ライフサイエンスコーパス: experimentally

1 cellent agreement with reactivity determined experimentally.

2 nts constitute hypotheses that can be tested experimentally.

3 stable states, a prediction that we confirm experimentally.

4 ions over timescales that are not accessible experimentally.

5 to probe the dynamics of the coupled system experimentally.

6 types of exine structure could be simulated experimentally.

7 hysical modelling but are poorly constrained experimentally.

8 hypothesis of amyotrophic lateral sclerosis experimentally.

9 icals and Ni(I), both of which are supported experimentally.

10 gas phase concentration of methanol observed experimentally.

11 ues of kinetic constants are hard to uncover experimentally.

12 , and 53 top-ranked molecules were evaluated experimentally.

13 ein structures can be difficult to determine experimentally.

14 ation junctions, all of which were confirmed experimentally.

15 This prediction was confirmed experimentally.

16 Ni-N(4)) in Ni-SACs has not been determined experimentally.

17 e hard grain basal dislocations, as observed experimentally.

18 ive immunity that remain to be characterized experimentally.

19 n different cordierite filters is determined experimentally.

20 pedance model is validated theoretically and experimentally.

21 in operons, and we validate several of these experimentally.

22 ion because they are not directly observable experimentally.

23 on for mass transport over the full range of experimentally accessible parameters.

24 Here, we used the experimentally-accessible locust ear (male, Schistocerca

25 rtly understood because of difficulties with experimentally accessing the relevant time and length sc

26 umerical model characteristics coincide with experimentally achieved spectral width, pulse duration,

27 the alignment task is often simpler than in experimentally acquired samples.

28 In addition, we used arousing stimuli to experimentally activate participants' noradrenergic syst

29 the third breeding season, social cues were experimentally added at 10 formerly unoccupied sites wit

30 We show that the [Ca2+]i dynamics observed experimentally after sustained alkalinisation can be rep

31 top computational predictions were evaluated experimentally against asexual blood stages of both sens

32 The models were further validated experimentally against seven independent MeONPs (ACC = 8

33 Experimentally, airway vaccination induces greater effic

34 ssion of the pharyngeal arches and show that experimentally altering the timing of Hgf/Met signaling

35 Different ePCR regimes were experimentally analyzed to identify the most robust tech

36 imulations closely reproduced those observed experimentally and both measurements were sensitive to t

37 hich our strategy was compared with previous experimentally and computationally determined results.

38 Herein, we studied experimentally and computationally the formation, acidit

39 al properties of the probe have been studied experimentally and computationally, suggesting an inters

40 Here, we study, experimentally and computationally, the mechanics of gas

41 iochemical assays, we tested these compounds experimentally and found one, named CLK8, that specifica

42 We characterized these interactions experimentally and investigated the underlying principle

43 unodominant proteins were recognized by dogs experimentally and naturally infected with Bartonella sp

44 extended lifetime of pearls was studied both experimentally and numerically.

45 ractions have been extensively explored both experimentally and theoretically.

46 production potential remains to be confirmed experimentally, and further technological innovations ar

47 Experimentally, apparent reaction activation energies in

48 r, traditional chemical inhibitors cannot be experimentally applied with spatiotemporal precision sui

49 In this work, we demonstrate both experimentally as well as theoretically how the intrinsi

50 era where protein-DNA interactions have been experimentally assayed for thousands of DNA-binding prot

51 ineered nanomaterial (ENM) have been raised, experimentally assessing toxicity of various ENMs is cha

52 otein kinase activity are difficult to study experimentally because of challenges in isolating a part

53 We experimentally burned 102 plots, for which we measured v

54 ardinal features of human mitosis determined experimentally by numerous laboratories.

55 This structure is then confirmed experimentally by one- and two-dimensional dynamic nucle

56 nce of these in-silico findings is validated experimentally by site-directed mutagenesis of the key C

57 ents in limiting calcification was confirmed experimentally by treating human coronary artery smooth

58 face concept is tested, both numerically and experimentally, by embedding a total-internal-reflection

59 Experimentally calibrated in silico analysis of transcri

60 ion has remained obscure, largely due to the experimentally challenging nature of targeting this smal

61 he encoded information(3-7) has proved to be experimentally challenging, and the only realization rep

62 because metabolic networks are difficult to experimentally characterize in diverse extant organisms.

63 hain length and chain conformation are often experimentally characterized by ensemble averages.

