ライフサイエンスコーパス: experimentally

1 itions of lycopene extraction were confirmed experimentally.

2 cyclization mechanism has not been addressed experimentally.

3 protein, thus making it difficult to detect experimentally.

4 lectric performance but is difficult to dope experimentally.

5 processes but has been challenging to study experimentally.

6 is concept, but so far this has been elusive experimentally.

7 rane, their strength has never been assessed experimentally.

8 he effects that are difficult to investigate experimentally.

9 ) current, and this prediction was validated experimentally.

10 of DNA damage and genomic variation observed experimentally.

11 ble-arm configurations has been investigated experimentally.

12 onding/anti- bonding modes that are measured experimentally.

13 sorption, and these predictions are verified experimentally.

14 e underlying features have not been compared experimentally.

15 predictions for 12 compounds were evaluated experimentally.

16 r to the nonrisk allele, which was confirmed experimentally.

17 ctively validating 12 of the top key drivers experimentally.

18 ls have proven difficult cells to manipulate experimentally.

19 tennas has been investigated numerically and experimentally.

20 ave been demonstrated both theoretically and experimentally.

21 plains the formation of the species observed experimentally.

22 n within 3 hours post-infection, as observed experimentally.

23 mines in water are difficult to characterize experimentally.

24 Of 96 designs that were characterized experimentally, 21 were found to form stable monodispers

25 Here the authors demonstrate experimentally a three-qubit single-photon linear determ

26 ize the cardiac lincRNA transcriptome in the experimentally accessible zebrafish model by integrating

27 tudies demonstrate that single molecules are experimentally accessible.

28 To begin to experimentally address this knowledge gap, we asked whet

29 of 0, 8 and 20 sector Gabor zone plates were experimentally analyzed.

30 lar vesicle (GUV) membranes has been studied experimentally and by means of kinetic Monte Carlo model

31 ders of magnitude larger than those screened experimentally and can enable efficient optimization of

32 These factors were integrated with experimentally and computationally derived interactome d

33 Here we have experimentally and computationally evaluated the functio

34 ucleophilic probe, we have demonstrated both experimentally and computationally that a proper selecti

35 ir complex 3D conformational landscape, both experimentally and computationally.

36 n of the configuration, as demonstrated both experimentally and computationally.

37 ic heteroatoms in SNO-OCT were explored both experimentally and computationally.

38 enanthroline (phen) as a ligand was explored experimentally and computationally.

39 ies of ion channels is extremely challenging experimentally and even impossible in clinical applicati

40 We investigate experimentally and numerically the stochastic dynamics a

41 a suspended resistor both theoretically and experimentally and obtained consistent results.

42 has been investigated spectroscopically both experimentally and theoretically with some differences a

43 r allowed for a detailed investigation, both experimentally and theoretically, on the interplay betwe

44 electronic states are challenging to explore experimentally and theoretically-due to the large densit

45 ly substituted alkenes with BH3 was examined experimentally, and a classically unexpected trend is th

46 We observe experimentally, and validate theoretically, that the inw

47 between fatty liver from healthy liver in an experimentally arrived mouse model using noninvasive tec

48 Yet few studies exist that experimentally assess the degree to which environmental

49 In a K-ras transformed cell line we experimentally assessed glutamine-induced metabolic chan

50 the spall strength is proposed that fits the experimentally available values in the literature.

51 loped methods sensitive to the full range of experimentally-available wavenumbers q, we extract the l

52 roperty modulation has not been demonstrated experimentally because of the difficulty of realizing CN

53 uch transient species are difficult to study experimentally, but it has proven valuable to prepare an

54 t is supported by ab initio calculations and experimentally by a normalized crystallographic B-factor

55 Failure of phagocytosis could be induced experimentally by incubating healthy control neutrophils

56 Processing factors experimentally calculated were correlated to their octan

57 cyte HC computational model, we incorporated experimentally calibrated hMSC PS effects on cardiomyocy

58 y of the asymmetric growth patterns observed experimentally can be reproduced by our model, which inc

59 drive the formation of approximately 99% all experimentally captured interactions, in which approxima

60 he peak of clinical disease from beef cattle experimentally challenged with either bovine respiratory

61 Here we experimentally characterize the principal biogeochemical

62 Here, Lim et al. experimentally characterize the stability of whispering-

63 trion and biexciton for single-layer WS2 are experimentally characterized at 35 meV and 60 meV, respe

64 Finally, three metal-metal bonds in experimentally characterized compounds are examined: a [

65 To experimentally confirm isotope fractionation in thiomoly

66 forces that challenge underwater balance and experimentally confirm that larvae are subject to consta

67 using fluid-supported silicon membranes, and experimentally confirm the successful suppression of bot

68 We experimentally confirmed the catalytic function of the p

69 We identified and experimentally confirmed the function of two secreted gl

70 Our in silico predictions were experimentally confirmed using reconstituted MscL in a l

71 We use the experimentally constrained model to evaluate the correct

72 n culture is almost impossible to predict or experimentally control.

