1 To address these questions,
we performed 16S sequencing on fecal DNA samples from th
2 We performed 2-photon imaging to examine the representat
3 In this paper,
we perform 2D Fourier analysis of the full bunch longitu
4 We perform a broad analysis of the recorded data, compar
5 We perform a comprehensive analysis of DNA synthesis at
6 In this study,
we perform a comprehensive unbiased characterisation of
7 Here
we perform a CRISPR/Cas9-based functional screening of 5
8 In this work,
we perform a detailed analysis of the transverse DW moti
9 We perform a detailed characterization of our engineered
10 We perform a genetic study of three MRI markers of the d
11 Here,
we perform a genome-wide CRISPR screen using an endogeno
12 Here
we perform a massive analysis on near-real-time Italian
13 Here,
we perform a statistical simulation-based study on MDLs
14 We perform a symmetry analysis that recalls that an indi
15 Here,
we perform a systematic evaluation of 18 scRNA-seq imput
16 In the current study,
we performed a 1-year follow-up assessment of the same m
17 ssect social behavior of Galphai2(-/-) mice,
we performed a 3-chamber sociability assay and found tha
18 We performed a 3D movement analysis of runners in order
19 We performed a balanced parallel and crossover design ex
20 ability, biocompatibility, and transparency,
we performed a cell tracking experiment of prostate canc
21 In addition,
we performed a ChIP-Seq experiment that identified ANT b
22 Therefore,
we performed a clinical study to elaborate on the implic
23 We performed a cohort study in which the daptomycin resi
24 We performed a cohort study with 21 patients suffering f
25 Towards filling this gap,
we performed a combined analysis of metabolic and gene c
26 Here
we performed a comparative 16S rRNA gene survey of the r
27 To begin addressing this gap,
we performed a comparative analysis of gene expression v
28 al defects in Grn-deficient mouse microglia,
we performed a compound screen coupled with high through
29 We performed a comprehensive analysis of 14 epigenetic c
30 Here
we performed a comprehensive behavioral characterization
31 We performed a comprehensive evaluation of humoral immun
32 We performed a comprehensive immunomolecular biomarker a
33 We performed a comprehensive in silico analysis of viral
34 We performed a conceptual analysis of the general phenom
35 d MLL2-dependent transcriptional regulation,
we performed a CRISPR-based screen with an MLL2-dependen
36 Here
we performed a CRISPR-Cas9 screen in human SV589 cells f
37 this unique DNA damage response in ES cells,
we performed a CRISPR-Cas9-knockout screen.
38 We performed a CRISPR-Cas9-knockout selection designed t
39 We performed a cross-sectional analysis of endocrine sur
40 We performed a cross-sectional study in Kampala, Uganda,
41 We performed a cross-sectional study with 108 post-LT pa
42 We performed a cross-sectional survey in April-May 2018
43 erogeneity of cell types located in the PVH,
we performed a detailed analysis of the neurochemical id
44 In this study,
we performed a detailed characterization of strain-speci
45 We performed a double-blind phase 2 trial of 104 patient
46 ng prolonged mechanical ventilation.Methods:
We performed a focused ethnographic evaluation at eight
47 We performed a gene expression study using RNA sequencin
48 genetic components causing this deficiency,
we performed a genome-wide association study (GWAS) for
49 We performed a genome-wide association study and analyse
50 We performed a genome-wide association study in Arabidop
51 tion, functional genomic strategy, DEADPOOL,
we performed a genome-wide CRISPR screen and identified
52 In this study,
we performed a genome-wide identification and expression
53 To identify potential resistance mechanisms,
we performed a genome-wide RNAi screen in BRCA2-deficien
54 fying the genetic susceptibility to obesity,
we performed a GWAS on metabolically healthy thin indivi
55 We performed a high-throughput whole-genome RNAi screen
56 on increase signatures by natural selection,
we performed a laboratory evolution experiment on a pane
57 To achieve high accuracy,
we performed a large number of expert-based annotations,
58 Here,
we performed a large sequencing and culture-based analys
59 We performed a large, genome-wide association study (GWA
60 To fill this significant knowledge gap,
we performed a large-scale systems-level analysis of the
61 wn toxicological threats to aquatic animals,
we performed a literature search to evaluate the strengt
62 We performed a longitudinal assessment of individuals re
63 rch for pharmacological inhibitors of SOX10,
