ライフサイエンスコーパス: collision

1 so from there to human systems (deer-vehicle collisions).

2 molecules in real time during diffusion and collision.

3 f exit channels accessible upon their mutual collision.

4 ided with the early stages of the Asia-India collision.

5 ability one-year following the motor vehicle collision.

6 action, which is measured in an atom surface collision.

7 e assembled from the fragments of an ancient collision.

8 ation mechanisms of inelastic inter-particle collisions.

9 ss of habitat but also impacts fauna through collisions.

10 1 is a ZNF598-independent sensor of ribosome collisions.

11 omic swirl") created in relativistic nuclear collisions.

12 are activated by the same signal of ribosome collisions.

13 targets if they subsequently stall and incur collisions.

14 sumed to occur largely by diffusion-mediated collisions.

15 ese three DNA repair factors at sites of T-R collisions.

16 -early transcriptional response to ribosomal collisions.

17 t require modifying natural motions to avoid collisions.

18 ics via more efficient seeding of productive collisions.

19 he latitudinal distribution of arc-continent collisions.

20 or particles and anti-particles in heavy ion collisions.

21 n part to access carrion produced by vehicle collisions.

22 dominant angular momentum projections of the collisions.

23 -lived in-medium magnetic field in heavy ion collisions.

24 chanisms that animals use to avoid impending collisions.

25 ormation states, using soft molecule-surface collision (0.5-5.0 eV).

26 Inelastic losses in molecular collisions(2-5), however, have greatly hampered the engi

27 thermore, the ARHMD avoided potential tablet collisions (4.8 for 3.2 seconds in Task1; 3.8 for 1.3 se

28 njury most often resulted from motor vehicle collision (74%).

29 on and UV irradiation, we show that ribosome collisions activate the stress-activated protein kinase

30 lucuronide metabolites and BF(3) followed by collision-activated dissociation (CAD) in a linear quadr

31 drupole ion trap, isolated, and subjected to collision-activated dissociation (CAD; MS(2) experiments

32 s have emerged as a potential alternative to collision-activated dissociation in tandem mass spectrom

33 This may involve directed end-on collisions along a molecular bond axis or encounters in

34 llows us to quantify the extent of ribosomal collisions along the transcript and identify individual

35 tracking at the LC interface confirmed that collision and subsequent spreading of amphiphiles at the

36 nt processes that include lipid transfer via collision and upon direct particle tethering to the memb

37 n opposite directions along the RNA, risking collisions and abortive replication.

38 ng granular gases that exchange charges upon collisions and interact via the long-ranged Coulomb forc

39 K ZAK functions as the sentinel for ribosome collisions and is required for immediate early activatio

40 bL9 become compacted closer together during collisions and that the E-sites of the stalled ribosomes

41 pidly, making a minimal deviation to avoid a collision, and subsequently returning to its original pa

42 Using paired collision- and electron-based dissociation spectra, O-Pa

43 Here, we use methods that combine collision- and electron-based fragmentation to character

44 Persistent collisions are detected by ZNF598, a ubiquitin ligase th

45 Low-latitude arc-continent collisions are hypothesized to drive cooling by exhuming

46 d identify individual codons where ribosomal collisions are likely.

47 We propose that no matter how weak the collisions are, at large enough distances from the sourc

48 , fully incorporating friction and inelastic collisions, are designed to reproduce experimental behav

49 premolar positioning, facet orientation, and collision areas.

50 Genomic collision at this locus was associated with rejection of

51 lycero-3-phosphocholine) liposomes by single collisions at 10 mum diameter carbon and Pt ultramicroel

52 ical detection of single redox DMPC liposome collisions at polarized UMEs was investigated under diff

53 t high initiation rates occurs when ribosome collisions at stalls stimulate abortive termination of t

54 IMD significantly attenuated collision avoidance behaviors and impaired responses of

55 encoding aerodynamic information can enable collision avoidance by developing a quadcopter with a se

56 le, indicating a short-range, mechanosensory collision-avoidance mechanism.

