1 expressed in these sensory neurons, and that
experimental ablation of neuronal Shh expression causes
2 ans and macaques was increased following the
experimental addition of haemoglobin (Hb) or ferric iron
3 Using data from 7 years of
experimental Air and Soil warming in moist acidic tundra
4 rties, the authors have demonstrated by both
experimental analysis and numerical modeling that these
5 We evaluated our procedure on three
experimental and 300 simulated data sets and showed that
6 Our
experimental and analytical approaches are important alt
7 pe exchange is obtained from a comparison of
experimental and calculated NMR data.
8 reening and titration of infectious virus in
experimental and clinical samples, independent of ebolav
9 We demonstrate the combined
experimental and computational approach for de novo sequ
10 ow a systems pharmacology approach combining
experimental and computational methods can guide antibio
11 nd may have broad interest in combination of
experimental and computational methods for enantiosensin
12 Both
experimental and computational studies find that 2D CTGU
13 The
experimental and computational study here of a beta-keto
14 he etiology of EOC remains elusive; however,
experimental and epidemiologic data suggest a role for h
15 In agreement with previous
experimental and modeling studies, key factors influenci
16 essing fluorescent proteins and a multiscale
experimental and numerical approach.
17 istributions holds continentally by relating
experimental and observational data of drought-induced m
18 A comparison of
experimental and predicted drug release data revealed th
19 ation by a previously unknown native moth in
experimental and restored populations suggests the poten
20 Here, we present a detailed
experimental and theoretical investigation accounting fo
21 Both
experimental and theoretical results agree that ZnCu und
22 Here, we review a broad range of
experimental and theoretical results suggesting that goo
23 Combined
experimental and theoretical studies of electrosensory s
24 Experimental and theoretical studies of the C-H aminatio
25 The proposed mechanism is supported by both
experimental and theoretical studies.
26 iew also highlights the benefit of combining
experimental and theoretical studies.
27 e focus of this review is on the most recent
experimental and theoretical work on photoinduced transf
28 We compare
experimental (
and random phase approximation) reference
29 The parallel between
experimental animal and observational human data lends s
30 y counteracted acute lung eosinophilia in an
experimental animal model.
31 Increased levels of 20-HETE in
experimental animals and in humans are associated with h
32 ely applicable to supplement high-throughput
experimental antibody sequencing workflows.
33 O2 solubility was measured using a home-made
experimental apparatus based on changes of CO2 partial p
34 Our novel
experimental approach accurately models human NBL and es
35 membrane molecules and highlight a powerful
experimental approach to decipher specific influences on
36 sent study demonstrates the potential of our
experimental approach to study predator-prey relationshi
37 However, the
experimental approaches are not only time consuming, but
38 We combined computational and
experimental approaches to compare energy metabolism in
39 ion within a mutualism using theoretical and
experimental approaches with a synthetic anaerobic cocul
40 not only new insights but also a plethora of
experimental approaches, sometimes reaching conflicting
41 lesional inflammasome activation and reduced
experimental atherosclerosis.
42 ral stem/precursor cells (NPCs) in mice with
experimental autoimmune encephalomyelitis (EAE) impairs
43 ll as PLP138-151-induced relapsing-remitting
experimental autoimmune encephalomyelitis (EAE) mice.
44 We used a murine model of MS,
experimental autoimmune encephalomyelitis (EAE), to eval
45 vivo, RGC-32(-/-) mice display an attenuated
experimental autoimmune encephalomyelitis phenotype acco
46 leviate and even prevent signs of disease in
experimental autoimmune encephalomyelitis, as well as ma
47 it lesions in rhesus monkey brain induced by
experimental autoimmune encephalomyelitis, which is the
48 tant in the order of 10(-4) s(-1) despite an
experimental barrier of Ea =4.8 kcal mol(-1) and with on
49 ll, as is currently prevalent in preclinical
experimental biomedicine.
50 PA, it did not degrade fibrinogen or enhance
experimental bleeding.
51 e validity (%CV) was provided in half of the
experimental blocks to prompt updating of prior expectat
52 Experimental breakthrough curves further demonstrate the
53 sonators remains largely unexplored, and its
experimental characterization is challenging.
54 The
experimental characterization of wave motion in lattice
55 ons, which can facilitate and expedite their
experimental characterization.
