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1 hospholipids with gelsolin, an actin-capping/severing protein.
2 the gene that encodes spastin, a microtubule-severing protein.
3  the loss of adseverin, an actin capping and severing protein.
4  only known ATP-independent microtubule (MT)-severing protein.
5 reduce the levels of fidgetin, a microtubule-severing protein.
6  role for wild-type spastin as a microtubule-severing protein.
7 s than slow fibroblasts that lack this actin-severing protein.
8 and P60-katanin are two distinct microtubule-severing proteins.
9 abilizing them and providing protection from severing proteins.
10 vestigate, using molecular dynamics, how the severing protein, actin depolymerization factor (ADF)/co
11       We also found that loss of the F-actin-severing proteins ADF and cofilin-1 decreased barbed end
12 in filaments facilitates access of the actin-severing protein Adf1 and subsequent filament disassembl
13  By using mutants of the fission yeast actin severing protein Adf1, we observed that contracting AMRs
14 in, a known calcium-activated actin filament-severing protein, also impaired the wound response, indi
15 uced by muscle contractions relayed by actin-severing proteins and from formin homology 2 domain-cont
16 he sides of filaments and protects them from severing proteins and pointed-end depolymerization in vi
17 tively removed using gelsolin (thin filament severing protein), and the actin filament was reconstitu
18  suppresses expression of gelsolin, an actin-severing protein, and rescues spine deficits found in Ts
19 ere, we show that cofilin 1 (Cfl1), an actin-severing protein, and Vangl2, a core PCP protein, cooper
20 t-60L1) of the Katanin family of microtubule severing proteins are required for dendrite severing.
21 entify cofilin1, an actin depolymerizing and severing protein, as a downstream target of NRG1 signali
22 n as SPG4) gene that encodes the microtubule-severing protein called spastin, are the most common cau
23             Our findings show that the actin-severing protein CFL coordinates responses to TGF-beta t
24 sin Cdc8, bundling protein fimbrin Fim1, and severing protein coffin Adf1, we examined how their pair
25      Mutations in the muscle-specific, actin-severing protein cofilin (unc-60) suppress the axon phen
26  defect in mouse mutants that lack the actin-severing protein cofilin 1 (CFL1).
27 e lamellipodium where it activates the actin-severing protein cofilin [6, 7].
28 nes requires phosphorylation of the filament severing protein cofilin and is modulated by expression
29 d actin dynamics are connected via the actin severing protein cofilin and its slingshot phosphatase t
30 iously reported the involvement of the actin-severing protein cofilin and the Ca(2+) ATPase secretory
31 ctivities of Rac1 and the actin cytoskeleton-severing protein cofilin are low in JEB keratinocytes co
32                                  The F-actin severing protein cofilin has been implicated in the remo
33   The mechanistic role of the actin filament severing protein cofilin is now firmly established; howe
34 e that suppressing the activity of the actin-severing protein cofilin plays an important role in the
35 PO9) acts in concert with the actin filament-severing protein cofilin to transport actin into the nuc
36 A and phosphorylates (inactivates) the actin severing protein cofilin, a downstream target of RhoA.
37 ROCKI activity, phosphorylation of the actin severing protein cofilin, and a corresponding diminution
38 factor ARHGEF1, MLC20 , MYPT-1 and the actin-severing protein cofilin, but not of RhoA, ROCK2 or c-Sr
39 of Rac1 and its downstream target, the actin-severing protein cofilin, in alcohol consumption prefere
40 star, the orthologue of the vertebrate actin-severing protein Cofilin, to regulate F-actin levels and
41 -2 promotes activation of the actin filament-severing protein cofilin, which is crucial for the reorg
42                           The actin filament severing protein cofilin-1 (CFL-1) is required for actin
43  properties and modulation by the regulatory severing protein cofilin.
44  increased activity of the filamentous actin severing protein cofilin.
45 tigen receptor (BCR) by activating the actin-severing protein cofilin.
46 hanism of INF2 with that of the well-studied severing protein cofilin.
47 el role modulating the activity of the actin-severing protein cofilin.
48 s structurally related to the actin filament-severing protein cofilin.
49 tion via signaling through Rac1 to the actin-severing protein cofilin.
50 ta4 integrin signaling to Rac1 and the actin-severing protein cofilin.
51 ylation and activation of the actin filament-severing protein (cofilin) independently of Galpha(q)/Ca
52                               One such actin-severing protein, cofilin, is activated in detached PTEN
53                                          The severing protein, cofilin, renders filaments more compli
54  microvillar rootlets are decorated with the severing protein, cofilin, suggesting high levels of ADP
55                     Katanin, the microtubule-severing protein, consists of a subunit termed P60 that
56 cal contraction, increased activity of actin-severing proteins could release constraints on McTN form
57 redistribution of synaptic cofilin, an actin-severing protein downstream of Rac1.
58 us, and we evaluated the role of the vesicle severing protein dynamin.
