ライフサイエンスコーパス: by analyzing

1 s the safety of red light treatment of sperm by analyzing, (1) the levels of double-strand breaks in

2 of the proposed SEC-FD method was evaluated by analyzing 100 nm liposomes and albumin-FITC conjugate

3 By analyzing 101 mMTOR-related genes in a large ID patie

4 These conclusions are supported by analyzing 14 single-site HsIPMK mutants, some of whic

5 We demonstrate Perturb-seq by analyzing 200,000 cells in immune cells and cell line

6 f published effect sizes and estimated power by analyzing 26,841 statistical records from 3,801 cogni

7 ro could be used in a highly parallel screen by analyzing 288 different polymerase reaction condition

8 e times of all major lineages of Hymenoptera by analyzing 3,256 protein-coding genes in 173 insect sp

9 By analyzing 320 methylated genes from 26 studies on blo

10 H/MeCN/HCOOH) which we applied and validated by analyzing 46 common flavones and flavanones and exemp

11 A first study was conducted by analyzing 52 samples from two durum and common wheat

12 By analyzing 6,456 genomes from multiple tumor types, we

13 By analyzing 8,711 individuals, we showed that heterozyg

14 By analyzing 96 different genes in a panel of tumor samp

15 By analyzing a chemically induced mutant of Mimulus lewi

16 By analyzing a collection of Muscodor isolates with vary

17 nvestigate the genetic ancestry of wild rice by analyzing a diverse panel of rice genomes consisting

18 from the T2D case-control study are limited by analyzing a few number of SNPs at a time from a large

19 By analyzing a kinetic model, we uncovered a nonlinear i

20 Furthermore, by analyzing a large number of human antibody sequences

21 /beta-TREC ratio, in HIV disease progression by analyzing a large number of patients in 3 cohorts wit

22 ism of action of the SLAM family in NK cells by analyzing a mouse lacking the entire approximately 40

23 The proposed method is demonstrated by analyzing a National Institute of Standards and Techn

24 We demonstrate its use and interpretation by analyzing a publicly available cancer dataset with mo

25 This was accomplished, in part, by analyzing a quality control standard, matrix spiked w

26 explore some common methodological criticism by analyzing a sample of contemporary coronary stent tri

27 of glacier and ocean changes back 1700 years by analyzing a sediment core from Sermilik Fjord near He

28 f a many-body quantum system be extrapolated by analyzing a sequence of finite-size cases?

29 theory underlying the plasmoelectric effect by analyzing a simplified model system consisting of a s

30 Finally, the method was validated by analyzing a variety of different reactor effluents an

31 We exercise this approach by analyzing a version of the double-slit experiment aug

32 The method was evaluated by analyzing a wide range of milk powders produced by th

33 By analyzing actigraphy data obtained from members of 26

34 By analyzing activated murine wild-type and Rheb-deficie

35 families carrying a C9orf72 repeat expansion by analyzing age at onset, disease duration, and age at

36 This model was then validated by analyzing an additional 49 samples obtained by prepar

37 solated and in vitro-cultured CD11c(+) cells by analyzing an additional phenotype, the ability to sup

38 Method accuracy and precision was checked by analyzing an AFM1 certified reference material and di

39 OMAAT was evaluated by analyzing an MSI data set of a high-throughput glycos

40 Here, we address these statements by analyzing and projecting growth responses to climate

41 By analyzing approximately 1,000 breast cancer samples,

42 By analyzing approximately 15000 measurements from 18 pr

43 By analyzing available crystal structures, we observed t

44 Ripening and growth were monitored by analyzing berry technological parameters and weight.

45 eased during the Paleocene-Eocene transition by analyzing bioapatite of terrestrial mammals.

46 a central component of the exocyst complex, by analyzing both exoc5 zebrafish mutants, and photorece

47 By analyzing CA1 pyramidal neurons in mutant hippocampal

48 By analyzing cell line responses to 265 compounds, we un

49 By analyzing cell lines, genetically modified mice, and

50 The accuracy of the method was confirmed by analyzing certified reference material ERM BC-211 (ri

51 The accuracy of the method was verified by analyzing certified reference materials (CRMs) and pe

52 We demonstrated PIUMet by analyzing changes in metabolism of sphingolipids, fat

53 We addressed this uncertainty by analyzing changes in the local and average structures

54 cted high-pressure chemistry is rationalized by analyzing charge density and electron localization fu

55 We confirm our observations by analyzing ChIP-exo, chemical mapping, and ATAC-seq da

56 By analyzing chromosome and replisome localization, we d

57 treatment, apoptosis was readily detectable by analyzing cleavage of PARP and caspase-7.