73 omparative genomics methods, we identify and experimentally define a novel binding motif for the SOS

74 hitecture for computing heading has not been experimentally defined in any species.

75 Finally, we experimentally demonstrate >350% emission intensity enha

76 We experimentally demonstrate a fast adiabatic transportati

77 We experimentally demonstrate a highly efficient, broadband

78 We propose and experimentally demonstrate a metasurface device to gener

79 Here we experimentally demonstrate broadband, flexible, conforma

80 single-photon character of the input, and we experimentally demonstrate entanglement between over two

81 Here we experimentally demonstrate high-gain optical parametric

82 We experimentally demonstrate phase-matching-free second ha

83 h the nitrogen vacancy center in diamond, we experimentally demonstrate that quantum interpolation ca

84 Here we experimentally demonstrate that the electronic structure

85 We experimentally demonstrate that this terahertz source ca

86 Here, for the first time, we experimentally demonstrate the deep-UV SH generations (S

87 I hypersensitive sites in breast cancer and experimentally demonstrate they are regulatory elements

88 ce of our isolator far exceeds that of other experimentally demonstrated terahertz isolators, and ind

89 tes at strikingly low modulation voltages is experimentally demonstrated.

90 BioPlex 2.0 exceeds previous experimentally derived interaction networks in depth and

91 on have substantially greater agreement with experimentally derived networks, while remaining more pr

92 ve spike-stimulus delays are consistent with experimentally derived spike-timing-dependent plasticity

93 The value of Rs* must be experimentally determined and is dependent on the chemom

94 tome-wide mRNA 3' UTR interaction sites were experimentally determined at 72 h posteclosion and 24 h

95 with partial residence times consistent with experimentally determined atomic sites and fractional oc

96 he three proteins are in good agreement with experimentally determined B factors and with fluctuation

97 nonspherical (tailed) bacterial viruses were experimentally determined by measuring their flux across

98 of Deltaf to Deltam should be done using an experimentally determined characteristic constant (Cf,ex

99 Experimentally determined damage thresholds were compare

100 vements seen in vivo, using a minimal set of experimentally determined ingredients.

101 he use of highly methyl-labeled protein with experimentally determined intermolecular distances, a co

102 We present experimentally determined physical and chemical characte

103 Approximately half of proteins with experimentally determined structures can interact with o

104 h yields structural models that recapitulate experimentally determined structures with all-heavy-atom

105 We experimentally determined the full phase diagram of an I

106 ruses (EIVs), the ancestors of H3N8 CIV, and experimentally determined the impact of amino acid 186 i

107 Experimentally, DHI exerted comprehensive anti-inflammat

108 microscopy and subcellular fractionation is experimentally difficult and low throughput.

109 Birds with experimentally disabled tracheal membranes were still ab

110 e has been much research into predicting and experimentally discovering distinct classes of these mat

111 o date, it has remained a major challenge to experimentally disentangle the complex kinetic reaction

112 risk and ambiguity are formally distinct and experimentally dissociable, little is known about ambigu

113 Here, we experimentally eliminate environmental modifications fro

114 c cryptic splice variants, two of which were experimentally evaluated and confirmed.

115 The classes are defined as follows: experimentally evaluated effects of amino acid substitut

116 ously expressed dominant lethal D genes were experimentally evolved.

117 Experimentally exacerbated droughts further reduced the

118 ism through N-doping has not yet been proved experimentally, except for systems containing a high amo

119 ult from evolved differences in immunity, we experimentally exposed laboratory-reared fish from ecolo

120 permittivity, showing that this approach is experimentally feasible.

121 We validate this prediction experimentally, finding that the ablation of PDB leads t

122 15 protocols computationally and 4 protocols experimentally for batch-matched cell populations, in ad

123 able to reproduce the unbinding trends seen experimentally for both DNA and protein competitors.

