1 Lipid hydrolysis products
were identified by (
1)H NMR to validate lipid degradatio
2 Microbial taxa
were identified by 16S pyrosequencing.
3 isolated PGPR strains, named P1, P2, and P3,
were identified by 16S-rRNA gene sequencing as Bacillus
4 ation of a coumarin as a side product, which
was identified by 2D NMR experiments.
5 Here we show microhomologies
are identified by a scanning mechanism initiated from th
6 d UV-reduced cysteine-containing peptides to
be identified by a nontargeted database search.
7 Molecular heterogeneity
is identified by a fully unsupervised deconvolution of g
8 Mupirocin
was identified by a machine learning approach to be suit
9 for A(H7N9) infection in Chinese populations
was identified by a two-stage investigation involving 12
10 34 compounds
were identified by a combination of chemical analyses, i
11 Patients
were identified by a computerized search of the Emory Ey
12 lecule, NAD-dependent deacetylase Sirtuin 1,
were identified by a contest-based approach, in which pa
13 pecies implicated in snRNA pseudouridylation
were identified by a genome-wide approach based on ligat
14 The most promising derivatives
were identified by a multiparameter analysis of the comp
15 hepatitis B surface antigen (HBsAg) testing
were identified by a novel EHR-based population health t
16 Rearrangements
were identified by a PCR-based experimental strategy.
17 , and Western blot, and EV-associated miRNAs
were identified by a RT-qPCR-based profiling.
18 ine with (MA) and migraine without aura (MO)
were identified by a screener, which we validated agains
19 ening strategy with inclusion list; peptides
were identified by a semiautomated workflow for feature
20 Isolated bacteria
were identified by a series of biochemical tests using t
21 Low-level fetal variants
were identified by a statistical analysis adjusted for N
22 Parasitemia
was identified by active surveillance every 1-3 months u
23 populations expresses the Thrb gene and can
be identified by activity of the ThrbCRM1 cis-regulatory
24 ll lysate, and the protein conjugates formed
were identified by affinity chromatography-mass spectrom
25 Key residues for sugar binding and catalysis
were identified by alanine scanning, D36 being a critica
26 physician diagnosis, only three participants
were identified by all four criteria.
27 Notably, PTB-associated genes RAB31 and RBPJ
were identified by all three data types (WGS, RNA-seq, a
28 This hot-spot site
was identified by an experimental approach involving sel
29 (a human mutation-based Shank3 mouse model),
were identified by an innovative mass spectrometric meth
30 ne modules significantly associated with SOC
were identified by analyzing population transcriptomes f
31 Many of these anomalous tests could
be identified by applying machine learning techniques to
32 entified by BFPP, and 92 additional bacteria
were identified by BFPP alone, including 22/92 (23.9%) a
33 Risk factors for recurrence
were identified by binary logistic regression with adjus
34 CheRNAs can
be identified by biochemical fractionation of nuclear RN
35 stitis cases were cultured, and 181 isolates
were identified by biochemical testing, MALDI-TOF MS, an
36 e cluster responsible for their biosynthesis
was identified by bioinformatics and insertional mutagen
37 ed key innate immune signals, unique signals
were identified by both approaches.
38 singly, only half of the annotated cysteines
were identified by both iodoacetamide-desthiobiotin and
39 A total of 60 loci
were identified by both methods, but no specific genomic
40 yl radical adducts at nearby residues, which
were identified by bottom-up proteomics to detect residu
41 twenty-four participants with high-risk LVH
were identified by cardiac magnetic resonance.
42 A total of 167 polymorphic SSR alleles
were identified by CE with a mean value of polymorphic i
43 microarray analysis, and direct gene targets
were identified by Chromatin immunoprecipitation (ChIP).
44 threshold predictive of survival at 30 days
was identified by classification and regression tree ana
45 Rather, two distinct dyslexic subgroups
were identified by cluster analysis - one characterised
46 n and rural areas of Parintins City, Brazil,
were identified by cluster random sampling.
