ライフサイエンスコーパス: contraction

1 r activity-dependent form that supports ring contraction.

2 tion and abnormal airway smooth muscle (ASM) contraction.

3 cells (SMC) provide the Ca(2+) that triggers contraction.

4 the influence of activated monocytes on clot contraction.

5 eficit may result in drowning and/or lateral contraction.

6 ions including migration, proliferation, and contraction.

7 ting in minimal effects of MYPT1 knockout on contraction.

8 ates mitochondrial energy production to fuel contraction.

9 predominant response of W/W(V) stomachs was contraction.

10 mechanical and biochemical inputs to mediate contraction.

11 iates cardiac contractility and the force of contraction.

12 xercise pressor reflex in response to muscle contraction.

13 nal-regulated kinase and phospholamban), and contraction.

14 ry with the intensity and duration of muscle contraction.

15 GC response during its initiation, peak, and contraction.

16 m and are responsible for controlling muscle contraction.

17 CM signaling that is modulated by protrusion/contraction.

18 d a breathing mode with radial expansion and contraction.

19 coupling that regulated waves of propagating contraction.

20 p hypertension, reflecting systemic arterial contraction.

21 es to sustain cell growth and limit scaffold contraction.

22 appear to be primarily influenced by muscle contraction.

23 observed to scale linearly with the lattice contraction.

24 plays an important role in regulating muscle contraction.

25 require reversible guard cell elongation and contraction.

26 torques from 0% to 20% of maximum voluntary contraction.

27 sure downstream of the inlet valve following contraction.

28 nt stimulus and observe a front of increased contraction.

29 network organization during cell stretch and contraction.

30 periovulatory follicles and induces ovarian contraction.

31 ead to muscle fiber damage from the force of contraction.

32 reflect the intensity and duration of muscle contraction.

33 en released from the surface underwent rapid contraction.

34 trodes has been attempted to monitor uterine contraction.

35 p plays the dominant role in actomyosin ring contraction.

36 cardiac electrical activation and mechanical contraction.

37 f Gq/11-evoked Ca(2+) signaling and vascular contraction.

38 long-duration waves of airway smooth muscle contraction.

39 n but only HC-HA/PTX3 inhibited collagen gel contraction.

40 ing rate associated with sustained voluntary contractions.

41 ticularly active cell associated with muscle contractions.

42 g of titin stretched during eccentric muscle contractions.

43 sed the frequency of spontaneous non-voiding contractions.

44 uring ascending but not descending phases of contractions.

45 erred to be associated with fast propagating contractions.

46 etics of cardiomyocyte Ca(2+) transients and contractions.

47 generate appropriate intensities for muscle contractions.

48 nerates pulses and propagating waves of cell contractions.

49 57BL/6 mice (aged 3-4 months), brief tetanic contraction (100 Hz for 500 ms) evoked rapid onset vasod

50 release of internal stresses upon actomyosin contraction (800 +/- 100 Pa) and relaxation (600 +/- 100

51 during the ascending phase of the triangular contractions, 93% of the firing rate profiles were best

52 entricle outflow tract premature ventricular contraction ablation, an aortic valve closure artifact i

53 ated endurance times for sustained isometric contractions across a wide range of target levels.

54 A control neuronal signalling, smooth muscle contraction, airway and exocrine gland secretion, and rh

55 Then, active contraction along the anterior intestinal portal generat

56 ined by phosphoester elongation and siloxane contraction along the pulling axis in the respective rat

57 chain (RLC), NM myosin filament assembly and contraction, although it did not inhibit SM RLC phosphor

58 m internal stores and subsequent myofilament contraction, although these structures become disorganiz

59 ence of isoproterenol, Ca(2+) transients and contraction amplitudes were smaller in CD38(-/-) myocyte

60 e with longitudinal expansion and transverse contraction and a breathing mode with radial expansion a

61 promotes Orai1 hyperactivity, increased ASM contraction and airway hyperresponsiveness.

