ライフサイエンスコーパス: retractor

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 In 2 patients (13.3%), intrarectal retractor expansion failed, and conversion to convention

17 genioglossus; medial XIIth nerve branch) and retractor (hyoglossus and styloglossus; lateral XIIth ne

18 styloglossus and hyoglossus muscles (tongue retractors) in maintaining upper airway patency in human

19 mill protractor (LG) phase and maintains the retractor (Int1) phase duration by activating the same m

20 The use of iris retractors may facilitate posterior capsule staining by

21 hypoxia and hypercapnia, and that the tongue retractors may have a significant role in protecting upp

22 experiments on permeabilized anterior byssus retractor muscle (ABRM) of Mytilus edulis have shown tha

23 mooth muscles, including the anterior byssus retractor muscle (ABRM) of Mytilus edulis.

24 In the hamster retractor muscle (n=54), interactions between three leve

25 d venular ends of capillaries in the hamster retractor muscle before and after isovolemic hemodilutio

26 experiments, augmentations of protrudor and retractor muscle EMG activities were associated with par

27 ation in feed arteries and arterioles of the retractor muscle indicate that substantive differences c

28 The retractor muscle of anaesthetized hamsters was contracte

29 ts on thick filaments of the anterior byssus retractor muscle of Mytilus and the telson-levator muscl

30 The anterior byssus retractor muscle of Mytilus edulis was used to character

31 ted thick filaments from the anterior byssus retractor muscle of the blue mussel Mytilus edulis and t

32 eed arteries (diameter, 50-70 microm) of the retractor muscle secured at 100 % resting length or stre

33 Independent retractor muscle stimulation did not significantly alter

34 ction of arterioles and feed arteries of the retractor muscle that was constrained to the vicinity of

35 dynamics of isolated Mytilus anterior byssus retractor muscle thick filaments.

36 developed a novel preparation of the hamster retractor muscle to investigate whether passive changes

37 ting diameter 64 +/- 4 microm) supplying the retractor muscle was either stimulated by local microion

38 tery (observed 1000 microm upstream from the retractor muscle) in response to distal acetylcholine or

39 ; maximum = 99 +/- 2; n = 86) of the hamster retractor muscle, we tested the hypothesis that distinct

40 g; length approximately 4 mm) of the hamster retractor muscle, we tested the hypothesis that endothel

41 on along feed arteries and arterioles of the retractor muscle, which is contiguous with the cheek pou

42 etric parameters for the hamster cheek pouch retractor muscle.

43 ' contractile kinetics in their main humeral retractor muscle.

44 l vasodilatation was investigated in hamster retractor muscle.

45 were chosen for working hamster cheek-pouch retractor muscle.

46 ultaneous activation of tongue protrudor and retractor muscles (co-activation) would constrict and st

47 elated during co-activation of protrudor and retractor muscles (r2 = 0.63, P < 0.05), but not during

48 l fin consists of one pair of protractor and retractor muscles and 10 sets of muscles attaching to th

49 We conclude that the tongue protrudor and retractor muscles are coactivated in response to hypoxia

50 ce and the neural drive to the protrudor and retractor muscles could be measured during spontaneous b

51 e the response of human tongue protrudor and retractor muscles during a breathhold maneuver and in st

52 In permeabilized anterior byssus retractor muscles from Mytilus edulis, catch force was i

53 r muscles in mild hypoxia, and (3) extrinsic retractor muscles have a steeper rate of rise of activit

54 lusion increased the activities of intrinsic retractor muscles in mild hypoxia, and (3) extrinsic ret

55 tion on neural drive to tongue protrudor and retractor muscles in the rat.

56 Co-activation of tongue protrudor and retractor muscles increased VI, max (peak increase 44 %,

57 dependent activation of tongue protrudor and retractor muscles influence upper airway flow mechanics.

58 s a nonheme iron oxygen carrier found in the retractor muscles of marine "peanut" worms.

59 e that either co-activation of protrudor and retractor muscles or independent activation of protrudor

60 Co-activating the protrudor and retractor muscles produced tongue retraction, whereas in

61 sal motoneurons driving tongue protrudor and retractor muscles respond identically to these stimuli.

62 The results showed that the protrudor and retractor muscles were coactivated under both conditions

63 e lateral XIIth nerve branch (denervation of retractor muscles) the tongue either protruded (15/21 an

64 y-related co-activation of the protrudor and retractor muscles, and proportional changes in tongue re

65 The mesentoblast cell, 4d, contributes to retractor muscles, heart, larval kidney and intestine.

66 hridia, and eight sets of dorsoventral pedal retractor muscles.

67 ion of intrinsic and extrinsic protrudor and retractor muscles.

68 thin filaments from Mytilus anterior byssus retractor muscles.

69 ral muscles: the transversus penis (TPN) and retractor penis magnus (RPM).

70 Second, GPR directly excites the retractor phase neurons.

71 This selective action on the retractor phase results from two distinct GPR actions.

72 Stimulating GPR during each retractor phase selectively prolongs that phase and ther

73 ate pattern (active during each gastric mill retractor phase) influences an ongoing gastric mill rhyt

74 MCN1 transmitter release occurs during each retractor phase, these parallel GPR actions selectively

75 lation selectively prolongs the gastric mill retractor phase, via presynaptic inhibition of MCN1.

76 crom, maximal: 98 +/- 2 microm) from hamster retractor skeletal muscle, we investigated the contribut

77 ertently due to procedures such as incision, retractor stretch, and electrocauterization when perform

78 the tongue protrudor (genioglossus, GG) and retractor (styloglossus, SG and hyoglossus, HG) muscles

79 copes, we used a 5-mm curved or articulating retractor that was placed into the abdomen via a separat

80 ferent motor nerve activity to protrudor and retractor tongue muscles.