1 ction by performing 232 direct blood-feeding
experiments on 118 viremic patients with dengue in Vietn
2 ness of the proposed algorithm, we conducted
experiments on 16 binary classification tasks with diffe
3 a compendium to date, which includes 31 CLIP
experiments on 19 RBPs involved in splicing (such as hnR
4 onal correlation function obtained from PSPP
experiments on 2-SeCN-Bmim(+) exhibits two periods of re
5 Experiments on 25 chimeras, constructed from Kv1.2 and K
6 Pulsed EPR spectroscopy
experiments on 3 revealed quantum coherence up to room t
7 Conducting chromatographic
experiments on 4 cm long micromachined packed bed column
8 Here, we performed two
experiments on 48 volunteers to characterize perceptual
9 We performed kinetic folding and unfolding
experiments on 69 mutants (engineered every 2-3 residues
10 9th-11th years of an elevated CO2 (+200 ppm)
experiment on a maize-soybean agroecosystem, measured re
11 In a proof-of-principle
experiment on a university-scale system, we demonstrate
12 We report here the results of video-recorded
experiments on a congenitally blind child, beginning imm
13 e analysis of angular-resolved photoemission
experiments on a cuprate superconductor.
14 we performed synchrotron-based X-ray imaging
experiments on a decagonal phase with composition of Al-
15 re dramatic evidence of this phenomenon from
experiments on a fullerene-porphyrin dyad.
16 parameter for ligand donation, derived from
experiments on a high-valent chromium species, is now av
17 In this study,
experiments on a mouse model with two different cell typ
18 , recent time-resolved infrared spectroscopy
experiments on a photoswitchable PDZ domain (PDZ2S) have
19 of this instrument and results from VT-IM-MS
experiments on a range of model systems-IMS CCS standard
20 In-vivo
experiments on a rat show that the flexible ECoG system
21 This study reports a series of toxicity
experiments on a representative coastal marine diatom sp
22 Through supercomputer
experiments on a sample of the network, we study thousan
23 retation, complementary ATR-FTIR Kretschmann
experiments on a similar model system, which is exposed
24 Experiments on a single-celled ciliate reveal how mobile
25 Our model predictions fit well with recent
experiments on a single-stator motor.
26 FT-GGA-PW91) calculations, reaction kinetics
experiments on a SiO2-supported Pd catalyst, and mean-fi
27 Experiments on a subset of the clusters suggested a link
28 Comparison to
experiments on a water-soluble version of the metal carb
29 ed by computer simulations and verifiable in
experiments on active colloidal Janus particles and magn
30 For validation, we conduct
experiments on AD diagnosis by selecting mutually inform
31 Although the first
experiments on alpha-neurofeedback date back nearly six
32 results of this study and those from similar
experiments on an Al-2Cu alloy were consistent when the
33 Using a combination of models and
experiments on an amphibian species suffering extirpatio
34 s simulations, CD response calculations, and
experiments on an AT-sequence, we show that the ICD of m
35 Experiments on an expanded set of eight angiosperm speci
36 This simple NMR probe design allows
experiments on aqueous solutions to pressures correspond
37 Experiments on artificial membranes are revealing many d
38 Through tremendous
experiments on artificial networks, which can be control
39 differences, we performed an RNA sequencing
experiment on ARVMs from male and female rats and identi
40 A recent
experiment on Atlantic shearwaters (Cory's shearwater, C
41 Preliminary
experiments on bacteria cultures from pathogens causing
42 We conducted in situ three-point bending
experiments on beams with roughly square cross-sections,
43 The excellent agreement between theory and
experiment on bond dissociation energies, energy disposa
44 ings of laser-assisted atom probe tomography
experiments on boron carbide elucidate an approach for c
45 Performing real-time deformability cytometry
experiments on both model spheres of known elasticity an
46 Experiments on both simulated and real datasets showed t
47 We perform extensive
experiments on both simulated datasets and yeast dataset
48 Experiments on both synthetic data and real data show th
49 mation was obtained by coimmunoprecipitation
experiments on both transfected and infected cells and b
50 Microfluidic
experiments on budding yeast populations in space-limite
51 To address this problem, we combined
