ライフサイエンスコーパス: decay

1 cluding protein coding and nonsense-mediated decay.

2 ing mature rRNA formation and discarded rRNA decay.

3 that the mutation induces nonsense-mediated decay.

4 ets inflammatory mRNAs for deadenylation and decay.

5 measured in this region exhibit a power-law decay.

6 est life and are prone to postharvest fungal decay.

7 a substantial role in the photoluminescence decay.

8 to control mRNA maturation, translation and decay.

9 or circle formation, likely representing RNA decay.

10 mutation, indicating nonsense-mediated mRNA decay.

11 and coupling their RNA products to efficient decay.

12 y due to activation of nonsense mediated RNA decay.

13 anifest themselves as resonances that do not decay.

14 enger RNA by nonsense-mediated messenger RNA decay.

15 G cap that promotes rather than inhibits RNA decay.

16 erranean probably due to pelagic ecosystem's decay.

17 otion that evidence accumulates without much decay.

18 to estimate the effect of SLD on weighted LD decay.

19 he 3' untranslated region and promoting mRNA decay.

20 sulting mRNA is subject to nonsense-mediated decay.

21 targets the transcript for nonsense mediated decay.

22 ermination is followed by TRAMP-mediated RNA decay.

23 6c>u were degraded by nonsense-mediated mRNA decay.

24 s to a reduced calcium time to transient 50% decay.

25 g multiple steps in AGO2-miRNA-mediated mRNA decay.

26 rentiation, and m(6)A tagging promotes their decay.

27 n for degrading the poly(A) tail during mRNA decay.

28 ifetimes are required to fit the exponential decays.

29 h as atomic spontaneous emissions and cavity decays.

30 rom a 3-exponential approximation of the FAF decays.

31 s after almost all genes on the W Chromosome decayed.

32 ibitors (C' receptor-1 related isoform Y and decay accelerating factor), and an increase in local TUN

33 emic syndrome (aHUS), was defective in C3bBb decay-accelerating activity (DAA) and factor I cofactor

34 unction mutations in the gene encoding CD55 (decay-accelerating factor), which lead to loss of protei

35 mics of acetylene dication produced by Auger decay after X-ray photoionization of the carbon atom K s

36 rp47 and Mpp6 stimulate exosome-mediated RNA decay, albeit with unique dependencies on elements withi

37 i PI-7 displayed a longer lag phase prior to decay and a longer half-life compared with E. coli DSM11

38 a four-phase pattern of soil organic matter decay and carbon dioxide fluxes to the atmosphere, with

39 monstrated RRGD loci undergo cotranslational decay and identified changes in the ribosome stalling in

40 ew insights into the movement of ions during decay and illustrate how synchrotron-based XFM is unique

41 mportance of radioactivity, the basics of Np decay and its ramifications (including the radiochemical

42 1000mumol/L melatonin on attenuating fungal decay and maintaining nutritional quality of strawberry

43 were marked by m(6)A, exhibited slower mRNA decay and showed increased mRNAs and levels of protein e

44 ificant differences were shown in percentage decayed and filled teeth and decayed teeth in the primar

45 t include high systemic toxicity, rapid drug decay, and low efficacy (ca. 20%).

46 he fast rise of the light curves, subsequent decay, and rapid color evolution are consistent with mul

47 position; the earliest stages of leaf litter decay are associated with a net import of N from the soi

48 ng transcripts that escape nonsense-mediated decay are not actively translated.

49 cited via Landau damping (during the plasmon decay) are responsible for the photocatalytic property o

50 Linkage disequilibrium rapidly decayed around LanFTc1, suggesting that this deletion ca

51 rameter recovery variance exhibits power law decay as a function of the length of available ground tr

52 anscriptome analyses suggested nonsense mRNA decay as a main impact of mutations.

53 nm, we observe a final approximately 150 ps decay assigned to trapping by charge separation, and the

54 es inside the 2DMA dominates its fluorescent decay at a picosecond timescale.

