ライフサイエンスコーパス: deep cerebellar nuclei

1 ty of both Purkinje cells and neurons of the deep cerebellar nuclei.

2 g inhibition of cerebellar output neurons in deep cerebellar nuclei.

3 upts inhibition of the inferior olive by the deep cerebellar nuclei.

4 flexible selection of signals for output to deep cerebellar nuclei.

5 All injections labeled the deep cerebellar nuclei.

6 uced in Purkinje cells, but increased in the deep cerebellar nuclei.

7 otocols can drive synaptic plasticity in the deep cerebellar nuclei.

8 um without directly affecting neurons in the deep cerebellar nuclei.

9 stantia nigra pars reticulata, pallidum, and deep cerebellar nuclei.

10 enhanced hyperexcitability of neurons in the deep cerebellar nuclei.

11 sent in the olfactory bulb, red nucleus, and deep cerebellar nuclei.

12 es in the cerebellar cortex and in the lower deep cerebellar nuclei.

13 ulations vulnerable to weaver, including the deep cerebellar nuclei.

14 lum, it is expressed in Purkinje neurons and deep cerebellar nuclei.

15 ibular nuclei, inferior olivary complex, and deep cerebellar nuclei.

16 nsmission at synapses from Purkinje cells to deep cerebellar nuclei and at vestibular synapses in mic

17 onto discrete populations of neurons in the deep cerebellar nuclei and brainstem vestibular nuclei.

18 --'50/40 pS'--openings) in some patches from deep cerebellar nuclei and dorsal horn neurones.

19 amatergic premotor projection neurons in the deep cerebellar nuclei and GABAergic neurons that feed b

20 nuclei, and the rhombic lip, which generates deep cerebellar nuclei and granule cells.

21 ons from layers four and five of the cortex, deep cerebellar nuclei and other localized brain regions

22 clei, hypothalamus, midbrain, pons, medulla, deep cerebellar nuclei and spinal cord, with tau-immunor

23 The specific role of deep cerebellar nuclei and the cerebellar cortex in eyeb

24 localized to specific areas within both the deep cerebellar nuclei and the cerebellar cortex.

25 components simulating cerebellar cortex and deep cerebellar nuclei, and it received input from a mid

26 trogliosis and vacuolation of neurons in the deep cerebellar nuclei, and the severe vacuolation of th

27 basal forebrain, the vestibular complex, the deep cerebellar nuclei, and the trapezoid body, a patter

28 The projection neurons of the deep cerebellar nuclei are especially altered.

29 or motor recovery, and lesions affecting the deep cerebellar nuclei are not fully compensated at any

30 s onto a Purkinje cell or onto a cell in the deep cerebellar nuclei become eligible for plasticity on

31 Transduction was evident in the deep cerebellar nuclei, cerebellar Purkinje cells, the b

32 Results suggest that lateral deep cerebellar nuclei contribute to visuospatial proces

33 isinhibition of the cerebellar cortex on the deep cerebellar nuclei could treat oculopalatal tremor.

34 istributed among many unlabeled cells in the deep cerebellar nuclei (DCbN).

35 al lines of evidence have indicated that the deep cerebellar nuclei (DCN) are a site of memory storag

36 Neurons of deep cerebellar nuclei (DCN) are spontaneously active, a

37 The deep cerebellar nuclei (DCN) are the main output centers

38 The deep cerebellar nuclei (DCN) are the major output of the

39 In addition, we evaluated the use of the deep cerebellar nuclei (DCN) as a site for injection to

40 rat cerebellum, PNNs are found around large, deep cerebellar nuclei (DCN) neurons and Golgi neurons a

41 d the components of the neuropil in the four deep cerebellar nuclei (DCN) of the rat's brain.

42 Inhibitory projection neurons in the deep cerebellar nuclei (DCN) provide GABAergic input to

43 se, may be initiated by hyperexcitability of deep cerebellar nuclei (DCN) secondary to loss of inhibi

44 s within the mature fastigial pathway of the deep cerebellar nuclei (DCN), a region critical for bala

45 ween Purkinje neurons and the neurons of the deep cerebellar nuclei (DCN), a site that has been impli

46 reactive to several brain regions, including deep cerebellar nuclei (DCN), globus pallidus, and thala

47 requency bursting activity in neurons of the deep cerebellar nuclei (DCN), which comprise the bulk of

48 ination was examined with an emphasis on the deep cerebellar nuclei (DCN).

