of Drosophila nephrocytes requires balanced endocytosis and recycling to maintain its structural int

102 stabilizes the developing AIS by inhibiting endocytosis and removal of AIS proteins.

103 f AMOT on BMP-SMAD signaling is dependent on endocytosis and specific to the apical side of polarized

104 d in macrophages when the receptor undergoes endocytosis and switches signaling adaptor; surface TLR4

105 ing the Wnt, MAPK, the ribosome, proteasome, endocytosis and tight junction pathways.

106 e we show that macrophages take up HSV-1 via endocytosis and transport the virions into multivesicula

107 romotes the cellular uptake of polyamines by endocytosis and transports them into the cytosol, highli

108 LIM1 may be involved in the synaptic vesicle endocytosis and/or the presynaptic trafficking of synapt

109 ontology biologic process 'receptor-mediated endocytosis', and 52 TMPRSS2-correlated genes had known

110 in internode intercalary meristems, inhibits endocytosis, and alters the distribution of heteroxylan

111 tically contributes to GPCR desensitization, endocytosis, and downstream signaling, and GPCR-betaarr

112 had deficient SNX1 activity, impaired D(5) R endocytosis, and increased ROS compared with cells from

113 ated in the recognition, phagocytosis and/or endocytosis, and maintenance of algae, as well as in the

114 Relationships between immunity, endocytosis, and mRNA translation lead to hypothesize th

115 fine an axis of posttranscriptional control, endocytosis, and signal transduction that is important f

116 ins to control the distribution, clustering, endocytosis, and signaling of surface glycoproteins.

117 Intriguingly, we show that suppressed endocytosis appears to be a general feature of cells in

118 Synaptic vesicle exocytosis and endocytosis are tightly coupled, and their coupling is e

119 ms by which Rit2 controls PKC-stimulated DAT endocytosis are unknown.

120 tify albumin-associated macropinocytosis and endocytosis as an ApoE-independent LNP cellular uptake p

121 Unlike other imaging-based endocytosis assays, the ppH protocol detects EVs without

122 r delivery of chemotherapy via TFR1-mediated endocytosis, assessing this target for the first time in

123 effects on the expression of AD-related and endocytosis-associated genes.

124 The effect is due to increased Na(v)1.6 endocytosis at this neuronal compartment rather than a f

125 tingly, dextran-decorated NPs showing higher endocytosis at various concentrations in macrophages als

126 ell imaging of redox states in TfR1-mediated endocytosis, attesting a reducing environment in the end

127 regulation of protein-protein interactions, endocytosis, autophagy, DNA repair, and cell cycle regul

128 defines regulatory factors for alpha-Syn PFF endocytosis, but also reveals a previously unknown endoc

129 n types are efficiently internalized through endocytosis, but capsids fail to uncoat and accumulate w

130 ng fibrils enter cells via clathrin-mediated endocytosis, but the underlying mechanisms are unclear.

131 e their EPR as well as the receptor-mediated endocytosis by hepatocyte targeting-ligands.

132 n of endocytic proteins, TORC2 also controls endocytosis by modulating PM tension.

133 Conversely, inhibition of trans-endocytosis by silencing of the small GTPase TC21 or exp

134 , it is unclear whether the mechanism of BCR endocytosis changes in response to these factors.

135 as supported by pathway analyses (immunity, endocytosis, cholesterol transport, ubiquitination, amyl

136 ement for actomyosin in clathrin-independent endocytosis (CIE) has not been demonstrated.

137 Clathrin-mediated endocytosis (CME) and its core endocytic machinery are e

138 P-2), which is involved in clathrin-mediated endocytosis (CME) and synaptic vesicle recycling.

139 Clathrin-mediated endocytosis (CME) begins with the nucleation of clathrin

140 Clathrin-mediated endocytosis (CME) in mammalian cells is driven by resili

141 sable proteins of the core clathrin-mediated endocytosis (CME) machinery.

142 Clathrin-mediated endocytosis (CME) occurs via the formation of clathrin-c

143 pathway in yeast for early clathrin-mediated endocytosis (CME) proteins facilitated by the phase sepa

144 In plants, clathrin mediated endocytosis (CME) represents the major route for cargo i

145 an essential component for clathrin-mediated endocytosis (CME), display a loss of pluripotency and an

146 re governed mainly through clathrin-mediated endocytosis (CME), endosomal recycling, or degradation.

147 During clathrin-mediated endocytosis (CME), over 50 different proteins assemble o

148 ferrin as an indicator for clathrin-mediated endocytosis (CME), we find that alpha-Syn involvement in

149 Conserved proteins drive clathrin-mediated endocytosis (CME), which from yeast to humans involves a

150 Although endocytosis contributes to AIS turnover, how membrane pr

151 These results indicate that cadherin endocytosis coordinates cell polarity and migration cues

152 domain in miRNA-deficient cells reverses the endocytosis defect.