58 cidence, trends, and associated risk factors by analyzing consecutive adult patients who underwent HT

59 lustrate the power of this novel methodology by analyzing controlled experiments as well as genuine p

60 ion of CSMEN in electroporation is confirmed by analyzing crystallographic phases, multiferroic prope

61 By analyzing data from 68,496 individuals, we find that

62 The program was validated by analyzing data from a variety of samples, including m

63 fety of intensive BP reduction for acute ICH by analyzing data from several recent randomized control

64 f peptide antigen length on antibody binding by analyzing data on more than 900 peptides used for B-c

65 as compared with traditional fitting methods by analyzing datasets containing images from freshly res

66 We address this gap by analyzing descending fibers from injections of an ant

67 the universality of the assay was confirmed by analyzing different strains of influenza A virus.

68 )-methyladenosine (m(6)A) in RNA transcripts by analyzing different subcellular fractions.

69 capability of our biosensor was demonstrated by analyzing different urine samples spiked with either

70 This is exemplified by analyzing distinct features in the electrochemical re

71 ancestry to learn about health and disease, by analyzing DNA and protein sequences, but also through

72 We demonstrate the usefulness of EpiTools by analyzing Drosophila wing imaginal disc growth, revea

73 ensitivity to FGFR inhibitors was determined by analyzing drug screen data and conducting in vitro an

74 for lac repressor(R)-lac operator(O) binding by analyzing effects of RO-stabilizing and RO-destabiliz

75 M (HTM) model has been created and validated by analyzing effects of TGFbeta2 on transcellular pressu

76 ound to the functionalized array is achieved by analyzing either the intact protein mass or, after on

77 luence sleep medication prescribing patterns by analyzing Electronic Medical Records (EMRs) including

78 By analyzing enhancers during dorsal-ventral (DV) axis f

79 ost likely functional variants at each locus by analyzing epigenetic marks and gene expression data.

80 ng from ADHD and healthy control individuals by analyzing event-related potentials in the electroence

81 ature of urea-aromatic stacking interactions by analyzing experimental structures of urea transporter

82 Assessment of growth parameters by analyzing expression of cell-specific markers reveale

83 sis thaliana were functionally characterized by analyzing expression patterns, double mutant phenotyp

84 local entropy rate ([Formula: see text]) and by analyzing field and simulated deltas, we suggest that

85 By analyzing fragmentation patterns across the contiguou

86 By analyzing fusion transcriptome, we observed close clu

87 ertoire of receptor genes for each sensillum by analyzing GAL4 driver lines of Ir, Gr, Ppk, and Trp r

88 By analyzing genome sequence data from human populations

89 Here, by analyzing genome-wide translation efficiency estimate

90 By analyzing genomes and transcriptomes across 37 deuter

91 Here, we circumvent this limitation by analyzing genomes from mutator populations that arose

92 Here we show, by analyzing >2 x 10(8) TCRB sequences of circulating na

93 e conditions on astronauts were investigated by analyzing hair samples from ten astronauts who had sp

94 of heparan sulfate synthesized was confirmed by analyzing heparan sulfate content in tissues isolated

95 er, by extending the resolution to 1.1 A and by analyzing high-resolution complexes with the enantiop

96 lection operating at the HLA haplotype level by analyzing HLA A C B DRB1 DQB1 haplotype frequencies d

97 not function cooperatively can be identified by analyzing host cell transcription factor expression p

98 rsity relationships in the Brazilian Cerrado by analyzing how woody plant species richness changed wi

99 By analyzing human protein mRNA sequences, we found evid

100 portunities to decipher metabolic mechanisms by analyzing hundreds to thousands of metabolites.

101 By analyzing imputed data for a large number of human tr

102 By analyzing intracranial electrode data from humans, we

103 new mechanisms of KRAS-induced tumorigenesis by analyzing its effects on the components of the tumor

104 on the human immune system was investigated by analyzing its impact on monocyte-derived DCs.