62 bit repetitive cycles of rapid expansion and contraction and apply coordinated traction forces to the

63 Cell contraction and blebbing also frequently occur as part o

64 ane to antagonize RhoC signaling during cell contraction and blebbing.

65 bitors (nifedipine and nimodipine) on airway contraction and Ca(2+) oscillations and SOCE-mediated Ca

66 We therefore studied the ability of contraction and exercise to stimulate glucose transport

67 d to perform a molecular machine function of contraction and expansion utilizing the binding features

68 lasmic reticulum to initiate skeletal muscle contraction and is associated with muscle diseases, mali

69 s a significant role in alleviating vascular contraction and promoting vascular relaxation due to its

70 ously within 1 day of seeding; the speeds of contraction and relaxation and the peak amplitudes of th

71 Contraction and relaxation are prolonged in isolated myo

72 efficient physiological mechanism to enhance contraction and relaxation of the heart.

73 potentials, the electrical events underlying contraction and relaxation, respectively, in colonic mus

74 (DCM) cardiomyopathy by disrupting sarcomere contraction and relaxation.

75 cal changes leading first to cell growth and contraction and then cell deadhesion, scattering, and in

76 i ) must increase during systole to activate contraction and then fall, during diastole, to allow the

77 nism for the control of airway smooth muscle contraction and thus are a critical factor in airway hyp

78 epithelial dynamics, and that alterations in contraction and/or substrate adhesion can cause confluen

79 Prostaglandins stimulate uterine contractions and are clinically used for cervical ripeni

80 nsory feedback to control coordinated muscle contractions and body posture.

81 ions in Drosophila result in abnormal muscle contractions and cause embryo torsion.

82 space potentially promoting widespread range contractions and expansions.

83 e, and repair of the breaks can cause repeat contractions and expansions.

84 cope are likely the result of multiple range contractions and extinction events.

85 cterized by sustained or intermittent muscle contractions and its pathophysiological mechanisms are s

86 oles of oxytocin (OT) is in inducing uterine contractions and labor.

87 Gastric emptying, antral contractions and oro-cecal transit after ingestion of a

88 Antral contractions and oro-cecal transit were not different.

89 mple model to identify combinations of range contractions and price increases capable of causing exti

90 ance therapy, as it inhibits both myometrial contractions and the proinflammatory effects of OT witho

91 Phasic contractions and tone in the IAS were nearly abolished b

92 have a central role in SW generation, phasic contractions and tone, independent of stretch.

93 ing cytoskeleton, focal adhesion, actomyosin contraction, and actin and microtubule assembly have bee

94 ing F-actin flow, the contribution of myosin contraction, and actin polymerization at bundles' termin

95 h-induced NM myosin filament assembly and SM contraction, and also inhibits the assembly of membrane

96 g growth factor-beta, vascular smooth muscle contraction, and the hedgehog and Wnt signaling pathways

97 nesis, the frequency of airway smooth muscle contraction, and the rate of developmental maturation of

98 es affect myofibroblast differentiation, gel contraction, and wound healing via mitochondria stress t

99 MLCK activity, MLC phosphorylation, and cell contraction are increased.

100 scle (SM) tissues and their possible role in contraction are largely unknown.

101 derstand how the processes regulating atrial contraction are remodelled during ageing and provides a

102 Thus, factors causing range contraction as abundance declines may pose unexpectedly

103 n nanotube yarn muscles that provide tensile contraction as high as 16.5%, which is 12.7 times higher

104 cells showed repeated nuclear stretching and contraction as the chromosomes failed to separate.

105 of 5 muM, in a fibroblast-mediated collagen contraction assay, was less cytotoxic, and a more potent

106 ting that Myp2p plays a minimal role in ring contraction at these temperatures.