47 SV release sites could
be identified by clusters of Munc13, which allow SVs to
48 Ovalbumin-specific regulatory B cells
were identified by co-expression of fluorescence-conjuga
49 Finally, 62 unique loci
were identified by colocalization of haQTLs with the sub
50 Management priorities
were identified by combining scores for risk (derived fr
51 hypothesized that such rare mutations might
be identified by comparing broadly neutralizing and non-
52 Analytes can
be identified by comparing their theoretical isotopic si
53 Dysregulation of AA metabolism
was identified by comparing plasma metabolites from 516
54 A cell-surface marker
was identified by comparing the mRNA expression profile
55 556 differentially methylated regions (DMRs)
were identified by comparing the methylomes of dml3 and
56 The cellular metaphosphates
are identified by comparison with the (31)P chemical shi
57 One substance could easily
be identified by comparison to the IR spectra of referen
58 Relapse-specific mutations can
be identified by comprehensive genome sequencing and mig
59 Ganglia-specific transcriptional profiles
were identified by computationally subtracting muscle ge
60 tween January 1, 2000, and January 31, 2018,
were identified by conducting a systematic review regist
61 ETHOD: Journal articles published in English
were identified by conducting electronic searches in CIN
62 Transmission clusters
were identified by construction of phylogenetic trees ba
63 ypothesized that context-specific CREs could
be identified by context-specific non-coding RNA (ncRNA)
64 o undergo elective colon or rectal resection
were identified by convenience sampling.
65 Organisms
were identified by conventional microbiological methods,
66 incipal component scores of the data and can
be identified by convex-hull computation.
67 Human type 2 innate lymphoid cells (ILC2s)
are identified by coupled detection of CRTH2 and IL7Ralp
68 k factors for first and recurrent infections
were identified by Cox regression models.
69 and receptor in close physical proximity can
be identified by cross-linking/mass spectrometry.
70 RA or a noncoronary artery disease diagnosis
was identified by DE-CMR in 14% and 13%, respectively.
71 r a new noncoronary artery disease diagnosis
was identified by DE-CMR in 60% and 19% of patients, res
72 The medium-sized peptides
were identified by de novo and combination of de novo an
73 f 10 mul (>= 50 ng/ml), all positive results
were identified by densitometry at 10 and 20 min; howeve
74 Me(2))(3)}{kappa(2)-pinB-O(CMe(2))(2)OBH(3)}
are identified by detailed 1D and 2D (11)B SSNMR experim
75 Colonized patients
were identified by detecting the tcdB gene by polymerase
76 rios of the cooperative bond activation have
been identified by DFT and DLPNO-CCSD(T) calculations.
77 to the final grafted molecular complex have
been identified by DFT.
78 mineral dust and grit in natural diets might
be identified by DMTA, also in the fossil record.
79 rom 12 to 35 kDa, with possible bioactivity,
were identified by electrophoresis.
80 ensors and compounds of biological relevance
are identified by employing the largest reported library
81 ples of acute and chronic illnesses that can
be identified by employing a CLIA-waived test.
82 Of 89 ICM VTs, the isthmus could
be identified by endocardial entrainment in 55 (62%), co
83 neoadjuvant treatment for rectal cancer can
be identified by endoscopy at +/-9 weeks.
84 No gross lesions
were identified by endoscopy.
85 Stochastic networks for the clock
were identified by ensemble methods using genetic algori
86 l-defined clusters and small Au(I)SR species
was identified by ESI-MS and UV-vis spectroscopy.
87 us to identify many pathways that would not
be identified by existing approaches in these data.
88 tions and linkages of the detected O-glycans
were identified by exoglycosidase digestion facilitated
89 er homozygous truncating variant in FAM149B1
was identified by exome sequencing.
90 in control subjects (p = .039), of which all
were identified by exome sequencing.
91 or de novo (two) missense variants in DHX37
were identified by exome sequencing.
92 , segregating with the affected individuals,
were identified by exome sequencing.
93 The mutations
were identified by expanding the database search process
94 potential recurrence-associated SNPs, which
were identified by exploratory bioinformatics analyses o
95 iations from normal gene expression patterns
were identified by expression quantitative trait loci (c
96 Potential cases of Kawasaki disease
were identified by first-in-365-days International Class
97 c functional groups in the unreacted samples
were identified by fitting of high-resolution X-ray phot
98 We demonstrate that prostate cancer can
be identified by flow cytometric profiling of blood immu
99 2018, 131 adults waitlisted for LT with HEHE
were identified by free-text entry.
