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1 are exposed (e.g., compression, torsion, and stretch).
2 glike structures parallel to static uniaxial stretch.
3 by varying strain, length, and repetition of stretch.
4  the third lobe, consequently reducing flame stretch.
5 rofibril dynamics not seen during mechanical stretch.
6 tes assumed during activation via mechanical stretch.
7 ormation of strings along the orientation of stretch.
8  ratio over a wide range of applied uniaxial stretch.
9 0 nm and has a distinct Raman-active ethynyl stretch.
10 d cell divisions in the presence of uniaxial stretch.
11 do River, which was investigated for a 17 km stretch.
12 phasic contractions and tone, independent of stretch.
13  regions of low cell density where cells are stretched.
14 cle is held at a constant length after being stretched.
15 itting of the C horizontal lineC phenyl ring stretches.
16 sically disordered regions (IDRs) and acidic stretches.
17 ell correlated in all the investigated river stretches.
18 ng at many sequences, not limited to proline stretches.
19 ociated complexes under the applied membrane stretches.
20 crown pocket is strongly coupled with its OH stretches.
21  in homopolymeric (poly A or poly T) genomic stretches.
22 r preserving muscle integrity during passive stretching.
23 nt power even with repeated 70 cycles of 50% stretching.
24 on an east-northeast to west-southwest axis, stretching 230 km southwest and 140 km northeast of the
25 nges to molecular structures by mechanically stretching a single metal complex molecule via changing
26 he binding of histones at its largest acidic stretch (A2) via direct competition with both the C-term
27 rst amplitude scaled equally well to initial stretch acceleration or dF/dt, though later transients w
28 e; a proline-rich C-terminal hRpn2 extension stretches across a narrow canyon of the ubiquitin-bindin
29 ommunities from a large mangrove forest that stretches across southwestern India showed strong simila
30  biological phenomena, notably the gating of stretch activated ion channels.
31             Such Hechtian transduction opens stretch-activated Ca(2+) channels and activates H(+) -AT
32 on is diminished by pharmacological block of stretch-activated cation-nonselective channels.
33 ogical block of ATP-inactivated potassium or stretch-activated cation-nonselective channels.
34 is increased proliferation is induced by the stretch-activated channel Piezo1 and involves calcium-tr
35  cells become too crowded, they activate the stretch-activated channel Piezo1 to trigger extrusion of
36 tein cochlin with the cell surface bound and stretch-activated channel TREK-1.
37 -substrate contacts but only PIEZO1 mediates stretch-activated currents.
38 arise from abnormal repolarization caused by stretch activation of potassium channels.
39 eals a novel "pinched" SF configuration that stretch activation rapidly destabilizes.
40 ue deformation determines PVEM induction via stretch-activation of cation-nonselective channels, with
41                                         When stretched along the superhelical axis, all superhelices
42 t competition with both the C-terminal basic stretch and basic nuclear localization signal.
43 cKO) mice suggest, respectively, that radial stretch and cilia play little, if any, role in determini
44  actomyosin network organization during cell stretch and contraction.
45 illary flow but reduced by pathologic cyclic stretch and inflammatory stimuli.
46 s predict that the magnitude of the uniaxial stretch and the strength of the contractile forces regul
47  was decreased and might be due to decreased stretch and/or altered macrophage polarization.
48 rils were first placed in a rigor state then stretched and shortened at different displacements (0.1-
49  two states, in which the trans isomer has a stretched and the cis isomer a compact form.
50  Nlrp9b recognizes short double-stranded RNA stretches and forms inflammasome complexes with the adap
51 shared the same underlying shape, aside from stretching and compression (called "self-similarity").
