ライフサイエンスコーパス: analyses

1 to macroevolutionary as well as phylodynamic analyses.

2 s were included in the per-protocol efficacy analyses.

3 using summary statistics from standard eQTL analyses.

4 idelines for performing and interpreting PRS analyses.

5 er devices followed by interaction parameter analyses.

6 ETI was confirmed by genetic and biochemical analyses.

7 nal, and pathological significance in genome analyses.

8 y are unaccounted for in existing global MHW analyses.

9 a is poorly understood and confounds current analyses.

10 these loops is a critical part of most Hi-C analyses.

11 onitoring after inverse probability weighted analyses.

12 virus evolution and large-scale phylodynamic analyses.

13 lone or as care bundles were included in the analyses.

14 l data and can be used in cost-effectiveness analyses.

15 had baseline and week 12 data available for analyses.

16 ein as we show in biochemical and structural analyses.

17 pitation and analysed by NMR and methylation analyses.

18 nt, and often prevent rapid, high-throughput analyses.

19 atrophy using nested multivariate regression analyses.

20 t and quantitative polymerase chain reaction analyses.

21 ween groups using the t test and chi-squared analyses.

22 ime scales and by multiwavelength and target analyses.

23 q 2000 system and subjected to bioinformatic analyses.

24 y analyzed by both imaging and flow velocity analyses.

25 ttee using an adaptive approach with interim analyses.

26 A sequencing and reverse-phase protein array analyses.

27 , enzyme activity assays and gene expression analyses.

28 tion genetics, and structural bioinformatics analyses.

29 a pipeline that performs maximum likelihood analyses, a k-mer-based set difference algorithm, and ra

30 Detailed kinetic analyses across different time scales, that is, from the

31 equence dependence, we conducted correlation analyses across pairs of packaging events.

32 means of multilevel random effect regression analyses adjusting for clustering in health centres.

33 Analyses aggregating all 6 wk of posttax time points sho

34 ce pattern analyses, and logistic regression analyses) aimed to detect any combinations of events pre

35 ele-specific copy number and serial sampling analyses allowed for the detection and tracking of clona

36 Adjusted MSPHM survival analyses also found no significant difference in 28-day

37 ur metabolomics results, our transcriptomics analyses also revealed significant alterations in gene e

38 Genome-wide analyses also revealed that wild-type AID localized to M

39 g protocol and provide a guide to downstream analyses and allow for exclusion of samples of poor qual

40 g Bayesian skyline plots (BSP), multivariate analyses and Bayesian clustering.

41 se discrepancies could compromise downstream analyses and biological reproducibility, we built a more

42 nce is critical for downstream transcriptome analyses and can lead to precise molecular mechanisms fo

43 ss how these errors have affected downstream analyses and give recommendations for software developer

44 Descriptive analyses and multivariable binary logistic regression an

45 This report provides analyses and perspective of a survey of critical care wo

46 Meta-analyses and prospective comparisons of different formul

47 n and elaboration document, may guide future analyses and reporting of RCTs.

48 oothing (LOWESS) regression and change-point analyses and Spearman correlation coefficients.

49 alence were pooled using random-effects meta-analyses and were 0.32% (95% confidence interval [CI]: 0

50 We concluded that the combination of linkage analyses and WGS to search for disease genes still remai

51 viding spicy and fruity notes at the sensory analyses, and being appreciated for their body balance,

52 Retrospective studies, prospective analyses, and case series were included.

53 ed proteins, in vitro transcription, kinetic analyses, and in vivo cell viability assays, we report t

54 ical analysis (descriptive, sequence pattern analyses, and logistic regression analyses) aimed to det

55 synthesis of new evidence with existing meta-analyses, and studies had several methodological shortco

56 Here, the experimental and theoretical analyses are focused on single tetracenothiophene molecu

57 These analyses are important because they provide a starting p

58 However, such analyses are infrequently performed.

59 uses of sex-biased mortalities, more complex analyses are needed that incorporate various ecological

60 Several functional analyses are performed on this model to study MFS relate

61 Electrochemical analyses are presented together with the rational and pa

62 Subsequent differential expression analyses based on datasets integrated from different pla

63 We performed subgroup analyses by treatment or types of FLAIR-HAs defined by l

64 Our analyses confirm previously reported drivers(6,7), raise

65 cular docking, and site-directed mutagenesis analyses confirmed these compounds as active site-direct