experiments on burying beetles (Nicrophorus vespilloides
52 We start with optical imaging
experiments on CA1 in mice as they run along a virtual l
53 translation from numerous successful animal
experiments on cardioprotection beyond that by reperfusi
54 Our extensive
experiments on CDD, HOMSTRAD and BAliBASE benchmark data
55 We suggest model
experiments on cell assemblies on substrates that can te
56 Collagen gels are widely used in
experiments on cell mechanics because they mimic the ext
57 ar basis of TAD formation, we performed Hi-C
experiments on cells depleted for the Forkhead transcrip
58 astly, we performed fluorescence fluctuation
experiments on cells expressing a coactivator and two nu
59 Classification
experiments on cervical and tongue cancer datasets lead
60 Here, we performed laboratory
experiments on chemically different organic materials in
61 Additional
experiments on chemically modified graphene oxide membra
62 Here, we combine
experiments on chick embryos with computational modeling
63 Accelerated aging
experiments on co-melt mixtures ranging from 0% to 100%
64 nd Schultze (1825-1874) performed functional
experiments on coarse granular cells using a warm stage
65 Previous
experiments on colliding Bose-Einstein condensates have
66 By comparing our results to a number of
experiments on controlled migration through pores, we sh
67 Field-effect
experiments on cuprates using ionic liquids have enabled
68 n recent scanning tunneling microscopy (STM)
experiments on cuprates.
69 Nanomechanical
experiments on cylindrical samples, with diameters betwe
70 these earthquakes by performing deformation
experiments on dehydrating serpentinized peridotites (sy
71 Furthermore, parallel
experiments on Dgcr8 (+/-) mouse cultures reveal a signi
72 Experiments on dorsal root ganglion cells show that, for
73 h-clamp electrophysiology and Ca(2+) imaging
experiments on dorsal root ganglion neurons, NGF- and IL
74 Experiments on drug-sensitive versus resistant SW480 can
75 Until now, no
experiments on Earth could selectively suppress both oto
76 vior, and we give special attention to field
experiments on election participation, environmentally s
77 We designed the first functional
experiments on electrogenic transport in human ES and in
78 Subsequent
experiments on elite endurance athletes performing the s
79 Here, we provide a community-wide
experiment on emergent facilitation including natural pr
80 Results of
experiments on endocytosis in yeast show general agreeme
81 Using flow chamber
experiments on endothelial monolayers and tracking of th
82 We show semiquantitative agreement with
experiment on entry and exit rates and in the identifica
83 Comparative HDX/MS
experiments on enzyme dynamics should therefore be inter
84 We performed
experiments on ethyl crotonate and menthol, using three
85 s, a public combination dataset, and several
experiments on Ewing's Sarcoma.
86 ngle molecule imaging and rotor manipulation
experiments on F1-ATPase.
87 Recent
experiments on FeSe films grown on SrTiO3 (STO) suggest
88 to feeding and development, we conducted an
experiment on field-collected caterpillars of the model
89 We test our axioms using data from an
experiment on financial decisions.
90 e of the deformed rods which we compare with
experiments on flexible ferromagnetic nickel rods at the
91 Also, in the in vitro
experiments on fMLP-stimulated neutrophils and 5-LOX-tra
92 Here, single-molecule FRET
experiments on freely diffusing TFAM/LSP complexes conta
93 Experiments on fruit flies are shedding new light on the
94 Experiments on full-thickness skin revealed that the mic
95 action, we performed fluorescence microscopy
experiments on fungal cells treated with an ad-hoc synth
96 We report laser-driven shock
experiments on fused silica, alpha-quartz, and stishovit
97 t resonant inelastic x-ray scattering (RIXS)
experiments on Gd x Sc3-x N@C80 at Gd N 4,5-edges to dir
98 er (DEST) and relaxation dispersion (RD) NMR
experiments on gel-stabilized NP samples enables the acc
99 In addition, through
experiments on gram scale in palladium, mechanistically
100 tation by performing a reciprocal transplant
experiment on grasses that evolved for 14 years under am
101 A new field has been opened up by
experiments on H2 scattering from surfaces at fast grazi
102 As shown in single-channel patch clamp
experiments on HEK293 cells, selective activation of nat
103 g genetic variation in a long-term selection
experiment on high and low body weight of chickens.
