ライフサイエンスコーパス: decay of

1 m(-2) for 110 times at a negligible capacity decay of 0.01% per cycle.

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

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

4 er of 1 was revealed through the accelerated decay of 1 in the presence of the substrates, including

5 ction of single (136)Ba ions produced in the decay of (136)Xe ("barium tagging").

6 In particular, the neutrinoless double beta decay of (136)Xe could be established by detecting the d

7 excess radiation could be expected from the decay of (137)Cs produced by the US nuclear testing prog

8 the wide-angle lens to image light from the decay of (18)F-FDG emission signal.

9 obilized by alpha recoil associated with the decay of (222)Rn and short-lived progeny.

10 rtaking was based on the fact that the alpha decay of (238)Pu present in the investigated samples pro

11 ere found to be consistent with unimolecular decay of 3, and [2+1]-cycloaddition with radical clocks

12 As a result, the decay of 5-HT1A -IPSCs was independent of the intensity

13 Slight capacity decay of 6% in the battery using the electrode in stretc

14 bserved beta-delayed neutron production from decay of (9)Li, formed by the high-energy deuteron bomba

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

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

17 surements are made by recording the temporal decay of a carrier-concentration-dependent material prop

18 f the body-plan morphology together with the decay of a central biosignaling system, indicate that el

19 ithin 100-200 mus, followed by a much slower decay of a few seconds.

20 ecting a singular SO(3) line vortex from the decay of a non-singular spin texture in a ferromagnetic

21 llow direct observation of the formation and decay of a palladium(I) species during the reaction.

22 tly alter the impact of these factors in the decay of a particular mRNA.

23 depends on the balance between synthesis and decay of a particular transcript.

24 1,5-hydrogen atom transfer (1,5-HAT) in the decay of a PEGylated carbazyl (aminyl) radical in soluti

25 ransfer transition (PICTT), that enables the decay of a plasmon by directly exciting an electron from

26 ance depends on the balance of synthesis and decay of a population of mRNAs.

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

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

29 obtained from the kinetics of formation and decay of a tyrosyl radical.

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

31 tant mechanisms for the specific capacitance decay of activated carbon electrodes in this study.

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

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

34 light exposure accelerated significantly the decay of all the DNA markers.

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

36 th chlorophylls-f/d The data demonstrate the decay of an ~720-nm negative feature on the picosecond-t

37 We have analyzed the fluorescence decay of anthocyanins by fluorescence lifetime imaging m

38 st tumor cells by selectively enhancing mRNA decay of antiapoptotic gene transcripts, including Bcl2L

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

40 A first-order electron and hole decay of approximately 1 ps suggests a Shockley-Read-Hal

41 omplex and DCP2 overexpression induces rapid decay of APUM9 targeted mRNAs.

42 and pasteurization led to the most extensive decay of ARGs and intI1, often to levels similar to that

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

44 93T cells, GCaMP6fu revealed a 4-fold faster decay of ATP-evoked intracellular calcium transients tha

45 umulate endogenous NMD-elicited mRNAs, while decay of AU-rich instability element (ARE)-signal contai

46 ltilayer modeling demonstrates that the slow decay of BaP over long times can be simulated if there i

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

48 RNA sequencing (RNA-seq) revealed cell-wide decay of basal mRNAs accompanied by rapid accumulation o

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

50 Where the decay of both modes is slow compared to the rate of reso

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

52 Decay of bound states due to coupling with free particle

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

54 on the host cell surface by accelerating the decay of C3 convertase.

55 The degree of leak determines whether decay of Ca waves, biphasic or monophasic, occurs.

56 jective was to model the short and long-term decay of CA-HIV-DNA blood reservoir in patients initiati

57 The decay of CA-HIV-DNA over time while on successful cART w

58 ring impairment likely via nonsense-mediated decay of CABP2-mRNA.

59 In contrast, fluorescence decay of calcium-bound jRCaMP1a occurs by the reversal o

60 However, fluorescence decay of calcium-bound jRGECO1a follows a different path

61 Thr286 phosphorylation slows the decay of CaMKII and thus lowers the frequency required t

62 Ethosuximide's effect on rate of decay of CaV 3.2 was significantly less for P640L channe

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

64 are therefore consistent with time-dependent decay of cells and body fluids during incubation ex vivo

65 the impairment of the exosome-mediated 3'-5' decay of CER3 transcript in the cer7 mutant that trigger

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

67 iate species that promoted the autocatalytic decay of chlorine.

68 iques, it properly handles the Hi-C-specific decay of chromatin interaction frequencies with the incr

69 Hi-C datasets, adapted for the Hi-C-specific decay of chromatin interaction frequencies.

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

71 e initial Co(III) species concomitant to the decay of Co(I), thus closing the catalytic cycle.

