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1                                          CAD was assessed by (1) vessel score (>/=50% reduction in lu
2                                          HFC was assessed by (1)H MRS.
3       Fecal, urinary, and plasma metabolomes were assessed by (1)H-nuclear magnetic resonance.
4                                      Effects were assessed by 14 parameters representing sample size
5                    Twenty-three GBM patients were assessed by (18)F-fluoromisonidazole ((18)F-FMISO)
6                                Study quality was assessed by 2 independent reviewers.
7                                       Safety was assessed by 3 validated bleeding scales (Global Use
8                                       Images were assessed by 5 nuclear medicine physicians who had l
9            Early therapy response evaluation was assessed by (99m)Tc-duramycin SPECT and (18)F-FDG PE
10                                 NVC coupling is assessed by a wavelet metric estimation of percent ti
11                 The part 2 primary objective was assessed by a composite primary endpoint of clinical
12                                      Potency was assessed by a fluorescence-based assay measuring inh
13            Subjective utility of the stimuli was assessed by a matching task between the stimuli.
14                           Social integration was assessed by a simplified Berkman-Syme Social Network
15 lease from endothelial cells or erythrocytes were assessed by a luciferin-luciferase assay.
16                        Psychiatric disorders were assessed by a structured interview.
17 -CE assay to record dynamic, in vivo changes was assessed by administering an insulin stimulation via
18               In the same population, safety was assessed by adverse effect monitoring.
19                                       Safety was assessed by adverse event reporting.
20                           Mechanonociception was assessed by aesthesiometry, oedema by plethysmometry
21            The integrity of the isolated DNA was assessed by amplifying the 16S rRNA gene using Com1
22                               Hearing acuity was assessed by an objective hearing test (HearCheck han
23 nship between tumor hypoxia and angiogenesis was assessed by an overlap analysis of the volume of (18
24 ople in the non-clinical and clinical groups were assessed by an in-depth interview, and appraisals o
25 se was checked every 4 wk, and other effects were assessed by anamnesis.
26 ng-type hand dynamometers, and walking speed was assessed by asking respondents to walk 2.5 m at thei
27                              Social networks were assessed by asking participants to nominate people
28 by direct sequencing and cloning; phenotypes were assessed by assays of rod opsin in retinal extracts
29 lized microscopically, and bacterial killing was assessed by bacterial culture.
30                           Treatment efficacy was assessed by baseline risk for CV death/MI/iCVA, the
31 The classification accuracy of the new index was assessed by binary logistic regression and by receiv
32 ans of Passing & Bablok regression, and bias was assessed by Bland-Altman analysis.
33 Sensitivity and specificity of the algorithm were assessed by blinded analysis of a multinational coh
34              Plasmodium falciparum infection was assessed by blood smear microscopy at all visits.
35  consequences of Ca(2+)-induced mPTP opening were assessed by Ca(2+) retention capacity, using fluore
36                           Cell-cell coupling was assessed by calcein fluorescence recovery after phot
37                          Concurrent validity was assessed by calculating sensitivity, specificity and
38 pearman coefficient, and diagnostic accuracy was assessed by calculating the sensitivity and specific
39                                        Swine were assessed by cardiac magnetic resonance imaging and
40 rgeting efficacy of targeted liposomes (t-L) was assessed by cell uptake and cytotoxicity studies in
41                           Patients (n = 324) were assessed by clinical and histological (Kleiner scor
42                          Safety and efficacy were assessed by clinical, laboratory, and echocardiogra
43                        Prognostic discussion was assessed by coding transcribed audio-recorded visits
44           The agreement between SPT and sIgE was assessed by Cohen's kappa coefficient with different
45                        The collection device was assessed by collecting several concentrations of nan
46       Spousal health at patient HF diagnosis was assessed by comorbidity burden, self-reported diffic
47             Then the laser deflection method is assessed by comparing it with the hydrophone method.
48                                     Efficacy was assessed by comparing conjunctival provocation test
49        The fiber scaffold segmentation error was assessed by comparing fiber diameters from SEM and C
50                          Diagnostic accuracy was assessed by comparing image results with the standar
51                                  Calibration was assessed by comparing observed vs predicted probabil
52                  The implication of dopamine was assessed by comparing performance ON and OFF prodopa
53 e, Ca(2+)-bridging of BPS to clay edge sites was assessed by comparing sorption from 0.01 N KCl and 0
54          The accuracy of the proposed method was assessed by comparing the generated and acquired ima
55 ng a novel real-time controlled jet injector was assessed by comparison with intradermal and subcutan
56                     Serum antibody responses were assessed by competitive Luminex immunoassay.
57                         Antioxidant activity was assessed by complementary methods (ORAC-Fl, FRAP and
58 es, and subclinical coronary atherosclerosis was assessed by computed tomography.