104 e controversy surrounding 'gain-of-function'
experiments on high-consequence avian influenza viruses
105 rformed single-particle tracking time-course
experiments on hippocampal neurons during AIS developmen
106 ifications and compare both models to recent
experiments on histone methylation in fission yeast.
107 solid state nuclear magnetic resonance (NMR)
experiments on HIV-1 capsid protein (CA) assemblies with
108 Many recent
experiments on hot carriers using terahertz spectroscopy
109 A proof-of-concept
experiment on human pan-T cells showed significant (p <<
110 endency graph from approximately 3,000 CF-MS
experiments on human cell lines.
111 Many
experiments on human cooperation have revealed that indi
112 Our
experiments on human gene regulatory networks suggest th
113 In
experiments on human mesenchymal stem cells plated on so
114 and multivariate pattern analysis, in three
experiments on human participants (57% females), by mani
115 Through an in vivo murine model and in vitro
experiments on human red blood cells (RBCs), the study b
116 Experiments on hydroamination of aminodialkenes testing
117 Patch clamp
experiments on hypothalamic slices showed that the mean
118 ed amide hydrogen/deuterium exchange (HDXMS)
experiments on IkappaBalpha as well as IkappaBalpha boun
119 Experiments on image-guided photodynamic cancer ablation
120 Outgrowth
experiments on immobilized IgLON proteins revealed a rol
121 I started research in high school,
experimenting on immunological tolerance to transplantat
122 As shown in control
experiments on in vitro alphaB- and gammaD-crystallin, 2
123 Experiments on in vitro BMM cultures revealed that KCa3.
124 In situ compression
experiments on individual nanospheres show that the amor
125 1.2 x 10(-9) vs 2.7 x 10(-11) M, saturation
experiments on intact cells).
126 There is an extensive body of
experiments on interactions between DOM and ENPs and als
127 over, examples are presented of pseudo-MS(3)
experiments on ISD fragment ions from RNase B by collisi
128 In recent
experiments on isogenetic cancer cell lines, it was obse
129 sm, and use our ability to perform arbitrary
experiments on it to see if popular data analysis method
130 trophysiological and in vivo hormone profile
experiments on kisspeptin-specific ERalpha knock-out mic
131 We performed a 120 day OM decomposition
experiment on lake water, with an untreated control and
132 ated through examples obtained from physical
experiments on landscape evolution.
133 Animal
experiments on Langendorff-perfused rabbit hearts demons
134 Here we conducted deformation
experiments on lawsonite, while monitoring acoustic emis
135 nthamiana (tobacco) and particle bombardment
experiments on leaves from oilseed rape suggested that A
136 Small-angle x-ray scattering
experiments on lens tissue show colloidal gels of S-crys
137 ves the previous controversies of theory and
experiment on Li2N2.
138 For
experiments on liver tissue, calibration by spiked tissu
139 ehavioral results, taken together with prior
experiments on LTP, strongly support a critical role of
140 diffraction (ND) and x-ray diffraction (XRD)
experiments on magnetically-oriented fibers of Abeta1-28
141 Here we describe
experiments on magnetized DNA-modified electrodes to exp
142 Leaching
experiments on mare basalt 14053 demonstrate that isotop
143 Interestingly, electron microscopy
experiments on mature filopodia indeed frequently reveal
144 Additional
experiments on melting points of wine proteins reveal th
145 Our
experiments on metagenomes assembled from long reads sho
146 Sub-10 fs resolution pump-probe
experiments on methylammonium lead halide perovskite fil
147 m(3) in all cases), consistent with previous
experiments on methylglyoxal.
