1 We detected 1 episode of possible direct patient-to-pati
2 We detected 1,423 people with TB and 874 people living w
3 In living mice
we detect ~
10(5) fluorescent cells in deep tissues.
4 We detected 104 candidate genes in sweep regions involve
5 We detected 110 NT5C2 mutations in 75 (16.5%) of 455 B-c
6 Using the dengue lateral-flow rapid test
we detected 12 positive cases out of the 55 (21.8%) COVI
7 We detected 122 significant (P < 1.28 x 10(-11)) indepen
8 We detected 1287 Streptomyces rpoB operational taxonomic
9 Through an analysis of key PR genes,
we detected 129 individual variants and 72 unique varian
10 We detected 14,615 variant genotypes and built 93 associ
11 Using exome sequencing and read count data,
we detected 16 605 deletions and duplications that affec
12 We detected 171 fungal amplicon sequence variants (ASVs)
13 nd interconnected Ceramic Age population(7),
we detect 19 pairs of cross-island cousins, close relati
14 y coupled with mass spectroscopy (LC-MS/MS),
we detected 20 steroids within unfertilized eggs.
15 We detected 225,936 genomic Mu insertion sites and 41,08
16 ntrast, in NPCs derived from these ESC lines
we detected 29 RDCs, a large fraction of which were robu
17 We detected 3,400 full-length NLR loci, of which 1,560 w
18 We detect 310 neurons from mPFC and MTL from patients wi
19 We detected 320 independent signals in 276 loci for 27 d
20 We detected 346 fungal amplicon sequence variants domina
21 We detected 4.3.1 S. Typhi as early as 1991, the earlies
22 We detected 41 genes differentially spliced after NOVA2
23 Furthermore,
we detected 48% (95% CI 43-52%) increase in the chance o
24 Using this method,
we detect 5-bromodeoxyuridine (BrdU) incorporated by Sac
25 In genomes from these resistant lineages,
we detect 53 genes with evidence of convergent amino aci
26 We detected 543 putative viral-encoded auxiliary metabol
27 In total,
we detected 55 unique NA isomer groups, out of the 181 s
28 We detected 620 chemicals that matched 300 molecular for
29 cortical tissue samples of 233 subjects, and
we detected 816 genes with consistent differences betwee
30 protein spiked with 1000 ppm HCP standards,
we detected 83 HCPs, 61 out of which were not identified
31 We detect a high frequency of mutation in CTNNB1 (43%),
32 We detect a number of recurrent fusions, such as those i
33 In five patients
we detect a primary immunodeficiency or enteropathy, wit
34 We detect a shared G-rich DNA sequence signature that co
35 In human polymorphism
we detect a striking similarity between mutation types p
36 addition to a hydrated phyllosilicate band,
we detect a ubiquitous 3.4-micrometer absorption feature
37 ntibiotics post-ASP, and by days of therapy,
we detected a 4.3% (-5.4% - -3.1%) decrease in overall u
38 We detected a 40-pS and 20-pS potassium channel in the b
39 seq, single-molecule RNA FISH, and DNA FISH,
we detected a cancer sample with EML4-ALK fusion RNA wit
40 We detected a few Pdx1(+)/Ptf1a(-) lineage cells in addi
41 We detected a high frequency of genomic alterations typi
42 aining an EndoU catalytic-inactive mutation,
we detected a higher abundance of PUN RNA in the cytopla
43 -based repertoire sequencing [RACE-RepSeq]),
we detected a lambda LC monoclonal expansion in the bone
44 Conversely,
we detected a legacy effect of predators on plankton in
45 We detected a marginal effect on cognitive function in c
46 Here
we detected a more complex behavior with both proliferat
47 oronavirus disease 2019 (COVID-19) pandemic,
we detected a new immunofluorescence (IF) pattern in ser
48 More specifically,
we detected a number of changes in lower taxa reminiscen
49 We detected a replicable increase in brain BOLD signal v
50 that results are comparable between genera,
we detected a significant 283-fold increase in Anisakis
51 Using this approach,
we detected a significant release of MNPs after 3.5 minu
52 We detected a similar pattern of apoprotein cross-linkin
53 We detected a single candidate region on cattle chromoso
54 We detected a small decrease in ribosome occupancy on th
55 We detected a strong relationship between ACEs and a sel
56 Also,
we detected a structurally different rectangular neural
57 sing a machine learning prediction algorithm
we detected a subset of genes whose abundance could be u
58 We detected a total of approximately 9,000 subclonal mut
59 Concurrent with peak pDC frequency,
we detected a transient decline in the ability of pDCs t
60 Yet, in another subset of founder mice,
we detected aberrant integration events at the target si
61 Within this rich resource,
we detected aberrant trafficking of lysosomal proteases
62 n the largest longitudinal BD study to date,
we detected abnormal cortical changes with high anatomic
63 We detect abundant TCR sequences even after exclusion of
64 Moreover,
we detected activated ISG-expressing microglia envelopin
65 We detect activity time courses that follow the hypothes
66 Additionally,
we detected adaptive immune responses against the vector
67 We detected all four clades of C. auris without cross-re
68 We detect an age-dependent decrease in NSC O-GlcNAc leve
69 ned with information from the fossil record,
we detect an evolutionary signal of natural selection th
70 Notably,
we detected an association of Prevotellaceae and Ruminoc
71 In all analysed MJD models,
we detected an elevated calpain activity at baseline.
