コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 t terminals in the sensory lamina of the rat spinal cord dorsal horn.
2 e the major noradrenergic innervation of the spinal cord dorsal horn.
3 iated in part by alpha2-adrenoceptors in the spinal cord dorsal horn.
4 important elements in pain signaling in the spinal cord dorsal horn.
5 C-fiber axonal terminals in the superficial spinal cord dorsal horn.
6 nd intensely labeled laminae I and II of the spinal cord dorsal horn.
7 to neuroplastic changes that converge at the spinal cord dorsal horn.
8 regions, the dorsal root ganglion (DRG) and spinal cord dorsal horn.
9 la (RVM), known to modify nociception in the spinal cord dorsal horn.
10 l up-regulation of PTEN and Nedd4 within the spinal cord dorsal horn.
11 ynaptic plasticity in the CNS, including the spinal cord dorsal horn.
12 aces to reach target opioid receptors in the spinal cord dorsal horn.
13 en GABAergic and glycinergic synapses in the spinal cord dorsal horn.
14 on of GABAergic synaptic transmission in the spinal cord dorsal horn.
15 t of inhibitory synaptic transmission in the spinal cord dorsal horn.
16 unit of NMDAR, and PKCgamma within the rat's spinal cord dorsal horn.
17 n of both CB-1 and CB-2 receptors within the spinal cord dorsal horn.
18 he periphery first becomes integrated in the spinal cord dorsal horn.
19 dorsolateral pons (DLP) that project to the spinal cord dorsal horn.
20 nctly expressed in superficial layers of the spinal cord dorsal horn.
21 d phosphorylation of CREB in the ipsilateral spinal cord dorsal horn.
22 th excitatory and inhibitory synapses in the spinal cord dorsal horn.
23 on of the antiapoptotic Bcl-2 protein in the spinal cord dorsal horn.
24 s (EAAC1 and GLAST) in the rat's superficial spinal cord dorsal horn.
25 ulation of C-fibers and their targets in the spinal cord dorsal horn.
26 pons known to effect antinociception in the spinal cord dorsal horn.
27 iber-type neurons projecting to lamina II of spinal cord dorsal horn.
28 the action of alpha(2)-adrenoceptors in the spinal cord dorsal horn.
29 ia a different mechanism than that of NTS or spinal cord dorsal horn.
30 ct (NTS), and caudal thoracic/rostral lumbar spinal cord dorsal horn.
31 lerance is in the superficial laminae of the spinal cord dorsal horn.
32 by noradrenergic neurons that innervate the spinal cord dorsal horn.
33 thin the trigeminal nucleus caudalis and the spinal cord dorsal horn, 5-HT1D-IR fibers are concentrat
34 osphorylated CREB was upregulated within the spinal cord dorsal horn after chronic morphine, and a CR
35 genes have been shown to occur in the lumbar spinal cord dorsal horn after peripheral inflammation.
36 bstantially increased within the ipsilateral spinal cord dorsal horn after peripheral nerve injury.
37 he inflamed knee joint increases GABA in the spinal cord dorsal horn and activates GABA receptors spi
38 that many neurons in laminae I and V of the spinal cord dorsal horn and caudal spinal trigeminal nuc
39 e retrograde tracers Fluoro-Gold (FG) in the spinal cord dorsal horn and DiI in the DLP were used to
41 ciceptive transmission by projections to the spinal cord dorsal horn and indirectly by projections to
42 subunit underlies A-type K+ currents in the spinal cord dorsal horn and is modulated by the ERK sign
43 d in cells of the superficial laminae of the spinal cord dorsal horn and its extension into the medul
44 noradrenergic A7 neurons that innervate the spinal cord dorsal horn and modulate pain perception.
45 an result in sensitization of neurons in the spinal cord dorsal horn and produce physiological change
46 f glutamatergic synaptic transmission in the spinal cord dorsal horn and provide a possible mechanism
47 t also within pain-signalling neurons of the spinal cord dorsal horn and thalamic ventral posterolate
48 s detected in the superficial laminae of the spinal cord dorsal horn and the nucleus of the spinal tr
49 ere predominantly located in the superficial spinal cord dorsal horn, and most apoptotic cells also e
50 sue inflammation, neurochemical increases in spinal cord dorsal horns, and declines in fine motor con
51 trastructural level, 5-HT1D receptors in the spinal cord dorsal horn are localized exclusively within
53 ts from T10-L3 blocked viral spread into the spinal cord dorsal horn, but did not prevent infection o
54 oxious stimuli are sensed and carried to the spinal cord dorsal horn by A delta and C primary afferen
55 gp120 stimulates cytokine expression in the spinal cord dorsal horn by activating Wnt5a signaling.
