ライフサイエンスコーパス: stretch

1 e to mechanical stimulation (uniaxial cyclic stretch).

2 fractional pump flow are sensitive to axial stretch.

3 s high-magnification imaging of cells during stretch.

4 roterenol, phenylephrine, angiotensin II and stretch.

5 the vibrational frequency of the thiocyanate stretch.

6 d basolateral flow, and flow plus repetitive stretch.

7 rred from changes in the envelope of the C-H stretch.

8 target genes in response to uniaxial cyclic stretch.

9 t suffers reduced accuracy in homonucleotide stretches.

10 tions of floating sheets subjected to radial stretching.

11 s to apically constrict through mitotic cell stretching.

12 d role for the lamina in systemic chromosome stretching.

13 tiveness (SE) deteriorates consistently with stretching.

14 main tightly coupled, restricting chromosome stretching.

15 nd gene-regulatory networks are modulated by stretching.

16 tural motifs upon physiological twisting and stretching.

17 re decoupled from behavior or are temporally stretched across single trials.

18 Their distribution stretches across Latin America, with some species occurr

19 show that the MEF effects, depending on the stretch-activated channels' conductances and reversal po

20 to as mechanoelectrical feedback (MEF), via stretch-activated channels.

21 The majority of TM cells exhibited a delayed stretch-activated current that was mediated independentl

22 ear rate, occuring during repetitive passive stretching adminstration (passive stretching training) m

23 e 2.0% in the first survey were located in a stretch along a 2000 km of the Amazon river in the north

24 HBC arrays with the poly(ene-yne) backbones stretching along the column direction, based on a variet

25 and cell types that function as the primary stretch and pressure detectors in the urinary tract most

26 utive individual proteins need to reversibly stretch and recoil over long periods of time.

27 in cyclic deformation of TT during diastolic stretch and systolic shortening serves to mix TT luminal

28 surgeon manipulated the affected shoulder to stretch and tear the tight capsule while the participant

29 eripheral mechanical stimuli such as bladder stretch and urethral flow(4).

30 matory neuropathy, prone positioning-related stretch and/or compression injury, systemic neuropathy,

31 The pockets are stretched and elongated along with the jet, eventually r

32 We highlight mechanical stretching and bending of membranes and the importance o

33 devices by suppressing crack formation upon stretching and bending.

34 during the high-speed tank-treading induced stretching and compression process that a patch of the R

35 ghts into the chemical changes during tendon stretching and directly link these chemical changes to f

36 However, chromatin stretching and ensuing DHFR gene upregulation by the in-

37 Our experiments reveal that systematic stretching and folding of fluid elements are produced in

38 a straightforward competition between chain stretching and interfacial tension under the constraint

39 tive affinity, resulting in greater membrane stretching and rupturing, corroborating the theoretical

40 ch suggests that adsorbed NPs cause membrane stretching and squeezing.

41 g in the disorganization of microtubules and stretching and stiffening of the apical membrane.

42 peaks related to N-H bending vibration, C-N stretching and symmetric, and asymmetric vibration of th

43 Both stretching and torsional forces are considered, and thes

44 on of the kinase involves previously unknown stretching and twisting within individual solenoid segme

45 ion, in the femoral, popliteal (treated with stretching), and brachial arteries (untreated) of both s

46 PH oxidase 2 is activated by and responds to stretch, and finally the degree to which normalizing mec

47 s), how NOX2 is activated by and responds to stretch, and finally the degree to which normalizing X-R

48 in the mechanisms by which heat, mechanical stretch, and pharmacological modulators alter TREK1 chan

49 hes differences in cell stiffness, chromatin stretching, and DHFR gene upregulation under different f

50 odegradable scaffolds, incremental pulsatile stretching, and optimal culture conditions.

51 that the multicycle pulses are driven by the stretched aponeuroses (flat tendons that connect the son

52 Using an equiaxial stretching apparatus, we applied a step stress and measu

53 ve antinociceptive agents in the acetic acid stretch assay (AASA) at subcutaneous doses of 1 mg/kg.

