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1 Expression was analyzed by 1-way analysis of variance (significance

2 ipid and aqueous extracts of raw claw muscle were analyzed by (1)H NMR spectroscopy and MVA (multivar

3 iment, the composition of the gut microbiota was analyzed by 16 S rRNA gene high-throughput sequencin

4 tal biopsy-associated microbiota composition was analyzed by 16S ribosomal DNA sequencing.

5 m mice and the composition of the microbiota was analyzed by 16S ribosomal RNA sequencing.

6 graphy and the composition of the microbiota was analyzed by 16S rRNA sequencing and quantitative pol

7 Feces were collected and microbiota were analyzed by 16S rDNA sequencing.

8 Fecal samples were analyzed by 16s ribosomal RNA sequencing.

9 were collected and proportions of microbiota were analyzed by 16S rRNA amplicon sequencing and quanti

10 Each acquisition was analyzed by 2 different observers; first observer an

11 Hypodensities were analyzed by 2 independent blinded raters.

12 One hundred seventy OCT pullbacks were analyzed by 2 independent observers with intravascu

13 Images were analyzed by 2 interpreters in random order and sepa

14 beled methyl d-glucose-4,6-phosphates, which were analyzed by (31)P NMR spectroscopy.

15 and nasal samples of 86 school age children was analyzed by 454 pyrosequencing of the 16S rRNA gene

16 es from school-age farm and nonfarm children were analyzed by 454-pyrosequencing of the bacterial 16S

17 complex is dissected into subcomplexes that are analyzed by a three-dimensional gel electrophoresis

18 mplex with various telomeric DNA models have been analyzed by a combined ESI MS and X-ray diffraction

19 Each sample was analyzed by a standard pulse and by an experiment su

20 ND Leukocytes infiltrating the failing heart were analyzed by a multistep enzymatic procedure over a

21 d along the coast of Rio de Janeiro, Brazil, were analyzed by a nontargeted approach based on GCxGC/T

22 (68)Ga-PSMA-11 PET/CT images were analyzed by a nuclear medicine physician.

23 of Chamelea gallina and Tapes philippinarum were analyzed by a proteomic approach based on a two-dim

24 It has been shown that such situations can be analyzed by adding a binary indicator (exposed/nonexp

25 by absorption properties of the compounds to be analyzed by adjusting the excitation wavelength.

26 ty and major adverse cardiovascular outcomes were analyzed by age, sex, and CAD status.

27 In the vast majority of cases, these have been analyzed by aligning sequence reads to a single ref

28 Differences among lines were analyzed by ANOVA and shown to be significant (P <0

29 The experimental data were analyzed by ANOVA method and a well-predictive, sec

30 Payments from 2013 to 2014 were analyzed by anti-VEGF agent, payment category, and

31 sition of the gate dielectric and CuPc films are analyzed by atomic force microscopy, grazing inciden

32 The assembly of the immunochip surface was analyzed by atomic force microscopy (AFM) and the NS

33 nical properties and dynamics at equilibrium were analyzed by atomic force microscopy.

34 Subgroups were analyzed by basophil activation test (BAT) and CAP-

35 Proteins were analyzed by biochemical and proteomic approaches.

36 exposed to cigarette smoke, and their lungs were analyzed by biochemical, immunologic, and morphomet

37 Interobserver variability was analyzed by calculating intraclass correlation coeff

38 imation difference between CATCRP and CASimK was analyzed by calculating the arithmetic, absolute, an

39 ose fibers extracted from rice and oat husks were analyzed by chemical composition, morphology, funct

40 ation patterns and uronic acid epimerization were analyzed by chemical derivatization and LC-MS/MS.

41 Bacterial leakage was analyzed by chi(2) and Fisher exact tests (alpha = 5

42 Dichotomous variables were analyzed by chi2 test and continuous variables with

43 Development of allergic immune responses was analyzed by collecting draining lymph nodes and sera

44 species representing 10 Brassicaceae tribes were analyzed by comparative chromosome painting and/or

45 The sensitivity of the safety assessments was analyzed by comparing LLGR and 24-hour UFC in the pl

46 ochemical mechanisms of a few reactions have been analyzed by computational methods, including quantu

47 Abeta10-40 conformations were analyzed by computing secondary structure, backbone

48 olomics analyses, and mitochondrial function was analyzed by confocal microscopy and spectrofluoromet

49 global organization of protein binding sites is analyzed by constructing a weighted network of bindin

50 Data were analyzed by Cox regression, with adjustment for sex

51 te diastolic atrial contraction phases (SRa) were analyzed by dedicated software (EchoPAC, GE) and co

52 These reaction pathways were analyzed by density functional theory calculation.

53 Results were analyzed by descriptive statistics followed by gene

54 samples from the Yangtze River Delta region were analyzed by DRIFTS and chemical methods.

