1 ations, reaching 76 and 89% atom exchange in
experiments with 0.1 and 1 mM Fe(II), respectively.
2 ials, quasi-experimental studies, or natural
experiments with: (
1) a control group; (2) minimum follo
3 Experiments with (
13)C6 labelled Gal and Glc showed that
4 QC data and
experiments with 14 synthetic reference peptides indicat
5 In a soil incubation
experiment with (
15)NH4NO3, NH4(15)NO3, or Na(15)NO2 ame
6 SIP
experiments using (
15) N methylamine combined with metag
7 In a randomized field
experiment with 1540 children (average age 4.9 years) in
8 Ethylene induction
experiments using 2-(methylthio)ethanol versus sulfate a
9 Pretargeting
experiments with 2 and a novel (99m)Tc-labeled tetrazine
10 Quadrupolar-echo (2)H NMR
experiments with (
2)H-labeled samples showed that fast r
11 esponses to beverage stimuli.We performed an
experiment with 20 healthy-weight individuals who were r
12 resolution, we also performed preincubation
experiments with 5-hydroxy-L-tryptophan and serotonin.
13 An exhaustive spike-in
experiment with 79 metabolite standards demonstrated the
14 We test this argument through an online
experiment with 8,906 users of Airbnb, a leading hospita
15 ictions, we conducted a large-scale mesocosm
experiment using a natural gradient in the concentration
16 he samples were kept frozen during the whole
experiment using a nitrogen cooled sample holder.
17 During a long-term evaporation
experiment with a 15 wt % NaCl solution, the GO leaf dem
18 y 3 to >45 mmol Fe(II) kg(-1) d(-1) over the
experiment with a concomitant increase of an Fe(II) conc
19 tion on native plant fitness in a glasshouse
experiment with a forest invader that produces known ant
20 We conducted an
experiment with a host-parasitoid system to test the pre
21 A preliminary field
experiment with a natural phytoplankton community in the
22 on by comparing a typical quadrupling-of-CO2
experiment with a simulation driven by sea-surface tempe
23 dot patterns used in these roughness coding
experiments using a model of skin mechanics.
24 Experiments using a mutant form of ARF1 affecting GTP hy
25 Here, we review findings from elevated CO2
experiments using a plant economics framework, highlight
26 was estimated from energy-transfer quenching
experiments using a series of organic triplet donors (E(
27 Building on our previous
experiments using a single female pig-tailed macaque as
28 The conducted
experiments with a 10 nm indium tin oxide film, having p
29 Adhesion frequency
experiments with a biomembrane force probe could not det
30 We present a series of
experiments with a combination of promoters, fluorescent
31 two times higher than that for typical bulk
experiments with a commercial rotating ring disk electro
32 We present results from laboratory
experiments with a field portable oxidation flow reactor
33 quantum mechanical computations, comparative
experiments with a fluorocarbon-free alpha,omega-dihexyl
34 Experiments with a klinostat and with inverted stem orie
35 e find strong support for this prediction in
experiments with a marine diatom, Thalassiosira pseudona
36 lars on a regular grid, and complement these
experiments with a matching two-dimensional pore-network
37 r their ability to survive in all nine field
experiments with a mean survival rate of 0.57, ranging f
38 Perturbation
experiments with a miR-218-5p mimic or inhibitor demonst
39 Rescue
experiments with a MOF histone acetyltransferase domain
40 Next,
experiments with a paralyzed strain indicated that the s
41 that controlling the temperature during the
experiments with a precision below 1 K is of importance.
42 Experiments with a ribonuclease-inactive recombinant RNa
43 in the whole plant during independent uptake
experiments with a root-mean-square error (log predicted
44 In preparative electrolysis
experiments with a series of alcohol substrates and the
45 Trapping
experiments with a substituted 1,6-cyclodecadiyne using
46 Parallel
experiments with a trr allele that augments enzyme produ
47 ameters, phase diagram method, and quenching
experiments using acrylamide and iodide.
