1 Labeled molecules
were analyzed by (
1)H and (13)C solution NMR, IR spectro
2 t and end of the study, the fecal microbiome
were analyzed by 16S ribosomal DNA sequencing.
3 Feces from mice
were analyzed by 16s ribosomal RNA sequencing and compar
4 Samples
were analyzed by 16S ribosomal RNA sequencing, and diet-
5 Microbiota and metabolites
were analyzed by 16S rRNA gene amplicon sequencing and N
6 tool samples were collected, and microbiomes
were analyzed by 16S rRNA gene sequencing.
7 Stool samples
were analyzed by 16S rRNA V4 region sequencing, and GMB
8 gest aggregate comprising eight chromophores
was analyzed by 1D and 2D nuclear magnetic resonance spe
9 I detected by one (or more) of these systems
was analyzed by 2 reviewers to determine the presence of
10 The VF defects
were analyzed by 2 independent reviewers and classified
11 A mixture of phosphopeptides
was analyzed by 2DMS without any prior separation.
12 The cTns
were analyzed by 3 high-sensitivity (hs) cTn assays: hs-
13 artridge and, finally, the obtained peptides
were analyzed by ((
4)D) RPLC-MS.
14 Eleven type 3 OPV samples
were analyzed by 8 laboratories using their in-house NGS
15 s chloroform or acetonitrile, which can then
be analyzed by a number of analytical techniques includi
16 les immobilized on a glass coverslip surface
is analyzed by a Matlab code before and after the additi
17 as "positive controls." Insulin sensitivity
was analyzed by a 2-step hyperinsulinemic euglycemic cla
18 e subset of vision-related anxiety questions
was analyzed by a graded response model using the Cai Me
19 Copeptin
was analyzed by a sandwich immunoluminometric assay.
20 New York City hospitals were studied; images
were analyzed by a central core laboratory blinded to cl
21 nd at 30 days and 1 year after the procedure
were analyzed by a consortium of 2 echocardiography core
22 ic Transcatheter Valves) 2 SAPIEN 3 registry
were analyzed by a consortium of core laboratories and d
23 s for the entire circumference of the angle,
were analyzed by a single examiner, masked to the subjec
24 For this purpose, commercial beers
were analyzed by a validated UHPLC-HRMS method and sampl
25 Confirmed meningitis cases
were analyzed by age group and subregion (South-East and
26 d peptide-protein docking simulations, which
are analyzed by agglomerative hierarchical clustering.
27 Microbiota
were analyzed by amplicon sequencing.
28 Data
were analyzed by an individual hazard-based transmission
29 erapy (DOT) per 1,000 patient-days, and data
were analyzed by an interrupted time series.
30 hy scans from 172 patients waitlisted for LT
were analyzed by applying 6 morphometric muscle scores,
31 d gene expression in autologous CD4+ T cells
were analyzed by assays for transposase-accessible chrom
32 of patients tested positive for C. difficile
were analyzed by assessing alpha and beta diversity, Lef
33 spectrometry and the zinc and copper content
was analyzed by atomic absorption spectroscopy in an ins
34 Allergenicity
was analyzed by basophil activation test.
35 Discrepant results
were analyzed by bi-directional PCR/sequencing of residu
36 Bacteria in colonic and fecal samples
were analyzed by both 16S ribosomal RNA gene and transcr
37 PET/CT images
were analyzed by calculating percentage injected dose pe
38 CTA images
were analyzed by central core laboratory (HeartFlow, Inc
39 Additionally, mismatch-repair-deficiency
was analyzed by checking the microsatellite status using
40 Sequencing data
was analyzed by commercial software solutions and an in-
41 Data
were analyzed by comparing workflow and challenges (obse
42 residues in wax, honey and beebread samples
were analyzed by composite apiary samples.
43 Receptor-allergen-ligand interactions
were analyzed by computational modeling.
44 Spatiotemporal variability
was analyzed by correlating time-series of 2 and 24 h av
45 The association between PMI and mortality
was analyzed by Cox regression.
46 n to first major cardiovascular event (MACE)
were analyzed by Cox regression.
47 e cells settle on the support surface before
being analyzed by CRRC.
48 The self-assembly mechanism
is analyzed by cryo-transmission electron microscopy, wi
49 antly expanded the range of samples that can
be analyzed by cryoET.
50 f 2544 and three other antibodies with Pfs25
are analyzed by crystallography to understand structural
51 Cerebrospinal fluid specimens
were analyzed by culture and/or polymerase chain reactio
52 Colon contents from mice
were analyzed by culture-based microbiology assays.