59         The cellular uptake and localization was assessed by confocal microscopy.
60                                Reference MaR was assessed by contrast-multidetector computed tomograp
61                     Coronary atherosclerosis was assessed by coronary artery calcium (CAC) scoring do
62 SH) and oxidized (GSSG) forms of glutathione was assessed by CV studies at physiological pH.
63 ochemical behavior of the modified electrode was assessed by cyclic voltammetry (CV) to determine the
64  induced WAVE1 activation in striatum, which was assessed by dephosphorylation.
65 chastic model to calculate R0 and the latter was assessed by deriving a suitability indicator (SIG) t
66                            Virus infectivity was assessed by detection of virus antigen by flow cytom
67 tainment using predetermined asthma criteria was assessed by determining both criterion validity (cha
68 ens 5 of the most important Vespoidea groups were assessed by different diagnostic setups.
69              The presence of K-ras mutations was assessed by direct sequencing, locked nuclei acid (L
70 arly intervention oral immunotherapy (4-SU), was assessed by double-blinded, placebo-controlled food
71                     The antioxidant capacity was assessed by DPPH and ABTS(+) assays, beta-carotene/l
72                    The antioxidant potential was assessed by DPPH radical scavenging, FRAP and beta-c
73 one or in the presence of usual antioxidants were assessed by DPPH assay.
74 ular or population allele frequencies of L1s were assessed by droplet digital PCR or Taqman genotypin
75                    Neonatal body composition was assessed by dual X-ray absorptiometry at age 2 weeks
76 function in response to mechanical unloading was assessed by echocardiography during turndown of the
77 blood and myocardium, and diastolic function was assessed by echocardiography.
78  abdominal response to colorectal distension was assessed by electromyography.
79 l damage in atherosclerotic carotid arteries was assessed by electron microscopy and correlates with
80 se of tumor necrosis factor-alpha (TNFalpha) was assessed by ELISA.
81 infiltrated inflammatory cells and cytokines were assessed by ELISA.
82 in individuals with and without meat allergy were assessed by ELISA.
83 olecule (anti-OTC), purified and the quality was assessed by enzyme linked immuno sorbet assay.
84                         Urinary calprotectin was assessed by enzyme-linked immunosorbent assay in 328
85                                   Additivity was assessed by estimating the reduced excess risk due t
86                     Measles transmissibility was assessed by estimation of the reproduction number, R
87 ) model's ability to control confounding can be assessed by evaluating covariate balance across expos
88 d-dependent modulation of cutaneous reflexes was assessed by evoking and characterizing ipsilateral a
89 and year of anaphylaxis with incidence rates were assessed by fitting Poisson regression models.
90                        Their immunophenotype was assessed by flow cytometry and protein expression; a
91 -specific regulatory T (Treg)-cell induction was assessed by flow cytometry using a transgenic T-cell
92 escent-labelled exosomes in epithelial cells was assessed by flow cytometry.
93                                  Engraftment was assessed by flow cytometry.
94  performed as follows: BAT-CD63 upregulation was assessed by flow cytometry; HR-released histamine wa
95                Endothelial function (n = 82) was assessed by flow-meditated dilatation (FMD) at basel
96                  T cells and dendritic cells were assessed by flow cytometry, cytokines by multiplex
97 immunological markers and phagocytic ability were assessed by flow cytometry.
98 acilitated allergen binding and presentation were assessed by flow cytometry.
99                            MAF amplification was assessed by fluorescence in-situ hybridisation of tw
100                 Cell type-specific functions were assessed by fluorescence-activated cell sorting and
101          Hepatogenic potential of stem cells was assessed by functional assays at both genetic and pr
102 n a different day, brain insulin sensitivity was assessed by functional MRI.