72 Moreover, in the absence of AhR,
we detected an enhanced T helper type-2 (Th2) [increased
73 In NAFLD-HCC patients,
we detected an enrichment in pathogenic (p = 0.024), and
74 We detected an enrichment of the eQTLs from the glucose
75 Importantly,
we detected an expansion of SARS-CoV-2 nucleocapsid prot
76 In the subesophageal mass,
we detected an extensive filigree of TH-immunoreactive (
77 single nuclei data from adult brain neurons,
we detected an extrachromosomal circular DNA event.
78 Additionally,
we detected an increase in the rate of expansion induced
79 zygous knockouts housed at 30 degrees C, and
we detected an intact brown fat response through exogeno
80 We detected an interaction between COPA and STING, and m
81 Furthermore,
we detected an interaction between the MuV P protein and
82 monosomal and polysomal ribosome fractions,
we detected an invariant set of 72 of 79 core RPs, RACK1
83 Moreover,
we detected an ongoing diploidization process in this ge
84 In adjusted analyses,
we detected an overall increase of VRE infection followi
85 With X-ray crystallography,
we detected an unexpected photochemical intermediate tra
86 uorescent probe elsewhere in RNAP or in DNA,
we detect and characterize TL closing and opening in sol
87 l experts and we are constantly refining how
we detect and discriminate objects in the world around u
88 molecular mass, and fast acquisition rates,
we detect and image individual membrane-attached actin f
89 molecular complexes such as the proteasome,
we detect and quantify assemblies invisible to nsEM.
90 iagnostics with the potential to improve how
we detect and treat neurological pathologies.
91 dorsal CA1-DG axis from sleeping male mice,
we detected and classified two types of LFP events in th
92 data from the PsychENCODE BrainGVEX project,
we detected and corrected 201 (12.5% of total data gener
93 In the present study,
we detected and quantified 16-O-methylated diterpenes (1
94 se improved mass spectrometric capabilities,
we detected and quantified 216 isotope-labeled synthetic
95 We detected and quantified clear wall thinning around pl
96 effect relative to the immunological signal
we detect,
and demonstrate that immune-amnesia is largel
97 -scale RNA-seq data across many individuals,
we detect ASAS events associated with genome-wide associ
98 participants using a weighted genetic score
we detect associations with CKD stages and complications
99 We detected associations between multiple environmental
100 We detected at least one virus in 89% of the ant samples
101 We detected AURKA-dependent phosphorylation of RPS6KB1 i
102 In this study,
we detected autoantibodies against AGE-modified proteins
103 In IBD + CDI,
we detect both metabolites associated with inflammation/
104 More precisely,
we detect bursts of adaptive evolution in thermal sensit
105 in macrophages than in cycling T cells, and
we detected,
by coimmunoprecipitation assay, an interact
106 ing survey data of the human gut microbiome,
we detected C. difficile colonization and blooms in peop
107 tional two metastatic colon cancer patients,
we detected CD8(+) neoantigen-specific cells targeting t
108 We detected cell-to-cell variability using flow cytometr
109 Furthermore,
we detect changes in both amino acid and lipid metabolit
110 m a process-based biogeochemical model, here
we detect changes in ecosystem N cycle across the Tibeta
111 ry NSCs following decreased O-GlcNAcylation,
we detected changes in the STAT3 signaling pathway indic
112 We detected changes in virus particle density, suggestin
113 mining meiosis in cin8Delta kip3Delta cells,
we detected chromosome breakage in the meiosis II cells.
