ライフサイエンスコーパス: decay rate

1 rs) and small xi (0.14 on litter/soil carbon decay rates).

2 n the diffusion coefficient and the pathogen decay rate.

3 ield excitation and increasing the radiative decay rate.

4 e mechanical frequency, and the cavity-field decay rate.

5 n hosts and on the magnitude of the pathogen decay rate.

6 sity, flow chamber dimensions, and morphogen decay rate.

7 h the initial radical concentration and fast decay rate.

8 t the initial radical concentration and fast decay rate.

9 ticulum Ca2+ release, and intracellular Ca2+ decay rate.

10 characterized by faster signal rise time and decay rate.

11 lly increase attachment success and decrease decay rate.

12 osis factor (TNF) mRNA, and increasing their decay rates.

13 odes with strongly differing frequencies and decay rates.

14 ationship between metal fractions and oxygen decay rates.

15 ransitions, enhance as well the nonradiative decay rates.

16 contributing to allelic differences in mRNA decay rates.

17 do not directly impact NAD(P)H fluorescence decay rates.

18 red ones as confirmed by surface temperature decay rates.

19 issociated from location memory by different decay rates.

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

21 the formation of MPO intermediates and their decay rates.

22 ic structures and radiative and nonradiative decay rates.

23 e, CH(4) conversion to electricity) and four decay rates.

24 ecay (PD) with a Gamma distribution of power-decay rates.

25 at shape the transcriptome by regulating RNA decay rates.

26 trol output dynamics by altering output mRNA decay rates.

27 eam pathways are sensitive to target protein decay rates.

28 25W), affect agonist sensitivity and current decay rates.

29 l nitrogen content strongly predicting early decay rates (3 months) and initial melanin content deter

30 d it is not clear whether the bulk HIV-1 RNA decay rate actually represents a composite of the decay

31 oncentrations of dodecyl maltoside left this decay rate almost unaltered, whereas several other deter

32 possible to extract drug efficacy from viral decay rate alone.

33 Decay rate analysis in the laboratory revealed that aero

34 ge, better control of host metabolism, lower decay rate and a physical size that mimics bacterial pre

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

36 ecause of an increased nonradiative CT state decay rate and that this decay obeys an energy-gap law.

37 lastic mode in (Y,Lu)MnO3 and quantified its decay rate and the exchange-striction coupling term requ

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

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

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

41 A decay machinery with consequent effects on decay rates and mRNA abundance.

42 sian approach provided full distributions of decay rates and reduced the uncertainty, offering useful

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

44 ge), fluorescence decay curves, fluorescence decay rates, and histograms of estimated tear thickness

45 Tu.GTP.aa-tRNA ternary complex formation and decay rates are accelerated in the presence of the nucle

46 We now know that transcription and decay rates are coordinated, but the factors or molecula

47 It is shown that the decay rates are dependent on the interactions of the pro

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

49 The decay rates are greater for abiotic microcosms than biot

50 Faster excited-state decay rates are measured for the ChaM-capped QDs, highli

51 at least two, tight repression, and balanced decay rates are necessary for robust gates.

52 Sums of discrete exponential decay rates are often used, but we hypothesized that con

53 ability, the collection efficiencies and the decay rates are systematically investigated as a functio

54 monstrate that heritable differences in mRNA decay rates are widespread and are an important target f

55 n rules out Purcell enhancement of radiative decay rate as a possible explanation of the recently dis

56 These molecules exhibited reduced decay rates as part of the enzymatic factor Xa generatio

57 sults primarily from changes in nonradiative decay rates associated with exciton diffusion to quenchi

58 we found no significant difference in litter decay rate between mycorrhizal groups, and variation in

59 fields can be achieved with a low coherence decay rate between the two lower levels, high pump-field

60 se, only 4 exhibited significantly different decay rates between arsenite and control treatment.

61 The difference in decay rates between the faster and slower components was

62 set: mono-exponential (ME) with one discrete decay rate, bi-exponential (BE) with two rates, gamma-ex

63 Metallic structures can modify fluorophore decay rates but also have high losses.

64 rsely, in mice lacking the alpha7 nAChR, the decay rate, but not the amplitude, of nicotine-evoked ch

65 sulted from the reduced nitrifier endogenous decay rate by a low DO.