48 or amine-containing micropollutants in batch
experiments with activated sludge that has so far gone u
49 djusted by using the available data from the
experiment with adipose-derived stem cells subjected to
50 NMR
experiments using advanced bioreactors have advantages w
51 Results from
experiments using AGO2-loaded miRNAs in duplex with targ
52 Experiments with alpha-boryl acetals containing a latent
53 Additional
experiments with altered oxygen concentrations in condit
54 Experiments using ambient pressure X-ray photoelectron s
55 ChIP-sequencing
experiments using an anti-O-GlcNAc antibody revealed sig
56 Here authors perform
experiments using an in situ scanning electron microscop
57 We perform
experiments using an in situ scanning electron microscop
58 However, lineage-tracing
experiments using an inducible Tbx18-CreERT2 line reveal
59 Analogous
experiments with an antagonist (prochlorperazine) and a
60 curs despite the presence of antiscalants in
experiments with and without shale contact and is driven
61 Experiments using antibiotics to cure the endobacterium
62 Experiments using antibody transfer indicate that antibo
63 Meat binding
experiments with beef and pork were performed using a te
64 By combining in vitro
experiments with bioinformatic and RNA-seq data, metabol
65 Mass spectrometry-based affinity capture
experiments with biotin-linked derivatives revealed a nu
66 Other
experiments with bone marrow chimeras revealed that infl
67 Experiments with both synthetic and our real data demons
68 polymorpha and Physcomitrella patens UVR8 in
experiments with bryophyte tissue and expression of gree
69 In addition,
experiments with Btk-null B cells revealed off-target ef
70 We performed three separate
experiments with bumblebees (Bombus terrestris), where t
71 Kinetic and circular dichroism
experiments with C69G-GES-5 demonstrate that this small
72 We designed an in vitro
experiment with calcium phosphate with different SDF con
73 Rescue
experiments with catalytically inactive mutants of MOF s
74 On the basis of these experiments and on an
experiment with CBZ-10,11-epoxide a transformation pathw
75 Experiments using CD11b/CD18 integrin-deficient (CD11b(-
76 Experiments with cell culture medium showed that virus i
77 Single-forcing
experiments with changed inputs, temperature, and moistu
78 Experiments with clusters of tumor cells compartmentaliz
79 We perform a reactive transport
experiment using CO2-saturated brine at reservoir condit
80 ies are using research interfaces to conduct
experiments with cochlear-implant (CI) users.
81 n model, we performed co-immunoprecipitation
experiments with combinations of ARTEMIS mutants.
82 n blot experiments and compared to analogous
experiments using commercially available antibody-conjug
83 global vortex structure, we match theory and
experiment using computer vision methodologies to determ
84 e, we combine insights from recent microbial
experiments with concepts from lattice-field theory and
85 In
experiments with conditional ATOH1 mouse mutants crossed
86 20 equiv NH3 per Os center in a single batch
experiment using Cp*2Co and [H2NPh2][OTf] as reductant a
87 hnical difficulties in performing controlled
experiments with currently available neuroimaging method
88 y comparing the results from this laboratory
experiment with data compiled from 210 soils representin
89 Optical pulse-chase
experiments with Dendra2-tagged aSyn versions indicated
90 series of primordial-soup Miller-Urey style
experiments with deuterated gases and reagents to compar
91 Experiments with deuterated substrates are also shown he
92 In situ NMR
experiments with deuterated substrates show that H2 is f
93 MS(2)
experiments using different ion activation techniques va
94 Internalization
experiments with different cell lines, well-differentiat
95 Crossflow rejection
experiments with dilute feed composition indicate that b
96 Experiments with DNA containing abasic sites and polyeth
97 e Forster resonance energy transfer (smFRET)
experiments using donor-labeled Rev and acceptor-labeled
98 ct mechanism by conducting photoinactivation
experiments with eight health-relevant bacterial species
99 On the basis of
experiments using either soft or less-intense hard X-ray
100 y dTL as an important variable in thin-layer
experiments with electrochemical reactions and FTIR read
101 However, in practical
experiments using electrons either the maximum collectio
102 Control
experiments using enantioenriched 3-hydroxy-2-oxindole s
103 t studies have attempted to merge ecological
experiments with epigenetic analyses to elucidate the co
104 or populations that arose during a long-term
experiment with Escherichia coli, in which populations h
105 velopmental ontogeny, we conducted a mapping
experiment using Euphrates poplar (Populus euphratica),
106 trometry of exhaled breath and UHPLC-HRMS/MS
experiments using exhaled breath condensate, respectivel
107 Practical
experiments with extraction time 16.00min, ethanol conce
108 F(ab')2 targets, as confirmed by inhibition
experiments with F(ab')2 fragments and hinge peptides.
