ライフサイエンスコーパス: medial geniculate body

1 t station to A1, the ventral division of the medial geniculate body.

2 C, as well as IC axon collaterals within the medial geniculate body.

3 thalamus, and the medial subdivision of the medial geniculate body.

4 ulus and the suprageniculate division of the medial geniculate body.

5 al (but not polysensory) subdivisions of the medial geniculate body.

6 t origins, in the dorsal division of the cat medial geniculate body.

7 l medulla, the parabrachial nucleus, and the medial geniculate body.

8 tionally connected cell pairs in the ventral medial geniculate body and primary auditory cortex.

9 ay-tuned neurons in the inferior colliculus, medial geniculate body, and auditory cortex.

10 perior olivary complex, inferior colliculus, medial geniculate body, and primary auditory cortex.

11 and temporal cortices, inferior colliculus, medial geniculate body, and some of the nuclei of the su

12 njection site in the ventral division of the medial geniculate body as well as the anterogradely labe

13 butyric acidergic (GABAergic) neurons in the medial geniculate body, from <1% (bat and rat) to 25% or

14 n exists from the inferior colliculus to the medial geniculate body in cats.

15 ons from the inferior colliculus (IC) to the medial geniculate body (MGB) and from the MGB to the aud

16 ry cortex, but no detectable response in the medial geniculate body (MGB) and inferior colliculus (IC

17 reaches the inferior colliculus (IC) and the medial geniculate body (MGB) en route to the cortex.

18 The medial geniculate body (MGB) has three major subdivision

19 Despite the functional importance of the medial geniculate body (MGB) in normal hearing, many asp

20 culus (IC) to thalamocortical neurons of the medial geniculate body (MGB) in the rat.

21 However, the putative role of the medial geniculate body (MGB) in tinnitus has not been pr

22 The medial geniculate body (MGB) is a thalamic structure tha

23 The medial geniculate body (MGB) is a thalamic structure tha

24 The flow of auditory information through the medial geniculate body (MGB) is regulated, in part, by c

25 colliculus (IC), the ventral division of the medial geniculate body (MGB) of the thalamus, and the pr

26 l activity from the auditory cortex (AC) and medial geniculate body (MGB) simultaneously with electri

27 density of retrogradely labeled somas in the medial geniculate body (MGB) were examined as a function

28 nucleus of the brachium of the IC (BIN), the medial geniculate body (MGB), and the primary auditory c

29 se in the first-order auditory thalamus, the medial geniculate body (MGB), is increased when rapidly

30 projections from the three subnuclei of the medial geniculate body (MGB), namely, its ventral (MGv),

31 tral (MGv) and dorsal divisions (MGd) of the medial geniculate body (MGB), the reticular thalamic nuc

32 amine the human inferior colliculus (IC) and medial geniculate body (MGB).

33 tory cortex (AC) and its thalamic input, the medial geniculate body (MGB).

34 or inhibitory neurotransmitter acting in the medial geniculate body (MGB).

35 ABA(A)R function in auditory thalamus or the medial geniculate body (MGB).

36 nction of the auditory sensory thalamus, the medial geniculate body (MGB).

37 input from the ventral nucleus (MGBv) of the medial geniculate body (MGB).

38 athways originating in various nuclei of the medial geniculate body (MGB).

39 ystem, including the inferior colliculus and medial geniculate body (MGB).

40 rease or increase of GABAergic inhibition in medial geniculate body (MGB).

41 units were recorded from auditory thalamus [medial geniculate body (MGB)] of young awake, aged awake

42 hibition homeostasis, possibly convergent on medial geniculate body (MGB, auditory thalamus) and rela

43 signal processing in the auditory thalamus (medial geniculate body, MGB) is poorly understood.

44 thin the circuitry of the auditory thalamus (medial geniculate body, MGB).

45 C) to another via the dorsal division of the medial geniculate body (MGBd) by analyzing the degree of

46 The ventral and medial divisions of the medial geniculate body (MGBv and MGBm) respectively are

47 s in the ventral and medial divisions of the medial geniculate body (MGBv and MGBm, respectively).

48 mes propose that the ventral division of the medial geniculate body (MGBv) is a single functionally h

49 nucleus, but not the ventral division of the medial geniculate body (MGBv), in all experiments (n = 9

50 iculate nucleus (SG) and ventral division of medial geniculate body (MGBv), respectively.

51 es of neurons in the ventral division of the medial geniculate body (MGBv).

52 cortex (A1) and the ventral division of the medial geniculate body (MGBv).

53 ensory input from the ventral nucleus of the medial geniculate body (MGBv); whereas belt cortex recei

54 mammals, the ventral division of the rabbit medial geniculate body (MGV) has cellular laminae visibl

55 ade tracers into the ventral division of the medial geniculate body (MGV) of both rats and rabbits la

56 Single units in the ventral division of the medial geniculate body (MGV) were characterized extracel

57 vision, i.e., the ventral subdivision of the medial geniculate body (MGv).

58 ry neocortex and the ventral division of the medial geniculate body (MGV).

59 terized sites in the ventral division of the medial geniculate body of New Zealand white rabbits.

60 mic acid decarboxylase was undertaken in the medial geniculate body of the adult cat.

61 ties of cells in the ventral division of the medial geniculate body of the rabbit.

62 the ventral and the dorsal divisions of the medial geniculate body of the thalamus, but they also br

63 ) to the more rostral structures such as the medial geniculate body (P6) were prolonged 2h after NTG

64 dial nucleus and the ventral division of the medial geniculate body resulted in three distinct respon

65 ts in which D-[3H]aspartate, injected in the medial geniculate body, retrogradely labeled neurons in

66 In the central auditory pathway, only the medial geniculate body shows this arrangement; the relat

67 In the bat, some medial geniculate body subdivisions have no GABAergic ce

68 e differences in inhibitory processing among medial geniculate body subdivisions.

69 fuse labeling was found ipsilaterally in the medial geniculate body, superior colliculus, and dorsola

70 sions of the auditory thalamus including the medial geniculate body, suprageniculate nucleus, and ret

71 Furthermore, cells in the medial geniculate body that had been retrogradely prelab

72 reticularis of the thalamus, the lateral and medial geniculate bodies, the basilar pontine nucleus, t

73 idline and intralaminar thalamic nuclei, the medial geniculate body, the periaqueductal gray, the ven

74 from the medial and dorsal divisions of the medial geniculate body to the external nucleus of the ip

75 ons arising from the ventral division of the medial geniculate body to the primary auditory cortex ar

76 The present findings demonstrate that medial geniculate body units from awake rats show an age

77 on from 12 auditory cortical fields onto the medial geniculate body was investigated in adult cats by

78 ation in the three major subdivisions of the medial geniculate body were analyzed.

79 conjugated biotinylated dextran amine in the medial geniculate body were applied to these slices.

80 inferior colliculus project to parts of the medial geniculate body whose closest auditory affiliatio