55 with varying Ce(3+):Ce(4+) are produced and are analyzed by electrochemical methods.

56 Optimization and characterization steps were analyzed by electrochemical techniques such as elec

57 fect content of the resultant solid Ge films were analyzed by electron backscatter diffraction, scann

58 flow cytometry, the production of cytokines was analyzed by ELISA or intracellular staining and flow

59 IL-4, and IL-6 and endothelial cell markers were analyzed by ELISA.

60 om baseline in pulmonary function at Week 48 were analyzed by emphysema extent.

61 ol study with 99 survivors, 99 nonsurvivors) were analyzed by enzyme-linked immunosorbent assay with

62 Visfatin levels were analyzed by enzyme-linked immunosorbent assay, and

63 Salivary levels of analytes were analyzed by enzyme-linked immunosorbent assay.

64 Compounds 1-3 were analyzed by EPR and NMR spectroscopy, DFT calculati

65 ions at110 degrees C for 3h and the residues were analyzed by ESI/qTOF/MS using MS/MS and isotope lab

66 ceiver operating characteristic (ROC) curves were analyzed by evaluating the area under the curve (AU

67 Moriles" and "Vinagre de Condado de Huelva", were analyzed by excitation-emission fluorescence spectr

68 The residues of the four sulfonamides (SAs) were analyzed by extraction process and liquid chromatog

69 Phonon-electron interaction is analyzed by finding the phonon features involved in t

70 Phenotype of immune cells was analyzed by flow cytometry, and cytokines by enzyme-

71 culating CD4+ T cells from infected children was analyzed by flow cytometry, and disease severity was

72 s detected by EB/AO staining, and cell cycle was analyzed by flow cytometry.

73 Cells were analyzed by flow cytometry and sorted from species

74 henotype, and cytokine production by T cells were analyzed by flow cytometry or enzyme-linked immunos

75 . nucleatum strains and neutrophil apoptosis were analyzed by flow cytometry.

76 from ischemic and contralateral hemispheres were analyzed by flow cytometry.

77 or seronegative and HIV-uninfected controls were analyzed by flow cytometry.

78 Biofilm samples were analyzed by FLX+ pyrosequencing of the V1 to V4 hyp

79 aining) analytes found in low-concentrations were analyzed by Fourier transform ion cyclotron resonan

80 u Marc.) nectar, honey sac content and honey were analyzed by FTIR-ATR spectroscopy and reference met

81 eptides), and the output (captured peptides) were analyzed by G12 and R5 competitive ELISA as well as

82 of Adult Men, buttock fatty acid composition was analyzed by gas-liquid chromatography in 1992 to 199

83 arked by dried fruit and cooked fruit aromas were analyzed by gas chromatography coupled to olfactome

84 Skeletal muscle, liver, and plasma samples were analyzed by gas chromatography time-of-flight mass

85 Fatty acids were analyzed by gas chromatography, and retinol and alp

86 The acetonitrile extract was analyzed by GC-MS/MS.

87 3)C]glucose, (13)CO2, or D2O supplementation were analyzed by GC-MS and/or LC-MS over time courses du

88 Overlap of functional profiles was analyzed by gene set enrichment analysis profiles.

89 our mutations detected, the two HA mutations were analyzed by generating recombinant viruses.

90 EGC-conditioned media was analyzed by high-sensitivity liquid-chromatography t

91 Active constituents of respective extracts were analyzed by high performance liquid chromatography

92 fibrosis in wild-type and miR-155(-/-) mice was analyzed by histology, collagen, and profibrotic gen

93 Liver tissues were analyzed by histology and by immunoblotting.

94 ted; hepatocytes and liver mononuclear cells were analyzed by histology, immunoblots, and confocal mi

95 Monoamines are analyzed by HPLC with coulometric electrochemical de

96 tric electrochemical detection (ED), pterins are analyzed by HPLC with coupled coulometric electroche

97 chemical and fluorescence detection, and PLP is analyzed by HPLC with fluorescence detection.

98 ration of phenolic compounds in each extract was analyzed by HPLC.

