ライフサイエンスコーパス: spinothalamic tract

1 he DC at T10, but not by interruption of the spinothalamic tract.

2 influenced by interfering with the ascending spinothalamic tract.

3 hose in the cervical cord also belong to the spinothalamic tract.

4 ing peripheral nociceptive sensation via the spinothalamic tract and brainstem nuclei to the thalamus

5 ll tissues caudal to the neck eliminates the spinothalamic tract and the transmission of somatosensor

6 ensory neuronal circuits of nociception (the spinothalamic tract) and proprioception (the dorsal spin

7 s in C6 and 17% of those in L5 belong to the spinothalamic tract, and these apparently project exclus

8 This review focuses on the spinothalamic tract, but other pathways are excited as w

9 Excitation of spinothalamic tract cells in the upper thoracic and lowe

10 la and then descend to excite upper cervical spinothalamic tract cells.

11 Our results demonstrate that the spinothalamic tract contains mutually exclusive populati

12 07, P = 0.0440, R2 = 0.20) and cervical cord spinothalamic tract fractional anisotropy associated wit

13 width of ventral tissue bridges-a proxy for spinothalamic tract function-at 1 month post-spinal cord

14 tic or demyelinating lesions centered on the spinothalamic tract in rats.

15 ntact animals, electrical stimulation of the spinothalamic tract induces increases in thalamic CCL21

16 st that GRPR+ neurons are different from the spinothalamic tract neurons that have been the focus of

17 We examined the responses of spinothalamic tract neurons to histaminergic and, for th

18 pinocervical, postsynaptic dorsal column and spinothalamic tract neurons was used to simulate the pop

19 n of the sensory component of pain along the spinothalamic tract, or stereotactic cingulotomy (n = 7)

20 linical outcome groups in the left and right spinothalamic tracts (p = 0.003 and 0.020) and MTRh (p =

21 prion protein in the substantia gelatinosa, spinothalamic tracts, posterior columns and nuclei and i

22 The spinothalamic tract projects to the medial and lateral t

23 al spinal cord to inhibit activity of lumbar spinothalamic tract (SST) cells and dorsal horn (DH) cel

24 ed neuron, indicating the termination of the spinothalamic tract (STT) axon.

25 oposed to contribute to the sensitization of spinothalamic tract (STT) cells and hyperalgesia.

26 ted NR1 subunits (pNR1) are expressed in the spinothalamic tract (STT) cells and immunohistochemistry

27 The responses of spinothalamic tract (STT) cells were recorded before and

28 The spinothalamic tract (STT) is an integral pathway in the

29 Nociceptive spinothalamic tract (STT) neurones in lamina I of the lu

30 Central sensitization of spinothalamic tract (STT) neurons in anesthetized monkey

31 ogy and distribution of retrogradely labeled spinothalamic tract (STT) neurons in lamina I (the margi

32 c pain, central sensitization of dorsal horn spinothalamic tract (STT) neurons is a major underlying

33 mine the effects of central sensitization of spinothalamic tract (STT) neurons produced by intraderma

34 perior sagittal sinus (SSS) can excite C1-C2 spinothalamic tract (STT) neurons receiving thoracic vis

35 Spinothalamic tract (STT) neurons respond to itch-produc

36 We found a class of lamina I spinothalamic tract (STT) neurons selectively excited by

37 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in macaqu

38 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in monkey

39 Lamina I spinothalamic tract (STT) neurons were identified by ret

40 Fifty-seven primate spinothalamic tract (STT) neurons were identified using

41 by disruption of the DC pathway, but not the spinothalamic tract (STT).

42 in the pain-signaling pathway to the brain [spinothalamic tract (STT)] that respond only to painful

43 ified itch-specific neuronal pathways in the spinothalamic tract that are distinct from pain pathways

44 s in each of these populations belong to the spinothalamic tract, which conveys nociceptive informati