52 ensin-depleted cells showed repeated nuclear stretching and contraction as the chromosomes failed to
53  fraction reflecting the ratio of myocardial stretching and contraction during systole diminished (P=
54 mentally observe this buckling transition by stretching and imaging the lamina of isolated cell nucle
55 nd hard skin layers after multiple cycles of stretching and releasing revealed that the soft skin lay
56 ctuation of pore opening via both mechanical stretching and temperature, along with their potential a
57 ring shortening was greater than that during stretching and the difference depended on speed (31% at
58 RZ and BRZ regimes is governed by the vortex-stretching and viscous dissipation contributions, simila
59 e EC cell model released 5-HT in response to stretch, and had Piezo2 mRNA and protein, as well as a m
60 espond to lipids, temperature and mechanical stretch, and influence pain, temperature perception and
61 8 MAPK signaling is activated in response to stretch, and inhibition of p38 MAPK abrogates stretch-in
62 ngs suggest that myocyte stretch, fibroblast stretch, and matrix stiffening following MI may separate
63 (3) A N-N distance and the 1644 cm(-1) Raman stretch are consistent with the presence of an (N horizo
64 ater concentrations over a 100-m-long stream stretch as a consequence of remobilization from introduc
65 uccessfully explains the red-shift of the CN stretch as a function of the dielectric constant and is
66  F-actin dismantling, enabling the glands to stretch as they accumulate secreted products in the lume
67 e in both the tail-immersion and acetic acid stretch assays.
68  resistive torques from the repeated passive stretch at velocities of 5 degrees /s and 100 degrees /s
69 -up where a reconstituted chromatin fibre is stretched at its two ends (e.g., by laser tweezers), whi
70     These results indicate that proline-rich stretches attenuate the potential of stem cell active ho
71 etch, which oriented cell divisions with the stretch axis irrespective of the orientation of the cell
72            The change in intensity of the CH stretching bands as a function of temperature was used t
73 onsistent with harmonic expectations, the OH stretching bands of H3O(+) are surprisingly broad, appea
74                              Although the NH stretching bands of the CH3NH3(+) ion are consistent wit
75 mechanical interactions, including pressing, stretching, bending, and twisting.
76                     The Mediterranean shores stretching between Sicily, Southern Italy and the Southe
77 ude that targeted alpha-therapy regimens may stretch beyond the realm of micrometastatic disease and
78  ultrastructure with the potential to extend stretch-buffering capacity and support a revised model f
79 eart muscle cells generate higher force when stretched, but despite intense efforts the underlying mo
80 the length of the entire organ, and could be stretched by approximately 10% without apparent damage.
81     During ovulation, spermathecal cells are stretched by oocyte entry and then coordinately contract
82 , the firehose of data generated by the time stretch camera requires optical data compression.
83 n and found that 1) paracrine signaling from stretched cardiomyocytes induces CFB proliferation under
84 orce, with its ability to distort, bend, and stretch chemical bonds, is unique in the way it activate
85 The protein ataxin-3 carries a polyglutamine stretch close to the C-terminus that triggers a neurodeg
86                                              Stretching coiled yarns generated 250 watts per kilogram
87  paths in various networks are significantly stretched compared to their shortest counterparts.
88  can be well-maintained under many different stretched conditions and after hundreds of stretching-re
89 nal stretchability, and poor stability under stretched conditions.
90 loromethane, the macrocycles prevail in wide-stretched conformations and upon photoexcitation exhibit
91 of these two molecules: the threefold softer stretching constant obtained for dsRNA, the opposite twi
92 stant obtained for dsRNA, the opposite twist-stretch coupling, and its nontrivial force dependence.
93                                      Biaxial stretch damage induced shrunken neurites and cell death.
94 d flour based doughs revealed that the dough stretching depended on the wheat protein fraction, TG am
95  is isotropic relative to the orientation of stretch, depends on Arf6, Cav1, and Cavin1.
96 alls by atomic force microscopy (AFM) with a stretching device and endoglucanase treatment that induc
97 physiological tremor as a function of muscle stretch differs from that of the stretch reflex amplitud
98                                              Stretch distributions are also found to be extremely sim
99  emphysematous areas are subject to abnormal stretch during respiration, and this biomechanical stres
100 ce, and Ca(2+)-dependent stiffening of titin stretched during eccentric muscle contractions.
101 d intron configurations interrupting the DNA stretch encoding a conserved peptidic sequence.
102  this locus to a 5 kb region that overlaps a stretch-enhancer active in islets.
103 ifically and significantly enriched in islet stretch enhancers.
104 fibre undergoes a sharp transition between a stretched, epigenetically disordered, state and a crumpl
105                            By experimentally stretching epithelia, we find that mechanical stretch it
106  the WL + S group incorporated breathing and stretching exercises.