100 onal groups involved in bacterial Zn binding
were identified by FT-IR spectroscopy and elemental Zn i
101 The hot spots
are identified by FTMap, a computational analogue of exp
102 Antifibrotic drug candidates
were identified by functional screening of 480 chemicall
103 Most known oncogenes
were identified by gain-of-function mutations in cancer,
104 chemical composition of the encapsulated EO
was identified by gas chromatography (GC) and nuclear ma
105 etate, (E)-2-undecanal and (S)-germacrene D,
were identified by GC-mass spectrometry and quantified b
106 E/MYC-driven tumors that would otherwise not
be identified by gene amplification or translocation alo
107 Specimens with MSI
were identified by genetic analyses.
108 g increased varying degrees of VTE risk have
been identified by genome-wide association studies (GWAS
109 currently 90 independent risk variants have
been identified by genome-wide association studies.
110 Sixty-four candidate genes
were identified by genome-wide association study (GWAS),
111 ms for exceptional responses to therapy have
been identified by genomic analysis of tumor biopsies fr
112 n humans, thousands of crossover events have
been identified by genotyping related family members.
113 rall, 60 volatile organic metabolites (VOMs)
were identified by headspace solid-phase microextraction
114 GC Tfh
are identified by high expression of the chemokine recep
115 The isolation and local environment
was identified by high-angle annular dark-field scanning
116 compounds from different styles craft beers
were identified by high performance liquid chromatograph
117 Products
were identified by HPLC, ESI-MS, FT-IR, and [Formula: se
118 43 metabolites
were identified by HPLC-DAD-ESI-QTOF (8 betaxanthins, 8
119 A total of 46 phenolic compounds
were identified by HPLC-DAD-ESI/MS(n) and quantified by
120 Phenolic compounds
were identified by HPLC-DAD-ESI/MS(n), twenty-two flavon
121 ydroxycinnamic acid amides and lignanamides,
were identified by HPLC-ESI-QTOF-MS/MS.
122 HL and most (7/8; 87.5%; 95% CI, 46.6-99.7)
were identified by HS.
123 in 815 plant RIPs in the Pfam database that
were identified by HUMMR as containing a RIP domain.
124 surface and exposes a variable region, which
is identified by hydrogen-deuterium exchange as the comm
125 ature of their action in the genome that can
be identified by hydrolytic end sequencing, we show that
126 Acute cardiovascular events
were identified by ICD discharge codes and may be subjec
127 ingle-cell) RNA sequencing; RNA and proteins
were identified by imaging mass cytometry.
128 Specimens with dMMR
were identified by immunohistochemistry analyses of tiss
129 Cells responsible for SS1P removal
were identified by immunohistochemistry and intravital t
130 CD163+ perivascular macrophages
were identified by immunohistochemistry in brain parench
131 Proteins that interact with PAF1 in CSCs
were identified by immunoprecipitations and mass spectro
132 To verify this model, H1s
were identified by immunoreactivity for GABA and 95% of
133 Twf1
was identified by in silico analysis as a common target
134 PL3 peptide (amino acid sequence: AGRGRLVR)
was identified by in vitro biopanning on recombinant TNC
135 ar pathways that are common to elevated miRs
were identified by in silico analysis.
136 Pathogenic missense coding mutations
were identified by in silico tools and the ClinVar datab
137 elevation MI and non-ST-segment-elevation MI
was identified by International Classification of Diseas
138 ients with cirrhosis undergoing an endoscopy
were identified by International Classification of Disea
139 ts with select ophthalmic immune-related AEs
were identified by International Classification of Disea
140 Hydrogen gas
was identified by its subsequent use to hydrogenate an a
141 .Measurements and Main Results: Elevated PZP
was identified by label-free liquid chromatography/mass
142 e probe in enriching modified targets, which
were identified by label-free quantitative proteomics an
143 Furthermore, similar separations
were identified by LC-mass spectrometry with non-labeled
144 s responsible for the antioxidant activities
were identified by LC-MS, including phenolic acids, anth
145 Metabolites
were identified by line-fitting of 1D 1H-NMR spectra and
146 The outbreak
was identified by linking multiple independent illness r
147 Cardiomyopathy cases
were identified by linking the Medical Birth Register to
148 ution mass spectrometry (LC-HRMS) and lipids
were identified by Lipostar software.
