1 In this study, we performed a controlled
experiment on 10 polydomous wood ant (Formica lugubris)
2 In
experiments on 15 benchmark BioNER datasets, our multi-t
3 onal correlation function obtained from PSPP
experiments on 2-SeCN-Bmim(+) exhibits two periods of re
4 We made observations and conducted
experiments on 23 native and cultivated flowering plant
5 A rescue
experiment on 47 tools that were published from 2019 onw
6 dversarial images are robustly related: In 8
experiments on 5 prominent and diverse adversarial image
7 Third, we ran a series of
experiments on 74 distinct olfactory qualities and showe
8 9th-11th years of an elevated CO2 (+200 ppm)
experiment on a maize-soybean agroecosystem, measured re
9 lection, we performed a laboratory evolution
experiment on a panel of artificial hybrids to measure T
10 J(CH) values collected from a single HSQMBC
experiment on a sample of strychnine were used in the CA
11 a recycling reactive flow-through transport
experiment on a sandstone under geologic reservoir condi
12 ne expression profiles obtained from RNA-Seq
experiments on a collection of tissue samples, consideri
13 s were 6.58 +/- 0.42 min when performing the
experiments on a conventional qPCR instrument (n = 41).
14 we performed synchrotron-based X-ray imaging
experiments on a decagonal phase with composition of Al-
15 Moreover, the
experiments on a dynamic engine test bench focus on the
16 parameter for ligand donation, derived from
experiments on a high-valent chromium species, is now av
17 es for combating these challenges during IMS
experiments on a hybrid QhFT-ICR MS.
18 f S. mansoni sirtuin 2 (SmSirt2) and kinetic
experiments on a myristoylated peptide demonstrated lysi
19 These observations are compared with imaging
experiments on a normal yeast strain and two condensin-m
20 , recent time-resolved infrared spectroscopy
experiments on a photoswitchable PDZ domain (PDZ2S) have
21 angevin dynamics, we performed computational
experiments on a prototypical ternary system modeled aft
22 In-vivo
experiments on a rat show that the flexible ECoG system
23 This study reports a series of toxicity
experiments on a representative coastal marine diatom sp
24 f optimal human GRI dynamics not captured by
experiments on a rodent population (false negatives).
25 of the Getz Ice Shelf system and laboratory
experiments on a rotating platform.
26 tistep well-designed quasistatic compression
experiments on a series of nanopores/nonwetting liquid m
27 retation, complementary ATR-FTIR Kretschmann
experiments on a similar model system, which is exposed
28 Experiments on a subset of the clusters suggested a link
29 Using extensive computational docking
experiments on a test set of 241 protein complexes, we f
30 Comparison to
experiments on a water-soluble version of the metal carb
31 Further, we perform in vitro perturbation
experiments on a widely replicated asthma gene, GSDMB, s
32 For validation, we conduct
experiments on AD diagnosis by selecting mutually inform
33 Our first two
experiments on adapting a high-structure course model to
34 We demonstrate that two independent
experiments on adhered cells of different types fall on
35 9 person-to-person spread treated as natural
experiments on air pollution and population health.
36 Here in a 5-year field
experiment on Alexander Island in the southern maritime
37 Although the first
experiments on alpha-neurofeedback date back nearly six
38 l was tested using a 5 yr drought/heat field
experiment on an established pinon-juniper stand with ro
39 We
experimented on an in vitro coculture system to determin
40 results of this study and those from similar
experiments on an Al-2Cu alloy were consistent when the
41 Using a combination of models and
experiments on an amphibian species suffering extirpatio
42 s simulations, CD response calculations, and
experiments on an AT-sequence, we show that the ICD of m
43 Experiments on an expanded set of eight angiosperm speci
44 erase activities and are valuable for future
experiments on animals and humans.
45 gnature genes, we performed new localisation
experiments on ARMC3, EFCAB6, FAM183A, MYCBPAP, RIBC2 an
46 differences, we performed an RNA sequencing
experiment on ARVMs from male and female rats and identi
47 ort attoclock and momentum-space imaging(16)
experiments on atomic hydrogen and compare these results
48 rajectories, and visualizing high throughput
experiments on available experimental data.