107 CSE), anomalous exponent (alpha) obtained at stretched exponential DWI, ADC obtained with DKI modelin
108 rived from conventional monoexponential DWI, stretched exponential DWI, diffusion kurtosis imaging (D
109 tions shows that using parameter beta of the stretched exponential function (1-exp(-(t/tau)(beta)) a
110                             Particularly the stretched exponential is favoured in approximately 60% o
111                                    Thus, the stretched exponential may be utilized as a potential opt
112 noexponential fit (ADCME), ADC obtained with stretched exponential modeling (ADCSE), anomalous expone
113 ntial, the intravoxel incoherent motion, the stretched exponential, and the statistical model.
114 naptic current (EPSC), has been updated as a stretched-exponential function with voltage factors in a
115 ture of the effect of landmines and UXO that stretches far beyond injury and mortality prevalence, ma
116          These findings suggest that myocyte stretch, fibroblast stretch, and matrix stiffening follo
117                  We show that, by tuning the stretching force and the binding affinity of the readers
118 using pull and release experiments, when the stretching force applied to a single-layer graphene nano
119 n the sub-second timescale when subject to a stretching force of 1-2 nN (depending on isomer).
120 stic relaxation response upon release of the stretching force.
121 t cells are subjected to prolonged cycles of stretch forces, caveolae are destabilized and the plasma
122 rotect the plasma membrane from damage under stretch forces.
123                                              Stretching forces induce local changes in the molecule s
124 he structure of dsDNA and dsRNA subjected to stretching forces up to 20 pN.
125 es but exhibited increased stability against stretching forces.
126                                  RV systolic stretch fraction reflecting the ratio of myocardial stre
127 alculations were used to establish the v(CO) stretching frequencies and energetics of key redox inter
128  but the net effect is the same: to lower CH stretching frequencies by hundreds of wavenumbers.
129 for determination of the Fe horizontal lineO stretching frequencies of high-valent iron(IV)-oxo compl
130                      It is found that the CN stretch frequency red-shifts with increasing dielectric
131  the FT-IR spectra show an unusually low N-N stretching frequency (2019 cm(-1)), suggesting that the
132                                          The stretching frequency, nu(Cu-O), of the [CuOH](2+) core i
133 so found in the form of an intervening strip stretching from the posterior OFC through the anterior a
134 h species of intermediate geometry featuring stretched Ga-H and compressed M-H/M-Ga bonds, to a fully
135                                              Stretched histone regions, such as super-enhancers and b
136 t IFRs in muscle spindle Ia afferents during stretch (i.e., lengthening) of passive muscle, including
137 alysis method was applied to an example time stretch imaging system via simulation and validated with
138 ndamental challenges are addressed with time stretch imaging, which has been used for ultrafast conti
139 zinc ion binding site, binds to a 28 residue stretch in SMRT comprising a GSI motif followed by an al
140                                           CH stretches in hydrocarbon cations often shift to lower fr
141                   In particular, lysine-rich stretches in the linker, which resemble the positively c
142  the influences of large amplitude, membrane stretching in the neutral plane, and the interactions of
143 grees with our micromanipulation experiments stretching individual nuclei.
144 (1 mum) diminished myogenic tone and blocked stretch-induced cation currents in cerebral arteries fro
145  native cerebral arterial myocytes, membrane stretch-induced cation currents were blocked by the TRPM
146             This was associated with reduced stretch-induced CD147 expression on lung epithelial cell
147 tretch, and inhibition of p38 MAPK abrogates stretch-induced cytoskeletal reorganization.
148 assessment revealed a high predisposition to stretch-induced damage in fiber bundles of R349P mice.
149 duced muscle strength, but is protected from stretch-induced eccentric damage with age.
150 pproved for treating heart failure, inhibits stretch-induced hypertrophy, and predict further efficac
151 mbedded rigid inclusions markedly facilitate stretch-induced membrane disruptions while mechanically
152 though many pathways have been implicated in stretch-induced remodeling, the control structures by wh
153 pe of mechanical force controls the outcome: stretch induces cell division, whereas crowding induces
154           The effects of a series of biaxial stretch injuries (BSI) on a neuronal derived cell line,
155 ize distribution and spatial dispersion were stretched into uniformly dispersed and sized Sn nanopart
156 h the hydro-oleophobic perfluorocarbon chain stretching into air bubbles and the polar head in water.
