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1 cularly pronounced in the narrow part of the trapezoid.
2 s, however, cell-shape refinement results in trapezoids.
3 lot each matching region as colored lines or trapezoids.
4 rough a panel displaying local alignments as trapezoids.
5 distorts in polarizing environments, such as trapezoids.(26)(,)(27) If grid cells support distance es
9 incipal neurons of the medial nucleus of the trapezoid body (MNTB) and lateral superior olive (LSO);
10 ansmission between the medial nucleus of the trapezoid body (MNTB) and the lateral superior olive (LS
12 eld synapse in the rat medial nucleus of the trapezoid body (MNTB) are stimulated by the activation o
13 incipal neurons of the medial nucleus of the trapezoid body (MNTB) as a model system for examining vo
14 urons in the mammalian medial nucleus of the trapezoid body (MNTB) convey precise, faithful inhibitio
15 of Held synapse in the medial nucleus of the trapezoid body (MNTB) demonstrated strongly altered syna
16 incipal neurons of the medial nucleus of the trapezoid body (MNTB) express a spectrum of voltage-depe
19 f principal neurons in the medial nucleus of trapezoid body (MNTB) in preterm and term baboon brainst
21 neuron synapses at the medial nucleus of the trapezoid body (MNTB) in the auditory brainstem of male
22 zation of Kv1.3 in the medial nucleus of the trapezoid body (MNTB) in the auditory brainstem, a nucle
23 s such as those in the medial nucleus of the trapezoid body (MNTB) in the auditory brainstem, Kv3.1 p
25 gene expression in the medial nucleus of the trapezoid body (MNTB) in the brainstem during the critic
30 rogenitor cells in the medial nucleus of the trapezoid body (MNTB) located in the rat auditory brains
31 ordings were made from medial nucleus of the trapezoid body (MNTB) neurones during 1 s excitatory pos
32 in nAChR expression in medial nucleus of the trapezoid body (MNTB) neurons and presynaptic calyx of H
36 ic gradient within the medial nucleus of the trapezoid body (MNTB) of the auditory brainstem, where K
38 ated in neurons of the medial nucleus of the trapezoid body (MNTB) of the auditory system in the CNS.
39 of Held synapse in the medial nucleus of the trapezoid body (MNTB) of the rat auditory brainstem.
40 ct from the VCN to the medial nucleus of the trapezoid body (MNTB) on the contralateral, but not the
41 ormally project to the medial nucleus of the trapezoid body (MNTB) only on the contralateral side.
42 tory synapses from the medial nucleus of the trapezoid body (MNTB) onto medial olivocochlear (MOC) ne
43 es from neurons of the medial nucleus of the trapezoid body (MNTB) onto neurons of the lateral superi
44 napse in the mammalian medial nucleus of the trapezoid body (MNTB) plays an important role in sound l
45 ncipal neurones of the medial nucleus of the trapezoid body (MNTB) revealed a low-threshold dendrotox
46 or VCN (PVCN), and the medial nucleus of the trapezoid body (MNTB) shortly before the onset of sound-
47 ray recording from the medial nucleus of the trapezoid body (MNTB) showed longer latency and decrease
48 rgic inhibition to the medial nucleus of the trapezoid body (MNTB) specific to the tonotopic location
49 incipal neurons of the medial nucleus of the trapezoid body (MNTB) through the giant glutamatergic sy
50 incipal neurons in the medial nucleus of the trapezoid body (MNTB) to provide inhibition that is both
51 ation pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO
52 nergic inputs from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO
53 ergic pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO
54 ry projection from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO
55 ergic pathway from the medial nucleus of the trapezoid body (MNTB) to the LSO, while leaving the exci
56 incipal neurons of the medial nucleus of the trapezoid body (MNTB) was assessed in the context of the
57 ransmission to the rat medial nucleus of the trapezoid body (MNTB) was studied in an in vitro brain s
58 principal cells of the medial nucleus of the trapezoid body (MNTB) with NADPH-diaphorase histochemist
59 cal stimulation of the medial nucleus of the trapezoid body (MNTB), a known glycinergic projection in
60 utamate release in the medial nucleus of the trapezoid body (MNTB), an auditory brainstem nucleus cri
61 ainstem neurons in the medial nucleus of the trapezoid body (MNTB), and also impairs the functional r
62 ralateral ear, via the medial nucleus of the trapezoid body (MNTB), and excitatory input from the ips
63 ibitory input from the medial nucleus of the trapezoid body (MNTB), specific elimination and strength
64 rincipal neuron of the medial nucleus of the trapezoid body (MNTB), to examine the NMDAR-mediated EPS