103                    Vaccine-virus relatedness was assessed by gene sequencing and hemagglutination inh
104                        Risk factors for RTIs were assessed by generalized linear mixed method regress
105                                MATS coverage was assessed by geographical region and age group.
106                                 Liver damage was assessed by hematoxylin and eosin and alanine aminot
107           Inflammation and fibrosis of lungs were assessed by histologic, flow cytometric, and quanti
108  of tumors, and intestinal barrier integrity were assessed by histologic, immunohistochemical, quanti
109                             Bone marrow will be assessed by histology or immunohistochemistry and cyt
110                      Alcohol's effect on BAT was assessed by histology, qPCR, HPLC, LC/MS and measure
111    Cardiac fibrosis and ventricular function were assessed by histology and echocardiography.
112 ys post-loading and whole knee joint changes were assessed by histology, immunostaining, micro-CT, an
113 structure, gene expression, and MMP activity were assessed by histology, real-time reverse transcript
114 ts transplanted perivascular to jugular vein were assessed by HPLC/MS/MS, and retention of the fat de
115      At the final step of VEPART, robustness is assessed by identifying and analyzing the optimal the
116 meat extract and bovine gamma globulin (BGG) was assessed by immunoblotting and ELISA, respectively.
117 opy and mitochondrial function and autophagy were assessed by immunoblotting, immunohistochemistry, a
118                        Alpha-gal-sIgE levels were assessed by ImmunoCAP assay.
119  vivo and in vitro and in patients with COPD was assessed by immunofluorescence staining, Western blo
120              DNA double-strand breaks (DSBs) were assessed by immunofluorescence analysis of 53BP1 fo
121                        Nur77 protein amounts were assessed by immunofluorescence and flow cytometry i
122   Cardiovascular inflammation and senescence were assessed by immunohistochemical and immunofluoresce
123                          Tissue inflammation was assessed by immunohistochemistry and flow cytometry.
124                            Notch1 activation was assessed by immunohistochemistry for Notch1 intracel
125                      Thus, nKIFC1 expression was assessed by immunohistochemistry in 163 African Amer
126                   Localization of miR-218-5p was assessed by in situ hybridization.
127 2 integrins in ILC2 trafficking to the lungs was assessed by in vivo blocking of these integrins befo
128                                     Outcomes were assessed by independent raters and self-report at b
129                           The final analysis was assessed by intention to treat.
130  computed and the detected language networks were assessed by intra-operative stimulation mapping to
131 rocessed by 2 observers, and reproducibility was assessed by intraclass correlation coefficient and B
132 lity of echocardiographic reports and images were assessed by investigators blinded to the external l
133                              Iron absorption was assessed by isotope incorporation in erythrocytes 14
134 om-effects model, and quality of the studies was assessed by JADAD scale.
135                      Radiologist reliability was assessed by kappa; a Hui-Walter model was used to es
136 l Prognostic Index (MIPI), and proliferation is assessed by Ki67.
137                  Dermal-epidermal separation was assessed by light microscopy studies and quantified
138                                     CT scans were assessed by local radiologists according to Respons
139 =3 mo with the identified trajectory classes was assessed by logistic regression.
140  as 4-year and 10-year risks for fatty liver were assessed by logistic regression.
141    Predictive factors for erosive tooth wear were assessed by logistic regression.
142 e of innate, TH1, and TH17 immune responses, were assessed by Luminex in acute and convalescent sera
143                       Paneth cell deficiency was assessed by lysozyme staining of ileum tissues and l
144                          Retinal sensitivity was assessed by Macular Integrity Assessment microperime
145 ion, lipid core, and intraplaque hemorrhage) was assessed by magnetic resonance imaging.
146 and the superior rectus and the orbital roof was assessed by masked review of computed tomography or
147 on was open label but endpoints at 12 months were assessed by masked investigators.
