ライフサイエンスコーパス: submembranous

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1 teins with IgG-coated erythrocytes triggered submembranous actin assembly.

2 cortical cytoskeleton, the topography of the submembranous actin cytoskeleton (100-300 nm depth) was

3 bryogenesis, is coincident with a pattern of submembranous actin filament bundles in the epithelial c

4 Concomitantly observed was reorganization of submembranous actin filaments correlating directly with

5 of neural cell adhesion molecules, with the submembranous actin-spectrin skeleton.

6 New 'super-resolution' imaging of the submembranous axonal cytoskeleton reveals that it is org

7 ealed that formin IV is primarily found in a submembranous band that co-localizes with the actin cyto

8 ich are thought to link membrane proteins to submembranous bundles of actin filaments.

9 calmodulin-dependent kinase CaMKII and local submembranous Ca(2+) elevation.

10 Submembranous Ca(2+) increases were detected during the

11 Activation of a submembranous Ca2+ sensor, just beneath sites of Ca2+ en

12 g interference reflection microscopy and the submembranous calcium signal was assessed using total in

13 ive CB interacts with gephyrin, inducing the submembranous clustering and the postsynaptic accumulati

14 a spatial redistribution of calponin to the submembranous cortex.

15 n of volume control and reduced actin in the submembranous cortex.

16 a specialized cytoskeleton consisting of two submembranous cytoskeletal and scaffolding proteins, ank

17 Here, we demonstrate that the submembranous cytoskeletal proteins alphaII and betaII s

18 ding protein (ABP-280) is a component of the submembranous cytoskeleton and interacts with the glycop

19 Thus, the paranodal spectrin-based submembranous cytoskeleton comprises the paranodal barri

20 Spectrins form a submembranous cytoskeleton proposed to confer strength a

21 d of actin, but proteins of the erythrocytic submembranous cytoskeleton were present.

22 reak symmetry, they assemble a distal axonal submembranous cytoskeleton, comprised of ankyrinB (ankB)

23 s a linker protein connecting SNAP-25 to the submembranous cytoskeleton.

24 homolog of dystrophin and a component of the submembranous cytoskeleton.

25 so colocalized in endothelial cells in focal submembranous dorsoventral protrusions.

26 in turtle hair cells and utilized to monitor submembranous intracellular Ca2+ and to evaluate the con

27 or the activation of NHE1 and an increase in submembranous intracellular pH occurring during macropin

28 Ultrastructural analysis revealed submembranous localization of Ank-G at nodes of Ranvier

29 presence of sodium channels, along with the submembranous location of Ank-G is consistent with the r

30 chanism underlying the dynamic regulation of submembranous macromolecular complex formation between g

31 -containing molecule acts as an organizer of submembranous molecular complexes that control the coord

32 caused by confinement of TMP mobility by the submembranous MreB network.

33 and translocation of actin filaments to the submembranous network is observed.

34 thelial surface layer and its linkage to the submembranous scaffold.

35 ne conductance regulator associates with the submembranous scaffolding protein EBP50 (ERM-binding pho

36 ed synaptically where they interact with the submembranous scaffolding protein gephyrin, receptors co

37 g microtubules or modulate the size range of submembranous septin disks-a prevalent septin structure

38 enterocyte reduced pHi locally in the apical submembranous space.

39 oreactivity were discretely localized to the submembranous surfaces of dendrites forming slight protr

40 PAK1 is detected in submembranous vesicles in both unstimulated and stimulat

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