54 on for ~120 min/wk) schedule compared with a stretching attention control group for 16 consecutive we

55 oridges formed by precursor fusion along the stretch axis, which computational modeling explained as

56 Additionally, our data showed that stretched axons do not respond to BDNF signaling, sugges

57 Moreover, stretched axons showed increased microtubule (MT) densit

58 Enhanced growth in stretched axons was also accompanied by endoplasmic reti

59 um isoscape development, that such practices stretch back into the late Middle Stone Age.

60 ar vibrational spectroscopy of the water O-H stretching band over a temperature range of 10-75 degree

61 after being normalized to the neighboring CH stretching band.

62 ers in early mitosis, while interkinetochore stretch becomes important after biorientation.

63 easure the locations, magnitudes, and modes (stretch, bend, or press) of mechanical deformation.

64 approach by visualizing single DNA molecules stretched between microspheres at various heights.

65 tant mechanism to build a cognitive map that stretches beyond direct experience, thus supporting flex

66 We induced mechanical stretch by centrifuging or culturing Kv1.5-expressing HE

67 apparent deformation index (DI) of the cells stretched by extensional flow at the stagnation point of

68 s and Holliday junctions are synthesized and stretched by fluid flow.

69 , amino acid residue (~1396 cm(-1)), and C=O stretching carboxylic esters (1745 cm(-1)).

70 ms of ataxin-1 containing expanded glutamine stretches cause the movement disorder spinocerebellar at

71 the CTD showed that a serine/threonine-rich stretch causes a backbone twist in the N-terminal beta s

72 Moreover, the stretch causes an immediate illusion of touching a harde

73 cells (hemocytes) and ovarian somatic cells (stretched cells) during their brief phagocytic role in n

74 In anisotropically stretched cells, microridges formed by precursor fusion

75 ur present research suggests that mechanical stretch changes the components of EMPs, which in turn mo

76 l alcohol/polyaniline hydrogel can work as a stretching/compressing/bending electrode, maintaining it

77 by monitoring the red-shifts of carboxylate stretches coupled to anharmonic metal-carboxylate oscill

78 are constantly exposed to mechanical cyclic stretch (CS) following blood pressure.

79 t bending deformations are reversible, while stretching deformation may be irreversible, leading to m

80 eme distances and are subject to significant stretch deformations during limb movements or sudden hea

81 This approach includes membrane bending and stretching deformations into the model, producing a more

82 n reversible physiological swelling, whereas stretching deformations should also be considered in pat

83 We show that mechanical stretch deforms the nucleus, which cells initially count

84 Cyclic stretch did not have any significant effect beyond that

85 erful spectral measurement technique, a time-stretch dispersive Fourier transformation (TS-DFT) has b

86 tial bending-dominated softening regime to a stretching-dominated stiffening regime, which occurs bef

87 lish a phase diagram for compression-driven, stretching-dominated stress propagation and jamming in u

88 Mechanical stretch due to muscle overload causes a restoration of f

89 Transitional cells undergo extensive stretching during differentiation, making them vulnerabl

90 r to the presumptive nose and then extend by stretching during embryo elongation.

91 While stretch-elicited X-ROS primes intracellular calcium (Ca(

92 ith reduced eQTL effect size observed in the stretch enhancers most strongly implicated in GWAS signa

93 mer micelles that are limited in size by the stretching entropy of the polyglutamine region.

94 a single chain scission per triggering chain stretching event, and the loss of stress transfer that r

95 Pressure-induced cell stretch evoked a rapid increase in transmembrane current

96 pochs per subject were averaged to produce a Stretch Evoked Potential (StretchEP).

97 Selective TRPV4 activation without stretch evoked significant ATP release-key urothelial se

98 th a second feature, which indicates that OH stretch excitation of these molecules drives low-frequen

99 15eGFP fluorescence anisotropy decays with a stretched exponential decay model (<E(FRET)(exp)> = 0.25

100 f time-resolved fluorescence anisotropy, the stretched exponential decay model, and molecular dynamic

101 g(2)(q, t) exhibits either a compressed or a stretched exponential decay, depending on the size of th

102 and on the bead-tip distance according to a stretched exponential relationship.