105 ion of Chinese artichoke (S. affinis tubers) by analyzing its polar constituents and its macro- and m

106 By analyzing kidney biopsy specimens of patients with ex

107 lly, we demonstrate the power of the package by analyzing lag phase growth with single cell resolutio

108 of cultural change over periods of centuries by analyzing large textual time series, specifically dig

109 approach that predicts RNA binding activity by analyzing large-scale affinity precipitation-MS prote

110 By analyzing ligation events involving three or more loc

111 Arabidopsis thaliana growth and development by analyzing lines with decreased and increased CRF func

112 By analyzing local and systemic immune responses in peri

113 on of the various materials to be determined by analyzing local dissolution kinetics.

114 By analyzing longitudinal tumor biopsies from 17 metasta

115 By analyzing loss-of-function variants of both SirA and

116 We investigated conservation in mammals by analyzing LZA element function in human cultured cell

117 its performance on real experimental traces by analyzing macroscopic calcium-current traces elicited

118 We show, by analyzing many acoustic emission events during rock d

119 the human ortholog of Doa10, MARCH6 (TEB4), by analyzing MARCH6 autoregulation of its own degradatio

120 By analyzing metabolic flux in mouse retinas, we also fo

121 Here, by analyzing mice with juxtamembrane or kinase domain po

122 By analyzing micro-RNA expression profiles in a set of p

123 ed in 1972 and repeated the full C inventory by analyzing more than 4 decades of data on the number o

124 Finally, by analyzing more than 4,300 primary patient specimens v

125 umatic brain injuries in adults and children by analyzing mortality rates, neurologic outcomes, and a

126 We tested synaptic disruption in vivo by analyzing motor defects and binding of a positron emi

127 le of the threonine string on PrP conversion by analyzing mouse Prnp(a) and Prnp(b) polymorphism that

128 By analyzing multiple enzymes involved in sphingolipid m

129 By analyzing multitissue gene expression and genome-wide

130 By analyzing mutant allele frequency distributions in tu

131 By analyzing mutation levels, it was possible to disting

132 By analyzing nanodiffraction patterns medium-range order

133 t the single-molecule level are demonstrated by analyzing nanomechanically induced DNA denaturation.

134 e examined IgH isotype-specific BCR function by analyzing naturally switched B cells from wild-type m

135 d be observed either by inactivating Ltn1 or by analyzing NCs with limited ubiquitylation potential,

136 By analyzing online breath measurements of 146 healthy i

137 By analyzing optical spectra and by DFT computations we

138 By analyzing over 23,000 publicly available RNA-Seq data

139 inkling estimated from digital facial images by analyzing over eight million SNPs in 2,693 elderly Du

140 Finally, by analyzing patterns of coexpression, we were able to p

141 sms of dynamic sensorimotor feedback control by analyzing patterns of neural activity in the midbrain

142 By analyzing phonon mean free paths and lifetimes, we fu

143 By analyzing physiological parameters and proteome profi

144 Cell signaling is dominated by analyzing positive responses to stimuli.

145 By analyzing post-mortem gene expression data from the A

146 We test a key tenet of this hypothesis by analyzing predatory drill holes in fossil marine shel

147 patterns in a way that could not be resolved by analyzing present-day genomes alone.

148 stic systems were firstly reviewed, followed by analyzing pros and cons of cell penetrating peptides.

149 d-facing (IF) and outward-facing (OF) states by analyzing purified preparations of apo- and ion-bound

150 By analyzing radiative-convective equilibrium simulation

151 MiRNAs can be identified by analyzing reads from high-throughput deep sequencing.

152 a large community-based screening population by analyzing recall rate, positive predictive value, and

153 We also discuss the scheme feasibility by analyzing recent experiment parameters.

154 localization and excision of breast lesions by analyzing reflector placement, localization, and remo

155 sured part of the in-hive pesticide exposome by analyzing residues from live in-hive bees, stored pol

156 By analyzing results of a study of an extensive deployme

157 A retrospective study was performed by analyzing RI administrative data and findings from su

158 The analytical performance was evaluated by analyzing RNA modifications from 100 ng of RNA from h

159 By analyzing RNA-seq data combined with quantitative RT-

160 By analyzing RNA-sequencing data from The Cancer Genome

161 gnostic performance of bile EV concentration by analyzing samples from the 30 consecutive patients wi

162 Further studies could improve on ours by analyzing samples of breastmilk and formula and by in

163 By analyzing SCRS of these mutants, it provides insights

164 but also reveal different metabolic pathways by analyzing SCRS.