56 Experimental CMV-based vaccine vectors expressing a sing
57 sion and severity of autoimmune diseases and
experimental colitis.
58 e good agreement between the theoretical and
experimental collision frequency of individual Pt nanopa
59 il induces tumor-suppressing effects against
experimental colon cancer.
60 ity to predict nitrate concentrations in the
experimental columns.
61 To test for such influences, we assembled
experimental communities of wood-decomposing fungi using
62 This detailed
experimental comparative study represents a fundamental
63 tion of immortalized cell lines and relevant
experimental components.
64 ions and reliable dynamic predictions in new
experimental conditions (i.e. not used in the training).
65 previous models included a broad spectrum of
experimental conditions and dealt only with loading, her
66 strains were grown in culture under the same
experimental conditions and identified by molecular PCR
67 is work demonstrates for the first time that
experimental conditions optimized for SRM 955c (caprine
68 The results indicate that under
experimental conditions the catalytically active species
69 d yield), in short reaction times under mild
experimental conditions using a slight excess (1.5 equiv
70 Under the optimal
experimental conditions, the preconcentration factors in
71 ved in ensemble measurements under analogous
experimental conditions.
72 hydrophilic/phenolic antioxidants under our
experimental conditions.
73 aided drug discovery methods under identical
experimental conditions.
74 ng among the very few publications providing
experimental confirmation to the theory describing react
75 We outline some
experimental consequences of our results.
76 eks/months) without the need for restrictive
experimental control.
77 ate our model, we systematically manipulated
experimental correlates of parameters in the model: subs
78 Experimental crystallization textures closely resemble t
79 calibrated by existing in vivo and in vitro
experimental data and can be used over a wide range of f
80 Despite enthusiastic agreement that
experimental data are directly relevant for determining
81 The
experimental data are supported by a model to show how o
82 Diffusivity was extracted from
experimental data based on "regular regime approach".
83 The model predictions were compared with the
experimental data for specific porous media and good agr
84 vide insight into binding modes in line with
experimental data for these receptors.
85 APSIM accurately reproduced
experimental data from the Soybean Free-Air CO2 Enrichme
86 mately 6.5 provides an excellent fit for the
experimental data of liquid argon, for a range of thermo
87 All of our
experimental data stay within these physical boundaries
88 data and analysis tools with other types of
experimental data such as RNA-seq or ChIP-seq.
89 Our clinical and
experimental data suggest a correlation between age at d
90 Overall, our
experimental data suggest that CLIP170 serves as an intr
91 Genetic and
experimental data suggest that efferocytosis is impaired
92 Our
experimental data suggest that reversible protonation of
93 e in better agreement with the benchmark and
experimental data than are the NSF results in all studie
94 ction has been gained from the comparison of
experimental data to receptor models.
95 ionally heterogeneous systems by integrating
experimental data with a priori information.
96 d compare biological networks, inferred from
experimental data, in a fast and principled way.
97 phic modelling, grounded in observational or
experimental data, is therefore necessary to better unde
98 Consistent with
experimental data, MD runs in the absence of Ca(2+) and
99 hods for physics-based, knowledge-based, and
experimental data-directed modeling for RNA structures a
100 nd to predict morphologies in agreement with
experimental data.
101 benchmarking the method against independent
experimental data.
102 that satisfies the many constraints from our
experimental data.
103 ion accessibility from the analysis of these
experimental data.
104 or power-law rheology (PLR), best suits the
experimental data.
105 distance, both in polymer simulations and in
experimental data.
106 a bi-layer structure qualitatively fits the
experimental data.
107 comparisons between several theoretical and
experimental datasets, we assign an error of 1.1-1.2 log
108 From whole organ to single fibre levels,
experimental demands and hardware requirements increase,
109 Serious problems in the
experimental design and data interpretation raise concer
110 Furthermore, we discuss key
experimental design considerations, including the choice
111 Using a longitudinal
experimental design, we quantified the ontogenetic profi
112 Our results suggest that new
experimental designs targeting a majority of inhibitory
113 ives that may suit various biological goals,
experimental designs, and laboratories' preferences.
114 ods to reduce the number of subjects, refine
experimental designs, and replace live animals.
115 studies using rigorous experimental or quasi-
experimental designs.
116 of electrons generated by CRAND provides an
experimental determination of the neutron density in nea
117 Experimental discovery of such solitons is hindered by t
118 Here we report the
experimental discovery of two structure types by computa
119 aking WSMs, despite numerous theoretical and
experimental efforts, few examples have been reported.