109 Here we present X-ray diffraction
experiments with femtosecond resolution that capture in
110 Experiments with ferrous iron or anthrahydroquinone-2,6-
111 development of the example qAOP was based on
experiments with FHMs exposed to the aromatase inhibitor
112 e, and Mg- and Ca-bearing siderite formed in
experiments with flood basalt.
113 Analysis of DC maturation markers, tracking
experiments with fluorescently labeled cells, and use of
114 ched particle beams as well as time-resolved
experiments with free-electron beams.
115 Leaching
experiments with freshly crushed granodiorite, the domin
116 Interestingly, co-culture
experiments with FTD astrocytes revealed increased oxida
117 Our
experiments with full-length Cya and its cytosolic domai
118 can provide useful frameworks for testing by
experiment with fundamental insights provided by theory.
119 the same experimental conditions in separate
experiments using Fura-4AM.
120 DNA binding
experiments using gel-shift and ChIP assays demonstrated
121 A series of adoptive transfer
experiments with genetically engineered donors and recip
122 We initiated laboratory evolutionary
experiments with genotypes carrying different versions o
123 m calls using a combination of lab and field
experiments with great tits (Parus major), a songbird th
124 Localization
experiments using green fluorescent protein fusion const
125 Experiments using HDAC11 knockout (KO) mice revealed tha
126 We performed coculture
experiments using healthy monocytes with exosome-package
127 Prolonged presence of S(-II)aq in
experiments with hematite in combination with a larger r
128 Experiments with heterologous expression systems show th
129 Two independent brain imaging
experiments using high-resolution fMRI revealed that the
130 ying conditionally essential genes in Tn-Seq
experiments with high detection sensitivity and specific
131 es allows one to perform competition binding
experiments with high sensitivity while avoiding signal
132 ine state of the art laboratory permeability
experiments with high-resolution X-ray computed tomograp
133 Rejection
experiments with higher ionic strength and different com
134 elucidate mechanisms, we conducted in vitro
experiments with HSCs infected with adenoviral vectors e
135 lly important for designing and interpreting
experiments with Hsp90.
136 We performed a co-culture
experiment with human metastatic melanoma cell line (SKM
137 g regions derived from ChIP-seq/ChIP-exo-seq
experiments using human and mouse cells.
138 Experiments using human genotyped livers showed an inter
139 ation including animal research and in vitro
experiments using human vascular cells and plasma from s
140 (55)Fe-radiolabeling
experiments with human cells depleted of CIA1, CIA2A, CI
141 Using batch
experiments with human fecal material as substrate, we a
142 Rescue
experiments with human tau expression restored MT bundli
143 he predictions made by macaque studies in an
experiment with humans with frontal lobe lesions, asking
144 Experiments with IEC organoids demonstrated that IEC exp
145 Eight
experiments using incentivized real effort tasks found t
146 Competition
experiments using increasing ethanol concentrations on n
147 Here, different
experiments with individual NTs coupled with first-princ
148 Experiments with inhibitors of protein kinase G (PKG), p
149 ay rule" for embryo research stipulates that
experiments with intact human embryos must not allow the
150 curve in small-angle X-ray scattering (SAXS)
experiments using isolated GluA2 ligand-binding domain (
151 ProteoModlR is intended for the analysis of
experiments using isotopically labeled reference peptide
152 Analogous
experiments with K2PtCl4/K2PdCl4 mixtures show PdCl2 tra
153 to execute and analyze live-cell microscopy
experiments using KTRs.