148                         Neuronal development was assessed by means of electrophysiological, optical,
149                               Liver fibrosis was assessed by means of liver biopsy, transient elastog
150                             Spectral quality was assessed by means of region-of-interest analysis.
151                                       Safety was assessed by means of serial cardiac and thoracic ima
152                                    Tolerance was assessed by means of suppression of contact hypersen
153  antihyperalgesic activity of such compounds was assessed by means of the paw-pressure and incapacita
154               Health-related quality of life was assessed by means of the Short Form-36.
155 nhibition on the same intracellular pathways was assessed by means of Western blotting, and the final
156       Inflammatory parameters in the airways were assessed by means of flow cytometry, ELISA, Luminex
157 cytokine and transcription factor expression were assessed by means of flow cytometry.
158      Tissue volume and hepatic PDFF accuracy were assessed by means of linear regression with the res
159  annulus fibrosus regions of all lumbar IVDs were assessed by means of principal frequency analysis.
160                          Functional outcomes were assessed by means of Western blotting, real-time PC
161                                    Arthritis was assessed by measurement of joint swelling and histol
162   The pharmacodynamic profile of lanadelumab was assessed by measurement of plasma levels of cleaved
163                           Periodontal status was assessed by measurement of probing depth, clinical a
164                                       It can be assessed by measuring the acetazolamide-induced chang
165 ore, the toxicity of LbL-assembled nanofilms was assessed by measuring cell viability.
166     Exposure to mites at age 6 and 18 months was assessed by measuring Der p 1 weight/weight concentr
167                                     Efficacy was assessed by measuring engraftment of gene-modified h
168                              Vascular status was assessed by measuring flow-mediated vasodilation (FM
169                                Consolidation was assessed by measuring performance on the same task 2
170 ys, and the growth rates of cell populations were assessed by measuring areas of the same individual
171 d in H pylori strains during human infection were assessed by measuring release of interleukin 8 from
172                 Objective imaging parameters were assessed by measuring the SUV and coefficient of va
173    The reliability of the established method was assessed by method validation and comparison with th
174 domonas aeruginosa and Staphylococcus aureus was assessed by microdilution assay.
175                                     Progress was assessed by monthly sensory and motor function tests
176                      Brain neurodegeneration was assessed by MRI and fludeoxyglucose-18 positron emis
177 ydrogen were measured and intestinal content was assessed by MRI before and at various time points af
178                           Muscle involvement was assessed by MRI, muscle strength testing and muscle
179 diac effects of ELA-32 and [Pyr(1)]apelin-13 were assessed by MRI and cardiac catheterization in anes
180 (OXA) EoE mouse model, and GM-CSF production was assessed by mRNA and protein analyses.
181                 Reference myocardium at risk was assessed by multidetector computed tomography during
182 r patient survival before and after Share 35 was assessed by multivariable Cox proportional hazards a
183 ons, and chloride concentration with outcome was assessed by multivariate analysis in the whole cohor
184 I with pancreas and kidney allograft failure were assessed by multivariate Cox regression adjusted fo
185                     Clinical characteristics were assessed by mutation status.
186                                          RNA was assessed by nanostring.
187 uronal loss, and protein deposition that can be assessed by neuroimaging (ie, MRI and PET) or CSF ana
188                   The quality of the library was assessed by next-generation sequencing and detailed
189                                 Cardiac risk was assessed by noting baseline coronary artery disease
190                      Circulating amino acids were assessed by nuclear magnetic resonance spectroscopy
191                                           CA was assessed by ophthalmologists using slit-lamp biomicr
192                      The effect of treatment was assessed by paired pretreatment and posttreatment li
193                               Asthma control was assessed by parent report and child report (primary
194                                          ICP was assessed by placing a fluid-filled 25 gauge butterfl
195                                    Each case was assessed by PMCTA, followed by autopsy.
196 roup, sympathetic/parasympathetic modulation was assessed by power spectral analysis.
197                     Visual field progression was assessed by PROGRESSOR software version 3.7 (Medisof
198                                    BER genes were assessed by quantitative RT-PCR.
199 T2 gene (RNASET2) expression and methylation were assessed by quantitative trait loci analyses.
200  depression, and childhood wheezing episodes were assessed by quarterly questionnaires beginning at b
201 nonspecific symptoms, and sleep disturbances were assessed by questionnaire.
