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 sity, flow chamber dimensions, and morphogen decay rate.

3 h the initial radical concentration and fast decay rate.

4 t the initial radical concentration and fast decay rate.

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

6 characterized by faster signal rise time and decay rate.

7 duces the level of p27Kip1 by increasing its decay rate.

8 Complementation restored the wild-type decay rate.

9 the donor excitation relative to a slow FRET decay rate.

10 l rapid decay, which was followed by a lower decay rate.

11 n the diffusion coefficient and the pathogen decay rate.

12 ield excitation and increasing the radiative decay rate.

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

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

15 red ones as confirmed by surface temperature decay rates.

16 issociated from location memory by different decay rates.

17 the formation of MPO intermediates and their decay rates.

18 necessary for optimal RNA function or proper decay rates.

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

20 g an over 100-fold increase in the radiative decay rates.

21 odes with strongly differing frequencies and decay rates.

22 igments had significant alterations in their decay rates.

23 ationship between metal fractions and oxygen decay rates.

24 contributing to allelic differences in mRNA decay rates.

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

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

27 lines to identify transcripts with different decay rates, after serum stimulation and actinomycin D t

28 as biolabels because their long luminescence decay rates allow time-gated detection, which separates

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

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

31 rganizational principles in the variation of decay rates among functional classes.

32 Decay rate analysis in the laboratory revealed that aero

33 ons depletion is mainly determined by a slow decay rate and fragmentation efficiency curves for des-A

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

35 biosynthetic proteins have decreased average decay rates and are deficient in fast-decaying mRNAs.

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

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

38 hermore, we propose methods for inferring LD-decay rates and recombination hotspots on the basis of D

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

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

41 Although mRNA decay rates are a key determinant of the steady-state co

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

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

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

45 mRNA decay rates are dictated by cis-acting elements within t

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

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

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

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

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

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

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

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

54 fferences in the reactivation process or the decay rate between the young and old age groups.

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

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

57 s estimates of first- and second-phase viral decay rates between treatment arms and sex.

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

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

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

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

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

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

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

65 cription factor mRNAs have increased average decay rates compared with other transcripts and are enri

66 re, for the bulk population of vesicles, the decay rate constant and vesicle intensity (dependent on

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

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

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

70 The corresponding decay rate constants and lifetimes are incompatible with

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

72 Nonradiative decay rate constants and the luminescence maxima follow

73 ved for the azide-accelerated decay, and the decay rate constants are proportional to the concentrati

74 ss the normally large magnitude nonradiative decay rate constants characteristic of (porphinato)iron(

75 The formation and decay rate constants for an E47A variant of 2Fe-SOR are

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

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

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

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

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

81 determination of nonradiative and radiative decay rate constants.

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

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

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

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

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

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

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

89 Viral decay rates did not differ by sex.

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

91 mage dynamically scattered light fluctuation decay rates (dynamic light scattering microscopy) is dev

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

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

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

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

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

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

98 Viral decay rates for 115 evaluable subjects were estimated fr

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

100 (20 microm) to Ca+ significantly accelerated decay rates for both WT and MH, but their effect was sig

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

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

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

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

105 has appeared to improve with time, with the decay rates for viral DNA being at the lower end of valu

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

107 Biologic decay rates from 24 to 168 h after injection were only s

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

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

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

111 uantum yield, and radiative and nonradiative decay rates have been difficult or impossible to measure

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

113 tween 12 and 70 weeks postchallenge, the low decay rates have had half-lives of about 20 weeks for vi

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

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

116 ay shows the same functional organization of decay rates, implying that it is a general organizationa

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

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

119 These data strongly suggest: 1) the decay rate in skeletal myotubes is related in part to Ca

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

121 This disequilibrium and its decay rate in the pfcrt-flanking region are consistent w

122 show that the BSM predicts slowing of the SF decay rate in the presence of exogenous Ca(2+) buffers,

123 elation between the CTL number and the virus decay rate in therapy and predict that individuals with

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 Sbp1p overexpression restores normal decay rates in decapping-defective strains and increases

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

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

129 e used microarray technology to measure mRNA decay rates in resting and activated T lymphocytes in or

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

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

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

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

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

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

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

137 We decided to measure mRNA decay rates in two human cell lines with high-density ol

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

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

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

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

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

143 For the anion charge transfer, the decay rates increased by factors of 1.4, 4.2, and 5.1, r

144 d 5.1, respectively, and for the cation, the decay rates increased by factors of 5, 276, and 470.