49 For biologically triplicate
experiments, on average 953 N-glycosylation sites on 393
50 Sequential soaking
experiments on BbZIP crystals clarified the process of m
51 lem through nuclear magnetic resonance (NMR)
experiments on BiCu[Formula: see text]PO[Formula: see te
52 and chromatin immunoprecipitation-sequencing
experiments on BMP9 (bone morphogenetic protein 9)-stimu
53 a common mechanism for phenomena observed in
experiments on both atrial and ventricular cardiac cells
54 rious ISVAID-derived peptides in competition
experiments on both female and male mouse and rats hippo
55 Here, we combine FRAP
experiments on both in vitro reconstituted droplets and
56 underlying circuit processes and comparable
experiments on both spatial scales are rare.
57 We start with optical imaging
experiments on CA1 in mice as they run along a virtual l
58 layers are -7.6 and -6.6 cm/s, and that from
experiment on cadaver skin is -6.65 cm/s).
59 Using an extensive set of machine learning
experiments on cancer omics data, we find that current p
60 Here, through an
experiment on carbon nanotubes, we present a new approac
61 translation from numerous successful animal
experiments on cardioprotection beyond that by reperfusi
62 -enhanced 2D (113)Cd-(113)Cd correlation NMR
experiments on CdS NPs and natural isotropic abundance 2
63 lenging homonuclear and heteronuclear 2D NMR
experiments on CdS, Si, and Cd(3)P(2) NPs.
64 ar basis of TAD formation, we performed Hi-C
experiments on cells depleted for the Forkhead transcrip
65 Laboratory
experiments on centimetre-scale meteorites(3) have been
66 Benchmarking
experiments on challenging simulated and real datasets s
67 Here, we performed laboratory
experiments on chemically different organic materials in
68 Here, we combine
experiments on chick embryos with computational modeling
69 identified that were not found in individual
experiments, on chromosomes 3, 4, 9 and 11.
70 Accelerated aging
experiments on co-melt mixtures ranging from 0% to 100%
71 Experiments on cohesin have shown that cohesins walk dif
72 Previous
experiments on colliding Bose-Einstein condensates have
73 Experiments on confidence reports have almost exclusivel
74 By comparing our results to a number of
experiments on controlled migration through pores, we sh
75 easures gas yields from laboratory pyrolysis
experiments on core samples.
76 We combine
experiments on critical Casimir colloidal suspensions, n
77 proach is demonstrated with proof of concept
experiments on crude mixtures including egg white, unpur
78 Field-effect
experiments on cuprates using ionic liquids have enabled
79 these earthquakes by performing deformation
experiments on dehydrating serpentinized peridotites (sy
80 Furthermore, parallel
experiments on Dgcr8 (+/-) mouse cultures reveal a signi
81 The model is validated with wicking
experiments on different hemiwicking surfaces in conjunc
82 nucleic acid barcode sequence, thus allowing
experiments on different molecules in parallel.
83 The results allow one to rationalize
experiments on diffusion in two-dimensional systems.
84 We simulated single-molecule pulling
experiments on dimers, the minimal oligomer, and compare
85 Furthermore, we conducted case study
experiments on diseases including breast cancer, glioma
86 Steady state microwave conductivity
experiments on doped aggregates confirm that holes in th
87 Experiments on dorsal root ganglion cells show that, for
88 h-clamp electrophysiology and Ca(2+) imaging
experiments on dorsal root ganglion neurons, NGF- and IL
89 d using both simulated data (calibrated from
experiments on Drosophila melanogaster) and real data fr
90 Experiments on drug-sensitive versus resistant SW480 can
91 Previous
experiments on edge states in photonics were carried out
92 vior, and we give special attention to field
experiments on election participation, environmentally s
93 Using flow chamber
experiments on endothelial monolayers and tracking of th
94 Comparative HDX/MS
experiments on enzyme dynamics should therefore be inter
95 We performed
experiments on ethyl crotonate and menthol, using three
96 Systematic
experiments on European eel (Anguilla anguilla) in their
97 e methods with numerical simulations and new
experiments on ex vivo ovine skeletal muscle (n = 3).