we performed a mass spectrometry-based screen in human m
64 tematically resolve their functional status,
we performed a massively parallel screen in human cells
65 We performed a meta-analysis of primary data from labora
66 d transcriptomic components in a microbiome,
we performed a meta-omic survey of extremophile communit
67 We performed a modified intention-to-treat analysis on 2
68 edication use for patients with IPF.Methods:
We performed a multicenter RCT in newly treated patients
69 We performed a multicenter study comparing 13 commonly u
70 We performed a multicenter, double-blind trial in which
71 We performed a multicenter, double-blind, placebo-contro
72 We performed a multicenter, open-label, randomized contr
73 ta from 2,658 cancers across 38 tumor types,
we performed a multidimensional, integrated characteriza
74 We performed a nationwide retrospective cohort study on
75 In this study,
we performed a phase 1 clinical trial to assess the safe
76 We performed a post hoc analysis of patients enrolled in
77 We performed a prespecified post hoc analysis of ischemi
78 We performed a pressure and chemical tracer monitoring e
79 We performed a prospective study of 180 severely obese p
80 We performed a prospective trial of SRL monotherapy with
81 Towards this end,
we performed a protein-protein interaction (PPI) network
82 We performed a random effects meta-analysis to determine
83 We performed a randomized phase 2 study in 90 patients (
84 We performed a randomized, controlled trial comparing sy
85 We performed a randomized, controlled trial to investiga
86 We performed a retrospective analysis of consecutive adv
87 We performed a retrospective cohort of encephalitis case
88 or duration for patients with shock.Methods:
We performed a retrospective cohort study of adults admi
89 We performed a retrospective cohort study of Kaiser Perm
90 ion (IUGR) as independent predictors of ROP,
we performed a retrospective cohort study of patients wh
91 We performed a retrospective longitudinal cohort study o
92 We performed a retrospective multicenter cohort study of
93 We performed a retrospective multicenter study of 712 pa
94 We performed a retrospective review of consecutive patie
95 We performed a retrospective study of 986 019 adults who
96 We performed a retrospective study of HRIs who underwent
97 We performed a scoping review of empirical evaluations o
98 We performed a single-center retrospective study of stem
99 ell carcinoma (IASCC) in persons with HIV-1,
we performed a single-center, retrospective analysis of
100 We performed a single-center, retrospective review of ch
101 We performed a small molecule screen based on competitio
102 We performed a systematic review of all risk factors ass
103 ive system to regulate somatic proteostasis,
we performed a tissue targeted genetic screen for germli
104 We performed a transcriptome-wide analysis during in vit
105 standing of APOE4's role in AD pathogenesis,
we performed a transcriptomics analysis of APOE4 vs. APO
106 We performed a trial to evaluate the efficacy and safety
107 We performed a two-stage individual participant data (IP
108 We performed a two-step positive end-expiratory pressure
109 Here,
we perform additional temporal transcription factor mani
110 Herein,
we perform an unbiased interrogation of tumor mesenchyma
111 We performed an autopsy on a single patient who died of
112 We performed an evidence-based narrative review of the l
113 Herein,
we performed an exome-wide association study of systemic
114 its impact on population abundance estimates
we performed an experiment under controlled conditions i
115 deprivation per day for 5 consecutive days,
we performed an extensive analysis of topographical NREM
116 We performed an extensive validation of all deletions in
117 We performed an extracellular vesicle array to find prot
118 We performed an in-depth analysis of the SNCA locus to i
119 We performed an individual participant data meta-analysi
120 Methods:
We performed an individual patient data meta-analysis, i
121 ts of late-onset Alzheimer's Disease (LOAD),
we performed an integrative network analysis of multi-om
122 We performed an intensive coring study within a sub-trop
123 We performed an inversion association analysis including
124 local anesthesia on longer-term AVF patency,
we performed an observer-blinded randomized controlled t
125 quantitative intestinal permeability assay,
we performed an unbiased GWAS screen (using 156 strains
126 e operation of the on-line SDE-GC/MS system,
we performed analyses of selected real samples (beer).