202                          Baseline heart rate was assessed by quintiles and as a continuous variable.
203  households incurring catastrophic costs and were assessed by quintiles of household income.
204 A, -C, and VEGF receptor 2 (VEGF-R2) in VECs was assessed by real-time PCR.
205                      Safety of the procedure was assessed by recording the number of adverse events.
206                           Temporal variation was assessed by repeated measurements over hours and day
207       The prognostic value of MRI biomarkers was assessed by retrospective correlations with patholog
208 ar regulation of glucocorticoid-mediated ST2 was assessed by RT-qPCR, ChIP assay and luciferase repor
209 ts from a dry eye clinic and normal controls were assessed by Schirmer's test for tear flow.
210                       Occupational exposures were assessed by self-reported VGDF exposure and by job-
211            The composition of gut microbiota was assessed by sequencing the 16S rRNA gene.
212                                     Efficacy was assessed by serial CT tumor volumetry and (18)F-FDG
213                                  LV function was assessed by serial echocardiography, 2,3,5-triphenyl
214  The biodistribution and radiation dosimetry were assessed by serial whole-body PET/CT scans (10 min,
215 low obstruction with smoking characteristics was assessed by sex using regression analysis.
216 th use of solid fuels for cooking or heating was assessed by sex, within each site, using regression
217                                        Atopy was assessed by skin prick test (SPT) using inhalant and
218 ty of MDSC to differentiate into osteoclasts was assessed by staining for tartrate-resistant acid pho
219  epithelial cells from healthy and CF donors was assessed by surface biotinylation and subsequent Wes
220 evels in serum and PBMC culture supernatants were assessed by suspension array multiplexed immunoassa
221                    Vision-related disability was assessed by the 25-item National Eye Institute Visua
222 ive, longitudinal study, disease progression was assessed by the ALS Functional Rating Score-Revised
223                                Heterogeneity was assessed by the Cochran Q statistic and quantified b
224 e-dependent covariate; its effect on outcome was assessed by the Cox proportional hazard regression m
225                                Bleeding risk was assessed by the HAS-BLED, ATRIA, ORBIT and HEMORR2HA
226                              Bioavailability was assessed by the quantitative analysis of urinary fla
227 igh-molecular-weight kininogen, and efficacy was assessed by the rate of attacks of angioedema during
228                    Clinical disease response was assessed by the Severity-Weighted Assessment Tool (s
229 vivors from consecutive Ewing sarcoma trials was assessed by the Toronto Extremity Salvage Score, Sho
230                          Platelet reactivity was assessed by the VerifyNow point-of-care assay; high
231 ic characteristics of nixtamalized corn masa were assessed by the dynamic oscillatory test.
232 E gels and by ELISA whereas Amadori products were assessed by the fructosamine method.
233 , width, and thickness of keratinized tissue were assessed by the same masked examiners as after the
234                     Jam formulations 3 and 4 were assessed by the sensory panel as more spreadable si
235                             These models can be assessed by their overall fit to the experimental dat
236               Thirdly, inclusion eligibility was assessed by title, abstract, and full text.
237  and infection of human gut epithelial cells was assessed by Tn-insertion site sequencing (Tn-seq).
238       In fact, their relative importance can be assessed by tracking past population fluctuations ove
239             The (18)F-FMISO uptake on PET/CT was assessed by trained experts.
240                            Systolic function was assessed by transthoracic echocardiogram, and systol
241 tudinal strain and flow propagation velocity were assessed by transthoracic echocardiography during a
242 ontrol groups (saline, free dox, and Caelyx) was assessed by tumor growth measurements.
243                      Interobserver agreement was assessed by two separate observers who reviewed 100
244                                  Carotid IMT was assessed by ultrasonography at baseline and 12 and 2
245                               Fetal biometry was assessed by ultrasound at each research visit.
246                      Carotid atherosclerosis was assessed by ultrasound, whereas plaque composition (
247  involvement) status and associated survival were assessed by uni- and multivariable analyses.