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

146 f these motifs are strong predictors of mRNA decay rate, indicating that the regulation of mRNA decay

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

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

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

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

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

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

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

154 s of dynamically scattered light fluctuation decay rates is presented.

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

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

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

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

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

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

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

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

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

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

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

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

167 Under equilibrium conditions the decay rate of (213)Bi was used to determine the concentr

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

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

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

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

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

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

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

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

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

177 ss surrounding focal quadrats illustrate the decay rate of assemblage similarity with distance and th

178 The amount and decay rate of asynchronous release, two measures sensiti

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

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

181 d to form at rate constants identical to the decay rate of F(peroxo).

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

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

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

185 Surprisingly, the decay rate of MPO Compound II remained unaltered as NO c

186 bout 27 Myr, which corresponds to a per site decay rate of mu approximately 1.3 x 10(-8)/year and a r

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

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

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

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

191 d Cul4A, because DDB1 failed to increase the decay rate of p27Kip1 in cells deficient in CSN1 or Cul4

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

193 ral model to assess the daily changes in the decay rate of short-term memory, motivation, and motor a

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

195 The initial decay rate of the [2Fe-2S](2+) cluster is about 1 order

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

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

198 ng by the sarcoplasmic reticulum, slowed the decay rate of the Ca(2+) transient.

199 n rate of the mechanical contraction and the decay rate of the calcium transient increased with littl

200 Furthermore, the decay rate of the calcium transient was significantly re

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

202 vations to the dominance of a fast radiative decay rate of the donor excitation relative to a slow FR

203 old nanoparticles, as manifested by a faster decay rate of the excited electronic distribution at pro

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

205 250 h) matrix sites were revealed, with the decay rate of the former in close agreement with first-p

206 Based on the length-scale dependence of the decay rate of the measured correlation functions, the na

207 larization pattern of P700+A1-, in which the decay rate of the pattern is assumed to be negligibly sm

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

209 At all concentrations of denaturant, the decay rate of the W29 triplet of the unfolded protein is

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

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

212 -free mRNAs, and (2) significantly slows the decay rate of transiently induced nonsense-containing bu

213 ding activity demonstrate a markedly reduced decay rate of wild type compared with mutant transcripts

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

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

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

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

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

219 e used microarray technology to compare mRNA decay rates of approximately 7000 transcripts in normal

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 However, the decay rates of mRNAs encoding groups of proteins that ac

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

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

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

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

232 First- and second-phase decay rates of plasma HIV-1 were compared in men and wom

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

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

235 Decay rates of subsets of latently HIV-infected cells pa

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

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

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

239 silver islands have increased the radiative decay rates of the fluorophore.

240 or each animal after the second inoculation, decay rates of the infected cells were only minimally af

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

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

243 The decay rates of the Q316H and Q316H/M539L mutants, but no

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

245 not contribute significantly to the rise or decay rates of these transients.

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

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

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

249 Moreover, expression of Cul4A increases the decay-rate of p53 and delays the accumulation of p53 in

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

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

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

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

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

255 itionally, we investigated the dependence of decay rates on sequence composition, that is, the presen

256 ed motivation by 50% without altering memory decay rate or motor ability.

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

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

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

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

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

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

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

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

265 eotide arrays that enable the measurement of decay rates simultaneously for thousands of mRNA species

266 various levels of resolution and compare the decay rate statistics between these classes.

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

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

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

270 d 3TC/ZDV/EFV had a more rapid phase 1 viral decay rate than those who received 3TC/ZDV/NFV or other

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

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

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

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

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

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

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

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

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

280 The decay rate was governed by accessibility of the electroc

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

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

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

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

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

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

287 Decay rate was slowest in dystrophic water and fastest i

288 single APs, the Ca2+ transient amplitude and decay rate were similar at boutons and bottleneck region

289 When decay rates were analyzed after actinomycin D treatment,

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

291 ence was eliminated in Ca-, and the relative decay rates were faster for both genotypes than in Ca+.

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 The differential decay rates were not a consequence of differential nucle

295 Viral decay rates were not significantly different in men and

296 Phase 1 viral decay rates were positively correlated with baseline RNA

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

298 lished between plasma RNA levels and phase 1 decay rates, which has worrisome implications for infant

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

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