ライフサイエンスコーパス: decay

1 K increasing to indicate very high hazard of decay.

2 e saturated receptor-catalyzed rate of virus decay.

3 ine biosynthetic pathways because of genomic decay.

4 e removed much more rapidly via unimolecular decay.

5 lex, that catalyzes the first step of 5'mRNA decay.

6 A substrates that can undergo 5'-3' mediated decay.

7 nd examined their roles in the process of NO decay.

8 result in escape from nonsense-mediated mRNA decay.

9 ic splice site, leading to nonsense mediated decay.

10 ssociation of key NMD factors to elicit mRNA decay.

11 me composition and be associated with dental decay.

12 he DCP2 decapping enzyme and stimulates mRNA decay.

13 fore relaxing to equilibrium as the carriers decay.

14 nsistent with a more pronounced nonradiative decay.

15 slation, which triggers messenger RNA (mRNA) decay.

16 bserved trends of urban scaling and distance decay.

17 ed by the balance between mRNA synthesis and decay.

18 r B5/B5R levels modulating the process of NO decay.

19 anisms that balance mRNA synthesis with mRNA decay.

20 the 3.5-keV line originates from dark matter decay.

21 of RNA metabolism, ranging from synthesis to decay.

22 excited state with subsequent phosphorescent decay.

23 ive organization strategy for bacterial mRNA decay.

24 ion plumes, although with different temporal decays.

25 Following the rapid decay (0.6 ns) of a small spectral side band, the broad

26 ronic states resulting in reasonably fast PL decays (~1 ns), large vibrational energy spacing, small

27 the time to over-threshold macroevolutionary decay(4) (shared fraction of species between two times <

28 Here, we show that podocyte expression of decay-accelerating factor (DAF/CD55), a complement C3 co

29 emonstrated long-range temporal dependencies decaying according to a power law across trials, a hallm

30 n and analysis of time-resolved fluorescence decays acquired with a vertically polarized excitation a

31 (<90 mV) and high durability (no performance decay after 75 h and annealing at 400 degrees C).

32 measure half-life by quantifying the rate of decay after experimental intervention (e.g., pulse label

33 This study introduces a global fluorescence decay analysis that substantially simplifies the acquisi

34 re natural products of RNase E-mediated mRNA decay and associate with major RNA-binding proteins (RBP

35 at an increase in strain rate results in the decay and disappearance of the serrated response.

36 y levels rapidly declined due to radioactive decay and environmental processes, but chronic lower dos

37 of how the fungus is able to facilitate wood decay and nutrient cycling as well as tolerate latex and

38 critical reason for Li-ion battery capacity decay and short circuit.

39 ropose a link between CCR4-NOT-mediated mRNA decay and T cell selection in the thymus.

40 elaxation, accounting for the delay in force decay and the initial delay in recovery of resting head

41 on RNA-binding proteins that influence mRNA decay and translation.

42 The exciton then decays and creates a single optical photon within 100 ps

43 ual RPE area followed a trend of exponential decay as a function of patient age.

44 al iron- and sulfur-based intermediates that decay as the [2Fe-2S] cluster signal developed.

45 rrency projects-predictability irrecoverably decays as a function of sampling, unveiling predictabili

46 ess requires factors involved in mutant mRNA decay, as in zebrafish and mouse.

47 RNA immunoprecipitation (RIP) and mRNA-decay assays reveal that QKI-7 binds and promotes mRNA d

48 Using RNA immunoprecipitation and RNA decay assays, we demonstrate that ZAP directly and speci

49 omycota fungi are causing extensive soft rot decay at all sites regardless of climate and local envir

50 The field decays at a rate of ~5 Gauss per second for 2 minutes, a

51 d states emitting with distinct luminescence decays at different wavelengths.

52 area, will cause periods of intensified SOM decay; (c) changing tidal regimes in mangroves due to se

53 Age-related decay can eventually lead to pathology such as cardiovas

54 el, caused by developmental defects or tooth decay (caries), affect health and quality of life, with

55 level rise might attenuate increases in SOM decay caused by global warming.

56 s latter strategy of inhibiting unproductive decay channels was pursued to improve the release effici

57 tions by thwarting competitive excited state decay channels.