55 gain associated to changes in limb position decayed at a faster rate than the velocity-dependent gai

56 ng an experimental system comprising 18 wood decay basidiomycete fungi, we test this possibility by q

57 Fungal decay, biochemical properties, quality and sensory attri

58 raditionally described by simple exponential decay, but there is increasing recognition that some pat

59 RNA 3'-end processing, gene looping and mRNA decay, but they have also been shown to enter the nucleu

60 act single-cell information from radioactive decays, but the stochastic nature of the process preclud

61 ectrics can cause emitters to preferentially decay by the emission of pairs of phonon polaritons, ins

62 s in adult tissues are tasked with replacing decaying cells and regenerating tissue after injury to m

63 n) reaction, which is the major nonradiative decay channel of uGFPc.

64 the empirically derived apparent exponential decay coefficients (kexp) was indeed continuous.

65 The slowest decay constant increases from 140 ps in the bulk to 504

66 s with acceptors over a limited depth with a decay constant of 10-20 nm by post-process immersion int

67 luminescent method using the light intensity decay constant.

68 cross mussel densities, but that first-order decay constants varied between experimental treatments.

69 ogic evaluation (radiochemical purity > 95%, decay-corrected radiochemical yield = 31.6%, specific ac

70 ith a radiochemical yield of 56% +/- 8% (non-decay-corrected), and the radiochemical purity was great

71 was obtained in 15%-40% radiochemical yield (decay-corrected), with a specific activity of 279 +/- 75

72 esponse is not well understood, a decline in decay could alter the amount, as well as biochemical com

73 aelectronvolts) is cosmic-ray albedo neutron decay (CRAND).

74 l studied pesticides fitted to a first-order decay curve in both types of cereals.

75 In previous methods, only the decay curve of weighted LD between pairs of sites whose

76 rcome these drawbacks, we proposed to filter decay curves instead of images.

77 In this novel scheme, decay curves were averaged in a local window, each with

78 , thus leading to pre-mRNA stabilization, or decay depending on the occurrence and extent of editing.

79 ifferences were seen in primary or permanent decay (dt, DT) when compared with controls.

80 that population rates showed no significant decay during UP periods.

81 -, shape-, and composition-dependent exciton decay dynamics and photoinduced energy transfer of QDs i

82 servables under the reservoir-induced atomic decay effect both with and without quantum memory.

83 ce, but confirm the orthodox view of rapidly decaying electronic quantum coherence on a timescale of

84 fluorophore, diffusing in the exponentially decaying evanescent excitation field.

85 overy caused by alpha-particles during alpha-decay events has not been possible, as the recovery proc

86 damage, created by alpha-recoils from alpha-decay events, on the diffusion of radiogenic elements (e

87 smissions as sum of monotones modulated by a decaying exponential, with angular attenuation by a modi

88 robiotas of allopatric mammalian populations decayed exponentially with the geographic distance separ

89 howed that the speed of judgment propagation decayed exponentially with the social distance from the

90 ing energy for the target DNA, with the gain decaying exponentially such that binding energy saturate

91 ch persists in a steady state phase and then decays exponentially upon depletion of the peroxo oxidan

92 act as mRNA storage depots rather than mRNA decay facilities.

93 components eIF4E, eIF4G, and PABP and of the decay factor DDX6 in human cells.

94 pathogens demonstrate a biphasic pattern of decay-fast followed by slow.

95 ormula: see text] Systems whose fluctuations decay faster, [Formula: see text] with [Formula: see tex

96 vealing the fine details of the mechanism of decay for these species.

97 for estimating the rate of differential mRNA decay from RNA-seq data and model mRNA stability in the

98 imilar yields for nonradiative excited-state decay from the photoacids and the Ru(II) dyes, suggest t

99 of biotrophic capacity in saprotrophic wood-decay fungi and which systems may be useful models, we i

100 tro using an array of 201 basidiomycete wood-decay fungi.

101 1 functions in promoting miRNA-mediated mRNA decay globally.

102 oved, the amplitude of oscillations start to decay immediately, since there is no means to restitute

103 ing solutions, multiexponential fluorescence decays imply separate solute populations in the aqueous

104 re the extent to which declines in microbial decay in a long-term (ca. 20 yrs.) N deposition experime

105 PA receptor EPSCs of approximately 1 nS that decay in approximately 1 ms and mildly voltage-dependent

106 receptor EPSCs of approximately 0.6 nS that decay in approximately 7 ms.

