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1 oncurrent studies were performed on in vitro muscle strips.
2 tion effect of the mutant peptide on skinned muscle strips.
3  of spontaneous activity (SA) in SCI bladder 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 cells impaled with microelectrodes in intact muscle strips.
9 d dose-dependent reductions in tone of N-LES muscle strips.
10 low wave propagation in canine antral smooth muscle strips.
11  of HCCSMCs and fresh human colonic circular muscle strips.
12 ts were performed on jejunal circular smooth muscle strips.
13  was markedly depressed in paxillin-depleted muscle strips.
14  sum with responses of ICC in intact jejunal muscle strips.
15 tility was investigated in canine trachealis muscle strips.
16 ine (ACh) than in extracts from unstimulated muscle strips.
17 ere used to measure vasopressin responses in muscle strips.
18 ontraction was lower in atria than ventricle muscle strips (0.36 vs. 1.54 microM).
19 lin-stimulated glucose transport in skeletal muscle strips; 2) chronic ET-1 administration in vivo le
20 ased insulin-stimulated glucose transport in muscle strips (-23%).
21 -actin content was 30 % lower in extracts of muscle strips activated with 10-4 M acetylcholine (ACh)
22           NH(2)Cl also hyperpolarized intact muscle strips, an effect blocked by iberiotoxin.
23 lation triggered contraction of cells in the muscle strip and net locomotion of the bio-bot with a ma
24                                           In muscle strips and adipocytes, exposure to both calpain i
25 tractions of isolated urinary bladder smooth muscle strips and exposed high affinity effects of the b
26 nalysis; passive stiffness was studied in LV muscle strips and isolated cardiac myocytes before and a
27                   NKA-induced contraction in muscle strips and single cells was virtually abolished b
28 adder relaxation was measured in vitro using muscle strips and single muscle cells.
29 d relaxation of the stretched bladder smooth muscle strips and triggered small-amplitude spontaneous
30 lectrode recordings were performed in intact muscle strips and whole-cell voltage clamp experiments w
31  unloaded shortening velocity in t/t skinned muscle strips, and dramatically reduced myofilament stif
32  glucose transport was measured in incubated muscle strips, and PC-1 content, enzymatic activity, and
33       In thiophosphorylated porcine tracheal muscle strips at pCa 9 + 2.1 mM ATP, H(2)O(2) caused a a
34 mere length relations were obtained in small muscle strips before and after KCl-KI treatment, which u
35 ical field-induced contraction of esophageal muscle strips, but not acetylcholine-induced contraction
36 illin antisense or sense was introduced into muscle strips by reversible permeabilization and strips
37 tyrosine sites 31, 118) into tracheal smooth muscle strips by reversible permeabilization, and incuba
38  Cdc42, were introduced into tracheal smooth muscle strips by reversible permeabilization, and tissue
39              These machines are powered by a muscle strip composed of differentiated skeletal myofibe
40  transport of [3H]2-deoxyglucose into soleus muscle strips confirmed the insulin resistance following
41  Mechanical performance of skinned papillary muscle strips derived from mutant and wild-type hearts a
42  direct excitatory effect on circular smooth muscle strips derived from the human colon.
43                                        E-LES muscle strips developed lower in vitro tone (0.78 g) tha
44                                      Pyloric muscle strips developed spontaneous phasic contractions
45                   Conversely, the IAS smooth muscle strips developed spontaneous tone.
46                      Gastrointestinal smooth muscle strips devoid of enteric nerve cells can contract
47                Mechanical measurements on LV muscle strips dissected from these hearts (n=8) revealed
48 EA enhanced fatty acid oxidation in skeletal muscle strips, dissociated hepatocytes, and primary card
49     Ex vivo contractility testing of bladder muscle strips exposed to electrical stimulation or solub
50  in skinned left ventricular (LV) epicardial muscle strips from 5 MR and 5 nonfailing (NF) control he
51                        In terms of function, muscle strips from allografts only generated 23% of the
52 ic muscle recordings of colonic longitudinal muscle strips from mice that do not express TLR4 (Tlr4(L
53 erties of skinned left ventricular papillary muscle strips from mouse hearts bearing the R403Q mutati
54                                   All smooth muscle strips from normal and Ls/Ls mice produced relaxa
55 hearts and beta-agonist responsiveness using muscle strips from patients undergoing transplantation.
56 rein, we used skinned, ventricular papillary muscle strips from rats to investigate the effects of [O
57                                     However, muscle strips from SM2(-/-) bladder showed increased con
58                    Consistently, ventricular muscle strips from Tg-CTGF mice stimulated with isoprote
59 paration of interior and submucosal circular muscle strips from the dominant (myenteric) pacemaker re
60                              Circular smooth muscle strips from the internal anal sphincter (IAS) and
61                                       Smooth muscle strips from the LES and the body of the esophagus
62 e transport was reduced by 32% (P < 0.05) in muscle strips from the pregnant control group and even f
63 SM), and studies of porcine carotid arterial muscle strips have shown that mechanical stretch leads t
64 udies in single myofibrils and permeabilized muscle strips highlighted faster cross-bridge cycling, a
65 and increased contractions of ileal circular muscle strips in ex vivo experiments (P < .05).