120 cell fate computation, in order to influence
experimental efforts, which may in turn influence the ou
121 Computational simulation of the
experimental EPR spectra, using a developed algorithm fo
122 use of a nonaqueous matrix solution allowed
experimental error to be minimized to within 1% RSD.
123 eover, the fitted parameter values represent
experimental evaluation of the magnitudes of most physic
124 re and the walls of the container, clear-cut
experimental evidence for this prediction is lacking.
125 Despite such interest in nano-optics, no
experimental evidence of Fano interference was reported
126 and fluorescence measurements, and obtained
experimental evidence suggesting a complex mechanism in
127 Experimental evidence supporting this hypothesis shows t
128 for a central pattern generator, and recent
experimental evidence that proprioception drives locomot
129 Here we use
experimental evolution to test the predictability of evo
130 Despite long theoretical and
experimental exploration, the nature of the triplet-pair
131 The
Experimental Factor Ontology (EFO) is an application ont
132 BAL-H in its aggregation states support this
experimental finding.
133 These
experimental findings are rationalized by transport calc
134 Our
experimental findings are supported by quantum chemical
135 The interpretation of the
experimental findings was supported by state-of-the-art
136 rrier and rate constants are consistent with
experimental findings.
137 of 1.5 typhoons/decade) impacting the Fushan
Experimental Forest, Taiwan.
138 Using a quantitative
experimental framework to determine in vivo tumorigenic
139 with TP53 mutations should be considered for
experimental frontline trials exploring novel agents.
140 e NMDA-DeltaCa(2+) responses between the two
experimental groups.
141 We have developed an
experimental growth system that enables the collection a
142 thors, reviewers, editors and funders to put
experimental guidelines into practice.
143 Experimental heats of formation and enthalpies obtained
144 Experimental hemimandibles exhibited lower rates of memb
145 Using simulated and
experimental Hi-C data, we show that domains identified
146 Using
experimental HIC data along with the estimated surface a
147 t important threats to genome stability, but
experimental identification of these gaps has proved cha
148 ent response model, fully parameterized with
experimental imaging data, to describe doxorubicin uptak
149 behavior in realistic physical models and in
experimental implementations.
150 lent cations upon A.C protonation, providing
experimental indication of the preferential localization
151 A quasi-
experimental instrumental variables probit model of the
152 We present systematic,
experimental investigations of this effect in four field
153 established infection and improve outcome in
experimental IPA.
154 assign one specific molecular formula to an
experimental isotopic pattern.
155 h resource abundances (leaf litter) using an
experimental landscape of mesocosms, and assayed coloniz
156 c structure of ST12-Ge (tP12, P43212) due to
experimental limitations in sample preparation and varyi
157 Experimental manipulations that reduced ambient levels h
158 sults obtained are quite consistent with the
experimental map.
159 Experimental measurements and bioinformatic analyses sug
160 new method (called REPPS) for incorporating
experimental measurements of growth rates and extracellu
161 have been investigated by making a series of
experimental measurements, coupled with simulations in Z
162 From the model and the
experimental measurements, the shear stress exerted by t
163 reflections have been perfectly verified by
experimental measurements.
164 phasize the power of direct observational or
experimental measures of recovery over indirect statisti
165 ody, lung, kidney and liver metastases in an
experimental metastases mouse model.
166 These results provide an
experimental method for determining the polaron relaxati
167 Tn-Seq is an
experimental method for probing the functions of genes t
168 Here we use a novel in situ
experimental method involving olivine micro-reactors and
169 ry to characterization due to the paucity of
experimental methods able to probe the mobility and dens
170 However,
experimental methods to identify associations between ln
171 Two different
experimental mixtures composed of fluorescent and nonflu
172 ung squamous cell carcinoma (LSCC) and in an
experimental model of lung TLS induction.
173 Our unique
experimental model which incorporates genetic effect, na
174 ion of HDAC6 improved established PAH in two
experimental models and can be safely given in combinati
175 uantify occurrence of extracellular traps in
experimental models and human samples.
176 Studies in
experimental models of anti-MPO GN suggest that, after A
177 Here, we used theoretical considerations and
experimental models of immune responses in vitro and in
178 and conditionally delete C5aR2 expression in
experimental models of inflammation.
