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1 nance of mechanical hyperalgesia of inflamed masseter muscle.
2 duces significant edema formation in the rat masseter muscle.
3 on, failed to produce edema formation in the masseter muscle.
4 nt inhibition of the MO-induced edema in the masseter muscle.
5 , complete Freund's adjuvant (CFA), into the masseter muscle.
6 muscle spindle isolated from the murine deep masseter muscle.
7 ateral to the mandible and reflection of the masseter muscle.
8  increase in the cross-sectional area of the masseter muscle.
9 is present in the cortical representation of masseter muscles.
10 ase (HRP) injections into the temporalis and masseter muscles.
11 eurokinin 1 (NK1) receptor antagonist in one masseter muscle 15 min prior to the MO injection in the
12 erties of Vi neurons that receive input from masseter muscle afferents by characterizing their respon
13 results suggest that the inflammation of the masseter muscle, an injury of orofacial deep tissue, res
14 l hypersensitivity after administration into masseter muscle and dura, respectively.
15  agent, complete Freund's adjuvant, into the masseter muscle and perfused at 2 hours postinflammation
16  primary afferent neurons that innervate the masseter muscle and the overlying skin.
17  mapped premotor neurons for the jaw-closing masseter muscle and the tongue-protruding genioglossus m
18 s located anteriorly to the insertion of the masseter muscle and varies among individuals, we hypothe
19 ic (e.g., sternocleidomastoid, temporal, and masseter muscles) and artifactual (e.g., dental implants
20  to determine how trigeminal motoneurons and masseter muscles are switched off during REM sleep in ra
21 1-actin, cardiac alphaalpha-tropomyosin, and masseter muscle beta-myosin complexes; masseter myosin,
22 y salivary glands located on the apex of the masseter muscle, close to the oral angle.
23                  We conclude that the rabbit masseter muscle contains an 'alpha-cardiac' fibre type t
24           Rats were sacrificed 2 h later and masseter muscles dissected and weighed.
25                           In particular, the masseter muscle is highly specialised, having extended a
26                                  While human masseter muscle is known to have unusual co-expression o
27 jected complete Freund's adjuvant (CFA) into masseter muscle (MM).
28 these results suggest that the activation of masseter muscle nociceptor alters spindle afferent respo
29 cal facilitation (ICF) were evaluated in the masseter muscles of 12 subjects and the cortical silent
30 ntensity/area) and higher sensitivity of the masseter muscle pain.
31    MK-801 (0.3 mg/kg) preadministered in the masseter muscle significantly reduced the peak and overa
32 ptive signals from periodontal ligaments and masseter muscle spindles.
33 ically active neurons that function to lower masseter muscle tone, whereas unilateral optogenetic act
34 of complete Freund's adjuvant (CFA) into the masseter muscle under methohexital anesthesia after a sm
35              Ninety cells were identified as masseter muscle units in 11 adult cats.
36                   Ongoing pain from inflamed masseter muscle was also reduced in KI mice, and was fur
37 ing respirometry and electromyography of the masseter muscle, we demonstrate that chewing by human su
38 icantly (p < 0.01) greater body (by 18%) and masseter muscle weight (by 83%), compared with wild-type
39  Significant correlations were noted between masseter muscle weight and mandibular body length (r = 0
40 nd the resulting reflexes in the ipsilateral masseter muscle were examined electromyographically.
41 instem neurons following the inflammation of masseter muscle were examined in order to differentiate
42                              Regeneration of masseter muscles, which normally regenerate much less co
43  challenge (hypertonic saline infused in the masseter muscle) with and without placebo administration