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1 ic nervous system (ENS), particularly in the submucosal plexus.
2 rgic secretomotor/vasodilator neurons in the submucosal plexus.
3 d noncholinergic secretomotor neurons in the submucosal plexus.
4 neurons, but was abundantly expressed in the submucosal plexus.
5 throughout the gut: the myenteric plexus and submucosal plexus.
6 sensory elements did not lie adjacent to the submucosal plexus.
7  immunoreactivity was rarely observed in the submucosal plexus.
8  present in any of the ganglion cells in the submucosal plexus.
9 ecessary for excitation to spread within the submucosal plexus.
10 noreactivity (SP-li), in nerve fibers of the submucosal plexus.
11 l as by TTX, hexamethonium or removal of the submucosal plexus.
12  reduction of CGRP-li in nerve fibers of the submucosal plexus.
13 ve ganglion cells, in both the myenteric and submucosal plexus.
14 retrograde tracer, FluoroGold (FG), into the submucosal plexus.
15 ack and destroy neurons of the myenteric and submucosal plexus.
16 tions, circuit dynamics and formation of the submucosal plexus.
17 or mRNA, but not CRF2, in both myenteric and submucosal plexuses.
18 ressed in nerve fibers in both myenteric and submucosal plexuses.
19  the levels of the presumptive myenteric and submucosal plexuses.
20 ng was quite dense in both the myenteric and submucosal plexuses.
21 CRF-IR cell bodies were more abundant in the submucosal plexus (29.9-38.0%) than in the myenteric ple
22 CRF-IR fibers persisted in the myenteric and submucosal plexuses after 7 days in organotypic culture.
23 even per cent of CSE positive neurons in the submucosal plexus and 50% of CSE positive neurons in the
24 cites secretomotor neurons in the guinea pig submucosal plexus and increases motility.
25 gic or sympathetic markers terminated in the submucosal plexus and mucosa of the duodenum.
26 ry revealed CaR expression in regions of the submucosal plexus and myenteric neurons.
27 y in calbindin-immunoreactive neurons in the submucosal plexus and not in myenteric ganglia.
28 ant labeling of neurons occurred only in the submucosal plexus and not in myenteric ganglia.
29  primary afferent neurons are located in the submucosal plexus and that N-type Ca2+ channels play a r
30               TRPC3-IR was found only in the submucosal plexus and was expressed exclusively by neuro
31                            The myenteric and submucosal plexuses and DVC were processed for detection
32 imarily stained neurons of the myenteric and submucosal plexuses, and abundant fibers distributed to
33               mGluR5-containing cells in the submucosal plexus are predominantly noncholinergic and c
34 so inhibited the spread of excitation in the submucosal plexus, assessed by measuring the uptake of F
35                                       In the submucosal plexus, CRF1 receptor immunoreactivity was fo
36 testinal tract, neurons of the myenteric and submucosal plexuses developed profound pathology, demons
37                                       In the submucosal plexus, DOReGFP was detected in neuropeptide
38 acing revealed that neuron identities in the submucosal plexus emerge through an initial binary fate
39 oglial structures similar to a myenteric and submucosal plexus, had functional interstitial cells of
40  small intestine and ICC associated with the submucosal plexus (ICC-SMP) in the colon.
41 al populations of both the myenteric and the submucosal plexuses in the chick, caudal to the level of
42  the hindgut in large numbers, myenteric and submucosal plexuses in the hindgut almost entirely compo
43 rve fibers were present in the myenteric and submucosal plexuses, in the circular muscle coat, and su
44 e also observed in the myoenteric plexus and submucosal plexus, involving enteric neurons with enteri
45  Absence of NF145 from ganglion cells in the submucosal plexus is an example of differences between m
46 calized in nerve fibers of the myenteric and submucosal plexuses, muscularis externa and lamina propr
47 urons, while being on axonal compartments of submucosal plexus neurons.
48 n morphologically identified neurones in the submucosal plexus of guinea-pig small intestine.
49 together, these results suggest that, in the submucosal plexus of the guinea-pig caecum, release of n
50 ach and small and large intestine and in the submucosal plexus of the small and large intestine.
51  was expressed in both the myenteric and the submucosal plexuses of all regions of the large and smal
52 anglia, and the ganglia of the myenteric and submucosal plexuses of the duodenum following intraperit
53 ally identified neurons in the myenteric and submucosal plexuses of the guinea pig enteric nervous sy
54 sence of ganglion cells in the myenteric and submucosal plexuses of the intestine.
55 mucosa-submucosa preparations (including the submucosal plexus) of rat proximal colon, carbachol (CCh
56 e enteric nervous system (ENS; myenteric and submucosal plexuses) of the gastrointestinal (GI) tract
57                                  The enteric submucosal plexus regulates essential digestive function
58 tions of adult (8-12-week old) myenteric and submucosal plexus stained with NADPH diaphorase (neurons
59 preferentially localize to the myenteric and submucosal plexuses suggesting potential role for this c
60 nduced slow EPSP-like response in guinea pig submucosal plexus, suggesting that CaMKII activity is re
61 trast, human stomachs have a clearly defined submucosal plexus that contains a variety of transmitter
62                                       In the submucosal plexus, TRPC4/6-IR was expressed exclusively
63                                Myenteric and submucosal plexuses were isolated from all 4 groups of m
64 o the myenteric plexus, and then back to the submucosal plexus, which is closer to the lumen.