57 ber and duration of potential surgeon-tablet collisions avoided by the ARHMD.

58 ases of ultracold atoms can be created using collision-based cooling schemes such as evaporative cool

59 ntain multiple O-glycosites, indicating that collision-based fragmentation alone is not sufficient.

60 e O-glycoproteomic methods to rely solely on collision-based fragmentation rather than electron-drive

61 s products and internal products relative to collision-based methods.

62 nt of the elasticity of the limbs, inelastic collision between a soft body and rigid surface, and uni

63 re that in the simplest case of an inelastic collision between an atom and a nearly homonuclear diato

64 ication fork and can be triggered by head-on collision between the restarted fork and RNA Polymerase

65 Ongoing arc-continent collision between the Sunda-Banda arc system and Austral

66 cule-molecule scattering in great detail for collision between two CO molecules.

67 appears to be a directly imaged catastrophic collision between two large planetesimals in an extrasol

68 s are available to study the consequences of collisions between DNA-bound molecular machines.

69 In heterogeneous collisions between healthy and stiff RBC pairs, it is fo

70 strand with a 5'-3'-directionality, head-on collisions between Pif1 and polymerase delta or gamma re

71 The ellipsoidal shape also directs random collisions between proteins away from sites that would p

72 For homogeneous collisions between RBC pairs, a decrease in final displa

73 The influence of RBC deformability on collisions between RBCs and platelets was found to be ne

74 Collisions between the DNA replication machinery and co-

75 RQC factor Hel2/ZNF598 generally recognized collisions but did not induce degradation of endogenous

76 nt with the expectation for complex-mediated collisions, but that the rate is lower than the limit of

77 The use of the AR visual aid reduced collisions by 50% in mobility testing (p = 0.02), and by

78 ing obstacles and can recover from in-flight collisions by exploiting material robustness and vehicle

79 and other highly cognitive vertebrates avoid collisions by perceiving the relationship between the la

80 irradiation creates lattice defects through collision cascades.

81 ed R loops lead to transcription-replication collisions, causing DNA damage and genomic instability.

82 triples it (to m/z 22 000) using a hexapole collision cell and yields a 3-10x increase in SID sensit

83 Pt(-) , and methane, CH(4) and CD(4) , in a collision cell shows the preferred generation of [PtCH(4

84 e CID and SID sensitivity by lengthening the collision cell, and (3) increase the mass range of the d

85 replace the entrance lens of a Bruker FT-ICR collision cell, the dynamic range enhancement (DRE) lens

86 is unclear whether this system distinguishes collision complexes formed on defective mRNAs from those

87 Instead, they allow the nonspecific collision complexes to evolve more efficiently into the

88 esis that pairs of molecules form long-lived collision complexes.

89 ental chemical dynamics studies under single-collision conditions and the outcome of trajectory simul

90 on the doublet C(7)H(7) surface under single collision conditions.

91 (CH)-with diacetylene (HCCCCH) under single-collision conditions.

92 e formation of C(9)H(8) isomers under single-collision conditions.

93 CCH) and allene (H(2) CCCH(2) ) under single-collision conditions.

94 ave been limited with only a small amount of collision cross section (CCS) data available.

95 Collision cross section (CCS) databases based on single-

96 A wide range of collision cross section (CCS) databases for different fa

97 structures through the generation of glycan collision cross section (CCS) identifiers.

98 The collision cross section (CCS) is an important property t

99 n AED identification using accurate mass and collision cross section (CCS) measurements.

