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1 by rapid cytoskeletal rearrangement, even in non-muscle cells.
2 l building blocks of the cytoskeleton in all non-muscle cells.
3 functional roles of actomyosin in muscle and non-muscle cells.
4 length of actin filaments in both muscle and non-muscle cells.
5 ), and is also associated with cell cycle in non-muscle cells.
6 ochemical characteristics of both muscle and non-muscle cells.
7 d for different actin dynamics in muscle and non-muscle cells.
8 -calponin is found in both smooth muscle and non-muscle cells.
9 activate this enhancer in some, but not all, non-muscle cells.
10 pha-MHC gene by preventing its expression in non-muscle cells.
11 s a silencer of alpha-MHC gene expression in non-muscle cells.
12 iation program when ectopically expressed in non-muscle cells.
13 tural basis of its functioning in muscle and non-muscle cells.
14 cle cells, despite substantial DNA uptake by non-muscle cells.
15 ntraction and other contractile processes in non-muscle cells.
16 ecting a subset of both striated muscles and non-muscle cells.
17 ed muscles, 16 non-striated muscles, and two non-muscle cells.
18 ion of mouse AChR subunits and calnexin into non-muscle cells.
19 nt mechanism for the activation of myosin in non-muscle cells.
20 nd MEF2C stimulate RGMc promoter function in non-muscle cells.
22 the mechanical function of alpha-actinin in non-muscle cells: alpha-actinin-microinjected cells are
23 sassembly of the actin-based cytoskeleton in non-muscle cells and clears the circulation of filaments
24 for global actin cytoskeleton remodeling in non-muscle cells and provide insight into cellular respo
25 s the presence of a skelemin-like protein in non-muscle cells and provides evidence that it may be in
26 lso binds to F-actin in smooth muscle and in non-muscle cells and stabilizes and regulates the filame
27 ulate the contractility of smooth muscle and non-muscle cells, and there is evidence that this occurs
29 n mouse myogenic cells, we found that, as in non-muscle cells, Bax co-immunoprecipitated with the mul
30 activity of myosin II, in smooth muscle and non-muscle cells, by modulating the Ca2+ sensitivity of
36 other SH3-containing proteins in muscle and non-muscle cell extracts were validated with peptide arr
40 ed by exon 9d expressed in smooth muscle and non-muscle cells increases the affinity of unacetylated
42 normally in muscle cells and ectopically in non-muscle cells is dependent upon the integrity of the
43 ssion of c6orf32 in C2C12 or HEK293 cells (a non-muscle cell line) promoted formation of long membran
45 iadin-1 as a series of glycoform variants in non-muscle cell lines and neonatal heart cells using pla
46 nsitization of smooth muscle contraction and non-muscle cell motility is through inhibition of the sm
48 the major intracellular reservoir of Ca2+ in non-muscle cells, sequestering Ca2+ for use in intracell
49 induce myogenic differentiation in cultured non-muscle cells, suggesting that they might be function
51 myosin (RLC) controls motility of mammalian non-muscle cells, the functional significance of RLC pho
52 to caffeine and halothane when expressed in non-muscle cells, their influence on EC coupling can onl
53 wo mutations inhibit myosin self-assembly in non-muscle cells, they do not prevent incorporation of t
54 ogene has been shown to induce myogenesis in non-muscle cells, to promote muscle hypertrophy in postn
57 ity without transdifferentiation to multiple non-muscle cell types and tested dystrophin restoration
59 cle terminal differentiation in a variety of non-muscle cell types, MyoD activity itself is highly re
62 new regulatory pathway in smooth muscle and non-muscle cells whereby ROCK1 phosphorylates and regula
63 olin-1 is required for caveolae formation in non-muscle cells, while the expression of caveolin-3 dri
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