248  that is, no, partial, or complete response, were assessed by use of the urticaria activity score, ph
249         In particular, quality of assemblies is assessed by using CLC Genomics Workbench read mapping
250    Protein (total, animal, vegetable) intake was assessed by using a food-frequency questionnaire in
251 Dietary intake during the previous 12 months was assessed by using a semiquantitative food-frequency
252                               Dietary intake was assessed by using a validated food-frequency questio
253   Diagnostic performance on a quadrant basis was assessed by using areas under the receiver operating
254 ssociation of serum potassium with mortality was assessed by using comprehensive state-of-the-art reg
255 nd specificity of Cre-mediated recombination was assessed by using Cre-reporter mice, polymerase chai
256                       The risk of meningioma was assessed by using data from the Swedish Cancer Regis
257                          Survival prediction was assessed by using difference in median survival time
258                             Clinical outcome was assessed by using follow-up imaging studies, medical
259              The effect of endogenous cysLTs was assessed by using human mast cell supernatants.
260 ucus hypersecretion, and airway inflammation was assessed by using in vivo models of IL-13-induced lu
261    Interobserver and interprotocol agreement was assessed by using kappa statistics.
262                                    Agreement was assessed by using kappa statistics; prevalence ratio
263  role of miR-146a in patients with psoriasis was assessed by using miR-146a(-/-) mice in conjunction
264          Agreement between density estimates was assessed by using Pearson correlation, linear regres
265                     Population heterogeneity was assessed by using principal component analysis, foll
266                         Discriminatory value was assessed by using receiver operating characteristic
267 , alcohol consumption, and physical activity was assessed by using the Chi-square test.
268                    The effectiveness of PCCs was assessed by using the International Society of Throm
269             Intra- and interreader agreement was assessed by using the intraclass correlation coeffic
270  parameters that reflect fracture resistance was assessed by using the intraclass correlation coeffic
271 odule (including initial treatment failures) was assessed by using the Kaplan-Meier method.
272                              Reproducibility was assessed by using the kappa test, correlation was as
273 der agreement on venous contamination grades was assessed by using the linearly weighted Cohen kappa
274 ssessed by using the kappa test, correlation was assessed by using the Spearman coefficient, and diag
275                             Measurement bias was assessed by using the sum of the mean signed errors
276  1 year in relation to length of RBC storage were assessed by using 3 independent analytic approaches
277                Nutritional habits at age 8 y were assessed by using a 3-d nutritional diary.At age 8
278 natal 25(OH)D3 concentrations in DBS samples were assessed by using highly sensitive chromatography-t
279                                  Human lungs were assessed by using immunohistochemistry for SIRT3 ac
280 FF intra- and interexamination repeatability were assessed by using intraclass correlation and coeffi
281                            Correlates of MAN were assessed by using log-binomial models.
282     Transcriptomes of sorted tonsillar ILC3s were assessed by using microarray analysis.
283  >/=45%), and HFrEF (ejection fraction <45%) were assessed by using multivariable adjusted Cox models
284 us primary care provider (PCP)-directed care-were assessed by using multivariable logistic regression
285                             Dietary patterns were assessed by using principal components analyses.Amo
286 e components in gene expression and activity were assessed by using quantitative PCR and the telomere
287 xpression and IL-12 and IL-35 protein levels were assessed by using quantitative RT-PCR and ELISA and
288 tigen level and circulating tumor cell count were assessed by using Spearman correlation (r).
289 coefficient (ADC) with response to treatment were assessed by using the Mann-Whitney test and logisti
290 spot sign and substantial hematoma expansion were assessed by using the Pearson chi(2) test.
291              Iodine and monochromatic errors were assessed by using the root sum of the squared error
292 hanges in MTRasym over time and between mice were assessed by using two-way repeated-measures analysi
293                               Dietary intake was assessed by validated food-frequency questionnaires.
294                      Conformational dynamics were assessed by variable-temperature NMR spectroscopy.
295                   Stabilities of the dipoles were assessed by various homodesmotic schemes and are co
296 e (maximum normalized wall index) and number were assessed by vessel wall magnetic resonance imaging.
297                              Quality of life was assessed by visual analogue scale.
298                        TJ protein expression was assessed by Western blotting (WB) and immunocytochem
299 Synaptic transmission at the endbulb of Held was assessed by whole-cell patch clamp recordings from a
300 tivity and macrophage marker CD68 expression were assessed by zymography and reverse-transcription po

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