72 2 and 3 T magnetic field and an exponential decay of coherence at high fields.

73 ilibrium two-dimensional bosonic gas, with a decay of coherence in both spatial and temporal domains

74 The decay of colinearity with other grass genomes correlates

75 In this study, the decay of coliphages, an indicator for enteric viruses, w

76 fect of temperature and trophic state on the decay of Common Carp (Cyprinus carpio) eDNA was evaluate

77 The rapid decay of compound 0 enabled calculation of the limits fo

78 he atmosphere, proceeds through unimolecular decay of Criegee intermediates.

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

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

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

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

83 ongitudinal analyses revealed an exponential decay of DRM (BF = 0.05) while genetic diversity increas

84 luded repression of EARLY FLOWERNG 4, slower decay of dusk components, and a slight phase delay at th

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

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

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

88 The overall rapid decay of eDNA and the effects of temperature and water q

89 However, the decay of enteric viruses is not well characterized, and

90 creased the peak amplitude and decreased the decay of evoked delta IPSCs but had no effect on delta o

91 ates evolutionary distances by measuring the decay of exact substring matches as a function of match

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

93 core nanocrystals to achieve unity radiative decay of excitons in single channel in comparison to oth

94 ant in EXOC2 that leads to nonsense-mediated decay of EXOC2 transcript, a severe reduction in exocyto

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

96 the Fe(III)-nitrite complex is limited, and decay of [Fe(III)(NO2)(N3PyS)](+) leads to {FeNO}(7) spe

97 ophores with free tryptophan, as well as the decay of fluorescence anisotropy of a labeled protein.

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

99 e can be consistently explained by radiative decay of free excitons, bound and trapped excitons as we

100 The generation, accumulation and decay of free radicals in six varieties of cheese, irrad

101 o exon 11 resulted in nonsense-mediated mRNA decay of full-length, but not the BRCA1-Delta11q isoform

102 ith the number of repeats, but with a slower decay of gain.

103 toxicity was found to relate to a decreased decay of gamma-H2AX foci and reduced induction of DNA do

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

105 d suggest that GABA co-release may speed the decay of glycine responses altering both temporal precis

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

107 These heterogeneities, caused by the decay of hafnium-182 in mantle domains with high hafnium

108 is the dominant 5' exoribonuclease mediating decay of HCV RNA and that miR-122 provides protection ag

109 ART was significantly associated with slower decay of HIV DNA (P= 0.011) but not with increased cellu

110 HIV-infected men was associated with slower decay of HIV DNA even during antiretroviral therapy (ART

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

112 tics of bictegravir and its association with decay of HIV-1 RNA in genital fluids and the rectum have

113 ong-term ART initiated from infancy leads to decay of HIV-1-infected cells to exceedingly low concent

114 IC vaccination resulted in slower decay of HIV-1-specific antibodies than did immunization

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

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

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

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

119 Finally, faster decay of implicit memory also characterized the impact o

120 Dyslexics showed a faster decay of implicit memory effects on both measures, with

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

122 deling of coarsening including diffusion and decay of individual NCs and unconventional coarsening pr

123 pses, we show that all mutations prolong the decay of inhibitory postsynaptic currents (IPSCs) and in

124 factors, P-body formation, and constitutive decay of instable mRNAs encoding mediators of inflammati

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

126 he major implication of our work is that the decay of intact proviruses in vitro is extremely rapid,

127 The decay of integrated intact proviruses was rapid and simi

128 Age-associated decay of intercellular interactions impairs the cells' c

129 In older adults, there was more rapid decay of intrinsic neuronal activity in multiple regions

130 ct gene expression through nonsense-mediated decay of intron-retained transcripts.

131 eir development into CD8alpha(+) cDCs due to decay of Irf8 autoactivation and diverted to the CD4(+)

132 The radioactive decay of isotopes of the heavy elements is predicted to

133 Whereas Xrn1 depletion significantly slowed decay of JFH1 and HJ3-5 RNAs, Xrn2 depletion marginally

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

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

136 TiO(4) coating greatly mitigates the voltage decay of Li-rich material with the degradation rate redu

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

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

139 an effective method to suppress the voltage decay of LLOs for further practical utilization in LIBs

140 rough energy transfer following the eventual decay of LSPRs.