165 utations driving the pathway were determined by analyzing sequences obtained from the DNA fraction of

166 By analyzing sequences of experimentally validated T-cel

167 the direct and indirect effectiveness of PCV by analyzing serotype-specific colonization prevalence a

168 However, by analyzing simulated and actual LFPs, here we question

169 We validated the accuracy of the method by analyzing simulated data.

170 We validated our method by analyzing simulated extension trajectories that mimic

171 By analyzing sleep architecture, we show that NPY regula

172 ated nucleotide patterns in plant small RNAs by analyzing small RNA sequencing libraries from Arabido

173 ue freezing and sectioning, which we address by analyzing smeared biopsy tissue.

174 By analyzing spectra recorded for different delays betwe

175 The method validation was performed by analyzing spiked samples at three concentrations (10,

176 concentrations in real samples was evaluated by analyzing spiked urine at different pg/mL concentrati

177 oncept of the MBL-GS muPADs was demonstrated by analyzing standard solutions of ethanol, sulfide, and

178 system on cognition functions were examined by analyzing synaptic integrity and performing animal be

179 By analyzing synchronized neuronal NMDAR-mediated excita

180 By analyzing T-cell receptor (TCR) sequence repertoires

181 dentify common molecular mechanisms of aging by analyzing tagged signatures from 244 studies that com

182 By analyzing telomerase-positive cells and their human T

183 By analyzing telopeptide and helical sequences, we ident

184 T-cell responses were assessed by analyzing Th1/Th2 cytokine production and the CD4(+)

185 In this article, by analyzing the accrued data in The Cancer Genome Atlas

186 Here, by analyzing the actin-related protein6 mutant, which is

187 n two experiments, we demonstrate the method by analyzing the activation of manipulable nouns as subj

188 lls result from increased expression of gcd1 By analyzing the activity of recombinant Gcd1 in vitro a

189 g affinity and selectivity toward the target by analyzing the binding kinetics recorded using the SAW

190 ve surface of the electrodes were elucidated by analyzing the calculated concentration profiles of th

191 By analyzing The Cancer Genome Atlas mRNA expression dat

192 HMDMs were investigated by analyzing the cell morphology, LPS-induced cytokine p

193 uorescent dihydroresorufin were investigated by analyzing the change in surface population of single

194 By analyzing the CLIPL data, many known and novel featur

195 Novel ITDs were validated by analyzing the corresponding RNA sequencing data.

196 proposed approach and further demonstrate it by analyzing the cross-population eQTL data from the GEU

197 By analyzing the distribution of PONDS-forming sequences

198 By analyzing the distribution of reported emotional stat

199 By analyzing the DNase I hypersensitive sites under 349

200 es risk prediction in the general population by analyzing the effect of 27 HNF1A variants identified

201 This was done by analyzing the effect of postnatal inactivation of miR

202 Here we extend these findings by analyzing the effect of the hGH minigene in TgC6hp55

203 Importantly, by analyzing the effect of the IYO/RIMA pathway on xylem

204 By analyzing the effects of conduction velocity restitut

205 We have explored these issues by analyzing the effects of the divalent strontium ion (

206 By analyzing the entropy content of different spectral c

207 s, by performing time-frequency analysis and by analyzing the evolution of the driving laser's electr

208 By analyzing the exomes of 12,332 unrelated Swedish indi

209 By analyzing the exon structure of the target transcript

210 been simply obtained about 10(-19) m(2)/V(2) by analyzing the experimental results.

211 By analyzing the expression of calretinin (CR), calbindi

212 These findings were validated by analyzing the expression of genes and signaling pathw

213 By analyzing the expression of miRNAs and miRNA-processi

214 By analyzing the expression of pRGA::GFP-RGA in the wild

215 -c cells in chicken, Xenopus, and zebrafish, by analyzing the expression of synthetic enzymes of DA a

216 By analyzing the expression of the three receptors of th

217 By analyzing the expression profiles of microRNAs combin

218 te measurements rely on the 2ApFold approach by analyzing the fluorescence response of riboswitch var

219 of droplet size for the three wetting modes by analyzing the free energy landscape with many local m

220 cation of naturally occurring bacteriophages by analyzing the full genomic sequences of over 100 isol

221 By analyzing the full phenotypic breadth of the EHR, com

222 under arms-crossed and -uncrossed conditions by analyzing the functional connectivity of the IPS.

