ライフサイエンスコーパス: zona incerta

1 he globus pallidus, subthalamic nucleus, and zona incerta.

2 input were mediated by GABA and activity in zona incerta.

3 ct to the caudate, the basis pontis, and the zona incerta.

4 thalamic area, dorsal hypothalamic area, and zona incerta.

5 butyric acid (GABA)-producing neurons of the zona incerta.

6 2R were found on dopaminergic neurons in the zona incerta.

7 the lateral and rostral PAG projected to the zona incerta.

8 nuclei of the thalamus, medial habenula, and zona incerta.

9 as low in the reticular thalamic nucleus and zona incerta.

10 ation and investigation nodes, including the zona incerta.

11 GCs, but not DRD4-DSGCs, also project to the zona incerta, a thalamic area not previously known to re

12 e ventromedial nucleus, arcuate nucleus, and zona incerta, all of which serve key roles in the neuron

13 Within the zona incerta, almost all the labelled neurons projected

14 A medial pathway innervates the zona incerta and dorsal hypothalamus (VLG and IGL); the

15 Neurons containing MCH are located in the zona incerta and in the lateral hypothalamus.

16 by medial hypothalamic areas as well as the zona incerta and projected to specific forebrain areas s

17 periaqueductal gray, caudal portions of the zona incerta and subparafascicular nucleus, and the late

18 w images for differentiation of STN from the zona incerta and substantia nigra, respectively, and was

19 nctional connections between the subthalamic zona incerta and thalamic reuniens (RE).

20 f labelled neurons were also observed in the zona incerta and the interstitial nucleus of the stria t

21 those rostral to this region, including the zona incerta and the pretectal nuclei, were labelled lar

22 nigra, inferior colliculus, locus coeruleus, zona incerta, and arcuate nucleus.

23 ipeduncular area, subparafascicular nucleus, zona incerta, and cuneiform area.

24 ion in the olfactory regions, dentate gyrus, zona incerta, and dorsal motor vagal nucleus.

25 erminalis, paraventricular thalamic nucleus, zona incerta, and medial subparaventricular zone, retrog

26 nucleus, ventral lateral geniculate nucleus, zona incerta, and nucleus of the fields of Forel) and of

27 example, inhibition from the basal ganglia, zona incerta, and pretectal regions, and chemical modula

28 lamus, including the posterior thalamus, the zona incerta, and the anterior pretectum.

29 ocessing, including the superior colliculus, zona incerta, and the visual and retrosplenial cortices.

30 he OMPFC also innervate the basal forebrain, zona incerta, and ventral midbrain.

31 d lateral geniculate nuclei of the thalamus; zona incerta; anterior, ventromedial, lateral, posterior

32 deep brain stimulation patients and identify zona incerta as a potential target for neuromodulation o

33 s), diencephalon (viz., subincertal nucleus, zona incerta as well as dorsal, dorsomedial, parafascicu

34 put to the superior colliculus (SC) from the zona incerta, as well as the organization of D1- and D2-

35 markably, the vgat l/vlPAG projection to the zona incerta bidirectionally controls approach towards f

36 tion of Lhx6-positive neurons in the ventral zona incerta bidirectionally regulate sleep time in adul

37 RE neurons act upstream of sleep-promoting zona incerta cells, and SD triggers plasticity of this c

38 oreactive neurons in the arcuate nucleus and zona incerta did not express Nurr1 mRNA.

39 roxylase-positive) neurons; however, <10% of zona incerta dopaminergic neurons (which are not hypophy

40 e in the magnocellular lateral hypothalamus, zona incerta dorsal, as well as the adjacent subthalamus

41 nd superior colliculus, and the subthalamus (zona incerta, fields of Forel) also project to the PHA.

42 mited area, which encompassed medial pole of zona incerta, Forel's field, and prerubral zone.

43 ted lesions and optogenetic manipulations of zona incerta GABAergic neurons during exploratory and go

44 Furthermore, zona incerta GABAergic neurons robustly code the occurre

45 othalamic groups (A12, A14), the prethalamic zona incerta group (A13), the preoptic groups (A15), and

46 The results showed that the zona incerta has a role in modulating the movement assoc

47 urred in other sites (e.g., suprageniculate, zona incerta, hypothalamic paraventricular n.).

48 ntred on the thalamus in seven cases, on the zona incerta in five cases and in the subthalamic nucleu

49 Stimulation of zona incerta in rodent models has been shown to modulate

50 amygdala, the lateral hypothalamus, and the zona incerta, interrupts the activity sequence pattern a

51 The zona incerta is a subthalamic nucleus made up mostly of

52 ld explain why deep brain stimulation of the zona incerta is beneficial to patients who suffer from P

53 mposed of the thalamic reticular nucleus and zona incerta, known to modulate thalamocortical communic

54 s, dopamine-containing cell region of medial zona incerta, lateral habenula, horizontal and vertical

55 were with the claustrum, reticular nucleus, zona incerta, lateral posterior and medial pulvinar nucl

56 neurons within the lateral hypothalamic area/zona incerta (LH) and the arcuate (Arc) nucleus.

57 supraoptic nucleus, paraventricular nucleus, zona incerta, medial and cortical amygdaloid nuclei, cer

58 region, a heterogeneous region of the medial zona incerta (mZI) containing dopaminergic, GABAergic, a

59 opamine (IHDA) neurons located in the medial zona incerta (MZI) project to the central nucleus of the

60 Zona incerta neurons distribute a broad corollary signal

61 To record the activity of zona incerta neurons during exploratory and cue-driven g

62 se few studies have measured the activity of zona incerta neurons in behaving animals under different

63 asalis of Meynert, medial habenular nucleus, zona incerta, neurosecretory arcuate nucleus, cranial mo

64 sensory cortex, paraventricular nucleus, and zona incerta; no regions were higher in maternal mice.