103 the same shapes as the SIR ones, but with a stretch factor applied to them across time that is relat

104 ate characteristic timescale, scaled by this stretch factor, that is universal to all SEIR models, wh

105 wist-torque profiles develop with increasing stretching force and show that they exhibit torsion stif

106 bining the twist-torque profiles for various stretching forces effectively results in a combined forc

107 in is under very low external tension (i.e., stretching forces less than ~1 pN).

108 of the molecule is subjected to torques and stretching forces using molecular dynamics simulations o

109 results (density functional theory), the NO stretching frequency (nu(NO)) is sensitive to the intram

110 relation between the high energy shift in NH stretching frequency and the electron withdrawing nature

111 1,2-peroxo)diiron(III) adduct with a low O-O stretching frequency of 825 cm(-1) and a short Fe...Fe d

112 additional red shift of 44 cm(-1) in the NH stretching frequency.

113 Thus, the proline-rich stretch from the glycine receptor alpha1 subunit represe

114 consisted of a staircase protocol and rapid stretches from slack length to increasing strains.

115 properties can be modulated by changing the stretching geometry and the number of interacting helice

116 hanical forces are physiologically relevant, stretch-growth could be an important endogenous mechanis

117 Stretch-growth has been defined as a process that extend

118 Stretch-growth was also found to stimulate axonal branch

119 ensity and MT assembly was key to sustaining stretch-growth, suggesting a possible role of tensile fo

120 e ability of the skin to grow in response to stretching has been exploited in reconstructive surgery(

121 Although the response of epidermal cells to stretching has been studied in vitro(2,3), it remains un

122 Tangential modulus was lower and peak stretch higher in POP III/IV compared to non-POP and POP

123 h both molecules and atoms prepared in their stretched hyperfine spin states.

124 mics of the curve shape showed a tendency to stretch (i.e. decrease of steepness), in the presence of

125 lity to accurately apply parallel mechanical stretch in a 96 well plate format in 576 well simultaneo

126 rapidly and locally activated by mechanical stretch in an actomyosin contractility-dependent manner.

127 .02) and negatively correlated with the peak stretch in both the main in vivo (r = -0.5, p = 0.02) an

128 The OH stretch in experimental infrared data, in agreement with

129 ningful viscoelastic resistance to diastolic stretch in human myocardium.

130 lowers viscoelastic resistance to diastolic stretch in human myocytes and myocardium.

131 esults demonstrate the significance of axial stretch in lymphatic contractile function, suggest that

132 wever, less is known about the role of axial stretch in regulating contraction.

133 ed by roughly 50 cm(-1) compared to the same stretch in the CF(3) analogue, indicating a significantl

134 by an expansion of a poly glutamine (polyQ) stretch in the huntingtin protein (HTT) that is necessar

135 A proline-rich stretch in this receptor domain forms a noncanonical rec

136 We observed that mechanical stretch increased I(Kv1.5), and this increase required t

137 We found that artificial skin-stretch increases the predictive grip force modulation i

138 ologically relevant tissue actions of TRPV4, stretch-independent responses, and underlying mechanisms

139 TRPV4 contributed to 50% stretch-induced ATP release.

140 ional modeling explained as a consequence of stretch-induced cortical flow.

141 and quantitative image analysis we find that stretch-induced nuclear elongation and alignment perpend

142 fied Yes-activated protein (YAP) as a cyclic stretch-induced regulator of HSPC formation.

143 G2F, HBB), which might play crucial roles in stretched-induced skin growth.

144 Passive stretching-induced improvements related to central mecha

145 issue of Cell, Nava and colleagues show that stretch induces rapid loss of heterochromatin that leads

146 Persistent, high-amplitude stretch induces supracellular alignment of tissue to red

147 and single-cell RNA sequencing, we show that stretching induces skin expansion by creating a transien

148 he flavin electronic absorption and carbonyl stretch infrared spectra in the light-adapted state.

149 ent also restored endothelial function after stretch injury (subfailure stretch), treatment with acid

150 ast ocean, with an active hydrological cycle stretching into the Amazonian.

151 Circumferential stretch is known to regulate contractile function in col

152 The thickness stretch is statically condensed to enforce vessel wall i

153 ibiting substantial increases of EMI SE when stretched is reported, which matches the EMI SE of metal

154 and keeps functioning after 10 000 cycles of stretching is fabricated.

