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1  the CM layer when it was separated from the myenteric plexus.
2 duced Fos expression in the small intestinal myenteric plexus.
3 enzymes were localized in the neurons of the myenteric plexus.
4 ting an inhibitory neural pathway within the myenteric plexus.
5 expression and nNOS synthesis in the gastric myenteric plexus.
6 suggesting mediation by NO released from the myenteric plexus.
7 ve neuronal fibers were found in the colonic myenteric plexus.
8 lex following vagotomy occurs in the gastric myenteric plexus.
9 ide synthase (NOS) expression in the gastric myenteric plexus.
10 ly by impaired NOS expression in the gastric myenteric plexus.
11 n of the stimulated formation of cAMP in the myenteric plexus.
12 on, akin to the developmental process of the myenteric plexus.
13 sion and recovery of neuronal density in the myenteric plexus.
14 d expression of IL-1R1 in the ganglia of the myenteric plexus.
15 nsity of the cytotoxic T-cell assault on the myenteric plexus.
16     Myenteric ganglia occupied 34% +/- 4% of myenteric plexus.
17 gic and nitrergic neurochemical codes in the myenteric plexus.
18 in the gut wall and in ganglion cells of the myenteric plexus.
19 trergic neuronal immunochemical codes in the myenteric plexus.
20 A was expressed in the villus epithelium and myenteric plexus.
21 tion to the gastric mucosa originates in the myenteric plexus.
22 tivate stretch-sensitive interneurons in the myenteric plexus.
23 e submucosal plexus (29.9-38.0%) than in the myenteric plexus.
24 peptide Y, serotonin, or somatostatin in the myenteric plexus.
25 pithelium, smooth muscle, and the submucosal myenteric plexus.
26 ne acetyltransferase, and substance P in the myenteric plexus.
27 o detected on neurons in both submucosal and myenteric plexuses.
28 e majority of neurons in both submucosal and myenteric plexuses.
29 cts on enteric neurons in the submucosal and myenteric plexuses.
30                                       In the myenteric plexus, 50% of muOR-immunoreactive neurons con
31 removed from progressively longer lengths of myenteric plexus, a graded reduction in the correlation
32 mice without colitis, NO was produced in the myenteric plexus almost completely via NOS1.
33    There are considerable differences in the myenteric plexus along different segments of the monkey
34 lexus and 50% of CSE positive neurons in the myenteric plexus also contained nNOS.
35               The PS contains ICC within the myenteric plexus and c-Kit immunopositive cells along th
36          COX-2 expression is enhanced in the myenteric plexus and cells within the smooth muscle laye
37  large, intensely immunofluorescent axons in myenteric plexus and circular muscle, and thinner varico
38 onged satiety action than CCK-8; and (3) the myenteric plexus and DVC may play roles in these differe
39 R), which binds laminin-beta1, in human HSCR myenteric plexus and EdnrB(NCC-/-) NCC.
40           The presence of clock genes in the myenteric plexus and epithelial cells suggests a role fo
41   Clock immunoreactivity was observed in the myenteric plexus and epithelial crypt cells.
42 ing neural network, exemplified by lack of a myenteric plexus and extensive overgrowth of fibers.
43 nes in the same plexus, from neurones in the myenteric plexus and from sympathetic postganglionic neu
44 nd all layers of the retina) and peripheral (myenteric plexus and innervating nerves) nervous system
45 a series of plexuses throughout the gut: the myenteric plexus and submucosal plexus.
46 was found in IC networks associated with the myenteric plexus and the deep muscular plexus.
47 r of NOS-immunoreactive cells in the gastric myenteric plexus and the NOS activity were significantly
48 CC that are distributed in the region of the myenteric plexus and throughout the circular muscle laye
49          Further, by directly modulating the myenteric plexus and thus mimicking meal ingestion, we i
50  in the postnatal rat gut are located in the myenteric plexus, and shows that these cells can be expa
51 llus epithelium are transmitted first to the myenteric plexus, and then back to the submucosal plexus
52 ties were present in both the submucosal and myenteric plexuses, and the OCTs were also located in th
53 of neurons projected predominantly to either myenteric plexus ( approximately 13%) or smooth muscle (
54 ely 100% of an arbor's varicose branches) to myenteric plexus ( approximately 2%) or smooth muscle (
55 ther, these data extend our understanding of myenteric plexus architecture in maturing zebrafish, the
56 lopment, however knowledge of its developing myenteric plexus architecture was unknown.
