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1 scission and producing a receptor-containing endocytic vesicle.
2 ion and the subsequent internalization of an endocytic vesicle.
3 ncurrently with the "touch" of a neighboring endocytic vesicle.
4 t mechanism and through contact with another endocytic vesicle.
5 cumulation of endoglin and beta-arrestin2 in endocytic vesicles.
6 sential for motility and processing of early endocytic vesicles.
7 protein directly involved in the assembly of endocytic vesicles.
8 d-bound RF receptor and its association into endocytic vesicles.
9  implicated in the formation and movement of endocytic vesicles.
10 , in which it spontaneously recycles through endocytic vesicles.
11 se upon HS degradation, and (4) leakage from endocytic vesicles.
12 may regulate the transition of early to late endocytic vesicles.
13 oated vesicles and in large, smooth-surfaced endocytic vesicles.
14 antibodies colocalized with virus-containing endocytic vesicles.
15  tail (M6tail) alone targeted to the nascent endocytic vesicles.
16 ponding to endoplasmic reticulum, Golgi, and endocytic vesicles.
17 st-translationally modified and localized to endocytic vesicles.
18 tivated beta1 integrins and L1 into distinct endocytic vesicles.
19 rect fusion with the plasma membrane and via endocytic vesicles.
20 als that specify incorporation of cargo into endocytic vesicles.
21 h other GPCRs and internalize with them into endocytic vesicles.
22 ses uptake of CpG (but not control) DNA into endocytic vesicles.
23 ion, hTLR9 and CpG DNA are found in the same endocytic vesicles.
24 d in vesicles suggest the caveolar origin of endocytic vesicles.
25 y, rtoA cells have a defect in the fusion of endocytic vesicles.
26 after activation of gp41 by the acidic pH of endocytic vesicles.
27 L,) a compartment thought to represent GLUT4 endocytic vesicles.
28 eplicative organelle that avoids fusion with endocytic vesicles.
29  viruses that penetrate cells by fusion with endocytic vesicles.
30  that acts to prevent clustering of Env into endocytic vesicles.
31  receptors specifically to different primary endocytic vesicles.
32 e was transient, but Raf-1 remained bound to endocytic vesicles.
33 flg22-dependent internalization of FLS2 into endocytic vesicles.
34  secretin and AT(1A) receptors colocalize in endocytic vesicles.
35 rane turnover than of active clustering into endocytic vesicles.
36  megalin is able to internalize insulin into endocytic vesicles.
37 d to be involved in downstream processing of endocytic vesicles.
38 esponse results in the accumulation of large endocytic vesicles.
39 rther illustrates the unique nature of these endocytic vesicles.
40 ndocytosis or loading of TfR into individual endocytic vesicles.
41  receptors from the plasma membrane and into endocytic vesicles.
42 t is believed to facilitate the formation of endocytic vesicles.
43 ributed by the VAMP7-dependent exocytosis of endocytic vesicles.
44  in vesicles/inclusion bodies, suggestive of endocytic vesicles.
45 bservable on the plasma membrane and also in endocytic vesicles.
46 tein PrP is confined to the cell membrane or endocytic vesicles.
47 he transport of polyplexes through important endocytic vesicles.
48  resulting in the redistribution of SAP97 to endocytic vesicles.
49 2 capsid proteins following acidification of endocytic vesicles.
50  thus serve as markers for discrete types of endocytic vesicles.
51 ation and was subsequently internalized into endocytic vesicles.
52  p85alpha knockdown enlarged SARA-containing endocytic vesicles.
53 the acidification and/or fusion with various endocytic vesicles.
54  major cargo protein of clathrin-independent endocytic vesicles.
55 dynamin 2, a protein involved in scission of endocytic vesicles.
56 t postendosomal trafficking, are sorted into endocytic vesicles.
57 ng proteins that recruit cargo proteins into endocytic vesicles.
58 ere subsequently taken up and accumulated in endocytic vesicles.
59 ontributing to neck formation in presynaptic endocytic vesicles.
60 resulting in accumulation of the material in endocytic vesicles.
61 sphosphate (PtdIns(4,5)P(2)) associated with endocytic vesicles.
62  the protein coats of certain post-Golgi and endocytic vesicles.
63 me when AIP4 co-localizes with arrestin-2 on endocytic vesicles.
64  envelope is induced by the acidic pH of the endocytic vesicle [1].
65 s thought to accompany the 'pinching off' of endocytic vesicles [1] [4].
66  entirely localised to the cytosolic face of endocytic vesicles [3] [4].