155 size deforms the nucleus, which expands and stretches its envelope.

156 We also show that there is an optimum stretching length, which results in the best separation

157 By targeting the S1-S2 linker, mechanical stretch may induce a change in the N-terminal conformati

158 tic contractile function, suggest that axial stretch may play an important role in regulating lymph t

159 tion or mutagenesis abolished the mechanical stretch-mediated increase in I(Kv1.5) Our results furthe

160 ine the step-by-step mechanisms that control stretch-mediated tissue expansion at single-cell resolut

161 vity modes are resonantly coupled to the O-H stretch mode of liquid water, the infrared spectrum show

162 r state predominantly to the C(beta)-C(beta) stretching mode of the thiophene heterocycle.

163 l lifetime (T(1)) of excited interfacial O-H stretching modes from T(1) ~ 600 fs to T(1) ~ 250 fs.

164 The peak positions of the CH(2) stretching modes indicate a progressive increase in the

165 Giant renormalization of plane Ni-O bond-stretching modes that modulate the volume around Ni appe

166 ctra of their -CN and -NC chromophore ligand stretching modes, were confirmed by (13) C and (15) N is

167 ular function in the feeding arteries of the stretched muscle have been extensively investigated; how

168 tion may not be appropriate when lung tissue stretch occurs heterogeneously and/or rapidly.

169 (40_70);2100_2110]) is predicted to insert a stretch of 13 or more lysines followed by either an in-f

170 The helix is characterized by a stretch of amino acids rich in alanine residues that are

171 For example, the OH stretch of an amino-substituted analogue is red-shifted

172 Mechanical stretch of baroreceptors in the wall of the aortic arch

173 t for association to the peroxisome, while a stretch of conserved positive charges and a central plec

174 The core-promoter, a stretch of DNA surrounding the transcription start site

175 scoelasticity was increased during diastolic stretch of HF cardiomyocytes compared with nonfailing co

176 fast dynamics of a vibrational probe (the CN stretch of phenyl selenocyanate) in poly(methyl methacry

177 In this work the Stark active C=N stretch of potassium thiocyanate is used as a molecular

178 We identified a stretch of residues in eIF5B, located close to the gamma

179 e that RGS2 associates with FBXO44 through a stretch of residues in its N terminus.

180 Here, we show that a short stretch of ribonucleotides at the 5' terminus stimulates

181 outhern Mexico and had an impact on a bigger stretch of the coast than previously suspected.

182 vity, a lipid-bilayer model, suggests that a stretch of the membrane induced by mechanical force alte

183 lecting lymphatic vessels are under an axial stretch of ~1.24 under normal physiological loads.

184 MYLK isoform, MYLK-L contains an additional stretch of ~919 amino acid at the N-terminus of unknown

185 tern--the incidence of peptide epitopes with stretches of 100% sequence identity bound to both dendri

186 ogous expression systems, RDE-3 can add long stretches of alternating non-templated uridine (U) and g

187 known danger-associated molecular pattern of stretches of anionic side chains strongly bound by CR4.

188 slow processive motion interrupted by short stretches of confined motion.

189 position of the altered triplets within long stretches of d(CGA) triplets.

190 on timing, but the latter can involve longer stretches of DNA.

191 an library of Lit alleles, we identified two stretches of functionally important amino acid residues

192 with CpG islands (CGIs), relatively CpG-rich stretches of generally several hundred nucleotides that

193 n a region of 200 kb, with conspicuous 20-kb stretches of highly conserved sequences among the four a

194 target cleavage, and a requirement for long stretches of homology between gRNA and DNA target.

195 Small stretches of information are transferred from a series o

196 ree nuclear membranes, whereas the adjoining stretches of membrane accumulate NPCs that are associate

197 These long stretches of repetitive DNA vary in length among human c

198 phase separation relative to other Arg-rich stretches of sequence, subsequently confirmed by mutagen

199 hat queries R-loops via the presence of long stretches of single-stranded DNA on their looped-out str

200 Higher rate stretching of membrane patch can result in a significant

201 Repetitive stretching of tendon cells activates the AKT and mTOR pa

202 heterogeneities in the vesicle size provoke stretching of the relaxation curves.