99 Phenolic content was analyzed by HPLC.

100 Phenolic compounds were analyzed by HPLC photodiode array detector, liquid

101 Aqueous supernatants were analyzed by HPLC-DAD and extractable anthocyanin co

102 ocyanins and flavanols-anthocyanins adducts, were analyzed by HPLC-DAD/ESI-MS.

103 h curves (BTCs) and retention profiles (RPs) were analyzed by ICP-MS.

104 and the concentrations of up to 18 elements were analyzed by ICP-OES.

105 LNs from 298 patients were analyzed by IHC; 41 (14%) were IHC-positive (42% in

106 membrane lipid rafts and adhesion receptors were analyzed by imaging flow cytometry.

107 ve polymerase chain reaction, protein levels were analyzed by immunoblot assays.

108 prevalence, and impact of thermal processing were analyzed by immunoblot with sera from 52 peanut-all

109 ent-invasive E coli or control agents; cells were analyzed by immunoblots and quantitative polymerase

110 LAP+ and LAP- fractions were analyzed by immunofluorescence and microarray.

111 Human pancreatitis tissues were analyzed by immunofluorescence.

112 Intestines and organoids were analyzed by immunohistochemical, in situ hybridizat

113 ession of LTB4R, LTB4R2, CYSLTR1 and CYSLTR2 was analyzed by immunohistochemistry (IHC) and quantitat

114 Liver was analyzed by immunohistochemistry and mRNA levels wer

115 choalveolar lavage (BAL); and alveolar SGLT1 was analyzed by immunohistochemistry.

116 fenib; tumor growth was measured and tissues were analyzed by immunohistochemistry and immunoblots.

117 Tumor tissues were analyzed by immunohistochemistry for levels of SMAD

118 ols, and participants of a vaccination trial were analyzed by immunohistochemistry, along with flow c

119 Age-matched nBmp2NLS(tm) and wild type mice were analyzed by immunohistochemistry, behavioral tests,

120 sues of different stages and isolated crypts were analyzed by in situ hybridization and immunohistoch

121 Liver biopsy specimens were analyzed by in situ hybridization.

122 lements such as Ca, Fe, K, Mg, Mn, Na and Zn were analyzed by inductively coupled plasma atomic emiss

123 effects (clinically significant improvement) were analyzed by intention to treat.

124 Data were analyzed by intention-to-treat basis.

125 een monocytes and cerebral endothelial cells were analyzed by intravital microscopy.

126 t are known not to contain caramel colorants were analyzed by isotope dilution LC-MS/MS to determine

127 Flow-weighted daily composites were analyzed by isotope dilution liquid chromatography

128 Data were analyzed by Kaplan-Meier log-rank test and Cox regr

129 Data were analyzed by Kruskal-Wallis and Mann-Whitney U tests

130 isons of biochemical and clinical parameters were analyzed by Kruskal-Wallis/Bonferroni-adjusted Mann

131 ted when the recombinant monoclonal antibody was analyzed by LC-MS to determine the molecular weights

132 assay), phenolic composition of each extract was analyzed by LC-MS.

133 Leaves were analyzed by LC-HRMS and a comprehensive statistical

134 by the ORAC method and the more active ones were analyzed by LC-MS/MS.

135 e of GA area growth in study and fellow eyes was analyzed by linear regression of square-root transfo

136 Data were analyzed by linear mixed models or generalized line

137 Data were analyzed by linear regression and independent sampl

138 ned, and the effective fraction (30-100 kDa) was analyzed by liquid chromatography-mass spectrometry,

139 IgG tryptic glycopeptides were analyzed by liquid chromatography electrospray ioni

140 luates from gel regions equivalent to 38 kDa were analyzed by liquid chromatography-tandem mass spect

141 by blinded researchers, and tissue sections were analyzed by local and blinded reference pathologist

142 Status of graft patency across time was analyzed by longitudinal nonlinear mixed-effects mod

143 sections of AD patients and healthy controls was analyzed by macro- and microautoradiography and by c

144 These fragments can then be analyzed by MALDI mass spectrometry, and the peptide

145 eudomonas aeruginosa, and E nterobacter spp. were analyzed by MALDI-TOF-MS in negative ion mode to ob

146 Storage compound distribution was analyzed by mass spectrometry imaging and morphologi

147 All bands were analyzed by mass spectrometry following cyanogen br

148 After elution and proteolysis, the peptides were analyzed by mass spectrometry to identify proteins

149 Eighty thermally treated soybean samples were analyzed by mass spectrometry to measure the concen

150 on, n = 15), and one control cohort (n = 20) were analyzed by mass spectrometry-based proteomics (n =

151 structures of antigenic glycans, which also were analyzed by mass spectrometry.

