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

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

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

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

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

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

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

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

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

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

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

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

19 5-HT may exert this effect on neurons of the laterodorsal tegmental (LDT) nuclei that are implicated

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

21 Distributed within the laterodorsal tegmental and pedunculopontine tegmental nu

22 The pedunculopontine-laterodorsal tegmental nuclear complex was identified as

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42 The laterodorsal tegmental nucleus receives inhibitory input

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 Laterodorsal tegmentum neurons preferentially synapse on

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

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

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

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

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

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

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