203 -inversion "umbrella" bending and asymmetric stretching of the SC(alpha) and C(alpha)O bonds.

204 y, we investigated the effects of mechanical stretch on Kv1.5 channels.

205 p a mouse model in which the consequences of stretching on skin epidermis can be studied at single-ce

206 We also discuss the effects of membrane stretching on swelling dynamics.

207 largely abrogated in cells lacking the Piezo stretch-operated channel; under load, these cells persis

208 protective mechanism during high mechanical stretch or loading.

209 whether crosslinking changes in response to stretching or relaxation.

210 After initial attachment was achieved, cells stretched out along with the directions of nanofibers.

211 the NADP(+) binding domain instead of being stretched out in the solvent.

212 the beta' zinc-binding domain (ZBD) of RNAP stretches out from its canonical position to interact wi

213 Many (>45) 20-km coastal stretches particularly those near cities receive more th

214 k provides a viscous impediment to diastolic stretch, particularly in HF.

215 ncorporation of EA in the cage significantly stretches Pb-I bonds, expands the cage, and induces a la

216 Within the high-frequency Ni-O bond stretching phonon dispersion, a softening at the propaga

217 dic device that can control the length via a stretching platform.

218 ons of roach (Rutilus rutilus) inhabit river stretches polluted with estrogenic WwTW effluents.

219 of molecules that either align or not within stretched polymers and the maximum absorption wavelength

220 and substrate could dominate the bending or stretching processes, leading to inefficiency strain tra

221 ore, direct force application via mechanical stretching promoted BMP-dependent mesoderm specification

222 Acute passive stretching (PS) effects on blood flow ( Q ), shear rate

223 Thus, here we report a numerical model of a stretched-pulsed Tm-doped fibre laser with hybrid mode-l

224 paramagnetic resonance (EPR) spectroscopy of stretched rat tail tendon, atomistic molecular dynamics

225 ctural engineering to accommodate mechanical stretching rather than imposing strain into the material

226 ape-morphing by programming the magnitude of stretch ratio in a thin LCE sheet with constant director

227 mechanisms, such as recurrent inhibition and stretch reflex, probably play a major role in the synerg

228 ibe optimized culture media and a mechanical stretching regimen to produce hiPSC-derived TEVGs with m

229 rface show that the vSFG response in the C=N stretch region originates from a SCN-H-O-Al complex, sug

230 sient vibrational spectra in the double-bond stretching region are recorded for subsets of electronic

231 y broad infrared spectrum of water in the OH stretching region is a manifestation of how profoundly a

232 tion (vSFG) measurements performed in the OH stretching region suggest that thiocyanate species organ

233 affect homopolymeric or dinucleotide A or T stretch regions of the genome.

234 maintained even under 30% strain and during stretch-release cycles without the need of extrinsic str

235 rpv1 null mice while the response to passive stretch remains intact.

236 ical deformations, especially high levels of stretching, represent key defining characteristics.

237 and 1139 cm(-1) CH(2), CH(3) bend and C-O-C stretch represented structural changes.

238 Imaging of actin dynamics during stretch revealed similar divergent trends, with F-actin

239 ciated with the finding of an intraoperative stretched scar (P < .001).

240 management of stretched scar -induced secondary strabismus by excision

241 21 consecutive and 6 recurrent cases of stretched scar -induced strabismus were identified and a

242 uced secondary strabismus by excision of the stretched scar and muscle fixation to the sclera using n

243 y consecutive or recurrent strabismus due to stretched scar from 2012 to 2017.

244 Patients with a stretched scar had significantly less correction per mil

245 The diagnosis of stretched scar was made in any case of late (>= 1 month)

246 After surgical correction of the stretched scar, consecutive deviations in the form of co

247 Adduction deficits indicate a stretched scar, which must be treated with resection and

248 ecutive or recurrent strabismus secondary to stretched scar.

249 ount of surgery is needed in patients with a stretched scar.

250 duction deficits were associated with larger stretched scars (P < .001).

251 ere it is required for low-threshold bladder-stretch sensing and urethral micturition reflexes.

