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3 rns and corresponding nerves, atrophy of the spinothalamic and spinocerebellar tracts and posterior c
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.
12 lls were distinguished from other classes of spinothalamic lamina I neurones by their peripheral inpu
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
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
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
31 urons with collaterals to the medulla and 2) spinothalamic neurons with collaterals to the midbrain.
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
37 ately 1%, indicating that spinomedullary and spinothalamic pathways arise from separate subpopulation
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
44 al spinal cord to inhibit activity of lumbar spinothalamic tract (SST) cells and dorsal horn (DH) cel
47 ted NR1 subunits (pNR1) are expressed in the spinothalamic tract (STT) cells and immunohistochemistry
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
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
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
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
73 pinocervical, postsynaptic dorsal column and spinothalamic tract neurons was used to simulate the pop
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
79 s in each of these populations belong to the spinothalamic tract, which conveys nociceptive informati
81 icroscope to examine lamina I trigemino- and spinothalamic (TSTT) terminations in the posterior part
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