67 mediate association with clathrin-containing endocytic vesicles: a putative dileucine motif at positi
68 pid trafficking defect, Tangier disease late endocytic vesicles accumulated both cholesterol and sphi
69 with the BCR on the cell surface and TLR9 in endocytic vesicles, achieving synergy must involve uniqu
70 ng with activated beta2AR, D1AR, and ETAR in endocytic vesicles, activation of AT1AR and NTR triggers
71       Agents that block the acidification of endocytic vesicles also arrest vesicular trafficking.
72 tween progression of clathrin-coated pits to endocytic vesicles and an activation-deactivation cycle
73 to redistribution of beta-arrestin2-GFP into endocytic vesicles and classical receptor desensitizatio
74 hat enzyme activity in fractions enriched in endocytic vesicles and cytosol was preferentially inhibi
75 presence of monensin, which raises the pH of endocytic vesicles and has been shown to inhibit FMDV re
76 g that myo6 has a transient association with endocytic vesicles and is released upon early endosome f
77 sis is elevated, which translocates Eiger to endocytic vesicles and leads to activation of apoptotic
78 rom mitochondria but colocalize in part with endocytic vesicles and lysosomes.
79 diate common to a subset of clathrin derived endocytic vesicles and macropinosomes.
80 or driving force for retrograde transport of endocytic vesicles and membranous organelles.
81 of early endocytic antigen 1 (EEA1)-positive endocytic vesicles and of vesicles containing internaliz
82 cterial and viral pathogens, and motility of endocytic vesicles and other membrane-bound organelles.
83                     TbCLH is present on both endocytic vesicles and post-Golgi elements, suggesting a
84 showed further that TTP is localized to late endocytic vesicles and that it facilitates the intracell
85 owed that these vesicles were newly uncoated endocytic vesicles and that myo6 was recruited to these
86 rect fusion with the plasma membrane and via endocytic vesicles and that this is not dependent on the
87 lipoprotein acceptors, traffics between late endocytic vesicles and the cell surface.
88 results in the depletion of alpha5 from both endocytic vesicles and the recycling compartment, provid
89 ong-standing question in cell biology is how endocytic vesicles and tubules detach from the plasma me
90 -enhanced green fluorescent protein-positive endocytic vesicles and tubulovesicular structures underg
91 nt capsid accumulated in caveolin-1-mediated endocytic vesicles and was then translocated to the endo
92 g G protein coupling, targeting receptors to endocytic vesicles, and initiating G protein-independent
93 asma membrane proteins to define all primary endocytic vesicles, and labelling of specific proteins w
94  its internalization and localization to the endocytic vesicles, and pretreatment of cardiomyocytes w
95  transiently interact with one another, late endocytic vesicles, and the cell surface.
96 re not rapidly replenished from recycling of endocytic vesicles; and (iv) exocytosis of vesicles in r
97 /3 complex activation to assemble F-actin as endocytic vesicles are being formed.
98 that at least 95% of the earliest detectable endocytic vesicles arise from clathrin-coated pits.
99 bedded ErbB-2, through endocytosis using the endocytic vesicle as a vehicle, importin beta1 as a driv
100 ast endocytosis can retrieve a single, large endocytic vesicle as fast as 50-100 ms after synaptic ve
101 ab5 interacting protein that may function on endocytic vesicles as a receptor for rab5-GDP and partic
102 e plasma membrane, prior to the formation of endocytic vesicles, as it is insensitive to dansylcadave
103 hosphomimetic mu2 mutant increases levels of endocytic vesicle-associated AP2.
104 e detailed proteomic analysis and mapping of endocytic vesicle-associated proteins.
105 sibly inhibited, permitting the isolation of endocytic vesicles at defined stages of maturation.
106 er surface proteins), perhaps by focusing of endocytic vesicles at the Golgi complex.
107 s most important for the initial movement of endocytic vesicles away from the plasma membrane, which
108 s been implicated in the docking of incoming endocytic vesicles before fusion with early endosomes.
109                 These studies suggested that endocytic vesicles bind to and travel along microtubules
110                           Thus, NO regulates endocytic vesicle budding by S-nitrosylation of dynamin.
111                 The GTPase dynamin regulates endocytic vesicle budding from the plasma membrane, but
112 ons may have implications for the process of endocytic vesicle budding in general.
113  living synapse has implicated endophilin in endocytic vesicle budding.
