ライフサイエンスコーパス: circular muscle

1 ve cells along the submucosal surface of the circular muscle.

2 longitudinal muscle contraction leading the circular muscle.

3 sduction of lower esophageal sphincter (LES) circular muscle.

4 confined to the axes of the longitudinal or circular muscle.

5 pacemaker cells populate all regions of the circular muscle.

6 ach have pacemaker capability throughout the circular muscle.

7 bitory junction potentials (IJPs) in colonic circular muscle.

8 xcitatory neurotransmitters in human sigmoid circular muscle.

9 itudinal muscle contracts independent of the circular muscle.

10 y induced contraction of human sigmoid colon circular muscle.

11 ential was examined in canine proximal colon circular muscle.

12 ngitudinal muscles and the activation of the circular muscles.

13 ves were recorded from canine proximal colon circular muscles.

14 and H2O2 levels were 4 times higher in E-LES circular muscle (0.85 nmol/mg protein) than in N-LES (0.

15 association between a suppression in jejunal circular muscle activity and a massive extravasation of

16 and intracellular microelectrodes to record circular muscle activity occurring spontaneously or foll

17 Circular muscle activity was assessed using mechanical a

18 In circular muscle, activity of choline acetyltransferase w

19 ited by SNP after removal of a thin strip of circular muscle along the myenteric edge.

20 transcript was predominantly present in the circular muscle and in the collagenous connective tissue

21 mach and varicose simple-type endings in the circular muscle and mucosa.

22 ing contraction and descending relaxation of circular muscle and release of serotonin and calcitonin

23 tive localization of FP receptor mRNA in the circular muscles and collagenous connective tissues of t

24 founders are of two classes: those that seed circular muscles and those that seed longitudinal muscle

25 s running from the myenteric plexus into the circular muscle, and in fibers and cells in intrapancrea

26 Nerve fibre density was not altered in the circular muscle, and pre-contracted rings of inflamed co

27 e propagation occurred in all regions of the circular muscle, and propagation velocities were similar

28 s could be evoked in interior and submucosal circular muscles at rates above normal antral frequency

29 okes descending inhibition of the intestinal circular muscle below an activation point, and contracti

30 C-alpha, -betaII, and -gamma isozymes in LES circular muscle, but only PKC-betaII translocated from t

31 Junctional conductance was greater between circular muscle-cell pairs from rats delivering either a

32 a second messenger in contraction of colonic circular muscle cells and if this role is altered by inf

33 on factor NF-kappa B is activated in colonic circular muscle cells by inflammation and oxidative stre

34 Electrical recordings from circular muscle cells confirmed the absence of slow wave

35 caine, bupivacaine and acidic pH depolarized circular muscle cells in intact muscles and decreased am

36 +) channel current are down-regulated in the circular muscle cells of the inflamed canine colon.

37 activity from either side of a fecal pellet, circular muscle cells oral and anal of a pellet, and in

38 acellular recordings were then obtained from circular muscle cells to examine excitatory and inhibito

39 Dissociated colonic circular muscle cells were obtained by enzymatic digesti

40 fiber tracts evoked biphasic IJPs in colonic circular muscle cells.

41 c receptor-activated contractions of colonic circular muscle cells.

42 tcracker esophagus [NCE]) show asynchrony of circular muscle (CM) and longitudinal muscle (LM) contra

43 Recordings were made from the circular muscle (CM) and longitudinal muscle (LM) in fla

44 The tension in the circular muscle (CM) and longitudinal muscle (LM) was re

45 ve movements of longitudinal muscle (LM) and circular muscle (CM) and the role that nerves play in co

46 mmals, ICC also line septa (ICC-SEP) between circular muscle (CM) bundles, suggesting they might be n

47 Recordings were made from circular muscle (CM) cells and myenteric neurons in the

48 lectrical recordings were made from pairs of circular muscle (CM) cells during colonic MMC activity i

49 ordings were made from myenteric neurons and circular muscle (CM) cells in isolated, stretched segmen

50 were made from longitudinal muscle (LM) and circular muscle (CM) cells of guinea-pig distal colon du

51 acellular recordings were made from pairs of circular muscle (CM) cells to map the region of smooth m

52 acellular recordings were made from pairs of circular muscle (CM) cells, at the oral and anal ends of

53 estigated the involvement of muscle tone and circular muscle (CM) contraction in peristalsis in isola

54 wever, the role of the longitudinal (LM) and circular muscle (CM) in transducing these mechanosensory

55 esponses of the longitudinal muscle (LM) and circular muscle (CM) layers activated by mucosal stimula

56 esponses of the longitudinal muscle (LM) and circular muscle (CM) layers of the guinea-pig ileum foll

57 in the ICC network and longitudinal (LM) and circular muscle (CM) layers of the isolated guinea-pig g

58 tify the boundaries of longitudinal (LM) and circular muscle (CM) layers.

59 traction of the longitudinal muscle (LM) and circular muscle (CM) oral to, and transient relaxation o

60 rk lying along the submucosal surface of the circular muscle (CM).

61 reflex pathways to the longitudinal (LM) and circular muscle (CM).

62 he mucosa, submucosal blood vessels, and the circular muscle coat also showed P2X(7) receptor immunor

63 he myenteric and submucosal plexuses, in the circular muscle coat, and surrounding submucosal arterio

64 at neuromuscular junctions in the intestinal circular muscle coat; this action of ATP is mediated by

65 , we observed a decrease in in vitro jejunal circular muscle contractility and gastrointestinal trans

66 nificantly improved postoperative intestinal circular muscle contractility in vitro and gastrointesti

67 nted the manipulation-induced suppression of circular muscle contractility in vitro, and significantl

68 In vitro circular muscle contractility was assessed in a standard

69 In vitro circular muscle contractility was assessed in a standard

70 Postoperative in vitro small intestinal circular muscle contractility was impaired by 42% compar

71 ansit assessed in vivo motility, and jejunal circular muscle contractility was measured in vitro.