152 Stool samples were analyzed by mass spectrometry.

153 respectively, and their releasate proteomes were analyzed by mass spectrometry.

154 e, and then both specificity and sensitivity were analyzed by matched inference.

155 The enriched phospho- moieties are analyzed by matrix-assisted laser desorption ionizat

156 The results are analyzed by means of bifurcation diagrams.

157 tors, symptoms, and noninvasive test results was analyzed by means of logistic regression.

158 Viral infectivity was analyzed by means of microscopy, immunofluorescence,

159 The function of naive or treated mast cells was analyzed by means of RNA sequencing, quantitative RT

160 Factors with a potential influence on LLGR were analyzed by means of ANOVA and the Levene test of h

161 phils, irrespective of whether the specimens were analyzed by means of conventional flow cytometry or

162 Samples were analyzed by means of liquid chromatography-quadrupo

163 es of a set of 36 samples of Spanish paprika were analyzed by means of parallel factor analysis (PARA

164 amples from 121 children with acute wheezing were analyzed by means of serology.

165 id, lung tissue, or human nasal polyp tissue were analyzed by means of Western blotting, immunoassays

166 Potential moderators of efficacy were analyzed by meta-regression.

167 ting blood samples were collected and plasma was analyzed by Metabolon, Inc.

168 Batech and Malus domestica were analyzed by methods such as inductively coupled pla

169 and to different concentrations of ammonium were analyzed by microarray and reverse transcription qu

170 Gene expression patterns were analyzed by microarrays and clinical data were coll

171 ning the lymphatic microvascular network can be analyzed by microscopy (stage 5).

172 n and memory scores over 8 years (2002-2010) were analyzed by mixture models among 10,241 adults aged

173 The binding of bicyclic compounds was analyzed by molecular dynamics simulations based on

174 solates and their virulence-associated genes were analyzed by multilocus sequence typing (MLST) and s

175 Wine volatiles were analyzed by multiple techniques, including headspac

176 ESR1 mutations were analyzed by multiplex digital polymerase chain reac

177 magnetic resonance (CMR) and tissue samples were analyzed by multiplexed quantitative proteomics.

178 e association between CHD and growth indices was analyzed by multivariable linear regression, adjuste

179 arkers significantly correlated with outcome were analyzed by multivariable Cox regression and correl

180 Antigenic determinants on Bla g 2 were analyzed by mutagenesis based on the structure of t

181 om nine cultivars of different qualities and were analyzed by nanoUPLC and Ultra Definition Mass Spec

182 l (non-affected) anterior myocardial regions were analyzed by next generation sequencing (NGS) and po

183 irradiated Wistar rat lungs and whole blood were analyzed by next-generation sequencing and the chan

184 e structures of these poly-alpha-truxillates were analyzed by NMR, FT-IR, and HRMS.

185 from incubations of HDL with CHO-SR-B1 cells were analyzed by non-denaturing PAGE, size-exclusion chr

186 ical variables, VT recurrence, and mortality were analyzed by NYHA IV status using Kaplan-Meier analy

187 The modified Rankin Scale score was analyzed by ordinal logistic regression, which yield

188 ontaining octapeptides derived from glycinin was analyzed by oxygen consumption measurements, absorba

189 DATA EXTRACTION: Extracted data were analyzed by pairwise and network meta-analysis.

190 nd DNA methylation of their promoter regions was analyzed by PCR and pyrosequencing.

191 lected 14 months after delivery; genomic DNA was analyzed by PCR to detect the Dnajb1-Prkaca fusion,

192 Collected data were analyzed by principal-component analysis to identif

193 he solution structure of the switch I region is analyzed by pulsed electron-electron double resonance

194 Fecal and ileal microbiota were analyzed by pyrosequencing of 16S rRNA genes and en

195 expression levels in humanized mouse livers were analyzed by qPCR and Nanostring.

196 d from subjects undergoing bariatric surgery were analyzed by qRT-PCR for expression of WNT/PCP genes

197 m hypochlorite, and these reaction solutions were analyzed by QTOF.

