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1 iaqueductal and pontine gray matter, and the red nucleus.
2 nd motor structures, including contralateral red nucleus.
3 as paired with electrical stimulation of the red nucleus.
4 rm, dorsal tenia tecta, bed nucleus, and the red nucleus.
5 dle cerebellar peduncle or the contralateral red nucleus.
6 ssion in the cerebellum, locus ceruleus, and red nucleus.
7 ncentrate in the ventrolateral region of the red nucleus.
8 brain nuclei: the oculomotor complex and the red nucleus.
9 ing inputs to motor signal generation in the red nucleus.
10 aration in the absence of the cerebellum and red nucleus.
11  substantia nigra (0.25% increase, P = .01), red nucleus (0.25% increase, P = .01), cerebellar pedunc
12 A in the substantia nigra (-45%; p < 0.001), red nucleus (-31%; p = 0.03), and locus coeruleus (-17%;
13 th controls in the putamen (-74%; P = .025), red nucleus (-61%; P = .018), and entire basal ganglia s
14                                          The red nucleus, a large brainstem structure, coordinates li
15 ddress this, we recorded from neurons in the red nucleus, a motor region thought to be important for
16 her nuclear output neurons projecting to the red nucleus also collateralize to the cerebellar cortex,
17 conditioned responses to be elicited via the red nucleus and accessory abducens motorneurons.
18 homogeneous excitatory SPNs from the cortex, red nucleus and cerebellum with somatotopic spinal termi
19 dbrain that was located ventrolateral to the red nucleus and corresponded to the SNc.
20             Ventral striatum Ki was 81% with red nucleus and globus pallidus Ki values of approximate
21 taucipir correlated with tau lesion score in red nucleus and midbrain tegmentum across patients, but
22 ial arc rostrally coordinately move both the red nucleus and oculomotor complex anlagen.
23 ely parallel inductions or expansions of the red nucleus and oculomotor complex primordia.
24 s well as in the hippocampus, dentate gyrus, red nucleus and pontine nucleus.
25 ating somatic muscle, lateral vestibular and red nucleus and pontine/medullary reticular nuclei.
26 nd extended to the pedunculopontine nucleus, red nucleus and subthalamic nucleus.
27 he axonal restructuring on the de-afferented red nucleus and the denervated spinal motoneurons (p<0.0
28 s the midline to innervate the contralateral red nucleus and the ipsilateral cervical spinal cord; th
29 oticed in the lateral vestibular nuclei, the red nucleus and the motor cortex whose spinal projection
30 e emergence of a de novo circuit between the red nucleus and the nucleus raphe magnus.
31 al ventral midbrain, which extended over the red nucleus and the substantia nigra.
32 l motor structures (basal ganglia, thalamus, red nucleus, and cerebellum; Cohen d >1) consistent with
33 eactivity was present in the olfactory bulb, red nucleus, and deep cerebellar nuclei.
34 tamen, globus pallidus, subthalamic nucleus, red nucleus, and midbrain.
35  and iron deposition in the globus pallidus, red nucleus, and substantia nigra.
36 ficantly less iron deposition in the GP, SN, red nucleus, and temporal cortex.
37 trigeminal ganglia, the medial habenula, the red nucleus, and the caudal region of the inferior oliva
38 he paraventricular hypothalamic nucleus, the red nucleus, and the motor cortex.
39 t are not courting: interpeduncular nucleus, red nucleus, and ventrolateral thalamus (VL).
40  the cerebellum and its connections with the red nucleus are essential for the acquisition of the con
41                                Although some red nucleus cells were also filled, they were only singl
42 in the posterior thalamus, substantia nigra, red nucleus, cerebellar peduncle, colliculi, dentate nuc
43 apparent susceptibility was increased in the red nucleus compared to all other groups, and in globus
44 site of sciatic nerve inoculation and in the red nucleus contralateral to HY TME inoculation.
45    Collectively, these findings suggest that red nucleus contributes to modulating motor behavior dur
46 r colliculus, dentate gyrus (increases), and red nucleus (decreases).
47  of the medial arc to oculomotor complex and red nucleus development by perturbing arc pattern format
48 ebellum, the substantia nigra pars compacta, red nucleus, dorsal motor nucleus of X cranial nerve, an
49 nitors generates a cohort that populates the red nucleus, Edinger Westphal nucleus, and supraoculomot
50 k, Slick is expressed in the olfactory bulb, red nucleus, facial nucleus, pontine nucleus, oculomotor
51 es (n > 14,000 studies) to precisely examine red nucleus function.
52                                     Notably, red nucleus functional connectivity with motor-effector
53                Our results suggest the human red nucleus implements goal-directed behavior by integra
54  the involvement of the interpositus and the red nucleus in extinction.
55  the cerebral cortex, in pons nuclei, in the red nucleus, in all cranial nerve nuclei, in the cerebel
56 e development of sensory ganglia, as well as red nucleus, inferior olive, and nucleus ambiguus.
