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1 c induction and mechanical ventilation via a tracheal tube.
2 ration values necessitating uncapping of the tracheal tube.
3 cent of tracheal intubation were with cuffed tracheal tubes.
4 of the lumen matrix during maturation of the tracheal tubes.
5 ide full barrier function and produce normal tracheal tubes.
6 o asphyxiation brought on by fluid-congested tracheal tubes.
7 nd causes expansion forces that elongate the tracheal tubes.
8 sponding to the membrane-driven expansion of tracheal tubes.
9 e pressure ventilation by an endotracheal or tracheal tube, a PaO2:FiO2 less than 200 mm Hg with at l
10 ed fifty-two adult patients intubated with a tracheal tube allowing subglottic secretion suctioning w
11 ow and pressure measured at the inlet of the tracheal tube and expressed as resistance (Rrs) and reac
12 ted of deflating the cuff on the fenestrated tracheal tube and occluding the tube.
13 ed using calibrated syringes and appropriate tracheal tubes and connections.
14 of mechanical ventilation, the prevalence of tracheal tubes, and behavioral "learned nonuse" may all
15 tory systems, plant vascular systems, insect tracheal tubes, and other distribution networks.
16      Anatomical details of the spiracles and tracheal tubes are described, images presented, and new
17                      The total length of the tracheal tubes are seventy times the length of the entir
18 n produce some ventilation with or without a tracheal tube, because the straight upper airways of ani
19             In all three mutants, developing tracheal tubes bud and extend normally, but the epitheli
20                          After replacing the tracheal tube by a double-lumen one, we initiated latera
21   Second, Yorkie controls water tightness of tracheal tubes by transcriptional regulation of the delt
22 xchange respiratory gases in their system of tracheal tubes by using either diffusion or changes in i
23 membrane size, which are required for proper tracheal tube elongation.
24 s the mechanical stress on the matrix during tracheal tube expansion.
25 ression appeared in late-stage embryos after tracheal tube formation, with individual PPK genes showi
26 AP kinase, is hyper-activated throughout the tracheal tube in the Pu mutant.
27                                              Tracheal tubes in mutant larvae are often crushed or twi
28 osis included transplant stricture (n = 13), tracheal tube injury (n = 10), inflammation (n = 6), tra
29                              Whether using a tracheal tube introducer ("bougie") increases the likeli
30  intervention may be precluded by changes in tracheal tube leak during the procedure.
31  the remaining 13 patients, the magnitude of tracheal tube leak increased by > or = 10% after delayed
32 claudins act in the same pathway controlling tracheal tube length.
33 r the Mucus Slurper (study group) or a Hi-Lo Tracheal Tube (Mallinckrodt, St.
34 thway in promoting cell intercalation during tracheal tube morphogenesis in Drosophila embryogenesis,
35   Here we show that three genes required for tracheal tube morphogenesis in Drosophila melanogaster e
36 e underlying mechanisms using the developing tracheal tube network of Drosophila indirect flight musc
37                                            A tracheal tube occlusion protocol can predict clinically
38                                          The tracheal tube occlusion protocol consisted of deflating
39                   All patients underwent the tracheal tube occlusion protocol followed by bronchoscop
40 r, those patients who failed to tolerate the tracheal tube occlusion protocol had clinically importan
41 was undertaken to test the hypothesis that a tracheal tube occlusion protocol predicts clinically imp
42 xty-three (84%) of 75 patients tolerated the tracheal tube occlusion protocol.
43 or without cardiac arrest, with or without a tracheal tube, showed essentially no ventilation by ster
44 o not disrupt several processes required for tracheal tube size control, including septate junction f
45 netic program and cellular events underlying tracheal tube size control.
46 al extracellular matrix proteins involved in tracheal tube size control: Crumbs, Uninflatable, Kune-K
47 tinct from other known processes involved in tracheal tube size regulation.
48 s support epithelial SJ barrier function and tracheal tube-size control.
49 known septate junctions genes cause the same tracheal tube-size defects as ATPalpha and nrv2 mutation
50 sophila Dorsal Air Sac Primordium (ASP) is a tracheal tube that grows toward Branchless FGF-expressin
51 pgant35A) are recessive lethal and result in tracheal tubes that are irregular in diameter and morpho
52 larval development, which generate the adult tracheal tubes, the spiracle and the epidermis surroundi
53  sinuous have previously been shown to cause tracheal tubes to be elongated and have diameter increas
54 bunits of the Na+/K+ ATPase cause Drosophila tracheal tubes to have increased lengths and expanded di
55  who developed respiratory distress when the tracheal tube was occluded were deemed to have failed th
56      emp mutants also display over elongated tracheal tubes with increased levels of the apical prote