65 polaris, posteromedial thalamic, and ventral zona incerta nuclei, are only weakly modulated by touch.

66 subsequently targeted the caudal part of the zona incerta nucleus (cZI).

67 n of the pallidofugal fibres and the rostral zona incerta) or at the junction between the dorsal bord

68 paraventricular and posterior hypothalamus, zona incerta, periaqueductal gray, intermediate layers o

69 iative thalamic nuclei, superior colliculus, zona incerta, pontine nucleus, multiple other brainstem

70 imulated, with peak p values in superior STN/zona incerta (quantified bradykinesia), dorsal STN (mood

71 20 Hz, the physiological firing frequency of zona incerta, reduces experimental heat pain by a modest

72 By demonstrating that the zona incerta regulates communication between the superio

73 jections of the A13 region, highlighting the zona incerta's role as a crucial hub for the rapid selec

74 ients to directly investigate the effects of zona incerta stimulation on human pain perception.

75 brain, including those found in the medulla, zona incerta, substantia nigra or olfactory bulb, receiv

76 uclei of the hypothalamus; lateral habenula; zona incerta; substantia innominata; posterior thalamic

77 und in layer II of cortex, cingulate cortex, zona incerta, thalamus and hypothalamus.

78 amen, diagonal band, amygdala, hypothalamus, zona incerta, thalamus, periaqueductal gray, raphe nucle

79 rgic subpopulation of neurons in the ventral zona incerta that promote sleep.

80 edial and posterior hypothalamic nuclei, the zona incerta, the intergeniculate leaflet and the ventra

81 a, the hippocampus, the medial habenula, the zona incerta, the paraventricular and supraoptic nuclei

82 lar and reuniens nuclei of the thalamus, the zona incerta, the subthalamic nucleus, the central gray,

83 ic nuclei in the mammalian brain include the zona incerta, the ventral lateral geniculate nucleus, an

84 chiasmatic, and tuberal hypothalamic nuclei, zona incerta, ventral tegmental area, cerebellum (Purkin

85 l diagonal band/magnocellular preoptic area, zona incerta, ventromedial hypothalamus, lateral mammill

86 tical inhibition, we performed recordings in zona incerta, where 10, but not 40, Hz stimulation evoke

87 anterodorsal nucleus, lateral habenula, and zona incerta, where labeling was much more extensive tha

88 et of GABAergic neurons in the mouse ventral zona incerta, which express the LIM homeodomain factor L

89 on of somatostatin-expressing neurons in the zona incerta (ZI(SST)) of preweaning mice that responds

90 ), parafascicular nucleus (PF), ventromedial zona incerta (ZI) and at the border of the locus coerule

91 erminals from anterior pretectal nucleus and zona incerta (ZI) are each abundant in specific Po regio

92 The subthalamic nucleus (STN) and the zona incerta (ZI) are two major structures of the subtha

93 rt that ablation of dopamine (DA) neurons in zona incerta (ZI) but not ventral tegmental area potentl

94 ea that receives dense GABA projections from zona incerta (ZI) for the regulation of feeding behaviou

95 5-HT inhibits GABA release from zona incerta (ZI) GABA terminals in PVT.

96 e find that optogenetic stimulation of mouse zona incerta (ZI) gamma-aminobutyric acid (GABA) neurons

97 cleus (VPM), neurons of the ventral thalamus zona incerta (ZI) have been shown to exhibit multiwhiske

98 Zona incerta (ZI) is a largely inhibitory subthalamic re

99 The zona incerta (ZI) is a subcortical structure primarily i

100 The zona incerta (ZI) is involved in mediating survival beha

101 Afferents from the zona incerta (ZI) of the ventral thalamus contribute to

102 ssential for motor coordination, whereas the zona incerta (ZI) plays a key role in modulating sensori

103 We found that mouse zona incerta (ZI) projection neurons form a GABAergic ax

104 ith DBS of the ventro-oralis posterior (VOP)/zona incerta (ZI) region, and subsequently underwent bli

105 Transsynaptic labeling identifies zona incerta (ZI) to thalamic posterior medial nucleus p

106 ear generalization could be modulated by the zona incerta (ZI), a subthalamic brain region that influ

107 and terminates in the ventral region of the zona incerta (ZI), a subthalamic structure previously li

108 on of activity in the GABAergic nucleus, the zona incerta (ZI), and concomitant increased activity in

109 ntrast, the ETI (arising from basal ganglia, zona incerta (ZI), anterior pretectum, and pontine retic

110 located in the lateral hypothalamus (LH) and zona incerta (ZI), but MCHR1 mRNA is widely expressed th

111 AAV-orexin gene delivery into neurons of the zona incerta (ZI), or the lateral hypothalamus (LH) bloc

112 hibitory inputs from the subthalamic nucleus zona incerta (ZI), POm responses were of significantly h

113 eus, the posterior medial (POm) nucleus, the zona incerta (ZI), the reticular nucleus (nRT) of the th

114 responding neurons preferentially target the zona incerta (ZI), which suppresses the superior collicu

115 was found in a circumscribed portion of the zona incerta (ZI)-a region assigned to the hypothalamus

116 lidofugal fibres (H2 field of Forel) and the zona incerta (ZI).

117 velty seeking in monkeys is regulated by the zona incerta (ZI).

118 ir neurons), midline raphe (26%), LHA (22%), zona incerta (ZI, 15%), CeA (5%), paraventricular nucleu

119 colliculus terminated densely in the ventral zona incerta (ZIv), but did not overlap the labeled neur

120 ensory cortex (SSp) to the ventral sector of zona incerta (ZIv).