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1 pital cortex, superior colliculi and lateral geniculate body).
2 la, the parabrachial nucleus, and the medial geniculate body.
3  the left acoustic radiation near the medial geniculate body.
4  not polysensory) subdivisions of the medial geniculate body.
5 on to A1, the ventral division of the medial geniculate body.
6 nsitive planum temporale and the left medial geniculate body.
7 ell as IC axon collaterals within the medial geniculate body.
8 us, and the medial subdivision of the medial geniculate body.
9 d the suprageniculate division of the medial geniculate body.
10 ) IPSPs in the ventral nucleus of the medial geniculate body.
11 s outside of the hypothalamus in the lateral geniculate body.
12 ns, in the dorsal division of the cat medial geniculate body.
13 the hypothalamus at the level of the lateral geniculate body.
14 djacent to the dorsal nucleus of the lateral geniculate body.
15 tion for the anterior nucleus, pulvinar, and geniculate bodies.
16 les in the optic tract overlying the lateral geniculate body and in the superior colliculus.
17 y connected cell pairs in the ventral medial geniculate body and primary auditory cortex.
18 erminal arbors are elaborated in the lateral geniculate body and superior colliculus and as myelinati
19 teral lemniscus, inferior colliculus, medial geniculate body, and auditory cortex all being in their
20 d neurons in the inferior colliculus, medial geniculate body, and auditory cortex.
21 gions (bilateral inferior colliculus, medial geniculate body, and primary and secondary auditory cort
22 olivary complex, inferior colliculus, medial geniculate body, and primary auditory cortex.
23 mporal cortices, inferior colliculus, medial geniculate body, and some of the nuclei of the superior
24  2 in the midbrain tegmental nuclei, lateral geniculate body, and thalamus for nonsmokers (n = 9) but
25 n site in the ventral division of the medial geniculate body as well as the anterogradely labeled tha
26  acidergic (GABAergic) neurons in the medial geniculate body, from <1% (bat and rat) to 25% or more (
27  0.07 in the anteroventral thalamus, lateral geniculate body, frontal cortex, and subiculum, respecti
28  include the anteroventral thalamus, lateral geniculate body, frontal cortex, subiculum, and cerebell
29 s from the inferior colliculus to the medial geniculate body in cats.
30 ojects to the auditory cortex via the medial geniculate body in the thalamus.
31    Post-training lesions of both the lateral geniculate body (LG) and lateral posterior nucleus (LP)
32                                   The medial geniculate body (MG) receives a large input from the ips
33 m the inferior colliculus (IC) to the medial geniculate body (MGB) and from the MGB to the auditory c
34 ex, but no detectable response in the medial geniculate body (MGB) and inferior colliculus (IC).
35  the inferior colliculus (IC) and the medial geniculate body (MGB) en route to the cortex.
36                                   The medial geniculate body (MGB) has three major subdivisions, vent
37 pite the functional importance of the medial geniculate body (MGB) in normal hearing, many aspects of
38 IC) to thalamocortical neurons of the medial geniculate body (MGB) in the rat.
39     However, the putative role of the medial geniculate body (MGB) in tinnitus has not been previousl
40                                   The medial geniculate body (MGB) integrates ascending inputs with d
41                                   The medial geniculate body (MGB) is a thalamic structure that is th
42                                   The medial geniculate body (MGB) is a thalamic structure that provi
43 w of auditory information through the medial geniculate body (MGB) is regulated, in part, by choliner
44 lus (IC), the ventral division of the medial geniculate body (MGB) of the thalamus, and the primary a
45 on of the projections from either the medial geniculate body (MGB) or primary auditory cortex (ACx) t
46 ity from the auditory cortex (AC) and medial geniculate body (MGB) simultaneously with electrical sti
47 ting sound with low modulation depth, medial geniculate body (MGB) single units show a switch from ad
48 c) inferior colliculus neurons to the media] geniculate body (MGB) was discovered in the cat using ax
49  of retrogradely labeled somas in the medial geniculate body (MGB) were examined as a function of the
50  of the brachium of the IC (BIN), the medial geniculate body (MGB), and the primary auditory cortex (
51 he first-order auditory thalamus, the medial geniculate body (MGB), is increased when rapidly varying
52 tions from the three subnuclei of the medial geniculate body (MGB), namely, its ventral (MGv), dorsal
53 roperties of CT axon terminals in the medial geniculate body (MGB), the auditory thalamus, in normal
54 Gv) and dorsal divisions (MGd) of the medial geniculate body (MGB), the reticular thalamic nucleus an
55 nferior colliculus (IC) inputs to the medial geniculate body (MGB).
56 activity in the auditory thalamus-the medial geniculate body (MGB).
57 r increase of GABAergic inhibition in medial geniculate body (MGB).
58 he human inferior colliculus (IC) and medial geniculate body (MGB).
59 rtex (AC) and its thalamic input, the medial geniculate body (MGB).
60 bitory neurotransmitter acting in the medial geniculate body (MGB).