154 However,
experiments with Kv1.3 KO rats and Kv1.3 siRNA knockdown
155 we have performed a comprehensive proteomics
experiment using label-free quantitative mass spectromet
156 Here we conduct a microcosm
experiment with laboratory protist community subjected t
157 e substances were assessed in targeted batch
experiments using laboratory-scale biofilm reactors oper
158 ailable soil nitrogen (N) by combining field
experiments with laboratory manipulations from sites exp
159 In addition, during coinfection
experiments with Legionella pneumophila, we found that d
160 m are limited because they largely come from
experiments using limited numbers of species [3], mesoco
161 ver, this mechanism was challenged, based on
experiments with lipid vesicle-incorporated gA under con
162 Cross-linking
experiments with liposome bound Atg18 yielded several PE
163 In neutron scattering
experiments with liposomes in the presence or absence of
164 ystem very efficient for instance for 2D NMR
experiments with long mixing times.
165 Relaxation and self-diffusion
experiments using low-field NMR spectrometry provided im
166 of the current understanding comes from the
experiments with low levels of chemotactically active li
167 Experiments using LPS-activated primary macrophages reve
168 e-substrate complex as indicated by cleavage
experiments with lysosomal enzymes (Tritosomes).
169 ibrated and validated with 2-year lysimetric
experiment with maize.
170 Control
experiments using maleic acid (cis-butenedioic acid) and
171 rnation causes reduced synaptic activity and
experiments with mammals reveal that this can have adver
172 By mirroring each
experiment with MD simulation, including "simulating syn
173 otolysis experiment is confirmed by trapping
experiments with methyl 1-methylpyrrole-2-carboxylate (6
174 plified by a D2-like receptor antagonist and
experiments with mice with targeted deletion of D2 recep
175 increases toward the equator, using a global
experiment with model caterpillars to measure predation
176 Experiments with model sensitizers and DOM isolates reve
177 Here we combine PELDOR
experiments with molecular dynamics (MD) simulations to
178 Here we combine nanoscale
experiments with molecular-level simulation to study the
179 In contrast to
experiments with monochromatic radiation, data from only
180 study, we conducted SILAC mass spectrometry
experiments with mononucleosomes and identified multiple
181 1, DPY19L3, and DPY19L4) and complementation
experiments with mouse homologs showed that DPY19L1 pref
182 Data mining of RNA-Seq
experiments with mouse models of intestinal HIF-2alpha o
183 s the detection of DMRs in large methylation
experiments with multiple groups of samples in minutes r
184 fy as specific gaps in current understanding
experiments with multiple levels of modifier species and
185 Experiments using murine macrophages showed that FPW ext
186 Rescue
experiments with mutated KRas 3'UTR showed very signific
187 In patch-clamp
experiments using native cerebral arterial myocytes, mem
188 We selected studies that conducted
experiments with native and NIS under common environment
189 Experiments with natural accessions and crosses between
190 Ex vivo microperfusion and in vitro
experiments with NEFA-bound albumin at concentrations th
191 Our
experiments with non-dissociating mutants of fluorescent
192 2PPM
experiments with non-mutated fluorescently labeled Galph
193 Finally,
experiments with often used penetration enhancer thymol
194 Magnesite formed in
experiments with olivine, and Mg- and Ca-bearing siderit
195 In our
experiments with Ononis spinosa, alpha-onocerin was dete
196 It is shown from theory and
experiment using open-air whole-season elevation of atmo
197 in pathophysiology and controlled laboratory
experiments with other living systems, which can flip fr
198 ons with cyanide as nucleophile, preliminary
experiments with other nucleophiles foreshadow the broad