58 es between two times <= 0.1), counted by the decay clock, reveals saw-toothed fluctuations around a P

59 stored immune responses, and slowed response decay compared to the 6-month vaccination.

60 ts on endonucleolytic nonsense-mediated mRNA decay components, suggesting that de novo CNOT1 variants

61 full intensity simulated sunlight, the mean decay constant was 0.29 +/- 0.09 min-1, equivalent to a

62 The values of the self-decay constants change within 1.4 x 10(-4) s(-1) for the

63 [(18)F]28) have been prepared in 10 and 1.7% decay corrected radiochemical yield, respectively, and i

64 uzumab in less than 15 min, with an isolated decay-corrected radiochemical yield (RCY) of 24.8%, a ra

65 ing a radiochemical yield of 51.7% +/- 4.7% (decay-corrected to starting (11)C-methyl iodide).

66 d radiochemical yield was 20 +/- 2% (n = 10, decay-corrected) based on [(11)C]CO(2) with a radiochemi

67 This trend persists after decay correction.

68 Proposals to explain this line include decaying dark matter-in particular, that the decay of st

69 ther a compressed or a stretched exponential decay, depending on the size of the Se nano-crystallites

70 al trait by demonstrating that its effect on decay depends on experiment duration and sampling freque

71 DIS3L2-mediated decay (DMD) is a surveillance pathway for certain non-co

72 Fungal decay dominates and hyphae penetrate the outer 2-4 mm of

73 optical gain suffer from nonradiative Auger decay due to multi-excitonic nature of light amplificati

74 nting for differential diffraction intensity decay due to the nonuniform illumination by the X-ray be

75 the global landscape of cotranslational mRNA decay during Arabidopsis (Arabidopsis thaliana) seedling

76 and anatomical reservoirs that show minimal decay during ART.

77 rgets are largely subject to cotranslational decay during plant development.

78 lowed the determination of a cotranslational decay efficiency that could be an alternative to other m

79 wing to a tightly-confined and exponentially-decaying electromagnetic field.

80 ored LLOs exhibit noticeably reduced voltage decay, enhanced rate performance, improved cycle stabili

81 cs and can independently explain the typical decaying envelope and the progressive spacing of the spi

82 ies from a Windkessel model (consisting of a decaying exponential plus a dampened cosine, with an int

83 The response then decayed exponentially.

84 by phosphorylation and inactivation of mRNA decay factor, Tristetraprolin (TTP) in G0.

85 Interestingly, the decay factors could differentiate between SAGA- and TFII

86 es among protective RNA-binding proteins and decay factors, PTBP1 promotes displacement of UPF1 alrea

87 ted to protect cellular RNAs by sequestering decay factors.

88 to Ag oscillations evolving into stochastic decaying fluctuations.

89 PFA decay followed first-order kinetics and the inactivation

90 we report the use of fluorescence anisotropy decay for measuring the rotation of six shape-persistent

91 inverted region behavior associated with the decay from the CSS to the ground state through charge re

92 sing methods, and a set of tunable threshold decay functions.

93 uld induce serious capacity loss and voltage decay, further hindering its practical application.

94 )H(3)) that features suppressed nonradiative decays, giving rise to a robust narrow-band green lumino

95 h salivary microbiome composition and dental decay in 61 children and adults.

96 The rate of decay in linkage disequilibrium was fast, and no signifi

97 ements with G-quadruplexes as marks for mRNA decay in P-bodies.

98 trate the prevalence of cotranslational mRNA decay in plant development and its role in translational

99 f new technologies for caries control, tooth decay in primary teeth remains a major global health pro

100 val of selection pressure generally leads to decay in resistance.

101 NO decay in SMCs was measured following bolus addition of N

102 Both methods revealed an exponential decay in the kinetic rate of depolymerization correspond

103 ecovery produced a simple single-exponential decay in the spatial Fourier domain, in excellent agreem

104 u = 4-11 ns) was shorter than its anisotropy decay in well-matched duplex DNA (theta = 20 ns), yet lo

105 P2RX7-deficient Trm cells progressively decayed in non-lymphoid tissues and expressed dysregulat

106 d that experienced 6.3-98.8% mass loss while decaying in common garden 'rotplots' in a temperate oak-

107 of thermodynamics: entropy of microstructure decays in isolated systems.

