ライフサイエンスコーパス: incerta

1 and investigation nodes, including the zona incerta.

2 obus pallidus, subthalamic nucleus, and zona incerta.

3 t were mediated by GABA and activity in zona incerta.

4 the caudate, the basis pontis, and the zona incerta.

5 mic area, dorsal hypothalamic area, and zona incerta.

6 ic acid (GABA)-producing neurons of the zona incerta.

7 re found on dopaminergic neurons in the zona incerta.

8 ateral and rostral PAG projected to the zona incerta.

9 i of the thalamus, medial habenula, and zona incerta.

10 w in the reticular thalamic nucleus and zona incerta.

11 is clearly revealed one unique candidate, C. incerta.

12 but not DRD4-DSGCs, also project to the zona incerta, a thalamic area not previously known to receive

13 tromedial nucleus, arcuate nucleus, and zona incerta, all of which serve key roles in the neuronal ci

14 Within the zona incerta, almost all the labelled neurons projected to th

15 ilar gene contents, although the 129.2 Mb C. incerta and 130.2 Mb C. schloesseri assemblies are more

16 ons and structure are likely conserved in C. incerta and C. schloesseri.

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

18 urons containing MCH are located in the zona incerta and in the lateral hypothalamus.

19 edial hypothalamic areas as well as the zona incerta and projected to specific forebrain areas such a

20 aqueductal gray, caudal portions of the zona incerta and subparafascicular nucleus, and the lateral p

21 ges for differentiation of STN from the zona incerta and substantia nigra, respectively, and was 22.7

22 nal connections between the subthalamic zona incerta and thalamic reuniens (RE).

23 elled neurons were also observed in the zona incerta and the interstitial nucleus of the stria termin

24 e rostral to this region, including the zona incerta and the pretectal nuclei, were labelled largely

25 , inferior colliculus, locus coeruleus, zona incerta, and arcuate nucleus.

26 ncular area, subparafascicular nucleus, zona incerta, and cuneiform area.

27 n the olfactory regions, dentate gyrus, zona incerta, and dorsal motor vagal nucleus.

28 alis, paraventricular thalamic nucleus, zona incerta, and medial subparaventricular zone, retrogradel

29 us, ventral lateral geniculate nucleus, zona incerta, and nucleus of the fields of Forel) and of epit

30 ple, inhibition from the basal ganglia, zona incerta, and pretectal regions, and chemical modulation

31 , including the posterior thalamus, the zona incerta, and the anterior pretectum.

32 ing, including the superior colliculus, zona incerta, and the visual and retrosplenial cortices.

33 PFC also innervate the basal forebrain, zona incerta, and ventral midbrain.

34 eral geniculate nuclei of the thalamus; zona incerta; anterior, ventromedial, lateral, posterior, sup

35 brain stimulation patients and identify zona incerta as a potential target for neuromodulation of pai

36 iencephalon (viz., subincertal nucleus, zona incerta as well as dorsal, dorsomedial, parafascicular,

37 o the superior colliculus (SC) from the zona incerta, as well as the organization of D1- and D2-recep

38 bly, the vgat l/vlPAG projection to the zona incerta bidirectionally controls approach towards food l

39 of Lhx6-positive neurons in the ventral zona incerta bidirectionally regulate sleep time in adult mic

40 ur Chlamydomonas species (C. reinhardtii, C. incerta, C. moewusii and C. eugametos) and five independ

41 monas reinhardtii (CC-621) and Chlamydomonas incerta (CC-1870/3871)-that these modules are prone to m

42 neurons act upstream of sleep-promoting zona incerta cells, and SD triggers plasticity of this circui

43 ular C. reinhardtii relatives: Chlamydomonas incerta, Chlamydomonas schloesseri, and the more distant

44 tive neurons in the arcuate nucleus and zona incerta did not express Nurr1 mRNA.

45 ase-positive) neurons; however, <10% of zona incerta dopaminergic neurons (which are not hypophysiotr

46 the magnocellular lateral hypothalamus, zona incerta dorsal, as well as the adjacent subthalamus in t

47 perior colliculus, and the subthalamus (zona incerta, fields of Forel) also project to the PHA.

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

49 esions and optogenetic manipulations of zona incerta GABAergic neurons during exploratory and goal-di

50 Furthermore, zona incerta GABAergic neurons robustly code the occurrence o

51 amic groups (A12, A14), the prethalamic zona incerta group (A13), the preoptic groups (A15), and the

52 The results showed that the zona incerta has a role in modulating the movement associated

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

54 on the thalamus in seven cases, on the zona incerta in five cases and in the subthalamic nucleus in

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

56 dala, the lateral hypothalamus, and the zona incerta, interrupts the activity sequence pattern and su

57 The zona incerta is a subthalamic nucleus made up mostly of GABAe

58 plain why deep brain stimulation of the zona incerta is beneficial to patients who suffer from Parkin

59 d of the thalamic reticular nucleus and zona incerta, known to modulate thalamocortical communication

60 pamine-containing cell region of medial zona incerta, lateral habenula, horizontal and vertical limbs

61 with the claustrum, reticular nucleus, zona incerta, lateral posterior and medial pulvinar nuclei, n

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

63 optic nucleus, paraventricular nucleus, zona incerta, medial and cortical amygdaloid nuclei, cerebell

64 n, a heterogeneous region of the medial zona incerta (mZI) containing dopaminergic, GABAergic, and gl

65 ne (IHDA) neurons located in the medial zona incerta (MZI) project to the central nucleus of the amyg

66 Zona incerta neurons distribute a broad corollary signal of m

67 To record the activity of zona incerta neurons during exploratory and cue-driven goal-d

68 w studies have measured the activity of zona incerta neurons in behaving animals under different cond

69 s of Meynert, medial habenular nucleus, zona incerta, neurosecretory arcuate nucleus, cranial motor n

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

71 is, posteromedial thalamic, and ventral zona incerta nuclei, are only weakly modulated by touch.

