戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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 entation of selectively nociceptive lamina I spinothalamic activity.
2                        Thus, the overlapping spinothalamic and cerebellar inputs may provide a substr
3 rns and corresponding nerves, atrophy of the spinothalamic and spinocerebellar tracts and posterior c
4                     The question whether the spinothalamic and spinoreticular fibres cross the cord t
5 n C7 and over one-fourth of those in L4 were spinothalamic, and at each level some projected to both
6 dial SPFp receives unique inputs from lumbar spinothalamic cells and brain regions involved in proces
7 d the significance of a population of lumbar spinothalamic cells for male sexual behavior in rats.
8 hese results suggest that this population of spinothalamic cells plays a pivotal role in generation o
9 lamina I projection cells per side, and that spinothalamic cells therefore make up approximately 42%
10 ounted for only on the assumption that these spinothalamic fibres are crossing the cord transversely.
11                                          The spinothalamic input was directed mostly to the ventral p
12 lls were distinguished from other classes of spinothalamic lamina I neurones by their peripheral inpu
13 racteristics of warming-specific lumbosacral spinothalamic lamina I neurones.
14                           We have shown that spinothalamic lamina I neurons are infrequent in rat lum
15                                Virtually all spinothalamic lamina I neurons at both levels were label
16                                              Spinothalamic lamina I neurons differed from those label
17 p of their collaterals that results in every spinothalamic neurone receiving an input from several do
18 olecystokinin as a marker for this subset of spinothalamic neurons and Fos-immunoreactivity as a mark
19  PAG and LPb, to determine the proportion of spinothalamic neurons at lumbar and cervical levels that
20                                              Spinothalamic neurons have generally been associated wit
21 mina I and lamina III/IV NK1r-immunoreactive spinothalamic neurons in cervical and lumbar segments co
22  investigate the involvement of these lumbar spinothalamic neurons in conveying copulation-related in
23  into the thalamus to estimate the number of spinothalamic neurons in each of these two populations,
24 This pathway originates from a population of spinothalamic neurons in the lumbar spinal cord containi
25 esults demonstrated that activation of these spinothalamic neurons is triggered by stimuli associated
26            The numbers of spinomedullary and spinothalamic neurons on the left side were comparable,
27 r results suggest that there are 90 lamina I spinothalamic neurons per side in C7 and 15 in L4 and th
28 demonstrate that a specific subpopulation of spinothalamic neurons signals information associated wit
29                   Second, spinomedullary and spinothalamic neurons were compared in retrograde double
30                              Moreover, these spinothalamic neurons were not activated by vaginocervic
31 urons with collaterals to the medulla and 2) spinothalamic neurons with collaterals to the midbrain.
32 mation conveyed by both these populations of spinothalamic neurons.
33  more ventrally located within lamina I than spinothalamic neurons.
34 ly, the recent identification of a candidate spinothalamic pathway involved in relay of ejaculation-s
35 d others has demonstrated the existence of a spinothalamic pathway that is a candidate to relay infor
36                               Intact crossed spinothalamic pathways are unable to support the normal
37 ately 1%, indicating that spinomedullary and spinothalamic pathways arise from separate subpopulation
38 nd that this projection is distinct from the spinothalamic projection.
39                             Classically, the spinothalamic (ST) system has been viewed as the major p
40 us results in monkeys show that mid-cervical spinothalamic (STT) neurons are activated by groups II a
41 ion of rat lumbar laminae VII and X putative spinothalamic (STT) neurons that co-contain cholecystoki
42 otopically organized lamina I trigemino- and spinothalamic terminations in a cytoarchitectonically di
43                  In addition, the patches of spinothalamic terminations intermingled and partly overl
44 al spinal cord to inhibit activity of lumbar spinothalamic tract (SST) cells and dorsal horn (DH) cel
45 ed neuron, indicating the termination of the spinothalamic tract (STT) axon.
46 oposed to contribute to the sensitization of spinothalamic tract (STT) cells and hyperalgesia.
47 ted NR1 subunits (pNR1) are expressed in the spinothalamic tract (STT) cells and immunohistochemistry
48                             The responses of spinothalamic tract (STT) cells were recorded before and
49                                          The spinothalamic tract (STT) is an integral pathway in the
50                                  Nociceptive spinothalamic tract (STT) neurones in lamina I of the lu
51                     Central sensitization of spinothalamic tract (STT) neurons in anesthetized monkey
52 ogy and distribution of retrogradely labeled spinothalamic tract (STT) neurons in lamina I (the margi
53 c pain, central sensitization of dorsal horn spinothalamic tract (STT) neurons is a major underlying
54 mine the effects of central sensitization of spinothalamic tract (STT) neurons produced by intraderma
55 perior sagittal sinus (SSS) can excite C1-C2 spinothalamic tract (STT) neurons receiving thoracic vis
56                                              Spinothalamic tract (STT) neurons respond to itch-produc
57                 We found a class of lamina I spinothalamic tract (STT) neurons selectively excited by
58     The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in macaqu
59     The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in monkey
60     The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in monkey
61                                     Lamina I spinothalamic tract (STT) neurons were identified by ret
62                          Fifty-seven primate spinothalamic tract (STT) neurons were identified using
63 by disruption of the DC pathway, but not the spinothalamic tract (STT).
64  in the pain-signaling pathway to the brain [spinothalamic tract (STT)] that respond only to painful
65 ll tissues caudal to the neck eliminates the spinothalamic tract and the transmission of somatosensor
66                                Excitation of spinothalamic tract cells in the upper thoracic and lowe
67 la and then descend to excite upper cervical spinothalamic tract cells.
68             Our results demonstrate that the spinothalamic tract contains mutually exclusive populati
69 tic or demyelinating lesions centered on the spinothalamic tract in rats.
70 ntact animals, electrical stimulation of the spinothalamic tract induces increases in thalamic CCL21
71 st that GRPR+ neurons are different from the spinothalamic tract neurons that have been the focus of
72                 We examined the responses of spinothalamic tract neurons to histaminergic and, for th
73 pinocervical, postsynaptic dorsal column and spinothalamic tract neurons was used to simulate the pop
74                                          The spinothalamic tract projects to the medial and lateral t
75 ified itch-specific neuronal pathways in the spinothalamic tract that are distinct from pain pathways
76 ensory neuronal circuits of nociception (the spinothalamic tract) and proprioception (the dorsal spin
77 s in C6 and 17% of those in L5 belong to the spinothalamic tract, and these apparently project exclus
78                   This review focuses on the spinothalamic tract, but other pathways are excited as w
79 s in each of these populations belong to the spinothalamic tract, which conveys nociceptive informati
80 he DC at T10, but not by interruption of the spinothalamic tract.
81 icroscope to examine lamina I trigemino- and spinothalamic (TSTT) terminations in the posterior part
82                 PHA-L-labeled trigemino- and spinothalamic (TSTT) terminations were identified immuno

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。