57  sensitive, whereas those located within the myenteric plexus are also thought to respond to changes
58                                   Within the myenteric plexus are neurons that contain neuronal nitri
59 g fast and slow synaptic transmission in the myenteric plexus are organized in a polarity- (ascending
60 rs old, suggest age-dependent changes in the myenteric plexus area, ENS ganglion area, percentage of
61 ochemical changes in CGRP-li or SP-li in the myenteric plexus at any time.
62 oreactive for trk could be visualized in the myenteric plexus at ED 16.
63 responsive neurons were distinguished in the myenteric plexus because of the hyperpolarization and de
64 r messenger RNA was expressed in the colonic myenteric plexus but not in the smooth muscle cells, sug
65 in cholinergic neurons in the submucosal and myenteric plexuses, but not in enterocytes.
66  dense neuronal networks at the level of the myenteric plexus by embryonic week (EW) 12, with express
67 nfirmed expression of PAR-1 and PAR-2 in the myenteric plexus by RT-PCR using primers based on sequen
68 riginates in pacemaker cells surrounding the myenteric plexus, called interstitial cells of Cajal (IC
69 y neuromuscular signaling is involved in the myenteric plexus circuitry that controls intestinal moti
70                         Dissected muscle and myenteric plexus contained transcripts encoding D1-D3 an
71            Moreover, the longitudinal muscle myenteric plexus content of PKC alpha and PKC beta is su
72 rebral cortex, pituitary, spinal cord, colon myenteric plexus, dorsal root ganglion, and prenatal cor
73      Normally, a dominant pacemaker near the myenteric plexus drives slow waves that actively propaga
74                         NO released from the myenteric plexus enhances colonic transit and facilitate
75 on of ENs and govern the architecture of the myenteric plexus for reinnervating ENs, as shown by nerv
76 ical, or electrical stimuli to the mucosa of myenteric plexus-free preparations (+/- extrinsic denerv
77 s from the muscularis propria containing the myenteric plexus from adult rats.
78 lcium imaging experiments in whole mounts of myenteric plexus from Wnt1(Cre2GCaMP5g-tdTom) mice revea
79  measures identified two hubs (the bilateral myenteric plexus ganglia that control digestive tract fu
80 rder characterized by the functional loss of myenteric plexus ganglion cells in the distal esophagus
81                  ICC within the plane of the myenteric plexus (ICC-MY) arise from KIT-positive progen
82           Quantitative analyses demonstrated myenteric plexus in 24.5% +/- 2.4% of flattened colon Z-
83 he mediation of NOS synthesis in the gastric myenteric plexus in rats.
84  thick bundles of fibers in proximity to the myenteric plexus in the longitudinal muscle and in assoc
85 d NOS messenger RNA (mRNA) expression of the myenteric plexus in the proximal and the distal colon in
86 ricose efferent axons throughout the gastric myenteric plexus (including that of the fundus).
87 The proportions of CRF-IR cell bodies in the myenteric plexus increased progressively from the stomac
88  neurones, enhanced synaptic activity in the myenteric plexus, increased serotonin (5-HT) availabilit
89     By late larval stages, complexity of the myenteric plexus increases such that a layer of axons is
90 ng and projection patterns in the guinea pig myenteric plexus, indicate that OFQ-IR is expressed pref
91 neurons in ganglia of the submucosal but not myenteric plexus; injections of (125)I-NT-3 into myenter
92 he enteric nervous system, including reduced myenteric plexus innervation density and reduced gastroi
93 also seen in thin processes running from the myenteric plexus into the circular muscle, and in fibers
94 e that synaptic facilitation in the inflamed myenteric plexus involves a presynaptic increase in PKA
95 s suggest that NOS expression in the gastric myenteric plexus is controlled by the vagal nerve and ni
96 oncluded that neuronal NOS expression in the myenteric plexus is independent of vagus nerve and is ne
97 y whether the total number of neurons of the myenteric plexus is reduced with aging.
