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1 receives orofacial nociceptor afferents, the spinal trigeminal nucleus.
2 minal ganglion, and central terminals in the spinal trigeminal nucleus.
3 nucleus and superficial layer of the caudal spinal trigeminal nucleus.
4 ct to non-gustatory hindbrain regions, i.e., spinal trigeminal nucleus.
5 bserved in other brainstem areas such as the spinal trigeminal nucleus.
6 he amygdala, the reticular formation and the spinal trigeminal nucleus.
7 ir is also present on afferents entering the spinal trigeminal nucleus.
8 solitary tract, ventral tegmental area, and spinal trigeminal nucleus.
9 d its extension into the medulla, the caudal spinal trigeminal nucleus.
10 rficial layers of the dorsal horn and caudal spinal trigeminal nucleus.
11 timulation reduces the responsiveness of the spinal trigeminal nucleus.
13 r and depressor areas of the medulla and the spinal trigeminal nucleus and contralaterally in the CPA
14 citatory and inhibitory projections from the spinal trigeminal nucleus and dorsolateral hump of the i
16 V of the spinal cord dorsal horn and caudal spinal trigeminal nucleus and in the nucleus of the soli
17 e tracer biotinylated dextran amine into the spinal trigeminal nucleus and studied the resulting ante
18 cus ceruleus, nucleus of the solitary tract, spinal trigeminal nucleus and superficial laminae of the
19 ion demonstrated inputs from portions of the spinal trigeminal nucleus and the nucleus of the solitar
23 dorsal column nuclei, the area postrema, the spinal trigeminal nucleus as well as identified motor ne
26 tral subnuclei of nucleus tractus solitarii, spinal trigeminal nucleus caudalis, and inferior olivary
27 also found in many other regions such as the spinal trigeminal nucleus, cerebellum and basal ganglia.
29 c-Fos in the laterally adjacent mediodorsal spinal trigeminal nucleus (DMSp5), but this trigeminal a
30 in the ventral medullary reticular nucleus, spinal trigeminal nucleus, dorsal horn, ventral horn and
31 e of the synaptic organization in the feline spinal trigeminal nucleus, emphasizing specific neurotra
32 ether anatomical changes were present in the spinal trigeminal nucleus in subjects with chronic orofa
33 ok advantage of the fact that lesions of the spinal trigeminal nucleus interpolaris (SpVi) significan
35 ocampus, principal and oral divisions of the spinal trigeminal nucleus, islands of Calleja and presub
36 -sensitized trigeminovascular neurons in the spinal trigeminal nucleus of anesthetized male and femal
39 fied a novel region of trigeminal brainstem, spinal trigeminal nucleus pars muralis, which contains a
40 ascending pain pathway, including within the spinal trigeminal nucleus, somatosensory thalamus, thala
41 inputs from somatosensory nuclei, including spinal trigeminal nucleus (Sp5) and cuneate nucleus (Cu)
42 unit activity in the presence and absence of spinal trigeminal nucleus (Sp5) electrical activation.
43 mostly nonoverlapping: projections from the spinal trigeminal nucleus (Sp5) terminate primarily in t
44 tions from the cochlear nucleus (CN) and the spinal trigeminal nucleus (Sp5) to the inferior collicul
45 e number of Fos-positive neurons in the DCN, spinal trigeminal nucleus (Sp5), dorsal raphe nucleus (D
46 s, and mean diffusivity decreases within the spinal trigeminal nucleus, specifically the subnucleus o
47 hypothesized there were star patterns in the spinal trigeminal nucleus subnuclei interpolaris and cau
48 uclear neurons in the caudal division of the spinal trigeminal nucleus that project to the principal
50 Details concerning the pathways from the spinal trigeminal, nucleus tractus solitarius, raphe mag
52 ied at 500 microns rostrocaudal intervals in spinal trigeminal nucleus (Vsp) of adenalectomized (ADX)
53 ositive neurons were identified in bilateral spinal trigeminal nucleus (VSP), nucleus tractus solitar
55 ctron microscopic immunochemistry in the rat spinal trigeminal nucleus, we show that PKCgamma-immunor
56 t activation was observed in the ipsilateral spinal trigeminal nucleus within the medulla and lower p
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