149 Active antifungal components
were identified by liquid chromatography-electrospray io
150 The major organs that remove RIT
were identified by live mouse imaging of RIT labeled wit
151 findings show that functional DNA motifs can
be identified by machine learning analysis of a comprehe
152 Bacteria
were identified by MALDI-TOF, antimicrobial susceptibili
153 aberrantly spliced genes that had previously
been identified by manual curation efforts.
154 WTK2
was identified by map-based cloning and validated by tra
155 or the selected mutant and the relevant gene
was identified by map-based cloning.
156 Eighty-seven drugs and compounds
were identified by mapping global phosphorylation profil
157 he novel protein tyrosine phosphatase PTPN14
was identified by mass spectrometry analysis exclusively
158 of 2-arachidonoyl-lysoPI oxidation by 15-LO
were identified by mass spectrometry (MS), and they acti
159 Lrp6 proximity targets
were identified by mass spectrometry, and revealed that
160 NTM
were identified by matrix-assisted laser desorption ioni
161 Bacteria
were identified by matrix-assisted laser desorption/ioni
162 Global priority areas can only
be identified by means of an integrated prioritization a
163 Nonpolio enterovirus (NPEV) serotypes
were identified by means of VP1 sequencing.
164 Sensitization
was identified by measuring sIgE levels.
165 Candidate genes
were identified by measuring growth as a readout of repo
166 Ischemia
was identified by metrics of retinal vessel density.
167 amples of the PTB and healthy control groups
were identified by microarray and reverse transcription-
168 Eighteen ST types
were identified by MLST, among these ST types, forty-sev
169 When an additional organism(s)
was identified by mNGS, antimicrobials were changed 26%
170 When additional organisms
were identified by mNGS, there was no change in manageme
171 Promising candidates
were identified by modification of two or three amide bo
172 The important residues
are identified by monitoring structural data from ensemb
173 Excited-state symmetry breaking
is identified by monitoring several spectroscopic signat
174 Strain F2
was identified by morphological observations, physiologi
175 ve saRNA interacting protein candidates that
were identified by MS were knocked-down with siRNAs to i
176 Predictors of outcomes
were identified by multivariable logistic regression.
177 as identified by EORTC QLQ-C30 and QLQ-OG25
were identified by multivariable regression analysis and
178 A point mutation
was identified by MutMap in the encoding region of Quino
179 DRG neuronal populations
were identified by neurofilament H-chain 200, I-B(4) iso
180 aspects of brain dysfunction in NF1 that can
be identified by neuroimaging and ameliorated by NOS inh
181 vity, and the antigens mediating recognition
are identified by next-generation sequencing.
182 er bacteria and archaea (without filtration)
were identified by next-generation sequencing.
183 d to standard and additional media; bacteria
were identified by NGS16S analysis of DNA extracted dire
184 velengths (250 and 350 nm), and key products
were identified by NMR spectroscopy and X-ray crystallog
185 A definite or possible culprit lesion
was identified by OCT in 46.2% (67/145) of participants,
186 Target genes of OsMYB30
were identified by one-hybrid assays in yeast and electr
187 lysis, and lack of workflows, as they cannot
be identified by ordinary peptidomics strategies and cov
188 Meis homeobox 2 (Meis2) gene family members
were identified by our approach, and double knockouts of
189 Symptomatic malaria episodes
were identified by passive surveillance.
190 Unique IR and Raman spectral signatures
were identified by pattern recognition analysis and clus
191 s cases, and MuV-specific CD8+ T cells could
be identified by peptide/dextramer staining.
192 Drug sensitivity biomarkers
were identified by performing an association analysis be
193 utritional immunity and host immune response
were identified by performing microLESA at the infectiou
194 Candidate peptides
were identified by phage display and deep sequencing, an
195 Natural substrates
were identified by physiological aglycone libraries prep
196 uding 1 with a focus of only 80 tumor cells)
were identified by PLG.
197 At-risk individuals for incident depression
were identified by polygenic risk scores or by reported
198 vealed acid-fast bacteria and M. haemophilum
was identified by polymerase chain reaction (PCR) and se
199 ajor pneumococcal lineages in the PCV period
were identified by pooled incidence rate using a random
200 high expression levels of key mediators that
were identified by proteomic analysis.