141 Lack of METTL3/WTAP phosphorylation reduces decay of m(6)A-labeled pluripotent factor transcripts an

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

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

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

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

146 More rapid decay of maternal antibodies was a major predictor of EB

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

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

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

150 are known to accurately describe growth and decay of modulationally unstable waves in conservative s

151 rtain kinetic parameters, like diffusion and decay of morphogens, could play a role in formation of a

152 Here we examine the decay of motor adaptation following the learning of nove

153 sed the adenosine triphosphate (ATP) content decay of mouse liver grafts after cold ischemia, warm is

154 AUF1 promotes rapid decay of mRNAs containing 3' untranslated region (3'UTR)

155 factor 1-like protein Dom34/Pelota to direct decay of mRNAs with ribosomal stalls.

156 criptional silencing or post-transcriptional decay of mRNAs.

157 lase, a ribonuclease that is responsible for decay of mtRNA transcripts.

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

159 haploinsufficiency through nonsense-mediated decay of mutant transcripts, or loss-of-function missens

160 Tristetraprolin promotes the decay of MyoD mRNA, which encodes a transcriptional regu

161 UPF1 promotes the decay of MYOD protein, a transcription factor that is a

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

163 ague pandemic that likely contributed to the decay of Neolithic populations in Europe.

164 tive function, in the presence of more rapid decay of neural activity.

165 all networks, as expressed by an accelerated decay of neural information.

166 les together help us understand the rise and decay of news stories from a network perspective.

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

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

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

170 visual cortex and resulted in an accelerated decay of OD plasticity.

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

172 y over 100 hours of operation with a voltage decay of only 15 % at 600 mA cm(-2) under H(2) /air (CO(

173 lgaris L.) on the shelf-life and Penicillium decay of oranges during cold storage.

174 r treatment since it causes a quick, drastic decay of organic matter content.

175 meter, known as phase slips, which cause the decay of persistent current in superconducting rings and

176 We present a detailed analysis of the decay of persistent photoconductivity in STO single crys

177 opy, is used to probe the ultrafast coherent decay of photoexcitations into charge-producing states i

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

179 athogen's genes with a predicted role in the decay of plant cell wall polymers, in the utilization of

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

181 Decay of plasmons to hot carriers has recently attracted

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

183 (Escherichia coli) triggers ribonucleolytic decay of primary transcripts by 5'-monophosphate-depende

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

185 as an alternative platform to manipulate the decay of quantum emitters, possibly leading to the explo

186 rom slow cooling), and perhaps heat from the decay of radioactive isotopes.

187 an unicellular bacteria, evolved to dominate decay of recalcitrant, nutrient poor substrates such as

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

189 We conclude that the thermal decay of Rho primarily proceeds through spontaneous brea

190 s adaptation is accompanied by Ccr4-mediated decay of ribosomal protein mRNAs.

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

192 SF as measured by the decay of S1 has been shown to occur efficiently and inde

193 for retarding bio-dissolution and mechanical decay of scaffolds in vitro.

194 indle densities were associated with reduced decay of schema-related memories.

195 irectly visualize the real-time creation and decay of screened magnetic charge configurations in a tw

196 The decay of sewage-sourced Escherichia coli and enterococci

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

198 lation of their targets but also accelerated decay of short-tailed target molecules.

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

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

201 The decay of SOC in these plots has been monitored for decad

202 impairments are characterized by accelerated decay of spatial memories.

203 We also discover a strengthening distance decay of spread over the life-cycle indicating high frac

204 However, the thermal decay of sterically overcrowded tertiary amines was not

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

206 The rate of decay of superlattice reflections of the (SnSe(2))(1+gam

207 o play important roles in the production and decay of surface active materials; however, the details

208 hreitol and ascorbic acid, assuming that the decay of surrogates corresponds to ROS formation.

209 The faster decay of synaptic currents mediated by mutant heteromeri

210 e would decrease the peak and accelerate the decay of synaptic NMDA receptor currents during normal s

211 iction errors on the two pathways and a weak decay of synaptic weights over trials.

212 free Ca(2+) transient amplitude and rate of decay of systolic Ca(2+) decrease with age, whereas sarc

213 on phosphorescence, which is produced by the decay of T(1) excitons, more effective use of these exci

214 The biexponential decay of T1rho and T2 relaxations was detected in 30% an

215 TTP promotes the deadenylation and ultimate decay of target transcripts.

216 ytic kinetics are measured by monitoring the decay of the AC voltammetry signal from the ferrocene la

217 The growth and decay of the Antarctic Ice Sheet reshapes the solid Eart

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

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

220 es and biographies, to describe the temporal decay of the attention received by cultural products.

221 uctuations of the membrane shape enhance the decay of the average force on a bond, but also lead to f

222 This periodic signal allows to detect the decay of the binary orbit due to gravitational wave emis

223 e of isoproterenol, leak produced a biphasic decay of the Ca transient in the majority of cells while

224 on, RyR-mediated Ca leak produces a biphasic decay of the Ca transient with a fast early phase and a

225 duced by ryanodine) and both induce biphasic decay of the Ca transient.

