ライフサイエンスコーパス: laterodorsal

1 o-localized in some granular cell subsets in laterodorsal and dorsolateral regions, and in some Purki

2 ignificantly elevated at 2 h after ST in the laterodorsal and peduculopontine tegmentum, up to 4 h in

3 yltransferase (ChAT)-positive neurons in the laterodorsal and pedunculo-pontine tegmental nuclei (LDT

4 tive neurons were distributed throughout the laterodorsal and pedunculopontine tegmental nuclei (LDT

5 The laterodorsal and pedunculopontine tegmental nuclei (LDT-

6 posterior commissure, parabrachial nucleus, laterodorsal and pedunculopontine tegmental nuclei, nucl

7 ucleus, the locus coeruleus, and the dorsal, laterodorsal, and ventral tegmental nuclei.

8 e gyrus and hippocampus, in the mediodorsal, laterodorsal, anteroventral, and parateanial thalamic nu

9 n VTA, NAC shell, central amygdala (ceA) and laterodorsal bed nucleus of the stria terminalis (BSTLD)

10 imate anxiety, provides evidence of a CeL to laterodorsal bed nucleus of the stria terminalis circuit

11 hat a subset of these neurons project to the laterodorsal bed nucleus of the stria terminalis.

12 lness to non-REM sleep in the left and right laterodorsal frontal gyri, right medial prefrontal corte

13 r, ventrolateral, mediodorsal, ventromedial, laterodorsal (LD) and lateral posterior (LP) nuclei.

14 The laterodorsal (LD) nucleus of the thalamus has been consi

15 ast cells in the lateral intralaminar (Lat), laterodorsal (LD), ventrolateral (VL) and lateral genicu

16 n spinal cord laminae V-VIII, as well as the laterodorsal motoneuronal group of lamina IX (which inne

17 In the thalamus, ventrolateral and laterodorsal nuclei were most strongly stained, whereas

18 ved input from the ventrolateral part of the laterodorsal nucleus of the thalamus (LDVL).

19 lex, and periventricular areas including the laterodorsal nucleus, locus coeruleus and dorsal raphe.

20 ecific forms of the fruitless protein in the laterodorsal region of the brain.

21 Autoregulation of cholinergic neurons in the laterodorsal tegmental (LDT) and pedunculopontine (PPT)

22 ic neurons of the pedunculopontine (PPN) and laterodorsal tegmental (LDT) nuclei indirectly influence

23 5-HT may exert this effect on neurons of the laterodorsal tegmental (LDT) nuclei that are implicated

24 ocated within the pedunculopontine (PPT) and laterodorsal tegmental (LTD) nuclei of the mesopontine t

25 Distributed within the laterodorsal tegmental and pedunculopontine tegmental nu

26 ivities, and role of GABA neurons within the laterodorsal tegmental and sublaterodorsal tegmental nuc

27 The pedunculopontine-laterodorsal tegmental nuclear complex was identified as

28 egmentum, including the pedunculopontine and laterodorsal tegmental nuclei (PPN and LDT), provides ma

29 Neurons of the pedunculopontine and laterodorsal tegmental nuclei synapse with striatal chol

30 nd to medial tegmentum, pedunculopontine and laterodorsal tegmental nuclei, dorsal raphe, and locus c

31 r region, in the caudal pedunculopontine and laterodorsal tegmental nuclei, dorsomedial pontine retic

32 ger-Westphal, the lateral habenular, and the laterodorsal tegmental nuclei.

33 pontine reticular nucleus, oral part (131%); laterodorsal tegmental nucleus (56%); pedunculopontine t

34 binding, was significantly increased in the laterodorsal tegmental nucleus (75.7%), caudal pontine r

35 GABAergic neurons in the laterodorsal tegmental nucleus (LDT(GABA)) encode aversi

36 entials (EPSPs) evoked by stimulation of the laterodorsal tegmental nucleus (LDT) and spontaneous EPS

37 ound in the nucleus raphe dorsalis (RD), the laterodorsal tegmental nucleus (LDT) and the locus coeru

38 ry an associative/motor signal, those of the laterodorsal tegmental nucleus (LDT) convey limbic infor

39 ic neurons of the pedunculopontine (PPN) and laterodorsal tegmental nucleus (LDT) send long-ranging a

40 esopontine cholinergic (MPCh) neurons of the laterodorsal tegmental nucleus (LDT), a target group who

41 edunculopontine tegmental nucleus (PPT), the laterodorsal tegmental nucleus (LDT), and the parabrachi

42 sites implicated in producing REM sleep: the laterodorsal tegmental nucleus (LDT), dorsal raphe nucle

43 (orexin) neurons in the hypothalamus to the laterodorsal tegmental nucleus (LDT), which is a critica

44 The laterodorsal tegmental nucleus (LDTg) expresses GLP-1Rs

45 The laterodorsal tegmental nucleus (LDTg) is a hindbrain cho

46 Here, we show that tonic input from the laterodorsal tegmental nucleus (LDTg) is required for gl

47 ha7 nAChR subtype is highly expressed in the laterodorsal tegmental nucleus (LDTg), a brainstem choli

48 ral tegmental area and is connected with the laterodorsal tegmental nucleus and the rostral raphe in

49 ically, the dorsal tegmental nucleus and the laterodorsal tegmental nucleus appeared to be closely as

50 retin)-producing neurons that project to the laterodorsal tegmental nucleus in the hindbrain.

