ライフサイエンスコーパス: pontomedullary

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1 expression of GAD67 and PV by neurons at the pontomedullary border implies that PV may not be a valid

2 D67-ir cells were found at the ventrolateral pontomedullary border in areas adjacent to the A5 noradr

3 al tone depends upon at least 3 sites of the pontomedullary brainstem and that a significant proporti

4 Previous studies suggested that unilateral pontomedullary brainstem lesions cause ipsiversive roll-

5 ds on neurons in at least three sites of the pontomedullary brainstem, and much of it arises independ

6 n of 5-HT2A receptor-like protein in the rat pontomedullary brainstem.

7 The distinct pontomedullary distribution of 5-HT2A receptors, combine

8 tary tract and in the locus caeruleus at the pontomedullary junction as well as in the fastigial nucl

9 Just over half of them are found at the pontomedullary junction within raphe obscurus, raphe mag

10 m the level of the area postrema (AP) to the pontomedullary junction.

11 from the mesencephalic locomotor region and pontomedullary medial reticular formation responsible fo

12 hese results identify a key component of the pontomedullary network controlling REM sleep.

13 the ESOc and ESOt activate different sets of pontomedullary nuclei and different physiological respon

14 mulation are mediated through a relay in the pontomedullary raphe magnus (RM) and adjacent nucleus re

15 The pontomedullary raphe magnus (RM) contains two physiologi

16 These neurons target selectively the pontomedullary regions implicated in generating the resp

17 ndrites along the VMS and they innervate key pontomedullary respiratory centers.

18 situ preparation in young rats that retained pontomedullary respiratory circuits and spinal pathways

19 on, and (4) use a computational model of the pontomedullary respiratory network to suggest neuronal m

20 nvestigated how single unit discharge in the pontomedullary reticular formation (PMRF) modulated duri

21 Pontomedullary reticular formation (PMRF) neurons (309)

22 ribed previously, suggesting that individual pontomedullary reticular formation neurons may coordinat

23 urons, were observed in several areas of the pontomedullary reticular formation.

24 d effects are SEROTONERGIC, the responses of pontomedullary SEROTONERGIC-LIKE cells to PAG stimulatio

25 f GABAergic signaling at these ventrolateral pontomedullary sites.

26 REM sleep and motor control circuitry in the pontomedullary structures cause REM sleep behaviour diso

27 as a result of degeneration of olfactory and pontomedullary structures could theoretically begin many

28 s of the ventral medulla, ventral and dorsal pontomedullary structures, basal forebrain, and cerebell

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