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1 le fibers as myoblast fusion targets (dorsal longitudinal muscles).
2 ands, blood vessels, submucosal ganglia, and longitudinal muscle.
3 nce is a putative stretch receptor in dorsal longitudinal muscle.
4 innervate other myenteric ganglia and/or the longitudinal muscle.
5 the external muscle layers, particularly the longitudinal muscle.
6 terogeneity in the distribution of ICC-IM in longitudinal muscles.
7 ensory feedback from both ventral and dorsal longitudinal muscles.
8 at seed circular muscles and those that seed longitudinal muscles.
10 in proximity to the myenteric plexus in the longitudinal muscle and in association with blood vessel
12 timated delay time between relaxation of the longitudinal muscles and the activation of the circular
13 avel within the hindgut between circular and longitudinal muscles and within the submucosa and serosa
14 Neuro-pharmacologic controls of circular and longitudinal muscle are different, which provides an opp
15 eural and seemed to be common precursors for longitudinal muscle cells and ICs of the myenteric plexu
22 mine temporal synchrony between circular and longitudinal muscle contraction in healthy subjects and
23 gating segments during peristalsis, with the longitudinal muscle contraction leading the circular mus
26 ited in ileal segments from P2X3-/- mice but longitudinal muscle contractions caused by nicotine and
27 ited in ileal segments from P2X2-/- mice but longitudinal muscle contractions caused by nicotine and
30 lower esophageal sphincter (LES) relaxation, longitudinal muscle contracts independent of the circula
31 between the giant fiber (GF) and the dorsal longitudinal muscles (DLM) showed no overt defect due to
33 recorded in indirect flight muscles [dorsal longitudinal muscles (DLMs)] of the giant fiber (GF) pat
34 gmented body with repeated cuticular plates, longitudinal muscles, dorsoventral muscles, and ganglia.
35 he stretch receptors associated with ventral longitudinal muscles encode the information of muscle co
36 in such a way that each of five specialized longitudinal muscle fascicles are monitored by at least
38 nds of the midgut form by the coalescence of longitudinal muscle fibers on the midgut surface, appare
39 olic acid inhibited contractility of colonic longitudinal muscle from tgr5-wt but not tgr5-ko mice.
41 es the response of the giant fiber to dorsal longitudinal muscle (GF-DLM) connection to 20 +/- 13.9%
42 nteric ganglia, and a subset (41%) of antral longitudinal muscle IMAs formed specialized net endings
43 o summarize what is known of the role of the longitudinal muscle in health, as well as in sensory and
44 provided novel insights into the role of the longitudinal muscle in LES relaxation and descending rel
45 f putative stretch receptors associated with longitudinal muscles in midbody segments of medicinal le
46 increased target volume, as the reduction in longitudinal muscle innervation persisted after correcti
47 mming; (2) stretch receptors associated with longitudinal muscles interact with the central oscillato
48 ating collective, and an increased number of longitudinal muscles is found at anterior sections of th
49 is case the motor neuron that innervates the longitudinal muscles (L-cells) that contributes to a def
50 W(V) mice, but functional innervation of the longitudinal muscle layer by these nerves in the corpus
53 ochemistry was used to examine ICC-IM in the longitudinal muscle layer of the murine corpus and antru
55 haped ICC were found within the circular and longitudinal muscle layers (IC-IM) throughout the stomac
57 preparations of gut tissue consisting of the longitudinal muscle layers with the adherent myenteric p
58 ic region (ICC-MY), between the circular and longitudinal muscle layers, generate and propagate elect
68 eous intracellular recordings were made from longitudinal muscle (LM) and circular muscle (CM) cells
69 ultaneous mechanical reflex responses of the longitudinal muscle (LM) and circular muscle (CM) layers
70 pathways underlying reflex responses of the longitudinal muscle (LM) and circular muscle (CM) layers
71 rs elicited a synchronous contraction of the longitudinal muscle (LM) and circular muscle (CM) oral t
72 r model that describes the coupled layers of longitudinal muscle (LM) and interstitial cells of Cajal
73 show asynchrony of circular muscle (CM) and longitudinal muscle (LM) contraction during peristalsis.
74 were made from the circular muscle (CM) and longitudinal muscle (LM) in flat sheet preparations usin
75 The tension in the circular muscle (CM) and longitudinal muscle (LM) was recorded with force transdu
76 contributes to larval structure, forming the longitudinal muscles, mesenchyme, and probably endoderm.
77 in through the recording microelectrode: (i) longitudinal muscle motor neurones, (ii) short circular
78 rats, we monitored activation of the colonic longitudinal muscle myenteric plexus (LMMP) neurons and
80 of AC (type II family) was observed in ileum longitudinal muscle myenteric plexus preparations obtain
81 ne, acute morphine treatment of opioid naive longitudinal muscle myenteric plexus tissue attenuates P
82 d PLCbeta3 phosphorylation in the guinea pig longitudinal muscle myenteric plexus tissue revealed sub
85 timulatory mu-opioid signaling in guinea pig longitudinal muscle/myenteric plexus (LMMP) preparations
87 tatory and nitrergic inhibitory responses in longitudinal muscles of the corpus, but not in the antru
88 lation between prolonged contractions of the longitudinal muscles of the esophagus and esophageal 'an
93 Here we show that mixing movements within longitudinal muscle result from spontaneously generated
94 ship between longitudinal muscle tension and longitudinal muscle shortening, and the contribution of
95 , and isometric muscle recordings of colonic longitudinal muscle strips from mice that do not express
96 of circular muscle, the relationship between longitudinal muscle tension and longitudinal muscle shor
100 sa and submucosa were removed, and strips of longitudinal muscle were peeled away to reveal the ICC-M
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