100 investigated for their distinguishability by collision cross section (CCS) values and their character

101 Rotationally averaged collision cross section (CCS) values for a series of pro

102 We measured a series of high precision collision cross section (CCS) values for protein and pro

103 its ability to separate isomers and provide collision cross section (CCS) values that facilitate str

104 n of chromatographic retention times (RT) or collision cross section (CCS) values when using ion mobi

105 The mobility of an ion is related to its collision cross section (CCS) with the buffer gas, a phy

106 IM-MS yields collision cross section (CCS, Omega) values that provide

107 ratic dependency of the ion-neutral particle collision cross section and polarizability (R(2) > 0.999

108 haride substitutions, alter both the overall collision cross section and the gas-phase stability of t

109 compact "native" folds can be preserved, the collision cross section distributions are highly sensiti

110 In this study, we explore the use of collision cross section distributions to allow compariso

111 ted in an ion mobility mass spectrometer and collision cross section values of fragments measured.

112 sets, which allowed statistically identical collision cross section values to be directly determined

113 cal reference libraries (e.g., mass spectra, collision cross section, and other measurable property l

114 their gas-phase size and shape (reflected by collision cross section, CCS) and their mass-to-charge (

115 analytical measurements derived from IM-MS (collision cross section, CCS), mass-to-charge (m/z), and

116 key based on slight variation of a fragment collision cross section.

117 Collision cross sections (CCS) can be obtained from meas

118 MS analyses provided a link between mass and collision cross sections (CCS) for specific PFAS familie

119 e a structural database of 456 mass-resolved collision cross sections (CCS) of sphingolipid and glyce

120 In structural biology, collision cross sections (CCSs) from ion mobility mass s

121 rometry and ion mobility were used to assess collision cross sections and confirm that the quaternary

122 Also, collision cross sections of MD structures were in good a

123 Changes in the charge state and collision cross sections of these species indicate that

124 The resulting collision cross sections were found in agreement with th

125 Additionally, no significant differences in collision cross sections were observed using ion mobilit

126 The collision cross-section (CCS) value provided by IMS is u

127 ehensive lipidome atlas with retention time, collision cross-section and tandem mass spectrometry inf

128 The information regarding accurate mass, collision-cross-section values in nitrogen ((DT)CCS(N2))

129 We did not find evidence of ribosome collisions curbing the protein output of yeast transcrip

130 ns-triggered electron-transfer/higher-energy collision dissociation (EThcD) mass spectrometry.

131 n (ETD), and electron-transfer/higher-energy collision dissociation (EThcD).

132 By adjusting higher-energy collision dissociation (HCD) normalized collisional ener

133 its stoichiometry confirmed by higher energy collision dissociation (HCD).

134 dentified by electron-transfer/higher-energy collision dissociation tandem mass spectrometry.

135 al energy surface (PES) that HF-HF inelastic collisions do not obey the energy and angular momentum g

136 Here, we report on ultracold collision dynamics of the hydroxyl free-radical OH with

137 of a set of tandem mass spectroscopy (MS/MS) collision energies and automated combination of all avai

138 higher energy fragments generated at higher collision energies as deposited in the METLIN MS/MS libr

139 h elastic and inelastic rate coefficients at collision energies below [Formula: see text].

140 relationships among fragmentation patterns, collision energies, structures, and retention times of a

141 Collision energy (CE) is a crucial instrument parameter

142 ts, manage stable isotope labeling, optimize collision energy and generate in silico spectral librari

143 ed fragmentation of the glycopeptides at low collision energy CID to produce linkage-specific Y-ions.

144 With its help, we investigated collision energy dependence of confirmed sequence covera

145 ments reveal that this resonance state has a collision energy of ~5 meV and a lifetime of ~80 fs, whi

146 ing molecular beam geometry that permits the collision energy to be tuned from above room temperature

147 species independent of instrument settings, collision energy, and employed internal standards.

148 tion pattern, and the same precursor m/z and collision energy.

149 a function of both atomic quantum state and collision energy.

150 simplest organosulfur molecules via a single-collision event affords persuasive evidence for a likely

151 The collision events of single Lactococcus lactis bacteria a

152 e systematically studied the electrochemical collision events with carbon black particle suspension s

153 age from increased transcription-replication collision events.

154 te and subsequent medical assessment of head collision events.