98 ooth muscle, while simultaneously contacting myenteric plexus, is consistent with the view that these
99 P-IR, but not VIP-IR, projects mainly to the myenteric plexus itself and the external muscle layers,
100  was expressed by enteric glial cells in the myenteric plexus layer, and cultured primary enteric gli
101 longitudinal muscle layers with the adherent myenteric plexus (LM-MP).
102 ctivation of the colonic longitudinal muscle myenteric plexus (LMMP) neurons and localization of CRF(
103  signaling in guinea pig longitudinal muscle/myenteric plexus (LMMP) preparations after chronic in vi
104                          Longitudinal muscle myenteric plexus (LMMP) tissues were collected, analyzed
105 the electrically stimulated guinea pig ileum myenteric plexus-longitudinal muscle preparation.
106 (fl/fl); Wnt1Cre+) caused a dramatic loss of myenteric plexus MET-IR neurites and 1-1'-dioctodecyl-3,
107 xide dismutase (MnSOD) is rapidly induced in myenteric plexus neurons (MPNs) in acute colitis and may
108 there was a progressive and profound loss of myenteric plexus neurons accompanied by changes in enter
109 de synthase (NOS)- and calretinin-containing myenteric plexus neurons and non-cholinergic secretomoto
110                           A subpopulation of myenteric plexus neurons expressed VGLUT2 protein and mR
111 vating colorectum; and 3) a subpopulation of myenteric plexus neurons expressing VGLUT(2).
112 nin gene-related peptide-immunoreactive (IR) myenteric plexus neurons thought to be intrinsic primary
113          CD8 T cells homed to submucosal and myenteric plexus neurons, 60% of which were lost, clinic
114 ndritic surfaces of neurochemically distinct myenteric plexus neurons, while being on axonal compartm
115 r the alpha4-5 subunits was only detected in myenteric plexus neurons.
116                                   Defects in myenteric plexus neurotransmission occur both in mice wi
117 lexus area, ENS ganglion area, percentage of myenteric plexus occupied by ganglia, neurons/mm(2), and
118 mistry indicated that LAMB4 localizes to the myenteric plexus of colonic tissue and patients harborin
119 AR-1 and PAR-2 in > 60 % of neurons from the myenteric plexus of guinea-pig small intestine in primar
120  NOS messenger RNA expression in the gastric myenteric plexus of spontaneously diabetic biobreeding/W
121 opulation of mechanosensory S-neurons in the myenteric plexus of the distal colon which appear to be
122                   (2) Possible roles for the myenteric plexus of the duodenum and the dorsal vagal co
123                                          The myenteric plexus of the enteric nervous system controls
124       Most enteric neurons reside within the myenteric plexus of the enteric nervous system in the mu
125  by central pattern generators housed in the myenteric plexus of the enteric nervous system.
126  of Kit-positive cells is evident within the myenteric plexus of the entire GI tract.
127 raganglionic laminar endings (IGLEs), in the myenteric plexus of the esophagus, and 70-90% in the sto
128                    CRF-IR cell bodies in the myenteric plexus of the ileum expressed IR for choline a
129 nd nodose ganglia, as well as ganglia in the myenteric plexus of the intestine.
130                             Here, we examine myenteric plexus of the maturing zebrafish larval fish h
131 vity was confined to enteric glia within the myenteric plexus of the mouse colon; the Cx43 inhibitors
132          Intestinal epithelial cells and the myenteric plexus of the mouse gastrointestinal tract con
133 ns and the NOS activity are increased in the myenteric plexus of the proximal colon compared with the
134 o study network-level activity in the intact myenteric plexus of the proximal colon.