107 eep deprivation experiment by evaluating the decay in autocorrelation and the scaling exponent of the

108 at amlexanox inhibits nonsense-mediated mRNA decay in cells from patients with RDEB that respond to r

109 burst stimulation (TBS) that alleviates the decay in cholinergic synaptic transmission effectively p

110 response-outcome conditioning caused a later decay in goal-directed responding-that is, mice were una

111 s and tomographic location of beta cell mass decay in individual islets as well as at the entire isle

112 us, the question of increased risk of dental decay in individuals with oral clefts or their unaffecte

113 Gravity model estimates indicate a sharp decay in influenza transmission with the distance betwee

114 pproach to single-molecule assessment of RNA decay in living cells by exploiting the ability of flavi

115 mically relevant parameter range and a steep decay in orientation selective activation that is consis

116 de of human immunodeficiency virus (HIV) RNA decay in semen.

117 found that different mechanisms dominate ASQ decay in the different protein environments, producing l

118 on and thus many patients suffer progressive decay in the heart's pumping capacity to the point of he

119 properties of the excitonic reservoir, which decay in time much slower with respect to the polariton

120 The discovery of Higgs-boson decays in a background of standard-model processes was a

121 nherent assumption of linear combinations of decays in global analysis means the technique is unable

122 nit lead to the acceleration of nonradiative decays, in conjunction with the narrowing of the singlet

123 Knockout of Cygb greatly prolongs NO decay, increases vascular relaxation, and lowers blood p

124 The unavoidable energy loss from plasmon decay, initially seen as a detriment, has now expanded t

125 vivirus RNA structural elements to trap XRN1 decay intermediates in dual-labeled reporter constructs.

126 that requires extensive uridylation of mRNA decay intermediates.

127 f this assumption, recent studies of B-meson decays involving the higher-mass tau lepton have resulte

128 tures of polymers using infrared multiphoton decay (IRMPD) and electron capture dissociation (ECD) as

129 The decay is accompanied by coherently excited vibrational d

130 We find that the time-scale of this decay is in line with the time-scale of the dispersion o

131 alkane, and show that the large conductance decay is intrinsic to the nature of the Si-O bond.

132 ing the simplifying assumption that distance decay is isotropic.

133 olled by the structural changes, whereas the decay is limited by the charge recombination step.

134 llulosic cell walls and fungal hyphae during decay is not known.

135 Dental caries (tooth decay) is a polymicrobial biofilm disease driven by the

136 peptide release during nonsense-mediated RNA decay, is critical for assembly of stalled polysomes in

137 A decaying isotope scan was obtained over 5 half-lives on

138 Although radioactive decay itself cannot be easily modulated, the associated

139 itory nerve and also balanced differences in decay kinetics between responses to different stimulatio

140 Mathematical modeling, which included the decay kinetics of the fluorescence of the miRNA sensors,

141 trum of W32(*) is presented, and analysis of decay kinetics show that W32(*) persists approximately 1

142 Additionally, the luminescence decay kinetics transform from multiexponential decays ty

143 fluorescence (k(0)F), S1 --> S0 nonradiative decay (knr), S1 --> T1 ISC (kISC), and T1 --> S0 relaxat

144 on a length scale that is comparable to the decay length of the LSPR-induced electromagnetic field e

145 ence (PL) intensity and the time-resolved PL decay lifetime increase after electrical stress, indicat

146 iple kinetic problems, such as fast capacity decay, low rate capacities and low Coulombic efficiencie

147 mechanistic link between the RNA and protein decay machineries in human cells.

148 NA, we investigated whether the 5' to 3' RNA decay machinery participated in the regulation of this p

149 l RNAs must successfully evade this host RNA decay machinery to establish a productive infection.

150 ibonuclease component of the cytoplasmic RNA decay machinery.

151 ternative splicing-coupled nonsense-mediated decay mechanism.

152 Despite the importance of ions in fungal decay mechanisms, the spatial distribution and quantific

153 al examination included: 1) dental findings (decayed, missing, and/or filled adult teeth [DMF-T] inde

154 in the house; prosthetic needs; or number of decayed, missing, or filled teeth (DMFT).

155 ear, and 149 378 (45 231-262 013; 2.4) fewer decayed, missing, or filled teeth annually.