155 ificant for particle transport in stochastic collision experiments in solutions of low ionic strength

156 Correlated microscopy of collision experiments of L. lactis using a 5 mum radius

157 urrent-time (i-t) curves recorded during the collision experiments showed transients that occurred wh

158 The model established that, in stochastic collision experiments with steady-state oxidation at dis

159 es, and a remarkably high probability of the collision flipping the rotational orientation.

160 The noise floor is dominated by collisions from molecules in the gas within which the ac

161 We generalize this band-collision gel electrophoresis (BCGE) approach to other r

162 er, the global cellular response to ribosome collisions has not been explored.

163 es, and compare our findings with the sticky collision hypothesis that pairs of molecules form long-l

164 hus increasing the potential for ship strike collisions; (iii) the soundscape is dominated by biologi

165 nvestigation of the roles played by ribosome collisions in eukaryotic translation and cellular homeos

166 Here, we uncover a function for ribosome collisions in signal transduction.

167 ferential cross sections for inelastic NO-He collisions in the 0.2 to 8.5 centimeter(-1) range with 0

168 is is caused by the combination of cell-cell collisions in the corners of the microchannel and the ex

169 n the extent of glaciation and arc-continent collisions in the tropics.

170 their projected frontal width and mitigating collisions; in extreme cases, bees flew entirely sideway

171 Collision induced dissociation (CID) is a widely used te

172 Collision induced dissociation (CID) of these phosphoryl

173 The method utilized in-source collision induced dissociation in conjunction with multi

174 ipt we harvest an overlooked property of the collision induced dissociation of amino acid adducts to

175 A hybrid collision induced dissociation/193 nm UVPD (CID/UVPD) ap

176 bines high-energy source optics for improved collision induced unfolding (CIU) experiments and an ele

177 ial interest in native ion mobility (IM) and collision induced unfolding (CIU) mass spectrometry (MS)

178 Ion mobility-mass spectrometry and collision induced unfolding experiments have recently ga

179 es are elongated, these results suggest that collisions induced by the orientation-dependent settling

180 In the analysis of MCF7 cell lysate, we show collision-induced dissociation (CID) and electron-transf

181 er-energy collisional dissociation (HCD) and collision-induced dissociation (CID) are employed to pro

182 series of on-board traps in which we perform collision-induced dissociation (CID) at pressures in the

183 le of surface-induced dissociation (SID) and collision-induced dissociation (CID) for Fourier transfo

184 s in the interface of tandem-TIMS results in collision-induced dissociation (CID) of avidin tetramers

185 t work has shown that fragments generated by collision-induced dissociation (CID) of disaccharides ca

186 Collision-induced dissociation (CID) of MALDI-generated

187 Collision-induced dissociation (CID) of the resulting de

188 ed FA complex cations fragment upon ion-trap collision-induced dissociation (CID) to generate product

189 structure-indicative fragments generated by collision-induced dissociation (CID) together with a flo

190 Reliant on low-energy collision-induced dissociation (CID), traditional ESI-MS

191 ( m-CPBA) epoxidation reaction coupling with collision-induced dissociation (CID)-MS/MS strategy prov

192 nt peptide backbone fragmentation when using collision-induced dissociation (CID).

193 based on sustained off-resonance irradiation collision-induced dissociation (SORI-CID).

194 Vc(50) values determined via collision-induced dissociation experiments enabled the e

195 ions and acquisition of structure-diagnostic collision-induced dissociation mass spectra, while minim

196 and sphingoid backbone (SB) was inferred by collision-induced dissociation multiple-stage mass spect

197 The collision-induced dissociation of the charge-inverted co

198 Collision-induced dissociation of the triply tagged, tri

199 human cerebellum and upon use of low-energy collision-induced dissociation tandem MS.

200 for subsequent fragmentation via low energy collision-induced dissociation.

201 nated ions, from GBPs in the gas phase using collision-induced dissociation.

202 confirmed via tandem mass spectrometry using collision-induced dissociation.