66 edge effects into account would decrease the decay rate by nearly one quarter, compared with estimate

67 ondary structures within mRNAs dictates mRNA decay rates by recruiting specific enzyme complexes that

68 y of temporal context vectors with different decay rates calculates the Laplace transform of real tim

69 ng an effect of GRK1 on light-activated PDE* decay rate can satisfactorily account for the changes in

70 ontinuous probability distributions (CPD) of decay rates can describe the data more parsimoniously an

71 hich may influence permeability, control how decay rates change through time.

72 ot significantly change the quantum yield or decay rate constant of P(s), relative to those of holo-E

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

74 The observed decrease in decay rate constant, increase in steady-state concentrat

75 salt used, due to a decrease in the (3)NOM* decay rate constant.

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

77 The corresponding decay rate constants and lifetimes are incompatible with

78 These states have the following first-order decay rate constants and quantum yields: 2.2 x 10(3) s(-

79 OC dynamics has been implicitly described by decay rate constants in most conventional global carbon

80 First order decay rate constants of both enterococci and E. coli wer

81 The decay rate constants of radical cations, determined by L

82 Decay rate constants of short-tailed mRNAs vary broadly

83 First-order decay rate constants ranged from 0.055 to 0.101 per hour

84 First order decay rate constants were well correlated to the daily a

85 eased MEPP frequency, and increased rise and decay rate constants.

86 determination of nonradiative and radiative decay rate constants.

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

88 The excimer decay rates correlate well with the SF efficiencies and

89 decays logarithmically with time t and that decay rates decrease approximately as 0.2 x t(-1) until

90 However, the luminescence-decay rate decreases with increasing pH over a biologica

91 ntial on the nanosecond time scale, with the decay rate depending linearly on temperature.

92 ssive intra-oral aroma decrease at different decay rates depending on compound type and panellist was

93 nstant drug efficacy, we show that the viral decay rate depends not just on drug efficacy, but also o

94 iurnal temperature variations as the thermal decay rate derived by using satellite daytime and nightt

95 Viral decay rates did not differ by sex.

96 ey photoluminescence properties, such as the decay rate, directionality and polarization.

97 Al2O3 HMM shows 18-fold spontaneous emission decay rate enhancement of dye molecules with respect to

98 Here we demonstrate an OLED that uses the decay rate enhancement(18) of a plasmonic system to incr

99 a pattern of exponential decay, and observed decay rates exceeded previously published values for aqu

100 ntal approaches, we show that target protein decay rates filter p53 pulses: Distinct target protein e

101 changes in steady-state mRNA levels and mRNA decay rates following 24-hr exposure to noncytotoxic con

102 excellent cycling stability (0.04% capacity decay rate for 500 cycles at 0.5C) and high rate capabil

103 ths based on the exponential constant of the decay rate for each protein.

104 a filter downstream of the ESP increased the decay rate for particles in the same size range.

105 Fluorescence decay rate for the low concentration condition was not s

106 objective of this work was to determine the decay rates for ARGs and class 1 integrons following sim

107 (20 microm) to Ca+ significantly accelerated decay rates for both WT and MH, but their effect was sig

108 We propose that clinically observed viral decay rates for HAART regimens should be evaluated in th

109 utilized to compute the thermal unimolecular decay rates for selectively and fully deuterated syn met

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

111 Median (interquartile range (IQR)) decay rates for UFP were 1.26 (0.82-1.83) h(-1); for FP

112 for unbiased estimation of differential mRNA decay rate from RNA-sequencing data by modeling the kine

113 Moreover, whereas the radiative decay rate, gamma(r), scales with N and is therefore sup

114 sions with spatially heterogeneous growth or decay rates, greater mixing reduces growth.

115 ual oscillatory behavior of the intermediate decay rate has been identified and attributed to specifi

116 Quantum yield and radiative decay rates have been observed to decrease for the metab

117 nificant allele-specific differences in mRNA decay rates have higher levels of polymorphism compared

118 Relative humidity alone did not affect the decay rate; however, minor interactions between relative

119 llectively, these results indicate that mRNA decay rates impact transcription and that gamma-herpesvi

120 re found to be elevated because of a reduced decay rate in primary macrophages from TTP(-/-) mice.

121 The decay rate in set point plasma virus recipient animals i

122 no relationship in 2011/2012 between pH and decay rate in summer.

123 on SRFA irradiation as well as the O(2)(*-) decay rate in the presence of SRFA, suggesting that the

124 measured allele-specific differences in mRNA decay rates in a diploid yeast hybrid created by mating

125 ut not E. coli, showed significantly smaller decay rates in beach sand than in seawater.