65 slices containing the medial nucleus of the trapezoid body (MNTB), where neurons are topographically
66 nucleus (DCN) and the medial nucleus of the trapezoid body (MNTB), which project in two distinct aud
82 e medial, lateral, and ventral nuclei of the trapezoid body (MNTB, LNTB, and VNTB) were examined 14 d
84 including the rostral ventral nucleus of the trapezoid body (rVNTB) and ventrolateral parts of PnC or
85 (SPN), the ventral and lateral nuclei of the trapezoid body (VNTB and LNTB, respectively), and the ve
86 s from neurons of the ventral nucleus of the trapezoid body (VNTB), so control of neuronal excitabili
88 chlear neurons in the ventral nucleus of the trapezoid body and blocking cholinergic input to small c
89 ere identified in the ventral nucleus of the trapezoid body and documented with the light microscope
90 ted bilaterally in the medial nucleus of the trapezoid body and periolivary cell groups in the superi
91 y were located in the ventral nucleus of the trapezoid body and the anteroventral periolivary nucleus
92 riolivary nuclei, and lateral nucleus of the trapezoid body and the contralateral medial and ventral
95 s were located in the ventral nucleus of the trapezoid body and the ventral nucleus of the lateral le
97 ynaptic neurons of the medial nucleus of the trapezoid body at the mouse calyx of Held synapse expres
98 ate Ca(2+) influx into medial nucleus of the trapezoid body axon terminals, resulting in reduced syna
101 incipal neurons of the medial nucleus of the trapezoid body did not change after P14, indicating that
103 If plugged during adulthood, the thickest trapezoid body fibers also showed a decrease in myelin.
105 t of the contralateral medial nucleus of the trapezoid body following a cochlear ablation, even in th
106 ic transmission in the medial nucleus of the trapezoid body in cDKO was impeded during development an
109 munoreactivity in the lateral nucleus of the trapezoid body may be generalizable to other populations
112 incipal neurons in the medial nucleus of the trapezoid body showed that a rise from 25 degrees C to 3
113 the mammalian CNS: the medial nucleus of the trapezoid body to lateral superior olive glycinergic syn
117 ic innervation in the lateral nucleus of the trapezoid body were revealed in which glycine-immunoreac
118 e tonotopic map in the medial nucleus of the trapezoid body with neurons responding best to high-freq
120 cterize the development of myelin within the trapezoid body, a central auditory fiber tract, and dete
121 complex, the deep cerebellar nuclei, and the trapezoid body, a pattern that parallels the distributio
122 inal nucleus, and the ventral nucleus of the trapezoid body, also contained perikarya that synthesize
124 ons of the ipsilateral medial nucleus of the trapezoid body, and small multipolar neurons of the cont
125 ucleus, the medial and lateral nuclei of the trapezoid body, and the lateral superior olive, whereas
126 high frequency electrical stimulation of the trapezoid body, and we determined that the recovery proc
127 e calyx of Held in the medial nucleus of the trapezoid body, by the use of in vivo electrophysiology,
128 hree subnuclei of the lateral nucleus of the trapezoid body, called the posteroventral subnucleus.
129 and one of these, the lateral nucleus of the trapezoid body, contains cell bodies exhibiting a spectr
130 two subnuclei of the lateral nucleus of the trapezoid body, its main and hilus subnuclei, contained
131 ntralateral medial and ventral nuclei of the trapezoid body, lateral lemniscal nuclei, and inferior c
132 bcortical auditory nuclei (cochlear nucleus, trapezoid body, lateral lemniscus and nucleus of lateral
134 coustic information by the medial nucleus of trapezoid body, the most prominent source of inhibition
135 limited to, the deep cerebellar nuclei, the trapezoid body, the red nucleus, the oculomotor nucleus,
136 ding the contralateral medial nucleus of the trapezoid body, were beaded, en passant type terminal va
137 were traced into the ventral nucleus of the trapezoid body, where they were observed terminating on
155 n, human positional memory was degraded in a trapezoid environment compared with a square environment
156 rk, crease patterns composed of more general trapezoid faces are considered and their low-energy line
158 nal repositioning was raised consisting of a trapezoid flap with de-epithelialization of papillae, an
159 e auditory system, the medial nucleus of the trapezoid had a robust signal consistent with staining o
160 AUCs of OP and IVMP were determined by the trapezoid method; pharmacokinetic parameters were obtain
162 ld structures of various lengths, made up of trapezoid-shape capsomeres, provide a basis for icosahed
164 assic and CLS tapers feature deeply threaded trapezoid-shaped profiles with thread heights over 65 um