ライフサイエンスコーパス: decay with

1 0 nm (near the red edge of the bulk antenna) decays with 590 fs kinetics; the corresponding anisotrop

2 lifetime of 1-21 days accompanied by a slow decay with a 1/e lifetime of 21-5028 days (47% of sample

3 ravitreal moxifloxacin showed an exponential decay with a half-life of 1.72 hours.

4 ng over weeks 60 to 384: an initial phase of decay with a half-life of 39 weeks and a subsequent phas

5 Y21F mutant protein exhibits a fluorescence decay with a lifetime of 0.6 ns.

6 ollection shows monoexponential fluorescence decay with a lifetime of 1.0 ns.

7 -1) to give C60 singlet excited states which decay with a lifetime of 1.2 ns to give very long-lived

8 t not Y21F also exhibits slower fluorescence decay with a lifetime of 1.7 ns.

9 olecules are produced within 100 fs and then decay with a lifetime of 400 ps or more.

10 1.7 mus) accounts for only 3-8% of the total decay with a longer-lived component having a time consta

11 ng replication-competent HIV-1 were found to decay with a mean half-life of approximately 6 months, c

12 The miniature EPSCs decay with a time constant of 13.0 +/- 1.1 ms whereas th

13 ctra of the S(1) state of the porphyrin that decay with a time constant of 17 ps (M = Mg) or 24 ps (M

14 nm that is best fit to a single-exponential decay with a time constant of 55 +/- 6 ns.

15 nts showed a fast-rising phase followed by a decay with a time constant of approximately 2-3 sec.

16 arization to +10 mV led to triphasic [Ca2+]i decay, with a fast-slow-fast pattern.

17 tion of any of the absorption peaks: a rapid decay, with a time constant of 1 ps or less, and a slow

18 a time constant of 1 ps or less, and a slow decay, with a time constant that can be longer than 300

19 larization the ensemble-averaged LCC current decayed with a fast and a slow exponential component.

20 me constant of 7.2+/-0.7 ms, while the mIPSC decayed with a fast time constant of 5.3+/-0.4 ms in the

21 The evoked IPSC decayed with a fast time constant of 7.2+/-0.7 ms, while

22 The VA.+ signal decayed with a first-order decay constant of 1.76 s-1, i

23 to 0.021 Hz) in <10 s after stimulation and decayed with a half time <20 s, indicating that the time

24 virion production, assessed by p24 release, decayed with a half-life of 2 days.

25 ranosylbenzimidazole, tyrosinase mRNA levels decayed with a half-life of 4-5 h.

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

27 ose per gram [%ID/g]) at 2 h was 7 %ID/g and decayed with a half-life of 72 h, whereas blood %ID/g ra

28 ec after the start of the depolarization and decayed with a mean time constant of 8.5 msec.

29 th a rate constant of 4.0 +/- 0.2 s (-1) and decayed with a rate constant of 3.7 +/- 0.2 s (-1).

30 te formed with a rate constant of 32 s-1 and decayed with a rate constant of 6.6 s-1.

31 nt of 140 s-1; the QB semiquinone EPR signal decayed with a rate constant of about 5 s-1.

32 Eye movement velocity decayed with a similar exponential trajectory (time cons

33 yme or was generated using hydrogen peroxide decayed with a t1/2 of 2 days compared with 6 min for wi

34 in dendritic regions <1 microm in length and decayed with a time constant of 0.35 +/- 0.03 s.

35 The AMPA receptor-mediated EPSC decayed with a time constant of 1.99+/-0.16 ms (n = 8).

36 his "resurgent" current peaked in 8 msec and decayed with a time constant of 30 msec.

37 um was seen after each action potential, and decayed with a time constant of about 200 ms in the soma

38 The facilitation decayed with a time constant of approximately 100 msec.

39 n an approximately 2.5-fold enhancement that decayed with a time constant of approximately 200 msec,

40 xotomy-induced synaptic withdrawal phenotype decayed with a time constant of approximately 30 days.

41 and a weaker, but more persistent, form that decayed with a time constant of several seconds.

42 n and in adult neocortical pyramidal neurons decayed with a time constant of tau = 8.0 +/- 2.8s.

43 nt conditions, the evoked EPSC in aniracetam decayed with a time course intermediate between deactiva

44 ransfected beta-globin mRNA was very stable, decaying with a half-life of >360 min.

45 (-H)(*) decay is biphasic with one component decaying with a lifetime of approximately 2.2 ms and the

46 ith the fused bifunctional wild type enzyme, decaying with a t1/2 of 10 min at 37 degrees C.

47 This exocytosis was transient in nature, decaying with a time constant of approximately 30 ms.

48 als, appearing within a few milliseconds and decaying with a time constant of approximately 50 ms.