72 ented SITx-induced suppression of intestinal circular muscle contractility.

73 e or in combination with GW274150C increased circular muscle contractility.

74 as examined histologically, and its in vitro circular muscle contraction and production of inflammato

75 Esophageal shortening was coordinated with circular muscle contraction such that each propagated di

76 termine the relationship between shortening, circular muscle contraction, and generation of propulsiv

77 egment occurred after shortening, during the circular muscle contraction, with the magnitude of propu

78 ulation leads to a significant inhibition of circular muscle contraction.

79 osal surface of upper GI tract to record the circular muscle contractions in eight dogs.

80 OFQ (10(-10) to 10(-6) mol/L) caused circular muscle contractions that were blocked by tetrod

81 Jejunal circular muscle contractions were measured in an organ b

82 ontaneous and bethanechol-stimulated jejunal circular muscle contractions were measured in an organ b

83 aris and a functional suppression in jejunal circular muscle contractions.

84 mplanted on the gastric antrum to record the circular muscle contractions.

85 tatory nerves to couple the longitudinal and circular muscles during the CMMC.

86 into the muscularis and also averted jejunal circular muscle dysfunction.

87 Leukocyte infiltration and in vitro jejunal circular muscle function were quantified in controls and

88 A subset (32%) of circular muscle IMAs issued specialized polymorphic coll

89 action were simultaneously recorded from the circular muscle in the presence of drugs to block adrene

90 ing contraction and descending relaxation of circular muscle induced by mucosal stimulation were inhi

91 purinergic inhibitory neuronal input to the circular muscle is selectively reduced in regions of the

92 dles and along the submucosal surface of the circular muscle layer (IC-SM).

93 circular smooth muscle cells throughout the circular muscle layer and abolished the transwall gradie

94 d vascular structures, and surrounding inner circular muscle layer fibers.

95 from muscle cells at different depths of the circular muscle layer from wild-type and heme oxygenase-

96 bundance along the submucosal surface of the circular muscle layer in the colon.

97 g membrane potential (RMP) exists across the circular muscle layer in the mouse colon.

98 cal role in enteric neural regulation of the circular muscle layer in the stomach, but no studies hav

99 dings were made from isolated bundles of the circular muscle layer of mouse and guinea-pig gastric fu

100 Kir2.1 was expressed in the circular muscle layer of the canine proximal colon, duod

101 pacemaker frequency was investigated in the circular muscle layer of the gastric antra of wild-type

102 The circular muscle layer of the IAS was divided into five t

103 w waves were identified in the human colonic circular muscle layer which arise at or near the submuco

104 immunopositive nerve fibers was observed in circular muscle layer while substance P immunoreactivity

105 IP-IR but not GRP-IR projects heavily to the circular muscle layer, the muscularis mucosae, and to ot

106 the presence of the myenteric region of the circular muscle layer, which contains cell bodies of ent

107 graft-derived neurons formed a plexus in the circular muscle layer.

108 of cells along the submucosal surface of the circular muscle layer.

109 sal half (SCM) and the interior (ICM) of the circular muscle layer.

110 dipine-insensitive slow waves throughout the circular muscle layer.

111 n of the myenteric plexus and throughout the circular muscle layer.

112 arbor expanded between the longitudinal and circular muscle layers, a region occupied by small unide

113 r neurons projecting to the longitudinal and circular muscle layers, as well as a small subgroup of d

114 n contrast, lower esophageal sphincter (LES) circular muscle maintains spontaneous tone and relaxes i

115 ngitudinal muscle motor neurones, (ii) short circular muscle motor neurones, and (iii) ascending inte

116 Circular muscle of the esophagus (ESO) is normally relax

117 ncy, delayed colonic emptying, and decreased circular muscle relaxation.

118 , long rectilinear arrays of neurites within circular muscle/secondary plexus or longitudinal muscle/

119 Separation of interior and submucosal circular muscle strips from the dominant (myenteric) pac

120 contractile activity was observed in colonic circular muscle strips in the absence of external stimul

121 TNFalpha treatment of circular muscle strips pretreated with ICAM-1 sense ODNs

122 ally quantify alterations in leukocytes, and circular muscle strips were used to assess organ bath mu

123 Transient transfection of human colonic circular muscle strips with antisense oligonucleotides t

124 circular smooth muscle cells and rat colonic circular muscle strips.

125 s and freshly obtained human and rat colonic circular muscle strips.

126 cultures of HCCSMCs and fresh human colonic circular muscle strips.

127 which the active and "passive" components of circular muscle tension are separately extracted from co

128 nics including the space-time stimulation of circular muscle, the relationship between longitudinal m

129 y dorsal and ventral ectoderm as well as the circular muscles; the third quartet forms only small clo

130 , LTD4, and LTE4) was measured in esophageal circular muscle tissue.

131 The responses of intact circular muscles to CCh and stimulation of intrinsic exc

132 partly account for the inhibition of colonic circular muscle tone and phasic contractions observed du

133 Tension of the circular muscle was measured in all three chambers.

134 The activity of whole circular muscle (WCM) was compared with that of the myen

135 Projections into the presumptive circular muscle were first observed at E14.5.

136 ted predominantly with the vascular zone and circular muscle within the cervical region.