179 On the basis of a number of
experimental models, several alternative cell types have
180 ble vascular scaffold [BVS]) using different
experimental models.
181 ed informatics or can only be used in single
experimental models.
182 ical inhibition, ameliorate skin fibrosis in
experimental mouse models.
183 Validation against approximately 600
experimental mutations indicated that our meta-predictor
184 accumulated in oPOM at a greater rate under
experimental N deposition, relative to the ambient treat
185 task for computing professionals rather than
experimental neuroscientists.
186 This is the first
experimental observation of Bi-B double and triple bonds
187 their internal dynamics have escaped direct
experimental observation.
188 Based on
experimental observations and DFT calculations, evidence
189 Overall, our
experimental observations and physical model establish g
190 retical calculations allow us to explain the
experimental observations and to give experimentally tes
191 for the visual and accurate determination of
experimental one-bond proton-carbon coupling constants (
192 and prevented retinal ganglion cell loss in
experimental optic neuritis, with reduced inflammation a
193 n (EGFP) as a model protein, we carry out an
experimental optimization of the ITP-based immunoassay a
194 needed, particularly studies using rigorous
experimental or quasi-experimental designs.
195 ance imaging included a resting state and an
experimental paradigm focusing on the anticipation of ac
196 After systematic optimizations of
experimental parameters (the components of running buffe
197 Moreover, we showed that sFRP5 blocks
experimental periodontal inflammation and bone loss, sug
198 and their stabilities for a wide variety of
experimental photoelectrodes for water reduction.
199 ed between fish and mammals and establish an
experimental platform for studying how evolutionarily di
200 To explore these questions,
experimental platforms are needed that can extensively a
201 To date, however, there has been no direct
experimental probe of these dark excitons.
202 are all detected and identified in a single
experimental procedure.
203 As researchers design their
experimental projects, one major challenge is to find th
204 This work presents the
experimental proof which validates the hypothesis of a p
205 negative effects have been criticized as the
experimental protocol did not perfectly simulate real-li
206 We demonstrate that currently existing
experimental protocols allow the measurement of an IR sp
207 Furthermore, standard
experimental protocols are insufficient to quantify the
208 an arbitrary pattern into DNA sequences and
experimental protocols, our assembly method is readily a
209 fusions are limited by tedious and prolonged
experimental protocols, thus limiting their use as rapid
210 ce of long-lasting forms of LTP for multiple
experimental protocols.
211 osteochondral defects of the knee joints of
experimental rats and calvarial defects of Jax mice.
212 We observed similar results with
experimental reads for NA24385, an individual whose germ
213 The
experimental regimens kill M. tuberculosis much more rap
214 iency, extraction yields of metabolites, and
experimental reproducibility.
215 nformatics research methods and traditional,
experimental research methods have strengths and weaknes
216 However, in two-dimensional materials,
experimental research on nodal line fermions is still la
217 Our combined
experimental results and density functional theory (DFT)
218 We present the
experimental results and the simulations regarding pairs
219 Preliminary
experimental results are obtained for generating 1.8-4.2
220 matical model shows excellent agreement with
experimental results for silk with various diameters: 50
221 Our
experimental results identify differences in the binding
222 Because the
experimental results reported in the literature are high
223 The analysis and
experimental results show the observed error is the resu
224 The
experimental results showed that the one-calibrant kinet
225 Experimental results suggest that the reaction likely pr
226 The opposed defined-pathway model stems from
experimental results that show that proteins are assembl
227 nescence measurements were conducted and the
experimental results were compared to molecular docking
228 We combined these
experimental results with anatomical data to create a mu
229 Together with
experimental results, a combination of theoretical model
230 The
experimental results, compared with four benchmark metho
231 on state model is also in agreement with the
experimental results.
232 lose resemblance between the simulations and
experimental results.
233 olding cyclic amplification (PMCA), by using
experimental scrapie and human prion strains as seeds an
234 Through a combination of rigorous
experimental screening and in silico virtual screening,
235 To limit degeneracy and increase
experimental sensitivity, we combined specific and segme
236 MS and 11 healthy controls (HCs) underwent 3
experimental sessions (baseline, real-rTMS, sham-rTMS),
237 g electrical activity from single neurons in
experimental sessions.
238 were rigorously investigated in an in vitro
experimental setup that mimics the human circulation.
