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1 pital cortex, superior colliculi and lateral geniculate body).
2 on to A1, the ventral division of the medial geniculate body.
3 ell as IC axon collaterals within the medial geniculate body.
4 us, and the medial subdivision of the medial geniculate body.
5 not polysensory) subdivisions of the medial geniculate body.
6 d the suprageniculate division of the medial geniculate body.
7 s outside of the hypothalamus in the lateral geniculate body.
8 ns, in the dorsal division of the cat medial geniculate body.
9 the hypothalamus at the level of the lateral geniculate body.
10 djacent to the dorsal nucleus of the lateral geniculate body.
11 la, the parabrachial nucleus, and the medial geniculate body.
12 tion for the anterior nucleus, pulvinar, and geniculate bodies.
15 erminal arbors are elaborated in the lateral geniculate body and superior colliculus and as myelinati
18 mporal cortices, inferior colliculus, medial geniculate body, and some of the nuclei of the superior
19 2 in the midbrain tegmental nuclei, lateral geniculate body, and thalamus for nonsmokers (n = 9) but
20 n site in the ventral division of the medial geniculate body as well as the anterogradely labeled tha
21 acidergic (GABAergic) neurons in the medial geniculate body, from <1% (bat and rat) to 25% or more (
22 0.07 in the anteroventral thalamus, lateral geniculate body, frontal cortex, and subiculum, respecti
23 include the anteroventral thalamus, lateral geniculate body, frontal cortex, subiculum, and cerebell
25 Post-training lesions of both the lateral geniculate body (LG) and lateral posterior nucleus (LP)
26 m the inferior colliculus (IC) to the medial geniculate body (MGB) and from the MGB to the auditory c
30 pite the functional importance of the medial geniculate body (MGB) in normal hearing, many aspects of
32 However, the putative role of the medial geniculate body (MGB) in tinnitus has not been previousl
35 w of auditory information through the medial geniculate body (MGB) is regulated, in part, by choliner
36 lus (IC), the ventral division of the medial geniculate body (MGB) of the thalamus, and the primary a
37 ity from the auditory cortex (AC) and medial geniculate body (MGB) simultaneously with electrical sti
38 c) inferior colliculus neurons to the media] geniculate body (MGB) was discovered in the cat using ax
39 of retrogradely labeled somas in the medial geniculate body (MGB) were examined as a function of the
40 of the brachium of the IC (BIN), the medial geniculate body (MGB), and the primary auditory cortex (
41 he first-order auditory thalamus, the medial geniculate body (MGB), is increased when rapidly varying
42 tions from the three subnuclei of the medial geniculate body (MGB), namely, its ventral (MGv), dorsal
43 Gv) and dorsal divisions (MGd) of the medial geniculate body (MGB), the reticular thalamic nucleus an
53 were recorded from auditory thalamus [medial geniculate body (MGB)] of young awake, aged awake, young
54 n homeostasis, possibly convergent on medial geniculate body (MGB, auditory thalamus) and related neu
57 nother via the dorsal division of the medial geniculate body (MGBd) by analyzing the degree of recipr
58 e ventral and medial divisions of the medial geniculate body (MGBv and MGBm) respectively are the lem
60 pose that the ventral division of the medial geniculate body (MGBv) is a single functionally homogeno
65 input from the ventral nucleus of the medial geniculate body (MGBv); whereas belt cortex receives pre
66 s, the ventral division of the rabbit medial geniculate body (MGV) has cellular laminae visible in ro
67 cers into the ventral division of the medial geniculate body (MGV) of both rats and rabbits labels te
68 units in the ventral division of the medial geniculate body (MGV) were characterized extracellularly
74 ntral and the dorsal divisions of the medial geniculate body of the thalamus, but they also branched
76 e more rostral structures such as the medial geniculate body (P6) were prolonged 2h after NTG adminis
77 cleus and the ventral division of the medial geniculate body resulted in three distinct response clas
78 hich D-[3H]aspartate, injected in the medial geniculate body, retrogradely labeled neurons in the IC
79 he central auditory pathway, only the medial geniculate body shows this arrangement; the relative num
82 beling was found ipsilaterally in the medial geniculate body, superior colliculus, and dorsolateral p
83 f the auditory thalamus including the medial geniculate body, suprageniculate nucleus, and reticular
85 aris of the thalamus, the lateral and medial geniculate bodies, the basilar pontine nucleus, the hori
86 logical sections at the level of the lateral geniculate body, the cross-sectional area of each nucleu
88 and intralaminar thalamic nuclei, the medial geniculate body, the periaqueductal gray, the ventral te
89 he medial and dorsal divisions of the medial geniculate body to the external nucleus of the ipsilater
90 sing from the ventral division of the medial geniculate body to the primary auditory cortex are also
91 The present findings demonstrate that medial geniculate body units from awake rats show an age-relate
92 rried out on sections containing the lateral geniculate body using [35S]-labeled antisense riboprobes
93 12 auditory cortical fields onto the medial geniculate body was investigated in adult cats by using
96 or colliculus project to parts of the medial geniculate body whose closest auditory affiliations are
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