98 pole excitations, as a guide to numerics and
experiments on existing materials.
99 stigated in vitro by binding and competition
experiments on FAP-transfected HT-1080 (HT-1080-FAP) or
100 e model gives results that strongly resemble
experiments on FeSe(1-x)S(x) across the nematic transiti
101 to feeding and development, we conducted an
experiment on field-collected caterpillars of the model
102 In the last few decades,
experiments on fission yeast have revealed different mol
103 Experiments on five manually curated collections of TRs
104 Experiments on flies suggest that a gain-of-function mec
105 Also, in the in vitro
experiments on fMLP-stimulated neutrophils and 5-LOX-tra
106 We performed detailed
experiments on formaldehyde (H(2)CO) photodissociation a
107 Experiments on four interaction networks, including drug
108 Here, single-molecule FRET
experiments on freely diffusing TFAM/LSP complexes conta
109 lanine's role in condensate assembly because
experiments on FtoA and tyrosine-to-phenylalanine mutant
110 of small-angle x-ray and neutron scattering
experiments on fully hydrated lipid vesicles in the pres
111 t resonant inelastic x-ray scattering (RIXS)
experiments on Gd x Sc3-x N@C80 at Gd N 4,5-edges to dir
112 These include the first such
experiments on genome-scale GI datasets in multiple spec
113 , we perform CO[Formula: see text] reduction
experiments on Gold at neutral to acidic pH values to el
114 In addition, through
experiments on gram scale in palladium, mechanistically
115 amics simulations and fluorescence-quenching
experiments on gramicidin A (gA).
116 a psychological treatment rationale in three
experiments on healthy subjects.
117 ndscape scale with a long-term ant-exclusion
experiment on hickory saplings in the context of spatial
118 tion of a cryogenic solid hydrogen target in
experiments on high-power laser-driven proton accelerati
119 This research should inspire further
experiments on how humans assign confidence judgments in
120 cium imaging, and multielectrode array (MEA)
experiments on human (h)iPSC-derived 2D cortical neurona
121 endency graph from approximately 3,000 CF-MS
experiments on human cell lines.
122 and multivariate pattern analysis, in three
experiments on human participants (57% females), by mani
123 Finally, we conduct extensive
experiments on human SL datasets and the results demonst
124 me-dependent behavior observed in controlled
experiments on humans, (b) the findings of a recent stud
125 Patch clamp
experiments on hypothalamic slices showed that the mean
126 As shown in control
experiments on in vitro alphaB- and gammaD-crystallin, 2
127 Experiments on in vitro BMM cultures revealed that KCa3.
128 to the total SOA mass, varied for different
experiments on individual parent PAHs: PHE and 6 quantif
129 There is an extensive body of
experiments on interactions between DOM and ENPs and als
130 Earlier neutron-scattering
experiments on iron-based 123 ladder materials, where OS
131 Here, we performed ATAC-seq
experiments on isolated E9.5 tailbud tissue, which revea
132 The role of anchoring was highlighted by
experiments on isolated fission yeast rings, where secti
133 magnitude higher than the values observed in
experiments on isolated outer hair cells.
134 Ex vivo
experiments on isolated rat tail collecting lymphatics s
135 We also performed cell biology
experiments on isolated SMC-derived cells, conducted int
136 sm, and use our ability to perform arbitrary
experiments on it to see if popular data analysis method
137 Small-angle X-ray scattering (SAXS)
experiments on JBP1 and JDBD in the presence or absence
138 trophysiological and in vivo hormone profile
experiments on kisspeptin-specific ERalpha knock-out mic
139 Results of
experiments on knotted protein fusions with a highly sta
140 We performed a 120 day OM decomposition
experiment on lake water, with an untreated control and
141 ated through examples obtained from physical
experiments on landscape evolution.