198 Microbial community structure can be analyzed by quantifying cell numbers or by quantifyin

199 of PRP and PPP on HPLSC bone differentiation was analyzed by quantifying calcium deposition after 14

200 tal of 7,924 sets of ultrasound measurements were analyzed by quantile regression to establish longit

201 RNA from cell lines and tissues was analyzed by quantitative polymerase chain reaction,

202 Monoglyceride lipase (MGLL) expression was analyzed by quantitative RT-PCR, Western blot, and i

203 ithout colon inflammation (controls, n = 23) were analyzed by quantitative polymerase chain rection t

204 Clinical outcomes from the ABSORB III trial were analyzed by randomized treatment assignment cumulat

205 ases acting on RNA (ADAR)(rs1127309TC) genes were analyzed by real-time PCR.

206 -59 months and living in rural Zanzibar, and were analyzed by real-time polymerase chain reaction tar

207 ated to cardiac differentiation and function were analyzed by real-time quantitative polymerase chain

208 Data were analyzed by repeated measures ANOVA and post hoc Bo

209 trans- and cis-beta-Carotenes were analyzed by reversed-phase HPLC method using a mobi

210 m a single donor treated with or without UVR were analyzed by RNA-seq, exome-seq, and H3K27ac ChIP-se

211 LNs from 256 patients were analyzed by RT-PCR; 176 (69%) were PCR-positive (52

212 applied: Transformation of the bulk material was analyzed by Scanning Electron Microscopy (SEM), X-ra

213 ent for 0 min, 30 min and 2 h, the pellicles were analyzed by SDS-PAGE.

214 Mitochondria were analyzed by semi-quantitative confocal imaging.

215 The intratumoral TSL and dox distribution were analyzed by single-photon emission computed tomogra

216 on of each element to CAT2 promoter activity was analyzed by site directed mutagenesis.

217 GR salivary levels were analyzed by spectrophotometry.

218 ial membrane, and proximity-labeled proteins were analyzed by stable isotope labeling with amino acid

219 liferative and cytokine-producing capacities were analyzed by stimulation with overlapping peptides s

220 al distribution of recruitment/derecruitment was analyzed by subtracting subsequent images.

221 a Thaumatin-like protein purified from wine, was analyzed by Synchrotron Radiation Circular Dichroism

222 In top-down proteomics, intact proteins are analyzed by tandem mass spectrometry and proteoforms

223 ally essential proteins identified by Tn-seq were analyzed by targeted proteomics, and 70% of them we

224 de of the most potent STAT3 inhibitor Erasin was analyzed by the investigation of structure-activity

225 The effectiveness of each approach was analyzed by the root mean square error (RMSE) measur

226 sh blood cultures received in the laboratory were analyzed by the Accelerate Pheno system within 0 to

227 eaf leachate and two humic-rich lake waters, were analyzed by the direct method presented here and in

228 erwent resting-state fMRI scans and the data were analyzed by the fALFF approach.

229 ry VT or VT storm at 5 international centers were analyzed by the International Cardiac Sympathetic D

230 ed experimentally and their bonding features were analyzed by theoretical calculations.

231 this respect, a new set of olive oil samples was analyzed by these three techniques.

232 Data were analyzed by three investigators using qualitative i

233 ency variants (minor allele frequency </=5%) were analyzed by three types of aggregating motifs defin

234 Collected spectra were analyzed by three-dimensional positive matrix facto

235 Orodental status was analyzed by trained dental practitioners blinded to

236 ectra available for 828 of these annotations were analyzed by translating experimentally known fragme

237 Infectious particles were analyzed by transmission electron microscopy.

238 Imaging was analyzed by two readers.

239 from contrast-enhanced spectral mammography were analyzed by two fellowship-trained breast imagers w

240 S ReST Committee following laser vitreolysis were analyzed by type to gain an understanding of the sp

241 es are ultrafiltrated and resulting extracts are analyzed by UHPLC-MS/MS.

242 light, medium, medium-dark and dark roasted) were analyzed by ultra-performance liquid chromatography

243 rent concentrations of SO2 added at pressing were analyzed by ultrahigh resolution mass spectrometry

244 amplicon sequencing, and metabolite profiles were analyzed by ultrahigh-performance liquid chromatogr

245 Associations with survival were analyzed by univariate and multivariate analyses.

246 Factors were analyzed by univariate and multivariate logistic re

247 f the active compounds and their metabolites were analyzed by UPLC-TWIMS-QTOF-MS.

248 a produced by our algorithm can subsequently be analyzed by use of relevant specialized software.

