1 ss than 100 kb, and chromosome structures to
be validated.
2 tionship to tumor growth or progression must
be validated.
3 termination of T. aestivum in Triticum spp.,
was validated.
4 that specifically target 6 of these proteins
was validated.
5 agreement among studies and few factors have
been validated.
6 iR-483-5p in ACC relative to ACA samples has
been validated.
7 arker for belatacept-resistant rejection has
been validated.
8 These findings
were validated 24 hours after removal of GNPs by flow cy
9 The developed method has
been validated according to EU regulation N.
10 The method
was validated according the European Commission Decision
11 The developed method
was validated according to the Commission Decision 2002/
12 changes enhancing the target electrostatics
are validated against drug-target affinity data, yieldin
13 Our model predictions
are validated against experimental (1)H NMR data, demons
14 hich describes the dynamics in the data, and
is validated against other stimulus protocol experiments
15 (four parameters), and its descriptive power
was validated against the data, including consistency in
16 Strikingly, the HS models
were validated against experimental data showing a remar
17 Models from Basel and The Netherlands
were validated against repeated 24 h outdoor measurement
18 Case-finding criteria
were validated against Sepsis-3 criteria using medical r
19 Obtained results
were validated against the response measured with ELISA
20 because there are few outcome measures that
are validated and reliable in patients with Barrett's oe
21 The system has
been validated and optimized for free sulfur dioxide det
22 lar targets, and therapeutic approaches have
been validated and translated into clinical practice.
23 e the automated continuous monitoring system
is validated and commercially available, some other tech
24 Further, RACER
is validated and optimized using a simulated annealing p
25 The method
was validated and applied for the determination of K, Ca
26 ) and a clean-up step with Envi-Carb sorbent
was validated and applied to the quantification of 24 PF
27 This condition
was validated and the performance of experimental extrac
28 The proposed method
was validated and used to analyse a variety of baby food
29 LC), using a new column of faster resolution
was validated and used to characterize commercial produc
30 oci associated with lateral root development
were validated and further investigated.
31 The model parameters and framework
were validated and the fitted parameters demonstrated to
32 expression of NLRP3 and NLRP12 inflammasomes
was validated,
and the clinical association was evaluate
33 m cell molecules CD44 and EZH2, all of which
are validated as direct and functionally relevant target
34 Cell stiffness
was validated as a sorting parameter as nonviable cells
35 s express FGFR3-TACC3 fusion proteins, which
were validated as drivers of the resistant phenotype by
36 RPLP1/2
were validated as essential host factors for DENV, YFV,
37 Candidate genes from these pathways
were validated at the mRNA and protein level.
38 In cases where computational methods can
be validated based on performance, they may be considere
39 This approach has
been validated both in flow injection and chromatographi
40 edictions of standing, feeding, and drinking
were validated,
but not locomotor activities.
41 These predictions
are validated by analyzing the invasion of melanoma cell
42 genes are identified, and most of the genes
are validated by cDNA and RNA-seq data.
43 imulations are performed and on the way they
are validated by comparison to values Q(exp) of experime
44 The QCGD simulations
are validated by demonstrating the capability to retain
45 These computational findings
are validated by kinetic studies across a range of hydro
46 This p53-mediated repression of GMPS could
be validated by immunoblotting in Sk-Hep1, HepG2, and Hu
47 Finally, the packaged OF immunosensor has
been validated by a preliminary test on human lung biops
48 High efficiency of the substitution has
been validated by MALDI-TOF MS analysis of the functiona
49 The reconstruction algorithms have
been validated by reconstructing two stacked Co-Ni-Ga si
50 The accuracy of such a model
is validated by a faithful replication of the experiment
51 It
is validated by comparison with stochastic simulations o
52 The method
is validated by determining the density (0.1-1% relative
53 The presented methodology
is validated by directly connecting the non-covalent int
54 Predicted cathode performance
is validated by experimental synthesis, characterization
55 The calculation
is validated by our experiments on the breakup of Fe3C-p
56 The model
is validated by predicting concentrations measured in th
57 This
is validated by quantifying the mitochondrial alteration
58 This approach
is validated by quantitative measurements of enzyme acti
59 The model
is validated by several methods that include a genetic a
60 ve model for site-selectivity and this model
is validated by various substrates.
61 The enzyme conformational change
was validated by 3D fluorescence and CD spectrum.
62 This prediction
was validated by a combination of simulation experiments
63 ma INS-1E cells, and the binding specificity
was validated by a CRISPR/Cas9 mediated ZnT8 knock-out.
