ライフサイエンスコーパス: masseter

1 ical threshold to noxious stimulation of the masseter.

2 he anatomy and muscle fiber phenotype of the masseter.

3 anatomical regions of male and female mouse masseters.

4 decrease to a non-detectable level in mouse masseter, (2) an increase to become the sole TnT in shee

5 an increase to become the sole TnT in sheep masseter, (3) an increase of the total level as well as

6 om contralateral (cMM) and ipsilateral (iMM) masseters, activated at 10% of maximal voluntary contrac

7 SupV BPNs is sufficient to induce bilateral masseter activation both during resting state and during

8 toxin light chain (TeNT) increases bilateral masseter activation during chewing, an effect driven by

9 ter and cutaneous inputs project to the MDH, masseter afferents provide an additional input to the Vi

10 rds were made of the electromyogram (EMG) in masseter and anterior digastric muscles and of the unloa

11 These results indicate that while both masseter and cutaneous inputs project to the MDH, masset

12 and slow skeletal muscle fibres such as the masseter and is an important source of reference work fo

13 nd MHC isoform content of fibres from rabbit masseter and soleus muscles.

14 sor tooth were recorded from the jaw closing masseter and temporal muscles of 21 human subjects.

15 Subjects were trained to record masseter and temporalis electromyography over 3 days and

16 rce calibrations determined subject-specific masseter and temporalis muscle activities per 20-N bite-

17 , on intramuscular hemodynamics in the human masseter and temporalis muscles following a sustained is

18 anesthesia during maximum stimulation of the masseter and temporalis muscles in each of five condylar

19 Three days after injury, masseter and tibialis anterior (TA) muscles in wild-type

20 every other hour at the level of the thenar, masseter, and deltoid muscles along with central hemodyn

21 eft and right anterior digastric (LAD, RAD), masseter, buccinator, and genioglossus (GG) muscles with

22 es had distinct gene expression profiles and masseter cells usually proliferated more and differentia

23 Samples of superficial masseter contained a few type I fibres, with the majorit

24 Generally, masseter-derived clones were larger and took longer to d

25 erties was preserved in both EDL-derived and masseter-derived satellite cells from old mice, although

26 When transplanted, however, masseter-derived satellite cells regenerated limb muscle

27 was masked by bilateral reflex depression of masseter EMG caused by auditory input from the coil disc

28 ack-test recordings of single, skinned human masseter fibers at 15 degrees C revealed maximum shorten

29 V0 in masseter fibers forms a continuum in which no clear rela

30 Analysis by gel electrophoresis found 63% of masseter fibers to contain pure type I MyHC and the rema

31 Some rabbit masseter fibres express the alpha-cardiac myosin heavy c

32 In masseter fibres the V(zero) values were (in muscle lengt

33 Masseters from male and female CD-1 mice (2-4 months old

34 cid led to the elimination or attenuation of masseter hyperalgesia/allodynia developed after masseter

35 ne blue (MB), and ODQ, in the Vc, attenuates masseter hypersensitivity induced by intramuscular injec

36 in the subnucleus caudalis (Vc) in mediating masseter hypersensitivity under acute inflammatory condi

37 seter hyperalgesia/allodynia developed after masseter inflammation (P<0.05-0.01).

38 ein immunohistochemistry, we show that after masseter inflammation, a population of neurons in the do

39 In response to masseter inflammation, there was an upregulation of glia

40 did not show Fos-like immunoreactivity after masseter inflammation.

41 ist, AP-5, into the Vi/Vc and MDH attenuated masseter inflammatory hyperalgesia.

42 alization of muscle fiber types in the mouse masseter is consistent with the functional compartmental

43 After 13 days of space flight, 1 masseter (MA) and tibialis anterior (TA) were frozen rap

44 ions of the tracers into the masseter-Vi/Vc, masseter-MDH, or the skin-MDH.

45 se, intracellular records were obtained from masseter motoneurons before and after carbachol-induced

46 nucleus pontis oralis (NPO) induced IPSPs in masseter motoneurons following, but never prior to, the

47 In addition, masseter motoneurons were significantly hyperpolarized a

48 eurokinin 1 (NK1) receptor antagonist in one masseter muscle 15 min prior to the MO injection in the

49 erties of Vi neurons that receive input from masseter muscle afferents by characterizing their respon

50 agent, complete Freund's adjuvant, into the masseter muscle and perfused at 2 hours postinflammation

51 primary afferent neurons that innervate the masseter muscle and the overlying skin.