126 ed placental transcripts exhibited decreased decay rates in differentiated trophoblast stem cells der

127 eased mycelial activity and possibly greater decay rates in ecosystems.

128 nown to be the major factor controlling mRNA decay rates in Saccharomyces cerevisiae.

129 subsequently measured fish eDNA shedding and decay rates in seawater mesocosms.

130 ochemical parameters, such as thresholds and decay rates in signaling pathways.

131 Decay rates in the 4-drug EFV group were intermediate.

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

133 th two bacterial species with very different decay rates in the environment, confirm the difference i

134 Comparison of decay rates in the two cell types led to the discovery o

135 rs also caused the greatest increase in leaf decay rates in the upstream reach containing only killif

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

137 der PCR method, and fecal concentrations and decay rates in water under qPCR method.

138 of the transient during K(+) depolarization (decay rate) in Ca+ was 50% slower for MH.

139 These total decay rates included, on average, about a 25% contributi

140 Results showed that the monochloramine decay rate increased with decreasing pH and increasing b

141 Studies of the mRNA decay rate indicated that alpha(1)-AR activation enhance

142 The mesocosm-derived shedding and decay rates inform the interpretation of eDNA concentrat

143 eamidation after accounting for unimolecular decay rates, internal energy of reactant ions, and multi

144 ssion into the guided mode and Gamma' is the decay rate into all other channels.

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

146 Modulation of the luminescence-decay rate is independent from the concentration of Eu(I

147 Control of messenger RNA (mRNA) decay rate is intimately connected to translation elonga

148 d rpsT P1 and yfcZ mRNA indicates that their decay rate is limited by cleavage of the monophosphoryla

149 or greater quantitative accuracy because the decay rate is measured more directly, with no dependency

150 n rate of resistance emergency or resistance decay rate is not known.

151 When the mechanical decay rate is small, the Bogoliubov modes can be effecti

152 ndependent modulation of singlet and triplet decay rates is highly desirable for the design of effici

153 breviated Pt(pop-BF(2))), yields a radiative decay rate (k(r) = 1.7 x 10(8) s(-1)) an order of magnit

154 includes two key parameters: the first-order decay rate (k) and methane production potential (L0).

155 y parameters within LandGEM, the first-order decay rate (k) and the methane production potential (L0)

156 Detritus decay rates (k, mass loss) increased threefold, and the

157 quality (median R(2) value >98%) exponential decay rates lasting from 30 min to 10 h.

158 The enhanced radiative decay rate leads to high fluorescence efficiencies and d

159 he response of soil nutrient cycling, litter decay rates, litter chemistry and fungal community struc

160 ically realistic values for the polaron pair decay rate, local hyperfine magnetic field and triplet c

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

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

163 stead arose from 50% increased IL-1beta mRNA decay rates, mediated by Hsp27.

164 e plasmons, which can increase the radiative decay rates, modify the spatial distribution of emission

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

166 For most mRNAs in which AUF1 affects their decay rates, mRNA degradation requires AGO2.

167 xponential decay, with the flux equal to the decay rate multiplied by the intracellular metabolite co

168 opical, and investigated relationships among decay rates, mycorrhizal association, phylogeny and clim

169 In contrast, neither the ydfG decay rate nor the fraction of ydfG transcripts that are

170 Decay rates, nutrient release and the change in total de

171 Decay rates observed are about two orders of magnitude l

172 a sensitive radiotracer assay to measure the decay rate of ([(14)C]glucosyl)-diphytanylglyceroldiethe

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

174 /discharge cycles, with an ultralow capacity decay rate of 0.0126 % at a high current density of 0.5

175 ability with a dramatically reduced capacity decay rate of 0.03% per cycle for 1000 cycles.

176 ediate Fe(III)-OOH adduct characterized by a decay rate of 11 s(-1).

177 an in 1978/1979, with an average increase in decay rate of 18.1%.

178 Interestingly, the decay rate of 2 is comparable to that of product formati

179 "rapid progressors" (32% of eyes) had a mean decay rate of 52.2%/year.

180 ith [O(2)] obtained from the phosphorescence decay rate of a palladium phosphor.

