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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  revealed the expression of rLFPs across the pontomedullary brainstem.
7 n of 5-HT2A receptor-like protein in the rat pontomedullary brainstem.
8 er areas, such as the midbrain and bilateral pontomedullary contributions.
9                                 The distinct pontomedullary distribution of 5-HT2A receptors, combine
10 tary tract and in the locus caeruleus at the pontomedullary junction as well as in the fastigial nucl
11      Just over half of them are found at the pontomedullary junction within raphe obscurus, raphe mag
12  persists after brainstem transection at the pontomedullary junction, indicating that the circuitry t
13 m the level of the area postrema (AP) to the pontomedullary junction.
14  from the mesencephalic locomotor region and pontomedullary medial reticular formation responsible fo
15 hese results identify a key component of the pontomedullary network controlling REM sleep.
16 tilation.SIGNIFICANCE STATEMENT A network of pontomedullary neurons within the brainstem generates re
17 the ESOc and ESOt activate different sets of pontomedullary nuclei and different physiological respon
18 mulation are mediated through a relay in the pontomedullary raphe magnus (RM) and adjacent nucleus re
19                                          The pontomedullary raphe magnus (RM) contains two physiologi
20         These neurons target selectively the pontomedullary regions implicated in generating the resp
21 ndrites along the VMS and they innervate key pontomedullary respiratory centers.
22              Opioids inhibit this excitatory pontomedullary respiratory circuit by three distinct mec
23 situ preparation in young rats that retained pontomedullary respiratory circuits and spinal pathways
24 on, and (4) use a computational model of the pontomedullary respiratory network to suggest neuronal m
25 h these responses, RTN innervates the entire pontomedullary respiratory network, including expiratory
26 nvestigated how single unit discharge in the pontomedullary reticular formation (PMRF) modulated duri
27                                              Pontomedullary reticular formation (PMRF) neurons (309)
28 ade previously from the motor cortex and the pontomedullary reticular formation in the same task show
29 ribed previously, suggesting that individual pontomedullary reticular formation neurons may coordinat
30 urons, were observed in several areas of the pontomedullary reticular formation.
31                        Volumetric mapping of pontomedullary rLFPs in single preparations could become
32 d effects are SEROTONERGIC, the responses of pontomedullary SEROTONERGIC-LIKE cells to PAG stimulatio
33 f GABAergic signaling at these ventrolateral pontomedullary sites.
34 REM sleep and motor control circuitry in the pontomedullary structures cause REM sleep behaviour diso
35 as a result of degeneration of olfactory and pontomedullary structures could theoretically begin many
36 s of the ventral medulla, ventral and dorsal pontomedullary structures, basal forebrain, and cerebell