66 Through genetic and proteogenomic analyses, Davis and colleagues in this issue of Cancer R

67 Stable isotope analyses (delta(13)C and delta(15)N) indicated that the

68 These analyses demonstrate that D567/S566 and E491/S527, locat

69 romatin immunoprecipitation-sequencing-based analyses demonstrate that direct readout of H3K27me3 by

70 Our analyses demonstrate the effectiveness of public health

71 Clustering concordance analyses demonstrated some differences across analytical

72 Corrected post-hoc analyses demonstrated that patients had significant enla

73 The benchmark analyses demonstrates that the spectrum of the polymer n

74 The primary analyses detected no convergence across studies.

75 ing motif; subsequent genomic and functional analyses establish SERBP1 regulation role in metabolic r

76 Statistical analyses estimated the treatment delay times at which ha

77 with adjusted linear and logistic regression analyses examining associations with immune parameters a

78 nd scale of the early liver have constrained analyses examining its emergence during organogenesis.

79 In trans-ethnic meta-analyses for 15 hematological traits in 746,667 particip

80 validate the efficiency of this new version, analyses for GM12878 individual autosomes were performed

81 In adjusted analyses, for every 10 telestroke consults requested by

82 Meta-analyses found significant associations between violence

83 Based on more than 2000 gut content analyses from animals ranging over three orders of magni

84 environmental exposure is a binary variable, analyses from exposure-stratified models which consist o

85 Functional and lipidomic analyses further link AMPK regulation of ferroptosis to

86 Univariable and multivariable analyses generated differing inference for 11/30 (30.67%

87 On unadjusted analyses, Gulf State DSAs were associated with 3.52 fewe

88 perly include, in continuous phylogeographic analyses, H5N1 sequences that are only associated with l

89 While procedures for primary radiomic analyses have been established in recent years, processi

90 Genome-wide transcriptomic analyses have revealed abundant expressed short open rea

91 Extensive CT deletions and mutagenesis analyses helped us zoom in on three residues in the CT,

92 Systems biology analyses highlight both similarities and differences bet

93 no association with SCC in crude or adjusted analyses (HR 0.98, 95% CI 0.73-1.31, p=0.89).

94 Expression quantitative trait loci analyses identified multiple SNPs associated with expres

95 Our genome-wide analyses identified one novel gene (NDUFB9) associated w

96 ble for post-pregnancy viral load trajectory analyses (ie, had at least two viral loads in the year a

97 expanded these observations with replication analyses in a large biorepository database.

98 rinted carbon electrodes (SPCE) suitable for analyses in gaseous samples which are of course lacking

99 istical power in combination with orthogonal analyses in mice, we detected four main pathways that co

100 ansient transformation assays and expression analyses in mutants reveal that, in planta, the majority

101 Our analyses included 156 total effects drawn from 42 studie

102 Analyses included reward positivity (RewP) data from 118

103 We conducted various sensitivity analyses, including further adjusting for property value

104 As meta-analyses increase across HF science, interpreting and ha

105 Together, these analyses indicate increases in the likelihood of faster-

106 Our analyses indicate that DNA methylation patterns associat

107 Our analyses indicate that sea-level rise in recent decades

108 The analyses indicate that the base rate of true effects is

109 and receiver operating characteristic curve analyses indicated that amyloid-beta1-42 was equally eff

110 Secondary analyses indicated that this interaction was mirrored by

111 number of systematic reviews (SRs) and meta-analyses (MAs) have evaluated the effect of periodontal

112 In secondary analyses, normalized pT(308) AKT1 was positively correla

113 nalyses were undertaken, along with subgroup analyses of >=75% compliant patients, to compare the inc

114 We performed single-cell transcriptome analyses of 14,441 cells from embryonic day 12 submandib

115 Expression analyses of 23 genes involved in salinity stress reveale

116 We performed histomorphological analyses of 47 teeth from 15 individuals with known life

117 sease Neuroimaging Initiative study, and the analyses of 64 drug responses, we demonstrate that MKpLM

118 Mechanistically, single-cell RNA-sequencing analyses of a mesenchymal niche model showed that fibrob

119 Reported here are thermochemical and kinetic analyses of a new pincer-ligated rhenium complex ((tBu)P

120 These are secondary analyses of a randomized controlled trial in rural Malaw

121 ummary, the platform affords high-throughput analyses of antibodies, including bispecific antibodies

122 We performed shotgun proteomics analyses of aortas of transgenic mice with macrophage-sp

123 vant for future population-scale genome-wide analyses of blueberry.