64 The consensus process
was validated by an extended group (EG) of ISIC members
65 Finally, the method
was validated by analyzing a variety of different reacto
66 The clinical importance of these chemokines
was validated by association of CXCL1 and IL8 polymorphi
67 segregation of microbiota compositions which
was validated by Beta diversity analysis.
68 This new binding mode
was validated by cocrystallization, showing all binding
69 using surrogate signatures to train the ANN
was validated by comparing blood levels among cigarette
70 The model
was validated by comparing the envelopes of the wild-typ
71 Subsequently, measured diffusivity
was validated by comparing to available literature data,
72 The prepared immunosensor
was validated by determining TGF-beta1 in real saliva sa
73 The developed analytical method
was validated by determining the concentration of U in a
74 tem for the detection of lipid-laden plaques
was validated by ex vivo imaging of an atherosclerotic h
75 The method
was validated by intra- and inter-day precision studies
76 The radiochemical procedure
was validated by its application for the measurement of
77 The equation
was validated by measuring the 4 parameters by echocardi
78 nscriptional factors (emx2, lhx2, and hopx),
was validated by qRT-PCR and immunostaining in brain sec
79 ved macrophages ingesting modified LDL; this
was validated by quantitative PCR in human and murine ma
80 This prediction
was validated by results in the pertinent literature not
81 tial expression of miRNA-218-5p (miR-218-5p)
was validated by reverse-transcriptase quantitative poly
82 e fine-scale accuracy of crossover detection
was validated by Sanger sequencing for a subset of ten c
83 ation that the loop is relocated by pressure
was validated by site-directed mutagenesis and by inhibi
84 Assay
was validated by spiking OTC to antibiotic free milk sam
85 xpression, previously shown to target ROCK2,
was validated by target prediction using ingenuity pathw
86 The method
was validated by the analysis of blank plasma samples sp
87 The simulated extraction yield of 17.91%
was validated by the experimental result (16.67+/-0.30).
88 The method
was validated by the in terms of: selectivity, calibrati
89 xonomic profiling of zooplankton communities
was validated by the morphology-based method on a large
90 The versatility of this approach
was validated by the synthesis of other intermetallic ph
91 The MISPE method
was validated by UPLC-MS/MS for the determination of AOH
92 role of SOX18 in the differentiation process
was validated by using lineage-tracing experiments based
93 Finally, the POC FO-SPR immunoassay
was validated by using matching serum and plasma samples
94 The results
were validated by a conventional method involving solven
95 These CNVs
were validated by array comparative genomic hybridizatio
96 Candidate genes
were validated by bisulfite pyrosequencing (30 AGA, 21 S
97 The results
were validated by comparing sensor and potentiostat perf
98 9, genes not previously associated with CHD,
were validated by CRISPR-Cas9 genome editing in mice as
99 Phosphoproteomic results
were validated by demonstrating that CRF overexpression
100 The OCT observations
were validated by direct observations of sectioned speci
101 These results
were validated by electrophysiological recordings in rVL
102 iable by sequence alone and their activities
were validated by enzymatic assays with the recombinant
103 Our results
were validated by examination of postsurgical elovl6 gen
104 Subsequently, the theoretical models
were validated by experiments.
105 TFA protocols
were validated by homogeneous quantification of both cAM
106 The identified genes
were validated by immunohistochemistry.
107 These interactions
were validated by immunoprecipitation/Western blotting,
108 Furthermore, single-cell studies
were validated by in vitro quantification and evaluation
109 reveal 65 candidate sRNAs, a third of which
were validated by northern blot analysis.
110 Thirteen transcripts
were validated by qPCR to confirm cell specific expressi
111 The selected candidate miRNAs
were validated by qRT-PCR analysis of cohorts of 24 T1DM
112 owing a significant role on altered pathways
were validated by qRT-PCR analysis on 12 samples per gro
113 Expression changes identified by RNA-Seq
were validated by qRT-PCR open arrays.
114 7 genes involved in CPT biosynthetic pathway
were validated by qRT-PCR.
115 The discovery set data
were validated by quantification using digital quantitat
116 These observations
were validated by results from the back trajectory analy
117 Hits
were validated by surface plasmon resonance and X-ray cr
118 NAs for alcohol-dependency in patients which
were validated by the phase-shift in their expression sc
119 Results
were validated by using quantitative reverse transcripta
120 1, and excitatory amino acid transporter 3)
were validated by Western blot analysis.