108 ally in three phases characterized by abrupt decays in plant productivity, soil fertility, and plant

109 quencing in mutants defective in nuclear RNA decay including the exosome to reassess the existence of

110 We show that entropy of grain structure decays indeed as expected.

111 ay (RCP) scenarios to project future climate decay indices for the United Kingdom until the end of th

112 Two heuristic models for the tri-exponential decay involving defects are discussed.

113 We quantified how mangrove SOM decay is affected by predicted global warming (+4 degree

114 As cotranslational mRNA decay is interconnected with translation, we also assess

115 We demonstrated that cotranslational mRNA decay is regulated by developmental cues.

116 Observation of the neutrinoless double beta decay is the only practical way to establish that neutri

117 /ionization (MALDI), combined with in-source decay (ISD) fragmentation and Fourier-transform ion cycl

118 attern detection experiment-we show how this decay kernel improves the model's predictive performance

119 PL decay kinetics corroborated by DFT calculations reveal a

120 nt an initial demand followed by first-order decay kinetics in SEW.

121 rganisms to monitor bacterial concentration, decay kinetics in the presence of various antibiotics (c

122 creased glutamate reuptake, producing faster decay kinetics.

123 Our findings indicate a decay machinery removing AGO-associated miRNAs with an e

124 ndensate containing the RNA degradosome mRNA decay machinery, but the biochemical function of such or

125 cay (NMD) is an evolutionarily conserved RNA decay mechanism that has emerged as a potent cell-intrin

126 esting that this is an important step in the decay mechanism.

127 Here, we show that RNA decay mechanisms involving upstream frameshift 1 (UPF1),

128 axa after adjusting for dental plaque index, decayed missing filled teeth (DMFT) and the frequency of

129 The association of SSB intake with baseline decayed, missing, and filled tooth surfaces (dmfs) (inte

130 prevalence of ECC (based on the presence of decayed, missing, or filled tooth surfaces).

131 isotropy decays with a stretched exponential decay model (<E(FRET)(exp)> = 0.25 +/- 0.05) and those c

132 ary radiations themselves cause evolutionary decay (modelled co-occurrence probability and shared fra

133 lly, the rapid dynamics of IEG induction and decay motivates the common use of IEG expression as mark

134 The relaxed (3) MLCT state then decays much more slowly (7.6 ps) to the (3) MC state.

135 5 inclusion triggers nonsense-mediated mRNA decay (NMD) and unproductive translation of Bak1 transcr

136 tein L) protect mRNAs from nonsense-mediated decay (NMD) by preventing the UPF1 RNA helicase from ass

137 hanism is dependent on the nonsense-mediated decay (NMD) component, Upf1, which promotes histone mRNA

138 Nonsense-mediated mRNA decay (NMD) degrades EJC-bound mRNA, but the lack of sui

139 Nonsense-mediated mRNA decay (NMD) is a conserved translation-coupled quality c

140 Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved RNA decay mec

141 rns are likely mediated by nonsense-mediated decay (NMD) of splicing isoforms, with autism phenotypes

142 The nonsense-mediated mRNA decay (NMD) pathway degrades some but not all mRNAs bear

143 mental illnesses, the nonsense-mediated mRNA decay (NMD) pathway presents an unexplored regulatory me

144 s are degraded through the nonsense-mediated decay (NMD) pathway, we hypothesise that some fs-indels

145 eshift 1 (UPF1), including nonsense-mediated decay (NMD), are inhibited in c9ALS/FTD brains and in cu

146 ntrol pathway, termed nonsense-mediated mRNA decay (NMD), by phosphorylating the NMD factor UPF1.

147 Igh allele is degraded by nonsense-mediated decay (NMD).

148 ranslation termination and nonsense-mediated decay (NMD).

149 ranscripts by antagonizing nonsense-mediated decay (NMD).

150 transcript degradation via nonsense-mediated decay (NMD).

151 licit degradation via nonsense-mediated mRNA decay (NMD).

