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1 al (but not polysensory) subdivisions of the medial geniculate body.
2 t station to A1, the ventral division of the medial geniculate body.
3 tion-sensitive planum temporale and the left medial geniculate body.
4 C, as well as IC axon collaterals within the medial geniculate body.
5  thalamus, and the medial subdivision of the medial geniculate body.
6 ulus and the suprageniculate division of the medial geniculate body.
7  GABA(B) IPSPs in the ventral nucleus of the medial geniculate body.
8 t origins, in the dorsal division of the cat medial geniculate body.
9 l medulla, the parabrachial nucleus, and the medial geniculate body.
10 ophy of the left acoustic radiation near the medial geniculate body.
11 tionally connected cell pairs in the ventral medial geniculate body and primary auditory cortex.
12 lex, lateral lemniscus, inferior colliculus, medial geniculate body, and auditory cortex all being in
13 ay-tuned neurons in the inferior colliculus, medial geniculate body, and auditory cortex.
14 rded regions (bilateral inferior colliculus, medial geniculate body, and primary and secondary audito
15 perior olivary complex, inferior colliculus, medial geniculate body, and primary auditory cortex.
16  and temporal cortices, inferior colliculus, medial geniculate body, and some of the nuclei of the su
17 njection site in the ventral division of the medial geniculate body as well as the anterogradely labe
18 butyric acidergic (GABAergic) neurons in the medial geniculate body, from <1% (bat and rat) to 25% or
19 n exists from the inferior colliculus to the medial geniculate body in cats.
20  and projects to the auditory cortex via the medial geniculate body in the thalamus.
21                                          The medial geniculate body (MG) receives a large input from
22 ons from the inferior colliculus (IC) to the medial geniculate body (MGB) and from the MGB to the aud
23 ry cortex, but no detectable response in the medial geniculate body (MGB) and inferior colliculus (IC
24 reaches the inferior colliculus (IC) and the medial geniculate body (MGB) en route to the cortex.
25                                          The medial geniculate body (MGB) has three major subdivision
26     Despite the functional importance of the medial geniculate body (MGB) in normal hearing, many asp
27 culus (IC) to thalamocortical neurons of the medial geniculate body (MGB) in the rat.
28            However, the putative role of the medial geniculate body (MGB) in tinnitus has not been pr
29                                          The medial geniculate body (MGB) integrates ascending inputs
30                                          The medial geniculate body (MGB) is a thalamic structure tha
31                                          The medial geniculate body (MGB) is a thalamic structure tha
32 The flow of auditory information through the medial geniculate body (MGB) is regulated, in part, by c
33 colliculus (IC), the ventral division of the medial geniculate body (MGB) of the thalamus, and the pr
34 nhibition of the projections from either the medial geniculate body (MGB) or primary auditory cortex
35 l activity from the auditory cortex (AC) and medial geniculate body (MGB) simultaneously with electri
36 t repeating sound with low modulation depth, medial geniculate body (MGB) single units show a switch
37 density of retrogradely labeled somas in the medial geniculate body (MGB) were examined as a function
38 nucleus of the brachium of the IC (BIN), the medial geniculate body (MGB), and the primary auditory c
39 se in the first-order auditory thalamus, the medial geniculate body (MGB), is increased when rapidly
40  projections from the three subnuclei of the medial geniculate body (MGB), namely, its ventral (MGv),
41 aptic properties of CT axon terminals in the medial geniculate body (MGB), the auditory thalamus, in
42 tral (MGv) and dorsal divisions (MGd) of the medial geniculate body (MGB), the reticular thalamic nuc
43 rease or increase of GABAergic inhibition in medial geniculate body (MGB).
44 amine the human inferior colliculus (IC) and medial geniculate body (MGB).
45 tory cortex (AC) and its thalamic input, the medial geniculate body (MGB).
46 or inhibitory neurotransmitter acting in the medial geniculate body (MGB).
47 ABA(A)R function in auditory thalamus or the medial geniculate body (MGB).
48 nction of the auditory sensory thalamus, the medial geniculate body (MGB).
49 input from the ventral nucleus (MGBv) of the medial geniculate body (MGB).
50 athways originating in various nuclei of the medial geniculate body (MGB).
51 ystem, including the inferior colliculus and medial geniculate body (MGB).
52 nsory inferior colliculus (IC) inputs to the medial geniculate body (MGB).
