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1 tasis and has long been used as a marker for clathrin mediated endocytosis.
2 ted enhancement is impaired by inhibitors of clathrin-mediated endocytosis.
3 efine alternative mechanisms that facilitate clathrin-mediated endocytosis.
4 Fcho proteins during the earliest stages of clathrin-mediated endocytosis.
5 homology domain (ENTH) is a major player in clathrin-mediated endocytosis.
6 dophilin has been assigned as a component of clathrin-mediated endocytosis.
7 internalize small BCR clusters by classical clathrin-mediated endocytosis.
8 nase signalling pathways, but independent of clathrin-mediated endocytosis.
9 tis C virus (HCV) enters its target cell via clathrin-mediated endocytosis.
10 wth via its role as major adaptor module for clathrin-mediated endocytosis.
11 c cargoes, demonstrating its pivotal role in clathrin-mediated endocytosis.
12 nocytosis, without affecting phagocytosis or clathrin-mediated endocytosis.
13 trieved directly from the plasma membrane by clathrin-mediated endocytosis.
14 asma membrane to control Arf6 activation and clathrin-mediated endocytosis.
15 usion at the plasma membrane and enhance its clathrin-mediated endocytosis.
16 tion of the canonical eukaryotic pathway for clathrin-mediated endocytosis.
17 rrow-derived DCs was facilitated by TLR2 via clathrin-mediated endocytosis.
18 endophilin is a temporally regulated step in clathrin-mediated endocytosis.
19 Endophilin is a key protein involved in clathrin-mediated endocytosis.
20 -binding protein involved in a late stage of clathrin-mediated endocytosis.
21 ytosis; moreover, it is 200-fold faster than clathrin-mediated endocytosis.
22 n depletion was observed to severely inhibit clathrin-mediated endocytosis.
23 minal results in removal of transporters via clathrin-mediated endocytosis.
24 s to assemble, because it is internalized by clathrin-mediated endocytosis.
25 eved from the presynaptic plasma membrane by clathrin-mediated endocytosis.
26 vels that internalizes lipoprotein cargo via clathrin-mediated endocytosis.
27 role for PtdIns(4,5)P2 in the regulation of clathrin-mediated endocytosis.
28 ration, dynamin assembly, and fission during clathrin-mediated endocytosis.
29 erent ligands, including HA and heparin, via clathrin-mediated endocytosis.
30 AP-2 is the core-organizing element in clathrin-mediated endocytosis.
31 ese proteins is amphiphysin 1, implicated in clathrin-mediated endocytosis.
32 polyhedrovirus (AcMNPV), enter host cells by clathrin-mediated endocytosis.
33 1 or 3 in either bulk endosome formation or clathrin-mediated endocytosis.
34 s heparan sulfate proteoglycans, and engages clathrin-mediated endocytosis.
35 iphysin/Rvs (BAR) domains play a key role in clathrin-mediated endocytosis.
36 e abundance of CFTR is in part controlled by clathrin-mediated endocytosis.
37 he HIV-1 replication cycle is independent of clathrin-mediated endocytosis.
38 n by N-BAR domain-containing proteins during clathrin-mediated endocytosis.
39 embrane, binds clathrin, and plays a role in clathrin-mediated endocytosis.
40 bunit of the AP-2 complex and is involved in clathrin-mediated endocytosis.
41 ntegrin redistribution is thought to require clathrin-mediated endocytosis.
42 te [PI(4,5)P(2)] plays a fundamental role in clathrin-mediated endocytosis.
43 ans, and they are known to be key factors in clathrin-mediated endocytosis.
44 coordination of intracellular signaling and clathrin-mediated endocytosis.
45 l inhibited LGR5 internalization by blocking clathrin-mediated endocytosis.
46 carried out by adaptor protein-2 (AP-2) via clathrin-mediated endocytosis.
47 tion of tissues through mechanoregulation of clathrin-mediated endocytosis.
48 rus G rapidly recycles from the membrane via clathrin-mediated endocytosis.
49 (+) efflux and M1 protein internalization by clathrin-mediated endocytosis.
50 B1 surprisingly colocalized with the zone of clathrin-mediated endocytosis.
51 is A virus (HAV)-infected cells (exo-HAV) by clathrin-mediated endocytosis.
52 e apical membrane of PTECs, which determines clathrin-mediated endocytosis.