152 Open circuit photovoltage decay (OCVD), Mott-Schottky (MS) plot, and transient abs

153 Thus, it is not caused by the physical decay of (90)Sr and environmental diffusion, but implies

154 ults demonstrate that the broadband emission decay of (EDBE)PbBr(4) arises from a time-averaged singl

155 ve a stable long cycling with a low capacity decay of 0.014% per cycle and 0.16% per day over 1000 cy

156 performance, with a very low average voltage decay of 0.8 mV per cycle as well as a capacity retentio

157 YTHDC1 facilitates the decay of a subset of these m(6)A-modified RNAs, especial

158 in darkness; and an increase in the rate of decay of activated phosphodiesterase, with perhaps also

159 th nonalcoholic fatty liver disease, such as decay of bile canaliculi network and ductular reactions.

160 f fluctuations in the unbound TF levels, the decay of bound TFs leads to faster fluctuations and smal

161 tween liquids and solids and investigate the decay of CE charges on the solid surfaces after liquid-s

162 n, as well as increased amplitude and faster decay of CF-evoked EPSCs.

163 on nonlinear amplification of changes in the decay of dendritic synaptic currents when they reach the

164 d decomposition associated with the complete decay of ECD signals upon acidification.

165 The decay of Fe(VI) had second-order kinetics in PB while Fe

166 ere is a slight but significant delay in the decay of force relative to WT muscle while the return of

167 BIC/FTC/TAF led to rapid decay of HIV-1 RNA in genital and rectal fluids.

168 t cellular proliferation counterbalanced the decay of HIV-infected cells throughout therapy.

169 distribution is co-determined by the spatial decay of hydrodynamic lift and the global deficiency of

170 d sea level largely driven by the growth and decay of ice sheets in the Northern Hemisphere.

171 omic response well below the quantum-limited decay of individual atoms into free space.

172 We observed slow decay of intact proviruses but no changes in the proport

173 with perhaps also an increase in the rate of decay of light-activated visual pigment.

174 a repressor that binds MARF1 to prevent the decay of MARF1 target mRNAs.

175 By monitoring, offline, the color decay of MB in a series of IPA solutions with different

176 igase mediates TDMD by directing proteasomal decay of miRNA-containing complexes engaged with highly

177 with implications for RyR regulation and the decay of muscle function in aging.

178 n the Nordic seas, caused by the progressive decay of Northern Hemisphere ice-sheets.

179 energy electron emission following the Auger decay of O 2s hole is nearly as efficient as electron em

180 energy electron emission following the Auger decay of O 2s holes from adsorbed oxygen and oxide surfa

181 By monitoring the decay of Omega through rapid freeze-quench trapping at p

182 NOM) is the product of microbial and abiotic decay of plant and animal remains in terrestrial and aqu

183 increase of persistent current and a slowed decay of resurgent current.

184 family, but was not consistent with general decay of SHM targeting with increasing distance from the

185 sed technique can be used to correct for the decay of signal due to T2* effects to improve quantifica

186 impairments are characterized by accelerated decay of spatial memories.

187 decaying dark matter-in particular, that the decay of sterile neutrinos with a mass around 7 keV coul

188 riments, we conclude that rapid nonradiative decay of the anthracene-substituted derivatives, perhaps

189 Subsequent thermal decay of the chemisorbed state led molecules to the phys

190 in darkness; and (3) an accelerated rate of decay of the effector enzyme phosphodiesterase and perha

191 tributions beyond the conventional monotonic decay of the evanescent field.

192 to be the first molecular scale study of the decay of the interfacial friction force in rock, observe

193 The Fe(2)(III/III) cluster produced upon decay of the intermediate has a small Mossbauer quadrupo

194 n due to mutations causing nonsense-mediated decay of the mRNA leads to a wide spectrum of clinical p

195 sulted in rapid self-cleavage and subsequent decay of the mRNA.

196 his phenomenon is solely responsible for the decay of the neutral pion pai(0) into two photons (gamma

197 formation, further confirming the diagenetic decay of the original collagen structure and the antiqui

198 triplet annihilation and promoting radiative decay of the resulting singlet exciton.

199 ereby the I(VV)(t) and I(VH)(t) fluorescence decays of a series of oligoquinolines labeled at one end

200 ortion leads to a large rate of nonradiative decay, on the order of 10(8) s(-1).