72 quently targeted the caudal part of the zona incerta nucleus (cZI).

73 the pallidofugal fibres and the rostral zona incerta) or at the junction between the dorsal border of

74 ventricular and posterior hypothalamus, zona incerta, periaqueductal gray, intermediate layers of the

75 reporter genes, and the nearly identical C. incerta petD functioned for mRNA stability and translati

76 e thalamic nuclei, superior colliculus, zona incerta, pontine nucleus, multiple other brainstem areas

77 ted, with peak p values in superior STN/zona incerta (quantified bradykinesia), dorsal STN (mood, anx

78 , the physiological firing frequency of zona incerta, reduces experimental heat pain by a modest but

79 By demonstrating that the zona incerta regulates communication between the superior col

80 ons of the A13 region, highlighting the zona incerta's role as a crucial hub for the rapid selection

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

82 , including those found in the medulla, zona incerta, substantia nigra or olfactory bulb, received si

83 of the hypothalamus; lateral habenula; zona incerta; substantia innominata; posterior thalamic nucle

84 ith SNS outflow neurons to IBAT, the subzona incerta (subZI) to test whether IBAT thermogenesis could

85 n layer II of cortex, cingulate cortex, zona incerta, thalamus and hypothalamus.

86 diagonal band, amygdala, hypothalamus, zona incerta, thalamus, periaqueductal gray, raphe nuclei, la

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

88 and posterior hypothalamic nuclei, the zona incerta, the intergeniculate leaflet and the ventral sub

89 e hippocampus, the medial habenula, the zona incerta, the paraventricular and supraoptic nuclei of th

90 nd reuniens nuclei of the thalamus, the zona incerta, the subthalamic nucleus, the central gray, the

91 clei in the mammalian brain include the zona incerta, the ventral lateral geniculate nucleus, and the

92 matic, and tuberal hypothalamic nuclei, zona incerta, ventral tegmental area, cerebellum (Purkinje ce

93 gonal band/magnocellular preoptic area, zona incerta, ventromedial hypothalamus, lateral mammillary n

94 inhibition, we performed recordings in zona incerta, where 10, but not 40, Hz stimulation evoked spi

95 rodorsal nucleus, lateral habenula, and zona incerta, where labeling was much more extensive than pre

96 GABAergic neurons in the mouse ventral zona incerta, which express the LIM homeodomain factor Lhx6 a

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

98 rafascicular nucleus (PF), ventromedial zona incerta (ZI) and at the border of the locus coeruleus (L

99 als from anterior pretectal nucleus and zona incerta (ZI) are each abundant in specific Po regions an

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

101 at ablation of dopamine (DA) neurons in zona incerta (ZI) but not ventral tegmental area potently imp

102 at receives dense GABA projections from zona incerta (ZI) for the regulation of feeding behaviours.

103 5-HT inhibits GABA release from zona incerta (ZI) GABA terminals in PVT.

104 d that optogenetic stimulation of mouse zona incerta (ZI) gamma-aminobutyric acid (GABA) neurons or t

105 (VPM), neurons of the ventral thalamus zona incerta (ZI) have been shown to exhibit multiwhisker res

106 Zona incerta (ZI) is a largely inhibitory subthalamic region

107 The zona incerta (ZI) is a subcortical structure primarily invest

108 The zona incerta (ZI) is involved in mediating survival behaviors

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

110 ial for motor coordination, whereas the zona incerta (ZI) plays a key role in modulating sensorimotor

111 We found that mouse zona incerta (ZI) projection neurons form a GABAergic axon pl

112 BS of the ventro-oralis posterior (VOP)/zona incerta (ZI) region, and subsequently underwent blinded

113 Transsynaptic labeling identifies zona incerta (ZI) to thalamic posterior medial nucleus projec

114 eneralization could be modulated by the zona incerta (ZI), a subthalamic brain region that influences

115 terminates in the ventral region of the zona incerta (ZI), a subthalamic structure previously linked

116 activity in the GABAergic nucleus, the zona incerta (ZI), and concomitant increased activity in one

117 t, the ETI (arising from basal ganglia, zona incerta (ZI), anterior pretectum, and pontine reticular

118 ed in the lateral hypothalamus (LH) and zona incerta (ZI), but MCHR1 mRNA is widely expressed through

119 rexin gene delivery into neurons of the zona incerta (ZI), or the lateral hypothalamus (LH) blocked c

120 ory inputs from the subthalamic nucleus zona incerta (ZI), POm responses were of significantly higher

121 the posterior medial (POm) nucleus, the zona incerta (ZI), the reticular nucleus (nRT) of the thalamu

122 nding neurons preferentially target the zona incerta (ZI), which suppresses the superior colliculus (

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

124 ugal fibres (H2 field of Forel) and the zona incerta (ZI).

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

126 urons), midline raphe (26%), LHA (22%), zona incerta (ZI, 15%), CeA (5%), paraventricular nucleus (PV

127 culus terminated densely in the ventral zona incerta (ZIv), but did not overlap the labeled neurons o

128 y cortex (SSp) to the ventral sector of zona incerta (ZIv).