142 We performed
experiments on leaf reflectance, phytohormonal compositi
143 ff and its mechanistic basis is supported by
experiments on leaves of California woody species, and i
144 Small-angle x-ray scattering
experiments on lens tissue show colloidal gels of S-crys
145 Thanks to a combination of
experiments on lipid vesicles supported by colloidal sca
146 particular, we report (1)H DNP-enhanced NMR
experiments on liquid samples having a volume of about 1
147 ling, fluorescence resonance energy transfer
experiments on living cells, biochemical and mutational
148 Motivated by recent
experiments on magnetically frustrated heavy fermion met
149 diffraction (ND) and x-ray diffraction (XRD)
experiments on magnetically-oriented fibers of Abeta1-28
150 Leaching
experiments on mare basalt 14053 demonstrate that isotop
151 mples of Ghanaians and Ugandans, and similar
experiments on members of parliament, probe the effects
152 nally, we compare quantitatively our data to
experiments on membrane-catalyzed amyloid aggregation of
153 smission electron microscopy crystallization
experiments on metallic glass nanorods, and show that st
154 2018, 35 (4), 289-299] reported laboratory
experiments on methane-saturated oil droplets under emul
155 Sub-10 fs resolution pump-probe
experiments on methylammonium lead halide perovskite fil
156 m(3) in all cases), consistent with previous
experiments on methylglyoxal.
157 Experiments on mice have shown that developmental proces
158 Experiments on mice show that an enzyme called DNA methy
159 Experiments on mitochondrial DNA in worms highlight that
160 Recent laboratory
experiments on mixed micro- and macro-pore suggest that
161 Biophysical
experiments on model membranes show common properties of
162 Experiments on model systems have revealed that cytokine
163 s partially explained by the push to conduct
experiments on model systems under relevant reaction con
164 To test this, we perform
experiments on model wings in a wind tunnel to approxima
165 We first conducted brain slice and in vivo
experiments on monkey motor cortex to investigate the ou
166 Transport
experiments on monolayers of Calu-3 cells and studies of
167 raction displays gene-regulating activity in
experiments on mouse stem cells.
168 ate for an unambiguous signature that future
experiments on multi-petawatt laser facilities have trul
169 n density functional theory calculations and
experiments on multiple push-pull conjugated polymers, i
170 We use a controlled in vivo loading
experiment on murine tibiae to test this hypothesis, whe
171 nge of experimental findings from mechanical
experiments on muscle cells are consistent with nonlinea
172 superthin filaments were inferred from early
experiments on muscle, decades passed before their exist
173 Proof-of-principle
experiments on neuronal co-cultures and brain tissues re
174 Experiments on neutral self-assembled quantum dots yield
175 ural activity recorded during delays in four
experiments on nonhuman primates.
176 In
experiments on nonmotile E. coli exposed to polymyxin B,
177 Established sample preparations for DNP SENS
experiments on NPs require the dilution of the NPs on me
178 Through extensive
experiments on one synthetic and three real datasets wit
179 Control AFM
experiments on other lipids and at different temperature
180 We conducted comprehensive
experiments on over 90 large-scale TF-DNA datasets which
181 search into energetics arose from Meyerhof's
experiments on oxidation of lactate in isolated muscles
182 Lab-scale and pilot-scale
experiments on ozonation of WWTP effluents confirmed tha
183 hic optical tweezers (HOT) and poke-and-flow
experiments on particles deposited onto a glass substrat
184 Analogue
experiments on phyllosilicates formed under low temperat
185 In laboratory headspace
experiments on pig manure, we used proton-transfer-react
186 Experiments on plasma-liquid interaction and formation o
187 Using ex vivo peeling
experiments on porcine liver, we characterized the adhes
188 etter understand these effects, we conducted
experiments on Porolithon onkodes, a common crustose cor
189 Escalating dose-response
experiments on primary VS cells grown from 15 human tumo
190 Our siRNA knockdown
experiments on ProGENI-identified genes confirmed the ro
191 osecond time-resolved X-ray pump/X-ray probe
experiment on protein nanocrystals.