114                        RIDalpha localizes to endocytic vesicles but is not homologous to Rab7 and is
115  revealed that they block virion escape from endocytic vesicles but not virion binding or internaliza
116 trafficking of CD89 to lamp1-containing late endocytic vesicles, but not class II-containing vesicles
117  are believed to infect target cells through endocytic vesicles, but the details of this pathway are
118 ate from the cytoplasm and bind to incoming, endocytic vesicles carrying TrkA concentrated at the tip
119 l replication begins due to acidification of endocytic vesicles, causing the breakdown of the viral c
120 pe assay to observe the interaction of early endocytic vesicles containing fluorescent ASOR with fluo
121 xes, evidently by inhibiting pinching off of endocytic vesicles containing the clustered IgE receptor
122 n added to cells, both peptides are found in endocytic vesicles containing the transferrin receptor a
123                                              Endocytic vesicles containing these complexes are acidif
124                             The formation of endocytic vesicles containing transferrin at plasma memb
125                                              Endocytic vesicles corral a central exocytic zone, tight
126 ]Galbeta1-4Glcbeta1-1'-ceramide (G(M2)) into endocytic vesicles depends on the presence of NPC1 prote
127 titution of receptor-ligand sorting in early endocytic vesicles derived from rat liver.
128  On the other hand, normal processing of the endocytic vesicles does appear to require the elevation
129           Studies of receptor recycling from endocytic vesicles employing fluorescently and HRP-tagge
130 ions, with acidic pH similar to that seen in endocytic vesicles favoring the beta-oligomer and neutra
131 min 2, a Vav-interacting protein involved in endocytic vesicle fission, significantly blocked oxLDL u
132 us lysosomes via tethering and clustering of endocytic vesicles followed by exchange of their content
133                  Because TLR9 is observed in endocytic vesicles following exposure to CpG ODN, our da
134 eruloplasmin and sequesters excess copper to endocytic vesicles for further export out of the cell.
135 t it is packed after its action into visible endocytic vesicles for its disposal.
136 or complex is often rapidly internalized via endocytic vesicles for trafficking into various intracel
137                                        Thus, endocytic vesicle formation and capture of the newly rel
138 nstrate that exogenous C(6)-ceramide induces endocytic vesicle formation and causes enlarged late end
139 dynamin isoforms have redundant functions in endocytic vesicle formation, but can be targeted to and
140                                       During endocytic vesicle formation, distinct subdomains along t
141 ed in hyaluronic capsule production and host endocytic vesicle formation, GAS GTPases and host fibrin
142 ng live cell imaging techniques to visualize endocytic vesicle formation, we find that the N-terminal
143 nover is required for multiple stages during endocytic vesicle formation.
144 a2p positively regulates Sla2p for efficient endocytic vesicle formation.
145  concentration of Sjl2 during late stages of endocytic vesicle formation.
146 on and downstream signaling only occur after endocytic vesicle formation.
147           The GTPase dynamin is required for endocytic vesicle formation.
148 ors are differentially sorted at the time of endocytic vesicle formation.
149                    Here we show that nascent endocytic vesicles formed in mutant cells displaying rap
150 ynamin, a GTPase required for the fission of endocytic vesicles from plasma membrane.
151  for the efficient transportation of nascent endocytic vesicles from the actin-rich peripheries of ep
152               Here, we find that scission of endocytic vesicles from the plasma membrane (PM) provide
153  100 kDa GTPases involved in the scission of endocytic vesicles from the plasma membrane [1].
154                Defects in the trafficking of endocytic vesicles from the plasma membrane to the Golgi
155 Endophilins A1 and A2 promote the budding of endocytic vesicles from the plasma membrane, whereas end
156 pool that functions in the separation of the endocytic vesicles from the plasma membrane.
157 n family of GTPases mediates the scission of endocytic vesicles from the plasma membrane.
158     In mammalian cells, fusion between early endocytic vesicles has been shown to require the ubiquit
159 least one population of class II- containing endocytic vesicles (i.e., CIIV) has been identified and
160 nally, the mutant receptors are localized in endocytic vesicles, identical to wild-type receptors sti
161 ment in gene expression: (i) pH buffering in endocytic vesicles, (ii) displacement of polycations fro
162 he rates of mass transfer into and among the endocytic vesicles in a model cell line, 3T3 fibroblasts
163 orescein-labeled transferrin co-localized in endocytic vesicles in Fq/11 cells, indicating that endoc
164 s are direct precursors of indented pits and endocytic vesicles in intact cells.
165         We find that alpha5 and beta1 are in endocytic vesicles in PMNs and that alpha5 colocalizes w
166 he EGFR are internalized and co-localized in endocytic vesicles in response to EGF.
167 tion of large vacuoles originating from late endocytic vesicles in sensitive mammalian cells.