121 Both MED1 and CTCF
are validated conserved miR-122 targets.
122 The method
was validated (
Decision 2002/657/EC) and it was fit for
123 onses to different calcium signatures; these
were validated empirically using quantitative real-time
124 This model
was validated estimating appropriate figures of merit.
125 Radiotracer uptake
was validated ex vivo by gamma-counting and autoradiogra
126 The model
was validated experimentally with H2, N2, Ar and CH4 on
127 rectifier K(+) current, and this prediction
was validated experimentally.
128 Computational predictions
were validated experimentally in a novel parasite-erythr
129 Ten novel drug combinations
were validated experimentally, and seven of these exhibi
130 This model has not
been validated for AD, which has higher placebo response
131 sess asthma long-term control but have never
been validated for AD.
132 The new method presented here has
been validated for MDA quantification in industrial grea
133 The assay has
been validated for the quantification of 33 amino compou
134 medicinal chemistry optimization once it has
been validated for the system under consideration.
135 oviding an overview of how MTRs can and have
been validated for use in clinical decision making in ma
136 Simple sugar chromatographic analysis
was validated for linearity (R(2)>0.999), limits of dete
137 The assay
was validated for linearity, limit of detection, sensiti
138 The method
was validated for nine common natural ITCs.
139 In this work an analytical procedure
was validated for the determination of the actual lutein
140 eid Xpert Ebola assay for EBOV RNA detection
was validated for whole semen and blood using samples ob
141 Screen results
were validated for several effector mutants displaying d
142 trical model for the spun coat scaffold type
was validated from atomic force microscopy images by com
143 The new model
was validated further on the ENTHUSE M1 cohort with simi
144 tion data to create large superscaffolds; it
was validated genetically and superscaffolds were orient
145 enous imaging-based biomarkers still have to
be validated,
growing evidence highlights a potential co
146 The assay
was validated here using clinical samples collected from
147 These predictions
are validated in a spiking neural network model of the O
148 Finally, dominant-negative GusR variants
are validated in cell-based studies.
149 mal transition/pro-metastatic protein levels
are validated in NSCLC patient specimens.
150 These findings should
be validated in a larger study.
151 omprehensive comparison, these findings must
be validated in a randomized prospective comparison with
152 iated with a "not-cured" outcome that should
be validated in future studies.
153 biomarkers have been identified but need to
be validated in larger studies and different population
154 Multidimensional algorithms, which must
be validated in primary and urgent care settings, may he
155 These biomarkers should
be validated in prospective trials in MMel.The clinical
156 n recent large sample-size studies that have
been validated in a separate cohort in most cases.
157 ic significance of postinduction CSs has now
been validated in an independent cohort of patients (SIO
158 The method has
been validated in H3K4me3 ChIP-seq experiments, by the q
159 ld impact clinical practice, but has not yet
been validated in other studies.
160 Inhibitors of the proteasome have
been validated in the treatment of multiple myeloma, wit
161 Their utility
is validated in examining protein S-persulfidation.
162 In vivo detection of senescence
is validated in mice bearing tumor xenografts treated wi
163 This novel molecular regulation
is validated in mouse and human cancer specimens.
164 The biomarker
was validated in 19 ccRCCs and three public datasets.
165 a predictive biomarker for AsiDNA treatment
was validated in 43 tumor cell lines from various tissue
166 The protein panel
was validated in 93 patients with idiopathic or heritabl
167 excellent discrimination and calibration and
was validated in a different cohort from the one that wa
168 acity of the SMF stimulated oligodendrocytes
was validated in a dorsal root ganglion microfluidics ch
169 ich did not appear in the training data set,
was validated in a previous research work.
170 scranial magnetic stimulation-guided regions
was validated in a second sample of 108 patients and fou
171 The performance of the ABMR prognostic score
was validated in an independent cohort of 202 kidney rec
172 This finding
was validated in an independent cohort of 23 patients wi
173 The association of rs1595009
was validated in an independent cohort of CP of European
174 This signature
was validated in an independent cohort.