53 and immune populations in the spleen of mice
were analyzed by cytokine multiplex detection, qRT-PCR,
54 k and fibrolipidic, media and intima layers)
was analyzed by deep quantitative multiplexed proteomics
55 EpiSC specific phage
were analyzed by deep sequencing and bioinformatics anal
56 ng to (E)- and (Z)-1-cyano-1,3-butadiene (1)
were analyzed by density functional theory calculations,
57 lass variants on conserved dynamics can also
be analyzed by deploying the classifiers on variant MD s
58 when autocorrelation within that time series
was analyzed by detrending.
59 The localization of both proteins
was analyzed by different experimental methods such as i
60 The amino terminal dendrimers
were analyzed by diffusion-ordered spectroscopy experime
61 l, demographic, procedural, and outcome data
were analyzed by dividing patients into 2 groups; LRPV g
62 Transcriptional activity of c-Myc
was analyzed by DNA-binding, luciferase-assays, and expr
63 PDCs
were analyzed by DNA/RNA sequencing, DNA methylation pro
64 Wheat, whole wheat, potato and corn flour
were analyzed by DSS-EA.
65 roscopy, and the electrocatalytic properties
are analyzed by electrochemistry.
66 When metabolites
are analyzed by electrospray ionization (ESI)-mass spect
67 competitive antagonist osteoprotegerin (OPG)
were analyzed by ELISA, quantitative polymerase chain re
68 TREM-1 and PGLYRP1 levels
were analyzed by ELISA.
69 Biomarker levels in GCF
were analyzed by ELISA.
70 -telopeptide of type I collagen (NTx) levels
were analyzed by ELISA.
71 Mice
were analyzed by endoscopy and for intestinal epithelial
72 ognition molecule MBL, and antibody serology
were analyzed by enzyme-immunoassays; viral load by PCR.
73 TREM-1, PGLYRP1, IL-1beta, and calprotectin
were analyzed by enzyme-linked immunosorbent assay.
74 Droplets are split, one portion
is analyzed by ESI-MS, and the second portion is sorted
75 analyze time traces, which are too short to
be analyzed by existing methods, including FCS.
76 ned from organs intended for transplantation
were analyzed by expert pathologists, ATR-FTIR spectrosc
77 IR maps of the whole cell
were analyzed by exploiting the RE-AFM-IR overall signal
78 The resulting time domain signal
is analyzed by fast Fourier transformation; the oscillat
79 The expression of cell surface epitopes
was analyzed by flow cytometry.
80 and folliclular helper (T(FH)) cell subsets
was analyzed by flow cytometry.
81 ) and memory (not naive) CD154+ CD4+ T cells
were analyzed by flow cytometry after 5 hours of stimula
82 eripheral blood ILC2 abundance and phenotype
were analyzed by flow cytometry and correlated to clinic
83 ells from Peyer's patches and lamina propria
were analyzed by flow cytometry and IgA repertoire was d
84 CD4+ T cells in blood and the lower airway
were analyzed by flow cytometry and immunohistochemistry
85 In vitro ovalbumin-stimulated PBMC
were analyzed by flow cytometry for presence of ovalbumi
86 d lamina propria mononuclear cells from mice
were analyzed by flow cytometry or transferred to Rag1(-
87 ically (n = 12) SIV-infected rhesus macaques
were analyzed by flow cytometry using commercially avail
88 T cells
were analyzed by flow cytometry, and serum amyloid prote
89 sEVs secreted by Panc1 cell lines
were analyzed by flow cytometry, transmission electron m
90 Homing phenotypes of circulating lymphocytes
were analyzed by flow cytometry.
91 phenotype and chemokine receptor expression
were analyzed by flow cytometry.
92 with isolectin B4, and vascular permeability
was analyzed by fluorescein angiography.
93 The ADCC
was analyzed by focal expansion assay and CD107 cytotoxi
94 The interferograms
were analyzed by four-step phase shift algorithm to reco
95 A total of 18 vacuum gas oils have
been analyzed by Fourier transform ion cyclotron resonan
96 y both the heterogeneity of samples that can
be analyzed by FPOP and the myriad of applications for w
97 t, both of them with high and low crop load,
were analyzed by front-face fluorescence.