64 Designs were experimentally characterized for binding to a panel of h

65 It is essential to experimentally confirm the material properties of such p

66 Finally, we experimentally confirm the predictions of our computatio

67 based machine learning, as we demonstrate by experimentally confirming the predicted properties of pe

68 and bicyclic peroxy radical (BCP-peroxy) are experimentally constrained at 295 K to be 420 +/- 80 and

69 the other 111 circuits that have so far been experimentally constructed using the 2-input BLADE platf

70 ce beyond immediate reach mandates free, yet experimentally controlled movements.

71 Three aphid sublines were experimentally created from single aphid genotype suscep

72 te richness in response to global change, we experimentally crossed host diversity (biodiversity loss

73 Mushrooms were experimentally cultivated on substrate contaminated with

74 Yet, experimentally curated disorder information still does n

75 formation and transformation processes were experimentally deconvolved in a dedicated lysimeter stud

76 er time frames, this study establishes a new experimentally defined minimal length of protective ZIKV

77 Here, we establish a new experimentally defined minimal length of protective ZIKV

78 upport selection of thermostable variants of experimentally demanding GPCRs.

79 In this paper, we propose and experimentally demonstrate a reconfigurable electroacous

80 Here, we propose and experimentally demonstrate a spatio-temporally modulated

81 Here, we describe and experimentally demonstrate a strategy for the generation

82 For these parameters, we experimentally demonstrate a threshold in laser-to-proto

83 Here we experimentally demonstrate direct electric-field control

84 We experimentally demonstrate response times on the order o

85 In this study, we experimentally demonstrate simultaneous solvent regenera

86 We experimentally demonstrate that the system is uniquely r

87 ese observations, we chose the RAS family to experimentally demonstrate that the translation efficien

88 nating current (AC) field-effect electrodes, experimentally demonstrate the separation of particles a

89 of coarse-grained molecular simulations and experimentally demonstrated by imaging DNA-origami tiles

90 es, BnPMT6s, in two QTLs were identified and experimentally demonstrated to negatively regulate SOC.

91 broadband blackbody thermal source has been experimentally demonstrated with converted power densiti

92 idy that are commonly discussed, even if not experimentally demonstrated, and to highlight key issues

93 ediction, the designed 6 ML and 8 ML SLs are experimentally demonstrated.

94 lico systems of influenza neuraminidase with experimentally derived glycoprofiles consisting of four

95 interparticle forces and responses to relate experimentally derived interparticle potentials to the u

96 and in vivo microdosimetry was modeled from experimentally derived pharmacologic variables.

97 are routinely compared to computationally or experimentally derived protein structures.

98 Comparison with the experimentally derived real hydration free energy produc

99 cell lines show excellent agreement with the experimentally derived values and high correlation with

100 While it is not feasible to experimentally determine optimal growth temperature (OGT

101 forces and provide a conceptual framework to experimentally determine why they have survived selectio

102 S values are compared to previously reported experimentally determined and computationally calculated

103 c stability of several AOXD derivatives were experimentally determined and found that the AOXD scaffo

104 Their affinities for the A(2A) AR were experimentally determined and investigated through a cyc

105 -mediated transport alone cannot explain the experimentally determined auxin distribution in the root

106 compounds generally comparing one cluster of experimentally determined data (e.g., (13)C NMR chemical

107 19,000 annotated gene sets for resolving 52 experimentally determined developmental trajectories.

108 dicting half-lives in soil by regressing the experimentally determined half-lives in activated sludge

109 Currently, frequencies are experimentally determined in randomised controlled clini

110 The experimentally determined partition coefficient was vali

111 These agreed well with corresponding experimentally determined structural epitopes previously

112 ill does not currently scale to the level of experimentally determined structural information in fold

113 on actin-tropomyosin because high-resolution experimentally determined structures of filament-associa

114 alation of chlorophyll-a to pheophytin-a was experimentally determined to be 450 +/- 20 M(-2).s(-1) a

115 ls are in reasonably good agreement with the experimentally determined values.

116 structures for homologous proteins have been experimentally determined(7).

117 However, experimentally determining the whole-genome sequences of

118 acute remodeling during embryogenesis, it is experimentally difficult to determine whether basal turn

119 on-theoretic quantities that suggests how to experimentally disentangle the impacts of internal noise

120 fied this interaction in native grassland by experimentally eliminating temporal variability in growi

121 rvations, and provides a robust criterion to experimentally elucidate the underpinnings of both actom

122 ering both peptides predicted to bind MHC or experimentally eluted from infected cells, making this t

123 ernate bearing in Citrus trees that had been experimentally established as fully flowering or nonflow

124 for isopropyl-substituted derivative 10 was experimentally estimated to be 18.7 kcal/mol.