249 ption (including fried and unfried potatoes) was analyzed by using a Block Brief 2000 food-frequency

250 uct a repeat cross-sectional database, which was analyzed by using a difference-in-differences model

251 etween preterm birth and risk of incident HF was analyzed by using a Poisson regression model.

252 Childhood Origins of Asthma Study [n = 28]) was analyzed by using bisulfite sequencing or Illumina 4

253 rived dendritic cells from allergic patients was analyzed by using flow cytometry.

254 lation or interaction of signaling molecules was analyzed by using phospho flow cytometry, immunoblot

255 tion of antigen, HLA molecules, and tryptase was analyzed by using structured illumination microscopy

256 in enhancement of at least 30%, 50%, and 65% was analyzed by using the Akaike information criterion.

257 Study variation was analyzed by using the Cochran Q test of heterogeneit

258 d matched peripheral blood from 132 subjects were analyzed by using 16-color flow cytometry and confo

259 c compositions in the first 26 weeks of life were analyzed by using 16S rRNA gene sequencing.

260 tandard-dose mammograms and synthetic images were analyzed by using a fully automated algorithm.

261 Data were analyzed by using analysis of variance, t test, or

262 NET formation and proteins were analyzed by using confocal immunofluorescence micro

263 ytical performances in cancer cell detection were analyzed by using electrochemical impedance spectro

264 Cs), and moDC/naive CD4(+) T-cell cocultures were analyzed by using ELISA and flow cytometry.

265 Serum SplD-specific IgE levels were analyzed by using ELISA.

266 iferation and secreted immunoglobulin levels were analyzed by using flow cytometry and ELISA.

267 Cell markers were analyzed by using immunohistochemistry, the Luminex

268 Data were analyzed by using linear mixed-effects models.

269 ks, or both) and respiratory symptoms scores were analyzed by using logistic (asthma) and negative bi

270 Data were analyzed by using multistate models that estimate p

271 between fluke infection and immune responses were analyzed by using multivariable linear mixed-effect

272 challenge was performed, and cough responses were analyzed by using nonlinear mixed-effects modeling

273 Data were analyzed by using one-way or two-way analysis of va

274 y, fractional anisotropy, and 3D tractograms were analyzed by using paired t tests and analysis of va

275 Nuclear magnetic resonance (NMR) profiles were analyzed by using partial least-squares discriminan

276 Data were analyzed by using Pearson correlation, linear regre

277 Data were analyzed by using random effects analysis of varian

278 hanges in sensitization and total IgE levels were analyzed by using regression analysis corrected for

279 d samples-127 primary and 37 relapse samples-were analyzed by using RNA sequencing.

280 In total, 50 samples were analyzed by using SMRT sequencing.

281 Clinical data were analyzed by using Student t tests.

282 Differences in perfusion patterns were analyzed by using the Fisher exact test.

283 samples from Germany and all over the world were analyzed by using the newly developed multi-mycotox

284 Measures obtained at visual inspection were analyzed by using the Wald chi(2) test.

285 ery and diffusion-weighted imaging sequences were analyzed by using validated morphologic scales.

286 curcumin concentration in enriched DES phase was analyzed by UV-Visible spectrophotometer.

287 ntermediates, and final degradation products were analyzed by UV/vis, NMR, GC-MS, and EPR.

288 bjects in the Severe Asthma Research Program was analyzed by weighted gene coexpression network analy

289 Protein expression and mRNA levels were analyzed by Western blotting, flow cytometry, and r

290 Evolved strains can be analyzed by whole genome sequencing and an array of o

291 l response of AM roots under K(+) deficiency was analyzed by whole-genome RNA sequencing.

292 Tumors were analyzed by whole-exome, transcriptome, and/or T ce

293 isolates not associated with these outbreaks were analyzed by whole-genome sequencing (WGS) analysis.

294 Results were analyzed by Wilcoxon signed-rank test with Bonferro

295 Data were analyzed by Wilcoxon, Mann-Whitney U, and permutati

296 Both monomer and polymer single crystals are analyzed by X-ray diffraction, which is the first ca

297 [K(18-crown-6)(Et2O)][Cp''2ThH2]2, 3, which was analyzed by X-ray crystallography, electron paramagn

298 The crystalline nature of thiamine was analyzed by X-ray diffraction studies.

299 Binding modes of 3FMTDZ and HETDZ were analyzed by X-ray crystallography.

300 ns in degree of overlap were noted when data were analyzed by year.