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1 s, however, cell-shape refinement results in trapezoids.
2 lot each matching region as colored lines or trapezoids.
3 rough a panel displaying local alignments as trapezoids.
7 eld synapse in the rat medial nucleus of the trapezoid body (MNTB) are stimulated by the activation o
8 incipal neurons of the medial nucleus of the trapezoid body (MNTB) as a model system for examining vo
9 incipal neurons of the medial nucleus of the trapezoid body (MNTB) express a spectrum of voltage-depe
11 f principal neurons in the medial nucleus of trapezoid body (MNTB) in preterm and term baboon brainst
12 zation of Kv1.3 in the medial nucleus of the trapezoid body (MNTB) in the auditory brainstem, a nucle
13 s such as those in the medial nucleus of the trapezoid body (MNTB) in the auditory brainstem, Kv3.1 p
17 rogenitor cells in the medial nucleus of the trapezoid body (MNTB) located in the rat auditory brains
18 ordings were made from medial nucleus of the trapezoid body (MNTB) neurones during 1 s excitatory pos
20 ic gradient within the medial nucleus of the trapezoid body (MNTB) of the auditory brainstem, where K
22 ated in neurons of the medial nucleus of the trapezoid body (MNTB) of the auditory system in the CNS.
23 of Held synapse in the medial nucleus of the trapezoid body (MNTB) of the rat auditory brainstem.
24 ct from the VCN to the medial nucleus of the trapezoid body (MNTB) on the contralateral, but not the
25 ormally project to the medial nucleus of the trapezoid body (MNTB) only on the contralateral side.
26 es from neurons of the medial nucleus of the trapezoid body (MNTB) onto neurons of the lateral superi
27 napse in the mammalian medial nucleus of the trapezoid body (MNTB) plays an important role in sound l
28 ncipal neurones of the medial nucleus of the trapezoid body (MNTB) revealed a low-threshold dendrotox
29 or VCN (PVCN), and the medial nucleus of the trapezoid body (MNTB) shortly before the onset of sound-
30 ray recording from the medial nucleus of the trapezoid body (MNTB) showed longer latency and decrease
31 rgic inhibition to the medial nucleus of the trapezoid body (MNTB) specific to the tonotopic location
32 incipal neurons of the medial nucleus of the trapezoid body (MNTB) through the giant glutamatergic sy
33 incipal neurons in the medial nucleus of the trapezoid body (MNTB) to provide inhibition that is both
34 ergic pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO
35 ry projection from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO
36 ergic pathway from the medial nucleus of the trapezoid body (MNTB) to the LSO, while leaving the exci
37 incipal neurons of the medial nucleus of the trapezoid body (MNTB) was assessed in the context of the
38 ransmission to the rat medial nucleus of the trapezoid body (MNTB) was studied in an in vitro brain s
39 principal cells of the medial nucleus of the trapezoid body (MNTB) with NADPH-diaphorase histochemist
40 cal stimulation of the medial nucleus of the trapezoid body (MNTB), a known glycinergic projection in
41 ralateral ear, via the medial nucleus of the trapezoid body (MNTB), and excitatory input from the ips
42 ibitory input from the medial nucleus of the trapezoid body (MNTB), specific elimination and strength
43 rincipal neuron of the medial nucleus of the trapezoid body (MNTB), to examine the NMDAR-mediated EPS
44 nucleus (DCN) and the medial nucleus of the trapezoid body (MNTB), which project in two distinct aud
55 e medial, lateral, and ventral nuclei of the trapezoid body (MNTB, LNTB, and VNTB) were examined 14 d
57 including the rostral ventral nucleus of the trapezoid body (rVNTB) and ventrolateral parts of PnC or
58 (SPN), the ventral and lateral nuclei of the trapezoid body (VNTB and LNTB, respectively), and the ve
59 s from neurons of the ventral nucleus of the trapezoid body (VNTB), so control of neuronal excitabili
61 ere identified in the ventral nucleus of the trapezoid body and documented with the light microscope
62 ted bilaterally in the medial nucleus of the trapezoid body and periolivary cell groups in the superi
63 y were located in the ventral nucleus of the trapezoid body and the anteroventral periolivary nucleus
64 riolivary nuclei, and lateral nucleus of the trapezoid body and the contralateral medial and ventral
67 s were located in the ventral nucleus of the trapezoid body and the ventral nucleus of the lateral le
69 ynaptic neurons of the medial nucleus of the trapezoid body at the mouse calyx of Held synapse expres
72 incipal neurons of the medial nucleus of the trapezoid body did not change after P14, indicating that
74 If plugged during adulthood, the thickest trapezoid body fibers also showed a decrease in myelin.
76 t of the contralateral medial nucleus of the trapezoid body following a cochlear ablation, even in th
77 ic transmission in the medial nucleus of the trapezoid body in cDKO was impeded during development an
78 munoreactivity in the lateral nucleus of the trapezoid body may be generalizable to other populations
81 incipal neurons in the medial nucleus of the trapezoid body showed that a rise from 25 degrees C to 3
82 the mammalian CNS: the medial nucleus of the trapezoid body to lateral superior olive glycinergic syn
86 ic innervation in the lateral nucleus of the trapezoid body were revealed in which glycine-immunoreac
87 e tonotopic map in the medial nucleus of the trapezoid body with neurons responding best to high-freq
89 cterize the development of myelin within the trapezoid body, a central auditory fiber tract, and dete
90 complex, the deep cerebellar nuclei, and the trapezoid body, a pattern that parallels the distributio
91 inal nucleus, and the ventral nucleus of the trapezoid body, also contained perikarya that synthesize
93 ons of the ipsilateral medial nucleus of the trapezoid body, and small multipolar neurons of the cont
94 ucleus, the medial and lateral nuclei of the trapezoid body, and the lateral superior olive, whereas
95 high frequency electrical stimulation of the trapezoid body, and we determined that the recovery proc
96 e calyx of Held in the medial nucleus of the trapezoid body, by the use of in vivo electrophysiology,
97 hree subnuclei of the lateral nucleus of the trapezoid body, called the posteroventral subnucleus.
98 and one of these, the lateral nucleus of the trapezoid body, contains cell bodies exhibiting a spectr
99 two subnuclei of the lateral nucleus of the trapezoid body, its main and hilus subnuclei, contained
100 ntralateral medial and ventral nuclei of the trapezoid body, lateral lemniscal nuclei, and inferior c
101 bcortical auditory nuclei (cochlear nucleus, trapezoid body, lateral lemniscus and nucleus of lateral
102 limited to, the deep cerebellar nuclei, the trapezoid body, the red nucleus, the oculomotor nucleus,
103 ding the contralateral medial nucleus of the trapezoid body, were beaded, en passant type terminal va
104 were traced into the ventral nucleus of the trapezoid body, where they were observed terminating on
122 nal repositioning was raised consisting of a trapezoid flap with de-epithelialization of papillae, an
123 e auditory system, the medial nucleus of the trapezoid had a robust signal consistent with staining o
124 AUCs of OP and IVMP were determined by the trapezoid method; pharmacokinetic parameters were obtain
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