ライフサイエンスコーパス: actin-related protein 2

1 The Actin Related Protein 2/3 complex coordinated successive

2 sions are balanced by myosin IIA (NMIIA) and actin-related protein 2/3 (Arp2/3) activity.

3 To investigate this, we disrupted actin-related protein 2/3 (Arp2/3) and the WASP-family v

4 Actin-related protein 2/3 (Arp2/3) complex activation by

5 s in this activity and include the conserved actin-related protein 2/3 (Arp2/3) complex as well as a

6 nitiated by nucleation/branching through the actin-related protein 2/3 (Arp2/3) complex downstream of

7 tt-Aldrich syndrome protein (N-WASP) and the actin-related protein 2/3 (Arp2/3) complex have emerged

8 ve amounts of F-actin, free barbed ends, and actin-related protein 2/3 (Arp2/3) complex in lamellipod

9 lular component of polarized growth, and the actin-related protein 2/3 (ARP2/3) complex is an importa

10 Although the actin-related protein 2/3 (Arp2/3) complex is necessary

11 The actin-related protein 2/3 (Arp2/3) complex is the primar

12 The actin-related protein 2/3 (Arp2/3) complex mediates the

13 ion of N-WASP, which binds and activates the actin-related protein 2/3 (Arp2/3) complex, dramatically

14 mation by enhancing actin nucleation via the actin-related protein 2/3 (Arp2/3) complex, is activated

15 lescence of BCR microclusters depends on the actin-related protein 2/3 (Arp2/3) complex, which nuclea

16 of other actin-binding proteins, notably the actin-related protein 2/3 (Arp2/3) complex, which nuclea

17 hanges were accompanied by activation of the actin-related protein 2/3 (Arp2/3) complex, which stimul

18 rolin homologous protein 1 (WAVE1) regulates actin-related protein 2/3 (Arp2/3) complex-mediated acti

19 lated by actin-binding proteins, such as the actin-related protein 2/3 (Arp2/3) complex.

20 -actin is generated by the nucleation factor actin-related protein 2/3 (Arp2/3) complex.

21 ulating the actin-nucleating activity of the actin-related protein 2/3 (Arp2/3) complex.

22 Beads coated with actin-related protein 2/3 (Arp2/3)-activating proteins c

23 ing imposed by elevated viscosity induces an actin-related protein 2/3 (ARP2/3)-complex-dependent den

24 BAR domain-containing protein that inhibits actin-related protein 2/3 (Arp2/3)-dependent actin polym

25 Actin-related protein 2/3 complex (Arp2/3 complex) catal

26 selectively dependent on Ca(2+) signals and actin-related protein 2/3 complex (Arp2/3) activity.

27 nd that cancer cell motility mediated by the actin-related protein 2/3 complex (Arp2/3) is required f

28 ively regulates cortical localization of the actin-related protein 2/3 complex (Arp2/3), its regulato

29 , which induces actin polymerization through actin-related protein 2/3 complex (Arp2/3), to address t

30 tor of the dendritic spine cytoskeleton, the actin-related protein 2/3 complex (Arp2/3), we report he

31 ished cell junctions causes actin-driven and actin-related protein 2/3 complex (ARP2/3)-controlled la

32 Wiskott-Aldrich syndrome protein, promoting actin-related protein 2/3 complex activity.

33 WASp result in unregulated activation of the actin-related protein 2/3 complex and increased actin po

34 is an F-actin binding protein that activates actin-related protein 2/3 complex and is localized withi

35 kott-Aldrich syndrome protein (WASp) and the actin-related protein 2/3 complex generates forces at mu

36 aned animals, diazepam binding inhibitor and actin-related protein 2/3 complex mRNA levels were suppr

37 rited actin polymerization defects by either actin-related protein 2/3 complex subunit 1B or megakary

38 eins alpha-actinin-1 and alpha-actinin-4 and actin-related protein 2/3 complex subunit 3 (Arp3), are

39 ettsial invasion, including actin filaments, actin-related protein 2/3 complex, phosphatidylinositol-

40 Arp2/3 (actin-related protein 2/3) complex is a seven-subunit co

41 The Arp2/3 (actin-related protein 2/3) complex nucleates branched ac

42 Arp (actin-related protein) 2/3 complex nucleates actin filam

43 drich syndrome protein (N-WASp) and the Arp (actin-related protein) 2/3 complex, and activation of th

44 cently, formins have been identified as Arp (actin-related protein) 2/3-independent nucleators of act

45 yeast Vip1 and Asp1 proteins, regulators of actin-related protein-2/3 (ARP 2/3) complexes.

46 istent with this hypothesis, deletion of the actin-related protein-2/3 (ARP2/3) complex, which regula

47 on of dendritic actin filament arrays by the actin-related protein-2/3 complex is regulated, the in v

48 roteins, formins, profilin, cofilin, and the actin-related protein-2/3 complex.

49 By contrast, ablation of the Arp2/3 (actin-related protein-2/3) complex activator SCAR (suppr

50 The Arp2/3 (Actin-related proteins 2/3) complex is activated by WASP

51 on macrophage deformability is dependent on actin-related proteins 2/3, indicating that stress hormo

52 Actin related protein 2/actin related protein 3 (Arp2/3)

53 Actin-related protein 2 and 3 (Arp2/3) complex forms a d

54 t binds actin-filaments and colocalizes with actin-related protein 2 and 3 (Arp2/3) complex in the me

55 The actin-related protein 2 and 3 (Arp2/3) complex is a seve

56 Yeast actin-related proteins 2 and 3 (Arp2/3) accelerates the

57 CDC42-dependent conformational change of the actin-related proteins 2 and 3 (ARP2/3) actin polymeriza

58 -specific protein 1 (HS1) is an F-actin- and actin-related proteins 2 and 3 (Arp2/3)-binding protein

59 l GTPase dynamin, the cytoskeletal regulator Actin-related protein 2, and the protein kinase Casein k

60 Actin-related protein 2 (Arp2) and Arp3 are folded like

61 Phosphorylation of the actin-related protein 2 (Arp2) subunit of the Arp2/3 com