107 a larger TV annular area with weaker annular contraction (both P<0.001) but a smaller tethering angle

108 etween cortex and periphery during isometric contraction builds on the presence of approximately 20 H

109 ed at the base of the Bilateria not only for contraction, but also as the source of positional inform

110 methods to measure cardiomyocyte and muscle contraction, but these require customized hardware, expe

111 of EGF at that point increases spreading and contractions, but this can be blocked by myosin-II inhib

112 e to fully relax methacholine-induced airway contraction by abolishing the Ca(2+) oscillations, in a

113 n be used to predict the maximal velocity of contraction (by motility assay or sarcomeric shortening)

114 ole of these prostanoids in the PVAT-induced contraction can be explained by a greater release of thr

115 Much of the Ca needed for contraction comes from the sarcoplasmic reticulum and is

116 ly, PRP coacervate doubled the rate of wound contraction compared to all other treatments, including

117 sculature, collecting vessels generate rapid contractions coordinated along lymphangions to propel ly

118 al myocytes Ca(2+) release during excitation-contraction coupling (ECC) is strikingly different from

119 Approach to Understanding Cardiac Excitation-Contraction Coupling and Arrhythmias (3-4 March 2016), a

120 Approach to Understanding Cardiac Excitation-Contraction Coupling and Arrhythmias Symposium, a biannu

121 divergent mechanisms that impair excitation-contraction coupling and may be exemplary of their adver

122 l cardiac function-in particular, excitation-contraction coupling and normal electric rhythms.

123 important for modulating cardiac excitation-contraction coupling and pathophysiology.

124 Ca(2+) is central to cardiac excitation-contraction coupling and stimulates mitochondrial energy

125 Excitation-contraction coupling in atrial cells is mediated by calc

126 efective membrane trafficking and excitation-contraction coupling in muscle.

127 Excitation-contraction coupling is the bridge between cardiac elect

128 e T-tubule development and mature excitation-contraction coupling of hiPSC-CM when cultured on extrac

129 ns unknown whether all SFMs share excitation-contraction coupling pathway adaptations for speed, and

130 ctional adaptations that minimize excitation-contraction coupling transduction times.

131 Ca(2+) is the central element of excitation-contraction coupling, but also impacts diverse signaling

132 orchestrate cardiac architecture, excitation-contraction coupling, mitochondrial biogenesis, and oxid

133 sing RyR2 channel activity during excitation-contraction coupling, resulting in random bursts of Ca(2

134 ly to preserve functional myocyte excitation-contraction coupling.

135 elease, and more ventricular-like excitation-contraction coupling.

136 ensuring synchronous and uniform excitation-contraction coupling.

137 sic activity of the motoneurons that control contraction (DE-3 motoneurons) and elongation (CV motone

138 In turn, the resulting diaphragmatic contraction delayed and reduced the expiratory collapse

139 model of two-dimensional actomyosin meshwork contraction, demonstrating that actomyosin meshworks exh

140 ed protein kinase (ROCK) activation and cell contraction-dependent manner.

141 ores (both >1,000 genes), although this gene contraction did not appear to correlate with the reducti

142 (BER) is responsible for causing CAG repeat contractions downstream of Fcy1, but not fragility.

143 view that differential growth and actomyosin contraction drive formation of the foregut and heart tub

144 The loss of diaphragmatic expiratory contraction during mechanical ventilation and muscle par

145 An SK channel activator (SKA-31) decreased contractions during filling, and rescued the overactivit

146 at result in progressively stronger cortical contractions during ingression.

147 tive effects on RV mechanics, synchrony, and contraction efficiency.

148 re activated selectively during longitudinal contractions, elongations in response to light, and radi

149 he mitochondrial Ca(2+) microdomain is where contraction, energy and death collide.

150 aximus muscle of C57BL/6 mice, brief tetanic contraction evoked rapid onset vasodilatation (ROV) (<1

151 t into appropriate motor command to keep the contraction force steady.

152 already extensively reported) but also with contraction force.

153 Myocardial contraction fraction (MCF) was calculated by dividing le

154 membrane, is required for ROCK-mediated cell contraction from 2 hr post infection.

155 agastric DB switched the origin of phase III contractions from the stomach to the duodenum (P = 0.001

156 ate conditions as promoters of species range contractions from those in neighbouring locations facili

157 The contraction generates a spatially graded centripetal act

158 and evoke external urethral sphincter (EUS) contraction (guarding reflex) to maintain continence.

