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1 ve neurons were present in the mesencephalic trigeminal nucleus.
2 ranial nerves VII, IX and X project into the trigeminal nucleus.
3 xtension into the medulla, the caudal spinal trigeminal nucleus.
4 layers of the dorsal horn and caudal spinal trigeminal nucleus.
5 ion reduces the responsiveness of the spinal trigeminal nucleus.
6 anglion, and central terminals in the spinal trigeminal nucleus.
7 s orofacial nociceptor afferents, the spinal trigeminal nucleus.
8 as well as the proprioceptive mesencephalic trigeminal nucleus.
9 s and superficial layer of the caudal spinal trigeminal nucleus.
10 identified ventro-lateral to the ipsilateral trigeminal nucleus.
11 and a lateral band of the principal sensory trigeminal nucleus.
12 on-gustatory hindbrain regions, i.e., spinal trigeminal nucleus.
13 s also produced some Fos labeling within the trigeminal nucleus.
14 in other brainstem areas such as the spinal trigeminal nucleus.
15 dala, the reticular formation and the spinal trigeminal nucleus.
16 lso present on afferents entering the spinal trigeminal nucleus.
17 ry tract, ventral tegmental area, and spinal trigeminal nucleus.
18 present intracellularly in the mesencephalic trigeminal nucleus.
19 n named the tensor tympani part of the motor trigeminal nucleus (5TT) in rodent brain atlases, becaus
20 of 5HT in migraine relates to inhibition of trigeminal nucleus activity, just as it is likely that s
22 N fibers extended rostrally to the principal trigeminal nucleus and caudally to the cervical spinal c
24 leads to excitation of neurons in the caudal trigeminal nucleus and dorsal horns of the C(1/)C(2) cer
25 y and inhibitory projections from the spinal trigeminal nucleus and dorsolateral hump of the interpos
27 ere located ventral to the ipsilateral motor trigeminal nucleus and extended rostrally towards the me
28 he spinal cord dorsal horn and caudal spinal trigeminal nucleus and in the nucleus of the solitary tr
29 r biotinylated dextran amine into the spinal trigeminal nucleus and studied the resulting anterograde
30 uleus, nucleus of the solitary tract, spinal trigeminal nucleus and superficial laminae of the spinal
31 expression was significantly greater in the trigeminal nucleus and superior salivatory nucleus after
32 onstrated inputs from portions of the spinal trigeminal nucleus and the nucleus of the solitary tract
33 the total alpha-motoneuron pool in the motor trigeminal nucleus and the spinal cord lateral motor col
35 of a functional continuum between the caudal trigeminal nucleus and upper cervical segments involved
36 us, dorsal motor nucleus of the vagus, motor trigeminal nucleus, and facial nucleus, but not in most
38 us (DCN), sensory neurons from the principal trigeminal nucleus, and motoneurons of the facial nucleu
41 locus coeruleus area, the principal sensory trigeminal nucleus, and the lateral parabrachial nucleus
43 culopontine tegmental nucleus, the accessory trigeminal nucleus, and the ventral nucleus of the trape
44 ons in the LC area and the principal sensory trigeminal nucleus are glutamatergic neurons, whereas ma
46 column nuclei, the area postrema, the spinal trigeminal nucleus as well as identified motor neurons i
49 mined for Fos-like immunoreactivity were the trigeminal nucleus caudalis (TNC) and its caudal extensi
50 complex (elPB) but were absent from both the trigeminal nucleus caudalis (TNC) and the spinal cord.
51 single unit recordings were made in the rat trigeminal nucleus caudalis (Vc) from cells with Adelta
52 d the contribution of 5-HT3 receptors in the trigeminal nucleus caudalis (Vc), the homolog of the spi
53 al projections of these afferents within the trigeminal nucleus caudalis and the spinal cord dorsal h
54 rotransmitters in activating neurones in the trigeminal nucleus caudalis following stimulation of the
55 was identified in the superficial aspect of trigeminal nucleus caudalis of the New World owl monkey
58 bnuclei of nucleus tractus solitarii, spinal trigeminal nucleus caudalis, and inferior olivary subnuc
65 in the laterally adjacent mediodorsal spinal trigeminal nucleus (DMSp5), but this trigeminal activati
66 ventral medullary reticular nucleus, spinal trigeminal nucleus, dorsal horn, ventral horn and centra
67 e synaptic organization in the feline spinal trigeminal nucleus, emphasizing specific neurotransmitte
68 ral lemniscus, pontine nuclei, mesencephalic trigeminal nucleus, external cuneate nucleus, area postr
69 l area, raphe (pontine and medullary), motor trigeminal nucleus, facial nucleus, vestibular nucleus,
70 These data indicate that 5HT inhibits evoked trigeminal nucleus firing via the 5HT1B/1D receptor at w
72 of the descending tract of the mesencephalic trigeminal nucleus in Alligator and other jawed animals
73 natomical changes were present in the spinal trigeminal nucleus in subjects with chronic orofacial ne
74 s not observed at the level of the principal trigeminal nucleus, indicating that it originates within
75 The structures examined for fos were the trigeminal nucleus, infratrigeminal nucleus, reticular n
76 a subset of small motor neurons of the motor trigeminal nucleus innervating the tensor tympani muscle
78 ntage of the fact that lesions of the spinal trigeminal nucleus interpolaris (SpVi) significantly red
81 , principal and oral divisions of the spinal trigeminal nucleus, islands of Calleja and presubiculum.