199 Competitive inhibition
experiments with other pneumococcal hTSP-1 adhesins demo
200 However,
experiments with other soils and biochars will be requir
201 Both survival and competition
experiments with outbred CD1 mice demonstrated that PEG3
202 Finally, in vivo
experiment using OV202 Sh1 derived xenograft show that A
203 Additional in vivo
experiments using P. berghei infected mice showed that a
204 Experiments using parabiotic mice fed a high-fat diet (H
205 ere used for in vitro concentration-response
experiments with PB, cetacean and seal spp. immune cells
206 Experiments with permeabilized human myocardium demonstr
207 Experiments with pharmacologic inhibitors were performed
208 cule fluorescence and in vitro cross-linking
experiments with photo-activatable unnatural amino acids
209 mportance that the properties of DOM used in
experiments with PM, in particular the molecular weight
210 amine reactants are employed in competition
experiments using polar solvents, such as DMF, no "mixed
211 Here we combine extensive crossing
experiments with population and functional genomic data
212 ant-pathogenic virus, we performed evolution
experiments with Potato virus Y (PVY) in potato genotype
213 In co-culture
experiments with primary human T cells, epithelial cells
214 Extensive
experiments using publicly available gene expression pro
215 Here, in a series of
experiments using purified proteins from mammalian cells
216 Experiments with purified AQP0 reconstituted into liposo
217 In vitro reconstitution
experiments with purified cyt b6f and recombinant Stt7 k
218 In vitro
experiments with purified P450s were conducted as well.
219 In vitro
experiments with purified recombinant CYP46A1 indicated
220 ease of oxidized aliphatic chains from CL in
experiments with purified recombinant iPLA2gamma, germ-l
221 Biochemical
experiments with purified recombinant proteins show that
222 Experiments with purified sGC in the presence of Tween 2
223 Careful
experiments with purified water already show large inter
224 In vivo and in vitro labeling
experiments using radiolabeled GPI precursors showed tha
225 aracterized by in vitro displacement binding
experiments with rat brain membranes, in vitro autoradio
226 the MALDI/ESI interface has been employed in
experiments with rat brain sections and was shown to be
227 In
experiments with rat neuroendocrine cells, we find that
228 Kinetic
experiments using reaction progress kinetic analysis pro
229 estigated by integrating flow-through column
experiments with reactive transport modeling, and electr
230 asophil leukemia assay, T-cell proliferation
experiments using recombinant wildtype Cyp c 1, and over
231 in pigs in detail have been limited because
experiments with regular-sized pigs are difficult to per
232 these two Fe phases was tested using mixing
experiments with river water and artificial seawater.
233 R10J5, as demonstrated by receptor knockdown
experiments using RNA interference.
234 Complementary ex situ chemical oxidation
experiments with [
Ru(bpy)3](3+) furthermore indicate tha
235 Dynamic column
experiments with sediment from the Sellafield nuclear fa
236 We planted a common garden
experiment with seeds collected from natural populations
237 A field
experiment with seven precipitation treatments (i.e. fro
238 Experiments using several inhibitors of IGF-1 receptor s
239 O-SPR sensors were then subjected to sensing
experiments with several alcohol vapors to establish the
240 We perform microchannel
experiments with SHSs consisting of stream-wise parallel
241 Experiments with single plasmid topoisomers showed that
242 t chimeric constructs between BGT1 and GAT3,
experiments with site-directed mutated transporters, and
243 A refreshing empirical
experiment with snails supports this long-standing hypot
244 rganosulfur species formed in photooxidation
experiments with SO2 are present in the SOA particles.