124 also compared bacterial transmission across experimentally generated "daisy-chain" vs. "star" networ

125 ar species, yet revealing these correlations experimentally has proved extremely challenging.

126 ally predicated ethanol-binding proteins and experimentally identified ethanol tolerance genes.

127 We experimentally identify two competing mechanisms through

128 or all types of networks we study, including experimentally-imaged collagen and fibrin architectures,

129 We experimentally implement the phase shifter and demonstra

130 es use of abstract logical models of growth, experimentally implemented systems are governed by nanos

131 model recapitulates CCL21 gradients observed experimentally in B cell follicles and interfollicular r

132 here the 'harmonic phase', is shown to occur experimentally in spin ice, a dipolar lattice system.

133 n rather than directly released as was shown experimentally in starved cells.

134 that the topological feature could be tested experimentally in superfluids of cold fermionic atoms wi

135 We show theoretically, and demonstrate experimentally in the Ho2Ir2O7 pyrochlore iridate, that

136 is unique LL structure has not been observed experimentally in transition metal dichalcogenides.

137 ndamental issues that thus far have remained experimentally inaccessible.

138 processing, and confirm several predictions experimentally including a disease-causing mutation.

139 tatively captures a suite of trends observed experimentally, including the statistics of filament flu

140 We experimentally increased embryonic temperature in free-l

141 Experimentally increasing or decreasing intracellular Ca

142 died binocular interactions in macaques with experimentally induced amblyopia.

143 our knowledge, this study examined effect of experimentally induced anxiety in humans on generalizati

144 n devils, and regression followed therapy of experimentally induced DFTD tumours in three Tasmanian d

145 An experimentally induced increase in alpha power by means

146 We demonstrated that experimentally induced memory reactivation during sleep

147 In both genetically prone and experimentally induced mouse models of autoimmunity, inc

148 d a causal association between the timing of experimentally induced theta rhythms and episodic memory

149 icroparticles before and after 20 minutes of experimentally-induced oscillatory shear stress.

150 points of spectral sensitivity responding to experimentally-induced stress in desiccated mosses, indi

151 ) causes a mild and self-limiting disease in experimentally infected crab-eating macaques, while simi

152 We applied this to experimentally infected guinea pig lung sections and wer

153 ed during replication in cell culture and in experimentally infected macaques.

154 frontal lobes and optic nerves of a macaque experimentally infected with variant CJD.

155 We experimentally investigated the quantum motion of an imp

156 uctural priming offers a powerful method for experimentally investigating the mental representation o

157 ese annotations were analyzed by translating experimentally known fragmentation rules of lipids into

158 ntrations show reasonable agreement with the experimentally known values and with the results of a nu

159 We experimentally manipulated plant diversity in a Californ

160 We experimentally manipulated the Amount of food delivered

161 to be successful if the mounted locusts were experimentally manipulated to have a reduced capacity to

162 f neural maturation and experience cannot be experimentally manipulated.

163 Experimentally manipulating ADS strongly influences spin

164 By experimentally manipulating solar irradiance and nightti

165 Structural comparison of experimentally mapped Der f 1/Der p1 IgG epitopes to the

166 Our results pave the way to experimentally mapping the low-temperature phase diagram

167 astically varied for each condition based on experimentally measured alteration in elastic fiber comp

168 ic law derived from in-situ experiments, the experimentally measured and calculated stresses during c

169 assembly of one type of RNA granule based on experimentally measured binding interactions among three

170 Experimentally measured bond lifetimes (1/koff) and diss

171 We show that the experimentally measured coordinates and chemical species

172 ing the degree of energetic coupling between experimentally measured degrees of freedom and subunit r

173 pied molecular orbitals, in conjunction with experimentally measured N K-edge absorption spectra, rev

174 he asymmetric binding is consistent with the experimentally measured negative cooperativity of ketami

175 significant discrepancies when comparing to experimentally measured rates or state populations.

176 glass shell thickness is elucidated and the experimentally measured sensitivities for two different

177 ropic springs, is in good agreement with the experimentally measured shear modulus.

178 f free energy is in excellent agreement with experimentally measured stabilities (R(2) = 0.93).

179 argets of TC cells were observed to resemble experimentally measured stLFP signatures.

180 The model quantitatively captures the experimentally measured swell-burst parameters for singl

181 and OER kinetics, however, has not yet been experimentally measured.