157 e Piezo1 senses both mechanical crowding and stretch, it may act as a homeostatic sensor to control e
158 tretching epithelia, we find that mechanical stretch itself rapidly stimulates cell division through
159  can function to controllably and completely stretch lambda DNA in a two-dimensional nanofluidic netw
160  (fIPV) could increase IPV affordability and stretch limited supplies.
161                   In contrast, incubation of stretched macrophages with sodium hydrosulfide prevented
162 etic peptide (BNP) in response to mechanical stretching, making them useful clinical biomarkers of ca
163 ccounts for most of the broadening in the OH stretching manifold.
164 ted cells (N = 240,000) by optofluidic time-stretch microscopy with high throughput up to 10,000 cel
165 orter vibrational lifetime of the asymmetric stretch mode compared to the IL phase.
166  infrared absorption spectroscopy of the S=O stretching mode combined with molecular dynamics and qua
167  operates in hydrazides by analyzing the N-H stretching mode in gas phase infrared (IR) spectroscopy,
168 by the observation of a blue shift of the CO stretching mode in the IR spectrum of [B12 Cl11 CO](-) a
169 opically decoupled IR oxygen-deuterium (O-D) stretching mode of HDO water near small purely hydrophob
170 infrared (2D IR) spectroscopy, on a carbonyl stretching mode of tricarbonylchloro-9-octadecylamino-4,
171 ng injury model in vivo as well as in a cell stretch model in vitro in the absence or presence of hyd
172  the thermal evolution of the ester carbonyl stretching modes (1800-1700cm(-1)) and the comparative s
173 igned to the symmetric and the antisymmetric stretching modes in ECX(*) radicals.
174 intensity of the cardiolipin cis-double-bond stretching modes.
175 wing for a strong coupling with the C-C bond-stretching modes.
176 These supramolecular polymer networks can be stretched more than 100x their original length and are a
177 monstrate that bending, in addition to twist-stretch motions, underpin the sub-mus dynamics of DNA.
178 agonists was the same in stretched versus un-stretched muscles.
179  in the locked phase (matrix phase) in a pre-stretched Nafion sheet.
180 sion then leads to nuclear flattening, which stretches nuclear pores, reduces their mechanical resist
181  substantially, resulting, for example, in a stretch of 22 identical amino acids in cytochrome c oxid
182 eneration (VSFG) results of the nitrile (CN) stretch of 4-mercaptobenzonitrile (4-MBN) covalently att
183 moylation motif (NDSM) carries an additional stretch of acidic residues downstream of the consensus P
184                                   Mutating a stretch of C-terminal Ca(2+)-binding residues in PICK1 r
185 hose of the infarct border region; 2) direct stretch of CFBs mimicking the mechanical environment of
186               The NMR analysis showed that a stretch of guanine-rich sequence in the first exon of hT
187  Tone development in the IAS did not require stretch of muscles, and the sensitivity of contraction t
188  into close proximity, including a repulsive stretch of positively charged residues.
189 periments showed that TMAO red-shifts the OH stretch of the IR spectrum via a mechanism that was very
190 ical stimuli to primary murine chondrocytes, stretch of the membrane and deflection of cell-substrate
191 t EOC and EEM data were obtained for a 90 km stretch of the Simeto River, the main river in Sicily, a
192 San Leonardo River and in the alluvial plain stretch of the Simeto River, whereas sucralose, sulfamet
193 ich are enriched with motifs consisting of a stretch of thymine bases.
194 trict into a tight helix that grips an 80 A stretch of unfolded protein.
195  of Cas9 ribonucleoprotein complex and short stretches of DNA sequences into porcine zygotes.
196  forming complexes that may not involve long stretches of DNA-RNA hybrid.
197                 The ability to rewrite large stretches of genomic DNA enables the creation of new org
198 OSINE computes the context similarity of two stretches of nucleobases given the similarity over distr
199 beta sequences were deconstructed into short stretches of overlapping contiguous amino acids.
200                    During externally-imposed stretches of passive, i.e. electrically-quiescent, muscl
201  together in a hierarchical manner to create stretches of phosphorylated residues, which may be a mea
202 nction of this protein motif is dependent on stretches of rare codons, Leu(UUA)-Gly(GGU)-Val(GUA).
