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1 minal ganglion, and central terminals in the spinal trigeminal nucleus.
2  nucleus and superficial layer of the caudal spinal trigeminal nucleus.
3 ct to non-gustatory hindbrain regions, i.e., spinal trigeminal nucleus.
4 receives orofacial nociceptor afferents, the 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.
12 inhibition from MPOA and excitation from the spinal trigeminal nucleus.
13 n exerting direct central effects within the spinal trigeminal nucleus.
14                  The region encompassing the spinal trigeminal nucleus also displayed increased regio
15 B), caudal pressor area, and lamina I of the spinal trigeminal nucleus and all levels of the spinal c
16 r and depressor areas of the medulla and the spinal trigeminal nucleus and contralaterally in the CPA
17 citatory and inhibitory projections from the spinal trigeminal nucleus and dorsolateral hump of the i
18 paratrigeminal nucleus, and lamina II of the spinal trigeminal nucleus and entire spinal cord.
19  V of the spinal cord dorsal horn and caudal spinal trigeminal nucleus and in the nucleus of the soli
20 e tracer biotinylated dextran amine into the spinal trigeminal nucleus and studied the resulting ante
21 cus ceruleus, nucleus of the solitary tract, spinal trigeminal nucleus and superficial laminae of the
22 ion demonstrated inputs from portions of the spinal trigeminal nucleus and the nucleus of the solitar
23 ry afferents (nucleus of the solitary tract, spinal trigeminal nucleus, and dorsal horn [DH]).
24  solitary nucleus, nucleus ambiguous, caudal spinal trigeminal nucleus, and reticular formation.
25 ema, pontine raphe nucleus, gracile nucleus, spinal trigeminal nucleus, and spinal cord.
26                            These include the spinal trigeminal nucleus, area postrema, habenula, amyg
27 dorsal column nuclei, the area postrema, the spinal trigeminal nucleus as well as identified motor ne
28 ate central trigeminovascular neurons in the spinal trigeminal nucleus (C1-2).
29 l nociceptors and nociceptive neurons in the spinal trigeminal nucleus can prevent their sensitizatio
30 ly target neurons in the spinal cord and the spinal trigeminal nucleus caudalis (SpVc).
31 tral subnuclei of nucleus tractus solitarii, spinal trigeminal nucleus caudalis, and inferior olivary
32 also found in many other regions such as the spinal trigeminal nucleus, cerebellum and basal ganglia.
33 lar reticular nucleus (PCRt) and dorsomedial spinal trigeminal nucleus (dm-Vsp).
34  c-Fos in the laterally adjacent mediodorsal spinal trigeminal nucleus (DMSp5), but this trigeminal a
35  in the ventral medullary reticular nucleus, spinal trigeminal nucleus, dorsal horn, ventral horn and
36 e of the synaptic organization in the feline spinal trigeminal nucleus, emphasizing specific neurotra
37 ether anatomical changes were present in the spinal trigeminal nucleus in subjects with chronic orofa
38 ok advantage of the fact that lesions of the spinal trigeminal nucleus interpolaris (SpVi) significan
39 s, but the nature of the projection from the spinal trigeminal nucleus is unknown.
40 ocampus, principal and oral divisions of the spinal trigeminal nucleus, islands of Calleja and presub
41 ilateral pontine cluster consistent with the spinal trigeminal nucleus (n = 51).
42 -sensitized trigeminovascular neurons in the spinal trigeminal nucleus of anesthetized male and femal
43 orded from wide dynamic range neurons in the spinal trigeminal nucleus of anesthetized rats.
44 ones of the rat substantia gelatinosa of the spinal trigeminal nucleus pars caudalis.
45 fied a novel region of trigeminal brainstem, spinal trigeminal nucleus pars muralis, which contains a
46  of central trigeminovascular neurons in the spinal trigeminal nucleus revealed the ability of this s
47 ascending pain pathway, including within the spinal trigeminal nucleus, somatosensory thalamus, thala
48  inputs from somatosensory nuclei, including spinal trigeminal nucleus (Sp5) and cuneate nucleus (Cu)
49  the nucleus of the solitary tract (NTS) and spinal trigeminal nucleus (Sp5) and found that 20 and 10
50 unit activity in the presence and absence of spinal trigeminal nucleus (Sp5) electrical activation.
51  mostly nonoverlapping: projections from the spinal trigeminal nucleus (Sp5) terminate primarily in t
52 tions from the cochlear nucleus (CN) and the spinal trigeminal nucleus (Sp5) to the inferior collicul
53 e number of Fos-positive neurons in the DCN, spinal trigeminal nucleus (Sp5), dorsal raphe nucleus (D
54 ain regions and other brainstem nuclei (e.g. spinal trigeminal nucleus; Sp5).
55 s, and mean diffusivity decreases within the spinal trigeminal nucleus, specifically the subnucleus o
56 lso found that pre-treatment activity of the spinal trigeminal nucleus (STN) and coupling between the
57 hypothesized there were star patterns in the spinal trigeminal nucleus subnuclei interpolaris and cau
58       Recruitment of the hypothalamus, pons, spinal trigeminal nucleus, thalamus, and visual and pain
59 uclear neurons in the caudal division of the spinal trigeminal nucleus that project to the principal
60 leus of the solitary tract, spinal cord, and spinal trigeminal nucleus to the forebrain.
61     Details concerning the pathways from the spinal trigeminal, nucleus tractus solitarius, raphe mag
62        Specifically, responses to EBS in the spinal trigeminal nucleus (TRIG) and red nucleus (RN) in
63 ied at 500 microns rostrocaudal intervals in spinal trigeminal nucleus (Vsp) of adenalectomized (ADX)
64 ositive neurons were identified in bilateral spinal trigeminal nucleus (VSP), nucleus tractus solitar
65                            Activation in the spinal trigeminal nucleus was constant in location for a
66 ctron microscopic immunochemistry in the rat spinal trigeminal nucleus, we show that PKCgamma-immunor
67 t activation was observed in the ipsilateral spinal trigeminal nucleus within the medulla and lower p