201 ar combinations of the I(VV)(t) and I(VH)(t) decays or acquiring the I(VV)(t) and I(VH)(t) decays wit

202 urrent generation and prolonged photocurrent decay, originated from charge trapping in the MoS(2)-org

203 a strong influence of the Nonsense Mediated Decay pathway on CKI levels.

204 Here, we characterize a genome-wide RNA decay pathway that reduces the half-lives of mRNAs based

205 RNA decay (PPD) pathway and an ARS2-mediated decay pathway.

206 importance of translational control and mRNA decay pathways for the successful establishment of the n

207 els to further understand the roles of these decay pathways in KSHV gene expression.

208 the first time, suppression of non-radiative decay pathways of a chromophore was tested by anchoring

209 nanorods release energy through nonradiative decay pathways, locally generating heat that efficiently

210 is and were differentially regulated by mRNA decay pathways, raising the possibility that one distinc

211 re to at least two host-mediated nuclear RNA decay pathways, the PABPN1- and PAPalpha/gamma-mediated

212 te recovery is mediated by two distinct S(1) decay pathways: a reactive twisting pathway and an unrea

213 ct observed data, distinguish any growing or decaying patterns, and obtain a hierarchy of previously

214 g m(-3), and exposure during the postcooking decay phase exceeded that of the cooking period itself.

215 During the decay phase of Ca(2+), the Ca(2+)-dependent block is rel

216 ature neurons exhibit hallmark fast rise and decay phases, newborn neurons display slow GPSCs with ch

217 f Auger-stimulated ion desorption, Coulombic decay, photodynamic cancer therapies, and may yield impo

218 Streptacidiphilus sp. P02-A3a, isolated from decaying pinewood.

219 -living, with most having been isolated from decaying plant or fungal matter.

220 smonic nanostructures, generated via plasmon decay, play key roles in applications such as photocatal

221 the PABPN1- and PAPalpha/gamma-mediated RNA decay (PPD) pathway and an ARS2-mediated decay pathway.

222 Distance decay principles predict that species with larger geogra

223 e understanding of LPMO contribution to wood decaying process in nature and for the development of su

224 arriers, and heat through the excitation and decay processes, is still controversial.

225 eld (QY), accompanied by a faster population decay profile.

226 ith the stimulation of the sub-steps of mRNA decay provide an effective organization strategy for bac

227 identifying naturally long-lived states in a decaying quantum system.

228 m paradoxical because ancestral correlations decay rapidly.

229 We determine that the NI decays rapidly under optimal turnover conditions, and th

230 DAR were correlated positively with the seed decay rate (r = 0.41-0.53) and negatively with the survi

231 ening (DAR), and for SL measured by the seed decay rate and survivability in the soil of a rice field

232 tion curve was established between the color decay rate and the scavenging capacity.

233 The relationship between the thermal decay rate and vegetation depends on many factors includ

234 ns to the distal histidine (His211); (2) The decay rate constant of the ferryl intermediate is not st

235 ecreased and become lower than the radiative decay rate constants (k(r) = 10(5) s(-1)).

236 Decay rate constants of short-tailed mRNAs vary broadly

237 Carriage decay rate is analysed using non-linear regression.

238 satellite thermal measurements, the thermal decay rate may be a useful index for monitoring vegetati

239 f cathode and anode mass) and a low capacity decay rate of 0.0047 % per cycle over 600 cycles in a Zn

240 We set an upper limit on the decay rate of dark matter in this mass range, which is i

241 Results show that the decay rate summarizes both vegetation structure and func

242 Mean decay rate without simulated sunlight across all relativ

243 Ca(2+) transient amplitude, 50% decay rate, and sarcoplasmic reticulum Ca(2+) content we

244 creased [Ca(2+)](i) transients amplitude and decay rate, lower SR Ca(2+) load and depressed cellular

245 odel uncertainties (e.g., static GWP values, decay rate, moisture content, or gas collection efficien

246 a level rise is unlikely to decrease the SOM decay rate, suggesting that previous mangrove elevation

247 sotropy is also reflected in the hot carrier decay rate, which is a factor of two slower along the c-

248 Yet, those with intermediate decay-rate constants switched from reaction limitation t

249 Our calculations show that the radiative decay rates are dominated in all instances by the electr

250 On the other hand, the nonradiative decay rates in the case of TAA-PTM radicals that have hi

251 Consequently, the nonradiative decay rates of these ICT emitters are decreased and beco

252 g enough to test whether drivers change with decay rates through time, with unknown consequences for

253 Pinus-dominated site, only the Pinus litter decay rates were decelerated by EM fungi and were associ

254 Measured decay rates were dependent on the level of simulated sun

255 However, for slower pathogen decay rates, stigmergy-driven movement increased outbrea

256 ransitions, enhance as well the nonradiative decay rates.

