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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                                              Masseter activity was organized into two modes synchroni
10 de, mastication occurred as rhythmic (~5 Hz) masseter activity while the hands held food below the mo
11  bouts of higher-frequency (~13 Hz) rhythmic masseter activity, which was accompanied by eye displace
12 ter and cutaneous inputs project to the MDH, masseter afferents provide an additional input to the Vi
13 rds were made of the electromyogram (EMG) in masseter and anterior digastric muscles and of the unloa
14       These results indicate that while both masseter and cutaneous inputs project to the MDH, masset
15  and kilohertz kinematic tracking to analyze masseter and hand actions as mice of both sexes handled
16  and slow skeletal muscle fibres such as the masseter and is an important source of reference work fo
17 nd MHC isoform content of fibres from rabbit masseter and soleus muscles.
18 sor tooth were recorded from the jaw closing masseter and temporal muscles of 21 human subjects.
19              Subjects were trained to record masseter and temporalis electromyography over 3 days and
20  Laboratory tests were performed to quantify masseter and temporalis muscle activities (mV) per bite
21 rce calibrations determined subject-specific masseter and temporalis muscle activities per 20-N bite-
22 during the daytime versus nighttime for both masseter and temporalis muscles and 1.8- and 3.0-fold la
23 , on intramuscular hemodynamics in the human masseter and temporalis muscles following a sustained is
24 anesthesia during maximum stimulation of the masseter and temporalis muscles in each of five condylar
25                     Three days after injury, masseter and tibialis anterior (TA) muscles in wild-type
26 every other hour at the level of the thenar, masseter, and deltoid muscles along with central hemodyn
27 eft and right anterior digastric (LAD, RAD), masseter, buccinator, and genioglossus (GG) muscles with
28 es had distinct gene expression profiles and masseter cells usually proliferated more and differentia
29  were initially higher and increased more in masseter compared to cutaneous trunci (P < 0.05 for all)
30                       Samples of superficial masseter contained a few type I fibres, with the majorit
31 ncluding rhythmic proptosis, attributable to masseter contractions.
32                                   Generally, masseter-derived clones were larger and took longer to d
33 erties was preserved in both EDL-derived and masseter-derived satellite cells from old mice, although
34                  When transplanted, however, masseter-derived satellite cells regenerated limb muscle
35  55.8 C for cutaneous trunci and no peak for masseter (DSC), indicates that myosin in type II fibres
36 grees C for cutaneous trunci and no peak for masseter (DSC), indicates that myosin in type II fibres
37 was masked by bilateral reflex depression of masseter EMG caused by auditory input from the coil disc
38  bites occurred as lower-amplitude aperiodic masseter events that were precisely timed to follow regr
39 ack-test recordings of single, skinned human masseter fibers at 15 degrees C revealed maximum shorten
40                                        V0 in masseter fibers forms a continuum in which no clear rela
41 Analysis by gel electrophoresis found 63% of masseter fibers to contain pure type I MyHC and the rema
42 g were characterised and compared for bovine masseter (fibre type I) and cutaneous trunci (fibre type
43                                  Some rabbit masseter fibres express the alpha-cardiac myosin heavy c
44                                           In masseter fibres the V(zero) values were (in muscle lengt
45                                              Masseters from male and female CD-1 mice (2-4 months old
46 tion of proteins in cutaneous trunci than in masseter (FTIR), supported by a myosin associated peak a
47 tion of proteins in cutaneous trunci than in masseter (FTIR), supported by a myosin associated peak a
48 oteomic analysis was performed on fresh beef masseter (high type-I fibres) and cutaneous trunci (high
49 cid led to the elimination or attenuation of masseter hyperalgesia/allodynia developed after masseter
50 ne blue (MB), and ODQ, in the Vc, attenuates masseter hypersensitivity induced by intramuscular injec
51 in the subnucleus caudalis (Vc) in mediating masseter hypersensitivity under acute inflammatory condi
52 seter hyperalgesia/allodynia developed after masseter inflammation (P<0.05-0.01).
53 ein immunohistochemistry, we show that after masseter inflammation, a population of neurons in the do
54                               In response to masseter inflammation, there was an upregulation of glia
55 dulla neurons attenuates hyperalgesia during masseter inflammation.
56 did not show Fos-like immunoreactivity after masseter inflammation.
57 ist, AP-5, into the Vi/Vc and MDH attenuated masseter inflammatory hyperalgesia.
58 alization of muscle fiber types in the mouse masseter is consistent with the functional compartmental
59 lculi from the ostium, and distance from the masseter line (kappa = 0.98, 0.98, 0.97, respectively; p
60 (distance of obstruction from the ostium and masseter line) and the condition of the main duct at MRI
61             After 13 days of space flight, 1 masseter (MA) and tibialis anterior (TA) were frozen rap
62                                      Daytime masseter MBSs for +D TMJs in females were the largest ov
63 ions of the tracers into the masseter-Vi/Vc, masseter-MDH, or the skin-MDH.
64 se, intracellular records were obtained from masseter motoneurons before and after carbachol-induced
65 nucleus pontis oralis (NPO) induced IPSPs in masseter motoneurons following, but never prior to, the
66                                 In addition, masseter motoneurons were significantly hyperpolarized a
67 showed associations of low-magnitude daytime masseter motor load, PHQ-15, and CPI scores for cluster
68 jected complete Freund's adjuvant (CFA) into masseter muscle (MM).
69 eurokinin 1 (NK1) receptor antagonist in one masseter muscle 15 min prior to the MO injection in the
70 erties of Vi neurons that receive input from masseter muscle afferents by characterizing their respon
71 l hypersensitivity after administration into masseter muscle and dura, respectively.
