ライフサイエンスコーパス: muscle strip

1 of spontaneous activity (SA) in SCI bladder muscle strips.

2 oncurrent studies were performed on in vitro muscle strips.

3 cells impaled with microelectrodes in intact muscle strips.

4 in Triton-skinned rat caudal arterial smooth muscle strips.

5 smooth muscle cells and rat colonic circular muscle strips.

6 shly obtained human and rat colonic circular muscle strips.

7 d isometric muscle recording from intestinal muscle strips.

8 d dose-dependent reductions in tone of N-LES muscle strips.

9 low wave propagation in canine antral smooth muscle strips.

10 of HCCSMCs and fresh human colonic circular muscle strips.

11 ts were performed on jejunal circular smooth muscle strips.

12 was markedly depressed in paxillin-depleted muscle strips.

13 sum with responses of ICC in intact jejunal muscle strips.

14 tility was investigated in canine trachealis muscle strips.

15 ine (ACh) than in extracts from unstimulated muscle strips.

16 ere used to measure vasopressin responses in muscle strips.

17 ontraction was lower in atria than ventricle muscle strips (0.36 vs. 1.54 microM).

18 lin-stimulated glucose transport in skeletal muscle strips; 2) chronic ET-1 administration in vivo le

19 ased insulin-stimulated glucose transport in muscle strips (-23%).

20 -actin content was 30 % lower in extracts of muscle strips activated with 10-4 M acetylcholine (ACh)

21 NH(2)Cl also hyperpolarized intact muscle strips, an effect blocked by iberiotoxin.

22 lation triggered contraction of cells in the muscle strip and net locomotion of the bio-bot with a ma

23 In muscle strips and adipocytes, exposure to both calpain i

24 tractions of isolated urinary bladder smooth muscle strips and exposed high affinity effects of the b

25 nalysis; passive stiffness was studied in LV muscle strips and isolated cardiac myocytes before and a

26 NKA-induced contraction in muscle strips and single cells was virtually abolished b

27 adder relaxation was measured in vitro using muscle strips and single muscle cells.

28 d relaxation of the stretched bladder smooth muscle strips and triggered small-amplitude spontaneous

29 lectrode recordings were performed in intact muscle strips and whole-cell voltage clamp experiments w

30 unloaded shortening velocity in t/t skinned muscle strips, and dramatically reduced myofilament stif

31 glucose transport was measured in incubated muscle strips, and PC-1 content, enzymatic activity, and

32 In thiophosphorylated porcine tracheal muscle strips at pCa 9 + 2.1 mM ATP, H(2)O(2) caused a a

33 mere length relations were obtained in small muscle strips before and after KCl-KI treatment, which u

34 ical field-induced contraction of esophageal muscle strips, but not acetylcholine-induced contraction

35 illin antisense or sense was introduced into muscle strips by reversible permeabilization and strips

36 tyrosine sites 31, 118) into tracheal smooth muscle strips by reversible permeabilization, and incuba

37 Cdc42, were introduced into tracheal smooth muscle strips by reversible permeabilization, and tissue

38 These machines are powered by a muscle strip composed of differentiated skeletal myofibe

39 transport of [3H]2-deoxyglucose into soleus muscle strips confirmed the insulin resistance following

40 Mechanical performance of skinned papillary muscle strips derived from mutant and wild-type hearts a

41 direct excitatory effect on circular smooth muscle strips derived from the human colon.

42 E-LES muscle strips developed lower in vitro tone (0.78 g) tha

43 Pyloric muscle strips developed spontaneous phasic contractions

44 Conversely, the IAS smooth muscle strips developed spontaneous tone.

45 Gastrointestinal smooth muscle strips devoid of enteric nerve cells can contract

46 Mechanical measurements on LV muscle strips dissected from these hearts (n=8) revealed

47 EA enhanced fatty acid oxidation in skeletal muscle strips, dissociated hepatocytes, and primary card

48 Ex vivo contractility testing of bladder muscle strips exposed to electrical stimulation or solub

49 in skinned left ventricular (LV) epicardial muscle strips from 5 MR and 5 nonfailing (NF) control he

50 In terms of function, muscle strips from allografts only generated 23% of the

51 ic muscle recordings of colonic longitudinal muscle strips from mice that do not express TLR4 (Tlr4(L

52 erties of skinned left ventricular papillary muscle strips from mouse hearts bearing the R403Q mutati

53 All smooth muscle strips from normal and Ls/Ls mice produced relaxa

54 hearts and beta-agonist responsiveness using muscle strips from patients undergoing transplantation.

55 However, muscle strips from SM2(-/-) bladder showed increased con

56 Consistently, ventricular muscle strips from Tg-CTGF mice stimulated with isoprote

57 paration of interior and submucosal circular muscle strips from the dominant (myenteric) pacemaker re

58 Circular smooth muscle strips from the internal anal sphincter (IAS) and

59 Smooth muscle strips from the LES and the body of the esophagus

60 e transport was reduced by 32% (P < 0.05) in muscle strips from the pregnant control group and even f

61 SM), and studies of porcine carotid arterial muscle strips have shown that mechanical stretch leads t

62 le activity was observed in colonic circular muscle strips in the absence of external stimuli.

