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1 ojecting from ipsilateral auditory thalamus (medial geniculate nucleus).
2 re principal neurons that can project to the medial geniculate nucleus.
3 ventral nucleus of the lateral lemniscus and medial geniculate nucleus.
4 reased metabolism in the caudate/putamen and medial geniculate nucleus.
5                           Within the ventral medial geniculate nucleus, a modular organization, revea
6 phic defects that alter projections from the medial geniculate nucleus and from the caudal ventrobasa
7 e amygdala via two routes: directly from the medial geniculate nucleus and indirectly from the audito
8  lemniscus and nucleus of lateral lemniscus, medial geniculate nucleus and inferior colliculus) had a
9 he auditory thalamus [medial division of the medial geniculate nucleus and the adjacent posterior int
10 rior nucleus, and the ventral portion of the medial geniculate nucleus) and higher-order (pulvinar an
11 cortical areas like the inferior colliculus, medial geniculate nucleus, and amygdala in response to t
12          In addition, inputs from the dorsal medial geniculate nucleus (dMGN) increase, whereas those
13 aptic connections, minimum amplitude ventral medial geniculate nucleus-evoked EPSCs were recorded.
14 ted structures included the caudate putamen, medial geniculate nucleus, lateral geniculate nucleus an
15            Male rats received lesions of the medial geniculate nucleus, lateral or central nuclei of
16                     However, ablation of the medial geniculate nucleus (MG) of the thalamus revealed
17 n of the dorsal and ventral divisions of the medial geniculate nucleus (MGd and MGv) and evoked by st
18  most numerous in the dorsal division of the medial geniculate nucleus (MGd; 32.9% of all labeled tha
19 activity (TIA) in the medial division of the medial geniculate nucleus (MGm).
20 in vitro in thalamocortical slices of A1 and medial geniculate nucleus (MGN) in mouse from postnatal
21 ral geniculate nucleus (LGN), but not in the medial geniculate nucleus (MGN) of rats that explore a n
22                 Synaptic transmission in the medial geniculate nucleus (MGN) to lateral nucleus of th
23 in the principal auditory relay nucleus, the medial geniculate nucleus (MGN), and principal visual re
24 riginate in the medial division (MGm) of the medial geniculate nucleus (MGN), the posterior intralami
25 lamus induces retinal axons to innervate the medial geniculate nucleus (MGN).
26 he dorsal superficial subdivision of the cat medial geniculate nucleus (MGN).
27 nal axons have been induced to innervate the medial geniculate nucleus (MGN).
28 ions in ferrets are induced to innervate the medial geniculate nucleus (MGN).
29 arallel thalamocortical projections from the medial geniculate nucleus (MGN).
30 l complex (VB; somatosensory system) and the medial geniculate nucleus (MGN; auditory system), using
31        Repetitive stimulation of the ventral medial geniculate nucleus (MGv) evoked robust short-term
32 lus (ICC) and the ventral subdivision of the medial geniculate nucleus (MGV) of male and female Mongo
33                  The ventral division of the medial geniculate nucleus (MGv) receives almost all of i
34 with the intensity of the stimulation in the medial geniculate nucleus (MGv).
35 s to neurons in the medial subnucleus of the medial geniculate nucleus (mMG) for changes of synaptic
36 g in the CNIC remain largely separate in the medial geniculate nucleus of the gerbil.
37                                          The medial geniculate nucleus of the thalamus (MGN) and the
38 d mainly in the inferior colliculus (IC) and medial geniculate nucleus, whereas glycine receptors wer