ライフサイエンスコーパス: incerta

1 obus pallidus, subthalamic nucleus, and zona incerta.

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

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

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

5 re found on dopaminergic neurons in the zona incerta.

6 ateral and rostral PAG projected to the zona incerta.

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

8 w in the reticular thalamic nucleus and zona incerta.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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