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