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1 ion appears to mark cells of the prospective medullary reticular formation.
2  ventral magnocellular portion of the medial medullary reticular formation.
3  the inferior olive and in the ventrolateral medullary reticular formation.
4 rd and terminating in the ventral and medial medullary reticular formation.
5 uclei, as well as the vestibular complex and medullary reticular formation.
6 is review are ascending connections from the medullary reticular formation and descending connections
7  motoneurons were present in both the medial medullary reticular formation and nucleus retroambiguus.
8 was increased susceptibility in the inferior medullary reticular formation and the raphe pallidus and
9 urons projecting to the superior colliculus, medullary reticular formation, and central lateral nucle
10 tric bipolar stimulating electrodes into the medullary reticular formation, and implanted electroence
11 us, dorsal raphe, mesencephalic, pontine and medullary reticular formation, and the following nuclei:
12 the raphe nuclei, the parabrachial area, the medullary reticular formation, and the nucleus of the so
13 eir spinal projections, several parts of the medullary reticular formation as well as the spinally pr
14 belled cells were found in the parapyramidal medullary reticular formation, Barrington's nucleus, rap
15 rigeminal complex; the area postrema and the medullary reticular formation contained some labeled fib
16              These data show that the medial medullary reticular formation contains neurons influenci
17  (RTN), located in the rostral ventrolateral medullary reticular formation, contains a bilateral clus
18 ynaptic effects of cortical TMS on the ponto-medullary reticular formation in the brainstem, which is
19 ser extent MC3) has been demonstrated in the medullary reticular formation in the general area where
20  data suggest that the ventral magnocellular medullary reticular formation is not essential for respi
21 nd exclusively in the ventral portion of the medullary reticular formation, medial to the facial moto
22 (20-80 ng) in dextrose were delivered to the medullary reticular formation (MRF) by diffusion from a
23  low but not high threshold penile inputs to medullary reticular formation (MRF) neurons after acute
24 elvic/visceral convergent inputs onto single medullary reticular formation (MRF) neurons.
25 d have suggested that portions of the medial medullary reticular formation (MRF) participate in gener
26  that many bulbospinal neurons in the medial medullary reticular formation (MRF) provide inputs to ph
27 istribution in the magnocellular part of the medullary reticular formation (MRF).
28 ether, these results suggest that Lhx3/Chx10 medullary reticular formation neurons are involved in lo
29                                Lhx3-positive medullary reticular formation neurons express Fos follow
30          However, overlapping populations of medullary reticular formation neurons that participate i
31                                       In the medullary reticular formation of the mouse, we identifie
32 etinin-positive cells were identified in the medullary reticular formation of the rat by both immunoh
33                           In particular, the medullary reticular formation, periaqueductal gray (PAG)
34           The distribution of neurons in the medullary reticular formation (RF) activated by the inge
35   The pontine parabrachial nucleus (PBN) and medullary reticular formation (RF) are hindbrain regions
36 eniculate input, and the ventral NST (V) and medullary reticular formation (RF), a caudal brainstem p
37  of rNST, the parabrachial nucleus (PBN) and medullary reticular formation (RF).
38 s unclear but likely includes regions of the medullary reticular formation (RF).
39 injections restricted to a region of ventral medullary reticular formation, the medullary cerebral va
40  the same regions, which included the medial medullary reticular formation, the medullary raphe nucle