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1 tions within the destrin gene (also known as actin-depolymerizing factor).
2 ors, which was regulated by cofilin, a major actin depolymerizing factor.
3 vation of the Rho target protein cofilin, an actin-depolymerizing factor.
4 ivity through phosphorylation of cofilin, an actin-depolymerizing factor.
5 ics and by the inhibitor of cofilin, a major actin-depolymerizing factor.
6 actin, indicating that AtADF4 is a bona fide actin-depolymerizing factor.
7 ature-sensitive alleles of both profilin and actin-depolymerizing factor.
8 cofilin that is distinct from its role as an actin-depolymerizing factor.
9 WD-40 repeat domain 1 (WDR1), an enhancer of actin-depolymerizing factor activity, is downregulated i
17 NAi, we find that co-depleting cofilin-1 and actin depolymerizing factor (ADF) led to a large increas
29 age during synaptic plasticity, in which the actin depolymerizing factor (ADF)/cofilin family of acti
32 habditis elegans, UNC-60B, a muscle-specific actin depolymerizing factor (ADF)/cofilin isoform, is re
34 muscular junctions as a model, we found that actin depolymerizing factor (ADF)/cofilin regulated acti
36 nd UNC-60B, nonmuscle and muscle isoforms of actin depolymerizing factor (ADF)/cofilin, are expressed
37 ons (rods), composed of actin saturated with actin depolymerizing factor (ADF)/cofilin, are induced i
44 f actin-binding proteins, among which is the Actin-Depolymerizing Factor (ADF) family of proteins.
45 coexpressed reproductive profilin (PRF4) or actin-depolymerizing factor (ADF) isovariants (e.g., ADF
47 th the actin filament depolymerizing cofilin/actin-depolymerizing factor (ADF) proteins, our data sug
49 ously, we found that NGF treatment increases actin-depolymerizing factor (ADF)/cofilin activity and g
57 ated from two cell lines expressing chimeric actin-depolymerizing factor (ADF)/cofilin fluorescent pr
58 m ADP to ATP and recycle actin monomers from actin-depolymerizing factor (ADF)/cofilin for new rounds
59 s the severing activity of gelsolin, but not actin-depolymerizing factor (ADF)/cofilin microinjected
60 osphorylation directly blocks interaction of actin-depolymerizing factor (ADF)/cofilin proteins with
62 rent models for actin dynamics maintain that actin-depolymerizing factor (ADF)/cofilin removes ADP-ac
64 (AIP) 1 specifically enhances disassembly of actin-depolymerizing factor (ADF)/cofilin-bound actin fi
65 and Slingshot (SSH) phosphatase to regulate actin-depolymerizing factor (ADF)/cofilin-mediated actin
67 protein, capping protein, profilin, and the actin-depolymerizing factor (ADF, also known as cofilin)
68 the F-actin patches from disassembly by the actin-depolymerizing factor, ADF, and promotes long-live
72 ity is the activity of a conserved family of actin-depolymerizing factors (ADFs), whose primarily fun
73 ubiquitous family of actin binding proteins, actin-depolymerizing factors (ADFs)/cofilins, bind to ac
74 sting information about tropomyosin, myosin, actin-depolymerizing factor, and nebulin is considered,
75 ding proteins Cyclase-Associated Protein and Actin-Depolymerizing Factor are identified as key downst
76 cted the actin-binding proteins profilin and actin-depolymerizing factor, because they are essential
77 ociated with robust dephosphorylation of the actin depolymerizing factor cofilin by PP1 and PP2A seri
84 ibit enhanced sensitivity to severing by the actin depolymerizing factor, cofilin, suggesting that GT
85 seizures also resulted in activation of the actin-depolymerizing factor, cofilin, and a correspondin
86 kine coreceptor CXCR4 to activate a cellular actin-depolymerizing factor, cofilin, to overcome this r
88 enorhabditis elegans unc-60 gene encodes two actin depolymerizing factor/cofilin proteins which are i
90 n neocortical and thalamic neurons that were actin depolymerizing factor/cofilin-immunoreactive but o
91 anisms and has a conserved role in promoting actin depolymerizing factor/cofilin-mediated actin turno
95 A yeast two-hybrid analysis uncovered the actin-depolymerizing factor gelsolin, the membrane glyco
97 Saccharomyces cerevisiae Abp1 actin-binding actin depolymerizing factor homology (ADFH) domain and d
98 g partner that interacts with the N-terminal actin depolymerizing factor homology domain (ADFH) domai
99 be catalyzed by two different members of the actin depolymerizing factor homology protein family: cof
101 ame domain structure including an N-terminal actin-depolymerizing factor homology domain and a C-term
103 (tsr), which encodes Drosophila cofilin/ADF (actin-depolymerizing factor), is required for both of th
106 primary downstream target of PAK and a major actin depolymerizing factor, prevented Shank3 siRNA from
107 ied a novel SNRK target, DSTN, a member of F-actin depolymerizing factor proteins that directly bind
108 TM5 interacts with two non-MADS proteins, an actin depolymerizing factor (PtADF) and a novel leucine-
109 that the single allele of Toxoplasma gondii actin depolymerizing factor (TgADF) has strong actin mon
110 ly equal molar ratio to profilin and cofilin/actin depolymerizing factor, two other well characterize
111 11 pollen allergens, polygalacturonase, and actin depolymerizing factor were characterized for the f
112 of the proteins identified was cofilin-1, an actin depolymerizing factor which regulates neuronal den