72  agent, complete Freund's adjuvant, into the masseter muscle and perfused at 2 hours postinflammation
73  primary afferent neurons that innervate the masseter muscle and the overlying skin.
74  mapped premotor neurons for the jaw-closing masseter muscle and the tongue-protruding genioglossus m
75 s located anteriorly to the insertion of the masseter muscle and varies among individuals, we hypothe
76 1-actin, cardiac alphaalpha-tropomyosin, and masseter muscle beta-myosin complexes; masseter myosin,
77                  We conclude that the rabbit masseter muscle contains an 'alpha-cardiac' fibre type t
78                           In particular, the masseter muscle is highly specialised, having extended a
79                                  While human masseter muscle is known to have unusual co-expression o
80 these results suggest that the activation of masseter muscle nociceptor alters spindle afferent respo
81 ntensity/area) and higher sensitivity of the masseter muscle pain.
82    MK-801 (0.3 mg/kg) preadministered in the masseter muscle significantly reduced the peak and overa
83 ptive signals from periodontal ligaments and masseter muscle spindles.
84 ically active neurons that function to lower masseter muscle tone, whereas unilateral optogenetic act
85 of complete Freund's adjuvant (CFA) into the masseter muscle under methohexital anesthesia after a sm
86              Ninety cells were identified as masseter muscle units in 11 adult cats.
87                   Ongoing pain from inflamed masseter muscle was also reduced in KI mice, and was fur
88 icantly (p < 0.01) greater body (by 18%) and masseter muscle weight (by 83%), compared with wild-type
89  Significant correlations were noted between masseter muscle weight and mandibular body length (r = 0
90 nd the resulting reflexes in the ipsilateral masseter muscle were examined electromyographically.
91 instem neurons following the inflammation of masseter muscle were examined in order to differentiate
92  challenge (hypertonic saline infused in the masseter muscle) with and without placebo administration
93 results suggest that the inflammation of the masseter muscle, an injury of orofacial deep tissue, res
94 y salivary glands located on the apex of the masseter muscle, close to the oral angle.
95 ing respirometry and electromyography of the masseter muscle, we demonstrate that chewing by human su
96 muscle spindle isolated from the murine deep masseter muscle.
97  increase in the cross-sectional area of the masseter muscle.
98 ateral to the mandible and reflection of the masseter muscle.
99 nance of mechanical hyperalgesia of inflamed masseter muscle.
100 duces significant edema formation in the rat masseter muscle.
101 on, failed to produce edema formation in the masseter muscle.
102 nt inhibition of the MO-induced edema in the masseter muscle.
103 , complete Freund's adjuvant (CFA), into the masseter muscle.
104  to determine how trigeminal motoneurons and masseter muscles are switched off during REM sleep in ra
105           Rats were sacrificed 2 h later and masseter muscles dissected and weighed.
106 cal facilitation (ICF) were evaluated in the masseter muscles of 12 subjects and the cortical silent
107 ic (e.g., sternocleidomastoid, temporal, and masseter muscles) and artifactual (e.g., dental implants
108                              Regeneration of masseter muscles, which normally regenerate much less co
109 is present in the cortical representation of masseter muscles.
110 ase (HRP) injections into the temporalis and masseter muscles.
111  we show that the affinity of ADP for bovine masseter myosin in the absence of actin (represented by
112 , and masseter muscle beta-myosin complexes; masseter myosin, which shares sequence identity with bet
113                      Local anesthesia of the masseter nerve prevented the increase in GFAP and IL-1be
114  electrical stimulation of the caudal Vme or masseter nerve, mechanical stimulation of jaw muscles an
115 h the functional compartmentalization of the masseter observed in other species.
116 L) of the limb with satellite cells from the masseter of the head.
117 d horseradish peroxidase or cholera toxin B: masseter or overlying skin) in the same rat.
118 e compounds, and proteomic profiles, in beef masseter [oxidative muscle, all type I fibres) and cutan
119 ) with cold pressor stimulation, both in the masseter (p < 0.001) and in the temporalis (p < 0.001) m
120 ake value were found in the control muscles (masseter [P = 0.38] and pterygoid [P = 0.70]) and subcut
121 , and IIb--was determined within the defined masseter partitions by means of Western blot analysis an
122    We serendipitously detected an additional masseter-related action, tooth sharpening, identified as
123 we hypothesized that L(O) of rat superficial masseter (SM) would decrease with activation intensity,
124 ng characteristic curve analysis showed that masseter tissue oxygen saturation (area under the curve
125 ygen saturation was consistently higher than masseter tissue oxygen saturation (p = .04) and deltoid
126 that in the early 6-hr resuscitation period, masseter tissue oxygen saturation accurately identified
127                                         Both masseter tissue oxygen saturation and deltoid tissue oxy
128 g characteristic curves analyses showed that masseter tissue oxygen saturation was better predictor o
129 oid tissue oxygen saturation (p = .002), and masseter tissue oxygen saturation was consistently highe
130 muscles and 1.8- and 3.0-fold larger for the masseter versus temporalis muscle during the daytime and
131 led after injections of the tracers into the masseter-Vi/Vc, masseter-MDH, or the skin-MDH.
132 after inflammation of the skin overlying the masseter was attenuated by injection of AP-5 into the MD
133 ent was unaffected in all muscles except the masseter, where its expression was extinguished in the I
134  proteolysis, in bovine cutaneous trunci and masseter, which represent very different muscles types.

 
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