125 We experimentally evolved populations of Escherichia coli w

126 Here, under controlled conditions, we experimentally examine fourteen types of stone-tipped pr

127 ble architecture of its connectome, offering experimentally falsifiable predictions on the genetic fa

128 This has been demonstrated experimentally for a Coulomb crystal of [Formula: see te

129 Some of them can be seen experimentally, for example with x-ray crystallography o

130 have been described, both theoretically and experimentally, for steady-state crowding densities; how

131 Here we experimentally, for the first time, demonstrated a direc

132 d demonstrates that large disease-linked and experimentally generated C-terminal truncated KCNQ3 muta

133 In this paper we demonstrate experimentally how cavity cooling can be implemented to

134 Here we show experimentally how the unitary Fourier transform-based p

135 Here, we experimentally identified all eight centromeres in M. sy

136 For each, we experimentally identified spatial patterns of activity a

137 Using an independent test set of experimentally identified succinylation sites, our metho

138 gth scales; however, it remains difficult to experimentally image Li-ion diffusion at the atomistic l

139 We use electric circuits to experimentally implement a four-dimensional (4D) topolog

140 s showed no adjustment following 15 years of experimentally imposed moisture deficit.

141 s of proteins have DFLs, they were annotated experimentally in <200 proteins.

142 75% of HLA-bound peptides that were observed experimentally in 11 patient-derived tumor cell lines.

143 Here, we studied experimentally in detail the forces of the nonreciprocal

144 five human patients with acute lung injury, experimentally in five mice ventilated before and after

145 with increased alcohol drinking by women and experimentally in rodents.

146 This exposure is studied numerically and experimentally in this manuscript.

147 cterized structurally or by simulations than experimentally in water, and unfavorable interactions ar

148 the possible design space has been explored experimentally, in part because that space has not yet b

149 Experimentally, increasing crowding within the compact l

150 Glaucoma-like neuropathies can be experimentally induced by disturbing aqueous outflow fro

151 ased intramammary therapy in dairy cows with experimentally induced Staphylococcus aureus clinical ma

152 ecific models of arterial mechanics using an experimentally informed four-fiber constitutive model.

153 Blood culture bottles experimentally inoculated were used as controls.

154 Blood cultures experimentally inoculated with Enterobacteriaceae, Staph

155 Finally, we assign and experimentally interrogate cancer-associated hot-spot mu

156 fer mechanistic insights and explications of experimentally intriguing observations in the Au(I)-cata

157 Here, we experimentally investigate the thermodynamics of continu

158 effect on the soil strength improvement was experimentally investigated by performing unconfined com

159 We experimentally investigated the influence of co-dosed li

160 Here, we experimentally investigated the role of S18-2 in cell st

161 We experimentally investigated transgenic mice and performe

162 However, elucidating this influence experimentally is difficult because grains typically exh

163 pathogen that may cause severe encephalitis; experimentally, it can be transmitted within just 15 min

164 d sectors showing close correspondences with experimentally-known biochemical domains.

165 be further understood, and theoretically and experimentally leveraged, to elucidate AD pathophysiolog

166 We experimentally manipulated abundances of the largest art

167 In the present study, viewer engagement was experimentally manipulated in order to: (1) replicate pa

168 omposition at carrion between sites where we experimentally manipulated mesopredator abundance and pa

169 We experimentally manipulated the species richness of marin

170 sgenic zebrafish in which Hh levels could be experimentally manipulated under different foraging cond

171 Here we experimentally mapped the in vivo RNA-RNA interactome of

172 ifferent segments of chromatin such that the experimentally measured contact count probability constr

173 Here, we use 63 reconstructed and experimentally measured DNA methylation maps of ancient

174 ich both amino acid sequence information and experimentally measured lambdamax values are known.