98 n feces, whereas urine and fecal metabolites
were analyzed by gas chromatography and liquid chromatog
99 d by solid phase microextraction and results
were analyzed by gas chromatography-mass spectrometry qu
100 Seven UV compounds
were analyzed by gas chromatography-tandem mass spectrom
101 Fatty acids (FA)
were analyzed by GC-FID; tocopherols, sterols, squalene,
102 charide compositions and glycosidic linkages
were analyzed by GC-MS, hydrodynamic radius and proton m
103 Liquids and aerosols
were analyzed by GCMS, HPLC, and fluorescence.
104 The samples
were analyzed by gel electrophoresis to visualize a 4.5
105 Pancreatic cancer cell lines
were analyzed by gene-expression microarray, quantitativ
106 ormed colony-forming units (CFUs) per mL CSF
were analyzed by general linear regression versus day of
107 The fecal microbial composition
was analyzed by Genetic Analysis GA-map Dysbiosis test,
108 Serum samples
were analyzed by gliadin antibody enzyme-linked immunoso
109 Potential biological functions of SNPs
were analyzed by HaploReg v4.1, RegulomeDB, GTEx, IMPC a
110 Human vaccine sera and ferret antisera
were analyzed by hemagglutination inhibition (HI) and ne
111 In this work, fruit juices have
been analyzed by high-performance liquid chromatography
112 Although several ANTAR proteins have
been analyzed by high-resolution structural analyses, th
113 The fractions
were analyzed by high performance anion exchange chromat
114 The compounds
were analyzed by high performance liquid chromatography
115 Carbonyl compounds
were analyzed by High Performance Liquid Chromatography
116 dition to gamma-counting, the plasma samples
were analyzed by high-performance liquid chromatography
117 The host immune responses
were analyzed by histological scoring of the inflammatio
118 Liver biopsy samples
were analyzed by histology and scored centrally accordin
119 Colon tissues
were analyzed by histology for the presence of collageno
120 ed survival times of mice, and colon tissues
were analyzed by histology, immunofluorescence, and immu
121 Pancreata and lung tissues from mice
were analyzed by histology, immunohistochemistry, and/or
122 Human and mouse liver tissues
were analyzed by histology, immunohistochemistry, flow c
123 mouse gastric tissues and mouse macrophages
were analyzed by histology, immunohistochemistry, immuno
124 2 weeks before and immediately after CLE and
were analyzed by histology, immunohistochemistry, revers
125 Samples
were analyzed by histology, immunohistochemistry, wester
126 Intestinal tissues
were analyzed by histology, in situ hybridization, proli
127 Intestinal tissues
were analyzed by histology, multiphoton and confocal mic
128 Colon and tumor tissues
were analyzed by histology, quantitative polymerase chai
129 c acid to induce colitis; intestinal tissues
were analyzed by histology.
130 immunosorbent assay, and intestinal tissues
were analyzed by histology.
131 HMO composition in these milk samples
was analyzed by HPLC.
132 Blood polyphenol concentrations
were analyzed by HPLC coupled to tandem MS after enzymat
133 The extracts
are analyzed by IC-DRC-ICP-MS for Cr(VI).
134 onica) plus thirty adulterated flour samples
were analyzed by ICP OES.
135 The targeted domains of the 35 antibodies
were analyzed by immunoblot and by epitope mapping using
136 onolayers using small hairpin RNAs and cells
were analyzed by immunoblot and immunofluorescence micro
137 s, primary T cells, and HEK293T cells, which
were analyzed by immunoblot, mobility shift, and immunop
138 Cells
were analyzed by immunoblot, quantitative polymerase cha
139 Cells
were analyzed by immunoblots, flow cytometry, or RNA-seq
140 Cells
were analyzed by immunoblots, quantitative real-time pol
141 eroids were established; cells and spheroids
were analyzed by immunoblots, reverse transcription poly
142 Signaling pathways in cells
were analyzed by immunoblots.
143 d HCT116 colorectal cancer cell lines, which
were analyzed by immunoblotting and proliferation and co
144 Colonoids
were analyzed by immunofluorescence and for ion transpor
145 Biopsies from patients
were analyzed by immunofluorescence and histochemical an
146 I, and COL IV) and corresponding CEC density
were analyzed by immunofluorescence flat mount-staining.
