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1 teins with IgG-coated erythrocytes triggered submembranous actin assembly.
2 is restricted by transient entrapment within submembranous actin corrals.
3 cortical cytoskeleton, the topography of the submembranous actin cytoskeleton (100-300 nm depth) was
4 bryogenesis, is coincident with a pattern of submembranous actin filament bundles in the epithelial c
5 Concomitantly observed was reorganization of submembranous actin filaments correlating directly with
6 LYVE-1 dynamics are indeed restricted by the submembranous actin network.
7  of neural cell adhesion molecules, with the submembranous actin-spectrin skeleton.
8 ensed by integrin proteins and transduced by submembranous adhesion complexes to signaling pathways t
9        New 'super-resolution' imaging of the submembranous axonal cytoskeleton reveals that it is org
10 ealed that formin IV is primarily found in a submembranous band that co-localizes with the actin cyto
11 ich are thought to link membrane proteins to submembranous bundles of actin filaments.
12 calmodulin-dependent kinase CaMKII and local submembranous Ca(2+) elevation.
13                                              Submembranous Ca(2+) increases were detected during the
14                              Activation of a submembranous Ca2+ sensor, just beneath sites of Ca2+ en
15 g interference reflection microscopy and the submembranous calcium signal was assessed using total in
16 ive CB interacts with gephyrin, inducing the submembranous clustering and the postsynaptic accumulati
17 leads to the redistribution of gephyrin into submembranous clusters at nascent inhibitory synapses.
18              Cell shape is controlled by the submembranous cortex, an actomyosin network mainly gener
19 n of volume control and reduced actin in the submembranous cortex.
20  a spatial redistribution of calponin to the submembranous cortex.
21 l and to large multiprotein complexes in the submembranous cytoplasm.
22 a specialized cytoskeleton consisting of two submembranous cytoskeletal and scaffolding proteins, ank
23                Here, we demonstrate that the submembranous cytoskeletal proteins alphaII and betaII s
24 ding protein (ABP-280) is a component of the submembranous cytoskeleton and interacts with the glycop
25           Thus, the paranodal spectrin-based submembranous cytoskeleton comprises the paranodal barri
26                             Spectrins form a submembranous cytoskeleton proposed to confer strength a
27 d of actin, but proteins of the erythrocytic submembranous cytoskeleton were present.
28 reak symmetry, they assemble a distal axonal submembranous cytoskeleton, comprised of ankyrinB (ankB)
29 s a linker protein connecting SNAP-25 to the submembranous cytoskeleton.
30 homolog of dystrophin and a component of the submembranous cytoskeleton.
31 her with actin as obligatory subunits of the submembranous cytoskeleton.
32 so colocalized in endothelial cells in focal submembranous dorsoventral protrusions.
33 )R-a3(A343W) mutant induces the formation of submembranous gephyrin clusters independently of CB in C
34 in turtle hair cells and utilized to monitor submembranous intracellular Ca2+ and to evaluate the con
35 or the activation of NHE1 and an increase in submembranous intracellular pH occurring during macropin
36            Ultrastructural analysis revealed submembranous localization of Ank-G at nodes of Ranvier
37  presence of sodium channels, along with the submembranous location of Ank-G is consistent with the r
38 chanism underlying the dynamic regulation of submembranous macromolecular complex formation between g
39 -containing molecule acts as an organizer of submembranous molecular complexes that control the coord
40 caused by confinement of TMP mobility by the submembranous MreB network.
41  and translocation of actin filaments to the submembranous network is observed.
42 th a discoid flat morphology maintained by a submembranous peripheral ring of microtubules, named mar
43 thelial surface layer and its linkage to the submembranous scaffold.
44 ne conductance regulator associates with the submembranous scaffolding protein EBP50 (ERM-binding pho
45 ed synaptically where they interact with the submembranous scaffolding protein gephyrin, receptors co
46 g microtubules or modulate the size range of submembranous septin disks-a prevalent septin structure
47 enterocyte reduced pHi locally in the apical submembranous space.
48 oreactivity were discretely localized to the submembranous surfaces of dendrites forming slight protr
49                          PAK1 is detected in submembranous vesicles in both unstimulated and stimulat