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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
14 ogenin gene knock-in (ki) developed a normal rib cage and were viable, therefore demonstrating functi
16 the diaphragm (t(di)), circumference of the rib cage (c(di)), and CSA(di) increased with height and
20 the effects of two different types of manual rib cage compression on expiratory flow and mucus cleara
22 reased to 28.4+/-5.2L/min during hard manual rib cage compression vs. 15.9+/-2.2 and 16.6+/-2.8L/min
24 zed with early expiratory phase (hard manual rib cage compression) and soft and gradual rib cage comp
26 he lungs during no treatment and soft manual rib cage compression, -0.28 +/- 0.61 and -0.15+/-0.95mm/
29 l rib cage compression) and soft and gradual rib cage compressions applied during the late expiratory
30 age compressions were tested: Hard and brief rib cage compressions synchronized with early expiratory
36 these subjects necessitates abnormally large rib cage displacements during exercise, which may be a s
39 ely from somitic mesoderm, patterning of the rib cage is complicated by its derivation from two disti
40 arge frequencies of the SMUs were higher and rib cage movement greater during HF-SCS compared to spon
42 ge phenotype, chondrocytes isolated from the rib cages of developing rat embryos were evaluated for t
43 to the Myf5 locus (Myf5(myg-ki)) rescued the rib cage truncation in the Myf5-null mutant, hence demon
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