148 tal sites, and in situ infrared spectroscopy
experiments on Mg2(olz) and Ni2(olz) were used to determ
149 ulosis strains on the outcome of vaccination
experiments on mice and transcriptional responses on M.
150 Experiments on mice show that an enzyme called DNA methy
151 Results of Ni IEK
experiments on mineral phases are fitted with a pseudo-f
152 Recent laboratory
experiments on mixed micro- and macro-pore suggest that
153 Experiments on model systems have revealed that cytokine
154 s partially explained by the push to conduct
experiments on model systems under relevant reaction con
155 A simulation tool runs virtual
experiments on models encoded in CellML, and a website p
156 Transport
experiments on monolayers of Calu-3 cells and studies of
157 Cytotoxicity
experiments on MoS2 nanosheets and molybdate ion control
158 Finally, in vitro
experiments on mouse small intestine show that SGLT1 acc
159 superthin filaments were inferred from early
experiments on muscle, decades passed before their exist
160 ding important insight into a large range of
experiments on nanoscale and quantum plasmonics.
161 Results of
experiments on native Hb variants and engineered, recomb
162 ks from single molecule fluorescence in situ
experiments on nematode embryos where there can be subst
163 Proof-of-principle
experiments on neuronal co-cultures and brain tissues re
164 Our results pose a new challenge for the
experiments on non-Hermitian scattering that have recent
165 Recent
experiments on noncovalent interactions at the nanoscale
166 In
experiments on nonmotile E. coli exposed to polymyxin B,
167 are vital for understanding force unfolding
experiments on nucleosome arrays.
168 resent results from laboratory-based torsion
experiments on olivine aggregates with and without melt,
169 Control AFM
experiments on other lipids and at different temperature
170 We conducted comprehensive
experiments on over 90 large-scale TF-DNA datasets which
171 Here we conducted respirometry
experiments on peacocks and demonstrate that the exagger
172 Experiments on pellicles, or floating biofilms, of Bacil
173 Experiments on plasma-liquid interaction and formation o
174 We further apply the method to an
experiment on pluripotent mouse embryonic stem cells to
175 lectrically detected electron spin resonance
experiments on poly(styrene-sulfonate)-doped poly(3,4-et
176 Corresponding numerical calculations and
experiments on polymer structures made by 3D printing ar
177 ential complication in the interpretation of
experiments on polyproline, used as a molecular ruler fo
178 transcriptome sequencing with common garden
experiments on populations spanning geographical and env
179 A dehydration and re-watering
experiment on potted P. munitum plants corroborated the
180 Our siRNA knockdown
experiments on ProGENI-identified genes confirmed the ro
181 Our
experiments on protein-protein interaction networks demo
182 Recent
experiments on pure fluids have identified distinct liqu
183 We report on a natural field
experiment on quantity discounts involving more than 14
184 We perform several
experiments on raw microscopy image datasets from 8 SCD
185 (1)H and (2)H NMR spectroscopy
experiments on reactions using allylic phosphates showed
186 Experiments on real and simulated data show that the met
187 Our
experiments on real and synthetic networks demonstrate t
188 between many-body theory and low-temperature
experiments on real materials since the early days of qu
189 edictions are quantitatively consistent with
experiments on reconstituted tissues and actomyosin netw
190 Additional feeding
experiments on related silver birch confirmed the SOA re
191 lem, we performed protein binding microarray
experiments on representatives of canonical TF families
192 Predictions are in good agreement with
experiments on ribosomal concentrations and synthesis ra
193 Experiments on rubbing the sample surface using TR mode
194 lid-state nuclear magnetic resonance (SSNMR)
experiments on samples loaded with (13)C-labeled CO2, "u
195 monstrate that the combination of laboratory
experiments on sediment cores, stream reach-scale tracer
196 The methodology has been
experimented on several brain datasets.
