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1 reduce the levels of fidgetin, a microtubule-severing protein.
2 role for wild-type spastin as a microtubule-severing protein.
3 s than slow fibroblasts that lack this actin-severing protein.
4 hospholipids with gelsolin, an actin-capping/severing protein.
5 and P60-katanin are two distinct microtubule-severing proteins.
6 abilizing them and providing protection from severing proteins.
7 vestigate, using molecular dynamics, how the severing protein, actin depolymerization factor (ADF)/co
8 in, a known calcium-activated actin filament-severing protein, also impaired the wound response, indi
9 he sides of filaments and protects them from severing proteins and pointed-end depolymerization in vi
10 tively removed using gelsolin (thin filament severing protein), and the actin filament was reconstitu
11 suppresses expression of gelsolin, an actin-severing protein, and rescues spine deficits found in Ts
12 ere, we show that cofilin 1 (Cfl1), an actin-severing protein, and Vangl2, a core PCP protein, cooper
13 t-60L1) of the Katanin family of microtubule severing proteins are required for dendrite severing.
14 entify cofilin1, an actin depolymerizing and severing protein, as a downstream target of NRG1 signali
15 n as SPG4) gene that encodes the microtubule-severing protein called spastin, are the most common cau
17 sin Cdc8, bundling protein fimbrin Fim1, and severing protein coffin Adf1, we examined how their pair
21 nes requires phosphorylation of the filament severing protein cofilin and is modulated by expression
22 d actin dynamics are connected via the actin severing protein cofilin and its slingshot phosphatase t
23 iously reported the involvement of the actin-severing protein cofilin and the Ca(2+) ATPase secretory
24 ctivities of Rac1 and the actin cytoskeleton-severing protein cofilin are low in JEB keratinocytes co
26 The mechanistic role of the actin filament severing protein cofilin is now firmly established; howe
27 e that suppressing the activity of the actin-severing protein cofilin plays an important role in the
28 A and phosphorylates (inactivates) the actin severing protein cofilin, a downstream target of RhoA.
29 ROCKI activity, phosphorylation of the actin severing protein cofilin, and a corresponding diminution
30 factor ARHGEF1, MLC20 , MYPT-1 and the actin-severing protein cofilin, but not of RhoA, ROCK2 or c-Sr
31 -2 promotes activation of the actin filament-severing protein cofilin, which is crucial for the reorg
41 ylation and activation of the actin filament-severing protein (cofilin) independently of Galpha(q)/Ca
45 cal contraction, increased activity of actin-severing proteins could release constraints on McTN form
49 include myosin II motors, actin capping and severing proteins, formins, profilin, cofilin, and the a
50 ic for severin, the Mr 40,000 actin filament severing protein from Dictyostelium discoideum amoebae,
51 re accompanied by dysregulation of the actin-severing protein gelsolin and Pctaire1 (Cdk16) kinase, w
52 clone A cells by treatment with the F-actin- severing protein gelsolin and that alpha6beta4 immunosta
53 By this approach, we identified the actin-severing protein Gelsolin as binding partner for Nm23-H1
56 by the calcium-activated actin-capping and -severing protein gelsolin plays a key role in regulating
57 ilaments had been extracted (using the actin severing protein gelsolin) showed that the difference in
58 RPGR interacts with and activates the actin-severing protein gelsolin, and that gelsolin regulates a
59 ion-regulating proteins, including the actin-severing protein gelsolin, to disrupt actin filaments an
61 ombinant human DNase I or the actin-filament-severing protein, gelsolin, both previously found to dec
63 ontrol, based on depolymerizing kinesins and severing proteins, have been studied extensively, positi
64 putative function of AtKTN1 as a microtubule-severing protein, immunolocalization demonstrated that t
65 ta support differential roles of microtubule-severing proteins in regulating neuronal morphology and
66 toplasmic gelsolin (cGSN), an abundant actin-severing protein involved in the depolymerization of act
67 emonstrate a requirement for the microtubule-severing protein katanin p60-like 1 (Kat-60L1) in regula
70 sought to determine whether the microtubule-severing protein known as katanin mediates microtubule r
71 ces in the susceptibility of microtubules to severing proteins may be a critical factor in the genera
73 us egg extracts suggested that a microtubule-severing protein might play an important role in cell cy
75 analogy between the effects of TMR-actin and severing proteins on F-actin, and imply that TMR-actin m
76 the isolation of three different microtubule-severing proteins, p56, EF1alpha, and katanin, has only
77 gulates the stability and activity of the MT-severing protein p60-katanin in interneurons to promote
80 ering activity revealed that TgADF is a weak severing protein, requiring much higher concentrations t
81 s in the SPAST gene encoding the microtubule-severing protein spastin account for most HSP cases.
82 Although loss of the related microtubule-severing protein Spastin also reduces the class IV dendr
83 ns to the SPG4 gene encoding the microtubule-severing protein spastin are the most common cause of he
85 bule array by overexpressing the microtubule-severing protein Spastin or by inhibiting the C. elegans
86 two isoforms (M1 and M87) of the microtubule-severing protein spastin, is the chief gene mutated in h
88 moting factors such as WASp, WAVE2, and HS1; severing proteins such as cofilin; motor proteins such a
89 amily, which includes the actin-capping and -severing proteins such as gelsolin, scinderin, and sever
90 contain sufficient levels of the microtubule-severing protein termed katanin to completely break down
95 tin (the SPG4 gene product) is a microtubule severing protein that shares homology with katanin, the
96 amino-terminal end of villin and other actin-severing proteins, the results provide a structural basi
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