59                 Gelsolin is an actin-binding/severing protein expressed in intracellular and secreted
60  include myosin II motors, actin capping and severing proteins, formins, profilin, cofilin, and the a
61 ic for severin, the Mr 40,000 actin filament severing protein from Dictyostelium discoideum amoebae,
62 re accompanied by dysregulation of the actin-severing protein gelsolin and Pctaire1 (Cdk16) kinase, w
63 clone A cells by treatment with the F-actin- severing protein gelsolin and that alpha6beta4 immunosta
64    By this approach, we identified the actin-severing protein Gelsolin as binding partner for Nm23-H1
65                                    The actin-severing protein gelsolin binds LPA with an affinity (K(
66                     The Ca2+-sensitive actin-severing protein gelsolin concentrates in the Listeria r
67  by the calcium-activated actin-capping and -severing protein gelsolin plays a key role in regulating
68 ilaments had been extracted (using the actin severing protein gelsolin) showed that the difference in
69  RPGR interacts with and activates the actin-severing protein gelsolin, and that gelsolin regulates a
70 ion-regulating proteins, including the actin-severing protein gelsolin, to disrupt actin filaments an
71 t, through the actions of the actin filament-severing protein gelsolin.
72 ombinant human DNase I or the actin-filament-severing protein, gelsolin, both previously found to dec
73 tin dynamics in photoreceptors via the actin-severing protein, gelsolin.
74 ontrol, based on depolymerizing kinesins and severing proteins, have been studied extensively, positi
75 putative function of AtKTN1 as a microtubule-severing protein, immunolocalization demonstrated that t
76 ta support differential roles of microtubule-severing proteins in regulating neuronal morphology and
77 l importance of cofilin, a filamentous actin-severing protein, in actin dynamics and pathogen-trigger
78 toplasmic gelsolin (cGSN), an abundant actin-severing protein involved in the depolymerization of act
79                 Furthermore, the microtubule-severing protein Katanin and the minus-end-binding prote
80 identify a critical role for the microtubule-severing protein katanin p60 in regulating neuronal prog
81 emonstrate a requirement for the microtubule-severing protein katanin p60-like 1 (Kat-60L1) in regula
82        Increased activity of the microtubule severing protein katanin scales the X. tropicalis spindl
83                              The microtubule-severing protein katanin, a heterodimer of 60 and 80 kDa
84 des a AAA+ ATPase related to the microtubule-severing protein katanin.
85  sought to determine whether the microtubule-severing protein known as katanin mediates microtubule r
86 ces in the susceptibility of microtubules to severing proteins may be a critical factor in the genera
87               Gelsolin, as an actin filament-severing protein, may serve an important role in the rap
88 us egg extracts suggested that a microtubule-severing protein might play an important role in cell cy
89    Neurons express two different microtubule-severing proteins, namely P60-katanin and spastin.
90                 Cofilin is an actin filament severing protein necessary for fast actin turnover dynam
91 analogy between the effects of TMR-actin and severing proteins on F-actin, and imply that TMR-actin m
92                       The contribution of MT-severing proteins on MT lattice curvature is largely und
93 the isolation of three different microtubule-severing proteins, p56, EF1alpha, and katanin, has only
94 gulates the stability and activity of the MT-severing protein p60-katanin in interneurons to promote
95 tween Cul3, Ctb9/KLHDC5, and the microtubule-severing protein, p60/katanin.
96                            Cofilin, an actin-severing protein, plays key roles in muscle sarcomere ad
97                  Cofilin (CFL) is an F-actin-severing protein required for the cytoskeleton reorganiz
98 ering activity revealed that TgADF is a weak severing protein, requiring much higher concentrations t
99 s in the SPAST gene encoding the microtubule-severing protein spastin account for most HSP cases.
100     Although loss of the related microtubule-severing protein Spastin also reduces the class IV dendr
101 ns to the SPG4 gene encoding the microtubule-severing protein spastin are the most common cause of he
102            We show that cells lacking the MT-severing protein spastin had increased tubulation of and
103 bule array by overexpressing the microtubule-severing protein Spastin or by inhibiting the C. elegans
104 he SPAST gene, which encodes the microtubule-severing protein spastin, are the most common cause of h
105 two isoforms (M1 and M87) of the microtubule-severing protein spastin, is the chief gene mutated in h
106 uppressing the expression of the microtubule-severing protein Spastin.
107                                        Actin-severing proteins such as cofilin and contractile myosin
108 moting factors such as WASp, WAVE2, and HS1; severing proteins such as cofilin; motor proteins such a
109 amily, which includes the actin-capping and -severing proteins such as gelsolin, scinderin, and sever
110 contain sufficient levels of the microtubule-severing protein termed katanin to completely break down
111                 Hence, INF2 is a more potent severing protein than cofilin.
112       Cofilin is an essential actin filament severing protein that accelerates the assembly dynamics
113       Katanin is a heterodimeric microtubule-severing protein that is conserved among eukaryotes.
114           Gelsolin is a Ca2+-activated actin-severing protein that is expressed in neurons, wherein i
115                          Cofilin, an F-actin severing protein that is inactivated by phosphorylation,
116                    Fidgetin is a microtubule-severing protein that pares back the labile domains of m
117 tin (the SPG4 gene product) is a microtubule severing protein that shares homology with katanin, the
118 amino-terminal end of villin and other actin-severing proteins, the results provide a structural basi
119                                The mammalian severing protein was fully expressed in transformed LL/2
120 emonstrate that inhibiting cofilin, an actin-severing protein, with SZ-3 increases cellular stiffness

 
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