156 aminers; secondary outcome measures included decayed, missing, or filled teeth surfaces (dmfs); pain;

157 ency of PMGF was fit to a double exponential decay model selected by information-theoretic criteria.

158 while also directly causing disinfectant to decay more rapidly.

159 Nonsense-mediated decay (NMD) eliminates transcripts with premature termin

160 that depletion of the nonsense-mediated mRNA decay (NMD) factor SMG7 or UPF1 significantly induced p5

161 Nonsense-mediated mRNA decay (NMD) is a cellular surveillance pathway that reco

162 Nonsense-mediated mRNA decay (NMD) is an essential eukaryotic process regulatin

163 rved helicase required for nonsense-mediated decay (NMD) regulating mRNA stability in the cytoplasm.

164 As were not substrates for nonsense-mediated decay (NMD), even though they were detected in polysomes

165 l mechanisms, such as nonsense-mediated mRNA decay (NMD), which degrades both abnormal as well as som

166 idly degraded through nonsense-mediated mRNA decay (NMD).

167 pt for degradation by nonsense-mediated mRNA decay (NMD).

168 ndent RNA decay, with maximal Mtr4-dependent decay observed with both cofactors.

169 mated that most of the litter CO2 efflux and decay occurring in the dry season was due to nighttime m

170 ce a new concept for translating radioactive decays occurring stochastically within radiolabeled sing

171 One example of such a transition is the decay of a beauty quark into a strange quark.

172 fission process, including the formation and decay of a quintet state that precedes formation of the

173 gain-space trajectories for the learning and decay of adaptation and (2) for combined motion-state pe

174 ent of the CCR4-NOT complex and TTP-directed decay of an mRNA containing an AU-rich element in its 3'

175 and the largest length-dependent conductance decay of any molecular systems measured to date.

176 scopy to compare the rates and mechanisms of decay of ASQ generated photochemically in bifurcating NA

177 AS event leading to a nonsense-mediated mRNA decay of BARD1.

178 In vitro, recombinant TSN initiated the decay of both protein-free and Argonaute 2-loaded miRNAs

179 study also suggests a possible link between decay of cleaved target mRNAs and miRNA stability in RIS

180 ions: insufficient supply of electron donor, decay of dechlorinators' biomass, and reduction in bacte

181 rom single layer graphene as a result of the decay of deep holes in the valence band.

182 n in E cells paradoxically caused a marginal decay of E-rate but a marked decay of I-rate in UP perio

183 put resistance, enhanced spiking, and slowed decay of excitatory post-synaptic potentials (EPSPs).

184 ffusive processes likely govern the ultimate decay of geomagnetic spikes.

185 Exponential decay of gull marker in sand amended with live Catellico

186 used a marginal decay of E-rate but a marked decay of I-rate in UP periods, a prediction that we vali

187 ead of action potentials, can induce a rapid decay of junctional conductance, thus demonstrating spik

188 s of the feedforward motor output during the decay of learning.

189 light-activated rhodopsin, accelerating the decay of ligand-bound forms.

190 Ythdf2 in zebrafish embryos decelerates the decay of m(6)A-modified maternal mRNAs and impedes zygot

191 The rate of mutational decay of male competitive fitness is 0.17%/generation;

192 estimate of 1.5X faster rate of mutational decay of male fitness is nearly identical to the same ra

193 thway in which the nuclease TSN promotes the decay of miRNAs that contain CA and/or UA dinucleotides.

194 criptional silencing or post-transcriptional decay of mRNAs.

195 The decay of Na(+) /Ca(2+) exchanger current that followed a

196 l to increase soil C storage by reducing the decay of plant litter and soil organic matter (SOM).

197 Decay of plasmons to hot carriers has recently attracted

198 Our data suggest that the decay of platelet mRNAs is slowed by the natural loss of

199 control light-matter interactions (e.g., the decay of quantum emitters).

200 However, the decay of S1 and the formation of (1)(TT) occur on differ

201 ns challenging mainly due to the exponential decay of signal-to-noise ratio with increasing MW.