124 Whole-brain analyses of cortical thickness were conducted both with

125 In this study, functional analyses of CpRbp1 were performed by constructing a knoc

126 earch activities: 1) a series of descriptive analyses of cross-sectional data from demographic and he

127 bulk TCR sequencing and structural affinity analyses of cytomegalovirus-specific T cells, and throug

128 Structural analyses of DAD2(N242I) and DAD2(D166A) revealed only sm

129 In lung and pancreatic cells, gene ontology analyses of DM promoters show an enrichment for genes in

130 In analyses of empirical datasets, RTDT produced dates that

131 Although analyses of Fgf8 conditional knockout mice did not revea

132 We hypothesized that bivariate analyses of findings from a meta-analysis of genome-wide

133 However, longitudinal analyses of gene expression in healthy individuals-espec

134 Our candidate-gene association analyses of GWAS datasets suggested an increased risk of

135 However, analyses of HK phosphorylation in biochemical assays in

136 In RNA-Seq analyses of human brain samples from the NYGC ALS cohort

137 ctivity studies in rodents and imaging-based analyses of human brains.

138 Many analyses of hydrocarbon mixtures instead characterize th

139 m total human lungs, along with histological analyses of IAV binding.

140 ed integrated metabolomic and transcriptomic analyses of liver tissue from patients with AH or alcoho

141 Systematic analyses of MADS-box genes have been reported in many pl

142 Paired TCRalphabeta analyses of MAIT cells revealed large clonal expansions

143 However, recent evolutionary analyses of mammals, plants, and flies report pervasive

144 Economic analyses of medical scribes have been limited to individ

145 ent studies have justified the more powerful analyses of multi-platform data.

146 Conformational analyses of N-acyl isochalcogenouronium species and comp

147 ng, but the effects of the transformation on analyses of neural populations are not well understood.

148 Many available tools facilitate analyses of one of the two major mechanisms of transcrip

149 Meta-analyses of one-sample proportions were done in all pati

150 Genetic analyses of patients with severe spine segmentation defe

151 We performed microarray analyses of peripheral blood mononuclear cells (PBMC) RN

152 Through extensive simulation studies, the analyses of PET-imaging outcomes from the Alzheimer's Di

153 Analyses of plasma collected pre- and postadministration

154 dies as well as qualitative and quantitative analyses of proteins in complex matrices such as those f

155 Expression and functional analyses of PunPgp-2 and PunPgp-9 in Saccharomyces cerev

156 randomized controlled trials (RCTs) and meta-analyses of RCTs published from August 1, 2014, through

157 quantitative polymerase chain reaction analyses of representative genes validated the RNA-Seq r

158 Comparative analyses of S-locus sequences of these three S-haplotype

159 We performed bioinformatics analyses of SFRP1 expression in human cancer.

160 Analyses of skeletal-related events were also done in th

161 Structure-function analyses of SKIP reveal that the C-terminal region compr

162 pose-built software designed for large-scale analyses of splicing, and identified 13,149 high-confide

163 Ensemble analyses of surrounding groups for WT and mutant KSIs pr

164 Analyses of synteny across genomes of bioluminescent spe

165 using mathematical modeling and statistical analyses of T cell receptor sequencing data, we develop

166 ely linked to policy changes and descriptive analyses of the complementary survey domains.

167 patients are scarce hampering comprehensive analyses of the complex interaction between the gut micr

168 Petrographic analyses of the dated units characterize the crystal car

169 Our analyses of the genome, transcriptome, and functional as

170 Our analyses of the kinetics of the forward and reverse reac

171 Here, we combined analyses of the mitochondrial COI gene and 11 microsatel

172 X-ray structural analyses of the PIs complexed with wild-type Protease (P

173 Here, we use time series gene expression analyses of the rattlesnake venom gland in comparison wi

174 These single-cell transcriptomic analyses of the shoot apex yield insight into the proces

175 this study, we conducted spatially explicit analyses of the stromal-immune interface across 400 mela

176 Analyses of the transport cycle show that serine phospho

177 Genomic analyses of these isolates along with those isolated fro

178 Gene expression analyses of these plants reveal a trade-off between VTE

179 High-resolution analyses of these two types of QTLs reveal distinct posi

180 RNA- and ATAC-sequencing analyses of tumor-derived cell lines revealed downregula

181 Here, we present global analyses of viral transcript levels to further understan

182 escence lifetime imaging (FLIM) and spectral analyses offers the potential of detecting diseases of t

183 Overall pathway analyses on the multi-omics datasets showed significant

184 Immunogenicity analyses only included women with visits 28-35 days apar

185 In contrast to recent analyses, our results confirm that ecological niche diff

186 other domains where large-scale statistical analyses over encrypted data are needed.