114 We detect co-localisation of eBMD GWAS and osteoclast eQ
115 We detected coinfections in cases of severe rotavirus di
116 (3+)-heme bound to the HRMs and to the core,
we detected conformational changes in the catalytic core
117 We detected considerable differences in the extent, loca
118 We detected consistent and significant increase of RLIM
119 Among 4,689 HCP-seasons,
we detected coronavirus infection in 387 (8%).
120 Many of the tandem repeat loci that
we detected correlated with cytogenetic fragile sites.
121 Furthermore,
we detected corresponding dynamics in human biopsies fro
122 We detected cross-replicating associations with rs113859
123 We detected CXCR4-using (X4) strains in five of the eigh
124 Unexpectedly,
we detected deposition of the classical inhibitory histo
125 tion heterogeneity in these scenarios, while
we detected differences in susceptibility to technical b
126 We detect different clonal expansion of the adaptive imm
127 For both mi- and ra-siRNAs,
we detected differential expression patterns following g
128 On the other end of the continuum,
we detected diminished expression of genes repressed by
129 We detected distinct morphological changes in LX-2 cells
130 We detected DJ-1 and XLF interaction in ATII cells in em
131 In 2017,
we detected DNA from "Candidatus Mycoplasma haemohominis
132 We detect early changes in ECM structure and composition
133 ng at the low frequency side of the bandgap,
we detect efficiency and spectral nonlinear dependencies
134 Although
we detected elevated anti-Candida antibodies in placebo
135 By contrast,
we detected enhanced plasma levels of inflammatory media
136 In this study
we detect evidence of the effect of autozygosity in 4 ou
137 Using two-photon imaging,
we detected evoked and spontaneous neuronal activity in
138 reference to a robust phylogenomic tree [6],
we detected evolutionary transitions between heterothall
139 We detect explosive radiations of testes mass diversity
140 but not the Bly-4 anti-CD21 antibody clone,
we detected expression of CD21 on both CD4(+) and CD8(+)
141 We detect extensive fine-scale population structure at e
142 However, from these published data sets,
we detected few changes under most conditions and were u
143 Using single-cell RNA sequencing,
we detected FLiCRE transcripts among the endogenous tran
144 the genome-wide association analysis (GWAS),
we detected for most shape and size-related traits, QTL
145 We detected four conservation hotspots for parrots: two
146 We detected four different paternal lineages of domestic
147 ombination with orthogonal analyses in mice,
we detected four main pathways that contribute to SVAS r
148 At the 31K SNPs level,
we detected four QTL on three chromosomes (Omy1, Omy12 a
149 colorimetric formulations, and as an example
we detected gaseous ammonia with Cu(II).
150 ine the clinical relevance of fusion events,
we detect gene fusions from a cohort of 742 patients fro
151 We detected gene flow from Pleistocene Siberian wolves,
152 We detected gene flow from the Taimyr lineage to Arctic
153 At the 3-d time point,
we detected gene signatures for cell cycle regulation, i
154 We detect genetic overlap between brainstem volumes and
155 We detected genome-wide significant signatures of natura
156 We detected genomic regions harboring genes associated w
157 ration of (64)Cu-Macrin in rabbits and pigs,
we detected heightened macrophage numbers in the infarct
158 alysis of two different CRC patient cohorts,
we detected heterozygosity for NAT2 alleles targetable b
159 We detected high allelic diversity in microsatellites, b
160 We detected high ploidy diversity in Allium and a polypl
161 We detected high viral loads in swabs from the nose and
162 We detected homologous segments that span the first beta
163 We detected human papillomavirus (HPV)-clade-specific di
164 We detected hundreds of dysregulated genes in Mef2c-Het
165 We detected (
i) elevated IL6 levels in patients with bia
166 Furthermore,
we detect IdU label on single DNA molecules in the genom
167 We detected IL-9 levels and T(H)9 differentiation in pat