175 This signature
was validated in an independent patient set (59 PC, 36 a
176 Decreased pulmonary expression of miR-218-5p
was validated in an independent validation cohort, in ci
177 and GC-quadrupole MS (GC-qMS), where GC-qMS
was validated in an interlaboratory comparison between M
178 The method
was validated in breast milk and also in various types o
179 Using small hairpin RNA (shRNA), which
was validated in cultured neuronal cells, we found that
180 d, more importantly, Rab10-pThr73 inhibition
was validated in immune stimulated human PBMCs using two
181 Expression of key targets
was validated in independent LSE samples (quantitative R
182 e differential expression of select proteins
was validated in more than 300 tumors using immunohistoc
183 The method
was validated in oat-containing hot cereal and snack bar
184 tion (0.462-0.952 %), a modified methodology
was validated in order to reduce testing costs while spe
185 lity to detect vascular compromise with LSCI
was validated in parathyroidectomies.
186 based lignin quantification by py-GC-SIM-MS
was validated in reconstituted biomass model systems wit
187 The role of the dorsal mesocardium
was validated in Shh(-/-) mutants, which recapitulate he
188 The method
was validated in terms of linearity, limit of detection
189 The assay
was validated in terms of selectivity, sensitivity, accu
190 ssion of NLRP3 and of the IL-1R family genes
was validated in the Airway Disease Endotyping for Perso
191 ogenic development, including IFS formation,
was validated in the hemibiotroph Magnaporthe oryzae.
192 This evidence
was validated in the hippocampus of humans who died foll
193 and increased tensile strength in mice, and
was validated in the porcine model.
194 This
was validated in the two additional cohorts.
195 The correlation
was validated in the validation set (Pearson correlation
196 The prognostic value
was validated in two independent cohorts.
197 This
was validated in vivo, where deletion of trkB.T1 in astr
198 Its role in vascular development
was validated in zebrafish embryos using morpholino olig
199 Mutations
were validated in a luciferase-based membrane fusion ass
200 The established models
were validated in a Monte Carlo cross-validation scheme.
201 Findings
were validated in a separate multicenter cohort via pres
202 The newly identified groupings
were validated in a Surveillance, Epidemiology, and End
203 These findings
were validated in a testing cohort in which the associat
204 Results
were validated in an independent cohort of 398 patients
205 These findings
were validated in an independent cohort of 40 patients.
206 ge, and methylation-expression relationships
were validated in an independent cohort of children with
207 The results from the training group
were validated in an independent group of healthy human
208 Two hundred forty-seven of these proteins
were validated in an independent planned myocardial inju
209 Results
were validated in an independent population of asthmatic
210 These in vitro findings
were validated in archival brain tissues from Simian Imm
211 Our findings
were validated in both primary and metastatic models of
212 criptional networks specific to RB loss that
were validated in clinical samples demonstrated the abil
213 The model provided three predictions that
were validated in EEG recordings of 48 convulsive seizur
214 High-confidence predictions
were validated in electronic records significantly more
215 lts for plasma lipoprotein(a) concentrations
were validated in five independent studies involving 10
216 Results obtained
were validated in front of reference procedures based on
217 hromatin immunoprecipitation assays; results
were validated in functional rescue experiments using tr
218 These in vitro results in rats
were validated in human disease where myelin-positive hy
219 rs held in common between human OPTN and ANG
were validated in mammalian cells and zebrafish, MAP2K5
220 The involved pathways
were validated in primary CD4(+) T cells, target cells f
221 Results
were validated in real-time reverse-transcription quanti
222 Matrices
were validated in terms of their binding prediction and
223 These associations
were validated in the cross-sectional study (P < 0.0001)
224 These biological subgroups
were validated in the independent cohort.
225 The new criteria (Expanded-Baveno VI)
were validated in two additional cohorts from London (30
226 These results
were validated in unrelated cohorts of early infected su
227 (transmembrane) or HLA-G5 (soluble) isoforms
were validated in vitro.
228 These results
were validated in vivo by evidence that LZK silencing wa
229 one with the same data, these results should
be validated on new patient data.
230 in Aspergillus fumigatus Its performance has
been validated on bronchoalveolar lavage (BAL) fluid and
231 The framework has
been validated on thousands of cancer samples, using gen
232 The strategy
was validated on thousands of seasonal influenza A and B
233 The performances of the models
were validated on an independent validation set.
234 The on-line method
was validated over a concentration range of 0.1-0.6ngg(-
235 These cross-sectional findings remain to
be validated prospectively.
236 tient-centred models of palliative care must
be validated,
taking into account religious and cultural
237 ate entry into S phase of the cell cycle and
are validated targets for anticancer drug discovery.
238 If this function could
be validated,
then genetic variations may associate with
239 omputational resource overhead and accuracy,
are validated through comparison with well-known commerc
240 insights and structural details that can now
be validated through mutation experiments.