159 r that the actomyosin-driven circumferential contraction/hoop tension applies a squeezing force on th

160 iggers a signaling cascade, culminating with contraction impairment and myofibril disruption in cardi

161 5%, 45%, 62.5%, and 80% of maximal voluntary contraction in a hand-held dynamometer).

162 The reduction induces substantial contraction in all bond lengths around the metal centers

163 tagonist GR32191B inhibited the PVAT-induced contraction in arteries from females.

164 ntagonist AL8810 attenuated the PVAT-induced contraction in arteries from males, whereas the TP recep

165 ic target to mitigate the severity of airway contraction in asthma.

166 regain volitional, graded control of muscle contraction in his paralyzed limb.

167 Finally, we used the algorithm to quantify contraction in in vitro and in vivo arrhythmia models an

168 Myosin-powered force generation and contraction in nonmuscle cells underlies many cell biolo

169 o rapid decline is evidenced by recent rapid contraction in range, supporting an uplisting of the Int

170 he regulatory protein that initiates cardiac contraction in response to Ca(2+) TnC binding Ca(2+) ini

171 order characterized by loss of smooth muscle contraction in the bladder and intestine.

172 mbryonic cholecystitis and fetal gallbladder contraction in the early pathogenesis of congenital bili

173 stitutions compromise the full inhibition of contraction in the relaxed state.

174 During Drosophila gastrulation, actomyosin contraction in ventral cells generates a long, narrow ep

175 myo2-E1-Sup1 are defective in ATP-dependent contraction in vitro.

176 ns must consider their response to potential contractions in international support for HIV programs.

177 e, axonal connectivity defects, and abnormal contractions in POMT mutant embryos.

178 inbelt, orbital variations produce expansion/contractions in terms of the global zonal mean.

179 In contrast, VT or premature ventricular contractions in the setting of a structurally normal hea

180 Factors causing such range contractions include schooling, herding, or flocking beh

181 a concentration-dependent decrease in muscle contraction, increase in heart rate, and accelerated hat

182 Measurement of membrane potential and contraction indicated that ANO1 and CavL have a central

183 Moreover, contraction-induced increases in sarcolemmal GLUT4 conte

184 ed distinct pathways linked to smooth muscle contraction, inflammatory cytokines, immune mediators, e

185 Tetanic contraction initiates hyperpolarization that conducts al

186 forces have been thought to drive interface contraction, initiation of Rab35 compartments does not r

187 An important mechanism of lymphocyte contraction is clonal depletion of activated T cells by

188 he majority fraction of the myosin heads for contraction is controlled in part by the external load o

189 The extent of this airway contraction is proportional to the frequency of Ca(2+) o

190 When macroscopic contraction is restricted, relaxation dominates.

191 A key elementary step of contraction is sequential extension-retraction of platel

192 abilization of the dxy orbital due to c-axis contraction is shown to be essential to explain the insu

193 position of surface BK channels to stimulate contraction is unclear.

194 tissues, however the role of NM myosin in SM contraction is unknown.

195 actin-myosin system, responsible for muscle contraction, is also the force-generating element in dyn

196 hat (i) quadriceps volume, maximum voluntary contraction isometric torque and patellar tendon force w

197 measurement revealed superior expansion and contraction kinetics of micromolar affinity CAR T cells.

198 atriumm58 mutant (wea) with inhibited atrial contraction leading to a highly undeveloped ventricle an

199 al variation of EMG and muscle motion onset, contraction level and speed.

200 ed complexity, diminished larval peristaltic contractions, loss of neuromuscular junction bouton stru

201 identical to the current gold standards for contraction measurement, such as optical flow, post defl

202 al role for TBC1D1 in exercise tolerance and contraction-mediated translocation of GLUT4 to the plasm

203 cts of electrically evoked maximal-intensity contractions (MICs) on protein phosphorylation in mouse

204 out of electrically evoked maximal-intensity contractions (MICs).