66 le activity was observed in colonic circular muscle strips in the absence of external stimuli.
67 o the activity in stretched carotid arterial muscle strips in vivo.
68 anterior (TA) muscles (in situ) or diaphragm muscle strips (in vitro).
69 on of 5-HT receptor mRNA was investigated in muscle strips, in purified populations of ICC, and in id
70 els including cultured myotubes and isolated muscles strips incubated with exogenous fatty acids and
71 but not male HDL, promoted the relaxation of muscle strips isolated from C57BL/6 mice but not SR-BI n
72 r stimulate fatty acid oxidation in skeletal muscle strips isolated from PPAR-alpha mice.
73            Passive stiffness measurements on muscle strips isolated from the LV free wall revealed th
74   At 38 degrees C in vitro, left ventricular muscle strips isolated from the mild hypothermia group h
75 oline caused a decrease in G-actin in normal muscle strips, it caused little change in the G-actin co
76 as assayed in canine colonic circular smooth muscle strips labelled with 32P and stimulated with 10 m
77 n, and contraction in urinary bladder smooth muscle strips neurally stimulated for 3 s.
78 igated the effects of OFQ on contractions of muscle strips obtained from different regions of the gas
79 l and mechanical activities of human colonic muscle strips obtained from either the ascending, descen
80  stimulation were significantly increased in muscle strips obtained from rats treated with splanchnic
81 as used to produce contraction of the smooth muscle strips of distal colon to record a decrease in th
82 tension cost was significantly higher in the muscle strips of the three R403Q patients (2.93 +/- 0.25
83 cardiac myofibrils and multicellular cardiac muscle strips of three HCM patients with the R403Q mutat
84 mulated glucose transport in isolated soleus muscle strips of WKY rats.
85  purified, independently contracting cardiac muscle strips on two-dimensional elastomer substrates wi
86 elatively higher input impedance than larger muscle strips or sheets, we recorded an ongoing discharg
87               TNFalpha treatment of circular muscle strips pretreated with ICAM-1 sense ODNs or contr
88                                              Muscle strips released TNF-alpha in the absence of LPS (
89 id isotonic organ bath experiments to assess muscle strip sensitivities to exogenous acetylcholine.
90 ) Electrophysiology experiments on dissected muscle strips show that slow waves originate from specif
91         In addition, ex vivo study of soleus muscle strips showed decreased glucose transport into mu
92 derlying myocardial DD was obvious from high muscle strip stiffness, which was largely (+/-80%) attri
93 e G-actin concentration in paxillin-depleted muscle strips, suggesting that paxillin is necessary for
94 inhibited force in alpha-toxin-permeabilized muscle strips that were activated either by Ca2+ or by A
95 ctuation of an engineered mammalian skeletal muscle strip to result in net locomotion of the bio-bot.
96 phageal muscle cells (HEMCs), and esophageal muscle strips to eosinophil-derived products.
97 ylation in h-CaD in porcine carotid arterial muscle strips was at Ser(789); however, the amount of ph
98 opossum internal anal sphincter (IAS) smooth muscle strips was investigated.
99                     The basal tone of smooth muscle strips was measured by isometric force transducer
100 e response of permeabilized bronchial smooth muscle strips was significantly increased after incubati
101                          Human airway smooth muscle strips were contracted with methacholine in vitro
102    The mucosa and submucosa were removed and muscle strips were cut and pinned in cross-section so th
103                                          The muscle strips were incubated at 37 degrees C in 95% O2/5
104 eatment, electrically paced left ventricular muscle strips were incubated with PI(3,5)P2.
105                                   IAS smooth muscle strips were isolated from wild-type (WT), heme ox
106                                Permeabilized muscle strips were mounted between a piezoelectric lengt
107                             Left ventricular muscle strips were obtained from seven patients with end
108                       The data from in vitro muscle strips were similar to those in conscious dogs.
109                                              Muscle strips were stimulated electrically for 10 second
110                               Rabbit pyloric muscle strips were studied in vitro.
111                              Tracheal smooth muscle strips were treated with paxillin antisense oligo
112 tify alterations in leukocytes, and circular muscle strips were used to assess organ bath muscle func
113 man colonic circular smooth muscle cells and muscle strips were used.
114         Using permeabilized, arterial smooth muscle strips where membrane-associated pathways remain
115      This material enables formation of thin muscle strips whose biomechanical characteristics are ea
116 ctively propagated from end to end of antral muscle strips with a constant latency between two points
117 sient transfection of human colonic circular muscle strips with antisense oligonucleotides to p50 and
118 C2C12 cells (ACC2) and in rat epitrochlearis muscle strips with EC50s of 57 nm and 1.3 microm.
119                Treating myotubes or skeletal muscle strips with IL-18 activated AMPK and increased fa
120                                Incubation of muscle strips with insulin significantly increased membr
121 e-endothelialized rat caudal arterial smooth muscle strips with the pyrazolo[3,4-d]pyrimidinone inhib
122           On the contrary, incubation of the muscle strips with VIP antagonist for 24 hours suppresse
123 uman colonic circular smooth muscle cells or muscle strips with VIP for 24 hours enhanced the express

 
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