61  function in auditory thalamus or the medial geniculate body (MGB).
62 of the auditory sensory thalamus, the medial geniculate body (MGB).
63 rom the ventral nucleus (MGBv) of the medial geniculate body (MGB).
64  originating in various nuclei of the medial geniculate body (MGB).
65 including the inferior colliculus and medial geniculate body (MGB).
66 were recorded from auditory thalamus [medial geniculate body (MGB)] of young awake, aged awake, young
67 n homeostasis, possibly convergent on medial geniculate body (MGB, auditory thalamus) and related neu
68 died learning-related activity in the medial geniculate body (MGB; Auditory thalamus), targeting main
69 ponses in the left auditory thalamus (medial geniculate body, MGB) during speech processing in contra
70  processing in the auditory thalamus (medial geniculate body, MGB) is poorly understood.
71 In particular, the auditory thalamus (medial geniculate body, MGB) response is modulated by speech re
72 e circuitry of the auditory thalamus (medial geniculate body, MGB).
73  modulation of the auditory thalamus (medial geniculate body; MGB): there are higher responses in lef
74 nother via the dorsal division of the medial geniculate body (MGBd) by analyzing the degree of recipr
75 e ventral and medial divisions of the medial geniculate body (MGBv and MGBm) respectively are the lem
76 e ventral and medial divisions of the medial geniculate body (MGBv and MGBm, respectively).
77 pose that the ventral division of the medial geniculate body (MGBv) is a single functionally homogeno
78 , but not the ventral division of the medial geniculate body (MGBv), in all experiments (n = 9).
79  nucleus (SG) and ventral division of medial geniculate body (MGBv), respectively.
80 eurons in the ventral division of the medial geniculate body (MGBv).
81  (A1) and the ventral division of the medial geniculate body (MGBv).
82 input from the ventral nucleus of the medial geniculate body (MGBv); whereas belt cortex receives pre
83 s, the ventral division of the rabbit medial geniculate body (MGV) has cellular laminae visible in ro
84 cers into the ventral division of the medial geniculate body (MGV) of both rats and rabbits labels te
85  units in the ventral division of the medial geniculate body (MGV) were characterized extracellularly
86  i.e., the ventral subdivision of the medial geniculate body (MGv).
87 ortex and the ventral division of the medial geniculate body (MGV).
88  sites in the ventral division of the medial geniculate body of New Zealand white rabbits.
89 d decarboxylase was undertaken in the medial geniculate body of the adult cat.
90  cells in the ventral division of the medial geniculate body of the rabbit.
91  mice - the inferior colliculus (IC), medial geniculate body of the thalamus (MGB) and primary audito
92 s observed in auditory cortex and the medial geniculate body of the thalamus in the absence of any ex
93 ntral and the dorsal divisions of the medial geniculate body of the thalamus, but they also branched
94                     In contrast, the lateral geniculate body of the visual system has about the same
95 e more rostral structures such as the medial geniculate body (P6) were prolonged 2h after NTG adminis
96 cleus and the ventral division of the medial geniculate body resulted in three distinct response clas
97 hich D-[3H]aspartate, injected in the medial geniculate body, retrogradely labeled neurons in the IC
98 he central auditory pathway, only the medial geniculate body shows this arrangement; the relative num
99                      In the bat, some medial geniculate body subdivisions have no GABAergic cells.
100 rences in inhibitory processing among medial geniculate body subdivisions.
101 beling was found ipsilaterally in the medial geniculate body, superior colliculus, and dorsolateral p
102 f the auditory thalamus including the medial geniculate body, suprageniculate nucleus, and reticular
103             Furthermore, cells in the medial geniculate body that had been retrogradely prelabeled wi
104 aris of the thalamus, the lateral and medial geniculate bodies, the basilar pontine nucleus, the hori
105 logical sections at the level of the lateral geniculate body, the cross-sectional area of each nucleu
106                               In the lateral geniculate body, the parvo laminae showed extensive mixi
107 and intralaminar thalamic nuclei, the medial geniculate body, the periaqueductal gray, the ventral te
108 at carry visual information from the lateral geniculate bodies to the visual cortex.
109 he medial and dorsal divisions of the medial geniculate body to the external nucleus of the ipsilater
110 sing from the ventral division of the medial geniculate body to the primary auditory cortex are also
111 The present findings demonstrate that medial geniculate body units from awake rats show an age-relate
112 rried out on sections containing the lateral geniculate body using [35S]-labeled antisense riboprobes
113 ocessing stages-the thalamus (ventral medial geniculate body (vMGB)), and thalamorecipient (L4) and s
114 eft primary sensory thalamus (ventral medial geniculate body; vMGB) is more involved when recognizing
115  12 auditory cortical fields onto the medial geniculate body was investigated in adult cats by using
116 n the three major subdivisions of the medial geniculate body were analyzed.
117 ted biotinylated dextran amine in the medial geniculate body were applied to these slices.
118 or colliculus project to parts of the medial geniculate body whose closest auditory affiliations are

 
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