53 inated activity in the auditory thalamus-the medial geniculate body (MGB).
54  units were recorded from auditory thalamus [medial geniculate body (MGB)] of young awake, aged awake
55 hibition homeostasis, possibly convergent on medial geniculate body (MGB, auditory thalamus) and rela
56  We studied learning-related activity in the medial geniculate body (MGB; Auditory thalamus), targeti
57 ced responses in the left auditory thalamus (medial geniculate body, MGB) during speech processing in
58  signal processing in the auditory thalamus (medial geniculate body, MGB) is poorly understood.
59        In particular, the auditory thalamus (medial geniculate body, MGB) response is modulated by sp
60 thin the circuitry of the auditory thalamus (medial geniculate body, MGB).
61 nvolves modulation of the auditory thalamus (medial geniculate body; MGB): there are higher responses
62 C) to another via the dorsal division of the medial geniculate body (MGBd) by analyzing the degree of
63      The ventral and medial divisions of the medial geniculate body (MGBv and MGBm) respectively are
64 s in the ventral and medial divisions of the medial geniculate body (MGBv and MGBm, respectively).
65 mes propose that the ventral division of the medial geniculate body (MGBv) is a single functionally h
66 nucleus, but not the ventral division of the medial geniculate body (MGBv), in all experiments (n = 9
67 iculate nucleus (SG) and ventral division of medial geniculate body (MGBv), respectively.
68 es of neurons in the ventral division of the medial geniculate body (MGBv).
69  cortex (A1) and the ventral division of the medial geniculate body (MGBv).
70 ensory input from the ventral nucleus of the medial geniculate body (MGBv); whereas belt cortex recei
71  mammals, the ventral division of the rabbit medial geniculate body (MGV) has cellular laminae visibl
72 ade tracers into the ventral division of the medial geniculate body (MGV) of both rats and rabbits la
73  Single units in the ventral division of the medial geniculate body (MGV) were characterized extracel
74 vision, i.e., the ventral subdivision of the medial geniculate body (MGv).
75 ry neocortex and the ventral division of the medial geniculate body (MGV).
76 terized sites in the ventral division of the medial geniculate body of New Zealand white rabbits.
77 mic acid decarboxylase was undertaken in the medial geniculate body of the adult cat.
78 ties of cells in the ventral division of the medial geniculate body of the rabbit.
79 n awake mice - the inferior colliculus (IC), medial geniculate body of the thalamus (MGB) and primary
80 ivity is observed in auditory cortex and the medial geniculate body of the thalamus in the absence of
81  the ventral and the dorsal divisions of the medial geniculate body of the thalamus, but they also br
82 ) to the more rostral structures such as the medial geniculate body (P6) were prolonged 2h after NTG
83 dial nucleus and the ventral division of the medial geniculate body resulted in three distinct respon
84 ts in which D-[3H]aspartate, injected in the medial geniculate body, retrogradely labeled neurons in
85    In the central auditory pathway, only the medial geniculate body shows this arrangement; the relat
86                             In the bat, some medial geniculate body subdivisions have no GABAergic ce
87 e differences in inhibitory processing among medial geniculate body subdivisions.
88 fuse labeling was found ipsilaterally in the medial geniculate body, superior colliculus, and dorsola
89 sions of the auditory thalamus including the medial geniculate body, suprageniculate nucleus, and ret
90                    Furthermore, cells in the medial geniculate body that had been retrogradely prelab
91 reticularis of the thalamus, the lateral and medial geniculate bodies, the basilar pontine nucleus, t
92 idline and intralaminar thalamic nuclei, the medial geniculate body, the periaqueductal gray, the ven
93  from the medial and dorsal divisions of the medial geniculate body to the external nucleus of the ip
94 ons arising from the ventral division of the medial geniculate body to the primary auditory cortex ar
95        The present findings demonstrate that medial geniculate body units from awake rats show an age
96 tory processing stages-the thalamus (ventral medial geniculate body (vMGB)), and thalamorecipient (L4
97 t the left primary sensory thalamus (ventral medial geniculate body; vMGB) is more involved when reco
98 on from 12 auditory cortical fields onto the medial geniculate body was investigated in adult cats by
99 ation in the three major subdivisions of the medial geniculate body were analyzed.
100 conjugated biotinylated dextran amine in the medial geniculate body were applied to these slices.
101  inferior colliculus project to parts of the medial geniculate body whose closest auditory affiliatio

 
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