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1 al vestibular nucleus, cochlear complex, and gigantocellular and paragigantocellular nuclei of the re
2 cells compared to mouthbrooding females, and gigantocellular AVT cell size correlated with the number
3 numbers of parvocellular, magnocellular, and gigantocellular AVT cells in the preoptic area.
4 vulated females had larger magnocellular and gigantocellular cells compared to mouthbrooding females,
5 such as the subnucleus reticularis dorsalis, gigantocellular, dorsal paragigantocellular, lateral, pa
6 nsively include the brainstem parvocellular, gigantocellular, intermediate, and medullary (dorsal and
7  within the ventral gigantocellular nucleus, gigantocellular nucleus alpha, and medial reticular form
8  within the ventral gigantocellular nucleus, gigantocellular nucleus pars alpha, raphe obscurus, and
9 ion within raphe obscurus, raphe magnus, and gigantocellular nucleus pars alpha.
10 c reticular formation, median raphe, and the gigantocellular nucleus pars alpha.
11 c PS neurons were located within the ventral gigantocellular nucleus, gigantocellular nucleus alpha,
12 tral ventromedial medulla within the ventral gigantocellular nucleus, gigantocellular nucleus pars al
13  salivatory nucleus, A5 noradrenergic cells, gigantocellular nucleus, inferior olive, solitary tract
14 er, AVT-immunoreactive (IR) soma size in the gigantocellular POA (gPOA), but not in the magnocellular
15 l, intermediate, and rostral subdivisions of gigantocellular precentral cortex (areas 4c, 4i, and 4r)
16 indicate that features of AVT neurons in the gigantocellular preoptic area (gPOA) and axon varicositi
17 the raphe magnus and obscurus nuclei, in the gigantocellular region, in the caudal pedunculopontine a
18 es have suggested that the ventral medullary gigantocellular reticular nuclei (composed of the gigant
19                        The parvicellular and gigantocellular reticular nuclei were not responsive to
20          The pontine oral reticular nucleus, gigantocellular reticular nucleus (Gi) and dorsal paragi
21 ell bodies were localized exclusively to the gigantocellular reticular nucleus (Gi) of the rostral me
22                                    Medullary gigantocellular reticular nucleus (mGi) neurons have bee
23 ojections, many of them originating from the gigantocellular reticular nucleus (NRG), have been obser
24 as expressed in several large neurons of the gigantocellular reticular nucleus and the raphe magnus n
25 ease in the projection from the ipsilesional gigantocellular reticular nucleus in response to the inj
26 jections from cerebellar nuclei neurons onto gigantocellular reticular nucleus neurons, which might p
27 ions (secondary and primary motor cortex and gigantocellular reticular nucleus) and high-level cortic
28 ueductal gray, the nucleus raphe magnus, the gigantocellular reticular nucleus, and the nucleus of th
29 n the Botzinger region and caudal to it, the gigantocellular reticular nucleus, midline neurons and t
30 or neurons lying within the raphe magnus and gigantocellular reticular nucleus, pars alpha.
31 ith cardiorespiratory control, including the gigantocellular reticular nucleus, the lateral paragigan
32 estibular nucleus, the cochlear nucleus, the gigantocellular reticular nucleus, the motor trigeminal
33 the orbital frontal cortex, limbic thalamus, gigantocellular reticular nucleus, the somatosensory sys
34 l part of the periaqueductal gray matter and gigantocellular reticular nucleus, ventral part also sho
35 in an area extending from the central to the gigantocellular tegmental field and the periventricular
36 tocellular reticular nuclei (composed of the gigantocellular ventralis and pars alpha nuclei as well