49 ine were also studied, showing biexponential decays with a 1.1 ps component (5%) besides a sub-0.2 ps

50 ts and 2D IR spectra show a new feature that decays with a 110-fs time scale.

51 diate species: I1, which forms in <10 ns and decays with a 200-micros lifetime to I2, which itself su

52 Kinetic analysis shows that I0 decays with a 220 +/- 20 ps lifetime, forming another in

53 Idouble dagger0 decays with a 3 +/- 0.15 ns time constant to form I1.

54 This putative triplet state subsequently decays with a 4-micros time constant into a 390 nm-absor

55 DsrA decays with a half-life of 23 min at 25 degrees C and 4

56 the thermal stability of Rho showed that Rho decays with a half-life on the order of days.

57 blindness mutants, the T94I MII intermediate decays with a half-life that is approximately 8-fold slo

58 lmost equal to its initial value and finally decays with a half-time (approximately 20 s) longer than

59 ution for days, whereas [CoIIIH(2)2iPr(OH)]- decays with a kint=5.9x10-8 M min-1.

60 process, the hydroperoxy-ferric intermediate decays with a large solvent kinetic isotope effect, as e

61 orrespondingly formed radical ion pair state decays with a lifetime of 1.0 +/- 0.1 ns.

62 predict that the probability of self-renewal decays with a logistic kinetic over the life span of a n

63 e demonstrate here that the latent reservoir decays with a mean half-life of 6.3 months in patients w

64 Seventy percent of the initial complex decays with a rate constant greater than 0.05 s-1, and 3

65 Above 255 K, it slowly decays with a rate constant k = 10(7.7+/-0.4) s(-1) x ex

66 A minor component ( approximately 16%) decays with a rate constant of 170 micros.

67 ith a rate constant of 1.2 x 10(7) s(-1) and decays with a rate constant of 5.6 x 10(5) s(-1).

68 damax=450 nm) due to formation of T1K, which decays with a rate of 2.1 x 105 s-1 to form triplet alky

69 2 x 105 s-1 in methanol, whereas nitrene 2a decays with a rate of approximately 91 s-1.

70 onditions, the catalytically competent state decays with a second-order half-life of approximately 15

71 a single cysteine residue display spin-echo decays with a single phase-memory time T2M and conventio

72 urements indicate that novelty within groups decays with a stretched-exponential law, suggesting the

73 This rescue decays with a t1/2 of approximately 1-1.5 d after gene i

74 e (Q(B)) site is fully occupied, P(+)H(B)(-) decays with a time constant estimated to be in the range

75 ignal for photogenerated electrons on g-C3N4 decays with a time constant of 1/ke' = 660 ps in the mix

76 ing gives rise to a transient discharge that decays with a time constant of 100 msec or less.

77 20 fs after ultraviolet photoexcitation and decays with a time constant of 110 +/- 60 fs.

78 This final state decays with a time constant of 3.8 mus.

79 removed prematurely, the accumulated message decays with a time constant that correlates with the tim

80 exhibited biexponential decay with age in gray and white matter regions, except

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

82 the IkappaB-alpha and IkappaB-beta proteins decayed with an approximate t1/2 of 38 and 76 min, respe

83 the aged LIM/O3 SOA in the 450-600 nm range decayed with an effective half-life of <0.5 h.

84 latency of 1.2 s, a rise time of 2.5 s, and decayed with an exponential time constant of 15 s.

85 Facilitation decayed with an intrinsic time constant of approximately

86 dienylidene (4), and this absorption feature decays with an approximately 30 ps time constant in hexa

87 For the inactive protein state, C(t) decays with an ultrafast component, close to bulk-type b

88 otide or a duplex undergoes a bi-exponential decay with approximately 4 and approximately 1 ns lifeti

89 y, we find that most dORFs are substantially decayed, with approximately 90% having two or more disab

90 -6ANI-NI(-)(*)), and the total RP population decays with approximately 10 ns lifetime at 140 K, which

91 entials and quantitative recordings of their decay with averaging at multiple sites during propagatio

92 at cytoplasmic WHx has a short half-life and decays with bimodal kinetics (approximately 20 min and 3

93 mulation, macroscopic NMDA receptor currents decay with biphasic kinetics that is believed to reflect

94 ge excess of H2O2, this intermediate rapidly decays with both a zero- and first-order dependence on t

95 d vessel status were associated with ASPECTS decay, with collateral blood vessel status demonstrating

96 All clusters exhibited p-state population decay with concomitant s-state repopulation (internal co

97 ermediate formed quickly (53 s(-1)) and then decayed with concurrent buildup of ferric iNOSoxy.

