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1 icity of tractions depend on the activity of nonmuscle myosin IIA.
2 tor discovered in a screen for inhibitors of nonmuscle myosin IIA.
3 he identification of myosin (Myo) XVIIIA and nonmuscle myosin IIA.
4 vy meromyosin- (HMM-) like fragment of human nonmuscle myosin IIA.
5 illin, F-actin, and the major motor isoform, nonmuscle myosin-IIA.
6 zipper gene, appears to be similar to rabbit nonmuscle myosin-IIA.
7 on of the corresponding region of GFP-tagged nonmuscle myosin IIA also abolished this localization.
8                                              Nonmuscle myosin IIA and IIB distribute preferentially t
9                                Expression of nonmuscle myosin IIA and IIB was confirmed in both human
10 l stem cells-as a prototypical adherent cell-nonmuscle myosin IIA and vimentin are just two of the cy
11  we showed that S100A4 specifically binds to nonmuscle myosin-IIA and promotes the unassembled state.
12 on epithelial cadherin (E-cadherin), NMMIIA (nonmuscle myosin IIA), and p120-catenin.
13 CMIIB), Dictyostelium myosin II (DdMII), and nonmuscle myosin IIA, as well as myosin V.
14 n MYH9, lesions in the rod, cause defects in nonmuscle myosin-IIA assembly.
15 by Mg(2+) in myosin V, smooth muscle myosin, nonmuscle myosin IIA, CMIIB, and DdMII, although the ADP
16 reviously that NK-cell cytotoxicity requires nonmuscle myosin IIA function and that granule-associate
17 by which mutations in the rod region disrupt nonmuscle myosin-IIA function, we examined the in vitro
18 f our top hits-including Myh9, which encodes nonmuscle myosin IIa-have not been linked to tumor devel
19                                          The nonmuscle myosin IIA heavy chain (Myh9) is strongly asso
20                       Mutations in the human nonmuscle myosin IIA heavy chain gene (MYH9) have been l
21 tion, and result from mutations in the human nonmuscle myosin-IIA heavy chain gene.
22 trongly suggest that base-line expression of nonmuscle myosin IIA inhibits osteoclast precursor fusio
23                           We also found that nonmuscle myosin IIA is a major determinant of ROCK1 cor
24 y pharmacologic inhibition of myosin-II, but nonmuscle myosin-IIA (MIIA) mutations paradoxically caus
25 ons with specific protein targets, including nonmuscle myosin-IIA (MIIA).
26  the S2 domain in chicken gizzard myosin and nonmuscle myosin IIA (MYH-9) but exhibit little binding
27                                Inhibition of nonmuscle myosin IIA (NM-MHC-IIA) motor activity prevent
28     In studies initially focused on roles of nonmuscle myosin IIA (NMIIA) in the developing mouse epi
29                              It binds to the nonmuscle myosin IIA (NMIIA) tail near the assembly comp
30        In addition, MyoGEF co-localizes with nonmuscle myosin IIA (NMIIA) to the front of migrating c
31 -interacting protein, cofilin, Munc13-4, and nonmuscle myosin IIA (NMIIA).
32                                              Nonmuscle myosin IIA (NMM-IIA) is involved in the format
33 (2+)]i, and the association of gelsolin with nonmuscle myosin IIA (NMMIIA) at collagen adhesions are
34 recipitates showed that FliI associated with nonmuscle myosin IIA (NMMIIA), which was confirmed by im
35 tal muscle myosin, nonmuscle myosin IIB, and nonmuscle myosin IIA revealed three distinct regimes of
36 ling between nucleotide and actin binding to nonmuscle myosin IIA subfragment-1.
37 eavy meromyosin-like recombinant fragment of nonmuscle myosin IIA, which was expressed in baculovirus

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