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1 onse has previously not been demonstrated in autonomic ganglia.
2 However, HSV-2 has also been found latent in autonomic ganglia.
3 enteric neurons but not in glial cells or in autonomic ganglia.
4 n was not consistently altered in any of the autonomic ganglia.
5 entral and peripheral nervous systems in the autonomic ganglia.
6 3 and beta 4, which are the most abundant in autonomic ganglia.
7 iary neurons does not likely derive from the autonomic ganglia.
8 of intact sensory or major, posterior tongue autonomic ganglia.
9  pair was adjacent to the fat pad containing autonomic ganglia (AG) at the veno-left atrial (LA) junc
10 cific inhibition of synaptic transmission in autonomic ganglia and antibody levels correlate in a pre
11 ous agent primarily uses synaptically linked autonomic ganglia and efferent fibers of the vagus and s
12 cetylcholine receptor is widely expressed in autonomic ganglia and in some parts of the brain.
13 ssion across parasympathetic and sympathetic autonomic ganglia and in the adrenal medulla and, theref
14 ining alpha3 and beta2 subunits are found in autonomic ganglia and mediate ganglionic transmission.
15 substantia nigra, hypothalamus, hippocampus, autonomic ganglia and olfactory tracts.
16  to establish latent infection in sensory or autonomic ganglia and to reactivate on physical, hormona
17 aricella), becomes latent in dorsal root and autonomic ganglia, and reactivates decades later to caus
18 for nicotinic acetylcholine receptors in the autonomic ganglia are potentially pathogenic and may ser
19 ariety of derivatives, including sensory and autonomic ganglia, cartilage and bone of the face and pi
20  cranial ganglia, and peripheral sensory and autonomic ganglia during the embryonic and neonatal peri
21 ere present at high levels in nerve cells of autonomic ganglia, epithelial cells, intestinal smooth m
22 eral targets, modulates neurotransmission in autonomic ganglia, has an important role in local enteri
23                                        While autonomic ganglia have been extensively studied in rats
24                     We hypothesized that the autonomic ganglia have important roles in viral reactiva
25 0 connections among 52 of the 84 sensory and autonomic ganglia identified.
26 ocalized principally in epithelial cells and autonomic ganglia in gut and colon.
27       Using two-photon microscopy, we imaged autonomic ganglia in living mice infected with PRV strai
28 n of NO bioavailability from nNOS in cardiac autonomic ganglia in response to training is dependent o
29                     HO2 also occurs in other autonomic ganglia including the petrosal, superior cervi
30         HO-2 is also localized to neurons in autonomic ganglia, including the petrosal, superior cerv
31 ndings indicate that viral reactivation from autonomic ganglia is a feature of latent viral infection
32 ain disease states, synaptic transmission in autonomic ganglia is depressed and the periphery becomes
33    Neonatal neurodegeneration in sensory and autonomic ganglia is followed by loss of neurons from la
34 ory synaptic transmission through vertebrate autonomic ganglia is mediated by postsynaptic nicotinic
35      Fast synaptic transmission in mammalian autonomic ganglia is mediated primarily by nicotinic rec
36             In vivo, expression of Phox2a in autonomic ganglia is strongly reduced in Mash1 -/- embry
37 ations (brain, raphe nuclei, spinal cord and autonomic ganglia) may modulate rat sexual behavior in o
38 the incubation period in enteric ganglia and autonomic ganglia of splanchnic or vagus circuitry prior
39 -1 spread via the dorsal root ganglia to the autonomic ganglia of the enteric nervous system (ENS) in
40 omical features of a cell bridge linking two autonomic ganglia of the neck, namely, the nodose gangli
41 rgic synaptic transmission in adrenal gland, autonomic ganglia, pineal gland, and several nuclei in t
42                                  Synapses in autonomic ganglia represent the final output of various
43                                              Autonomic ganglia stimulation, without atrial excitation
44 present study measured nAChRs in several rat autonomic ganglia: the superior cervical ganglia (SCG),
45                                           In autonomic ganglia, they are responsible for fast synapti
46 terrupting neurotransmission at the level of autonomic ganglia to determine its effect on the QT inte
47 ls with prior supranodose de-efferentations, autonomic ganglia were stained with Fluoro-gold, and tis