192 Experiments on protein-protein interaction network with
193 Our
experiments on prototypical Au-alkanedithiol-Au junction
194 Recent
experiments on pure fluids have identified distinct liqu
195 We report the results of an
experiment on radio-tracking of individual grey field sl
196 We perform several
experiments on raw microscopy image datasets from 8 SCD
197 (1)H and (2)H NMR spectroscopy
experiments on reactions using allylic phosphates showed
198 Our
experiments on real and synthetic networks demonstrate t
199 Identical
experiments on representative samples of Ghanaians and U
200 Experiments on Ru(NH(3))(6)(3+) reduction to Ru(NH(3))(6
201 We describe an impact
experiment on Ryugu using Hayabusa2's Small Carry-on Imp
202 mework of the modulated rate model, existing
experiments on S. elongatus are consistent with the simp
203 DMPC vesicles and by propidium iodide influx
experiments on S. epidermidis.
204 is parameter space by comparison to existing
experiments on S180 cells.
205 This relationship also persisted in
experiments on second-generation animals, and larval lip
206 Experiments on select receptors in mammalian cells confi
207 Furthermore, ddPCR
experiments on serum samples and experiments with nuclea
208 An independent RT-qPCR
experiment on seven genes in twelve cancer cell lines sh
209 The methodology has been
experimented on several brain datasets.
210 Large-scale
experiments on simulations and real cancer high-throughp
211 ted this hypothesis by conducting laboratory
experiments on six Daphnia species using a soft water cu
212 es, fresh-frozen tissue sections and in vivo
experiments on skin.
213 Classic
experiments on social groups dealing with truth statemen
214 lie social information use, using a suite of
experiments on social insects as case studies.
215 Laboratory
experiments on solidified sugars in water show that need
216 imitation (from 1 to 60 species added across
experiments) on species richness and productivity.
217 rcurrents; and timeliness in light of recent
experiments on spin injection in proximitized supercondu
218 MALDI-MSI
experiments on spleen tissues from intravenously injecte
219 large set of equilibrium and nonequilibrium
experiments on squalane and extend them to higher [Formu
220 Indeed, previous
experiments on squirrel monkeys and macaque monkeys show
221 Applications of these ideas to the recent
experiments on stripe-ordered La(1.875)Ba(0.125)CuO(4) (
222 However, behavioural
experiments on subjects with only rod function reveals t
223 We describe chromosome conformation capture
experiments on Sulfolobus species.
224 mperature, analogous to the temperature-jump
experiments on SUVs.
225 Our
experiments on synthetic and empirical genomic data demo
226 Experiments on synthetic and real graphs show the effect
227 Extensive
experiments on synthetic and real-world networks show th
228 Experiments on synthetic data demonstrate that the propo
229 Here we perform systematic
experiments on synthetic sequences to reveal how CNN arc
230 ch we use in the present analyses for a 21-d
experiment on the back reef of Mo'orea, French Polynesia
231 ication with a national sample and one field
experiment on the BBC News website (total n = 5,780)-to
232 ency of 1.2 mm monsoon-type watering events)
experiment on the Colorado Plateau, USA.
233 In particular, the
experiment on the Earth Microbiome Project dataset (~2.2
234 Experiment on the ground, the bone mass of humerus, femu
235 fluidic chip reactor in a proof-of-principle
experiment on the Hantzsch cyclization reaction forming
236 We carried out a mining
experiment on the International Space Station to test hy
237 Here we used a reciprocal design
experiment on the wild population to test whether BFDV m
238 Experiments on the Al+CuO nanocomposite system reveal a
239 models to data from individual-based culture
experiments on the aquatic invertebrate, Brachionus manj
240 Benchmarking
experiments on the benchmark dataset and comparisons wit
241 The calculation is validated by our
experiments on the breakup of Fe3C-plates in Fe matrix.
242 Experiments on the catalytic reaction indicated that NaO
243 Our
experiments on the decorated bilayer edge reveal an addi
244 nting for both processes and performed batch
experiments on the desorption kinetics of typical wastew
245 ined will be useful for understanding future
experiments on the diffusion and clustering of hydrogen-
246 However, evidence from community
experiments on the effect of restoration practices on ec
247 We also perform comparative
experiments on the efficiency of RTFC, 2D-RT and IT in q
248 gions, we conducted a battery of biophysical
experiments on the EGFR and HER3 tails.