168 utosomal mosaic chromosomal alterations that
we detected in 179,417 Japanese participants in the BioB
169 g the phase velocity of the waveguide modes,
we detect incoherent A-exciton bleaching along with a co
170 In support of these data,
we detected increased circulating tissue factor and thro
171 We detected increased expression of both tumor-associate
172 We detected increased expression of phosphorylated eIF4E
173 We detected increased Trpm3 mRNA levels in dorsal root g
174 We detected inflammation in the cerebrospinal fluid and
175 In the experiments,
we detect instability and localize its source, implement
176 Here,
we detect intrinsic instability in DNA flanking the RNA-
177 We detected KIT and/or NRAS mutation, known as frequentl
178 of three replicates from each of two donors,
we detected large clusters of integration sites with mul
179 We detected large introgressed Manihot glaziovii genome-
180 We detect leukemic variants in the blood and bone marrow
181 Further,
we detected light-induced phosphorylation in the minor l
182 r xCT expression, and reactive astrocytosis,
we detected local Iba1+ microglial inflammation that int
183 Here,
we detected LPS-derived lipid A from the Gram-negative p
184 xpressed in muscle tissue, and, accordingly,
we detected METTL21C-catalyzed methylation of AARS1 in m
185 We detected microglia regional heterogeneity using a hyb
186 We detect minimal admixture among neighboring groups bet
187 Although
we detected more genes associated with developmental dis
188 Investigating further,
we detected mTOR activation at the mechanistic nexus of
189 First,
we detect no bunching of results just above the classica
190 Using super-resolution microscopy
we detect no change in dendritic spine morphology, indic
191 Despite this divergence,
we detect no large-scale structural rearrangements, homo
192 Unlike other European Neolithic populations,
we detect no resurgence of hunter-gatherer ancestry at a
193 During this time,
we detected no acclimation of respiration rates, no ther
194 We detected no binding to mannan and BSA.
195 We detected no cytotoxicity of Gd-lip in human liver cel
196 In the primary analysis,
we detected no difference in eGFR for the intervention a
197 We detected no evidence of horizontal transmission via i
198 Here
we detected NO in the living brain using carbon fiber mi
199 We detected no major intrinsic cytotoxicity dysfunction
200 neralists did not decline after logging, and
we detected no overall changes in relative abundance or
201 We detected no significant elevations in a broad range o
202 Throughout the observing period,
we detected no single dispersed pulsed emission coincide
203 We detected no somatic L1 insertions in single cells of
204 We detected nominal significant interactions between PRS
205 t disrupts Gle1 nucleocytoplasmic shuttling,
we detected nuclear accumulation of specific mRNAs with
206 Surprisingly,
we detected only minor changes in the translational prof
207 We detected over 1.8 billion individual trees (13.4 tree
208 We detected over-representation in 13 Pfam terms includi
209 We detected phenotypic differences among the engineered
210 We detected planktonic foraminifera eDNA down to 30 cm a
211 antibodies recognizing SARS-CoV-2 proteins,
we detected preexisting humoral immunity.
212 Interestingly, here
we detected profound mechanistic differences among these
213 In addition,
we detected rare coding variants in the C9, SPEF2 and BC
214 We detected RBC (GPA(+))-engulfed material in circulatin
215 We detected reduced relative numbers of helper T cells a
216 large-scale genome-wide association studies,
we detected relevant tissues/cell types and candidate ge
217 ns from livers of mice globally lacking LAL,
we detected residual acid hydrolytic activities against
218 We detected RNA-seq profiles in 96 of 100 of samples (96
219 Additionally,
we detect robust and sustained neutralizing antibody res
220 We detected SARS-CoV-2 plasma RNA in 27% of hospitalized
221 Importantly,
we detected SARS-CoV-2-reactive CD4(+) T cells in ~40%-6
222 ning to answer a series of questions: How do
we detect scientific innovations?