205 sensor was constructed based on an extension-contraction movement of DNA interconversion for the appl

206 Similar enhancement of contractions occurred in bladders of Trpv4 (-/-) mice du

207 industrial development via the expansion and contraction of a city's infrastructure.

208 that cleavage furrow ingression initiates by contraction of an equatorial actin network with randomly

209 In contrast, biaxial contraction of an inflated and axially extended excised

210 lpha-SMA, production and assembly of FN, and contraction of collagen matrices.

211 e demonstrate that the dynamic expansion and contraction of electrode films formed by restacking chem

212 ABSTRACT: Contraction of heart muscle is triggered by a transient

213 We found that prior in situ contraction of m.

214 Analyzing contraction of mesenteric resistance arteries supported

215 ort herein a photoinduced carboborative ring contraction of monounsaturated six-membered carbocycles

216 ABSTRACT: Contraction of muscle evokes the exercise pressor reflex

217 ry-adrenal axis leads to splenic atrophy and contraction of NK cell numbers in the periphery through

218 sed microscopic asymmetry leads to effective contraction of random 1D actomyosin arrays.

219 filaments, it is likely that in its absence, contraction of smooth muscle cells is impaired.

220 nd allocation, suggesting a disproportionate contraction of the belowground ecosystem components; thi

221 , resulting in the experimentally verifiable contraction of the collagen structures.

222 whether decreased excretory function due to contraction of the extracellular fluid volume (vAKI) or

223 c changes were associated with a significant contraction of the fecal microbiome and were partially r

224 errant smooth muscle formation and defective contraction of the fetal gallbladder.

225 dral tilting upon Cs-substitution but only a contraction of the lattice, leading to progressive reduc

226 In particular, our results showed contraction of the Olfactory Receptor (OR) gene repertoi

227 ding a specific accounting for the expansion/contraction of the skeleton that may occur via anchor pr

228 o motor neurons (MN); ultimately these drive contraction of the tail and limb muscles.

229 dge, relative to DNA, and (ii) expansion and contraction of the transcription bubble.

230 Compared with calcium phosphate control, a contraction of the unit cell in the a-direction but not

231 This beaming causes flux enhancement and contraction of the variability timescales, so that most

232 ults from successive bouts of elongation and contraction of the whole leech body.

233 ver fir and Scots pine portend dieback and a contraction of their species distribution areas through

234 Continuing global contraction of top predator ranges could promote further

235 equire a liquid electrolyte, provide tensile contractions of 11.6% and 5%, respectively.

236 nergy to power jumping was generated by slow contractions of hind leg depressor muscles and then stor

237 manent rhythmic and bilaterally synchronized contractions of inspiratory pump muscles.

238 effect on free cytosolic [Ca(2)(+) ] during contractions of isolated muscle fibres.

239 a peristaltic wave driven by cross-sectional contractions of tubes.

240 ever, the impact of large-scale IR expansion/contraction on plastid nucleotide substitution rates amo

241 -driven reduction in blood clot volume (clot contraction or retraction) has been implicated to play a

242 l (AP) waveform initiates and modulates each contraction, or heartbeat.

243 Premature ventricular contractions originating in the left ventricle outflow t

244 Contractions peak after 15-20 min, but diminish by tenfo

245 Nevertheless, the SOV of FAs during rhythmic contractions persisted until inhibition of nitric oxide

246 Teff cells stopped dividing just before the contraction phase.

247 y diastolic (SRe), and late diastolic atrial contraction phases (SRa) were analyzed by dedicated soft

248 POINTS: In tonic, isometric, plantarflexion contractions, physiological tremor increases as the ankl

249 The defective gallbladder contraction positively correlated with the severity of e

250 The models account for isotropic contraction proportional to myosin density, viscous stre

251 Variability in premature ventricular contraction (PVC) coupling interval (CI) increases the r

252 Premature ventricular contraction rate increased with exercise, and within ana

253 The ring contraction reaction of methoxy- or phenylthio-diazepino

254 Effective labour contractions require synchronization of myometrial cells

255 Effective contractions require the molecular coupling between myos

256 TGF-beta on RhoA and Rho-kinase activity and contraction, respectively.

257 Hz frequencies, even during steady isometric contractions.SIGNIFICANCE STATEMENT Accurate motor actio

258 Smooth muscle cell contraction significantly increased the ratio of radial

259 During rhythmic twitch contractions, slow onset vasodilatation (10-15 s) in FAs

260 ctivation onset, which decreased with higher contraction speed (Spearman rho >/= 0.45, P < 0.001).