127 We performed analyses to assess system sensitivity; exam
128 We performed analysis of covariance, adjusted for model
129 We performed behavioral and brain-based experiments, wit
130 To address this question,
we perform benchmark studies on simulated and real scRNA
131 We performed bioinformatics analyses of SFRP1 expression
132 ad to transcript instability, in this study,
we performed BruChase-Seq to experimentally monitor the
133 te to enhanced natural scene representation,
we performed calcium imaging of excitatory neurons in th
134 new therapeutic targets in CIC-DUX4 sarcoma,
we performed chromatin immunoprecipitation sequencing an
135 We performed chronic social defeat stress (CSDS) in mice
136 We perform circuit tracing in the D. sechellia brain, an
137 We performed co-immunoprecipitation experiments and foun
138 ld exist in A1 organization between strains,
we performed comparative analysis of neuronal population
139 We performed comparative studies in a puromycin aminonuc
140 We perform comprehensive analyses for patients from The
141 gate viral infection history in KD patients,
we performed comprehensive serological profiling using a
142 We perform computational experiments using four well-kno
143 We performed computational studies of these reactions wi
144 naive patients in the Swiss HIV Cohort Study.
We performed Cox regression models adjusted for demograp
145 We performed cross-sectional and time-to-event analyses
146 We perform CTCF ChIP-seq in multiple mouse species to cr
147 We performed CyTOF analysis of colonic mucosa samples (n
148 We perform deep sequencing across the DAP1 genomic segme
149 Here,
we perform deep transcriptomic profiling at high tempora
150 To support the experimental studies,
we performed density functional theory studies on large
151 We performed detailed characterization of B cell respons
152 of KLF4-mediated monocytic differentiation,
we performed detailed genetic studies in acute myeloid l
153 As a proof of concept,
we performed digital LAMP on a sp-SlipChip to quantify h
154 ognition and identification occur in humans,
we performed direct intracranial recordings, in a large
155 Here,
we performed Direct RNA Sequencing (DRS) using the lates
156 Here,
we performed disome and trisome footprint profiling in y
157 We perform DNA copy number profiling on mixtures of cell
158 We performed dose-response, synergism, P-glycoprotein in
159 t benefited from a nutritional intervention,
we performed endoscopy in 80 children who had biopsy-con
160 To address this,
we performed enhanced ultraviolet (UV) cross-linking and
161 We performed epigenetic analyses of BE and EAC tissues a
162 e how altered PP-InsP levels affect the ESR,
we performed epistasis experiments with mutations in rpd
163 killer (NK) cell activation by both species,
we performed ex vivo whole-blood infection assays and co
164 We perform experiments on vanadium dioxide VO(2) films,
165 In this study,
we performed extracellular recordings in adult female mi
166 the MEC also activates in a traveling wave,
we performed extracellular recordings of local field pot
167 We performed extracellular vesicle (EV) analysis to iden
168 We performed fecal transplant gavage 3 days after middle
169 ic and experimental datasets for comparison,
we perform FLOW-MAP analysis side by side with other sin
170 As a replication,
we performed follow-up targeted sequencing of ASH1L in a
171 Here,
we performed force-ramp and force-jump experiments, in c
172 In 940 mother-offspring pairs,
we performed gas chromatography-mass spectrometry and id
173 ted kinase 1 (BAK1) conformational ensemble,
we performed Gaussian accelerated molecular dynamics sim
174 Here,
we perform gene expression analysis and ChIP followed by
175 Here,
we perform genome-wide assessment of chromatin accessibi