197 other DTE analysis methods in our extensive
experiments on simulated data and real data with qPCR va
198 Numerical
experiments on simulated datasets show that DICEseq yiel
199 strain recovery on unloading, while the same
experiments on single-crystalline silver nanowires do no
200 With final functional
experiments on six selected compounds, we confirmed four
201 ethylene hydrogenation, investigated through
experiments on size-selected Ptn (n=8-15) clusters soft-
202 Such oligomers are commonly observed in
experiments on small heat-shock proteins, but their conn
203 Classic
experiments on social groups dealing with truth statemen
204 lie social information use, using a suite of
experiments on social insects as case studies.
205 By testing the theory against
experiments on spherically shaped surfaces, we find quan
206 Indeed, patch-clamp
experiments on split-open tubular segments from the tran
207 large set of equilibrium and nonequilibrium
experiments on squalane and extend them to higher [Formu
208 Indeed, previous
experiments on squirrel monkeys and macaque monkeys show
209 force f, obtained in single-molecule pulling
experiments on src SH3 domain, exhibits upward curvature
210 reference lists of retrieved studies and/or
experiments on SSEP use in postoperative outcomes follow
211 f optimizing future computed tomography (CT)
experiments on still-unrolled Herculaneum scrolls to imp
212 ted by numerical simulations and by in vitro
experiments on straight capillaries, the complex analyti
213 However, behavioural
experiments on subjects with only rod function reveals t
214 performed single-molecule force spectroscopy
experiments on SUMO1/SBM complexes.
215 further validate the phase diagram with our
experiments on surface instabilities induced by mismatch
216 in interpreting the results, from any given
experiment on synaptic plasticity, can be the intrinsic
217 Extensive
experiments on synthetic and real-world networks show th
218 We evaluate our method via
experiments on synthetic data and perform a proof-of-con
219 Using
experiments on synthetic data, we demonstrate that pathw
220 confirm the percolation threshold in static
experiments on synthetic salt samples with x-ray microto
221 spin-spin distance histograms from ESR/DEER
experiments on T4 lysozyme are accurately reproduced.
222 Chromatin immunoprecipitation (ChIP)
experiments on T84 cells, which endogenously express Ano
223 Additionally, a metabolomics
experiment on the central nervous system (CNS) of the fr
224 ency of 1.2 mm monsoon-type watering events)
experiment on the Colorado Plateau, USA.
225 Using a noisy dataset from a pump-probe
experiment on the Coulomb explosion of nitrogen molecule
226 protein structure in the 11th Community Wide
Experiment on the Critical Assessment of Techniques for
227 (Grain Impact Analyser and Dust Accumulator)
experiment on the European Space Agency's Rosetta spacec
228 However, making quantitative contact between
experiment on the one hand and model-parameter dependent
229 e Americas-allows the equivalent of a repeat
experiment on the relation between geography and phyloge
230 within a reaction norm framework by using an
experiment on the three-spined stickleback (Gasterosteus
231 Our neutron-scattering
experiments on the 4f-electron metal Yb2Pt2Pb overturn t
232 analyzed urea-induced folding and unfolding
experiments on the alpha-helical membrane protein Mistic
233 More than two decades ago,
experiments on the antiviral mechanisms of IFNs led to t
234 nanometer ("picocavities"), enabling optical
experiments on the atomic scale.
235 Recent
experiments on the bacterial flagellar motor have shown
236 The calculation is validated by our
experiments on the breakup of Fe3C-plates in Fe matrix.
237 Experiments on the catalytic reaction indicated that NaO
238 We conducted repeat bleaching and recovery
experiments on the coral Montastraea cavernosa, and used
239 High-resolution inelastic neutron scattering
experiments on the cyanobacterium Synechocystis sp. PCC
240 nting for both processes and performed batch
experiments on the desorption kinetics of typical wastew
241 Recent
experiments on the double knockout mice showed, however,
242 However, evidence from community
experiments on the effect of restoration practices on ec
243 gions, we conducted a battery of biophysical
experiments on the EGFR and HER3 tails.