245 mine the recorded signatures, we carried out
experiments with spheres impacting at the surface of a w
246 Experiments using stabilized pH conditions revealed the
247 Control
experiments with stiffer, gel-phase 1,2-dipalmitoyl-sn-g
248 ulations to reconcile recent single-molecule
experiments with structural data and provide a consisten
249 The results of DFT calculations and
experiments with substituted styrenes indicate that the
250 Despite its small scale, an
experiment with such high resolution data allows us to b
251 doping in electric double-layer (EDL) gating
experiments with superconducting cuprates, our work show
252 novel methodology that iteratively combines
experiments with systems modeling analysis is essential
253 pable of influencing interpretations of many
experiments using targeted genome manipulations such as
254 A trapping
experiment with TEMPO is consistent with C-N bond format
255 ng and reimprisonment, we leverage a natural
experiment using the random assignment of judges with di
256 s became fixed early while bees continued to
experiment with the order of later visits.
257 reatest soil water loss was observed for the
experiment with the smallest spacing where competition d
258 We carried out glasshouse
experiments using the California-native shrub Baccharis
259 ions of generosity in a series of controlled
experiments using the dictator game.
260 Experiments using the model system Arabidopsis thaliana
261 Early preclinical
experiments using the non-obese diabetic (NOD) mouse mod
262 In fact, based on
experiments using the self-interacting FM domain, it app
263 Culturing
experiments with the alga showed that host glutamine may
264 gene drives due to recent proof of principle
experiments with the CRISPR-Cas9 system as a drive mecha
265 In two evolution
experiments with the facultatively sexual rotifer Brachi
266 ts kappaobs) were collected from competition
experiments with the faster reactions of 2 in THF and th
267 challenged by ultrafast optical spectroscopy
experiments with the Fenna-Matthews-Olson protein, in wh
268 st dynamic range in ratiometric FRET imaging
experiments with the G-protein sensor.
269 Experiments with the green alga Chlorella vulgaris prese
270 By conducting in vivo and ex vivo
experiments with the immunocompetent TC-1 murine tumor m
271 Experiments with the use-dependent NMDAR blocker, MK-801
272 g the effects of As on plants should include
experiments with thiolated As species.
273 Time courses for biological
experiments using this hydrogel are variable, and thus t
274 Initial
experiments using this method to sequence E. coli genomi
275 we apply these models to a data set from an
experiment with three mixed blocks of pro- and antisacca
276 Experiments using TM domains from other receptors, EGFR
277 results were validated in functional rescue
experiments using transgenes expression in EPCs from ret
278 Experiments with trapped ions demonstrate how spectral l
279 Experiments using Trib1 (-/-) mice that had a depleted a
280 Notably, in vitro
experiments with trophoblasts showed increased productio
281 Experiments with truncated forms of talin confirm the me
282 Our TUNEL
experiments using tunicamycin, an apoptosis inducer, and
283 cture, we generated a RNA-sequencing mixture
experiment using two cell lines of the same cancer type.
284 Here, we perform mixture
experiments using two different sets of spike-in RNA to
285 findings were confirmed with pharmacological
experiments using two selective NOP antagonists, SB-6121
286 Fluorescence
experiments with two hydrophobic fluorescent probes esta
287 We demonstrate, in closed-loop
experiments with two rhesus macaques, that after the los
288 The
experiments with two segmentation workflows show that th
289 Second, we consider thought
experiments using universal linear optical machines, whi
290 through simulation and in a proof-of-concept
experiment using unstructured peptides under slow-exchan
291 Control HX-MS
experiments using unstructured peptides labeled at pD 4.
292 on the degree of cross-linking by performing
experiments with varying formaldehyde concentrations.
293 We analyzed over 4,000 samples in
experiments with varying near-physiological GnRH concent
294 Further
experiments with varying regeneration and adsorption con
295 confirm the predicted exponential growth in
experiments using vibrated grains under microgravity, an
296 Through mathematical modelling and
experiments with Vibrio cholerae, we show how killing ad
297 For
experiments with water flow containing a disinfectant to
298 Experiments with wild-type seeds extended by mutant mono
299 vironmental changes, we conducted a mesocosm
experiment with wood frogs (Rana sylvatica) in the Canad
300 edicted computationally and confirmed in our
experiments using X-ray diffraction and atomic resolutio