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1 he DC at T10, but not by interruption of the spinothalamic tract.
2 ll tissues caudal to the neck eliminates the spinothalamic tract and the transmission of somatosensor
3 ensory neuronal circuits of nociception (the spinothalamic tract) and proprioception (the dorsal spin
4 s in C6 and 17% of those in L5 belong to the spinothalamic tract, and these apparently project exclus
10 ntact animals, electrical stimulation of the spinothalamic tract induces increases in thalamic CCL21
11 st that GRPR+ neurons are different from the spinothalamic tract neurons that have been the focus of
13 pinocervical, postsynaptic dorsal column and spinothalamic tract neurons was used to simulate the pop
15 al spinal cord to inhibit activity of lumbar spinothalamic tract (SST) cells and dorsal horn (DH) cel
18 ted NR1 subunits (pNR1) are expressed in the spinothalamic tract (STT) cells and immunohistochemistry
23 ogy and distribution of retrogradely labeled spinothalamic tract (STT) neurons in lamina I (the margi
24 c pain, central sensitization of dorsal horn spinothalamic tract (STT) neurons is a major underlying
25 mine the effects of central sensitization of spinothalamic tract (STT) neurons produced by intraderma
26 perior sagittal sinus (SSS) can excite C1-C2 spinothalamic tract (STT) neurons receiving thoracic vis
29 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in macaqu
30 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in monkey
31 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in monkey
35 in the pain-signaling pathway to the brain [spinothalamic tract (STT)] that respond only to painful
36 ified itch-specific neuronal pathways in the spinothalamic tract that are distinct from pain pathways
37 s in each of these populations belong to the spinothalamic tract, which conveys nociceptive informati
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