168            We show that Delta is retained in endocytic vesicles in the mesoderm but expressed on the
169  that the formation, movement, and fusion of endocytic vesicles in the region between the extruding n
170                      Stat3 co-localizes with endocytic vesicles in transit from the cell membrane to
171 d did not reside in the cell surface derived endocytic vesicles, in PC-3 cells, suggesting impaired t
172  and the localization of the hook protein to endocytic vesicles indicate that the hook gene encodes a
173 le for maintaining a pH above 6 within early endocytic vesicles, inhibited the growth of C. trachomat
174 enhanced by Ca2+ ions, whereas transfer from endocytic vesicles into the cytosol requires endosomal a
175 acted by the cross-linker fimbrin before the endocytic vesicle is released from the plasma membrane.
176  the protein coats of certain post-golgi and endocytic vesicles is clathrin, which appears as a three
177               However, the fate of the large endocytic vesicles is not known.
178                                        Early endocytic vesicles loaded with Texas Red asialoorosomuco
179                                              Endocytic vesicle-mediated internalization of pre-formed
180                   In those epithelial cells, endocytic vesicle-mediated internalization was observed
181 via the action of FAK, thereby affecting the endocytic vesicle-mediated protein trafficking events th
182 nt manner such that the pool of myosin VI in endocytic vesicles, membrane ruffles, and cytosol migrat
183 ng and/or depolymerization are important for endocytic vesicle morphogenesis.
184                                Additionally, endocytic vesicles move toward early endosomes on actin
185 ely studied, as well as trafficking in early endocytic vesicles notably regulated by the small GTPase
186 ers were also used to measure the binding to endocytic vesicles of exogenously added Rab5 and to moni
187 r how pathogens that reside primarily within endocytic vesicles of infected macrophages, such as MTB,
188  fixed, this peptide is observed only in the endocytic vesicles of live cells.
189 ntigenic peptides is largely confined to the endocytic vesicles of specialized antigen-presenting cel
190 ct plasma membrane from other DC, generating endocytic vesicles of up to 1 microm in diameter.
191  microscopy and subcellular fractionation of endocytic vesicles on a Percoll gradient.
192                        At the short necks of endocytic vesicles, other factors leading to tension may
193  and ultrastructural 3D analysis, we tracked endocytic vesicles over time, "frame by frame." The firs
194 the optimal type of HK polymer and the pH of endocytic vesicles (P = 0.0058).
195 lized to prepare highly purified fluorescent endocytic vesicles, permitting validation of microscopy-
196 t study provides evidence that ABCA1 in late endocytic vesicles plays a role in cellular lipid efflux
197 pe beta2AR and endogenous beta-arrestin 2 to endocytic vesicles prepared from CHO fibroblasts was obs
198  studies demonstrated that fluorescent early endocytic vesicles prepared from rat liver after injecti
199                                              Endocytic vesicles prepared from rat liver that had been
200 iding a system in which factors required for endocytic vesicle processing can be identified and chara
201 rom a pit before abortive CCP termination or endocytic vesicle production.
202 ned by parasite-directed modification of the endocytic vesicle rather than by the route of internaliz
203  with beta-arrestins, and found localized in endocytic vesicles rather than at the plasma membrane in
204 the complex responsible for formation of the endocytic vesicle reduced the aggregation.
205 nding mutants of Rvs167 exhibited defects in endocytic vesicle release.
206 lation with the characteristics of a primary endocytic vesicle responsible for the recycling of synap
207 nterestingly, chemicals that raise the pH of endocytic vesicles resulted in a 30 to 50% decrease in H
208 e excess cholesterol in Tangier disease late endocytic vesicles retained massive amounts of NPC1, whi
209 m through the requirement of the pluripotent endocytic vesicle scission enzyme, dynamin 2 GTPase, in
210 alizes to endosomal subdomains and regulates endocytic vesicle scission in an Arp2/3-dependent manner
211 The self-assembling GTPase dynamin catalyzes endocytic vesicle scission via membrane insertion of its
212 on parallels that of prototypical dynamin in endocytic vesicle scission.
213   Endocytosis of these coated pits generates endocytic vesicles selectively enriched in B2ARs, which
214 sential role of kinesin-based MT motility in endocytic vesicle sorting, providing a system in which f
215 ediated endocytosis, polarized blebbing, and endocytic vesicle sorting.