203 at SDH6 and SDH7 substitute missing sequence stretches of SDH3 and SDH4 in plants.
204  TRXL domain being encoded by nonconsecutive stretches of sequence.
205  Stalling at DNA replication forks generates stretches of single-stranded (ss) DNA on both strands th
206 undergo extensive processing, producing long stretches of single-stranded DNA (ssDNA).
207 ng strand, resulting in the exposure of long stretches of single-stranded leading-strand template.
208                                     As short stretches of subtelomeric synapsis emerged at early zygo
209 n in the mitochondrial genome and along long stretches of the nuclear genome.
210  of the catalytic cycle, implying that these stretches of the protein sample various structural micro
211  opening of FNIII domains contributes to the stretching of fibronectin matrix fibrils.
212    Multiple biological processes involve the stretching of nucleic acids (NAs).
213 ift in the redox potential due to mechanical stretching of the metal-ligand bond, and perform model c
214                For helical vortices that are stretched or compressed by a second vortex, we found con
215           Strikingly, when keratinocytes are stretched or hypo-osmotically shocked, alpha6beta4 integ
216  that can buffer mechanical stresses such as stretching or osmotic swelling [12].
217              A recent study shows that, upon stretching or wounding, epithelia display a fast prolife
218     Interestingly, most of the strain in the stretched organ is localized in the cap cells, which acc
219 bond orthogonal to the pulling axis, whereas stretching organosiloxanes inhibits dissociation of the
220 ies enhance the nanoscale z fluctuations but stretch out the membrane laterally.
221 iscrimination sensitivity over a long period stretching over >1 s before and after saccade execution.
222 micropipette shows that chromatin aligns and stretches parallel to the pore.
223 tailed kinetic measurements demonstrate that stretching phosphotriesters accelerates dissociation of
224                                              Stretching polymer chains accelerates dissociation of a
225 ubfailure damage to collagen in mechanically stretched rat tail tendon fascicle.
226  contribute to maintain or even increase the stretch reflex after nerve crush and by difference to ne
227 lly replicating the concomitant reduction in stretch reflex amplitude.
228 n of muscle stretch differs from that of the stretch reflex amplitude.
229 naptic connections with motoneurons form the stretch reflex circuit.
230 s the amplitudes of physiological tremor and stretch reflex to be decoupled.
231 as calf muscles shortened in contrast to the stretch reflex whose amplitude decreases as muscle short
232  nerve transection, Ia afferent synapses and stretch reflexes are permanently lost, even after regene
233 ellular shape was the repetition of a chosen stretch regimen, indicating that the engineered shape an
234    Glycine also caused a red shift in the OH stretch region, whereas betaine minimally impacted this
235 nt in the HD2O(+) isotopologue, while the OD stretching region displays a regular progression involvi
236                     Analysis of the carbonyl stretching region for chlorophyll a excitations indicate
237  of the TREK-2 channel to probe how membrane stretch regulates the SF gate.
238 t stretched conditions and after hundreds of stretching-release cycles.
239 e of cultured fibroblasts to uniaxial cyclic stretch results in an actin stress fiber reinforcement r
240 ese wavelengths due to the nearby asymmetric-stretch rovibrational band of atmospheric carbon dioxide
241 ell-cell junctions analogous to release of a stretched rubber band (recoil), or in groups of few cell
242                             Because block of stretch-sensitive ATP-inactivated potassium channels cur
243                                              Stretch-sensitive Ia afferent monosynaptic connections w
244 We determine that prestin itself possesses a stretch-sensitive, non-selective conductance that is lar
245   A regulator of intracellular chloride is a stretch-sensitive, non-selective conductance within the
246    Our data suggest that Piezo2 is an airway stretch sensor and that Piezo2-mediated mechanotransduct
247                                           CH stretching signals increased with polymorph stability, i
248 these fibers regulate the intrafusal fiber's stretch so that they retain proper tension and sensitivi
249  that exhibit new features that we coin the "stretched" solid effect.
250 uclease genome editing, display an abrogated stretch-stimulated actin reinforcement response and incr
251  tails" that emanate from focal adhesions in stretch-stimulated cells.