249 Interestingly, colonization
experiments on the eight polymers revealed a large core
250 We report on infrared spectroscopy
experiments on the electronic response in (Sr1-x La x )2
251 Experiments on the folding and tetramerization of the 26
252 Earlier CO flow-flash
experiments on the fully reduced Thermus thermophilus ba
253 hese findings by conducting siRNA knock-down
experiments on the highly migratory MDA-MB-231 cell line
254 nly, surface plasmon resonance (SPR) binding
experiments on the immobilized control antibody, and sma
255 d-state counterparts of high-energy collider
experiments on the induced fission of composite particle
256 Examples from
experiments on the NIF in each regime are given.
257 The
experiments on the paper indicated that in the presence
258 Experiments on the re-establishment of place fields in d
259 oscopy and electron energy-loss spectroscopy
experiments on the recovered sample and computer simulat
260 Targeted virtual cooling
experiments on the recurrent deep network models further
261 In
experiments on the same bacterial strain exposed to ampi
262 ferently when different laboratories perform
experiments on the same cell line.
263 streams from laboratory-scale and microscale
experiments on the same chemical system can provide comp
264 ecule fluorescence resonance energy transfer
experiments on the same constructs.
265 med complementary multiple particle tracking
experiments on the same particles, extending significant
266 We have run
experiments on the shell formation in foraminifera, unic
267 This model is derived from psychophysical
experiments on the upper limit for circular auditory mot
268 Further
experiments on the zebrafish showed that this vertebrate
269 Additionally, we perform
experiments on thermally driven stochastic switching in
270 We perform a rigorous set of
experiments on these models in matched GI datasets from
271 photosynthetic systems and describe selected
experiments on these systems.
272 ms, which may have implications for other IM
experiments on these time scales.
273 further conduct the numerical simulation and
experiments on these two applications.
274 ed second-order nonlinear optical scattering
experiments on thiolate-protected gold clusters (Au130(S
275 Experiments on three benchmark datasets suggest that the
276 We use transgenerational common garden
experiments on three populations 'resurrected' from a bi
277 er, we present a proof-of-concept validation
experiment on top-view images of 24 Arabidopsis plants i
278 Experiments on top-down mass spectrometry datasets showe
279 Furthermore, recent
experiments on trampling animals and biting crocodiles h
280 used mutagenesis and whole-cell patch clamp
experiments on TRPV3 channels endogenously expressed in
281 Recent
experiments on twisted bilayer graphene have shown a hig
282 te and validate it through synthetic polling
experiments on Twitter data.
283 Experiments on two benchmark datasets for biomedical ent
284 Extensive
experiments on two datasets corresponding to multiple sc
285 ffs, suggesting melanoma, we carried out our
experiments on two dermoscopy image datasets, which cons
286 (salty, sweet, sour, and bitter) in two fMRI
experiments on two different days to test for task- and
287 Flow cytometry and immunohistochemistry
experiments on two independent cohorts confirm the co-ex
288 Experiments on two real-world datasets illustrate that o
289 We validated the complete workflow with
experiments on two simple planar structures; the results
290 This finding unambiguously bridges
experiments on ultrathin SnTe films with predictions of
291 A field
experiment on urea and ammonium nitrate (UAN) treated wi
292 Of note,
experiments on vacuolar membrane-enriched vesicles isola
293 We perform
experiments on vanadium dioxide VO(2) films, which exhib
294 Computational
experiments on various datasets indicate that our OMC me
295 Initial
experiments on water oxidation by well-defined molecular
296 The advantages of future X-ray
experiments on water oxidation catalysts, which include
297 e and repair on 3D genome folding using Hi-C
experiments on wild type cells and ataxia telangiectasia
298 solution NMR, and pre-steady-state kinetics
experiments on wild-type and five WPD loop mutants to id
299 are known to be induced by wounding, further
experiments on wounded and non-wounded leaf samples were
300 Experiments on zebrafish show that the regeneration of t