176 To identify underlying molecular mechanisms,
we performed genome-wide association studies of the urin
177 mediated by cytotoxic T lymphocytes (CTLs),
we performed genome-wide CRISPR screens across a panel o
178 Here
we performed genome-wide CRISPR screens in Vero-E6 cells
179 In the discovery phase,
we performed genome-wide miRNA expression profiling of 1
180 stem cells are generated during development,
we performed genome-wide RNA tomography sequencing on ze
181 Here,
we performed global metabolite screening with metabolite
182 osis, development, and progression of FXTAS,
we performed global metabolomic profiling of premutation
183 In this study,
we performed high-resolution measurements of CH(4) flux
184 We performed high-resolution time-lapse microscopy of mo
185 Here,
we performed high-throughput CRISPR screening using a ub
186 We performed high-throughput screening (HTS) of a chemic
187 We performed histomorphological analyses of 47 teeth fro
188 To discern the SAN's contribution,
we performed HRV analysis on canine electrocardiograms c
189 We performed identical analyses of EEG recorded over the
190 We performed immunohistochemical analyses of 26 PDACs an
191 We performed immunoprecipitation-mass spectrometry analy
192 Here
we perform in situ transmission electron microscopy anal
193 To address these issues,
we performed in utero electroporation into the developin
194 ity of different parts of the spike protein,
we performed in vitro antibody selection for the spike a
195 Here,
we performed in vitro integration assays, finding that f
196 Methods:
We performed in vivo FME and quantification of fluoresce
197 After radiolabeling with (99m)Tc,
we performed in vivo SPECT imaging, biodistribution, and
198 We performed integrated metabolomic and transcriptomic a
199 We performed integrative methylomic, genomic, and transc
200 Using the BAL fluid,
we performed isotope dilution mass spectrometry to measu
201 We performed lineage tracing experiments to determine th
202 In addition,
we performed linear regression to identify clinical fact
203 We performed longitudinal multi-omic profiling of plasma
204 We performed machine-learning-based analyses on function
205 We performed measures on four of the most studied tendon
206 ry intake on the risk of metabolic diseases,
we performed meta-analysis, CPT1A transcription analysis
207 In this study,
we performed metabolite profiling in both brain (n = 109
208 We performed methylation-sensitive restriction enzyme-qu
209 We performed microarray analyses of peripheral blood mon
210 As) may serve as noninvasive markers of TBI,
we performed miRNA-seq to study TBI-induced changes in r
211 We performed mobile sampling using an advanced single-pa
212 To investigate this further
we performed molecular dynamic simulations of CD81 with
213 We performed molecular, histological, and metabolic anal
214 We performed morphometric quantification of the capillar
215 We performed multicolor flow cytometry to investigate CD
216 Here,
we perform multiple all-atom MD simulations of the homom
217 For the ES events,
we performed multiple functional annotations.
218 We performed multiple linear and logistic regression ana
219 We performed multistate analyses, incorporating weights
220 We performed multistep biochemical, structural, and comp
221 rgeted food fingerprint analysis of samples,
we performed multivariable data analyses, including prin
222 To define the signature,
we performed network deconvolution of transcriptomics da
223 We performed nonsupervised clustering using latent class
224 We perform operations on these analog values by manipula
225 We perform optical mapping and transmission electron mic
226 e of myopia on OCT parameters and RGC count,
we performed Pearson's correlation.