147 d distribution of caveolae regulated by flow
were analyzed by immunofluorescence staining and transmi
148 Gastric tissues from mice and human patients
were analyzed by immunofluorescence to verify findings a
149 om mice (with and without disruption of Crt)
were analyzed by immunofluorescence, immunoblots, and/or
150 ed down or overexpressed in T84 cells, which
were analyzed by immunofluorescence, immunoblots, high-p
151 Islets in human and rat pancreases
were analyzed by immunohistochemistry for immune cell in
152 In this study, nerves
were analyzed by immunohistochemistry in a cohort of 260
153 Liver tissues
were analyzed by immunohistochemistry, immunofluorescenc
154 Human HCC specimens
were analyzed by immunohistochemistry, quantitative poly
155 MMP1 protein and mRNA levels
were analyzed by immunosorbent assay, Western blotting a
156 with different durations of stay in the ICU
were analyzed by immunostaining and digital image analys
157 mechanism of lesion at the cell layer scale
is analyzed by impedance spectroscopy.
158 Implant-related complications
are analyzed by implant composition and operative indica
159 expression profiles of invading microtumors
were analyzed by incorporating a gold nanorod-locked nuc
160 The same tissues
were analyzed by indirect immunofluorescence and immunop
161 N application, SO(2) addition and oak ageing
were analyzed by inductively coupled plasma mass spectro
162 Efficacy
was analyzed by intention-to-treat in all randomized pat
163 he primary endpoint, delayed graft function,
was analyzed by "
intention-to-treat" evaluation.
164 Survival
was analyzed by Kaplan-Meier method.
165 Seminal proteins
were analyzed by label free mass spectrometry, with the
166 dividual rice grains at every polishing step
were analyzed by laser ablation ICP-MS to generate eleme
167 nel of 44 ACs including several oxidized ACs
was analyzed by LC-MS in plasma and urine samples collec
168 ved myofibroblast specimens from each rabbit
were analyzed by LC MS/MS iTRAQ technology using an Orbi
169 Plasma (poly)phenol metabolites
were analyzed by LC-MS.
170 N- and O-glycans present in each compartment
were analyzed by LC-MS.
171 Samples
were analyzed by LC/MS to determine the alpha-tocopherol
172 Renal functional status
was analyzed by levels of serum creatinine, urea, cystat
173 Samples
were analyzed by liquid chromatography-tandem mass spect
174 Treatment outcomes
were analyzed by logistic or Cox regression.
175 face morphology of [Formula: see text] films
was analyzed by low-energy electron microscopy and diffr
176 Brush cytology specimens
were analyzed by machine learning classifiers trained to
177 hologic features in the 1500-mum foveal zone
were analyzed by masked graders for disorganization of t
178 Oxidatively modified proteins by IV-FPOP
are analyzed by mass spectrometry (MS), and the extent o
179 real-time polymerase chain reaction; tumors
were analyzed by mass cytometry using markers to detect
180 a panel of engineered ACE2 glycoforms which
were analyzed by mass spectrometry to reveal the site-sp
181 the N-linked glycans from the native spikes
were analyzed by mass spectrometry, which revealed overa
182 after RLT, the proteome and phosphoproteome
were analyzed by mass spectrometry.
183 The mechanisms underlying the new technique
are analyzed by means of coarse-grained molecular simula
184 sitions between the [AlP(4) ](9-) tetrahedra
is analyzed by means of DFT calculations.
185 ases and 127 matched controls, fecal samples
were analyzed by means of FAIMS.
186 The samples
were analyzed by means of microcomputed tomography and h
187 These peptides
were analyzed by means of optical spectroscopies and mol
188 Excitation-emission matrices (EEMs)
were analyzed by means of unsupervised parallel factor a
189 ascular endothelial growth factor A (VEGF-A)
were analyzed by means of Western blotting.
190 Oxidative stress
was analyzed by measuring protein thiol oxidation and an
191 a meta-analysis; country-specific parameters
were analyzed by meta-regression.
192 Additionally, serum and PBMCs samples
were analyzed by metabolomics and transcriptomics, respe
193 Bioaerosols
were analyzed by metagenomic DNA sequencing and traditio
194 Alveolar bone loss
was analyzed by micro-computed tomography and scanning e
195 Choline uptake and metabolism in HCCs
were analyzed by micro-PET imaging of mice; livers were
196 y Western blot analysis, and mRNA expression
was analyzed by microarray.
197 After 2 and 4 weeks, postmortem samples
were analyzed by microcomputed tomography followed by ba
198 different MD groups and control individuals
were analyzed by miRNA microarray.
199 for failing SBC and post-ERCP complications
were analyzed by multivariate analysis.
200 Results
were analyzed by multivariate Cox regression and network
201 fecal microbiota composition between groups
were analyzed by multivariate factor analyses and cluste
202 The TCR repertoire
was analyzed by next-generation sequencing and cytokine
203 A total of 487 DCM patients
were analyzed by next-generation sequencing and categori
204 oth logarithmic and stationary phases, which
is analyzed by novel and existing software tools.