252 hat tentonin 3 (TTN3), a recently identified stretch-sensitive ion channel, was present at the vagus

253 o the actomyosin cortex via nuclear envelope stretch-sensitive proteins, up-regulating cell contracti

254 o1 channel as a key TM transducer of tensile stretch, shear flow and pressure.

255 ated by various mechanical stimuli including stretch, shear stress, and osmotic pressure.

256 e find that DNA denatures in the majority of stretching simulations, surprisingly including those wit

257 olecules and raises the possibility of using stretched spin states in the cooling of other molecules.

258 to soft human skin and cannot function under stretched states.

259 ane actin nuclear (TAN) lines are induced by stretch stimulation and nuclear envelope (NE) proteins i

260 nd their persistence requires maintenance of stretch stimulation.

261 ne hydrogel with a complete recovery of 100% stretching strain, 50% compressing strain and fully bend

262 NL-3 are required for preanaphase chromosome stretching, suggesting a role in pulling forces.

263 lysis methods, we show that the proline-rich stretch surrounding P366 mediates binding to syndapin I,

264 0.001; mediolateral, - 4.2%, P < 0.001) and 'stretch tall plus arm extension and thoracic cue' (anter

265 P < 0.001; thickness, + 19%, P < 0.001) and 'stretch tall plus arm extension and thoracic cue' (lengt

266 s abdominis contraction was greatest in the 'stretch tall plus arm extension' (length, - 15%, P < 0.0

267 us time window) in real-time using the time-stretch technique, we are able to resolve the transient

268 n and found that their levels are altered in stretched tendon.

269 ks of ABA amphiphiles are significantly less stretched than in the lamellar phases.

270 during active muscle contraction and muscle stretch that defy simple explanation.

271 ed regions, fraction of coils and tripeptide stretches that contain multiple histidines associate neg

272 mations relied on tethering to the lamina to stretch the chromosome; detachment from the lamina compa

273 One potential strategy to stretch the existing mOPV2 supply is to administer a red

274 ral could complicate transitions to hospice, stretch the limits of home hospice, and promote continue

275 with a programmable mechatronic device that stretches the skin of the fingertips to address this iss

276 Limb displacement causes muscle stretch; the corrective response has multiple activity b

277 re the tidal interaction with the black hole stretches them along the orbit) and they show both therm

278 er the cages of the 2D halide perovskites by stretching them.

279 ule (MT) mechanotransduction links diastolic stretch to generation of NADPH oxidase 2 (NOX2)-dependen

280 echanotransduction pathway linking diastolic stretch to NADPH oxidase 2-derived reactive oxygen speci

281 These extensible networks can be stretched to strains as large as 350% before failure and

282 aluated before and after 12 weeks of passive stretching training and after 6 weeks from training cess

283 ve passive stretching adminstration (passive stretching training) may constitute an effective stimulu

284 After passive stretching training, vascular function and arterial remo

285 al function after stretch injury (subfailure stretch), treatment with acidic Normal Saline (NS), and

286 longation and alignment perpendicular to the stretch vector are dependent on formin-regulated actin p

287 ependence, and nonlinear scaling with muscle stretch velocity - emerge from first principles of muscl

288 The frequency of the unique, Raman-active stretching vibration of this C2-D probe is a clear repor

289 ese oscillations originate from an Fe-ligand stretching vibrational wavepacket on a triplet metal-cen

290 The behavior of the OH stretching vibrations under pressure is profoundly affec

291 We stretched VSMCs in culture with cycle-by-cycle variabili

292 First, slow and rapid (diastolic) stretch was applied to intact cardiomyocytes from nonfai

293 were observed, and the loss of the carbonyl stretch was monitored at 1723 cm(-1).

294 Stretching was matched to exercise dosing arms on the ba

295 A new peak at 2144 cm(-1) (alkynyl C=C stretch) was also detected in the decolorized melanin.

296 compared to pressures generated by membrane stretching, when both membrane surface area and volume a

297 e C-terminus and a highly charged N-terminal stretch, which has been reported to bind to histone H3 a

298 nding pocket that accommodates a polyproline stretch within the N-terminal PDZD11 region.

299 ed amino acid residues in a highly conserved stretch within the regulatory region of yeast MTHFR to c

300 cell array can be readily bent, twisted and stretched without affecting its device performance.