181 wofold reduction of the transverse radiative decay rate of a superconducting artificial atom coupled

182 eled phenomenologically by assuming that the decay rate of an individual bond is a function of the re

183 The decay rate of an mRNA and the efficiency with which it i

184 An extremely fast decay rate of CH2OO was observed at high humidity.

185 e drug efficacy of antivirals from the viral decay rate of chronic infections.

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

187 We find that the capacity decay rate of electrodes in half cells is positively cor

188 BR-bodies stimulate the mRNA decay rate of enriched mRNAs, helping to reshape the cel

189 P-s and jRGECO1a-type GECI: the fluorescence decay rate of f-RCaMP1 was 21 s(-1), compared with 109 s

190 was markedly reduced (~11-fold), whereas the decay rate of FVIIIa due to A2 subunit dissociation was

191 Importantly, we show that the decay rate of LDLR mRNA is not affected by hnRNP K siRNA

192 The average capacity decay rate of LIB for 500 cycles was calculated to be ap

193 % smaller mode amplitude, while in light the decay rate of local fluctuations is 1.2-fold faster in i

194 e origination lambda and a constant per site decay rate of mu.

195 The decay rate of N-oxyl radicals follows first-order kineti

196 es but partly attenuated the relatively slow decay rate of nicotine-evoked cholinergic signals.

197 or over 1000 h at 600 mA cm(-2) with voltage decay rate of only 32-muV h(-1) - the best-reported dura

198 riole is transmitted very efficiently with a decay rate of only approximately 5% per 100 mum.

199 bilized around 500-550 mAh/g with a capacity decay rate of only ~0.25% per cycle.

200 duction in Escherichia coli by governing the decay rate of rne (RNase E) mRNA.

201 unneling is predicted to enhance the thermal decay rate of syn-CH3CHOO compared with the deuterated s

202 The observed twofold reduction in the decay rate of the atom allows the transverse coherence t

203 ate that the selected compounds increase the decay rate of the bis-Fe(IV) species by disrupting the e

204 The luminescence-decay rate of the complex is slow, due to a lack of wate

205 xane, and a million-fold acceleration in the decay rate of the Fe(III)-OOH intermediate at -40 degree

206 e initital velocity (DVmax = 1.8) and on the decay rate of the flavin intermediate (Dks = 2.3) in sin

207 250 h) matrix sites were revealed, with the decay rate of the former in close agreement with first-p

208 ing frequency of the relaxation mode and the decay rate of the local shape fluctuations.

209 te is, however, >10(2) times faster than the decay rate of the NI, demonstrating that this intermedia

210 harged defects that affects the nonradiative decay rate of the photoexcited species.

211 d sunlight and matrix significantly affected decay rate of the virus.

212 ill give an explicit characterization of the decay rate of these basis functions.

213 The decay rate of this species is accelerated upon mixing wi

214 Conversely, the decay rate of ydfG is limited by generation of the monop

215 The overall decay rate of ZnO NPs is significantly reduced in compar

216 , maximum growth rates of 2.5-3.8 d(-1), and decay rates of 0.04-0.05 d(-1).

217 uration, peak copy number, and expansion and decay rates of 1020 shedding episodes in 531 immunocompe

218 [Fe(II)]0 = 300 muM variation of pH yielded decay rates of about 70 s(-1) for pH 1 and 2 and of abou

219 with large-scale RNA sequencing to determine decay rates of all mRNAs in Saccharomyces cerevisiae.

220 equency of the coherent coupling exceeds the decay rates of atom and cavity excitations.

221 considered in a prediction of the radiative decay rates of atoms in squeezed vacuum.

222 The decay rates of both F+ coliphages (0.25 +/- 0.02 day(-1)

223 h abundant organic matter and nutrients, the decay rates of both isomers were not changed in the pres

224 The decay rates of coliphages and their uncertainties were a

225 an in shade (0.96 +/- 0.04 day(-1)), but the decay rates of male-specific (F+) coliphages were not si

226 nanocone antennas, we enhance the radiative decay rates of monoexcitons and biexcitons by 109 and 10

227 an host, we performed a global survey of the decay rates of MTB mRNA transcripts.

228 ted changes in synaptic currents, and faster decay rates of NMDA receptor-mediated currents in mice w

229 The decay rates of NoV in oysters as a function of the dista

230 It was found that the decay rates of photo excited cytosine and guanine were a

231 rom the summer experiments revealed that the decay rates of somatic coliphages were significantly hig

232 from content-free word usage, nonhomogeneous decay rates of stylistic influence, and an accelerating

233 The decay rates of T201(peroxo) were monitored in the absenc

234 o genetic algorithm to simulate the measured decay rates of TBA.

