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1 tr(-/-) mice the structural integrity of the myotendinous and neuromuscular junctions are maintained.
2                                   For the 59 myotendinous and the 48 osteochondral diagnoses, the sen
3 cle, beta 1D was concentrated in costameres, myotendinous, and neuromuscular junctions.
4 n skin deep; it extends to the depths of the myotendinous architecture and the mechanical basis for p
5 inding of its developing myotube to specific myotendinous attachment sites.
6 tilage disease, microinstability of the hip, myotendinous injuries, and athletic pubalgia.
7 colemma localization, SPN is enriched at the myotendinous junction (MTJ) and neuromuscular junction (
8                              Movement of the myotendinous junction (MTJ) of the gastrocnemius mediali
9 responding tendon cells to form a functional myotendinous junction (MTJ) that allows for the force ge
10 red for normal Laminin polymerization at the myotendinous junction (MTJ).
11 ular matrix (ECM) that anchors fibers to the myotendinous junction (MTJ).
12 the muscle-tendon complex, in particular the myotendinous junction (MTJ).
13                Electrical stimulation of the myotendinous junction activates antidromically MIF moton
14 last subtypes, including tenocytes along the myotendinous junction and fin mesenchymal cells in the f
15 of the muscle cell, including markers of the myotendinous junction and functionally validated factors
16 toward and subsequent differentiation of the myotendinous junction by priming formation of a protein
17 of muscle projections during early stages of myotendinous junction development.
18 rin expression during muscle development and myotendinous junction formation.
19 s normally confined to the neuromuscular and myotendinous junction in adult skeletal muscle.
20 le-specific protein that is localized to the myotendinous junction in skeletal muscle.
21 , thus suggesting the important influence of myotendinous junction integrity on the severity of muscu
22  mdx/utr-/- background is the restoration of myotendinous junction integrity.
23 njections of choleratoxin subunit B into the myotendinous junction of MR or IR in monkeys.
24               In three animals the IR and MR myotendinous junction of one eye was injected simultaneo
25  alpha7 integrin and utrophin in maintaining myotendinous junction structure and enabling force trans
26 ndary of fibroblast-derived myonuclei at the myotendinous junction that controls limb muscle patterni
27 d at the sarcolemma, neuromuscular junction, myotendinous junction, and in peripheral nerve, but not
28 n, loss of tension-mediating proteins at the myotendinous junction, and misshaped and internalized nu
29  revealed that electrical stimulation to the myotendinous junction, where palisade endings are locate
30  elastic element in series with titin at the myotendinous junction.
31  central nuclei at the perimysium and at the myotendinous junction.
32 ncluding Col22a1-expressing cells within the myotendinous junction.
33 ired for proper localization of PINCH at the myotendinous junction.
34  the myogenic lineage, preferentially at the myotendinous junction.
35 ole for dystrophin in maintaining vertebrate myotendinous junctions (MTJs) has been postulated previo
36 l muscle, talin 1 regulates the stability of myotendinous junctions (MTJs), but the function of talin
37 al for muscle attachment and ECM assembly at myotendinous junctions (MTJs).
38 e fiber cytoskeleton, and the maintenance of myotendinous junctions (MTJs).
39 unctions (NMJs) and, as shown here, abnormal myotendinous junctions (MTJs).
40  of those that underlie synapse formation at myotendinous junctions and that the outgrowth of seconda
41 unctions, which supports the hypothesis that myotendinous junctions are distinct domains in which the
42  underlying muscle guidance and formation of myotendinous junctions are poorly understood both in ver
43 table increase in myostatin concentration at myotendinous junctions during muscle unloading.
44      As assessed by atomic force microscopy, myotendinous junctions from normal and delta sgc-null mi
45 accumulates at the neuromuscular synapse and myotendinous junctions in adult skeletal muscle, and is
46 ues and is confined to the neuromuscular and myotendinous junctions in mature muscle.
47 is enriched at intersomitic junctions and at myotendinous junctions in somites and the myotome, where
48                                 However, the myotendinous junctions linking the DVM to the dorsal epi
49 ss tenocytes at multiple tendon entheses and myotendinous junctions reveals that their responses depe
50                                              Myotendinous junctions show adaptations to modified musc
51 keletal proteins that are highly enriched at myotendinous junctions that we hypothesize to be subject
52  enrichment at force transmitting sites, the myotendinous junctions, and costameres.
53   Ultrastructural analysis revealed abnormal myotendinous junctions, and functional tests showed a ni
54  confined in skeletal muscle to synapses and myotendinous junctions, and in kidney to the glomerular
55 zed tendon cells, resembling tendon cells at myotendinous junctions, form at the ends of these muscle
56 erentially concentrated at neuromuscular and myotendinous junctions, suggesting a role at sarcolemmal
57 hese territories were further specialized at myotendinous junctions, where both Dmd transcripts and d
58 hows that the mRNA is highly concentrated at myotendinous junctions, which supports the hypothesis th
59 ping muscle and cartilage, and xirp2a at the myotendinous junctions.
60 ncluding intercalated discs, costameres, and myotendinous junctions.
61 en muscle fibers and/or myofibrils or at the myotendinous junctions.
62 evelopment, repair, and at neuromuscular and myotendinous junctions.
63 ge from cell motility to formation of stable myotendinous junctions.
64 mplex to control the development of thoracic myotendinous junctions.
65                We selected individuals whose myotendinous or myofascial lesions could be classified a
66 extends beyond the classic neuromuscular and myotendinous populations.
67 We also found a positive correlation between myotendinous strain injury and ringed fibers in the HSA(
68                   We found that muscles with myotendinous strain injury had an increased expression o
69 olecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a micr
70  well characterized, the chronic response to myotendinous strain injury is less clear.
71                                              Myotendinous strain injury is the most common injury of
72 nd the formation of rings are adaptations to myotendinous strain injury that help to prevent muscle n