241 However, these scales have never
been validated through factor analysis.
242 In addition, it
is validated through the newly discovered lincRNA data s
243 y sensitive and more efficient immunosensors
was validated through selectivity, stability, reproducib
244 This
was validated through shRNA-mediated knockdown of the ta
245 o directly identify the causal variants that
were validated through complementation assays.
246 The analytical equations
were validated through the simulation of the respective
247 ich independent ChIA-PET data are available,
is validated to be RNAPII-, CTCF-, and RAD21-mediated.
248 Although digital nonlinearity compensation
was validated to be promising for mitigating Kerr nonlin
249 interviewer-administered questionnaire that
was validated to estimate typical dietary folate intake
250 igh precision acoustic dispensing technology
was validated to produce the DNA reference material with
251 Estimates of nitrate storage
are validated using basin-scale and national-scale estim
252 well as dose-dependent responses of the UPSS
are validated using in situ real-time atomic-force micro
253 SigSeeker has
been validated using established benchmarks for transcri
254 The method
is validated using calorimetry data for chicken egg lyso
255 The model
is validated using chronoamperometry and cyclic voltamme
256 tion procedures are included, and the system
is validated using measurements of tungsten light and a
257 hod to estimate the proportion of true zeros
is validated using precipitation data.
258 A simultaneous residue analysis method
is validated using QuEChERS extraction with acetonitrile
259 The accuracy and reliability of the method
is validated using simulated data sets.
260 This
was validated using a simulation of a two-joint planar r
261 ormance of the proposed cortisol sensor chip
was validated using an enzyme-linked immunosorbent assay
262 over recent years, and the model prediction
was validated using an independent data set from England
263 ymes such as prolyl endopeptidase (PREP) and
was validated using Fap-deficient mice.
264 The solution
was validated using field observations of recent earthqu
265 lastic-viscoelastic correspondence principle
was validated using finite element (FE) simulations and
266 The theoretical model
was validated using glycerol reference solutions.
267 Differential gene expression
was validated using NanoString technology.
268 This strategy
was validated using previously recalcitrant Fab-antigen
269 n of ten SDEGs involved in predation process
was validated using quantitative real-time PCR (qRT-PCR)
270 ALAT1 and depleted in breast cancer 1 (DBC1)
was validated using RNA pull-down and RNA immunoprecipit
271 The method
was validated using soybean oil samples spiked with CCs
272 The model
was validated using the 2013 American College of Surgeon
273 ied to any rotationally symmetric oligomers,
was validated using the structures of the Fas death rece
274 The results
were validated using a certified reference material (NIS
275 These results
were validated using a mathematical model of CSNs, inclu
276 Cut off levels for all three Fusarium toxins
were validated using blank wheat and wheat spiked either
277 These findings
were validated using data from colorectal cancer patient
278 s of remission, relapse and mortality, which
were validated using data from independent patients in T
279 WGRS97 and WGRS19
were validated using external data (n=369) from BHS (Bog
280 The binding results presented in this paper
were validated using fluorescent oligomers.
281 These studies
were validated using in vitro inhibition assays with pro
282 Findings
were validated using liver biopsies from 48 consecutive
283 The results of the analysis
were validated using mass balance by comparing the sum o
284 Model outcomes
were validated using the PBC Global Study.
285 These findings
were validated using two distinct, antigen-specific rcSs
286 The performance of the model
was validated,
using literature data for enzyme and micr
287 The effectiveness of the proposed method
is validated via the examples of two real-world power gr
288 himurium to H2O2L and H2O2H, and the results
were validated via phenotypic evaluation of 50 selected
289 Among the candidate targets that
were validated,
we identified PINK1, which is studied in
290 The predictions of the model
are validated with empirical data and with Monte Carlo s
291 e heterogeneity analysis results from THEMIS
are validated with single cell DNA sequencing from a cli
292 Inactivation protocols for HFV should
be validated with serum and whole blood.
293 of this method as a screening tool has also
been validated with arylation reactions of three differe
294 The algorithm
is validated with approximately 3 million rides extracte
295 The performance of the proposed technique
is validated with two different spectroscopic techniques
296 uares discriminant analysis, and the results
were validated with an independent patient set.
297 Observed genomic differences
were validated with experimental studies.
298 The physical maps
were validated with FISH and genetic mapping of SNP mark
299 ssed, using NanoString microArray profiling,
were validated with qPCR.
300 Both methods
were validated with respect to linearity, precision, acc