53 ion of ankyrin-B (AnkB) in coupling GLUT4 to clathrin-mediated endocytosis.
54 tomyosin cytoskeleton has been implicated in clathrin-mediated endocytosis, a clear requirement for a
55 g the concurrent activation of caveolae- and clathrin-mediated endocytosis, alongside macropinocytosi
57 DYCRV) that is an internalization signal for clathrin-mediated endocytosis and a determinant of NF-ka
58 icle recycling via interconnected actions in clathrin-mediated endocytosis and actin dynamics in neur
60 This protein complex is internalized via clathrin-mediated endocytosis and degraded in lysosomes,
62 ces AQP2 membrane accumulation by inhibiting clathrin-mediated endocytosis and increasing exocytosis.
64 onse to the needs of eukaryotic cells during clathrin-mediated endocytosis and intracellular traffick
65 ct rotational behaviors of nanocargos during clathrin-mediated endocytosis and intracellular transpor
66 We observed that INPP4A is dispensable for clathrin-mediated endocytosis and is undetectable in end
69 enveloped RNA viruses that infect cells via clathrin-mediated endocytosis and low-pH-triggered fusio
72 pressed PI4P 5-kinase PIP5K6 is required for clathrin-mediated endocytosis and polar tip growth in po
74 ABAR trafficking, this pathway requires both clathrin-mediated endocytosis and protein kinase C to re
75 in Lowe syndrome patient fibroblasts impacts clathrin-mediated endocytosis and results in an endocyti
78 ic adaptors function redundantly to regulate clathrin-mediated endocytosis and to recruit components
79 ate of transferrin receptors internalized by clathrin-mediated endocytosis and, more broadly, a mecha
80 ced interferon signaling or an inhibition of clathrin-mediated endocytosis, and PKD inhibitors do not
81 y and the nontranscriptional effect of SA on clathrin-mediated endocytosis are independent mechanisms
83 ssue of the JCI, Soda et al. have identified clathrin-mediated endocytosis as a central mechanism by
84 cellular internalization pathways identified clathrin-mediated endocytosis as the main route for eHEV
85 mplex AP-2 (CLAP), an essential component of clathrin-mediated endocytosis, as binding partners of ot
86 xin-9 (SNX9) and dynamins, key components of clathrin-mediated endocytosis, as binding partners of XL
87 cyon on NRG1 cleavage and shedding depend on clathrin-mediated endocytosis, beta-secretase 1, and int
90 c7 inhibitor H3 (SecinH3), and inhibitors of clathrin-mediated endocytosis but was unaffected by chlo
91 en alpha-Syn-bearing fibrils enter cells via clathrin-mediated endocytosis, but the underlying mechan
92 sorting proteins that are indispensable for clathrin-mediated endocytosis, but their precise functio
93 Both types of particles were internalized by clathrin-mediated endocytosis, but virions and ISVPs exh
94 lar mechanisms of cellular processes such as clathrin-mediated endocytosis, but, for quantitative mic
96 adaptors, stimulate ubiquitin-dependent and clathrin-mediated endocytosis by interacting with both a
97 dendritic spines and regulates postsynaptic clathrin-mediated endocytosis by positioning the endocyt
99 ate receptor (GluR) abundance at synapses by clathrin-mediated endocytosis can control synaptic stren
100 measure three different endocytic pathways: clathrin-mediated endocytosis, caveolae-mediated endocyt
101 ize nutrients and cell surface receptors via clathrin-mediated endocytosis, cells assemble at least 5
102 y homologous to PICALM and also functions in clathrin-mediated endocytosis, clathrin coat assembly pr
105 lectron microscopy indicated the presence of clathrin-mediated endocytosis (CME) and bulk endocytosis
106 niae invasion of HL-1 cells occurred through clathrin-mediated endocytosis (CME) and independently of
