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1 nd MEF2C stimulate RGMc promoter function in non-muscle cells.
2 l building blocks of the cytoskeleton in all non-muscle cells.
3 l for the regulation of actin homeostasis in non-muscle cells.
4 functional roles of actomyosin in muscle and non-muscle cells.
5 length of actin filaments in both muscle and non-muscle cells.
6 ), and is also associated with cell cycle in non-muscle cells.
7 ochemical characteristics of both muscle and non-muscle cells.
8 d for different actin dynamics in muscle and non-muscle cells.
9 -calponin is found in both smooth muscle and non-muscle cells.
10 activate this enhancer in some, but not all, non-muscle cells.
11 pha-MHC gene by preventing its expression in non-muscle cells.
12 s a silencer of alpha-MHC gene expression in non-muscle cells.
13 iation program when ectopically expressed in non-muscle cells.
14 y components of contractile stress fibers in non-muscle cells.
15 tural basis of its functioning in muscle and non-muscle cells.
16 cle cells, despite substantial DNA uptake by non-muscle cells.
17 ntraction and other contractile processes in non-muscle cells.
18 ecting a subset of both striated muscles and non-muscle cells.
19 ed muscles, 16 non-striated muscles, and two non-muscle cells.
20 ion of mouse AChR subunits and calnexin into non-muscle cells.
21 nt mechanism for the activation of myosin in non-muscle cells.
22 eres in muscles or as actomyosin networks in non-muscle cells.
23 by rapid cytoskeletal rearrangement, even in non-muscle cells.
24 egulation of total PP1calpha in myocytes and non-muscle cells, (3) the stability of cardiac MYPT1 and
25                                           In non-muscle cells, a shorter CaD isoform co-exists with m
26 hat ensures regular myosin-II spacing within non-muscle cell actomyosin bundles, and reveal how stres
27  an important component of smooth muscle and non-muscle cell actomyosin bundles, is an elongated prot
28  the mechanical function of alpha-actinin in non-muscle cells: alpha-actinin-microinjected cells are
29 sassembly of the actin-based cytoskeleton in non-muscle cells and clears the circulation of filaments
30  for global actin cytoskeleton remodeling in non-muscle cells and provide insight into cellular respo
31 s the presence of a skelemin-like protein in non-muscle cells and provides evidence that it may be in
32 lso binds to F-actin in smooth muscle and in non-muscle cells and stabilizes and regulates the filame
33 ulate the contractility of smooth muscle and non-muscle cells, and there is evidence that this occurs
34           Adhesion and morphogenesis of many non-muscle cells are guided by contractile actomyosin bu
35 n mouse myogenic cells, we found that, as in non-muscle cells, Bax co-immunoprecipitated with the mul
36  activity of myosin II, in smooth muscle and non-muscle cells, by modulating the Ca2+ sensitivity of
37                                           In non-muscle cells, CHC22 localizes to perinuclear vesicul
38 ed muscles, 16 non-striated muscles, and two non-muscle cells (coelomocytes).
39                                              Non-muscle cell contractility is critical for tissues to
40  step in the initiation of smooth muscle and non-muscle cell contraction.
41                Transdifferentiation of human non-muscle cells directly into myogenic cells by forced
42 ac myocytes, C2C12 myotubes, and transfected non-muscle cells expressing alpha1 subunits.
43  other SH3-containing proteins in muscle and non-muscle cell extracts were validated with peptide arr
44 n cell lineages are normally established and non-muscle cell fate markers begin to be expressed.
45  activity and force-balance are regulated in non-muscle cells have remained elusive.
46 fferentiated skeletal muscle (myoblasts) and non-muscle cells in culture.
47 al component of caveolae membrane domains in non-muscle cells, including mammary epithelia.
48 ed by exon 9d expressed in smooth muscle and non-muscle cells increases the affinity of unacetylated
49 division of mesodermal cells into muscle and non-muscle cells is crucial to animal development.
50  normally in muscle cells and ectopically in non-muscle cells is dependent upon the integrity of the
51 ssion of c6orf32 in C2C12 or HEK293 cells (a non-muscle cell line) promoted formation of long membran
52 nd differentiation of the diverse muscle and non-muscle cell lineages of the heart.
53 iadin-1 as a series of glycoform variants in non-muscle cell lines and neonatal heart cells using pla
54                     Finally, we confirmed in non-muscle cell lines that TBK1 phosphorylation occurs i
55 nsitization of smooth muscle contraction and non-muscle cell motility is through inhibition of the sm
56 ry tracts, thus raising the possibility of a non-muscle cell pacemaker.
57 ents of the lymphatic vessel wall identified non-muscle cell populations that shared some characteris
58 t high levels in muscle and at low levels in non-muscle cells, relative to CHC17.
59 the major intracellular reservoir of Ca2+ in non-muscle cells, sequestering Ca2+ for use in intracell
60  induce myogenic differentiation in cultured non-muscle cells, suggesting that they might be function
61                                              Non-muscle cells that expressed alpha(v) and beta1 integ
62  myosin (RLC) controls motility of mammalian non-muscle cells, the functional significance of RLC pho
63 actin filaments from overgrowing, whereas in non-muscle cells, their function has remained elusive.
64  to caffeine and halothane when expressed in non-muscle cells, their influence on EC coupling can onl
65 wo mutations inhibit myosin self-assembly in non-muscle cells, they do not prevent incorporation of t
66 trast to their role in muscle myofibrils, in non-muscle cells, Tmods bind actin-tropomyosin filaments
67 ogene has been shown to induce myogenesis in non-muscle cells, to promote muscle hypertrophy in postn
68                                           In non-muscle cells, tropomyosin additionally controls acce
69              Among multiple TMs expressed in non-muscle cells, tropomyosin-1 (TM1) isoform induces st
70 ity without transdifferentiation to multiple non-muscle cell types and tested dystrophin restoration
71  study investigated the role of infiltrating non-muscle cell types in FSHD signature expression and d
72                                           In non-muscle cell types, lysosomes are critical mediators
73 cle terminal differentiation in a variety of non-muscle cell types, MyoD activity itself is highly re
74 and smooth muscle differentiation markers in non-muscle cell types.
75 percentage of arginylated actin in migratory non-muscle cells under different physiological condition
76                         In smooth muscle and non-muscle cells, where troponin is absent, the precise
77  new regulatory pathway in smooth muscle and non-muscle cells whereby ROCK1 phosphorylates and regula
78 olin-1 is required for caveolae formation in non-muscle cells, while the expression of caveolin-3 dri