175 A total of 1062 experimentally measured load-dependent Vickers hardness

176 ctions improve most when conditioning on the experimentally measured local correlations in comparison

177 f colorectal cancer initiation together with experimentally measured mutation rates in colorectal tis

178 from the simulations are in correlation with experimentally measured observables, including viscositi

179 The experimentally measured packing configuration and inferr

180 cocoa beans are exposed to, with the aim of experimentally modelling changes to bean components (res

181 ting proteins and provide a valuable tool to experimentally modulate the subcellular distribution of

182 in this study, we performed BruChase-Seq to experimentally monitor the expression dynamics of nascen

183 We experimentally observe 113 individual heterostructured n

184 Using these image polaritons, we experimentally observe a record-high effective index of

185 We experimentally observe tunable topological transitions f

186 dimensional parameters to adequately explain experimentally observed adhesion weakening and strengthe

187 The experimentally observed alpha-selectivity was explored i

188 is subtype-dependent and correlates with the experimentally observed binding affinity of H1 subtypes,

189 r cell chemotaxis that is calibrated against experimentally observed cell trajectories in healthy and

190 We show that experimentally observed chromosome compaction and varian

191 tinuum-scale rate coefficients that produced experimentally observed colloid breakthrough-elution con

192 Taken together, our results explain experimentally observed data and shed light on the roles

193 sizer-oscillator" arrangement reproduces the experimentally observed features of multiple-fission cyc

194 ression noise, predicting bursty dynamics-an experimentally observed hallmark of eukaryotic transcrip

195 inhibition of Rac activation, which has been experimentally observed in recent years, facilitates thi

196 lipid species is sufficient to reproduce the experimentally observed increase in acyl tail saturation

197 roM potential, it is now possible to predict experimentally observed inter-chromosome contacts.

198 panying high-level quantum calculations, the experimentally observed intermolecular bands can be assi

199 eptible to humans, 0.42 m/s, is above 85% of experimentally observed landing speeds.

200 Our model captures experimentally observed peak to trough ratios, relative

201 xed alignment symmetries, which captures the experimentally observed phenomenology and provides a the

202 This model reproduces the experimentally observed regioselectivity and diastereose

203 ated absorption-difference spectra reproduce experimentally observed shifts in known chlorophyll abso

204 We experimentally observed solitons-waves that propagate wi

205 unt for the rich diversity of clinically and experimentally observed spatiotemporal patterns of seizu

206 Our model captures the experimentally observed temporal changes in the fraction

207 ed with the state transitions and reproduces experimentally observed variability in cell state by eit

208 Furthermore, we directly relate the experimentally observed yield of full-length protein in

209 corresponding Hall response has not yet been experimentally observed.

210 Interestingly, this signal is only experimentally obvious in thick films due to the differe

211 Further, we demonstrate our approach experimentally on a superconducting quantum processor, b

212 We experimentally parameterized conditional rate constants

213 udy demonstrates the potential utility of an experimentally parameterized continuum model as a predic

214 ning 143 circuits that have yet to be tested experimentally predict excellent performance of the 2-in

215 Here we experimentally prepare square and hexagonal GKP code sta

216 We have developed a technique to experimentally probe these phases of matter using a coll

217 The findings provide strong candidates for experimentally probing the molecular basis of synaptic p

218 trained using simulated biofilm images with experimentally realistic SBRs, cell densities, labeling

219 lcogenides (TMDs) offer an ideal platform to experimentally realize Dirac fermions.

220 Experimentally realized shapes are shown to agree closel

221 ll volume and large octahedral rotations are experimentally realized, which result in an enhancement

222 mary productivity (ANPP) under conditions of experimentally reduced versus naturally high rainfall va

223 hed in cells where the membrane's charge was experimentally reduced.

224 nformationally dynamic biological systems at experimentally relevant time resolutions, such as those

225 hort-term synaptic depression influences the experimentally reported dynamics of SWR events.

226 he existence of in-plane piezoelectricity is experimentally reported for multilayer BP along the armc

227 Finally, we experimentally reveal that the predicted non-classical f

228 extract moderately soluble NPs from soil and experimentally separate them from their dissolved fracti

229 yeast system (Saccharomyces cerevisiae), we experimentally show that communities with the greatest m

230 Here we experimentally show the successful implementation of a h

231 It is experimentally shown that the correction function is ind

232 base for 300 steroids allowed one to observe experimentally significant deviations of the expected CC

233 Additionally, we experimentally simulated previously reported ETV/3TC res

234 0 disease-associated genes using over 14,000 experimentally solved human protein structures.

235 l pest, Epiphyas postvittana (EposPBP3), and experimentally solved its apo-structure through X-ray cr

236 Four experimentally solved structures closely matched the des

237 Experimentally, studies confirmed that H-bonds and LA(II

238 Experimentally, such apparently G protein-biased opioids

239 Most putative G/U base pairs were experimentally supported by selective 2'-hydroxyl acylat

240 nd cell lines, including: (i) more than 2000 experimentally supported circulating, drug-resistant and

241 ature validation as well as validation using experimentally supported miRTarBase database.