63 o the activity in stretched carotid arterial muscle strips in vivo.

64 anterior (TA) muscles (in situ) or diaphragm muscle strips (in vitro).

65 on of 5-HT receptor mRNA was investigated in muscle strips, in purified populations of ICC, and in id

66 els including cultured myotubes and isolated muscles strips incubated with exogenous fatty acids and

67 but not male HDL, promoted the relaxation of muscle strips isolated from C57BL/6 mice but not SR-BI n

68 r stimulate fatty acid oxidation in skeletal muscle strips isolated from PPAR-alpha mice.

69 Passive stiffness measurements on muscle strips isolated from the LV free wall revealed th

70 At 38 degrees C in vitro, left ventricular muscle strips isolated from the mild hypothermia group h

71 oline caused a decrease in G-actin in normal muscle strips, it caused little change in the G-actin co

72 as assayed in canine colonic circular smooth muscle strips labelled with 32P and stimulated with 10 m

73 n, and contraction in urinary bladder smooth muscle strips neurally stimulated for 3 s.

74 igated the effects of OFQ on contractions of muscle strips obtained from different regions of the gas

75 l and mechanical activities of human colonic muscle strips obtained from either the ascending, descen

76 stimulation were significantly increased in muscle strips obtained from rats treated with splanchnic

77 as used to produce contraction of the smooth muscle strips of distal colon to record a decrease in th

78 tension cost was significantly higher in the muscle strips of the three R403Q patients (2.93 +/- 0.25

79 cardiac myofibrils and multicellular cardiac muscle strips of three HCM patients with the R403Q mutat

80 mulated glucose transport in isolated soleus muscle strips of WKY rats.

81 TNFalpha treatment of circular muscle strips pretreated with ICAM-1 sense ODNs or contr

82 Muscle strips released TNF-alpha in the absence of LPS (

83 id isotonic organ bath experiments to assess muscle strip sensitivities to exogenous acetylcholine.

84 ) Electrophysiology experiments on dissected muscle strips show that slow waves originate from specif

85 In addition, ex vivo study of soleus muscle strips showed decreased glucose transport into mu

86 derlying myocardial DD was obvious from high muscle strip stiffness, which was largely (+/-80%) attri

87 e G-actin concentration in paxillin-depleted muscle strips, suggesting that paxillin is necessary for

88 inhibited force in alpha-toxin-permeabilized muscle strips that were activated either by Ca2+ or by A

89 ctuation of an engineered mammalian skeletal muscle strip to result in net locomotion of the bio-bot.

90 phageal muscle cells (HEMCs), and esophageal muscle strips to eosinophil-derived products.

91 ylation in h-CaD in porcine carotid arterial muscle strips was at Ser(789); however, the amount of ph

92 opossum internal anal sphincter (IAS) smooth muscle strips was investigated.

93 The basal tone of smooth muscle strips was measured by isometric force transducer

94 e response of permeabilized bronchial smooth muscle strips was significantly increased after incubati

95 Human airway smooth muscle strips were contracted with methacholine in vitro

96 The mucosa and submucosa were removed and muscle strips were cut and pinned in cross-section so th

97 The muscle strips were incubated at 37 degrees C in 95% O2/5

98 eatment, electrically paced left ventricular muscle strips were incubated with PI(3,5)P2.

99 IAS smooth muscle strips were isolated from wild-type (WT), heme ox

100 Permeabilized muscle strips were mounted between a piezoelectric lengt

101 Left ventricular muscle strips were obtained from seven patients with end

102 The data from in vitro muscle strips were similar to those in conscious dogs.

103 Muscle strips were stimulated electrically for 10 second

104 Rabbit pyloric muscle strips were studied in vitro.

105 Tracheal smooth muscle strips were treated with paxillin antisense oligo

106 tify alterations in leukocytes, and circular muscle strips were used to assess organ bath muscle func

107 man colonic circular smooth muscle cells and muscle strips were used.

108 Using permeabilized, arterial smooth muscle strips where membrane-associated pathways remain

109 This material enables formation of thin muscle strips whose biomechanical characteristics are ea

110 ctively propagated from end to end of antral muscle strips with a constant latency between two points

111 sient transfection of human colonic circular muscle strips with antisense oligonucleotides to p50 and

112 C2C12 cells (ACC2) and in rat epitrochlearis muscle strips with EC50s of 57 nm and 1.3 microm.

113 Treating myotubes or skeletal muscle strips with IL-18 activated AMPK and increased fa

114 Incubation of muscle strips with insulin significantly increased membr

115 e-endothelialized rat caudal arterial smooth muscle strips with the pyrazolo[3,4-d]pyrimidinone inhib

116 On the contrary, incubation of the muscle strips with VIP antagonist for 24 hours suppresse

117 uman colonic circular smooth muscle cells or muscle strips with VIP for 24 hours enhanced the express