205 Metabolic profiles
were analyzed by nuclear magnetic resonance (NMR) spectr
206 Each peak
was analyzed by online MALS and then identified and conf
207 e assessed 6-30 months after transplantation
was analyzed by ordinal logistic regression.
208 Results
were analyzed by ordinal logistic regression, one-way an
209 Data
were analyzed by parametric test (ANOVA) with Tukey post
210 owed longitudinally, and livers of offspring
were analyzed by pathological evaluation, immunohistoche
211 Plasma samples from BoV+ subjects
were analyzed by PCR.
212 olyte pumping through the borehole electrode
was analyzed by performing anodic ethanol oxidation usin
213 Nasopharyngeal swabs
were analyzed by phenotypic and genotypic methods to det
214 ling pathways in multiple sclerosis (MS) can
be analyzed by phosphoproteomics in peripheral blood mon
215 Data from the 2 sets of images
were analyzed by placing regions of interest on lacrimal
216 stance Information Study (IRIS; NCT00884117)
were analyzed by polymerase chain reaction to determine
217 cally over an 8-37 h period, and each sample
was analyzed by powder X-ray diffraction.
218 George's Respiratory Questionnaire results
were analyzed by prior ICS use.
219 , the hydrophilic extract of the soft tissue
was analyzed by proton nuclear magnetic resonance ((1)H
220 esponse, including ACTA2, TGFBR1, and TGFBR2
were analyzed by qPCR.
221 cells of CRT-knockout mice and control mice
were analyzed by qRT-PCR, immunoblot, and transepithelia
222 The Th17 and Treg responses
were analyzed by quantifying the T-cell frequency and nu
223 binding to almond extract and the allergens
was analyzed by quantitative ELISA using sera from 18 su
224 ated to acquire opposite inflammatory states
was analyzed by quantitative PCR.
225 phatase (ALP) and collagen A I (COL I) genes
was analyzed by quantitative real-time polymerase chain
226 cytometry, and serum amyloid proteins (SAA)
were analyzed by quantitative real-time polymerase chain
227 hepatitis or individuals without disease and
were analyzed by quantitative reverse transcription poly
228 Organoids and adenomas
were analyzed by quantitative reverse-transcription PCR,
229 Clinical outcomes from ABSORB III
were analyzed by randomized device (intention to treat)
230 ping across the DDC locus on chromosome 7p12
was analyzed by re-sequencing guided by trait-associated
231 kidneys and high-glucose-treated HK-2 cells
was analyzed by real-time PCR, western blotting, and imm
232 Expression of CSF1 and IL34 mRNA in GF
was analyzed by real-time polymerase chain reaction and
233 important to electrophysiological properties
were analyzed by real-time polymerase chain reaction and
234 Median follow-up
was analyzed by reverse Kaplan-Meier.
235 s were collected during the CABG surgery and
were analyzed by reverse transcriptase polymerase chain
236 ng from a subsequent digestion using trypsin
were analyzed by reverse-phase liquid chromatography-mas
237 RNAome in primary human cardiac fibroblasts
were analyzed by RNA deep sequencing.
238 na propria and mesenteric lymph node tissues
were analyzed by RNA sequencing and flow cytometry.
239 enomic and non-genomic actions of budesonide
were analyzed by RNA-Seq analysis of 24 hours treated HA
240 (20 slow responders and 15 fast responders)
were analyzed by RNAseq.
241 Genomic DNA
was analyzed by Sanger sequencing or high-throughput seq
242 varieties (Guri, Irga 424, Puita, and Taim)
were analyzed by SD-LIBS.
243 carbonic anhydrase, and cytochrome c) could
be analyzed by SEC-ESI-MS using different column chemist
244 e association between treatment and outcomes
was analyzed by separate Cox models for each outcome.
245 d residence time in normal organs and tumors
were analyzed by serial SPECT/CT scans at 3 time points
246 Cross sections
are analyzed by several emergent mapping techniques.
247 cript amplicon sequencing; 285 fecal samples
were analyzed by shotgun metagenomics, and 60 fecal samp
248 The total cohort
was analyzed by site of care: intensive care (n = 170);
249 The same samples
were analyzed by six different techniques: Proton Transf
250 The recombinantly expressed enzyme
was analyzed by size-exclusion chromatography, gas-phase
251 two N-V centers and the two-mode cavity have
been analyzed by skew information, log-negativity, and B
252 4 and 48 h), and then the labelled volatiles
were analyzed by SPME-GC-MS.