242 FtsEX residues required for EnvC binding and experimentally test a proposed mechanism for amidase act

243 My model makes experimentally testable predictions, including how modul

244 equency of codon mutations of 10 Rho-GAP and experimentally tested biochemical and biological consequ

245 Lastly, Rosalind predictions were experimentally tested in a patient-derived in-vitro assa

246 ial to chlorophyte dominance are unclear, we experimentally tested phytoplankton responses to a gradi

247 inclusions, this theory is then extended and experimentally tested with nanoporous conductors that ar

248 rnatives whose activity on hPXR has not been experimentally tested.

249 at mediates ubiquitin transfer has yet to be experimentally tested.

250 Herein, we show experimentally that approximately 80 water molecules flo

251 We show experimentally that by fusing sequential and 3D genome d

252 In contrast, we found experimentally that gene expression patterns are highly

253 Conversely, we show here experimentally that gravity plays a negligible role: The

254 We show experimentally that natural aerial dispersal rate alters

255 Here we show experimentally that the often neglected optical magnetic

256 It has been demonstrated experimentally that the tracheal sound transmission gene

257 In this paper, we study theoretically and experimentally the effect of induced charging currents o

258 ion is the first unique evidence that proves experimentally the existence of diatropic currents, and

259 By simulating experimentally the extinction of three consumer species

260 Here we demonstrate experimentally the use of the recently developed techniq

261 e Slr1694 BLUF domain has been characterized experimentally, the identity of the light-adapted state

262 lenge for GB-property investigations is that experimentally they need to be performed at the top surf

263 rafish posterior lateral line primordium, an experimentally tractable model of complex self-organized

264 We experimentally tuned the optical-driver frequency by a f

265 The computational results were validated experimentally (up to 92:8 er), providing another succes

266 work evaluates the computational assignment experimentally using a series of related complexes.

267 ln levels despite Gln4p depletion, confirmed experimentally using tRNA Northern blotting.

268 ere computational and analytical models, and experimentally validate a novel non-transcriptional mech

269 In total, this study is the first to experimentally validate sulfur acquisition systems in S.

270 y identified PDAC growth-promoting genes and experimentally validate the effects of these APA events

271 y examined in the humanized mouse model, and experimentally validate the predicted function of an obe

272 Future work will be carried out to experimentally validate this framework in a controlled c

273 diction were inferred on a limited number of experimentally validated A. thaliana interactions and we

274 de material in kinetic states and provide an experimentally validated angstrom-level 3D picture of at

275 Finally, we found and experimentally validated bat-specific variation in micro

276 This aspect was then experimentally validated by modulating the zeta potentia

277 The results are experimentally validated for a given geometry over a wid

278 , requires the use of appropriate procedures experimentally validated in a systematic manner.

279 MTL-SGL to determine antigenic changes were experimentally validated in the H1N1 antigenic variants

280 internal mRNA m7G database containing 44 058 experimentally validated internal mRNA m7G sites, a sequ

281 In a case study, we discovered and experimentally validated new transcripts through the app

282 idates has been discovered and the number of experimentally validated target genes has increased cons

283 We experimentally validated that afatinib has the strongest

284 Among several novel SAN enhancers that were experimentally validated using transgenic mice, we ident

285 These mutations have never been experimentally validated, and no mechanisms of action ha

286 many novel interactions, some of which were experimentally validated, thus providing mechanistic ins

287 The model made novel predictions that were experimentally validated.

288 l regeneration-specific enhancers, which are experimentally validated.

289 In this work we present a novel and experimentally verified "True Random Number Generator" t

290 ng genes and lncRNAs defined using BGRDs are experimentally verified as required for cancer phenotype

291 h do not have (and are never likely to have) experimentally verified functional annotation.

292 Then, it is experimentally verified in the (Fe(0.83)Ga(0.17))(100-x)

293 We calculated and experimentally verified the excitation pulse energy to a

294 We predict and experimentally verify an entoptic phenomenon through whi

295 use of additives (anionic or cationic) is an experimentally viable strategy to implement external ele

296 een characterized, the long-standing goal of experimentally visualizing a CCD-carotenoid complex at h

297 be on the order of 0.1 electron per proton; experimentally, we also access this quantity via the pot

298 To demonstrate the sensor concept experimentally, we fabricated a microfluidic device with

299 Experimentally, we showed representation of four DNA tar

300 trated mostly by simulation and it struggles experimentally with the purity of the batches of buildin