57  of dopamine neurons directly underneath the red nucleus is considered a VTA region in humans but is
58 that a direct cerebral cortical input to the red nucleus is present only in the rat.
59 ere also increased in several brain regions (red nucleus, lateral geniculate nucleus, and cerebral co
60                                          The red nucleus, lateral reticular nucleus and cerebellum la
61 we investigated the effect of cerebellar and red nucleus lesions on the acquisition, extinction, and
62 otor projection density, suggesting that the red nucleus may contribute to functional recovery after
63 the corticospinal system in establishing the red nucleus motor map and rubrospinal tract connections.
64 nigra (n = 13), posterior thalamus (n = 12), red nucleus (n = 10), colliculi (n = 10), superior cereb
65  in vivo, but has no effect on oculomotor or red nucleus neurogenesis.
66 ebellorubral system, they differ in that the red nucleus of rats receives direct input from the motor
67  present study examined the circuitry of the red nucleus of the Sprague-Dawley rat and the freshwater
68 ding projection from the hypothalamus to the red nucleus of turtles has been described.
69 l neurons were higher than in neurons of the red nucleus or cranial nerve nuclei, but similar values
70 P = 0.04) and with astrocytic lesions in the red nucleus (P = 0.05).
71 lobus pallidus interna, subthalamic nucleus, red nucleus, periaqueductal gray, and locus coeruleus di
72 projected to the wFMNs: superior colliculus, red nucleus, periaqueductal gray, mesencephalon, pons, a
73 aratrochlear nucleus, paralemniscal nucleus, red nucleus, pontine nuclei, inferior colliculus and the
74 ergic neurons are greatly reduced in number, red nucleus precursors disappear from the ventral midbra
75 ia nigra (SNc), dentate and caudate nucleus, red nucleus, putamen and globus pallidus by T2* MRI at b
76 th volumes of putamen (r = -0.63, P < .001), red nucleus (r = -0.58, P = .001), globus pallidus (r =
77  ventral tegmental area, oculomotor nucleus, red nucleus, raphe nuclei, periaqueductal gray, locus co
78                    Consistent with this, the red nucleus responds to motor planning more than to actu
79 ons located in the magnocellular part of the red nucleus (RMC), a cell group that participates in bot
80                                          The red nucleus (RN) and rubrospinal tract (RST) are importa
81  in the spinal trigeminal nucleus (TRIG) and red nucleus (RN) increased as a positive function of sti
82  Histology confirmed that stimulation in the red nucleus (RN) inhibited RO profoundly.
83                                          The red nucleus (RN) is a midbrain premotor center that has
84                                          The red nucleus (RN) is essential for motor coordination, wh
85 more retrogradely labeled right (axotomized) red nucleus (RN) neurons were seen in Ch'ase ABC-treated
86 e robust increase in c-fos expression in the red nucleus (RN) than in other brain regions.
87 ynthase (nNOS) in opposition to those in the red nucleus (RN) that constitutively expresses nNOS.
88 ess this, we characterized neural signals in red nucleus (RN), a brain region linked to motor control
89                                          The red nucleus (RN), source of the rubrospinal tract, has b
90  show for the first time that the infant rat red nucleus (RN)-a brainstem sensorimotor structure-exhi
91 he corticorubral projection that reaches the red nucleus (RN).
92 romic activation from facial nucleus (FN) or red nucleus (RN).
93                            The magnocellular red nucleus (RNm), a brainstem premotor structure, is a
94 e their motor functions and, in turn, if the red nucleus/rubrospinal tract (RN/RST) compensates for d
95 lar formation, precerebellar nuclei, and the red nucleus (stage 2).
96 paraventricular thal n), the interpeduncular red nucleus, substantia nigra, parabrachial n; locus coe
97  specific (white matter, midbrain peduncles, red nucleus, temporal cortex) and correlated with change
98  to a common brain circuit with nodes in the red nucleus, thalamus, globus pallidus, and cerebellum.
99  ventrolateral thalamus and subnuclei of the red nucleus that were made from these same cases.
100  was five times that of controls, and in the red nucleus the number of contralaterally projecting axo
101 me cases, they were limited primarily to the red nucleus, the medullary raphe, and the adjacent retic
102 p cerebellar nuclei, the trapezoid body, the red nucleus, the oculomotor nucleus, the vestibular nucl
103      Among labeled neurons were those of the red nucleus, the vestibular nuclei, reticular formation,
104 al peduncle; the thalamus; the region of the red nucleus; the location of the central tegmental tract
105 oach, avoiding potential confounds of direct red nucleus-to-cerebellum projections.
106                                 We show that red nucleus tracks motor plans and that selectivity was
107 hs, 0.23 +/- 0.09; P < .001) and thalamus to red nucleus tract (mean number of tracts at baseline, 16
108 in the ablation core and in the thalamus and red nucleus tract, and a correlation between preablation
109                                 Finally, the red nucleus, which receives descending inputs from motor
110 w levels of [(18) F]Nifene binding while the red nucleus with alpha2beta2 nAChR had DVR approximately

 
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