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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
5                   This review focuses on the spinothalamic tract, but other pathways are excited as w
6                                Excitation of spinothalamic tract cells in the upper thoracic and lowe
7 la and then descend to excite upper cervical spinothalamic tract cells.
8             Our results demonstrate that the spinothalamic tract contains mutually exclusive populati
9 tic or demyelinating lesions centered on the spinothalamic tract in rats.
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
12                 We examined the responses of spinothalamic tract neurons to histaminergic and, for th
13 pinocervical, postsynaptic dorsal column and spinothalamic tract neurons was used to simulate the pop
14                                          The spinothalamic tract projects to the medial and lateral t
15 al spinal cord to inhibit activity of lumbar spinothalamic tract (SST) cells and dorsal horn (DH) cel
16 ed neuron, indicating the termination of the spinothalamic tract (STT) axon.
17 oposed to contribute to the sensitization of spinothalamic tract (STT) cells and hyperalgesia.
18 ted NR1 subunits (pNR1) are expressed in the spinothalamic tract (STT) cells and immunohistochemistry
19                             The responses of spinothalamic tract (STT) cells were recorded before and
20                                          The spinothalamic tract (STT) is an integral pathway in the
21                                  Nociceptive spinothalamic tract (STT) neurones in lamina I of the lu
22                     Central sensitization of spinothalamic tract (STT) neurons in anesthetized monkey
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
27                                              Spinothalamic tract (STT) neurons respond to itch-produc
28                 We found a class of lamina I spinothalamic tract (STT) neurons selectively excited by
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
32                                     Lamina I spinothalamic tract (STT) neurons were identified by ret
33                          Fifty-seven primate spinothalamic tract (STT) neurons were identified using
34 by disruption of the DC pathway, but not the spinothalamic tract (STT).
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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