51 hypothalamic cholinergic nuclei and a large laterodorsal tegmental nucleus of the pons that has both

52 phorase (NADPH-d) to identify neurons of the laterodorsal tegmental nucleus or for both CRF and NADPH

53 The laterodorsal tegmental nucleus receives inhibitory input

54 cephalic central gray (dorsal raphe nucleus, laterodorsal tegmental nucleus, and Barrington's nucleus

55 instem/forebrain sites: caudal raphe nuclei, laterodorsal tegmental nucleus, dorsal raphe nucleus, in

56 l area homologs, superficial mamillary area, laterodorsal tegmental nucleus, locus coeruleus, inferio

57 the rostral raphe complex, locus coeruleus, laterodorsal tegmental nucleus, nucleus pontis oralis, p

58 halamus, mesencephalic tectum and tegmentum, laterodorsal tegmental nucleus, reticular formation, spi

59 Only inputs from the laterodorsal tegmental nucleus, the principal extrinsic

60 MR was unchanged in the locus coeruleus, the laterodorsal tegmental nucleus, the supramammilary nucle

61 downstream orexin signaling to the hindbrain laterodorsal tegmental nucleus, thereby highlighting a n

62 croendoscopic Ca(2+) imaging in and near the laterodorsal tegmental nucleus, we found that many gluta

63 certus, supramammillary nucleus, septum, and laterodorsal tegmental nucleus.

64 minal nucleus, pedunculopontine nucleus, and laterodorsal tegmental nucleus.

65 downstream orexin receptor signaling in the laterodorsal tegmental nucleus.

66 ct from, the NADPH-d-reactive neurons of the laterodorsal tegmental nucleus.

67 stral-dorsomedial cholinergic neurons in the laterodorsal tegmental nucleus; lateral noradrenergic ne

68 , substantia nigra, dorsal and median raphe, laterodorsal tegmental, and incertus nuclei of the brain

69 ntine tegmental, dorsal raphe, median raphe, laterodorsal tegmental, and locus coeruleus nuclei.

70 eep mesencephalic, red, pedunculopontine and laterodorsal tegmental, cuneiform, parabrachial, and dee

71 ne tegmentum (MPT), which is composed of the laterodorsal tegmentum (LDT) and the pedunculopontine te

72 t activation of upstream GABA neurons in the laterodorsal tegmentum (LDT) as a key regulator of heter

73 in the pedunculopontine tegmentum (PPT) and laterodorsal tegmentum (LDT) in REM sleep generation.

74 The laterodorsal tegmentum (LDT) neurons supply most of the

75 Projections from the laterodorsal tegmentum (LDT) to the ventral tegmental ar

76 tic enhancement of cholinergic tone from the laterodorsal tegmentum (LDT) to the VTA restored normal

77 tal gray, pedunculopontine nucleus (PPT) and laterodorsal tegmentum (LDT).

78 einforcement and is tightly modulated by the laterodorsal tegmentum (LDT).

79 e that UII excites MPCh neurons of the mouse laterodorsal tegmentum (LDTg) by activating a slow inwar

80 ng the pedunculopontine tegmentum (PPTg) and laterodorsal tegmentum (LDTg) on the reward effectivenes

81 inhibitory IPN GABAergic projections to the laterodorsal tegmentum (LDTg), a key driver of reward-re

82 ation required the expression of NRG1 in the laterodorsal tegmentum (LDTg); LDTg-specific deletion of

83 ty, activation of inputs to the VTA from the laterodorsal tegmentum and the lateral habenula elicit r

84 on of neurons in the cholinergic zone of the laterodorsal tegmentum and the pedunculopontine nuclei,

85 present in the same cholinergic zone of the laterodorsal tegmentum and the pedunculopontine nuclei,

86 Laterodorsal tegmentum neurons preferentially synapse on

87 oma growth in pons, while stimulation of the laterodorsal tegmentum nucleus (LDT) drives proliferatio

88 lable sleep-relevant areas (pedunculopontine/laterodorsal tegmentum, nucleus basalis of Meynert, thal

89 tory bulb, parastrial nucleus, hypothalamus, laterodorsal tegmentum, superior colliculus, locus coeru

90 he thalamic nuclei investigated included LP, laterodorsal thalamic nucleus (LD), central lateral nucl

91 The laterodorsal thalamic nucleus (LD), with strong connecti

92 r cingulate/retrosplenial cortex (PCing) and laterodorsal thalamus (LDThal), areas implicated in spat

93 leus accumbens, lateral septum, hippocampus, laterodorsal thalamus, cingulate cortex, superior collic

94 In CA3, dentate gyrus, medial habenula, and laterodorsal thalamus, the density of apoptotic cells wa

95 edial amygdala, and V1aR in the anterior and laterodorsal thalamus.