109 otein complex 2 (AP-2), which is involved in clathrin-mediated endocytosis (CME) and synaptic vesicle
111 ptor, in particular, plays a central role in clathrin-mediated endocytosis (CME) by recruiting cargo
116 ve constructed here for proteins involved in clathrin-mediated endocytosis (CME) exhibits distinctive
117 hondrial uncoupler, is a potent inhibitor of clathrin-mediated endocytosis (CME) in different systems
118 axin-1, and superoxide dismutase-1) inhibits clathrin-mediated endocytosis (CME) in mammalian cells b
120 disputed the need for F-actin and Arp2/3 in Clathrin-Mediated Endocytosis (CME) in multicellular org
121 dings on the relative importance of actin in clathrin-mediated endocytosis (CME) in yeast versus mamm
122 rcome the cell's high turgor pressure during clathrin-mediated endocytosis (CME) in yeast, but precis
127 e receptors at the postsynaptic membrane via clathrin-mediated endocytosis (CME) is a key mechanism f
130 amin 1 and 3 double knock-out neurons, where clathrin-mediated endocytosis (CME) is dramatically impa
146 We show that cargo internalized either via clathrin-mediated endocytosis (CME) or independently of
148 lective autophagy pathway in yeast for early clathrin-mediated endocytosis (CME) proteins facilitated
151 upling was less efficient but not abolished; clathrin-mediated endocytosis (CME) was severely impaire
152 tion is important for vesicle fission during clathrin-mediated endocytosis (CME), and it has been pro
153 avy chain (Cltc), an essential component for clathrin-mediated endocytosis (CME), display a loss of p
155 activity of RTKs are governed mainly through clathrin-mediated endocytosis (CME), endosomal recycling
156 disassembly factor, Auxilin2, which inhibits clathrin-mediated endocytosis (CME), impaired the AtPep1
158 demonstrated that Ca(2)(+) is important for clathrin-mediated endocytosis (CME), the mechanistic rol
159 docytosis of transferrin as an indicator for clathrin-mediated endocytosis (CME), we find that alpha-
171 Myosin 1E (Myo1E) is recruited to sites of clathrin-mediated endocytosis coincident with a burst of
175 either fusion pore closure (kiss-and-run) or clathrin-mediated endocytosis directly from the plasma m
176 thrin revealed the dynamics of EGF-activated clathrin-mediated endocytosis during internalization.
177 known mechanism for endocytosis in yeast is clathrin-mediated endocytosis, even though clathrin-inde
181 adhesion molecule A (JAM-A), virions undergo clathrin-mediated endocytosis followed by proteolytic di
182 d the functional requirement of dynamin- and clathrin-mediated endocytosis for orthobunyavirus entry
183 s and RNAi specific for macropinocytosis and clathrin-mediated endocytosis had no effect on RVFV infe
185 LM (CALM) gene, whose product is involved in clathrin-mediated endocytosis, has been identified in tw
186 Given the diversity of proteins regulated by clathrin-mediated endocytosis, how this process may dist
187 otassium channel TASK-1 are internalized via clathrin-mediated endocytosis in a cooperative manner.
192 d paralogs remain elusive, and their role in clathrin-mediated endocytosis in mammalian cells is deba
195 ressed and catalyzes membrane fission during clathrin-mediated endocytosis in nonneuronal cells.
197 These findings emphasize the importance of clathrin-mediated endocytosis in regulating CTLA-4 traff
198 ified >50 proteins that assemble at sites of clathrin-mediated endocytosis in structures called actin
200 tide reduced run-down, suggesting a role for clathrin-mediated endocytosis in the regulation of the s
201 ved proteins appear sequentially at sites of clathrin-mediated endocytosis in yeast and mammals.