182 xtrusion kinetics, similar to those we found experimentally, model RT neurons are predisposed to an a

183 By experimentally modifying the level of stress hormones (c

184 Here we demonstrate experimentally not only elastic Rayleigh wave rainbow tr

185 We experimentally observe a threefold improvement in polari

186 nts are in size and symmetry compatible with experimentally observed Abeta assemblies.

187 s denote Ballesteros-Weinstein numbering) is experimentally observed and appears to be essential for

188 tide contributes to the stabilization of the experimentally observed antiparallel beta-sheet packing.

189 However, these models do not account for the experimentally observed dependency of angiogenic network

190 ntly non-random orientation, swimming in the experimentally observed direction from the corresponding

191 In addition, the lifetime broadening of the experimentally observed dispersions provides another mea

192 In addition, the DFT calculations reproduce experimentally observed effects on reaction rate, induce

193 ga, good correlations were found between the experimentally observed electrophilic reactivities of 44

194 hase at the interface region and explain the experimentally observed exchange bias.

195 ere 4-fold enriched with respect to improved experimentally observed expression levels.

196 The model reproduces experimentally observed features of membrane protein int

197 nsition (EMT), from which we identified four experimentally observed gene states, including the state

198 transcription) is superior in describing the experimentally observed gene-expression profile.

199 plausible mechanistic scenario based on the experimentally observed intermediates.

200 (i) A method is described for predicting the experimentally observed lifetime distribution of long bi

201 activation reproduce the preference for the experimentally observed major enantiomer.

202 These results identify the first experimentally observed MOF that exhibits band-like meta

203 /- 2 cm/s in a 100% cholesterol mimic of the experimentally observed noncrystalline cholesterol bilay

204 antoin series while correctly predicting the experimentally observed oxidation sites in various compl

205 ractome sizes for species with limited to no experimentally observed PPI, including Bacillus subtilis

206 repeats are intrinsically unfolded, and the experimentally observed radius of gyration (R g) is coin

207 file for a radical mechanism and support the experimentally observed regioselectivity.

208 ent, stresses the critical importance of the experimentally observed selective severing of the "cross

209 stent with previous theory, we predicted and experimentally observed that spatial diffusion increased

210 ative selection thresholds chosen to reflect experimentally observed thymic survival rates result in

211 was previously shown to accurately model the experimentally observed wall stress relaxation and expan

212 Circular dichroism as high as 0.6 is experimentally observed while the chirality switching is

213 for cells to perform the various classes of experimentally-observed motions.

214 evel were found between concentration values experimentally obtained and the certified values of two

215 Finally, an experimentally obtained anti-correlation momentum patter

216 MOLM16 cell lines and successfully validated experimentally our prediction that this resistance can b

217 The ability to experimentally perturb biological systems has traditiona

218 We tested this hypothesis by experimentally placing juvenile bird carcasses on the gr

219 Experimentally, polycyclic polymers with a layered struc

220 Here we experimentally probe hyper-complex quantum theories, stu

221 ng that such types of mixed anomaly could be experimentally probed in condensed matter systems known

222 ze distributions from a suite of natural and experimentally produced tephra to show that attrition is

223 geometrical modifications of an existing and experimentally proven phononic crystal design, the snowf

224 Naive ants that arrived at an experimentally provided feeder for the first time were c

225 t are surprisingly close to those determined experimentally, providing support for the dose-additive

226 KIE is a selective probe that identifies the experimentally reactive spin state.

227 Here, we introduce and experimentally realise a quantum network architecture, w

228 ns of hard core-soft shoulder particles with experimentally realistic interaction parameters.

229 Here, we analytically predict and experimentally realize a mixed-order equilibrium phase t

230 Discovering pathways to experimentally realize quantum phases of matter and exer

231 -capacitor transmission lines is designed to experimentally realize the transformation medium.

