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1 ves into the attachment sites for the dorsal abdominal muscles.
2 n of neuromuscular junctions (NMJs) at adult abdominal muscles.
3 ead eversion, in synchrony with death of the abdominal muscles.
4 f the first lumbar root (L1) innervating the abdominal muscles.
5 hila neuromuscular junction (NMJ) of ventral abdominal muscles.
6 n motor neuronal innervation of male ventral abdominal muscles.
7 with coordinated activation of the DIAm and abdominal muscles.
8 s muscle activity was strongly depressed and abdominal muscle activity showed potent expiratory modul
10 Variability in the postural strategy of the abdominal muscles and pain-related cognitions were evalu
11 neurons influencing the activity of multiple abdominal muscles, and support our hypothesis that this
15 ne and estradiol were associated with higher abdominal muscle area (1.74, 0.1-3.4, and 1.84, 0.4-3.3,
16 T cuts at L3 vertebra level to measure total abdominal muscle area (TAMA) and visceral fat area (VFA)
17 en fasting serum sex hormones and CT-derived abdominal muscle area and radiodensity in adult men.
18 Between these two CTs, the change in total abdominal muscle area index (TAMAI) was evaluated for pr
19 tosterone and estradiol were associated with abdominal muscle area, while only total testosterone was
24 ds (opioid-induced apnoea) in neonatal rats, abdominal muscles continue to contract at a rate similar
26 plitude intramuscular EMG activities of both abdominal muscles could be evoked with postural manoeuvr
27 the histolysis of salivary gland and midgut, abdominal muscle death occurs by apoptosis, and does not
28 roliferation and differentiation, leading to abdominal muscle defects; cleft palate; endochondral bon
29 omalies affecting the patterning of anterior abdominal muscles, demonstrating that Ubx isoforms are n
30 s responsible for rhythmic activation of the abdominal muscles during opioid-induced apnoea in the ne
31 deep residual U-Net (ResUNet) to segment 12 abdominal muscle groups including the left and right pso
32 sed to analyze samples extracted from shrimp abdominal muscle, hepatopancreas, gills and pleopods.
33 inal muscle IDPs and preliminarily determine abdominal muscle IDP variations with age and sex in a cl
34 lly automatic technique for assessment of CT abdominal muscle IDPs and preliminarily determine abdomi
38 n the size of the neuromuscular junctions on abdominal muscles in these animals suggests that one of
40 viors and protective reflexes, although each abdominal muscle is frequently activated differentially
42 their functions and those of the associated abdominal muscles of monotremes and marsupial mammals ha
43 enes display subtle migratory defects in the abdominal muscles of the ventral body wall and an enlarg
44 from upper airway muscles, the diaphragm and abdominal muscles or from the nerves that innervate thos
47 erse relationship was observed for SHBG with abdominal muscle radiodensity (0.3, 0.0-0.6, and - 0.33,
48 al circuitry controlling the activity of one abdominal muscle, rectus abdominis, was mapped using the
49 ng 3D abdominal muscle mass from 12 distinct abdominal muscle regions and groups using computed tomog
50 F produced a large increase in diaphragm and abdominal muscle responses to vestibular stimulation.
52 g neural control of airway, intercostal, and abdominal muscles that must be coordinated with DIAm act
53 network orientations matching those of host abdominal muscle tissue improved graft integration and t
54 usion and aspiration and the intercostal and abdominal muscles to appropriately stiffen the body cavi
56 e ribs and muscles of the trunk in which the abdominal muscles took on the primary ventilatory functi
57 of the motor neurons innervating the Ventral Abdominal Muscles (VAMs), we found that expression of mu
58 the associations of testosterone levels with abdominal muscle volume and density in men is limited, w
62 Petechial hemorrhages (PHs) in intestine and abdominal muscle were counted 15 min after exposure to c