257 showed little influence of Cu form on oxygen decay rates.

258 activation of regulated IRE1alpha-dependent decay (RIDD) without activating its canonical output med

259 The initial decay slope was significantly lower in SP than in RF and

260 The remainder decay slowly, at a rate consistent with equilibrium solv

261 damaging wood degraders have caused limited decay so far, probably due to unfavorable growth conditi

262 We discover exponentially decaying spatial modes in both hemispheres and discuss t

263 Virus-specific IgG decayed substantially in most individuals, whereas a dis

264 were corrected for scatter, attenuation, and decay supplemented by resolution recovery using dedicate

265 RNA helicase from associating with potential decay targets.

266 on between 2 and 6 hr/day did not affect SOM decay, the treatment without inundation led to a 60% inc

267 elds the nascent A-tail from uridylation and decay thereby protecting pre-mRNA upon KPAF3 displacemen

268 , and the rate at which those two quantities decayed; this finding raises interesting questions about

269 d on Floquet modes, which increases the Rabi decay time ([Formula: see text]) in a number of material

270 been found that the crystal exhibits a fast decay time constant of 1 ns at 7 K.

271 longer times we find an ambient temperature decay time of the Omega Fe-C5' bond of tau ~ 5-6 s, like

272 The rate of resistance decay to become fully susceptible from moderate-intensit

273 A warming of 4 degrees C caused SOM decay to increase by 21%, but longer inundation moderate

274 an initial peak (mean 1.6 pA/pF) followed by decay to the point that submembrane [Ca(2+)] reached ~10

275 rther determined rates of RNA biogenesis and decay to uncover RNA regulatory strategies during stepwi

276 tively (T(80) and T(70) represent efficiency decays to 80% and 70% of the initial value, respectively

277 se charge transfer complex that subsequently decays to eliminate thiocyanate.

278 t the center of the actuator and this strain decays to near zero at the edges of the actuator.

279 native intermediate (NI), which only slowly decays to the resting form.

280 e ability of the early and midstages of wood decay, to which our findings are most applicable.

281 ble electron-electron resonance spectroscopy decay traces and distance distributions between spin lab

282 ion reveals oscillations superimposed on the decay traces due to a vibrational wavepacket.

283 Moreover, decay traces generated from these distributions recapitu

284 rticipants to estimate protection curves and decay trajectories.

285 on of ER Ca(2+) stores, followed by a slower decay, typically reaching ~50% of initial dark-adapted l

286 It however suffers from a voltage decay upon cycling, urging for an in-depth understanding

287 concentration-dependent acceleration of its decay upon exposure to either l-NMA or N(delta)-hydroxy-

288 Oxidative decay via ozonolysis and product formation were monitore

289 e reducing systems that regulate cellular NO decay, we assessed the intracellular concentrations of C

290 Host density and rate of pathogen decay were also key predictors.

291 to a scattering state, become protected from decay whenever the relative phase is a multiple of pai.

292 ro95 hot spot mutations elicit enhanced mRNA decay, which is dependent on sequence-specific RNA bindi

293 wly at first but more quickly with advancing decay, which resolves ambiguity about the after-life con

294 ading to cytoskeletal unraveling and tension decay, which result in synapse breaking.

295 the cell-surface transporter density (n) may decay with cell radius (r) following the power rule n ~

296 nts of the phthalimide-N-oxyl radicals' self-decay with different electron-withdrawing or -donor subs

297 it of the eGFP15eGFP fluorescence anisotropy decays with a stretched exponential decay model (<E(FRET

298 e zone (<30 mum) where the hyperpolarization decays with increasing cell-electrode distance.

299 ecays or acquiring the I(VV)(t) and I(VH)(t) decays with static polarizers before fitting them global

300 pin-coated films show faster non-exponential decays with the slowest component of the crystal PL abse