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1  was abolished by optogenetic stimulation of cholinergic fibers.
2  large polysynaptic IPSCs by recruiting many cholinergic fibers.
3 he fimbria fornix, a major pathway of septal cholinergic fibers.
4                                              Cholinergic fiber activation revealed that CCK BCs were
5 n (NRTN), is established between sympathetic cholinergic fibers and bone-embedded osteocytes, which r
6  transmission between efferent olivocochlear cholinergic fibers and cochlea hair cells.
7                               By stimulating cholinergic fibers and making electrophysiological recor
8 sts that there might be synapses between the cholinergic fibers and the dendrites of SpL neurons.
9 icular acetylcholine transporter showed that cholinergic fibers apposed putative cortically projectin
10  MS/VDB neurite length, as well as increased cholinergic fiber density and synaptophysin pre-synaptic
11                                              Cholinergic fiber density in layer II of the prefrontal
12                      The treatment increased cholinergic fiber density in the hippocampus of both WT/
13                   No differences in parietal cholinergic fiber density or nucleus basalis cholinergic
14                                              Cholinergic fiber density within the hippocampus also is
15 l to dorsal and a rostral to caudal shift of cholinergic fiber distribution in mPFC.
16 s, we find that stimulation of intrastriatal cholinergic fibers evokes polysynaptic GABA(A) IPSCs in
17 , release of acetylcholine by stimulation of cholinergic fibers facilitates LTP via activation of M(1
18  implants also induced a robust sprouting of cholinergic fibers from subjacent basal forebrain neuron
19                                    Increased cholinergic fibers in asthmatic airway biopsies was foun
20  coupled temporally with the reappearance of cholinergic fibers in hippocampus, as assessed by the im
21  the first time, the presence of a plexus of cholinergic fibers in laminae II-III of the dorsal horn
22  In this study we optogenetically stimulated cholinergic fibers in rat neocortex and find that ACh en
23 crease in the total length of VAChT-positive cholinergic fibers in the IML after EC damage, along wit
24 r inhibits the release of acetylcholine from cholinergic fibers in the lungs and elsewhere.
25 viding evidence of compensatory sprouting of cholinergic fibers in the outer molecular layer of the d
26 ons in the nucleus basalis of Meynert and on cholinergic fibers in the prefrontal and parietal cortex
27 ive ChAT immunoreactivity was located in the cholinergic fibers in the SFO.
28 hibition of liver-projecting parasympathetic cholinergic fibers increases blood glucose levels.
29                                              Cholinergic fibers innervate hippocampal neuron axons, d
30 fferent (OE) nucleus is the likely source of cholinergic fibers innervating the ELL.
31 the IP are located in a region that receives cholinergic fiber inputs from the ventral MHb, and optog
32 ew stereological technique to estimate total cholinergic fiber length in hippocampal subregions of be
33                                      The new cholinergic fibers likely originate from the superior ce
34 ists or prolonged optogenetic stimulation of cholinergic fibers, may not reflect the effect of physio
35 nsistent with the hypothesis that descending cholinergic fibers modulate afferent auditory signals by
36 aled an age-related decline in the length of cholinergic fibers of 22%, which was similar across the
37 f efferent neurons precedes the formation of cholinergic fiber patches in the cat SC which is first i
38 diate gray layer which precisely overlap the cholinergic fiber patches in this region of the cat SC.
39 demonstrates that while AF64A damaged septal cholinergic fibers, periventricular GnRH-immunoreactive
40 unctional nicotinic receptors and receives a cholinergic fiber projection.
41                            Additionally, MOC cholinergic fibers release not only ACh but also GABA, a
42                          The fine network of cholinergic fibers running through the hippocampus forms
43                      The organization of the cholinergic fiber system was compared with that of stria
44                                  Clusters of cholinergic fibers that may be indicative of cortical pl
45 een thought of as an autoreceptor located on cholinergic fibers that originate from neurons in the nu
46 ors were also infiltrated by parasympathetic cholinergic fibers that promoted cancer dissemination.
47 eventing region-specific changes in cortical cholinergic fibers that result from the loss of circulat
48 at are strongly determined by the anatomy of cholinergic fibers, the distribution and the signaling m
49                    In addition to containing cholinergic fibers, this projection has been identified
50 the wakefulness-dependent activity of septal cholinergic fibers through the alpha7-nicotinic acetylch
51                      We found that ascending cholinergic fibers to the mPFC follow four pathways and
52 mistry that the MHb is cholinergic and sends cholinergic fibers to the Uva.
53 -immunopositive fibers in the SpL and in the cholinergic fiber tract lateral to the nucleus are assoc
54  revealed EPSPs evoked by stimulation of the cholinergic fiber tract lateral to the SpL.
55 precise overlap of striatal dopaminergic and cholinergic fibers underlies potent control of dopamine
56             It was found that the density of cholinergic fiber varicosities was higher in epileptic r
57                             To visualize the cholinergic fibers, we used brain sections immunostained
58  Two morphologically distinct populations of cholinergic fibers were labeled and classified according
59                                              Cholinergic fibers were observed in both the telencephal
60 nce of brain nitric oxide synthase (BNOS) in cholinergic fibers within the A-laminae of the lateral g
61 al genetic fate mapping, we demonstrate that cholinergic fibers within the mouse cortex exhibit remar