223 In nearly half of the diffracting waveforms,
we detected seismic waves scattered by three-dimensional
224 We detected serum vitamin A (VA) concentration in differ
225 In XRCC4/p53-deficient ESCs,
we detected seven RDCs, all of which were in genes and t
226 We detect several phenomena predicted to arise from the
227 Using next-generation sequencing,
we detected several candidate miRNAs from both EBOV and
228 By in situ hybridization,
we detected several of these RNAs in the cytoplasm of th
229 Within a single engram population,
we detected several sub-ensembles composed of neurons co
230 We detected shifts in relative abundances of marine and
231 Moreover,
we detected signals of antibiotic-resistance evolution o
232 In the African ape lineage,
we detect signatures of positive selection that occurred
233 In addition to non-homologous end joining,
we detect signatures of replication-associated processes
234 the genome for evidence of local adaptation,
we detected signatures of long-term balancing selection
235 We detected significant differences in rates of transmis
236 We detected significant differences in the protein decor
237 We detected significant genetic structure with an extrao
238 Intriguingly, by patch-clamp technique,
we detected significant NO(3) (-) conductance of OsPIP1;
239 We detected significant positive relationships between w
240 We detected significant responses to human disturbance a
241 We detected similar levels of complexes formed between D
242 In trigeminal primary sensory neurons,
we detected single-channel activity with biophysical and
243 in-associated proteins in endocytic patches,
we detected single-molecule residence times around 1 to
244 We detected six pathogenic/likely pathogenic variants an
245 We detected Sox9 expression in muscle progenitor cells u
246 We detected spike-reactive CD4(+) T cells not only in 83
247 We detect strong signals of polygenic adaptation for hei
248 In contrast, in turtles from Hawaii,
we detected strong antibody reactivity mainly in tumored
249 We detected strong signals associated with both flowerin
250 In addition,
we detected substantial differences between the cell-typ
251 We detected substantial variation in heat tolerance of a
252 However,
we detected T conversion into E2 in islets from two out
253 Furthermore,
we detected TDP-43 oligomers in these spALS spinal cord
254 posure prophylaxis program for Kenyan women,
we detected tenofovir-diphosphate in 61% (125/201) of ra
255 By employing gastrointestinal 3D organoids,
we detect that ERK3 protein levels steadily decrease dur
256 te altimetry and satellite ocean-color data,
we detect that when the strain rate of mesoscale surface
257 hroughout mouse embryonic brain development,
we detected that besides the endosomal localization it a
258 bin is treated as a new synthetic marker and
we detect the associations between bins and traits.
259 of 42 days, during which SOD1 fibrils form,
we detect the disappearance of the native monomeric spec
260 We detect the formation of an intermediate radical anion
261 We detect the presence of metallic tin among the degrada
262 Remarkably, proteins where
we detect the strongest evidence of clustering belong to
263 Using synthetic paper,
we detected the antibiotic enrofloxacin in whole milk wi
264 We detected the expression levels of APA isoforms in ind
265 Using stable isotope dilution LC-MS/MS,
we detected the formation of 3-bromotyrosine, a specific
266 We detected the formation of a long-wavelength band when
267 We detected the formation of acrylamide adducts with thi
268 We detected the most pronounced differences at 3 dpf, in
269 Specifically,
we detected the occurrence of prominent sleep-like TMS-e
270 Further, in wild-type GluA2 receptors,
we detected the population of a stable desensitized stat
271 We detected the presence of soluble organically bound io
272 d chromatography-mass spectrometry analysis,
we detected these flavonoids in the eye upon their intra
273 We detected these increases in egg volume and nestling s
274 We detect this encoded two-color fluorescence signature
275 We detected three classes of genomic architectures: trai
276 Within this QTL,
we detected three putative candidate genes, fgfa8, cyp17
277 We detected transfer of cytotoxic multiprotein complexes
278 Surprisingly,
we detected trivial FGF13 in adipose of wild-type mice f
279 At higher doping,
we detected two distinct current-carrying modes with zer
280 In all species,
we detected two distributed neuronal subsystems: the sub
281 ombined with PCR-based copy number analysis,
we detected two ecDNA elements that differ in migration
282 We detected two ground-state unprotonated retinal photop
283 We detected two main areas of high landscape permeabilit
284 In three out of eight participants,
we detected vaccine-binding germinal centre B cells up t
285 ross time points, protocols, and replicates,
we detect variability in cell proportions between differ
286 We detected variable effects of warm temperatures (negat
287 In STING V154M/WT mice
we detected variable expression of inflammatory infiltra
288 However,
we detected very little temporal synchronization of thes
289 ith a supported lipid bilayer (SLB) and MAG,
we detect vesicular GD1a and GT1b binding and determine
290 We detected viral contamination among all samples, suppo
291 Interestingly,
we detected virus in systemic tissues such as pancreas a
292 Notably,
we detected VZV- and HCMV-infected cells in the contrala
293 cells constitutively secrete antibodies, and
we detected VZV-specific PCs in the BM of all subjects.
294 Using the platform,
we detect widespread differences in cell type-specific g
295 We detected wild-type and single mutant viruses each pos
296 We detect,
without any corrections, correlations corresp
297 -type (WT) and mutant MESD in HEK293T cells,
we detected WT MESD in cell lysate but not in conditione
298 We detected ZEA in spiked and naturally contaminated mai
299 We detected ZIKV asRNA in semen of 9 of 19 men (47.4%) d
300 We detected zones where GEMs display especially low diff