153 ptake by BMVECs and that neither DMT1 nor an endocytosis-dependent pathway play any significant role

154 PAI-1 interacting with eNOS was shown to be endocytosis derived.

155 Disruption of clathrin-mediated endocytosis did not affect accumulation and nuclear tran

156 eptor endocytosis pathway, caveolin-mediated endocytosis, did not affect Wnt pathway activation in mE

157 closure (kiss-and-run) or clathrin-mediated endocytosis directly from the plasma membrane.

158 nous injection, penetrate into GBM cells via endocytosis, dissociate to be cytotoxic, and enhance the

159 Sym004 promoted EGFR endocytosis distinctly from EGF: it was asynchronous, no

160 eases featuring molecular defects in vesicle endocytosis, exocytosis, and recycling.

161 Loss of NAMPT impaired synaptic vesicle endocytosis/exocytosis in the NMJs.

162 the cKO mice were treated with NMN, vesicle endocytosis/exocytosis was improved and endplate morphol

163 During clathrin-mediated endocytosis, F-actin assembly initiated by the Arp2/3 co

164 pes enter by clathrin- and dynamin-dependent endocytosis, facilitated by integrin beta(1), and traffi

165 Together, these findings suggest that endocytosis followed by fusion with host membranes trigg

166 reast tumorigenesis by increasing E-cadherin endocytosis, followed by the activation of a beta-cateni

167 viruses enter their host cells by triggering endocytosis following receptor engagement.

168 zed signaling revealed a requirement of DOPr endocytosis for activation of PKC at the plasma membrane

169 way significantly impaired the activation of endocytosis for amino acid uptakes into chRCC cells.

170 NA directly through folate receptor mediated endocytosis for gene silencing has not, if any, been suc

171 ndent, mannose 6-phosphate receptor-mediated endocytosis from the cell surface.

172 endent, mannose-6-phophate receptor-mediated endocytosis from the cell-surface.

173 ion-approved drugs that inhibit viral entry, endocytosis, genome assembly, translation, and replicati

174 Live cell imaging of endocytosis has helped to decipher many of its mechanism

175 rs apically, and is compensated by subapical endocytosis, has been challenged in recent years.

176 type-specific cofactors may promote tetherin endocytosis.IMPORTANCE The mechanisms of tetherin's anti

177 We further show that interruption of Cx43 endocytosis in Abeta(25-35)-exposed astrocytes resulted

178 ther Rit2 is required for PKC-stimulated DAT endocytosis in DAergic terminals or whether there are re

179 lexes assemble at sites of clathrin-mediated endocytosis in human cells.

180 the first time a dynamin-dependent ultrafast endocytosis in IHCs.SIGNIFICANCE STATEMENT Otoferlin, a

181 However, the mechanism of IGF1R endocytosis in normal keratinocytes remains unclear.

182 p120-catenin (p120) and VE-cadherin (VE-cad) endocytosis in vascular development using mouse mutants

183 the discrepancy among reports on the role of endocytosis in Wnt signaling.

184 fast endocytosis and activity-dependent bulk endocytosis, in which SVs are regenerated from the inter

185 HSV enters many cell types by endocytosis, including epithelial cells, the site of pri

186 osed by functionalizing the aptasensors with endocytosis-inducing DSS peptides.

187 Treatment with the clathrin-mediated endocytosis inhibitor, Dyngo-4a, re-stored the plasma me

188 g was blocked in cells treated with clathrin endocytosis inhibitor.

189 Endocytosis inhibitors, immunofluorescence, immunoprecip

190 RNA transfer at the level of EV biogenesis, endocytosis, intracellular trafficking, and RNA delivery

191 oma brucei, occurs through receptor-mediated endocytosis involving the parasite's invariant surface g

192 Endocytosis is a fundamental process occurring in all eu

193 The reduced endocytosis is associated with impaired extracellular si

194 Synaptic vesicle (SV) endocytosis is coupled to exocytosis to maintain SV pool

195 membrane (PM) protein abundance by selective endocytosis is critical for cellular adaptation to stres

196 Endocytosis is critically dependent on intracellular Ca(

197 show that the rate of synaptic vesicle (SV) endocytosis is differentially affected by the alpha-Syn

198 our results indicate that regulated cadherin endocytosis is essential for both dynamic cell movements

199 Retrieval of synaptic vesicles via endocytosis is essential for maintaining sustained synap

200 While TBS-induced SK2 endocytosis is facilitated by PKA activation, SK2 recycl

201 Clathrin-mediated endocytosis is likely the main uptake mechanism.

202 results in multiple cell lines support that endocytosis is not a requirement for Wnt signal transduc

203 To examine whether this facilitation of endocytosis is related to the Na(+)-dependent vesicular

204 olved question in the field-whether receptor endocytosis is required for Wnt signal transduction.