232 Thus, we have experimentally realized a lyotropic liquid crystal syste

233 ation of free magnesium ([Mg2+]i), which was experimentally recorded in cells expressing connexin36,

234 Strikingly, when centrosome activity was experimentally reduced, the absence of KLP-7 or the mamm

235 Experimentally reducing Ocn(+) cell numbers suppresses t

236 We experimentally removed arthropods, foliar fungi and soil

237 Analyzing 19 compositions that are experimentally reported in both structure types, this ma

238 ncourage these interfacial interactions, but experimentally resolving how such weak interactions affe

239 iffraction technique, we for the first time, experimentally revealed the phase transition of ThC from

240 In particular, the keyhole pore formation is experimentally revealed with high spatial and temporal r

241 ly higher in NA than in EU and EA, and under experimentally short winter conditions NA species requir

242 We experimentally show that certain variants of mu-opioid a

243 This experimentally simple protocol provides structurally com

244 Experimentally, slight decrease in SO3 concentration was

245 By experimentally stretching epithelia, we find that mechan

246 We experimentally studied the power and robustness of the n

247 The lack of animal models to experimentally study how infectious agents transmit betw

248 light and excitations of the atoms, one can experimentally study phase transitions of open quantum s

249 ium Physiological analyses on SC-less plants experimentally support classic hypotheses that SCs permi

250 An experimentally supported model of the resulting complex

251 adical-transfer reactions in FnY-RNRs and to experimentally test and support the key prediction made.

252 reviously unexplained observations and makes experimentally testable predictions.

253 in the experimental observations and to give experimentally testable predictions.

254 We develop an experimentally testable theory, which reveals that late-

255 ng program and graphical interface have been experimentally tested in our laboratory for RNA domains

256 We experimentally tested whether algal polycultures could b

257 By experimentally testing a key model prediction we suggest

258 It was shown experimentally that Ca(2+)/CaM (holoCaM) binds to the Ca

259 These findings demonstrate experimentally that chimpanzees and bonobos can take int

260 Here we show experimentally that fine changes to molecular structures

261 In this study, we demonstrate experimentally that NN animals are highly susceptible af

262 application, we prove both theoretically and experimentally that the doughnut intensity profile at th

263 Here, we show experimentally that the spin current generated by the sp

264 h inducible expression of I-SceI, and showed experimentally that tobacco chloroplast DNAs insert into

265 We then show experimentally that turbulence generated by fine scale s

266 Here we measure experimentally this function in a system that is in loca

267 sion barrier for racemization was determined experimentally to be 29 kcal/mol and is supported by qua

268 is unique to humans or conserved in the more experimentally tractable mouse.

269 It allows the electrons to be cooled for an experimentally useful period of time to temperatures col

270 alloys (x 0.025 and y >/= 0.6) is studied experimentally using optical absorption, photomodulated

271 qualitatively novel results, which we tested experimentally using spatially diffusing laboratory popu

272 The activity of carbofuran was determined experimentally (using pseudo-first-order kinetics) and t

273 existence of an inverse energy cascade in an experimentally validated 3D active fluid model, describi

274 We experimentally validated candidates from two sets of pla

275 This study is the first to provide an experimentally validated complete crystallographic detai

276 to the training on updated, human specific, experimentally validated datasets.

277 Experimentally validated FE models are combined for that

278 Genomic data were experimentally validated for PSMA expression-by quantita

279 Different HPSDS implementations have been experimentally validated in the near-IR.

280 storical antigenic drift events, pointing to experimentally validated mutations.

281 miRBShunter was tested and experimentally validated on the in-house Ago2-dataset an

282 ed with the expression of miR-210, which was experimentally validated that miR-210 regulated GPD1L pr

283 We also predicted and experimentally validated the hybrid E/M status of certai

284 be used to generate hypothesis which can be experimentally validated to improve our understanding of

285 geable clusters that encapsulate many known, experimentally validated transcription factor interactio

286 RNAs, of which Ncr1071, Syr6 and NsiR7 were experimentally validated, and their putative targets wer

287 ackground particles in mixed systems is also experimentally validated, demonstrating both collision f

288 1-benzyl-1,2,3,4-tetrahydroisoquinoline, was experimentally validated.

289 harges of polyelectrolytes, resulting in the experimentally verifiable contraction of the collagen st

290 he extracellular domain was proposed but not experimentally verified.

291 imensional ceramic printing and the bandgaps experimentally verified.

292 We experimentally verify the predicted universal scaling fu

293 crotubule destabilizers, which was confirmed experimentally via cell-based assays.

294 n was probed using both DFT calculations and experimentally via halogen exchange.

295 We established experimentally warmed and nonwarmed common garden plots

296 Experimentally, we could detect small viral RNA polymera

297 Experimentally, we operated the microdevice in temperatu

298 The model was validated experimentally with H2, N2, Ar and CH4 on three classes

299 by 2D fingerprints and confirm three of them experimentally with ligand efficiencies from 0.442-0.637

300 intersubunit torsional flexibility measured experimentally with purified protein components.