235 The decay rates of the angle between the dipoles, dihedral a

236 The decay rates of the long-lived states decrease with incre

237 e points, which was accompanied by increased decay rates of the mRNAs of the inflammatory genes.

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

239 little is understood about what governs the decay rates of these transcripts.

240 The dependence of the formation and decay rates of this mixed-valent transient on pH and the

241 rate actually represents a composite of the decay rates of viral subpopulations compartmentalized in

242 A, a putative RNase, controls the transcript decay rates of virulence factors or their regulators acc

243 The amplitude, but not the decay rate, of nicotine-evoked transients was reduced by

244 of genes exhibit allelic differences in mRNA decay rates, of which 350 can be identified at a false d

245 of a strongly nonmonotonic dependence of the decay rate on the amplitude if one of the modes serves a

246 ar dependence of the intensity and radiative decay rate on the excitation power.

247 s the cavity-cavity hopping constant and the decay rate on the generated correlation dynamics.

248 The observed quadratic dependence of the decay rate on water concentration implied a predominant

249 roring the relative role of these factors on decay rates on the same pieces of wood even after 5 year

250 d to that of CA3 slow gamma by reducing IPSC decay rate or reducing interneuron activation through to

251 tially explicit trends in the annual thermal decay rates over Africa and discuss results.

252 Because XLRP carrier ERG amplitudes and decay rates over time were on average half of those of a

253 f miR-124 can be incorporated into the Notch decay rate parameter of our model.

254 omplex model, specifically in the redundancy decay rate parameter, is shown to generate mortality pla

255 s with FTO, and these mRNAs have accelerated decay rates potentially through the regulation by a spec

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

257 l equations with unknown parameters, such as decay rates, reaction rates, Michaelis-Menten constants,

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

259 Mean decay rates (+/- SD) in simulated saliva, under simulate

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

261 len belt can vary greatly, while the neutron-decay rate should be almost constant.

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

263 quantify effects of several factors on total decay rates, such as window opening behavior, home age,

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

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

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

267 a including light propagation, excited-state decay rates, temporal broadening or compression of ultra

268 extended periods of time and have late-time decay rates that are inconsistent with radioactivity.

269 in order to nullify the spontaneous emission decay rate, the system has to be electromagnetically clo

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

271 contribution of heritable variation in mRNA decay rates to gene expression variation has received fa

272 y, offering useful information for comparing decay rates under different conditions.

273 scale assay conditions showed comparable GFP decay rates upon CHX exposure, but the microfluidic data

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

275 Median decay rate was -10(6.2) HSV DNA copies/d during the fina

276 The second-phase viral decay rate was also faster in the 3-drug EFV group than

277 The HIV-1 RNA decay rate was assessed using nonlinear mixed-effects mo

278 The virus decay rate was biphasic (t1/2alpha= 0.4 h and t1/2beta =

279 The decay rate was governed by accessibility of the electroc

280 water and fastest in oligotrophic water, and decay rate was negatively correlated to dissolved organi

281 The decay rate was not affected by [K(+)] x [Cl(-)] product

282 The slowest decay rate was observed at 5 degrees C, with a T90 value

283 rescence from a Pd phosphor in solution; the decay rate was obtained by fitting the tail of the phosp

284 On the other hand, the decay rate was pronounced for deltorphin II, [d-Pen(2),

285 The Ca(2+) transient decay rate was similarly accelerated by Iso in Tg and no

286 Decay rate was slowest in dystrophic water and fastest i

287 between mycorrhizal groups, and variation in decay rates was best explained by litter phosphorus.

288 When decay rates were analyzed after actinomycin D treatment,

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

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

291 t (d1)-, second (d2)-, and, third (d3)-phase decay rates were estimated by mixed-effects models.

292 ample, for the high concentration condition, decay rates were higher than for the low concentration f

293 Decay rates were measured for 2139 of the ~4000 MTB gene

294 Median first-phase viral decay rates were significantly faster in subjects receiv

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

296 ecently produced cells show an initial rapid decay rate, which slows with age of the animal at which

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

298 produces a Ca(2+)-mediated decrease in PDE6 decay rate, with the novel feature that both spontaneous

299 SOA alkane and PAH decay rates within the sediment were similar to those at

300 Mean decay rate without simulated sunlight across all relativ