98 This method implements weight decay with conjugate gradient training and yields more s

99 results show that forward velocities rapidly decay with decreasing Re for all bell shapes when Re<10.

100 epidemics exists across the entire state and decay with distance (regional correlation=62%).

101 ronic coupling decreases and the exponential decay with distance becomes faster.

102 urrents in the apical shaft whose amplitudes decay with distance from the soma.

103 A marked exponential decay with distance was observed in the case of excitato

104 assumption that it describes an exponential decay with distance.

105 ion of transcription factor occupancies that decay with distance; distal coordination is also observe

106 oked changes in cGMP and Ca2+ concentrations decayed with distance from a site of steady focal activa

107 esent and revealed a small vasodilation that decayed with distance.

108 the dynamics of neighboring populations that decays with distance between patches.

109 ch a steady state in which the concentration decays with distance from the source of production.

110 r pairs, which is high for close markers and decays with distance.

111 om the increase in the amplitude of the fast decay with Dns-C6-Cho concentration with preincubation t

112 ibitory postsynaptic currents and potentials decayed with exponential time constants of 2.6 and 5.9 m

113 neous component, the FFCFs are biexponential decays with fast and slow time components of approximate

114 The hydroquinone decays with first order kinetics or pseudo first order k

115 This intermediate decays with first-order kinetics.

116 ose H(2)O(2), as occurs with 2(T252A)-a, but decays with formation of the epoxide of b.

117 exact exchange energy density for a density decaying with Gaussian-like behavior at long range.

118 Linkage-disequilibrium decay with genomic distance was less rapid in both the w

119 Beta-scale overlap decays with geographic distance fastest in the temperate

120 tance'-a phenomenon where genetic similarity decays with geographic distance.

121 The NR1 subunit showed a biphasic decay with half-lives of 2 and 34 h for the rapidly and

122 arming maximizes near the surface, gradually decays with height, and disappears in the upper troposph

123 y castrated rat were identified; their mRNAs decayed with identical kinetics.

124 ribution does not follow a clear exponential decay with increasing number of thiophene units in the c

125 f the decline in the rate constant of [Ca2+] decay with increasing stimulation duration as an index o

126 For most of the populations, pairwise LD decayed with increasing physical distance between loci i

127 LD in hybrids decays with increasing number of backcross generations a

128 eriodicity of approximately 10 basepairs and decays with increasing protein-protein distance.

129 mplexes making plus stands was also found to decay with inhibition of translation.

130 rm to a distance rule reflecting exponential decay with interareal separation.

131 the formation of 1 followed by a first-order decay with k(2) = 8.8 +/- 0.1 s(-1).

132 nce of benzaldehyde, the 348 nm intermediate decays, with k = 0.7 s(-1), to form a quasistable quinon

133 the dead time of the instrument, which then decays, with k = 210 s(-1), to form a transient intermed

134 stable as purified in dodecyl maltoside but decays with kinetics that require a double-exponential f

135 is recovers the positive correlation of mRNA decay with known AU-rich mRNA motifs, but we also uncove

136 -to-peak followed by a approximately 40 msec decay, with large spike counts (5.2 spikes per stimulus)

137 pen" state, characterized by monoexponential decay with lifetime approximately that of the free nucle

138 a single tryptophan, showed a biexponential decay with lifetimes of 4.33 and 17 ms, in contrast to p

139 e diazo compounds were detected and found to decay with lifetimes of less than 300 fs.

140 04-0.24, and triple exponential fluorescence decays with lifetimes of 4.4-6.6, 1.4-3.2, and 0.2-1.0 n

141 olesterol, and we noted an increase in tooth decay with longer periods of breastfeeding.

142 c activity of a single rhodopsin molecule to decay with low variability.

143 able quantum yield and a simple fluorescence decay, with marginal amounts of dark species.

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

145 oxidative Mn(3+) species at sites of active decay, with Mn eventually accumulating as insoluble Mn(3

146 ugging forces: AJs and tugging force grew or decayed with myosin activation or inhibition, respective

147 Unlike excitons, trions can radiatively decay with non-zero momentum by kicking out an electron,

148 ion, there was a differential rate in signal decay, with only half of the regions continuing to demon

149 assembly provides a means to coordinate mRNA decay with other cellular processes essential for growth

150 these deficiencies also cause mitochondrial decay with oxidant leakage and cellular aging and are as

151 , across all candidate genes, showed a rapid decay with physical distance.

152 n step with pK(a) of 4.6, while C formed and decayed with pK(a)s of 6.8 and 8.2, respectively.

153 s the additional advantage of energetic beta decay with potential therapeutic efficacy.