261 Rhythmic twitch contractions stimulate FA endothelium to release nitric

262 its (beta1beta2 KO) each partially decreased contraction-stimulated glucose transport in mouse soleus

263 with either AMPK beta1beta2 KO or alpha2KD, contraction-stimulated glucose transport was almost comp

264 early in life, are necessary for terminating contraction (systole) in aged animals, where their loss

265 optical spectra is attributed to the lattice contraction that accompanies the Pb(2+) for M(2+) cation

266 Fasciculation represents a brief spontaneous contraction that affects a small number of muscle fibres

267 myosin II plays a critical role in airway SM contraction that is independent and distinct from the fu

268 ry (SCI) are debilitating involuntary muscle contractions that have been associated with increased mo

269 after loss of dinitrogen and subsequent ring contraction, the corresponding sulfone in 83% yield.

270 drive blastoderm thinning by inducing tissue contraction through radial deep cell intercalations.

271 e added fatigue-related changes in MU force, contraction time, and firing rate associated with sustai

272 e stretch of muscles, and the sensitivity of contraction to ANO1 antagonists was the same in stretche

273 many cellular processes ranging from muscle contraction to learning and memory.

274 he heart has for autoregulating the force of contraction to maintain cardiac output under changes of

275 bbit occurs during transition from isometric contraction to shortening under low load.

276 (pHi) is critical to cardiac excitation and contraction; uncompensated changes in pHi impair cardiac

277 at Myo2p is the major motor involved in ring contraction, under most, if not all, conditions.

278 tile responses were confirmed by single-cell contraction using magnetic twisting cytometry (MTC).

279 nerve ultimately drive iris-sphincter-muscle contraction via excitatory cholinergic parasympathetic i

280 tal actin flow, which in turn reinforces the contraction via myosin redistribution and causes retract

281 of Arp2/3 actin nucleation) and Rho-mediated contraction (via ROCK phosphorylation of myosin light ch

282 The lanthanide contraction was employed to systematically vary the unit

283 VPC31143-induced AA contraction was sensitive to pertussis toxin (PTX), the

284 A significant increase in CAG repeat contractions was also observed, consistent with previous

285 hain-20, a key regulator of lymphatic muscle contraction, was observed in insulin-resistant LMCs.

286 of LECs may promote the rapid conduction of contraction waves along lymphatic muscle during lymph pr

287 riments demonstrated that coordinated muscle contraction waves are associated with asymmetric embryo

288 the benefits of their education due to wage contraction, welfare retrenchment, and generalized socia

289 entricle outflow tract premature ventricular contraction were included.

290 er capacity) above which flow-evoked bladder contractions were 252% larger and evoked phasic EUS acti

291 Contractions were also inhibited by activation of SK cha

292 te profiles for the descending phases of the contractions were best fitted with linear functions for

293 e calcium transients although no spontaneous contractions were observed in transdifferentiated cells.

294 myo2-E1 also affects actomyosin ring contraction when rings isolated from permissive temperat

295 elongations in response to light, and radial contractions, whereas an additional network is located n

296 EVS applied after pre-contraction with bethanechol caused relaxation of wild t

297 adhesion phosphorylation and IL-13-enhanced contraction, with no additional effect from chymase.

298 -containing peptide abrogated IL-13-enhanced contraction, with no further effect from chymase.

299 This method provides a fast border contraction without a need for extensive boolean operati

300 suppressed adhesome complex assembly and SM contraction without inhibiting NM myosin Ser1943 phospho