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1 the observed antinociception occurred at the subnucleus caudalis.
2 re localized to lamina II of the ipsilateral subnucleus caudalis.
3 r CGRP-LI and SP-LI increased in ipsilateral subnucleus caudalis.
4 rimary afferent profiles in lamina II of rat subnucleus caudalis.
5 tic axonal terminals within lamina II of the subnucleus caudalis.
6 inal trigeminal subnucleus interpolaris, and subnucleus caudalis.
7 ositive cells were counted in the trigeminal subnucleus caudalis.
8 These data demonstrate that in trigeminal subnucleus caudalis activation of either NK1 or NMDA rec
9 in trigeminal ganglia and associated spinal subnucleus caudalis and C1/C2 cervical dorsal spinal cor
10 n second-order neurons in the dorsal horn of subnucleus caudalis and cervical C1/C2 spinal cord (Vc/C
11 al to the obex (22% in C2, 22% in C1, 23% in subnucleus caudalis, and 18% in the transition zone betw
12 Fos expression can be induced in trigeminal subnucleus caudalis by NMDA or neurokinin-1 receptor act
13 audalis (Vi/Vc) transition or the trigeminal subnucleus caudalis-cervical cord (Vc/C1) junction regio
14 e immunoreactivity (SP-LI) were evaluated in subnucleus caudalis following induction of sinusitis.
17 t that neurons in superficial laminae of the subnucleus caudalis may be important for the reflex init
18 rve branches located in the main sensory and subnucleus caudalis of the brainstem and joints, respect
20 in other species, into cervical dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus
21 portion of the ipsilateral spinal trigeminal subnucleus caudalis (SVc) and interpolaris (SVi), and th
24 DPHd neurons were found predominantly in Vsp subnucleus caudalis (Vc) and in dorsomedial subnucleus o
25 inae of the dorsomedial aspect of trigeminal subnucleus caudalis (Vc) evoked by lingual application o
26 nvestigated the potential role of sGC in the subnucleus caudalis (Vc) in mediating masseter hypersens
28 eral medulla, and lamina V of the trigeminal subnucleus caudalis (Vc), exhibited FluoroGold/Fos doubl
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