244 Interestingly, colonization
experiments on the eight polymers revealed a large core
245 We report on infrared spectroscopy
experiments on the electronic response in (Sr1-x La x )2
246 Our technique points in a new direction for
experiments on the evolution of performance specialities
247 ions were confirmed with targeted validation
experiments on the functional requirements of nucleopori
248 We argue that
experiments on the Hall coefficient identify the latter
249 d-state counterparts of high-energy collider
experiments on the induced fission of composite particle
250 Contrary to current models,
experiments on the involvement of cyclophilins revealed
251 The results shed light on
experiments on the loss of variability at marker loci in
252 Based on kinetic
experiments on the O-O bond splitting transition of the
253 Laboratory release
experiments on the organochlorine pesticides DDT, DDE, D
254 hat the C8H7NCO anion radical was generated,
experiments on the oxidized product reveal the actual re
255 Experiments on the re-establishment of place fields in d
256 ld and transverse field muon spin relaxation
experiments on the recently discovered caged type superc
257 oscopy and electron energy-loss spectroscopy
experiments on the recovered sample and computer simulat
258 In the
experiments on the RNA-Seq data in The Cancer Genome Atl
259 Human
experiments on the rubber hand illusion implicate simila
260 In
experiments on the same bacterial strain exposed to ampi
261 ferently when different laboratories perform
experiments on the same cell line.
262 med complementary multiple particle tracking
experiments on the same particles, extending significant
263 ical Cell-substrate Impedance Sensing (ECIS)
experiments on the single cell level using morphological
264 Subsequent
experiments on the stoichiometric C(sp(2))-H bromination
265 Here we report our
experiments on the temperature and magnetic field depend
266 Further
experiments on the zebrafish showed that this vertebrate
267 Separate
experiments on thermal degradation of d5-ethyl linolenat
268 photosynthetic systems and describe selected
experiments on these systems.
269 Temperature jump relaxation
experiments on these three mutants reveal two different
270 ms, which may have implications for other IM
experiments on these time scales.
271 further conduct the numerical simulation and
experiments on these two applications.
272 Our
experiments on thin polymer films provide strong evidenc
273 ed second-order nonlinear optical scattering
experiments on thiolate-protected gold clusters (Au130(S
274 ulation trajectories are in accord with both
experiments on this protein, demonstrating that there is
275 hairpin form, giving results in harmony with
experiments on this system.
276 etail to understand previously contradicting
experiments on this topic.
277 Before
experimenting on thousands of potential DNA segments, we
278 er, we present a proof-of-concept validation
experiment on top-view images of 24 Arabidopsis plants i
279 Experiments on top-down mass spectrometry datasets showe
280 Furthermore, recent
experiments on trampling animals and biting crocodiles h
281 used mutagenesis and whole-cell patch clamp
experiments on TRPV3 channels endogenously expressed in
282 his study, we performed binding and blocking
experiments on TV with extended HBGA types and showed th
283 Experiments on two additional protein tyrosine kinases i
284 Experiments on two benchmark datasets for biomedical ent
285 ffs, suggesting melanoma, we carried out our
experiments on two dermoscopy image datasets, which cons
286 k metallic glasses is examined by conducting
experiments on two iron-based in situ metallic glass mat
287 our algorithms with extensive computational
experiments on two large-scale social network datasets.
288 line growth, and demonstrate its validity by
experiments on two well-known glass-forming alloy system
289 Interestingly, rheological
experiments on various in vitro biopolymer networks have
290 Experiments on various porous media including soil and e
291 Our extensive
experiments on various real-world networks, including a
292 Small-scale pilot
experiments on wastewater, thermal printing paper and co
293 Initial
experiments on water oxidation by well-defined molecular
294 The advantages of future X-ray
experiments on water oxidation catalysts, which include
295 The theory was verified by
experiments on well-characterized protein systems.
296 promising platform for transport and optics
experiments on Weyl semimetals.
297 Extensive numerical
experiments on widely-used benchmark functions show that
298 Secondly, we tested field-based eCa
experiments on woody plants across the globe for a relat
299 Using 2-microelectrode
experiments on Xenopus oocytes and patch-clamp electroph
300 ators, and we confirmed this prediction with
experiments on yeast harboring mutations in the Arp2/3 r