202 i(III) (mu-O)2 Ni(III) ](2+) complex and the decay of the asymmetric [Ni(III) (mu-O)2 Co(III) ](2+) c

203 Specifically, early in the decay of the charged droplet SP(3+) ions favor an extend

204 e dopant-related luminescence is ascribed to decay of the conduction-band electron following transfer

205 TA reveals a sub-100-fs blue shift and decay of the Franck-Condon bright state arising from rel

206 Decay of the HIV reservoir is slowed over time in part b

207 degrees C), we established that the measured decay of the intrinsic PDI fluorescence is appropriate f

208 rapies are being developed to accelerate the decay of the latent HIV reservoir, it will be important

209 how that such coupling can lead to anomalous decay of the modes where they go through nonlinear reson

210 eshift mutation results in nonsense-mediated decay of the mutant transcripts.

211 In an oscillatory system, it leads to the decay of the oscillation amplitude.

212 Notably, the observed decay of the over cut-off emission is found to be critic

213 Each mutation triggered nonsense-mediated decay of the respective mRNA transcript.

214 es translation repression and/or accelerated decay of this target mRNA (2) .

215 sical half-life of (225)Ac, assuming instant decay of unstable daughter nuclides.

216 l cells, which exhibits non-trivial temporal decay of velocity autocorrelation functions.

217 o consideration the resolving power (and its decay) of different mass analyzers.

218 ild-up (within less than one picosecond) and decay (on the several picosecond timescale).

219 fts in eye dominance are induced, the effect decays once the two eyes view stimuli equal in strength.

220 cruiting the CCR4-NOT complex, decapping and decay, or germ granule proteins.

221 population into a low-dimensional, periodic, decaying orbit - a spiral - in which it behaved as a tru

222 eed on microbial communities associated with decaying organic matter.

223 ble to describe monobromamine or dibromamine decay outside of the conditions for which it was calibra

224 the mutation rate in general, is expected to decay over time in individual bNAb lineages.

225 Levels of exogenous Cx30 decayed over time, but were still detectable four weeks

226 utive swimmers are anticorrelated, an effect decaying over time due to trail dispersion.

227 plication of traditional PageRank with fixed decay parameters.

228 and persister cell formation during the late decay phase, which may have accounted for its prolonged

229 icating that the kinetics of the major force decay (phase 2) upon rapid increase in [Pi] is determine

230 se 1) and a subsequent 3-5-fold faster major decay (phase 2).

231 ed on the kinematic observables of the Higgs decay photons, which we then use to construct a strong c

232 Regulated mRNA decay plays a vital role in determining both the level a

233 For safety consideration, these decayed potatoes should be systematically set aside.

234 Notably, we found that slowed EPSP decay preferentially enhanced temporal summation and fir

235 Additionally, we show that under decaying primary gradients, secondary gradients are more

236 The role of ions in the fungal decay process of lignocellulose biomaterials, and more b

237 The coupling between these decay processes and a chemical trajectory (nuclear motio

238 nic systems, our device converts the natural decay product of the plasmon-electronic heat-directly in

239 AUF1 overexpression implying that AUF1 is a decay-promoting factor influencing multiple steps in AGO

240 Geo-neutrinos produced by these decays provide important clues about the origin, formati

241 tween nearby PPC neurons was much weaker and decayed rapidly beyond approximately 200 mum.

242 +) (compound 0) accumulates within 5 mus and decays rapidly to CYP101Fe(3+), with a k440 nm of 9.6 x

243 In SP, the HIV-RNA decay rate with RPV was as fast as with EVGcobi; by week

244 Distance-decay rates and community structure also depended on spe

245 At pH 3 regardless of [Fe(II)]0 decay rates for the iron-peroxo complex of about 50 s(-1

246 shes radiative and nonradiative fluorescence decay rates in various solvent polarities.

247 The eDNA shedding and decay rates reported within are the first for freshwater

248 efficacy using only the observed viral titer decay rates seen in patients.

249 The analysis of signal decay rates suggests the existence of a partially folded

250 uch as cooperative Lamb shifts, superradiant decay rates, Van der Waals forces and resonance energy t

251 cit-induced memory impairment involves rapid decay rather than failure of memory acquisition.

252 The gamma-H2AX foci decay ratio correlated negatively with toxicity grade, w

253 A threshold foci decay ratio, determined in our retrospective study, corr

254 ility in prostate cancer for gamma-H2AX foci decay ratios and gene expression profiles derived from e

255 all relied on the detection of inverse beta decay reactions, which are insensitive to the contributi

256 thetical saturation levels and rates of gain decay, reflecting different repeat compositions, yielded

257 ls through the regulated IRE1alpha-dependent decay (RIDD) independent of XBP1.

