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1 reased metabolism in the caudate/putamen and medial geniculate nucleus.
2 ventral nucleus of the lateral lemniscus and medial geniculate nucleus.
3 phic defects that alter projections from the medial geniculate nucleus and from the caudal ventrobasa
4 e amygdala via two routes: directly from the medial geniculate nucleus and indirectly from the audito
5 lemniscus and nucleus of lateral lemniscus, medial geniculate nucleus and inferior colliculus) had a
6 he auditory thalamus [medial division of the medial geniculate nucleus and the adjacent posterior int
7 rior nucleus, and the ventral portion of the medial geniculate nucleus) and higher-order (pulvinar an
9 aptic connections, minimum amplitude ventral medial geniculate nucleus-evoked EPSCs were recorded.
10 ted structures included the caudate putamen, medial geniculate nucleus, lateral geniculate nucleus an
13 n of the dorsal and ventral divisions of the medial geniculate nucleus (MGd and MGv) and evoked by st
14 most numerous in the dorsal division of the medial geniculate nucleus (MGd; 32.9% of all labeled tha
16 in vitro in thalamocortical slices of A1 and medial geniculate nucleus (MGN) in mouse from postnatal
17 ral geniculate nucleus (LGN), but not in the medial geniculate nucleus (MGN) of rats that explore a n
19 in the principal auditory relay nucleus, the medial geniculate nucleus (MGN), and principal visual re
20 riginate in the medial division (MGm) of the medial geniculate nucleus (MGN), the posterior intralami
29 s to neurons in the medial subnucleus of the medial geniculate nucleus (mMG) for changes of synaptic
32 d mainly in the inferior colliculus (IC) and medial geniculate nucleus, whereas glycine receptors wer
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