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1  of MURC in shPAB cell cultures and in shPAB muscle bundle.
2 mesenchymal progenitors to the airway smooth muscle bundle.
3 ed with a spreading calcium wave in a dorsal muscle bundle.
4 ria of brown adipocytes interspersed between muscle bundles.
5 sting they might be necessary for activating muscle bundles.
6 re located at the origin and intersection of muscle bundles.
7 nce of collective cooperative contraction of muscle bundles.
8 sed the activity of RGD peptide on papillary muscle bundles.
9              Total creatine was localized to muscle bundles.
10  ventricular inflow and outflow by prominent muscle bundles.
11 e likely to interact with actin in cTnT-I79N muscle bundles.
12 ier, edematous lamina propria, and distorted muscle bundles.
13 structure connected the fibrin gels with the muscle bundles.
14 d increased passive mechanical properties of muscle bundles.
15 ere also found within septa (IC-SEP) between muscle bundles and along the submucosal surface of the c
16 med compact, longitudinally oriented cardiac muscle bundles and had cross-striations and vascularizat
17      These sites are in accord with anatomic muscle bundles and may have relevance for maintenance of
18 ng through the dermis, subcutis, orbicularis muscle bundles and nerve fibers; the tumour cells were n
19 duced birefringent collagen between detrusor muscle bundles, and atomic force microscopy showed a sig
20 s pigmentation around nerve fascicles, among muscle bundles, and in the hypodermis.
21        On supine radiographs, these discrete muscle bundles appeared as two or three large, arcuate i
22 antitative immunofluorescence, these cardiac muscle bundles can be used to parse orthogonal cues in e
23             Morphogenesis of all extraocular muscle bundles correlated highly with Pitx2 gene dose, b
24                    Transgenic I79N (Tg-I79N) muscle bundles displayed increased myofilament Ca(2+) se
25 ition is progressive and is due to anomalous muscle bundle hypertrophy or fibrosis, or both, which ma
26 xpression by mast cells in the airway smooth muscle bundle in bronchial biopsies from subjects with a
27 ts, endothelial cells, epithelial cells, and muscle bundles in Ad3- and Ad5-injected mice.
28 scle cells (ASMCs) were isolated from smooth muscle bundles in airway of rats.
29 ieved by incision of hypertrophied anomalous muscle bundles in all 17 patients, with prominent fibros
30 l microlocalization within the airway smooth muscle bundle is an important determinant of the asthmat
31 RX) and the SRX/DRX equilibrium in cTnT-I79N muscle bundles likely result in increased mobility of my
32 uggest that the second potential is from the muscle bundle (Marshall bundle) within the LOM.
33 n the mechanism for the thinning of skeletal muscle bundles observed in LRRC8A-deficient mice and hig
34  both the left and right atria and the major muscle bundles of the atria, including the crista termin
35 n pathway for spreading excitation deep into muscle bundles of the human jejunum, necessary for motor
36 epresses the force production from papillary muscle bundles, partly associated with changes in [Ca(2)
37                                We found that muscle bundle shapes and attachment sites were significa
38 emonstrate an increase in bladder wall mass, muscle bundle size, and a threefold increase in the cros
39                 Connective tissue and smooth muscle bundles suspended the pulley from the periorbita.
40 individual cells grow and self-assemble into muscle bundles that are integrated with micromechanical
41 re placed in the right ventricle, straddling muscle bundles that separated the apical VSD from the re
42                                           In muscle bundles, that have a relatively higher input impe
43 ellular microelectrode recording from corpus muscle bundles to characterize the roles of intramuscula
44 developed a platform of micron-scale cardiac muscle bundles to control biomechanics in arrays of thou
45 isms for, crucial events that enable nascent muscle bundles to reach their mature form and position w
46                            We show that some muscle bundles undergo splitting events to form individu
47                       Correlated activity in muscle bundles was linked with early twitching and event
48 e-frequency relationships of mouse papillary muscle bundles were measured in the presence or absence
49                                  However, CP muscle bundles, which include fibres in their constituen
50                              Abundant smooth muscle bundles with mature contractile phenotype were fo
51                      Excision of an injected muscle bundle within 10 min of DNA inoculation did not a
52                           Whether or not the muscle bundle within the ligament of Marshall (LOM) can
53  documented that the origin of AF was in the muscle bundle within the LOM.
54 odetected in nerve fascicles growing between muscle bundles within the human fetal bladder, directly