56 patterns of YAP and TAZ distribution in the spinal cord dorsal horn consistent with their distinctiv
57 at the morphology and number of cells in the spinal cord dorsal horn could change following periphera
60 ed by the release of substance P (SP) in the spinal cord dorsal horn from terminals of primary affere
61 cinergic inhibitory neurotransmission in the spinal cord dorsal horn gates nociceptive signaling, is
63 spartate (NMDA) receptor and PKCgamma in the spinal cord dorsal horn (immunohistochemistry; Western b
64 glion neurons and also within neurons of the spinal cord dorsal horn in a pattern complementing, yet
65 plitude in lamina II but not lamina I of the spinal cord dorsal horn in nerve-injured versus control
66 ly 2 h after either 4 Hz or 60 Hz SCS in the spinal cord dorsal horn in the cervical enlargement and
67 s elevated in the superficial laminae of the spinal cord dorsal horn in TOW mice, specifically in GAB
69 (RVL)) and in three regions of the thoracic spinal cord (dorsal horn, intermediate zone and ventral
71 ression of neuronal GRs primarily within the spinal cord dorsal horn ipsilateral to nerve injury, whi
73 hibition mediated by glycine and GABA in the spinal cord dorsal horn is essential for controlling sen
74 esses and is reciprocally connected with the spinal cord dorsal horn, it seems likely that peripheral
75 vious work, we hypothesized that the NTS and spinal cord dorsal horn labeling was due to activation o
76 ctrical stimulation of rat ACC depressed the spinal cord dorsal horn neuron activity in response to n
78 potential (FP) recordings were obtained from spinal cord dorsal horn neurons (laminae I-IV) in a rat
79 tral sensitization, increased sensitivity in spinal cord dorsal horn neurons after injuries, plays an
80 ethyl-D-aspartate (NMDA)-induced activity in spinal cord dorsal horn neurons and that this enhancemen
81 the Nav1.3 Na(+) channel within second-order spinal cord dorsal horn neurons and third-order thalamic
82 the potassium-chloride cotransporter KCC2 in spinal cord dorsal horn neurons are a major contributor
83 n-activated protein kinases are activated in spinal cord dorsal horn neurons in response to stimulati
86 ces transient inhibition of the responses of spinal cord dorsal horn neurons to higher intensity mech
87 ant transient inhibition of the responses of spinal cord dorsal horn neurons to higher intensity mech
89 study was to determine the responses of the spinal cord dorsal horn neurons to stimulation of the pr
91 We found that ATP induces ROS production in spinal cord dorsal horn neurons, an effect eliminated by
92 lular signal-regulated kinase in superficial spinal cord dorsal horn neurons, indicative of central s
93 preparation and patch-clamp recordings from spinal cord dorsal horn neurons, we examined excitatory
97 we found that 5-HT1D-IR is unchanged in the spinal cord dorsal horn of mice with a deletion of the g
98 ctivity of sensory neurons in the developing spinal cord dorsal horn of the intact postnatal rat has
100 d in the central nucleus of the amygdala and spinal cord dorsal horn only in mice with ongoing allody
101 osed to mediate synaptic transmission in the spinal cord dorsal horn, particularly in the pathway car
103 nilaterally in the superficial layers of the spinal cord dorsal horn, regions previously described as
104 IRK1 and/or GIRK2-containing channels in the spinal cord dorsal horn represents a powerful, albeit re
106 ed kinase 1 (ERK1) and ERK2 signaling in the spinal cord dorsal horn (SCDH) has been implicated in in
108 HIV-1 proteins in postmortem tissues of the spinal cord dorsal horn (SDH) from HIV-1/acquired immuno
109 s and in postsynaptic density fractions from spinal cord dorsal horns showed an increase in GluA4 exp
110 reotypic set of neurochemical changes in the spinal cord dorsal horn that receives sensory inputs fro
111 ically aligned mechanosensory columns of the spinal cord dorsal horn underlies the nervous system's e
112 neurons in the substantia gelatinosa of the spinal cord dorsal horn was examined by intracellular re
113 ative day 5 primarily within the ipsilateral spinal cord dorsal horn, which was followed by a GT down
114 atment and to produce depletion of NE in the spinal cord dorsal horn with N-(2-chloroethyl)-N-ethyl-2
115 ide dynamic range neurons in lamina V of the spinal cord dorsal horn with the behavioral hyperexcitab
116 ponents regulated by Hippo signaling, in the spinal cord dorsal horn would be altered by chronic cons
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。