49 function is rebound firing in neurons of the deep cerebellar nuclei (DCN).

50 , posterior parietal cortex (area 5) and the deep cerebellar nuclei (DCN).

51 by including in our study the neurons of the deep cerebellar nuclei (DCN).

52 halamus, contralateral cerebellar cortex and deep cerebellar nuclei (FDR q < 0.05).

53 We conclude that the deep cerebellar nuclei have a bilateral movement represe

54 For example, in the deep cerebellar nuclei, Hebbian patterns of coincident s

55 ibuted between the cerebellar cortex and the deep cerebellar nuclei; (ii) the cerebellar cortex plays

56 importance of the cerebellar cortex and the deep cerebellar nuclei in eyeblink conditioning is uncle

57 of the parabrachial, lateral lemniscal, and deep cerebellar nuclei, in addition to cerebellar granul

58 k comprising the inferior olive, vermis, and deep cerebellar nuclei including the dentate nucleus dur

59 ons but strikingly similar to neurons in the deep cerebellar nuclei, indicating a common role for int

60 making microelectrode penetrations into the deep cerebellar nuclei (mainly nucleus interpositus) of

61 f vestibular signals from the vestibular and deep cerebellar nuclei may be important components of fu

62 nput that can be achieved in this way in the deep cerebellar nuclei may be particularly important to

63 uit, with relative increases in perfusion in deep cerebellar nuclei (medial, interposed, lateral), th

64 ed largely to the olfactory bulbs, midbrain, deep cerebellar nuclei, medulla, and spinal cord.

65 At synapses from Purkinje cells to deep cerebellar nuclei neurons (PC-->DCN), light- and el

66 ABAA receptor-mediated monosynaptic IPSPs in deep cerebellar nuclei neurons by stimulation of Purkinj

67 Unlike vestibular and deep cerebellar nuclei neurons, where a mixture of respo

68 r Purkinje cells (which possess NR1 and 2D), deep cerebellar nuclei (NR1, 2A, 2B and 2D) and spinal c

69 ollowing bilateral lesions targeting lateral deep cerebellar nuclei, rats were subjected to a bridge

70 nular cell layer, and loss of neurons in the deep cerebellar nuclei; spheroids and loss of myelinated

71 um and to pinpoint the exact location in the deep cerebellar nuclei that is necessary.

72 inclusions at atypical sites (e.g. thalamus, deep cerebellar nuclei) that are not typical for Lewy bo

73 TXN1 messenger RNA levels were >/=30% in the deep cerebellar nuclei, the cerebellar cortex, inferior

74 -sensitive neurons in the most medial of the deep cerebellar nuclei, the rostral fastigial nucleus, w

75 In the deep cerebellar nuclei, the temporal increases in PBR pa

76 indbrain, including, but not limited to, the deep cerebellar nuclei, the trapezoid body, the red nucl

77 coding of information also allows neurons of deep cerebellar nuclei to use a simple averaging mechani

78 glutamatergic neurons, namely neurons of the deep cerebellar nuclei, unipolar brush cells, and the la

79 luorescent protein (rAAV1.miS1eGFP) into the deep cerebellar nuclei using magnetic resonance imaging

80 iple brainstem motor nuclei, inferior olive, deep cerebellar nuclei, vestibular nuclear complex, nucl

81 cleus, oculomotor nucleus, substantia nigra, deep cerebellar nuclei, vestibular nucleus, and the thal

82 es prior to E12.5, with the exception of the deep cerebellar nuclei, we find that Math1 cells migrate

83 binding and AT2 receptor mRNA levels in the deep cerebellar nuclei were also not affected by 3-acety

84 etected in the putamen, globus pallidus, and deep cerebellar nuclei, where the most dense areas of 8B

85 ction of Purkinje-cell axon terminals in the deep cerebellar nuclei, whereas the dendritic trees grew

86 Purkinje cells target the deep cerebellar nuclei, which are the output of the cere