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1 eletal defects in cervical vertebrae and the rib cage.
2 area of apposition of the diaphragm with the rib cage.
3 heating were examined in samples of porcine rib cage.
4 e zone of apposition of the diaphragm to the rib cage.
5 ity, supporting its role in the extension of rib cages.
6 elephants and manatees, which have extended rib cages.
9 alized along the entire vertebral column and rib cage and are linked to defective formation of cartil
10 ns regarding the nature of the ;Hox code' in rib cage and axial skeleton development are revealed.
11 e probably because of greater recruitment of rib cage and expiratory muscles (p = 0.004) and because
15 ogenin gene knock-in (ki) developed a normal rib cage and were viable, therefore demonstrating functi
16 wrist, elbow and arm, shoulder and clavicle, rib cage, and thoracolumbar spine) between July 2020 and
18 the diaphragm (t(di)), circumference of the rib cage (c(di)), and CSA(di) increased with height and
22 the effects of two different types of manual rib cage compression on expiratory flow and mucus cleara
24 reased to 28.4+/-5.2L/min during hard manual rib cage compression vs. 15.9+/-2.2 and 16.6+/-2.8L/min
26 zed with early expiratory phase (hard manual rib cage compression) and soft and gradual rib cage comp
28 he lungs during no treatment and soft manual rib cage compression, -0.28 +/- 0.61 and -0.15+/-0.95mm/
31 l rib cage compression) and soft and gradual rib cage compressions applied during the late expiratory
32 age compressions were tested: Hard and brief rib cage compressions synchronized with early expiratory
38 these subjects necessitates abnormally large rib cage displacements during exercise, which may be a s
40 otome, Kenya, along with its estimated adult rib cage, for comparison with H. sapiens and the Kebara
42 ely from somitic mesoderm, patterning of the rib cage is complicated by its derivation from two disti
44 arge frequencies of the SMUs were higher and rib cage movement greater during HF-SCS compared to spon
46 ge phenotype, chondrocytes isolated from the rib cages of developing rat embryos were evaluated for t
47 ) indices including phase angle ( ), percent rib cage (RC %), breaths per minute (BPM), and labored b
48 to the Myf5 locus (Myf5(myg-ki)) rescued the rib cage truncation in the Myf5-null mutant, hence demon
49 astic bands: one band (RC) placed around the rib cage under the upper armpit and another band (AB) ar