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1 cision aided by a specially designed sternal retractor.
2         All 5 cases involved the use of iris retractors.
3 ticularly in cases involving the use of iris retractors.
4 derwent phacoemulsification with use of iris retractors.
5 an earlier burst onset relative to intrinsic retractor activities in mild hypoxia.
6 percapnia revealed that phasic protrudor and retractor activity was initiated immediately before or d
7 ntraoperative complications, the use of iris retractors and operation time were recorded.Differences
8 rm was developed to incorporate instruments, retractors, and a controllable intra-abdominal camera.
9                             Accessory planta retractor (APR) motoneurons of the hawk moth, Manduca se
10 , Manduca sexta, individual accessory planta retractor (APR) motoneurons undergo a segment-specific p
11 he hawkmoth, Manduca sexta, accessory planta retractor (APR) motoneurons undergo a segment-specific p
12 he hawkmoth, Manduca sexta, accessory planta retractor (APR) motoneurons undergo a segment-specific p
13 holinergic connections with accessory planta retractor (APR) motoneurons.
14 fter phacoemulsification, 2 capsulotomy edge retractors attached to force transducers were used to st
15 ter CN VII lesion, and hypothesized that the retractor bulbi (RB) muscle assumes an important compens
16 f the rhythmic activity of active protractor-retractor CPG networks by individual stepping legs.SIGNI
17 tance-dependent activation of the protractor-retractor CPGs in different thoracic ganglia, there is n
18           In 2 patients (13.3%), intrarectal retractor expansion failed, and conversion to convention
19 ltration in 2-3 minutes by dissection of the retractors from the inferior margin of the tarsus via sk
20 genioglossus; medial XIIth nerve branch) and retractor (hyoglossus and styloglossus; lateral XIIth ne
21  styloglossus and hyoglossus muscles (tongue retractors) in maintaining upper airway patency in human
22 mill protractor (LG) phase and maintains the retractor (Int1) phase duration by activating the same m
23                              The use of iris retractors may facilitate posterior capsule staining by
24 hypoxia and hypercapnia, and that the tongue retractors may have a significant role in protecting upp
25 experiments on permeabilized anterior byssus retractor muscle (ABRM) of Mytilus edulis have shown tha
26 mooth muscles, including the anterior byssus retractor muscle (ABRM) of Mytilus edulis.
27                               In the hamster retractor muscle (n=54), interactions between three leve
28 d venular ends of capillaries in the hamster retractor muscle before and after isovolemic hemodilutio
29  experiments, augmentations of protrudor and retractor muscle EMG activities were associated with par
30 ation in feed arteries and arterioles of the retractor muscle indicate that substantive differences c
31                                          The retractor muscle of anaesthetized hamsters was contracte
32 ts on thick filaments of the anterior byssus retractor muscle of Mytilus and the telson-levator muscl
33                          The anterior byssus retractor muscle of Mytilus edulis was used to character
34 ted thick filaments from the anterior byssus retractor muscle of the blue mussel Mytilus edulis and t
35 eed arteries (diameter, 50-70 microm) of the retractor muscle secured at 100 % resting length or stre
36                                  Independent retractor muscle stimulation did not significantly alter
37 ction of arterioles and feed arteries of the retractor muscle that was constrained to the vicinity of
38 dynamics of isolated Mytilus anterior byssus retractor muscle thick filaments.
39 developed a novel preparation of the hamster retractor muscle to investigate whether passive changes
40 ting diameter 64 +/- 4 microm) supplying the retractor muscle was either stimulated by local microion
41 tery (observed 1000 microm upstream from the retractor muscle) in response to distal acetylcholine or
42 ; maximum = 99 +/- 2; n = 86) of the hamster retractor muscle, we tested the hypothesis that distinct
43 g; length approximately 4 mm) of the hamster retractor muscle, we tested the hypothesis that endothel
44 on along feed arteries and arterioles of the retractor muscle, which is contiguous with the cheek pou
45 etric parameters for the hamster cheek pouch retractor muscle.
46 ' contractile kinetics in their main humeral retractor muscle.
47 l vasodilatation was investigated in hamster retractor muscle.
48  were chosen for working hamster cheek-pouch retractor muscle.
49 ultaneous activation of tongue protrudor and retractor muscles (co-activation) would constrict and st
50 elated during co-activation of protrudor and retractor muscles (r2 = 0.63, P < 0.05), but not during
51 used an aberrant mirror-symmetric pattern of retractor muscles (RMs) in primary polyps.
52 l fin consists of one pair of protractor and retractor muscles and 10 sets of muscles attaching to th
53    We conclude that the tongue protrudor and retractor muscles are coactivated in response to hypoxia
54 ce and the neural drive to the protrudor and retractor muscles could be measured during spontaneous b
55 e the response of human tongue protrudor and retractor muscles during a breathhold maneuver and in st
56             In permeabilized anterior byssus retractor muscles from Mytilus edulis, catch force was i
57 r muscles in mild hypoxia, and (3) extrinsic retractor muscles have a steeper rate of rise of activit
58 lusion increased the activities of intrinsic retractor muscles in mild hypoxia, and (3) extrinsic ret
59 tion on neural drive to tongue protrudor and retractor muscles in the rat.
60        Co-activation of tongue protrudor and retractor muscles increased VI, max (peak increase 44 %,
61 dependent activation of tongue protrudor and retractor muscles influence upper airway flow mechanics.
62 s a nonheme iron oxygen carrier found in the retractor muscles of marine "peanut" worms.
63 e that either co-activation of protrudor and retractor muscles or independent activation of protrudor
64              Co-activating the protrudor and retractor muscles produced tongue retraction, whereas in
65 sal motoneurons driving tongue protrudor and retractor muscles respond identically to these stimuli.
66    The results showed that the protrudor and retractor muscles were coactivated under both conditions
67 e lateral XIIth nerve branch (denervation of retractor muscles) the tongue either protruded (15/21 an
68 y-related co-activation of the protrudor and retractor muscles, and proportional changes in tongue re
69    The mesentoblast cell, 4d, contributes to retractor muscles, heart, larval kidney and intestine.
70 hridia, and eight sets of dorsoventral pedal retractor muscles.
71 ion of intrinsic and extrinsic protrudor and retractor muscles.
72  thin filaments from Mytilus anterior byssus retractor muscles.
73 ral muscles: the transversus penis (TPN) and retractor penis magnus (RPM).
74             Second, GPR directly excites the retractor phase neurons.
75                 This selective action on the retractor phase results from two distinct GPR actions.
76                  Stimulating GPR during each retractor phase selectively prolongs that phase and ther
77 ate pattern (active during each gastric mill retractor phase) influences an ongoing gastric mill rhyt
78  MCN1 transmitter release occurs during each retractor phase, these parallel GPR actions selectively
79 lation selectively prolongs the gastric mill retractor phase, via presynaptic inhibition of MCN1.
80                                 Lower eyelid retractor recession without spacer yields significant pr
81 tion and Bell's phenomenon) and lower eyelid retractor recession without spacer.
82  retraction slightly, cutaneous lower eyelid retractor release (CLERR) eliminates this problem.
83 crom, maximal: 98 +/- 2 microm) from hamster retractor skeletal muscle, we investigated the contribut
84 ertently due to procedures such as incision, retractor stretch, and electrocauterization when perform
85  the tongue protrudor (genioglossus, GG) and retractor (styloglossus, SG and hyoglossus, HG) muscles
86 copes, we used a 5-mm curved or articulating retractor that was placed into the abdomen via a separat
87 ferent motor nerve activity to protrudor and retractor tongue muscles.