253 Some characteristics of the honey samples
were analyzed by standard laboratory methods.
254 Records
were analyzed by subgroup, based on the AMD status of th
255 After exposure, hair swatches
were analyzed by surface microscopy analysis, oxidation
256 Specimens
were analyzed by targeted next-generation sequencing int
257 ore, tryptic digests of regular and hay milk
were analyzed by targeting 26 non-enzymatic modification
258 ion carriers (n = 121 in total) and controls
was analyzed by techniques based on flow cytometry and e
259 ys via both tetrahedral and octahedral voids
are analyzed by temperature-dependent powder neutron dif
260 The versatility of the new method
was analyzed by the EIS analysis of a Caco-2 monolayer i
261 samples obtained from 17 healthy volunteers
were analyzed by the cell tracking velocimetry system, a
262 When OCT images alone
were analyzed by the system, accuracy of diagnosis was 7
263 More than 1200 TiO(2) nanoparticles
were analyzed by these techniques.
264 (C), inflammation (I), and heart failure (H)
were analyzed by this newly developed sensing platform a
265 alth Organization (WHO) grade II/III gliomas
were analyzed by three neuroradiologists blinded to tiss
266 issues collected and single-cell suspensions
were analyzed by time of flight mass spectrometry analys
267 Native peptides from sea bass muscle
were analyzed by two different approaches: medium-sized
268 Transcripts
were analyzed by two independent coders with a grounded
269 es, cereals, dairy products, meat, and offal
were analyzed by two LC-MS/MS methods and a microbiologi
270 CT images
were analyzed by two radiologists blinded to the RT-PCR
271 The samples
were analyzed by two-dimensional gas chromatography with
272 s from two community cohorts of 1,424 adults
were analyzed by ultra-performance liquid chromatography
273 The sulfopeptides
were analyzed by ultrahigh-performance liquid chromatogr
274 tes functionalized with chiral organic films
was analyzed by ultraviolet photoelectron spectroscopy a
275 smoking status, and potential risk variables
were analyzed by univariate and multivariate analysis, w
276 Predictive factors of survival
were analyzed by univariate and multivariate analysis.
277 sed on clean bedding or in contact with soil
was analyzed by using 16S rRNA gene sequencing, and the
278 ntermediate larvae, carnivorous late larvae)
was analyzed by using 16S rRNA-guided metabarcoding appr
279 a with or without nasal allergies (outcomes)
was analyzed by using 2-level logistic regression and 2-
280 hest-performing model, detection performance
was analyzed by using free-response receiver operating c
281 Swabs
were analyzed by using a manual, nonnested quantitative
282 te < 30 mL/min or graft loss at 1 y, n = 66)
were analyzed by using a multivariate logistic model.
283 Data
were analyzed by using generalized linear mixed models c
284 es) or control (37 degrees C for 10 minutes)
were analyzed by using mass spectrometry.
285 ifferences in performance between modalities
were analyzed by using the McNemar test.
286 , tissue remodeling, and the immune response
were analyzed by using wild-type and B-cell-deficient (m
287 , non-learned helpless, and non-shocked mice
were analyzed by V4 16S RNA sequencing to identify gut b
288 ould be improved, vaccine effectiveness must
be analyzed by vaccine and virus type.
289 Development and baseline contractility
were analyzed by video-optical recording.
290 For intramodality analyses, conspicuity
was analyzed by view, CC versus MLO, within the same mod
291 Proteomics data
was analyzed by volcano plot, hierarchical clustering, P
292 ce of platelet factor-4 in the rinse samples
was analyzed by Western blotting.
293 receptor (GR:NR3C1) and activation of NR4A1
was analyzed by western blotting.
294 ic perturbations on cilia-dependent pathways
were analyzed by Western and immunohistochemistry analys
295 TAT3 as well as proliferation and DNA repair
were analyzed by western blotting, electrophoretic mobil
296 of Barcelona Clinic Liver Cancer (BCLC) 0/A
were analyzed by whole-exome sequencing.
297 e internal assembled parts of each cartridge
were analyzed by X-ray imaging, before dissembling so th
298 These functionalized GNPs
were analyzed by Zeta potential, dynamic light scatterin
299 MMP-9 activity
was analyzed by zymography.
300 Plasma samples
were analyzed by Zymutest-HIA-IgG, HemosIL-AcuStar-HIT-I