203 This unexpected collision-induced transformation of individual CO(2) mol

204 Collision-induced unfolding (CIU) has emerged as a valua

205 Ion mobility (IM)-based collision-induced unfolding (CIU) has gained increasing

206 Collision-induced unfolding (CIU) of protein ions and th

207 ques, namely native ion mobility MS (IM-MS), collision-induced unfolding (CIU), and hydrogen-deuteriu

208 I-MS) and nano-ESI-ion mobility (IM)-MS with collision-induced unfolding (CIU), chemical labeling usi

209 med, which were used to obtain more detailed collision-induced unfolding pathways for Cytochrome C.

210 RNA in the A sites of all studied stall- and collision-inducing sequences.

211 ed from ZNF598-dependent sensing of ribosome collisions initiating RQC, another minor pathway contrib

212 ding site at the mRNA entry channel near the collision interface.

213 Inelastic collisions involving molecular species are key to energy

214 ular quantum state during a molecule-surface collision is a detailed descriptor of the interaction po

215 o the numerical ones when the molecular-wall collision is accounted, evidenced by the large deviation

216 Understanding and controlling collisions is crucial to the burgeoning field of ultraco

217 hieve more complex geometries and avoid self-collisions, it is critical to encode a spatial and tempo

218 We find the corresponding collision kernel [Formula: see text], where l, A, and [F

219 ential concentration, reducing the geometric collision kernel to the clearance rate, which we model a

220 ide valuable information about the preferred collision mechanism and reveal interesting quantum inter

221 presenting to EDs following a motor vehicle collision (MVC) and examine associations of participant

222 h year, whiplash injuries from motor vehicle collisions (MVC) affect millions worldwide, with no stro

223 t each optical "blinking" event results from collision of a single supramolecular assembly with the L

224 ous to Early Paleocene time, followed by the collision of India (plus Trans-Tethyan ophiolites) with

225 Collisional events began with collision of India and the Trans-Tethyan subduction zone

226 ropose an anti-shadowing mechanism where the collision of particles within the valleys of the surface

227 rolled molecular beam technique to study the collision of rotationally oriented ground state hydrogen

228 This commentary describes the risks of the collision of the COVID-19 and addiction epidemics.

229 rally associated with tectonic uplift during collision of the Panama volcanic arc with South America.

230 neutron-capture element associated with the collision of two extreme-density stars establishes the o

231 ry-free supersonic turbulence created by the collision of two laser-driven high-velocity turbulent pl

232 onolayer spreading on an empty space and the collision of two monolayers of different cells in an ant

233 cations for conservation efforts to mitigate collisions of birds with man-made obstacles.

234 e report our findings on the charge transfer collisions of cold [Formula: see text] ions and two isot

235 part, they result from stochastic, inelastic collisions of ejecta and coalescence of partially-sinter

236 has also allowed us to observe ground-state collisions of laser-cooled molecules both in the presenc

237 pplicable to understanding soft nanoparticle collisions on electrodes, vesicles in exocytosis and pha

238 est that Hel2 has a role in sensing ribosome collisions on endogenous mRNAs, and such events may be i

239 ndividual NEs containing ferrocene upon each collision onto a Pt ultramicroelectrode.

240 nd oxidation of its redox content during the collision onto UMEs.

241 via thermal self-disruption or giant planet collisions, or it could have avoided substantial gas acc

242 ned with advances in Rydberg-mediated photon collisions, our work will enable precision characterizat

243 Only when collisions persist is translation abandoned to initiate

244 Steric pressure generated by protein collisions plays a significant role in shaping and curvi

245 from solid surfaces in a two-step sequential collision process at hyperthermal incidence energies.

246 ops by suppressing transcription-replication collisions, promoting replication fork recovery, and enf

247 lar dissipation mechanism of inter-particles collisions, provided the size distributions of particles

248 e, N(2)O was used as the reaction gas in the collision reaction cell of the ICP-MS/MS.

249 (-2), revealing that the fraction of vesicle collisions resulting in fusion with the LC interface is

250 Collision risk from this orbital congestion is costly to

251 ount for costs they impose on each other via collision risk.

