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1 different rostrocaudal positions within the nucleus ambiguus.
2 activating GPER in cardiac vagal neurons of nucleus ambiguus.
3 es from cardiac vagal neurons located in the nucleus ambiguus.
4 transmission to cardiac vagal neurons in the nucleus ambiguus.
5 tatory nucleus of the solitary tract and the nucleus ambiguus.
6 cardioinhibitory vagal neurons (CVNs) in the nucleus ambiguus.
7 be localized within or ventrolateral to the nucleus ambiguus.
8 her or not aldosterone activates GPER in rat nucleus ambiguus.
9 of the dorsal motor nucleus of the vagus and nucleus ambiguus.
10 ular nucleus and the compact division of the nucleus ambiguus.
11 motoneurons of the compact formation of the nucleus ambiguus.
12 motoneurons were located just ventral to the nucleus ambiguus.
13 as well as red nucleus, inferior olive, and nucleus ambiguus.
14 ocated within, or in close proximity to, the nucleus ambiguus.
15 acer in visualized sections (250 microns) of nucleus ambiguus.
16 bilaterally in the external formation of the nucleus ambiguus, 5.6% were in the lateral extreme of th
21 aining the cardiovascular regulatory nuclei (nucleus ambiguus and dorsal motor nucleus of the vagus),
22 f nucleus tractus solitarii projected to the nucleus ambiguus and dorsal motor nucleus of the vagus.
23 and the regions of the retrofacial nucleus, nucleus ambiguus and nucleus retroambigualis during indu
24 at originate from two brain stem nuclei: the nucleus ambiguus and the dorsal motor nucleus of the vag
25 in the vicinity of nucleus retroambigualis, nucleus ambiguus and the retrofacial nucleus (ventral re
26 n the neuropil of the pre-Botzinger complex, nucleus ambiguus, and retrotrapezoid nucleus were high a
27 in the dorsal motor nucleus of the vagus and nucleus ambiguus are consistent with the presence of Trk
28 m sites near the lateral tegmental field and nucleus ambiguus at a more caudal level tested (1.3 mm a
29 F and TrkB: 1) in the pre-Botzinger complex, nucleus ambiguus, commissural and ventrolateral subnucle
30 ergic neurons of the brainstem motor nuclei, nucleus ambiguus, dorsal motor nucleus of the vagus, mot
31 (0.31, 0.62, 1.25 and 2.25 mmol/L) into the nucleus ambiguus elicited increases in heart rate (17.5
33 d nuclear groups (the pre-Botzinger complex, nucleus ambiguus, hypoglossal nucleus, and ventrolateral
34 In central lesions, the key lesion is in the nucleus ambiguus innervating the dilator muscles of the
36 ent of the compact and semicompact formation nucleus ambiguus, mGluRla was found in cell bodies and f
37 and entrain the activity of spinal (L1) and nucleus ambiguus motor pools located at positions where
38 ganglionic neurones (CVPNs and BVPNs) in the nucleus ambiguus (NA) and (b) are involved in pulmonary
39 otor cardiac vagal neurons (CVNs) located in nucleus ambiguus (NA) and dorsal motor nucleus of the va
40 carbocyanine methanesulfonate (DiI) into the nucleus ambiguus (NA) and used confocal microscopy to in
43 (DMN), nucleus tractus solitarius (NTS) and nucleus ambiguus (NA) with a sham control group (N=5).
44 ar nucleus (VN), parabrachial nucleus (PBN), nucleus ambiguus (NA), dorsal motor nucleus (DMN), and a
45 ibitory parasympathetic vagal neurons in the nucleus ambiguus (NA), from which originates control of
46 We injected the tracer DiI into the left nucleus ambiguus (NA), then used confocal microscopy and
47 al motor nucleus of the vagus (DMNX) and the nucleus ambiguus (NA), were consistently evoked upon sti
48 vagal preganglionic neurones (CVPNs) in the nucleus ambiguus (NA), which have respiratory modulated
54 l preganglionic neurons in the ventrolateral nucleus ambiguus (NA-VL) can be selectively labelled fro
58 n, to the fifth (MoV), seventh (VII), tenth (nucleus ambiguus, NA), and twelfth (XII) cranial nerve m
60 c-Fos expression, we examined activation of nucleus ambiguus (NAmb) neurons by EA, their relation to
61 dorsal motor nucleus of the vagus (DMV) and nucleus ambiguus (nAmb) that express the autism-associat
62 Aergic input to cardiac vagal neurons in the nucleus ambiguus occurred at a significantly lower frequ
63 ted by microinjections of glutamate into the nucleus ambiguus of an arterially perfused preparation i
64 eal motor control (rostral tip of the dorsal nucleus ambiguus, parvicellular reticular nucleus, retro
65 that microinjection of aldosterone into the nucleus ambiguus produced a dose-dependent bradycardia i
66 in the dorsal motor nucleus of the vagus and nucleus ambiguus retrogradely transported [125I]BDNF, [1
68 d depolarization of cardiac vagal neurons of nucleus ambiguus that was sensitive to antagonism of GPE
69 trogradely labelled cardiac vagal neurons of nucleus ambiguus; the response was abolished by pretreat
70 3 and 6 months), or DiI injections into the nucleus ambiguus to label vagal cardiac efferents (at 3,
72 and laryngomotor loose formations of the rat nucleus ambiguus was studied in single and serial sectio
73 teral caudal brainstem within and around the nucleus ambiguus was systematically explored for sites p
74 eptor like receptors (ORL1 receptors) in the nucleus ambiguus were studied in urethane-anesthetized,
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