154 B)-nitrosyl) transient dinitrosyl complex to decay with production of N2O at a rate of 0.7 s(-1) at 4

155 ciation of C3bBb complexes, because blocking decay with properdin and C3 nephritic factor did not res

156 up dental plaque and a vaccine against tooth decay with questionable potential for widespread applica

157 single-copy assay data revealed 3 phases of decay with RAL-containing ART, with a longer duration of

158 scan peaked within approximately 1 msec and decayed with rapid (tau(1) of 1.7 msec) and slow compone

159 e and magnesium, which undergoes first-order decay with rate constants independent of the concentrati

160 trast to previous reports of a biexponential decay with rates of 0.2 and 0.9 ms.

161 The transient intermediates decayed with rates of 80,000 s-1 and 11,000 s-1 in the p

162 mV were followed by three phases of [Ca2+]i decay with repolarization to both -110 and -50 mV.

163 at burst cells, whereas their activity level decays with residual gaze error.

164 eumelanin precursor 5,6-dihydroxyindole (1) decays with second-order kinetics to generate broad visi

165 distinct CXCR4 or CCR5 coreceptor phenotypes decayed with similar rates.

166 r supporting this proposal, each acetylation decays with similar kinetics when Htz1 transcription is

167 >/= 2 aftershocks showed a uniform power-law decay with slope -1.35 out to 50 km from the mainshocks.

168 in these subjects lead to nonsense-mediated decay with subsequent reduction of RNA expression and pr

169 converted to a NMR observable triplet state decaying with T(1), in the order of seconds.

170 We found ALT decays with t(1/2) = 12.7 hours.

171 au(1) = 3 ps time constant and excited state decay with tau(1) = 3 ps, tau(2) = 14 ps, and tau(3) = 1

172 ve comparison of the rates of Q(A)(-) and Z* decay with the decay of the 1478 cm(-1) line supported t

173 ion are strongly localized and exponentially decay with the network distance away from the perturbed

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

175 Trp fluorescence decay with the onset of solvation dynamics of the chromo

176 spontaneous spin coherences that precess and decay with the same characteristic energy and timescales

177 d versus time follow variants of exponential decay, with the flux equal to the decay rate multiplied

178 er 250 ms can be fit to a double exponential decay, with the intensity of the fast component roughly

179 bstituted nitrophenols showed an exponential decay, with the nitro-group on the aromatic ring found t

180 nd miRNAs work together to affect transcript decay, with the rescue of miRNA recognition sites via RB

181 The batho/bsi mixtures decayed with the following reaction scheme: batho/bsi <=

182 dence that viral evolutionary rate estimates decay with their measurement timescales and that the rat

183 zzle because magnetic fields are expected to decay with time but a cool surface suggests that the sta

184 eals changes that are fit by a biexponential decay with time constants of 2.4 +/- 0.2 and 36 +/- 0.2

185 as well approximated by a double exponential decay with time constants of 6-17 s and 2-3 min.

186 uptly decreased, followed by a biexponential decay with time constants of approximately 4 and 200 ms.

187 In ASCT2, these currents show biphasic decay with time constants, tau, in the 1-30 ms time rang

188 n and across individuals, showed the typical decay with time elapsed between encoding and testing, we

189 Relationship of rates of decay with time to worsening and eccentricity and agreem

190 e absence of the hippocampus, these memories decay with time, lacking the permanence that is a hallma

191 trend (increasing/decreasing) or exponential decay with time.

192 release permeability predicts an exponential decay with time.

193 The isolated glycinergic IPSC decayed with time constants of 7.8+/-0.3 and 38.3+/-1.7

194 The H2O2 gradually decayed with time due to the diffusion of H2O2-scavengin

195 ) and C(14) filtrates to elevate [Ca(2+)](i) decayed with time was consistent with this hypothesis.

196 rate that was modulated by an annual cycle, decaying with time.

197 n rates, seismic activity in the zone is not decaying with time.

198 Activity of FXase decays with time and reflects the lability of FVIIIa.

199 nent designated X-685 peaking at 685 nm that decays with time constants of 0.28 and 5.8 ns and does n

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

201 object's distance from the current focus and decays with time elapsed in the narrative since the item

202 nstrate that the production rate of deposits decays with time following a power law whose exponent li

203 ined helix fractions defined monoexponential decays, with time-constants of approximately 120 ns, ind

204 The anisotropy decayed with two correlation times near 5 and 370 ns, wi

205 illion years but follow a similar pattern of decay, with ultimately only 1.4% of chimeras preserved.

206 These transient IR bands decay with virtually identical lifetimes to those observ

207 umans, many promoters appear to be gradually decaying with weak transcriptional output and relaxed se

208 ate relaxation exhibiting a multiexponential decay with well-defined rate constants.