258 d their families do not have a higher dental decay risk as compared with the general population.

259 Also, few studies have assessed dental decay risk in unaffected relatives of children with clef

260 rgy barrier present on the main nonradiative decay route explains the 6-fold lengthening of the excit

261 The LFP signature is observed to decay sharply outside the cortical region receiving the

262 As would be expected, the radicals' decay, specifically probed by the oxyl's subsurface vibr

263 ons and sizes combined with longer transient decay stabilize integrals of diastolic Ca and NCX curren

264 ed platelet-like particles to show that mRNA decay strongly shapes the nascent platelet transcriptome

265 icase associated with nonsense-mediated mRNA decay, suggesting that amlexanox inhibits nonsense-media

266 1 triggers repression of translation or mRNA decay, suggesting that one factor may use two independen

267 esults were similar when the number of newly decayed teeth (OR = 0.86; 95% CI, 0.60 to 1.22) and toot

268 n in percentage decayed and filled teeth and decayed teeth in the primary dentition (dft, dt) and per

269 rial longitudinal systolic strain functional decay than those of men (P value for interaction, <0.05)

270 e Knight shift and the linear-in-T spin echo decay that increases with doping.

271 ets from vortex-induced reconnection rapidly decay through self-generated turbulence, leading to a ma

272 simple strategy to control and modulate the decay time of the functionalized Yb(3+)-doped nanopartic

273 ns is however limited by the relatively fast decay time of the hyperpolarized spin state together wit

274 ase channels regulates LCRs and Ca transient decay to insure fail-safe pacemaker cell operation withi

275 Interestingly, [(eta(1)-I2)BiI5](4-) decayed to ground state products with a first-order rate

276 We find a distinctive (1)(TT) state, which decays to 2xT1 with a time constant of 270 fs.

277 tates; the former is initially generated and decays to the latter, which repopulates the ground state

278 The higher-energy cis conformer decays to the lower-energy trans conformer via hydrogen-

279 ce analysis (EIS) and open-circuit potential decay transients (OCVD), which attributes to its higher

280 crococcal-like nuclease (TSN)-mediated miRNA decay (TumiD) as a cellular pathway in which the nucleas

281 cay kinetics transform from multiexponential decays typical of nanocrystalline semiconductors with a

282 ribution of trap sites, to a monoexponential decay, typical of single energy level emitters.

283 to the sum of a small number of exponential decays, typically on the order of 2-4, LDA uses a semi-c

284 dundant gene copies would undergo mutational decay unless preserved via selective or neutral forces.

285 The second phase of the biphasic force decay upon release of phosphate from caged phosphate was

286 stable in the absence of weak C-H bonds, but decay via N-O bond homolysis to ferrous or ferric iron h

287 of magnitude longer than that for 1-H, which decays via 1,5-HAT (tau1/2 = 48 s, DeltaH(double dagger)

288 the end of summer, while seasonal population decay was higher in YOY than in adults.

289 Decay was identified from in-person dental examinations

290 the ligase IIIalpha-XRCC1-nucleosome complex decays when ligation is complete, allowing the host nucl

291 functioned to mediate GM-CSF and IL-17 mRNA decay, which was confirmed by in vitro luciferase assay.

292 1.7 mus) accounts for only 3-8% of the total decay with a longer-lived component having a time consta

293 d increases in [Pi] induced a biphasic force decay with an initial slow decline (phase 1) and a subse

294 The energy requirements exponentially decay with the number of target nodes, suggesting that l

295 ffect of tracing on rate of return to clinic decayed with a half-life of 7.0 days after tracing (95%

296 lambdamax= 510 nm that first grows and then decays with time constants of 63 and 270 ns, respectivel

297 Rrp47 each contribute to Mtr4-dependent RNA decay, with maximal Mtr4-dependent decay observed with b

298 indicating that the integration process had decayed within 30 min.

299 The diet of decayed wood and crustaceans offered a substantial suppl

300 g environments: aerial litter caches, aerial decayed wood, organic root mounds and mineral soil.