52 mapped premotor neurons for the jaw-closing masseter muscle and the tongue-protruding genioglossus m

53 We conclude that the rabbit masseter muscle contains an 'alpha-cardiac' fibre type t

54 In particular, the masseter muscle is highly specialised, having extended a

55 While human masseter muscle is known to have unusual co-expression o

56 these results suggest that the activation of masseter muscle nociceptor alters spindle afferent respo

57 MK-801 (0.3 mg/kg) preadministered in the masseter muscle significantly reduced the peak and overa

58 ptive signals from periodontal ligaments and masseter muscle spindles.

59 ically active neurons that function to lower masseter muscle tone, whereas unilateral optogenetic act

60 of complete Freund's adjuvant (CFA) into the masseter muscle under methohexital anesthesia after a sm

61 Ninety cells were identified as masseter muscle units in 11 adult cats.

62 icantly (p < 0.01) greater body (by 18%) and masseter muscle weight (by 83%), compared with wild-type

63 Significant correlations were noted between masseter muscle weight and mandibular body length (r = 0

64 nd the resulting reflexes in the ipsilateral masseter muscle were examined electromyographically.

65 instem neurons following the inflammation of masseter muscle were examined in order to differentiate

66 challenge (hypertonic saline infused in the masseter muscle) with and without placebo administration

67 results suggest that the inflammation of the masseter muscle, an injury of orofacial deep tissue, res

68 y salivary glands located on the apex of the masseter muscle, close to the oral angle.

69 duces significant edema formation in the rat masseter muscle.

70 on, failed to produce edema formation in the masseter muscle.

71 nt inhibition of the MO-induced edema in the masseter muscle.

72 , complete Freund's adjuvant (CFA), into the masseter muscle.

73 ateral to the mandible and reflection of the masseter muscle.

74 to determine how trigeminal motoneurons and masseter muscles are switched off during REM sleep in ra

75 Rats were sacrificed 2 h later and masseter muscles dissected and weighed.

76 cal facilitation (ICF) were evaluated in the masseter muscles of 12 subjects and the cortical silent

77 ic (e.g., sternocleidomastoid, temporal, and masseter muscles) and artifactual (e.g., dental implants

78 Regeneration of masseter muscles, which normally regenerate much less co

79 is present in the cortical representation of masseter muscles.

80 ase (HRP) injections into the temporalis and masseter muscles.

81 we show that the affinity of ADP for bovine masseter myosin in the absence of actin (represented by

82 Local anesthesia of the masseter nerve prevented the increase in GFAP and IL-1be

83 electrical stimulation of the caudal Vme or masseter nerve, mechanical stimulation of jaw muscles an

84 h the functional compartmentalization of the masseter observed in other species.

85 L) of the limb with satellite cells from the masseter of the head.

86 d horseradish peroxidase or cholera toxin B: masseter or overlying skin) in the same rat.

87 ) with cold pressor stimulation, both in the masseter (p < 0.001) and in the temporalis (p < 0.001) m

88 ake value were found in the control muscles (masseter [P = 0.38] and pterygoid [P = 0.70]) and subcut

89 , and IIb--was determined within the defined masseter partitions by means of Western blot analysis an

90 ng characteristic curve analysis showed that masseter tissue oxygen saturation (area under the curve

91 ygen saturation was consistently higher than masseter tissue oxygen saturation (p = .04) and deltoid

92 that in the early 6-hr resuscitation period, masseter tissue oxygen saturation accurately identified

93 Both masseter tissue oxygen saturation and deltoid tissue oxy

94 g characteristic curves analyses showed that masseter tissue oxygen saturation was better predictor o

95 oid tissue oxygen saturation (p = .002), and masseter tissue oxygen saturation was consistently highe

96 led after injections of the tracers into the masseter-Vi/Vc, masseter-MDH, or the skin-MDH.

97 after inflammation of the skin overlying the masseter was attenuated by injection of AP-5 into the MD

98 ent was unaffected in all muscles except the masseter, where its expression was extinguished in the I