201 arallel, the CLV fragments bound to proteins
were identified by proteomic approaches.
202 The key volatiles
were identified by PTR-TOFMS.
203 The epitopes
were identified by quantitating the phage clones before
204 MUC5B (mucin 5B) polymorphisms
were identified by quantitative PCR.
205 The functional EcoToxModules
were identified by re-organizing KEGG pathways into biol
206 Symptomatic ZIKV infections (Zika cases)
were identified by real-time reverse transcription PCR a
207 The candidate neoepitopes
were identified by recalling memory T-cell responses in
208 Data cut-off points
were identified by receiver operating characteristic ana
209 Presumed GABA (pGABA) neurons
were identified by response to photostimulation and veri
210 all patients receiving a decompression tube
were identified by retrospective chart review and analyz
211 Patients with status epilepticus
were identified by retrospective search of electronic da
212 Reactions
were identified by reviewing records from the MRI techno
213 ogically distinct subtype of CSU that cannot
be identified by routine clinical parameters.
214 ions would have allowed 52% of infections to
be identified by sampling just 17.7% of households.
215 ptides derived from receptor TMDs, which can
be identified by screening or rationally developed on th
216 Participants
were identified by screening all SOF participants for ca
217 sidases and alpha-N-acetylgalactosaminidases
were identified by screening bacterial libraries in 2007
218 AF/AFL events
were identified by search of the safety database using M
219 this theory is that targets of immunity may
be identified by searching for non-overlapping associati
220 Common metabolites may
be identified by searching libraries of tandem mass spec
221 Potential incident cases
were identified by searching administrative data for per
222 dies published between 1950 and May 24, 2019
were identified by searching Embase and PubMed.
223 Relevant studies
were identified by searching PubMed and Embase databases
224 Suitable reports
were identified by searching PubMed, Scopus, and Web of
225 Studies
were identified by searching six databases and assessed
226 Relevant studies
were identified by searching the PubMed database up to 3
227 PRISMA recommendations, and relevant studies
were identified by searching the PubMed/MEDLINE, PsycINF
228 IL1RN gene variants
were identified by sequencing.
229 Most infections
are identified by serological assays including enzyme-li
230 Four hundred and seventeen proteoforms
were identified by sheathless CZE-MS, and one hundred an
231 more detail, and its calmodulin-binding site
was identified by specific mutations.
232 ity when induced, several of which could not
be identified by standard gene disruption approaches.
233 Although a single reaction pathway
was identified by static calculations, quasiclassical di
234 mber neutral loss of heterozygosity (CN-LOH)
were identified by STR and SNP arrays.
235 chlorinated, and organophosphorus compounds
were identified by suspect screening; 15 unique elementa
236 crosslinking time and printing configuration
were identified by systematic, parametric study.
237 An average of 362 protein groups
were identified by tandem mass spectrometry (MS/MS) from
238 marked grain size change, backwash deposits
are identified by terrestrial geochemical and mineralogi
239 Another 109 activities
were identified by testing against clinical safety targe
240 Such regimes
are identified by the breakdown of the rotating-wave app
241 At present, senescent cells
are identified by the combined presence of multiple trai
242 Replication foci, or 'bubbles,'
are identified by the presence of the incorporated nucle
243 stics with mammalian enteric glia but cannot
be identified by the expression of canonical glial marke
244 tors IL-23R, IL-7Ralpha, and IL-1R1; and can
be identified by the surface marker CXCR6.
245 Antimicrobial resistance (AMR) has
been identified by the World Health Organisation as a gl
246 The micro-structural source of elasticity
is identified by the l-balanced graph partition of the g
247 The onset of dissociation of chlorine
is identified by the observation of the incommensurate s
248 Complete PVD
was identified by the absence of these findings and cons
249 tients with a highly active B cell component
was identified by the ELISpot assay.
250 sialoglycan isomers, alpha2,3 and alpha2,6,
were identified by the characteristic MS/MS fragment ion
251 Cases
were identified by the combination of International Clas
252 ive specimens, whereas 83.6, 64.6, and 55.7%
were identified by the ePlex RPP, NxTAG RPP, and Mycopla
253 Subjects
were identified by the International Classification of D
254 Sclerotic hippocampi
were identified by the loss of Nissl-stained hilar neuro
255 p of the Rotterdam Study, lipid subfractions
were identified by the Nightingale biomarker platform.