216       In mutants, components of exocytic and endocytic vesicles, such as Vamp2, Clathrin and Dynamin,
217 ortical F-actin accumulation and scission of endocytic vesicles, such that membrane tubules remain te
218  Lymphocytes treated with FITC-CTB reveal an endocytic vesicle that is enriched in TCR and CD59, whil
219  EGFR, arresting functionally active EGFR in endocytic vesicles that consequently led to aberrant ERK
220                  alpha 5-GFP also resided in endocytic vesicles that emanated from the leading edge o
221                                              Endocytic vesicles that fail to lose their coat nucleate
222 ution in the cytosol but no association with endocytic vesicles, the Golgi apparatus or the endoplasm
223 s following the addition of glucose, and the endocytic vesicles then pinch off from the plasma membra
224 Notch and Wg pathway components within early endocytic vesicles, thereby controlling the amount of pr
225 f CpG DNA with toll-like receptor (TLR)-9 in endocytic vesicles, thereby preventing CpG-induced activ
226   Aggregates that enter cells somehow escape endocytic vesicles to contact cytosolic protein.
227 ponent of the fusion machinery for targeting endocytic vesicles to early endosomes.
228 ellular sterol transporter that localizes to endocytic vesicles to facilitate the redistribution of s
229                  CARP-2 acts at the level of endocytic vesicles to limit the intensity of TNF-induced
230 ker protein (CLIP)-170, a protein that links endocytic vesicles to microtubules.
231 ter internalization, exosomes shuttle within endocytic vesicles to scan the endoplasmic reticulum bef
232 toplasmic domain may target CD155-containing endocytic vesicles to the microtubular network.
233 mbrane proteins, before and after inhibiting endocytic vesicle traffic from the cell surface, either
234 tes the biogenesis of its phagosome to evade endocytic vesicle traffic.
235 in cytoskeleton, transcriptional control and endocytic vesicle trafficking [1-3].
236 lgi apparatus, (iii) occurs independently of endocytic vesicle trafficking along microtubules, and (i
237              The interaction is relevant for endocytic vesicle trafficking because overexpression of
238  various endocytosis pathways and subsequent endocytic vesicle trafficking have been shown to strongl
239  Overall, excess Hyal1 secretion accelerates endocytic vesicle trafficking in a substrate-dependent m
240 ulates acto-myosin ring contraction but also endocytic vesicle transport to the cleavage furrow and i
241      In contrast, the movement of late-stage endocytic vesicles, traveling through the cytoplasm en r
242 clathrin-coated pits and to ensuing uncoated endocytic vesicles (UCV).
243                                              Endocytic vesicles undergo fission to sort ligand from r
244 hich NHE3 is rapidly endocytosed from BBM to endocytic vesicles upon treatment with carbachol; (2) mu
245 o monitor the ATP-dependent acidification of endocytic vesicles using the fluorescent dye acridine or
246  were optimal transfection agents, the pH of endocytic vesicles was >6.0.
247 ct, enveloped HSV from the cell surface into endocytic vesicles was rapid (t(1/2) of 8 to 9 min) and
248 staining of the nucleus (nucleolus), but not endocytic vesicles, was abrogated by treating the cells
249                                         Some endocytic vesicles were acidified and colocalized with L
250 tudy, procedures to prepare fluorescent late endocytic vesicles were devised.
251 es appeared 4 s after stimulation, and these endocytic vesicles were located just above the active zo
252 h the linear HK was the optimal polymer, the endocytic vesicles were strongly acidic with a pH of <5.
253 to promote exit of vector/DNA complexes from endocytic vesicles were studied systematically to define
254 s compartment intersect class II proteins in endocytic vesicles where DM editing was facilitated.
255 pid-binding FYVE domain, CARP-2 localized to endocytic vesicles, where it interacted with internalize
256 nges and is known to directly associate with endocytic vesicles, which have been implicated in dsRNA
257 d steady-state levels of AP2 associated with endocytic vesicles, which is consistent with reduced unc
258 ncy provokes the accumulation of this NTF in endocytic vesicles, which leads to a B cell maturation a
259 he complex diffusive motions of newly formed endocytic vesicles, which move faster as the surrounding
260 required for recruitment of beta-arrestin to endocytic vesicles, which was dependent on co-expression
261 orescent protein conjugate internalizes into endocytic vesicles with agonist-activated neurotensin-1
262 ll-established role of Rab5 in the fusion of endocytic vesicles with endosomes, our results suggest t
263 beta2-adrenergic receptor that traffics into endocytic vesicles with receptors that lack serine/threo
264 thelial cells, allowing for timely fusion of endocytic vesicles with the early endosome.
265 ar, while generating large numbers of motile endocytic vesicles with which dynamin associates.
266  anti-gp60 antibody (Ab) were colocalized in endocytic vesicles within 5 min of gp60 activation.
267 arrestins and consequently, redistributed to endocytic vesicles without betaarr2-GFP, whereas interna
268 tered through endocytosis and accumulated in endocytic vesicles, without necessarily entering the cyt

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