226 The decay of the catalytic performance of Pt/C could be main

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

228 On the one hand, time dependent decay of the charging current mitigates its impact on th

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

230 owth kinetics, while the desorption mediated decay of the citrate signal followed a first-order model

231 obtained analytical solution to discuss the decay of the concentration difference across the curved

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

233 solar corona, thought to be produced by the decay of the coronal magnetic field strength.

234 experimentally bound the scrambling-induced decay of the corresponding OTOC measurement.

235 ucture is universal and leads to a power law decay of the currents distribution.

236 nd isotopic dilution clearly reveal that the decay of the dangling OH stretch excitation is almost en

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

238 op-gain mutations revealed nonsense-mediated decay of the endogenous mRNA.

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

240 spectral characteristics and a 2-fold slower decay of the excited-state absorption bands compared to

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

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

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

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

245 Phosphorylated ACT-5 accelerates decay of the intestinal subapical terminal web and impai

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

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

248 We observed decay of the latent HIV-1 cells in both T cell subsets a

249 Mean decay of the logarithm of the viral load was estimated a

250 d a stronger initial impression and a slower decay of the MAE than did the incongruent direction, whi

251 Decay of the MLCT excited-state absorption at 376 nm is

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

253 minescence that corresponds to the radiative decay of the molecular triplet state.

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

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

256 ' end of intron 2 leads to nonsense-mediated decay of the mRNA.

257 not be expected to lead to nonsense-mediated decay of the mRNA; nonetheless, both mutations are predi

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

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

260 he phonon energy decreases due to anharmonic decay of the optical phonons into acoustic phonons.

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

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

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

264 requires on-going translation to promote the decay of the petA mRNA.

265 On the other hand, the decay of the photoinduced conductivity in MAPbI3/PCBM is

266 itudinal subset of 64 individuals, continued decay of the plasma HIV-1 RNA level was observed, with a

267 The reduction was not due to passive decay of the potentiated pursuit signal because interlea

268 Here experimental decay of the priapulid Priapulus reveal consistent bias

269 probabilities of radiative and nonradiative decay of the QD exciton.

270 gamma-photons emitted during the radioactive decay of the radioisotope (31)Si produced via the neutro

271 or to earlier agents, but the rapid physical decay of the radionuclide poses logistic and regulatory

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

273 molecular differences in the activation and decay of the response may have each made a small contrib

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

275 were observed, reflecting an input from the decay of the short-lived fission products (95)Zr and (97

276 Second, we find that during decay of the signaling state an active-like, yet empty,

277 Both results may contribute to the slower decay of the size of the reservoir during CMV replicatio

278 coherence times indicates that dephasing and decay of the spin arise from single-phonon-mediated exci

279 se effects gives rise to anomalous power-law decay of the spin-structure factor, with continuously va

280 ndent manner by impairing the miRNA-directed decay of the SRF mRNA.

281 cting a reduced magnitude and an accelerated decay of the synaptic response, thus reducing the safety

282 The decay of the three fungicides was evaluated using an in-

283 T variant does not trigger nonsense-mediated decay of the ZSWIM6 mRNA in affected individual-derived

284 The study looked at four-body decays of the [Formula: see text] baryon.

285 c PTS system is also required for the normal decay of these sRNAs and that it acts by binding to the

286 Upon exposure to ozone, the decay of thin coatings of triolein was observed, accompa

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

288 The resulting genetic decay of those traits under relaxed selection reduces an

289 We monitored the formation and decay of transient electric fields that form upon photoe

290 triplet transfer ligand and that bimolecular decay of triplets is potentially a major loss pathway wh

291 be monitored in situ following the radiative decay of tunnelling-induced surface plasmons.

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

293 spin-dependent modulation on the spontaneous decay of valley excitons leads to tunable handedness and

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

295 rebound and participants who showed a faster decay of VRC01 in serum rebounded more rapidly.

296 ion and initiates differentiation; and RGS5, decay of which activates Sonic Hedgehog (SHH) pathway-me

297 ich promotes myoblast development; CyclinD1, decay of which blocks myoblast proliferation and initiat

298 gnetic fields in excess of 10(14) gauss, the decay of which powers a range of high-energy phenomena(5

299 point mRNAs targeted by AUF1 include Twist1, decay of which promotes myoblast development; CyclinD1,

300 ns (up to 13-34mg/kg) confirmed that quality decay of whole-wheat breadsticks is mainly associated to