205 Receptor-mediated endocytosis is responsible for reabsorption of transferr

206 Endocytosis is restored at kismet mutant synapses by pha

207 Intriguingly, the requirement for MYO7B in endocytosis is restricted to alpha-Syn PFFs and other po

208 (CME), we find that alpha-Syn involvement in endocytosis is specifically mediated through PI(4,5)P(2)

209 specifically regulates a specialized form of endocytosis known as macropinocytosis, without affecting

210 We also show that reduced endocytosis leads to increased cell size, which suggests

211 Rather than clathrin-mediated endocytosis, macropinosomes encapsulate F-actin in the c

212 off-target effects of a drug used to inhibit endocytosis may be one source of the discrepancy among r

213 , further indicating that effects of AFL1 on endocytosis may be related to actin filament organizatio

214 tosis, but also reveals a previously unknown endocytosis mechanism for HSPG-binding cargos in general

215 HSV-1 enters epithelial cells via an endocytosis mechanism that is low-pH dependent.

216 ce strongly supports a crosslinking-mediated endocytosis mechanism.

217 sical properties known to engage alternative endocytosis mechanisms, highlighting the importance of b

218 1 lysosomal degradation is independent of 1) endocytosis mediated by the clathrin adaptor AP2; 2) Tf,

219 ion of IGF1R promotes its clathrin-dependent endocytosis, mediated by two distinct adaptors, Flot-1 i

220 en a new avenue to study the interplay among endocytosis, metabolism and nanomedicine.

221 Clathrin-mediated endocytosis occurs via the assembly of clathrin-coated p

222 multiple epithelia, where it participates in endocytosis of a variety of ligands performing roles imp

223 NuMA1 inhibits the endocytosis of AIS NF186 by impeding Lis1's interaction

224 lial cells with BMP-9 triggers the extensive endocytosis of ALK-1, and it is mediated by caveolin-1 (

225 is the use of a novel means of achieving the endocytosis of aptasensors.

226 an early effector involved in regulating the endocytosis of C. pneumoniae in an EGFR- and SNX9-depend

227 ed that because of the force-dependent trans-endocytosis of CD80, the capacity of APCs to activate T

228 Endophilin plays key roles during endocytosis of cellular receptors, including generating

229 A better understanding of endocytosis of different cell surface receptors has impl

230 Following endocytosis of EBOV, the GP1 domain is cleaved by cellul

231 in patient cells and identified a defect in endocytosis of epidermal growth factor.

232 Decreased membrane tension facilitates the endocytosis of FGF signaling components, which activate

233 -wide screen now revealed that the selective endocytosis of four AATs during starvation required the

234 n multiple intracellular processes including endocytosis of hemoglobin, which is required for parasit

235 Thus, trans-endocytosis of membrane-associated IL-15Ralpha-IL-15 pro

236 ther show that P4 induces clathrin-dependent endocytosis of mPRbeta into signaling endosome, where mP

237 njugation of human NHE3 by Nedd4-2 regulates endocytosis of NHE3 but does not affect its cellular exp

238 tase, important in clathrin uncoating during endocytosis of presynaptic vesicles.

239 on, we showed that the YxxPhi motif triggers endocytosis of S proteins.

240 response to amino acid availability, through endocytosis of sugar- and amino acid transporters (AATs)

241 ceptor-related protein 1 (LRP1) controls the endocytosis of tau and its subsequent spread.

242 Because endocytosis of TGFbeta receptor II (TbetaRII), in respon

243 Using endocytosis of transferrin as an indicator for clathrin-

244 of TfR1, which has been widely used to study endocytosis, often not considering its function in iron

245 l internalization to STRIC is independent of endocytosis or an intact Golgi, but depends on Ltc1, a L

246 activity of NME was insufficient to promote endocytosis or inhibit EGFR signaling.

247 assembly or by rapid removal of MAC through endocytosis or shedding.

