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5 dies were numerous in the spinal trigeminal, cuneate and gracilis nuclei whilst rarer in the lateral
7 experiments was to define the topography of cuneate and spinal projections to the forelimb represent
9 ation of their inputs from the somatosensory cuneate and spinal trigeminal nuclei and by direct stimu
12 to 20 years, it was found that the brainstem cuneate and the thalamic ventral posterior nuclei had un
13 ll domain also receives projections from the cuneate and trigeminal nuclei, which are first-order nuc
14 t expansions of gracile projections into the cuneate and, in one case, external cuneate nucleus withi
16 ositus hypoglossi, all vestibular, abducens, cuneate, and lateral reticular nuclei, labeled neurons c
17 area 3b organization further show that some cuneate changes are preserved in area 3b, whereas other
18 nges are preserved in area 3b, whereas other cuneate changes are transformed before being expressed i
23 Finally, a complete but lower lesion of the cuneate fasciculus at C8 produced some abnormalities in
24 deafferented for two years by section of the cuneate fasciculus at the C1 level, there was extensive
25 cile fasciculus or a small percentage of the cuneate fasciculus did not produce changes in the gross
26 Six to 7 weeks after complete lesions of the cuneate fasciculus subserving the forelimb at cervical l
27 rently complete lesions of the contralateral cuneate fasciculus, but afferents from the digits may no
28 sal hand is represented directly beneath the cuneate fasciculus, in a region devoid of barrelettes.
30 rested in determining whether the spinal and cuneate inputs constitute a homogeneous afferent source,
31 of rDAO neurons, whereas input from rostral cuneate is most likely modulatory, probably inhibitory,
32 s neurons in the medial vestibular, external cuneate, lateral reticular, prepositus hypoglossi, supra
35 when dexterity had largely recovered, RFs of cuneate neurons could again be mapped within the cuneate
36 .6 imp/s) and durations (83.4+/-10.8 sec) of cuneate neurons excited by IB were significantly less th
38 he brainstem level, neonatally amputated rat cuneate neurons possessed the following responsivities:
40 o of short latency/long-lasting responses of cuneate neurons to IB (14/3) were significant higher tha
41 from the medial deep cerebellar and external cuneate neurons was affected in Unc5c(-/-) mice, as were
42 e that projecting neurons in the gracile and cuneate nuclei express predominantly the GluR3 subunit o
43 and densities of CTB-labeled patches in the cuneate nuclei of both sides were quantified and compare
50 instem organization of tactile inputs in the cuneate nucleus (CN) changes after acute injury of hand
52 ogical representation of the forelimb in the cuneate nucleus (CN) of forelimb-intact young adult rats
54 reshold or wide-dynamic range neurons in the cuneate nucleus (CN) were excited by peripheral stimulat
55 opposite, unaffected, side, the ipsilateral cuneate nucleus (CN), external cuneate nucleus (ECN), an
57 e ipsilateral cuneate nucleus (CN), external cuneate nucleus (ECN), and contralateral VPL showed redu
59 ry afferent terminals in the dorsal horn and cuneate nucleus after a restricted dorsal root injury.
60 tile inputs from the hand begins in the main cuneate nucleus and continues in the thalamus and area 3
62 lesions at a high cervical level deprive the cuneate nucleus and much of the somatosensory system of
63 e first injected anatomical tracers into the cuneate nucleus and plotted the distributions of labeled
64 ons, degeneration of neurons in the external cuneate nucleus and subdivisions of the inferior olivary
65 es the sprouting of digit 1 afferents in the cuneate nucleus and that this sprouting allowed these pr
67 cellular potentials of single neurons in the cuneate nucleus and upper thoracic (T3) spinal cord were
68 cardiac stimulus on neuronal activity in the cuneate nucleus and upper thoracic spinal cord in rats.
69 chanisms that operate from a distance in the cuneate nucleus and, in part, reflects supracuneate mech
72 he side of the lesion in the dorsal horn and cuneate nucleus at 15-25 weeks after the dorsal rootlet
73 n was assessed in the spinal dorsal horn and cuneate nucleus at 7 days and 15-25 postlesion weeks.
74 [RF] recordings) in the pars rotunda of the cuneate nucleus at either 1-2 weeks (short term) or 16-3
75 c transmission to the spinal grey matter and cuneate nucleus by providing a bridge for regeneration o
77 us of the brainstem sprout and grow into the cuneate nucleus in adult monkeys after lesions of the do
82 l enzyme chondroitinase ABC (chABC) into the cuneate nucleus of rats partially denervated of forepaw
84 utaneously-driven reorganization in both the cuneate nucleus of the brainstem and the ventroposterior
86 ting of remaining axons from the hand in the cuneate nucleus of the lower brainstem, we sought to inf
87 eptor subunits in somatosensory area 3b, and cuneate nucleus one week after median nerve compression
89 he gracile nucleus and the medial rim of the cuneate nucleus or the dorsomedial rim of the gracile nu
91 ued thereafter; and 3) in the nonrespiratory cuneate nucleus showed a gentle plateau throughout the f
92 revealed a small second-order pathway to the cuneate nucleus that survives high cervical dorsal colum
93 d second-order spinal cord neurons reach the cuneate nucleus through pathways that circumvent the dor
94 ntrols), a significantly greater area of the cuneate nucleus was occupied by physiologically active C
95 luence cortical reactivation by treating the cuneate nucleus with an enzyme, chondroitinase ABC, that
96 into the cuneate and, in one case, external cuneate nucleus within three months of the deafferentati
98 eus of the eighth nerve, nucleus Y, external cuneate nucleus, and lobules I, IV, V, IX, and X of the
99 , mesencephalic trigeminal nucleus, external cuneate nucleus, area postrema, and nucleus tractus soli
100 roduced anterograde labeling in the external cuneate nucleus, cuneate nucleus, nucleus X, central cer
101 lla, central amygdala, parabrachial nucleus, cuneate nucleus, nucleus tractus solitarii (NTS), parave
102 de labeling in the external cuneate nucleus, cuneate nucleus, nucleus X, central cervical nucleus, do
103 ate neurons could again be mapped within the cuneate nucleus, primarily in a region bordering the dep
104 also in other nuclei, including the external cuneate nucleus, the postpyramidal nucleus of the raphe,
105 l weeks following a unilateral lesion of the cuneate nucleus, the source of medial lemniscal (ML) axo
106 cal connection is known to exist between the cuneate nucleus, which is a first-order somatosensory nu
114 d primary afferents into the dorsal horn and cuneate nucleus; and 3) substantial although incomplete
117 ermined that the axonal projections from the cuneate region gave rise to mossy fiber terminals in the
118 ts from the hand form consistently organized cuneate representations that, in turn, relate to the par
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