135  HO2- and nNOS-containing neurons within the myenteric plexus of the rat ileum.
136 n dorsal root ganglia neurons but not in the myenteric plexus of the small and large intestine.
137                                       In the myenteric plexus of the small intestine, DOReGFP was pre
138 lly terminated in the hepatic artery and the myenteric plexus of the stomach and duodenum.
139  CRF1 receptor was distributed widely in the myenteric plexus of the stomach and small and large inte
140 n cells with Dogiel type I morphology in the myenteric plexus of the stomach and small and large inte
141 ons of the large and small intestine and the myenteric plexus of the stomach.
142 t contribute to synaptic facilitation in the myenteric plexus of the trinitrobenzene sulphonic acid-i
143 es for HO-2, nNOS, and VIP were found in the myenteric plexus of WT IAS.
144 sion in both the brains and small intestinal myenteric plexuses of control rats.
145 lyses of the small intestinal submucosal and myenteric plexuses of rats at various times after intest
146 the enteric nervous system, specifically the myenteric plexus, of the rhesus monkey (Macaca mulatta)
147 e majority of CM was sharp dissected off the myenteric plexus, ongoing neural activity was absent, or
148 t and Sema3d affecting survival, presence of myenteric plexus or intestine transcriptome.
149               The majority of ganglia in the myenteric plexus possess both HO2 and neuronal NO syntha
150 ation of enteric neuron and glia nuclei from myenteric plexus preparations from adult zebrafish intes
151 d microelectrode recordings from whole mount myenteric plexus preparations in guinea pigs.
152 y) was observed in ileum longitudinal muscle myenteric plexus preparations obtained from chronic morp
153                          Longitudinal muscle-myenteric plexus preparations of guinea pig intestines a
154 ssed survival by counting various genotypes, myenteric plexus presence by acetylcholinesterase staini
155 ptide immunoreactive (GRP-IR) neurons in the myenteric plexus, received vagal contacts.
156 for longitudinal muscle cells and ICs of the myenteric plexus region (IC-MY).
157 h multiple processes formed a network in the myenteric plexus region from corpus to pylorus.
158  Development and organization of ICCs of the myenteric plexus region into networks precedes the devel
159 ession of nitric oxide synthase (NOS) in the myenteric plexus remains unknown.
160  enzyme responsible for NO production in the myenteric plexus, remains unknown.
161 eganglionic fibers in the duodenal and cecal myenteric plexuses resembled the organization in the sto
162 early within the gastrointestinal mucosa and myenteric plexus, respectively.
163 ighly excitable, tonic S neurones within the myenteric plexus, since, in contrast to other S neurones
164 mically in neuronal perikarya (submucosal >> myenteric plexus; small intestine > stomach or colon).
165 ddition, to study age-related changes in the myenteric plexus, the stomachs, small intestines, and la
166      When the LM was sharp dissected off the myenteric plexus, the synchronized discharge of ascendin
167 reatment of opioid naive longitudinal muscle myenteric plexus tissue attenuates PLCbeta3 phosphorylat
168 lation in the guinea pig longitudinal muscle myenteric plexus tissue revealed substantial alterations
169 beta), in the guinea pig longitudinal muscle myenteric plexus tissue.
170                            In the developing myenteric plexus, trk immunoreactivity was present at em
171 smural electrical stimuli confirmed that the myenteric plexus was always present and intact in these
172 not express opioids; opioid synthesis in the myenteric plexus was not altered on induction of inflamm
173                                      Loss of myenteric plexus was observed only in all Ret null homoz
174 that the connectivity between the LM and the myenteric plexus was required for mechanotransduction.
175 he number of NOS-immunopositive cells in the myenteric plexus was significantly increased in tissues
176 tive cells and nNOS synthesis in the colonic myenteric plexus were significantly reduced in aged rats
177 r Hu was 100% in the P3 and 71% in the adult myenteric plexus, when submucosal neurons were also OTR-
178 ere located in the intestinal submucosal and myenteric plexuses where they were closely associated wi
179 ration of a robust expression of DPPX in the myenteric plexus, which strongly reacted with patients'

 
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