227 We performed peripheral blood mononuclear cell (PBMC) an
228 Using 18,514 sequences,
we perform phylogenetic, population genetics, and struct
229 We performed polygenic risk score (PRS) analyses to inve
230 We performed post hoc analyses to determine whether high
231 We performed pretraining using 494,364 labeled endoscopi
232 We performed Protect-seq on the human colon cancer cell
233 We performed quantitative in situ hepatic glutathione re
234 We performed Raman spectroscopy under pressure on this p
235 breadth of applicability of this technique,
we perform rapid synthesis of 20 tritiated and 10 carbon
236 We performed repeated structural and functional brain MR
237 We performed reverse-transcription polymerase chain reac
238 Hence,
we performed RNA-Seq of leaf infected with or without DB
239 We performed RNAseq of cell populations isolated using l
240 We performed RNAseq to understand how exposures alter ex
241 To systematically investigate this,
we performed robotic cancer cell line screens and discov
242 We performed scRNA-seq on skin and blood from a patient
243 Here,
we performed secondary analyses of the PRT data to inves
244 We performed segmented linear regression, adjusting for
245 Using these nanosensors,
we performed serial breath tests to monitor dynamic chan
246 We perform several tests to check for consistency and ro
247 We performed sex-specific GWAS of BE/EA in 3 separate st
248 better assess the diversity of MDV protists,
we performed shotgun metagenomics on 18 sites representi
249 We performed shotgun proteomics analyses of aortas of tr
250 We performed similar analyses with maternal second trime
251 In this study,
we performed simultaneous TG and PG analysis in blood pl
252 To fill these important knowledge gaps,
we perform single-cell RNA sequencing on two-day old sch
253 known dark zone and light zone compartments,
we performed single-cell (sc) transcriptomic analysis on
254 the development of CF lung disease.Methods:
We performed single-cell RNA sequencing of sputum cells
255 We performed single-cell transcriptome analyses of 14,44
256 an OR mechanism for the observed inhibition,
we performed single-cell transcriptomics on OSNs exhibit
257 In this study,
we performed single-nucleus RNA-Seq on the adult mouse S
258 We performed SisterC on mitotic Saccharomyces cerevisiae
259 ation on the structure and function of CHT7,
we performed site-directed mutagenesis of previously ide
260 We performed small-RNA sequencing (smRNA-Seq) and quanti
261 We performed small-RNA sequencing on liver of Tsc1-knock
262 Here,
we perform structural modeling of the SARS-CoV-2 spike g
263 To synthesize those findings,
we performed structural equation modeling, which showed
264 Here,
we performed structural studies and show that the cytoto
265 We performed studies with C57BL/6; RAG1(-/-) (C57BL/6);
266 We performed studies with male C57BL/6 mice that persist
267 We performed studies with primary mouse HSCs, human LX2
268 We performed subgroup analyses by treatment or types of
269 Finally,
we perform survival prediction using a hybrid method of
270 of pancreatic ductal adenocarcinoma (PDAC),
we performed tandem mass spectrometry analysis of HLA cl
271 In this retrospective omics study,
we performed targeted proteomics (N=625) of whole blood
272 plex role played by CYP2J2 in cardiac cells,
we performed targeted silencing of CYP2J2 expression in
273 Using immunohistochemistry,
we performed tau phenotyping of CTE neuropathologies and
274 Here
we perform TCRB sequencing, integration site analysis, a
275 With these new examples,
we perform the first cross-kingdom structural analysis o
276 We perform the structural analysis of the ComRS system f
277 To better understand how NTRs work,
we performed the first comprehensive investigation of th
278 e proof of concept and estimate effect size,
we performed the first epigenome-wide methylation analys
279 We performed the first randomized double-blind placebo-c
280 In the present study,
we performed the first rigorous assessment of the abilit
281 l profile of this airway immune dysfunction,
we performed the first single-cell transcriptome charact
282 We perform this analysis in the presence and absence of
283 We performed this test by tracking the emergence of soci
284 that are redox regulated by EGF stimulation,
we performed time-resolved quantification of the EGF-dep
285 identify novel cellular responses to stress,
we performed transcriptional analysis in acutely stresse
286 pression in the human fetal brain with which
we perform transcriptome-wide association studies (TWASs
287 ed with SARS-CoV-2 pathogenesis in macaques,
we performed transcriptomic analyses of bronchoalveolar
288 We performed transcriptomic, sphingolipid, and protein a
289 sic Fabry disease genotype and/or phenotype,
we performed unbiased quantitative morphometric electron
290 Here
we perform whole exome sequencing and gene expression an
291 Here
we perform whole-genome sequencing (WGS) of 103 UM from
292 We performed whole exome sequencing on this cohort and a
293 We performed whole genome sequencing for two American mi
294 We performed whole gut transit, bead latency, and geomet
295 We performed whole-cell patch-clamp recordings of medium
296 We performed whole-exome and shallow whole-genome sequen
297 We performed whole-exome sequencing in 222 OCD parent-ch
298 To address this gap,
we performed whole-exome sequencing in 58 men with unexp
299 ar characteristics of idiopathic NOA and SO,
we performed whole-exome sequencing of 314 unrelated pat
300 We performed whole-genome sequencing on food and clinica