202 ncreased transferrin uptake occurred through clathrin-mediated endocytosis, indicating that nanocompo
203 nscytosis was significantly inhibited by the clathrin-mediated endocytosis inhibitor Pitstop 2 or siR
205 approximately 90 nm) makes it unlikely that clathrin-mediated endocytosis internalizes as a unit the
212 en these sorting motifs are mutated, or when clathrin-mediated endocytosis is inhibited, MHC-II-Ii co
213 f the structural changes taking place during clathrin-mediated endocytosis is largely based on electr
216 The role of clathrin light chain (CLC) in clathrin-mediated endocytosis is not completely understo
217 ip between constitutive and ligand-triggered clathrin-mediated endocytosis is only poorly characteriz
219 on mediated by NEDD4-2 or NEDD4-1 leading to clathrin-mediated endocytosis is the common mode of regu
223 protein that participates in early stages of clathrin-mediated endocytosis, is downregulated as well
226 of endocytosis have been proposed including clathrin-mediated endocytosis, kiss-and-run endocytosis,
228 s as an uncoating factor and that defects in clathrin-mediated endocytosis likely contribute to patho
229 s) adapter proteins couple components of the clathrin-mediated endocytosis machinery with regulators
232 ytic membranes, including vesicles formed by clathrin-mediated endocytosis, macropinosomes, and Rab5
234 own to play an important role in the control clathrin mediated endocytosis of EGFR and other cell sur
235 nhibition increased exocytosis and inhibited clathrin-mediated endocytosis of AQP2, but exerted its e
237 1), Ca(2+), or protein kinase C (PKC) impair clathrin-mediated endocytosis of EGFR, the formation of
239 , and APSD levels were blunted by inhibiting clathrin-mediated endocytosis of GluA2 subunits with the
240 ns illuminate key host factors that regulate clathrin-mediated endocytosis of JCPyV, which is necessa
241 f-concept genetic evidence that blocking the clathrin-mediated endocytosis of LGR5 could be used to p
243 n-2 sigma subunit (AP2sigma2) is pivotal for clathrin-mediated endocytosis of plasma membrane constit
244 or adjusting excitatory synaptic strength is clathrin-mediated endocytosis of postsynaptic glutamate
248 4-(N)-GemC18-SLNs entered tumor cells due to clathrin-mediated endocytosis of the 4-(N)-GemC18-SLNs i
251 hese manipulations was without effect on the clathrin-mediated endocytosis of transferrin receptor (T
252 ) and their subsequent reformation either by clathrin-mediated endocytosis or budding from bulk endos
253 e at the plasma membrane and not involved in clathrin-mediated endocytosis or endosomal recycling, as
254 diated endocytosis but not macropinocytosis, clathrin-mediated endocytosis, or glycosphingolipid-enri
255 further characterize how JCPyV utilizes the clathrin-mediated endocytosis pathway to invade host cel
258 Independently, AP2M, a core component in clathrin-mediated endocytosis, plays a role in the forma
259 eletal dynamics, phosphoinositide signaling, clathrin-mediated endocytosis, polarized blebbing, and e
261 pathways, particularly flotillin-dependent, clathrin-mediated endocytosis, provide a new avenue for
262 Consistent with its role in participating in clathrin-mediated endocytosis, Rab14 localizes in nonlip
264 that PICALM, an adaptor protein involved in clathrin-mediated endocytosis, regulates APP internaliza
265 ension of BMPRII-LF accounted for its faster clathrin-mediated endocytosis relative to BMPRII-SF, acc
268 characterize a molecularly distinct mode of clathrin-mediated endocytosis requiring ligand ubiquityl
269 and the implications of the epsin's role in clathrin-mediated endocytosis resulting from the interpl
270 vesicles in primary cardiomyocytes, in which clathrin-mediated endocytosis seems to be the pre-domina
271 s of branched actin networks at the sites of clathrin-mediated endocytosis sheds light on the role of
273 to enter host cells through exploitation of clathrin-mediated endocytosis, the entry pathway for fil
274 of the dynamin helix is a critical stage in clathrin-mediated endocytosis, the mechanism for this re
275 pe are known to route surface receptors into clathrin-mediated endocytosis through interaction with t
276 lfate and was internalized by LRP1, LRP2 and clathrin-mediated endocytosis to be gathered in Rab11 ve
278 nociceptive neuronal excitability, the AP-2 clathrin-mediated endocytosis trafficking mechanism may
280 te that TbetaRI is targeted for constitutive clathrin-mediated endocytosis via a di-leucine (Leu(180)
281 e, we demonstrate high-resolution imaging of clathrin-mediated endocytosis, vimentin, the endoplasmic
282 ined by confocal microscopy, indicating that clathrin-mediated endocytosis was not involved in THY-1-
285 architecture of the protein machinery during clathrin-mediated endocytosis was visualized using a new
288 single-cell analysis of protein-folding and clathrin-mediated endocytosis, we show that both chapero
289 c actin filaments are a crucial component of clathrin-mediated endocytosis when endocytic proteins ca
291 athrin-coated vesicles (CCVs), is pivotal in clathrin-mediated endocytosis, which internalizes plasma
292 e in a number of essential pathways, such as clathrin-mediated endocytosis, which involve dramatic me
293 on of transferrin, a process that depends on clathrin-mediated endocytosis, while its ablation by CRI
295 kdown or knockout of essential components of clathrin-mediated endocytosis with quantitative assessme
297 While TfR1 constitutively traffics through clathrin-mediated endocytosis, with or without ligand, t
300 f the three major internalization motifs for clathrin-mediated endocytosis (YXXPhi, [DE]XXXL[LI], or