187 tial trial conducted in France, with interim analyses planned every 50 patients.

188 Additional analyses probed stress effects on the dorsal hippocampus

189 eliminary and observational in nature, these analyses provide support for a possible mechanistic link

190 rgeting the plant defense regulator NPR1 and analyses receptor FLS2.

191 In both genera, coalescent analyses recovered almost all nominal taxa as "species".

192 nge of ready-to-use workflows to run complex analyses requiring minimal intervention by users.

193 Similar findings were observed in analyses restricted to participants with a history of os

194 Mass spectrometry analyses reveal that HIPK2 is at least O-GlcNAc modified

195 Epigenetic analyses reveal that histone modifications, but not DNA

196 Our analyses reveal that not all traits are equally well-sui

197 Aerial-image analyses reveal that resulting "Sesarma-grazed" creekhea

198 Our computational analyses reveal that the receptive fields of human midge

199 Phylogenetic analyses reveal that these form-function associations re

200 These analyses reveal the noncanonical nature of the transform

201 Single-cell mutation and phospho-protein analyses reveal the segregation of oncogenic STAT5 and E

202 Comprehensive lipidomic analyses revealed a dramatic increase in membrane satura

203 Further metabolomic analyses revealed a marked reduction in storage lipids a

204 unoprecipitation (HITS-CLIP) and biochemical analyses revealed direct binding between endogenous TruB

205 Our systematic and comprehensive analyses revealed distinct genetic architecture of human

206 on features of forest edges and microclimate analyses revealed negative associations between minimum

207 Results of steady-state kinetic analyses revealed that AsFMO exhibited negligible activi

208 d mutagenesis and competitive ligand-binding analyses revealed that DPO and Ala-AA occupy the same bi

209 Pharmacokinetic analyses revealed that INT131 penetrates into the brain

210 RNA-Seq analyses revealed that ROCK2 controlled a unique transcr

211 Epigenetic analyses revealed that T(RM) cells align closely with co

212 Indirect calorimetry analyses revealed that the deletion of ALX dysregulated

213 Integrative analyses revealed that the HOXA5-9 transcription factors

214 Morphometric analyses revealed that Treg depletion blocked plaque rem

215 Flow cytometric and gene expression analyses revealed that VAT transplantation recapitulated

216 Phylogenetic analyses revealed that while a few genes cluster with th

217 Phylogenetic analyses revealed the cryptic introduction of at least s

218 Integrative analyses revealed the E+ microbiota correlated and co-va

219 In secondary analyses, saliva Mn, hair Cu, and saliva Cr were selecte

220 tent, suggesting that correlation and decile analyses should be conducted before applying any inflamm

221 Our genetic analyses show M. guttatus is highly dispersive and maint

222 Transcriptomic and metabolomic analyses show that alpha2-Na/K ATPase loss alters metabo

223 Evolutionary analyses show that in 17 out of 19 cases, the Hominidae

224 Detailed data analyses show that the major advantage of MAGELLAN is at

225 assays and caspase 3, caspase 7, and PARP-1 analyses show that these compounds activate apoptosis.

226 Theoretical analyses show that, although CAs could stimulate non- HC

227 Exploratory analyses showed similar associations across particle met

228 RNA sequencing, metabolomics, and molecular analyses showed that OXPHOS(high) BAP1 mutant UM cells u

229 In silico analyses showed that these five loci contained cell-spec

230 ta were analysed using independent component analyses, source localization and measure projection ana

231 Electrochemical corrosion analyses strongly suggested that Cr(0) in the corrosion

232 mpounds upon bioinformatics drug repurposing analyses, such as calcium folinate and betulin.

233 Genomic analyses suggest an average window of over three years b

234 Our analyses suggest diversification was largely driven by c

235 Experimental and mathematical modeling analyses suggest that active cargo loading reduces non-s

236 Retrospective analyses suggest that banding a sleeve using a silicone

237 In addition, our analyses suggest that genetic factors controlling circad

238 Our analyses suggest that the magnitude of sex differences i

239 Subsequent analyses suggest that these three regions may be especia

240 Interaction analyses suggested an association with road traffic nois

241 However, allergen-specific analyses suggested increased risks of sensitization to b

242 Clonal and anatomical analyses suggested that a single FC gradually recruits n

243 One-sample Mendelian randomization analyses suggested that the association between PTSD sym

244 om thermodynamic, kinetic, and computational analyses suggested that this 12-mer is highly labile and

