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1 -Fuse, periaqueductal gray, and intermediate reticular nuclei).
2 ibular and red nucleus and pontine/medullary reticular nuclei.
3 al nucleus, and dorsal paragigantocellularis reticular nuclei.
4 d the rostral parvicellular and intermediate reticular nuclei.
5  by cholinergic neurons in several motor and reticular nuclei.
6 y tract and the dorsal and ventral medullary reticular nuclei, and in fibers and terminals of known p
7  second-order premotor neurons were found in reticular nuclei, and sensory trigeminal, auditory, vest
8 ior and lateral vestibular nuclei, brainstem reticular nuclei, and several cranial nerve motor nuclei
9 ental nuclei, locus coeruleus, raphe nuclei, reticular nuclei, and the nuclei of the trigeminal motor
10 , the periaqueductal gray, several brainstem reticular nuclei, and the nucleus of the solitary tract.
11 mulation evoked dopamine release in all four reticular nuclei, but not in the spinal cord.
12 d that the ventral medullary gigantocellular reticular nuclei (composed of the gigantocellular ventra
13 r cortex (M1) strongly innervates brain stem reticular nuclei containing whisker premotor neurons, wh
14 within raphe magnus (RM) and the neighboring reticular nuclei, contains serotonin and is the source o
15     Specifically, this complex of paramedian reticular nuclei has been implicated in the inhibition o
16                                     Nineteen reticular nuclei have spinal projections: reticularis (r
17 ramatic decrease in immunoreactivity in most reticular nuclei in the old cats.
18 l vestibular, abducens, cuneate, and lateral reticular nuclei, labeled neurons commingled with unlabe
19 interpeduncular nucleus, superior and middle reticular nuclei, magnocellular vestibular nucleus, soli
20 MDAR1 and C.O. staining, such as the pontine reticular nuclei, motor and mesencephalic nuclei of the
21               Computer modelling of thalamic reticular nuclei neurons indicated that the altered gati
22 trigeminal nucleus, infratrigeminal nucleus, reticular nuclei, nucleus raphe magnus, pontine blink pr
23 innervate reticulospinal neurons in the four reticular nuclei of lampreys.
24 gdala, hippocampal formation, paratenial and reticular nuclei of the thalamus, medial habenula, and z
25 teraction between neurons of the primary and reticular nuclei of the thalamus, resulting in rhythmic
26 forebrain, medial raphe nucleus, and pontine reticular nuclei (PRN).
27  ZI has strong connections between brainstem reticular nuclei, sensory nuclei, and nonspecific thalam
28 nervate cortex, but not in axons of thalamic reticular nuclei, striatal nuclei, or cortical neurons t
29 d region of medullary raphe and ventromedial reticular nuclei that project to all areas of the spinal
30 l pontine, ventral pontine, and oral pontine reticular nuclei; the dorsomedial tegmental, subpeduncul
31 re in the lateral thalamic nuclei, medullary reticular nuclei, vestibular nuclei, inferior olivary co
32 epam (CZP) are restricted to either relay or reticular nuclei, we show that the enhancement of intra-
33 c, monoaminergic, cholinergic, and classical reticular nuclei were affected with varying degrees of s
34        The parvicellular and gigantocellular reticular nuclei were not responsive to bombesin.
35 inergic neurons release dopamine in the four reticular nuclei where reticulospinal neurons are locate
36 paminergic source using tracer injections in reticular nuclei, which retrogradely labeled dopaminergi
37                 The large number of distinct reticular nuclei with spinal projections corroborates th