83 as of the brain, including the mesencephalic trigeminal nucleus (meV), subfornical organ (SFO) and th
84 tivity was examined in the rat mesencephalic trigeminal nucleus (MTN), using orexin A immunohistochem
85 ized trigeminovascular neurons in the spinal trigeminal nucleus of anesthetized male and female rats.
87 R) within the feline trigeminal ganglion and trigeminal nucleus of normal adult subjects and in subje
88 ere we show that the face afferents from the trigeminal nucleus of the brainstem sprout and grow into
89 te that the majority of CGRP-IR found in the trigeminal nucleus originates from trigeminal primary af
91 novel region of trigeminal brainstem, spinal trigeminal nucleus pars muralis, which contains a class
93 reticulospinal neurons are excited through a trigeminal nucleus pathway and swimming starts first on
94 to 'win' because excitation from a shorter, trigeminal nucleus pathway becomes reliable and can init
95 11 is necessary for pattern formation in the trigeminal nucleus principalis (PrV), the requisite brai
97 inferior olive, abducens nucleus, and motor trigeminal nucleus; protein coexpression of CLR and RAMP
98 on, the persistence of CGRP-IR fibers in the trigeminal nucleus provides one possible explanation for
99 has been largely restricted to the principal trigeminal nucleus (PrV) and its ascending projections t
100 uclei, periaqueductal gray, locus coeruleus, trigeminal nucleus, reticular formation, area postrema a
101 ng pain pathway, including within the spinal trigeminal nucleus, somatosensory thalamus, thalamic ret
104 nonoverlapping: projections from the spinal trigeminal nucleus (Sp5) terminate primarily in the gran
105 rom the cochlear nucleus (CN) and the spinal trigeminal nucleus (Sp5) to the inferior colliculus (IC)
106 r of Fos-positive neurons in the DCN, spinal trigeminal nucleus (Sp5), dorsal raphe nucleus (DR) and
107 oinflammatory cytokine, in the region of the trigeminal nucleus specifically related to the processin
108 mean diffusivity decreases within the spinal trigeminal nucleus, specifically the subnucleus oralis.
110 sized there were star patterns in the spinal trigeminal nucleus subnuclei interpolaris and caudalis.
111 MOR ligands predominantly in the descending trigeminal nucleus suggested that the observed antinocic
112 These data demonstrate that the second order trigeminal nucleus synapse in the brainstem and upper ce
114 neurons in the caudal division of the spinal trigeminal nucleus that project to the principal nucleus
116 ails concerning the pathways from the spinal trigeminal, nucleus tractus solitarius, raphe magnus, ra
117 Specifically, responses to EBS in the spinal trigeminal nucleus (TRIG) and red nucleus (RN) increased
118 A direct projection from rat mesencephalic trigeminal nucleus (Vme) neurons to the hypoglossal nucl
119 ons closely apposed another 10 mesencephalic trigeminal nucleus (Vme) perikarya labeled from the jaw
120 pindle afferents (JMSA) in the mesencephalic trigeminal nucleus (Vme) project to the parvocellular re
121 500 microns rostrocaudal intervals in spinal trigeminal nucleus (Vsp) of adenalectomized (ADX), ADX +
122 neurons were identified in bilateral spinal trigeminal nucleus (VSP), nucleus tractus solitarius (NT
123 from those in the cat in that input from the trigeminal nucleus was confined rostrally, so that the c
126 icroscopic immunochemistry in the rat spinal trigeminal nucleus, we show that PKCgamma-immunoreactivi
127 cells and large neurons in the mesencephalic trigeminal nucleus were immunoreactive for p75 and all t
128 afferent axons located in the mesencephalic trigeminal nucleus were physiologically identified and i
129 played a laminar sequence that resembled the trigeminal nucleus, with V2 more rostral, V1 caudal, and
130 ation was observed in the ipsilateral spinal trigeminal nucleus within the medulla and lower pons in
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