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1 vestigate neuronal cell death in the nucleus ambiguus.
2 nt rostrocaudal positions within the nucleus ambiguus.
3 ing GPER in cardiac vagal neurons of nucleus ambiguus.
4 cardiac vagal neurons located in the nucleus ambiguus.
5 sion to cardiac vagal neurons in the nucleus ambiguus.
6 ucleus of the solitary tract and the nucleus ambiguus.
7 hibitory vagal neurons (CVNs) in the nucleus ambiguus.
8 lized within or ventrolateral to the nucleus ambiguus.
9 orsal motor nucleus of the vagus and nucleus ambiguus.
10 leus and the compact division of the nucleus ambiguus.
11 en identified in familial and sporadic situs ambiguus.
12 rons of the compact formation of the nucleus ambiguus.
13 ons were located just ventral to the nucleus ambiguus.
14 as red nucleus, inferior olive, and nucleus ambiguus.
15 ithin, or in close proximity to, the nucleus ambiguus.
16 visualized sections (250 microns) of nucleus ambiguus.
17 ot aldosterone activates GPER in rat nucleus ambiguus.
18 lly in the external formation of the nucleus ambiguus, 5.6% were in the lateral extreme of the dorsal
21 innervating neurons in the brainstem nucleus ambiguus (Amb) are comprised of two molecularly, anatomi
22 urons in the trigeminal (Mo5), facial (Mo7), ambiguus (Amb), and hypoglossal (Mo12) motor nuclei inne
25 he cardiovascular regulatory nuclei (nucleus ambiguus and dorsal motor nucleus of the vagus), but no
28 regions of the retrofacial nucleus, nucleus ambiguus and nucleus retroambigualis during induction of
30 vicinity of nucleus retroambigualis, nucleus ambiguus and the retrofacial nucleus (ventral respirator
31 uropil of the pre-Botzinger complex, nucleus ambiguus, and retrotrapezoid nucleus were high at P2-11
33 orsal motor nucleus of the vagus and nucleus ambiguus are consistent with the presence of TrkB and Tr
34 een the parabrachial nucleus and the nucleus ambiguus, are conserved among fast-click species, and sl
35 near the lateral tegmental field and nucleus ambiguus at a more caudal level tested (1.3 mm anterior
38 ortion of embryos lacking SPC4 develop situs ambiguus combined with left pulmonary isomerism or compl
39 kB: 1) in the pre-Botzinger complex, nucleus ambiguus, commissural and ventrolateral subnuclei of sol
41 urons of the brainstem motor nuclei, nucleus ambiguus, dorsal motor nucleus of the vagus, motor trige
42 0.62, 1.25 and 2.25 mmol/L) into the nucleus ambiguus elicited increases in heart rate (17.5 +/- 4, 3
45 r groups (the pre-Botzinger complex, nucleus ambiguus, hypoglossal nucleus, and ventrolateral subnucl
47 al lesions, the key lesion is in the nucleus ambiguus innervating the dilator muscles of the soft pal
50 he compact and semicompact formation nucleus ambiguus, mGluRla was found in cell bodies and fibers.
52 and dendritic spines were reduced in nucleus ambiguus MNs from 18 months (evaluated by confocal imagi
53 se behavioural weakness and death of nucleus ambiguus MNs will occur by age 24 months in F344 rats an
55 rain the activity of spinal (L1) and nucleus ambiguus motor pools located at positions where expirato
56 ic neurones (CVPNs and BVPNs) in the nucleus ambiguus (NA) and (b) are involved in pulmonary C-fibre
57 diac vagal neurons (CVNs) located in nucleus ambiguus (NA) and dorsal motor nucleus of the vagus (DMN
58 at Dbh(+) nTS neurons project to the nucleus ambiguus (NA) and that NA neurons are necessary and suff
59 nine methanesulfonate (DiI) into the nucleus ambiguus (NA) and used confocal microscopy to inventory
63 us (VN), parabrachial nucleus (PBN), nucleus ambiguus (NA), dorsal motor nucleus (DMN), and all subnu
64 parasympathetic vagal neurons in the nucleus ambiguus (NA), from which originates control of heart ra
66 njected the tracer DiI into the left nucleus ambiguus (NA), then used confocal microscopy and a Neuro
67 nucleus of the vagus (DMNX) and the nucleus ambiguus (NA), were consistently evoked upon stimulation
68 reganglionic neurones (CVPNs) in the nucleus ambiguus (NA), which have respiratory modulated activity
74 glionic neurons in the ventrolateral nucleus ambiguus (NA-VL) can be selectively labelled from the he
78 e fifth (MoV), seventh (VII), tenth (nucleus ambiguus, NA), and twelfth (XII) cranial nerve motor nuc
80 xpression, we examined activation of nucleus ambiguus (NAmb) neurons by EA, their relation to choline
81 motor nucleus of the vagus (DMV) and nucleus ambiguus (nAmb) that express the autism-associated MET r
83 the brainstem reticular formation and in the ambiguus nucleus as well as predominantly ipsilateral la
84 y (dorsal and ventral) reticular formations; ambiguus nucleus; and midbrain superior colliculus and d
85 nput to cardiac vagal neurons in the nucleus ambiguus occurred at a significantly lower frequency tha
86 icroinjections of glutamate into the nucleus ambiguus of an arterially perfused preparation in a grid
87 xy, expressed either as randomization (situs ambiguus) or complete reversal (situs inversus) of norma
88 mization of individual organ position (situs ambiguus) or to mirror-image reversal of all lateralized
89 r control (rostral tip of the dorsal nucleus ambiguus, parvicellular reticular nucleus, retrorubral a
90 croinjection of aldosterone into the nucleus ambiguus produced a dose-dependent bradycardia in consci
91 orsal motor nucleus of the vagus and nucleus ambiguus retrogradely transported [125I]BDNF, [125I]NT-3
94 rization of cardiac vagal neurons of nucleus ambiguus that was sensitive to antagonism of GPER but no
95 ly labelled cardiac vagal neurons of nucleus ambiguus; the response was abolished by pretreatment wit
96 months), or DiI injections into the nucleus ambiguus to label vagal cardiac efferents (at 3, 6, and
98 ngomotor loose formations of the rat nucleus ambiguus was studied in single and serial sections by me
99 udal brainstem within and around the nucleus ambiguus was systematically explored for sites producing
100 ke receptors (ORL1 receptors) in the nucleus ambiguus were studied in urethane-anesthetized, adult ma