256 Cases
were identified by the Ophthalmic Mutual Insurance Compa
257 Viral targets
were identified by the PN panel in 17.7% of specimens te
258 PCG helical chains in the enantiomeric BCPs*
were identified by the vibrational circular dichroism (V
259 Unpublished studies
were identified by the World Health Organization (WHO) E
260 uency sweep while the resulting product ions
are identified by their ejection time within a repeating
261 scription initiation regions (TIRs) that can
be identified by their distinctive patterns of actively
262 an counterparts of mouse DC progenitors have
been identified by their shared transcriptional signatur
263 g to take low-dose aspirin (14,205 patients)
were identified by their first filled prescriptions for
264 recruitment bias as the patient participants
were identified by their health professionals.
265 Experts
were identified by their respective societies based on r
266 charge localization at the central core has
been identified by theoretical calculations, which are i
267 Edema
was identified by thickening of the inner nuclear layer,
268 Neurodegeneration
was identified by thinning of the retinal nerve fiber la
269 rying eae and 2 O45 strains carrying stx (1)
were identified by this dPCR assay and verified by the t
270 sides, three more new multitarget inhibitors
were identified by this virtual screening approach.
271 apies for BRCA1-deficient cancers than would
be identified by traditional synergy analysis.
272 c mechanisms unique to KIT-independent GISTs
were identified by transcriptome sequencing, qRT-PCR, im
273 y (STCS), all clinically relevant infections
were identified by transplant-infectious diseases physic
274 Clonal Sezary cells
were identified by TRBC1 staining in 56 of 111 (50%) sam
275 Reference indeterminate pulmonary nodules
were identified by two nonreader thoracic radiologists.
276 xty-three LS cases (diagnostic yield, 1.62%)
were identified by universal screening, with only 5 (7.9
277 Five subgroups of patients with active EoE
were identified by unsupervised clustering based on expr
278 antibiotics, azlocillin and cefotaxime that
were identified by us earlier.
279 reased risk of incident gastric cancer could
be identified by use of our newly developed polygenic ri
280 second unknown substance could nevertheless
be identified by using computationally predicted IR spec
281 pler from January 2009 through December 2013
were identified by using a centralized imaging database.
282 first arteriovenous access placement in 2009
were identified by using billing codes in the 5% Limited
283 ational Health Service between 2010 and 2013
were identified by using data from the Cancer Registry,
284 Affinity-purified antigens
were identified by using mass spectrometry and validated
285 between October 1, 2007, and April 30, 2018,
were identified by using medical subject headings (MeSH)
286 icant changes in flow and KE during exercise
were identified by using t tests.
287 between March 17, 2020, and April 10, 2020,
were identified by using the electronic medical record (
288 Olmsted County, Minnesota from 2006 to 2015
were identified by using the Rochester Epidemiology Proj
289 ch hot spots in the period from 1976 to 2016
were identified by using the visualization of similariti
290 were simultaneously monitored, some of which
were identified by utilizing theoretically predicted ion
291 Fe(IV)(O)(Me(3)TACN)(S(2)SiMe(2)) (3), which
was identified by UV-vis (lambda(max) = 385, 460, 890 nm
292 ion sites, including the three found by WGS,
were identified by viral capture-based sequencing, indic
293 first GES-5 K. oxytoca isolate was delayed,
being identified by WGS.
294 nemase-positive Klebsiella oxytoca infection
was identified by whole genome sequencing (WGS) (later f
295 nemase-positive Klebsiella oxytoca infection
was identified by whole-genome sequencing (WGS; later fo
296 for whom heterozygous mutations within ANO5
were identified by whole exome sequencing (WES).
297 cies in individuals with higher CMI in blood
were identified by whole metagenomic analysis.
298 Candidate genetic variants
were identified by whole-exome sequencing of 2 patients
299 All stellar-mass black holes have hitherto
been identified by X-rays emitted from gas that is accre
300 A single JMS-053 binding site
was identified by X-ray crystallography in human serum a