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1 with retrograde movement of actin inside the filopodium.
2 p and the retrograde flow at the base of the filopodium.
3 dling and completed formation of the nascent filopodium.
4  12.0 +/- 2.5 motors [GeoMean +/- GeoSD] per filopodium.
5                                              Filopodium, a spike-like actin protrusion at the leading
6                          At the core of each filopodium an actin bundle forms and grows into the lame
7 and flow rate can vary with time in a single filopodium and between filopodia in a single growth cone
8 ibution of individual filaments in a growing filopodium and studied how it depends on various physica
9 rated by myosin IIA filaments at the base of filopodium and transmitted to the tip through actin core
10          Hundreds of Myo10s are in a typical filopodium, and their distribution across filopodia is l
11 eins, and heightened membrane tension as the filopodium attempts to retract but is held in place by a
12 he putative microtubule-based barrier at the filopodium base.
13                     We model the growth of a filopodium based on a stochastic description which incor
14 ated phosphoprotein (VASP) is active in many filopodium-based and cytoskeleton reorganization process
15 e polarized actin filament bundle within the filopodium becoming confined to a single point at the ti
16                 Recent work has shown that a filopodium begins deciding to become a stable branch wit
17 capping protein, the number of fibers in the filopodium bundle decreases down the length of the enclo
18  effect on P domain retrograde actin flow or filopodium bundle number.
19             Without external influences, the filopodium can extend indefinitely up to the buckling le
20                                         Each filopodium contains a rigid and organized bundle of para
21                              The tip of each filopodium crawls along ECM fibers, tugs the surrounding
22        A subset of PC12 cells displayed high filopodium density on PCD.
23      Mechanistically, Slit evokes changes in filopodium dynamics by increasing direct binding of its
24                                   Perturbing filopodium dynamics pharmacologically or genetically dis
25                                         This filopodium-ECM interaction is modeled as a stochastic pr
26 enerating FIT, despite its prominent role in filopodium elongation.
27  of a neuroblastoma cell line, we found that filopodium extension and retraction are governed by a ba
28 bolished neurabin I dimerization and induced filopodium extension.
29 ur study revealed a novel mechanism, whereby filopodium formation and cell migration are regulated th
30 actin regulator filamin-A (FLNa) to modulate filopodium formation and cell migration.
31 LNa and Arl4C is essential for Arl4C-induced filopodium formation and increases the association of FL
32 h-1 can activate PAK-1 and JNK-1, and induce filopodium formation and stress fiber dissolution.
33 P-binding protein Cdc42 is thought to induce filopodium formation by regulating actin polymerization
34                               Measurement of filopodium formation by time-lapse imaging of live cells
35 inity for TEM4 and producing Rac activation, filopodium formation, and cell motility.
36 ied and some of them have been implicated in filopodium formation, the precise role of Cdc42 in modul
37 lpha appeared to mediate Cdc42 signaling for filopodium formation, whereas Nckbeta mediated Rho signa
38 e formation of dendritic spines but inhibits filopodium formation.
39  and morphology and was linked to effects on filopodium formation.
40 bilizes actin filaments and is important for filopodium formation.
41 ogressive fiber end-capping occurring as the filopodium grows.
42      Realistic future dynamical theories for filopodium growth are likely to rely on an accurate trea
43 lly resolved protein concentration along the filopodium independent of bending, lateral shift, or til
44 ion of calcium concentration within a single filopodium induced new branch filopodia.
45 o, and in silico to unravel the mechanism of filopodium initiation driven by the membrane curvature s
46                            How cells control filopodium initiation on the plasma membrane remains elu
47 ensure a precise spatial-temporal control of filopodium initiation.
48                                            A filopodium is a cytoplasmic projection, exquisitely buil
49 umber of fibers down the length of a growing filopodium is found to have profound implications for th
50 e concentration profile of G actin along the filopodium is rather nontrivial, containing a narrow min
51         This surfing-like behavior along the filopodium is recorded by feedback-controlled interferom
52 riched in localized patches on the PM and in filopodium-like extensions.
53 PCs continuously extend and retract numerous filopodium-like processes as they migrate and settle int
54 n order to extend integrin beta1-containing, filopodium-like protrusions (FLPs), which enable them to
55 mbrane to generate and maintain F-actin-rich filopodium-like protrusions and promote cancer cell inva
56 n the thrombus shell, and are flattened with filopodium-like structures when in direct contact to col
57 ed levels of filamentous actin and inhibited filopodium mobility in the growth cones.
58 e lens pit stage--there is approximately one filopodium per epithelial cell.
59  is known to decrease down the length of the filopodium, presumably due to progressive fiber end-capp
60 thod we observed an increase in the spine-to-filopodium ratio from P9-P16, indicating a period of rap
61 ngly, actin bundles that are associated with filopodium roots elongated by approximately 83% after in
62            Any realistic future theories for filopodium stability are likely to rely on an accurate t
63 t a minimum number of fibers is required for filopodium stability.
64 m an actin patch elongating into a dendritic filopodium, which tip subsequently expands via Arp2/3 co
65                          This process endows filopodium with a finite lifetime.