239 ueen, and therefore cannot be used to devise
experimental setups.
240 An
experimental strategy has been developed to increase the
241 ntuition and insights that will inform their
experimental strategy.
242 beta-adrenergic receptor antagonism after
experimental stroke prevents loss of splenic MZ B cells,
243 -aromatic stacking interactions by analyzing
experimental structures of urea transporters and protein
244 Principal component analysis on 38 GroEL
experimental structures yields the most important motion
245 sociation parameters from a meta-analysis of
experimental studies (SSBs and weight change), a meta-an
246 larger spatial and temporal scales than most
experimental studies do.
247 Experimental studies in allo-HCT animal models have show
248 combines computational predictions with new
experimental studies in mice to identify plausible mecha
249 Experimental studies on the origin of the backward oxida
250 In vivo
experimental studies show that LOX overexpression in col
251 Preclinical and
experimental studies show that PDE5 inhibitors (PDE5is)
252 Insights from
experimental studies support causal effects of maternal
253 nd future climate; we highlight the need for
experimental studies to identify the mechanisms underlyi
254 Here we combine observational and
experimental studies to test this hypothesis for lowland
255 e the potential to improve the efficiency of
experimental studies, even when sample sizes are very sm
256 been complemented by a substantial suite of
experimental studies, now bridging to the wild through f
257 is generally low compared with that used in
experimental studies.
258 We report a theoretical and
experimental study of coupling between a whispering-gall
260 In auditory fear conditioning,
experimental subjects learn to associate an auditory con
261 with localized structure from simulated and
experimental substrate displacements.
262 Here, we provide both observational and
experimental support of critical slowing down along natu
263 d and seemingly conflicting theories require
experimental support which is difficult to obtain from t
264 In this
experimental survey, individuals from 11 US healthcare s
265 This renders YbMgGaO4 the first
experimental system where putative RVB correlations rest
266 s evident at different plant ages in various
experimental systems and appears to be genetically linke
267 AFB1 mutational signatures from all four
experimental systems were remarkably similar.
268 surface of cerebral cortex within 1 hour of
experimental TBI.
269 iments is currently limited by the available
experimental techniques for the generation and character
270 The
experimental techniques reported here will enable therma
271 curring in microdroplet environments require
experimental techniques that allow a reaction to be init
272 ly here the combination of two complementary
experimental techniques, simulations, and theory to the
273 Device fabrication is applicable via current
experimental techniques.
274 drogel scaffold, were injected into half the
experimental teeth.
275 However,
experimental tests of this cross-ecosystem theory are la
276 undaries, we obtain excellent agreement with
experimental thermal conductivity of nanocrystalline Si
277 Spin relaxation however limits the maximum
experimental time and prevents the use of this method wi
278 n metallic glass thin films are simulated at
experimental timescales using a metadynamics-based atomi
279 al phenotypes have been impeded by a lack of
experimental tools.
280 acaques and, potentially, their responses to
experimental treatments.
281 These findings outline parameters for the
experimental use of VOR to clear latent infection.
282 ntages over current therapeutic options, yet
experimental vaccines have not been successful to date,
283 Experimental validation of several novel microRNAs in C.
284 ographically characterized, hindering direct
experimental validation of the offline hypothesis and el
285 Extensive
experimental validation showed that AtRTD2 and its modif
286 ular, cellular, and human disease traits and
experimental validation to demonstrate that genetic vari
287 Supported by two parallel routes of
experimental validation, our results indicate that natur
288 Numerical simulations, supported by
experimental validation, predict that rare fixers will i
289 The
experimental values of lycopene with selected combinatio
290 in excellent agreement with well established
experimental values when such values exist, and they pro
291 tially higher than the only earlier reported
experimental values.
292 identification of factors that contribute to
experimental variability.
293 A number of
experimental variables (e.g., a composition and pH of th
294 l lines to organize and describe the diverse
experimental variables and data resided in the EMBL-EBI
295 y (EFO) is an application ontology driven by
experimental variables including cell lines to organize
296 must be examined carefully along with other
experimental variables, keeping in mind that the effects
297 variety of emergent topological properties,
experimental verification of these predictions can be ob
298 tronics systems that can address resolution,
experimental versatility and mostly, automation of force
299 ented here should form the basis for further
experimental work, which will in turn provide input to r
300 ure provided a significantly improved fit of
experimental x-ray reflectivity data.