248 ression does not affect clathrin-independent endocytosis or, surprisingly, AP1-dependent lysosomal tr

249 d rapid forms of endocytosis and facilitated endocytosis overshoot, but did not affect the readily re

250 Disruption of another receptor endocytosis pathway, caveolin-mediated endocytosis, did

251 ith immunofluorescence, confocal microscopy, endocytosis, PLD activity, and cell viability assays, we

252 with beta-arrestin recruitment and receptor endocytosis, promoting CCR3 internalization and degradat

253 Mutation of residues within the IFITM3 endocytosis-promoting Yxx motif converted human IFITM3 i

254 larly flotillin-dependent, clathrin-mediated endocytosis, provide a new avenue for drug targeting in

255 tracellular Na(+) concentration affected the endocytosis rate.

256 Following endocytosis, receptors that are internalized to sorting

257 ow that a mechanically triggered increase in endocytosis regulates early differentiation.

258 fy SLC35B2 and myosin-7B (MYO7B) as critical endocytosis regulators for alpha-Syn preformed fibrils (

259 tosolic protein transporters, exocytosis and endocytosis regulators, and proteins necessary for synap

260 studies demonstrated that PKC-stimulated DAT endocytosis requires both Ack1 inactivation, which relea

261 Increasing Rab5a-facilitated endocytosis rescues defective early differentiation.

262 nsfection efficiency was consistent with the endocytosis results.

263 hough the basic process of receptor-mediated endocytosis (RME) is well established, certain specific

264 Progranulin is involved in endocytosis, secretion and lysosomal processes, but its

265 including membrane protein characterization, endocytosis, secretion, protein folding, quality control

266 addition of latrunculin A to acutely inhibit endocytosis shows that rcy1Delta and snx4Delta single mu

267 that inactivation of both 2'-O-MTase and the endocytosis signal of the spike protein is an approach t

268 ane PI(4,5)P2 in cultured neurons impairs SV endocytosis, specifically in midbrain neurons, and furth

269 sure the rates of clathrin-mediated FAP-EGFR endocytosis stimulated with physiological EGF concentrat

270 a apparent nonvesicular pathways rather than endocytosis, suggesting applications of this activity-ba

271 lectively internalized via receptor-mediated endocytosis, suppressed invasion and epithelial-mesenchy

272 We propose that in B cells, the mechanism of endocytosis switches to accommodate large receptor clust

273 -conserved, large-scale, fluid-phase form of endocytosis that has been ascribed different functions i

274 Lowering the temperature slowed down endocytosis, thereby enhancing the temporal resolution o

275 0 expressed on the APCs, and underwent trans-endocytosis to deplete CD80.

276 ning relative to sites of bulk secretion and endocytosis to further characterize functions of these s

277 ecules as an amino acid source by activating endocytosis to sustain cell proliferation and survival.

278 lved in many cellular processes ranging from endocytosis to transcription.

279 mbly utilizes an adaptive mechanism enabling endocytosis under varying physical constraints.

280 nown role in normal receptor tyrosine kinase endocytosis, under basal conditions in monolayer keratin

281 receptor 1 (CD71) guarantees iron supply by endocytosis upon binding of iron-loaded transferrin and

282 However, unlike many receptors that trigger endocytosis upon ligand binding, HER2 is an internalizat

283 ts as well as dramatic shape changes such as endocytosis, vesicular trafficking, and cell division.

284 high-resolution imaging of clathrin-mediated endocytosis, vimentin, the endoplasmic reticulum, membra

285 ernalization into cells by receptor-mediated endocytosis was also studied.

286 with bafilomycin and found that the rate of endocytosis was not affected by regulating the vesicular

287 The concept of receptor-mediated endocytosis was proposed 40 years ago in a seminal revie

288 1 (GAPVD1), a protein required for efficient endocytosis, was consistently one of the most abundant i

289 pplying NERDSS to steps in clathrin-mediated endocytosis, we design multicomponent systems that can f

290 sis of protein-folding and clathrin-mediated endocytosis, we show that both chaperone-dependent cellu

291 App1 is postulated to be involved in endocytosis, whereas Dpp1 and Lpp1 may be involved in li

292 R) receptor BR INSENSITIVE1 (BRI1) undergoes endocytosis, which depends on clathrin and AP-2.

293 ation is modulated by mechanisms such as TCR endocytosis, which is thought to terminate TCR signallin

294 e of the TLR7/8 agonist in native form after endocytosis, which results in high in vitro TLR agonist

295 nals control both plasma membrane growth and endocytosis, which would ensure that the rates of each p

296 horylation is mainly involved in TBS-induced endocytosis, while ubiquitination predominantly inhibits

297 Inhibiting EV endocytosis with dynasore blocked the increase in cytoso

298 In support of this blocking endocytosis with inhibitors prevents the effects of Wnt5

299 of essential components of clathrin-mediated endocytosis with quantitative assessment of Wnt signal t

300 higher-valence conjugates induced more rapid endocytosis, with over 90% of the surface-bound conjugat