252 ias potential on the number and magnitude of collision spikes by changing the applied potential in ch

253 ease associated with exposure to contact and collision sports, including American football.

254 stall-containing endogenous mRNAs to escape collision-stimulated reduction in gene expression.

255 spects, including cohesion, coalignment, and collision suppression, none of which are explicitly enco

256 inum nanoparticles (NPs) using a microjet NP collision system.

257 rationalize our observations with a model of collisions that drive active fluctuations and activate t

258 ratio of elastic to inelastic molecule-atom collisions that is greater than 50-large enough to suppo

259 w that this phenomenon results from ribosome collisions that occur during translational stalling, whi

260 ation of mRNAs lead to ribosome stalling and collisions that trigger a series of quality control even

261 c potentials relevant for these non-reactive collisions, their diabatization procedure, as well as th

262 nslation of aberrant mRNAs induces ribosomal collisions, thereby triggering pathways for mRNA and nas

263 case action during replication-transcription collisions therefore promotes continued replication with

264 EDF1 stabilises GIGYF2 at collisions to inhibit translation initiation in cis via

265 ion of the Saharides involved no continental collisions until the end of their development.

266 eduled CIU method relying on diagnostic trap collision voltages or by implementing mAb-multiplexed SE

267 so occurred at this time, demonstrating that collision was a multistage process involving at least tw

268 cture of the left tibia from a motor vehicle collision was reported and was previously treated with c

269 ition of all major Phanerozoic arc-continent collisions was reconstructed and compared to the latitud

270 We suggest that collisions were common in the young Solar system and tha

271 isome footprint profiling in yeast and found collisions were enriched on diverse sequence motifs know

272 uality-control pathway triggered by ribosome collisions when membrane domain insertion and/or folding

273 synchronous movement can occur during CO-CO collisions, whereby a bump is followed by a move similar

274 restart of a eukaryotic replisome following collision with a cyclobutane pyrimidine dimer.

275 Upon collision with an electrode, alloy NPs are electrodeposi

276 nts that await further infection events upon collision with appropriate host cells.

277 , we previously showed that replication fork collision with DPCs causes their proteolysis, followed b

278 lies their motility across the cell surface, collision with each other, and ultimately clustering to

279 to Southeast Asia three times during India's collision with Eurasia, the first dispersal event occurr

280 rs, a decrease in final displacement after a collision with increasing membrane stiffness is observed

281 Upon collision with the cell border, waves may initiate the f

282 the reverse orientation, by transcriptional collision with the vector-derived Cas9 transcript.

283 d other soaring species to elevated risk via collision with vehicles and/or transmission lines.

284 Energetic collisions with background gas can cause structural chan

285 cross-sections, and result in more frequent collisions with background gas molecules.

286 corresponding to single redox DMPC liposome collisions with K(3)Fe(CN)(6)/K(4)Fe(CN)(6) as the encap

287 s, bats have to emit sounds rapidly to avoid collisions with near objects.

288 rmined in large part by its strength against collisions with other objects(1,2) (impact strength).

289 g a safe path through a busy street to avoid collisions with other people, and falls.

290 e primarily diffusively as a result of their collisions with short strings.

291 These robots can sense and withstand collisions with surrounding obstacles and can recover fr

292 province (southern Spain) erected to prevent collisions with the common chameleon (Chamaeleo chamaele

293 gulation of ciliary beating through physical collisions with the CP.

294 ccumulation of RNA:DNA hybrids (R-loops) and collisions with the replication machinery causing replic

295 lating ribosomes that slow excessively incur collisions with trailing ribosomes.

296 NAs can cause ribosomes to stall, leading to collisions with trailing ribosomes.

297 We have investigated replisome collisions with transcription complexes and R-loops usin

298 o micro- and nanokelvin temperatures through collisions with ultracold Na atoms, with both molecules

299 , possibly because of dynamical friction and collisions within the cloud or later gas drag.

300 This tiered response to ribosome collisions would allow cells to dynamically tune transla