252 rotein HspB1 (hsp25/27) is phosphorylated in stretch-stimulated mouse fibroblasts via a p38 MAPK-depe
253 ndles are associated with characteristics of stretch such as length and velocity.
254  by the entropic barrier for the chain to be stretched sufficiently to reach the distant receptor tar
255                                Activities to stretch supplies and to suppress demand have been ongoin
256          Structural modeling showed that the stretch surrounding Gly-457 is likely to form a pi-helix
257 helium with a computer-controlled mechanical stretching system to show that breathing-induced physiol
258                 By means of an emerging time-stretch technique, we resolve the evolution of femtoseco
259 gnificant negative relationships between the stretch test and the Myotonometer measurements (r < -0.5
260                         In addition, passive stretch tests indicated a significant increase of total
261 e, interchangeable, linear or 3D hydrophobic stretches that become available because of the unstructu
262 ly localized to and activated long chromatin stretches that were overloaded with transcriptional regu
263  offers a potential dose-sparing strategy to stretch the limited global IPV supply while further impr
264 teracting fermionic problems, problems which stretch the limits of existing high-performance computer
265                         As actomyosin forces stretch the spring network, simulations predict the resu
266 bly, the performance is preserved even after stretching the composite material for 100 nanotensile te
267                               By selectively stretching the droplet monolayer with nanolitre injectio
268 ution much finer than the nozzle diameter by stretching the extruded ink, and print various thickened
269                                              Stretching the model under gravity demonstrates that asy
270                                       During stretching, the myofibril stiffness was independent of b
271 ulum (ER) is a network of tubules and sheets stretching throughout the eukaryotic cells.
272 trix stiffness and application of mechanical stretch to multipotent mesenchymal cells stimulated the
273                           Applied mechanical stretch to RAW 264.7 macrophages resulted in increased e
274                          Cardiomyocytes were stretched to investigate titin distensibility.
275 ble as global water resources continue to be stretched to their limits and communities continue to de
276             The third step leads back to the stretched trans isomer.
277 ciples of the system include (1) time/warped stretch transformation and (2) the spatial dispersion of
278                       Consequently, uniaxial stretch triggered a polarized cortical distribution of L
279                  To stimulate cell division, stretch triggers cells that are paused in early G2 phase
280 t, our fabricated semiconducting film can be stretched up to 100% strain without affecting mobility,
281 re mechanically robust and can be reversibly stretched up to 40% strain for 100 cycles without failur
282 nitial bursts, increased dynamic response to stretch velocity if a muscle has been isometric, and rat
283 traction to ANO1 antagonists was the same in stretched versus un-stretched muscles.
284  a weak to moderate hydrogen bond with a C-H stretch vibration frequency blue-shifted by 14 cm(-1) an
285 onitoring the dynamics of the ester carbonyl stretching vibration in hydrated phosphocholine lipid bi
286 es ((10Os)CO-Au NPs) greatly enhanced the CO stretching vibration signal at 2100cm(-1), which is rel
287                                       The CO stretch vibrations are very sensitive to the redox chang
288 tive isotope editing to monitor the CO/CN(-) stretching vibrations in [FeFe]-hydrogenase HYDA1 from C
289 -independent technique dubbed 'teleportation stretching', we establish these capacities for many fund
290 o mechanical loading and in vitro mechanical stretch were shown to induce the profound up-regulation
291                                              Stretches were performed in myocardial strips, and an ex
292       However, no differences in endothelial stretching were observed between groups (37% versus 37%
293  is especially the case in their mountainous stretches, where harsh terrain is seen as an impediment
294 most approaches to tuning rely on mechanical stretching which cannot control phase locally, or by mod
295 ers was increased by a low level of uniaxial stretch, which oriented cell divisions with the stretch
296 at Lys-714 was located within a leucine-rich stretch, which resembles a nuclear export signal, and co
297 tems that can be bent, folded, crumpled, and stretched while maintaining their electrochemical functi
298 rtant, yet we are unable to control how they stretch with much more sophistication than inflating bal
299 m analyses of intensity parameters of linear stretches with deviations in heterozygous probes of sing
300 used by expansion of a polyglutamine (polyQ) stretch within the Huntingtin (Htt) protein.

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