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1 egulates the quiescent state of the skeletal muscle satellite cell.
2 o be the Drosophila equivalent of vertebrate muscle satellite cells.
3 ll cycle progression to regulate function in muscle satellite cells.
4 maged muscle fibers and within the activated muscle satellite cells.
5 ze to the myogenin promoter in primary adult muscle satellite cells.
6  we show that the growing tail contains many muscle satellite cells.
7 lls" that share several characteristics with muscle satellite cells.
8 ecific, further implicating a defect in FSHD muscle satellite cells.
9 ess that requires activation and division of muscle satellite cells.
10 ted the activation of Pax7-positive skeletal muscle satellite cells and increased its local populatio
11 ccurs between endothelial cells and skeletal muscle satellite cells and is mitogenic for both cell ty
12                                     Skeletal muscle satellite cells are adult stem cells responsible
13                                              Muscle satellite cells are mononuclear cells that remain
14                                              Muscle satellite cells are myogenic stem cells whose qui
15 argely Hh quiescent and that Pax7-expressing muscle satellite cells are not able to give rise to eRMS
16  show that the majority of, if not all, limb muscle satellite cells arise from cells expressing Pax3
17                               Using skeletal muscle satellite cells as a model and through myogenic c
18 he Pax7 transcription factor is required for muscle satellite cell biogenesis and specification of th
19                                     Skeletal muscle satellite cells can sense various forms of enviro
20     Although mitotically quiescent in mature muscle, satellite cells can be activated to produce myob
21 nomic profiles of preadipocytes and skeletal muscle satellite cells collected from irradiated mice.
22 mportantly, transplanted cells also seed the muscle satellite cell compartment, and engraftment is pr
23                                     Skeletal muscle satellite cells cultured on soft surfaces (12 kPa
24     Unexpectedly, expression of Pax3:Fkhr in muscle satellite cells did not produce tumors, but it di
25 and fibro/adipogenic progenitors (FAPs) from muscle; satellite cells did not differentiate into adipo
26                                              Muscle satellite cells express Pax7, but overexpression
27 tor, GO6983, promotes myogenesis in skeletal muscle satellite cells expressing oncogenic Ha-Ras.
28 shown concurrent activation and apoptosis of muscle satellite cells following a burn injury in paedia
29    The ongoing activation and recruitment of muscle satellite cells for myofiber regeneration results
30 om HG treated ECs cause impairments in human muscle satellite cell growth and differentiation in vitr
31                                        Adult muscle satellite cells have a principal role in postnata
32 ogenic program is repressed, suggesting that muscle satellite cells have undergone chondrogenic diffe
33                We have studied the origin of muscle satellite cells in embryos of Xenopus laevis.
34                                     Skeletal muscle satellite cells in their niche are quiescent and
35 factor Amphiregulin, which acted directly on muscle satellite cells in vitro and improved muscle repa
36 growth and differentiation of human skeletal muscle satellite cells in vitro.
37 e results imply that premature senescence of muscle satellite cells is an underlying pathogenic featu
38 nd immunostaining of in vitro differentiated muscle satellite cells isolated from Mkx-null mice revea
39 timulates proliferation of the MM14 skeletal muscle satellite cell line in the absence of exogenously
40                                              Muscle satellite cells make up a stem cell population th
41  model of replicative senescence, decline in muscle satellite cell-mediated regeneration coincides wi
42 between endothelial cells (ECs) and skeletal muscle satellite cells (MuSC) has been identified as an
43 ption factor that plays an essential role in muscle satellite cell (muscle stem cell) differentiation
44                                        Adult muscle satellite cells (MuSCs) are mostly quiescent in u
45                                              Muscle satellite cells (MuSCs) are the quiescent muscle
46 ation, proliferation, and differentiation of muscle satellite cells (MuSCs) that are normally quiesce
47      NOTCH signaling plays multiple roles in muscle satellite cells (MuSCs), but the regulation of NO
48 transition and their intrinsically deficient muscle satellite cells (MuSCs).
49  regulation of embryonic myoblasts and adult muscle satellite cells (MuSCs).
50 sion and function of all three Pitx genes in muscle satellite cells of adult mice.
51 owth defect and a moderately decreased Pax7+ muscle satellite cell pool, phenocopying Pax7 deficiency
52 ly elevated levels of TWEAK, which stimulate muscle satellite cell proliferation and tissue regenerat
53                                              Muscle satellite cells promote regeneration and could po
54              Previous studies showed porcine muscle satellite cells (PSCs) are important for postnata
55  burn trauma and we propose that an impaired muscle satellite cell response is key in the aetiology o
56 ntext dependence, and regulation of skeletal muscle satellite cell (SC) subsets remains poorly unders
57                                 The skeletal muscle satellite cells (SCs) mediate regeneration of myo
58  The functional study of lncRNAs in skeletal muscle satellite cells (SCs) remains at the infancy stag
59 eletal muscle health; however, its effect on muscle satellite cells (SCs) remains largely unknown.
60 ar response after muscle injury, focusing on muscle satellite cells (SCs), inflammatory reaction, fib
61        We found an increase in the number of muscle satellite cells (SCs), which are essential for mu
62                                     Skeletal muscle satellite cells (SMSCs), the major stem cells res
63 hese putative stem cells may be identical to muscle satellite cells, some of which lack myogenic regu
64 muscle reveal a marked decrease in quiescent muscle satellite cells suggesting a deregulation of post
65                           We show that chick muscle satellite cells that normally would undergo myoge
66    The stress-induced progression of BMDC to muscle satellite cell to muscle fiber results in a contr
67 s deleted and oncogenic Kras is activated in muscle satellite cells via a Pax7(CreER) driver followin
68 ovel, inducible Pax7-CreER line for tracking muscle satellite cells, we demonstrate the longitudinal