245 Mendelian randomization analyses suggested that triglycerides, interleukin-6 (IL

246 Fusarium-damaged kernels and deoxynivalenol analyses supported the findings of the field and greenho

247 inclusion of these factors in multivariable analyses that also adjust for the complex variance struc

248 al burden of disease, this systematic review analyses the evidence from rigorously evaluated programm

249 In multivariate analyses, the odds of having A-HSIL were >6 times higher

250 tion between payments and prescribing in all analyses; the remainder (n = 6) had a mix of positive an

251 er and were therefore excluded from efficacy analyses; the remaining 151 patients were included in th

252 In multivariable adjusted analyses, there was no significant association between b

253 In histological analyses, these changes manifested as larger lesion size

254 We performed analyses to assess system sensitivity; examine inter-rat

255 We used multidimensional statistical analyses to characterize the impact of age on the overal

256 , source localization and measure projection analyses to compare neural oscillations between individu

257 ed transcriptomic, sphingolipid, and protein analyses to evaluate sphingolipid metabolism and signali

258 owed-up our top findings using two-sample MR analyses to evaluate whether estimates may be biased due

259 We used principal component analyses to identify eating behavior patterns, twin mode

260 eptibility with multiple in-depth structural analyses to identify key ACE2 amino acid positions inclu

261 we used dynamic resting state functional MRI analyses to increase temporal resolution to seconds and

262 etic resonance imaging with semantic content analyses to investigate the neural mechanisms that under

263 We used multivariate pattern analyses to measure reactivation of initial pair memorie

264 munoprecipitation and genome-wide expression analyses to study a possible role of Rme1 in C. albicans

265 Analyses used 2-sided t tests, Wilcoxon rank sum tests,

266 Results varied in sensitivity analyses using different estimates of clinical trial suc

267 ct of corticosteroids by random-effects meta-analyses using the generic inverse variance method.

268 Based on structural and affinity analyses, we designed two cyclic peptide mimics of the T

269 , scanning electron microscopy, and sediment analyses, we document hundreds of rodent coprolites foun

270 In adjusted regression analyses, we examined associations of brain insulin sign

271 Using single-molecule analyses, we examined the mechanism by which E449K activ

272 ng comparative biochemical and physiological analyses, we found that mitochondrial function is mainta

273 Using complexome profiling and biochemical analyses, we have explored the structural rearrangements

274 Through sequence similarity network analyses, we identified 29 Opp and 19 Dpp sequences that

275 pectra, kinetics, biochemical assays, and MS analyses, we show that the conserved nucleophilic residu

276 approaches and immunofluorescence microscopy analyses, we sought to investigate the mechanisms that r

277 Analyses were adjusted for confounding by time, cluster

278 and multivariable binary logistic regression analyses were conducted on weighted data.

279 Subgroup and sensitivity analyses were conducted using an ICU cohort and Acute Ph

280 All analyses were descriptive.

281 Cerebrospinal fluid analyses were negative for SARS-CoV-2 in all patients te

282 Efficacy analyses were performed by applying RECIST 1.1 criteria

283 Standard fixed-effects meta-analyses were performed for each comparison, and a meta-

284 Bacterial 16S ribosomal RNA analyses were performed on stool samples from 405 HIV-in

285 Additional sensitivity analyses were performed to assess the effect of missing

286 ession and Kaplan-Meier), and center effects analyses were performed to examine the association of EC

287 riable and multivariable logistic regression analyses were performed to identify parameters that were

288 Mendelian randomization analyses were performed to infer phenome-wide effects of

289 Adjusted logistic regression models and meta-analyses were performed.

290 tartrate-resistant acid phosphatase [TRAP]) analyses were performed.

291 All analyses were stratified by race/ethnicity in the main a

292 The aims of the present exploratory analyses were to: (i) characterize the effect of verubec

293 tention-to-treat (ITT) and per-protocol (PP) analyses were undertaken, along with subgroup analyses o

294 Random effects dose-response meta-analyses were used to estimate summary relative risks (S

295 g 1959 external controls and performing meta-analyses with 2 independent EoE genome-wide association

296 ntire lung, and multiple logistic regression analyses with areas under the curve (AUCs) as outputs we

297 nd did one-way and probabilistic sensitivity analyses with determination of 95% credible intervals (C

298 We performed similar analyses with maternal second trimester tocopherol isofo

299 m ~10 to 780 mbsf by combining metabarcoding analyses with mid/high-throughput culturing approaches.

300 Comparative genomics and phylogenetic analyses within the Malassezia genus revealed that flavo