223 cal properties of the alloy was investigated by analyzing the grain refinement and microstructural ev

224 T)), but this prediction has not been tested by analyzing the GSK-3 phosphoproteome.

225 We illustrate the performance of our tool by analyzing the GWAS meta-analysis summary statistics f

226 ogical mechanisms underlying this phenomenon by analyzing the immunological mechanisms in patient ser

227 rease this mortality, we carried out a study by analyzing the infant mortality data from the Shenyang

228 ng the proliferative phase of cardiac repair by analyzing the infiltration of macrophages, Treg lymph

229 Then, by analyzing the information on the directionality of ph

230 er nature of the nanosheets were ascertained by analyzing the intensity ratio between two diffraction

231 We simulated this phenomenon by analyzing the interfacial energy of two bilayer foam

232 By analyzing the intrinsic mannose patch from a panel of

233 These predictions are validated by analyzing the invasion of melanoma cells in collagen

234 By analyzing the kinetics of Ub charging and discharging

235 icles as the SERS substrate, is investigated by analyzing the labels separately and in mixtures.

236 By analyzing the libraries subjected to selection in mic

237 By analyzing the localization of a Cdh2-EGFP fusion prot

238 that hyperconjugation operates in hydrazides by analyzing the N-H stretching mode in gas phase infrar

239 By analyzing the nucleation pathway, we conclude that fr

240 Here, by analyzing the outer layer composition of a series of

241 investigated the role of NBEAL2 in immunity by analyzing the phenotype of Nbeal2-deficient mice.

242 the various roles triplets can play in P3HT by analyzing the photoluminescence (PL) from isolated si

243 ts the origin of their structure is revealed by analyzing the PJT interaction between the frontier mo

244 and vertical retinotopic maps are generated by analyzing the response of each pixel during the perio

245 This observation is further confirmed by analyzing the results of Cyclic Voltammetry (CV), Sca

246 nm Dimer dissociation kinetics were measured by analyzing the shape of the sedimentation boundary and

247 By analyzing the sigmoid time course of CFTR current act

248 o examine the mechanism of XCI fate decision by analyzing the signaling regulatory circuit associated

249 polypharmacology of drugs can be anticipated by analyzing the similarity of binding sites across the

250 The values of Cf,exp are determined by analyzing the slopes of charge density versus Deltaf

251 f the locomotion ofDictyosteliumtandem pairs by analyzing the spatiotemporal evolution of their tract

252 onal components of environmental enteropathy by analyzing the specific metabolic and gut-microbiota c

253 A sexing accuracy of 90% was obtained by analyzing the spectra of blood circulating in the ext

254 By analyzing the spectra of the (13) C and (18) O isotop

255 By analyzing the spectra of the solvent (water) and a sp

256 role of guano on corals reefs across scales by analyzing the stable nitrogen isotopic (delta(15)N) v

257 The accuracy of the method was confirmed by analyzing the standard reference material (SRM 1640a)

258 The accuracy of the method was confirmed by analyzing the standard reference materials (BCR-482 L

259 review, we take a wide view of this problem by analyzing the strategies involved in setting up norma

260 By analyzing the structure factor and the radial distrib

261 By analyzing the structure-activity relationships of 35

262 universality of this conventional narrative by analyzing the structures of individual faculty produc

263 By analyzing the structures of SERMs and their incidenta

264 By analyzing the subcellular localization of truncated v

265 or of Y2O3:Er(3+) microtubes is investigated by analyzing the temperature and excitation power depend

266 Here, by analyzing the tension-dependent recruitment of vincul

267 By analyzing the time series RNA-seq data (days 5, 9, 13

268 to be targeted by ZIKV, which was confirmed by analyzing the transcript levels of the proteins of in

269 By analyzing the transient response of the SLG temperatu

270 By analyzing the UV and MS data, and comparison with aut

271 quare cyclobutadiene (C4H4) are investigated by analyzing the variations in isotropic magnetic shield

272 quantify the transverse momentum correlation by analyzing the visibility of this pattern.

273 By analyzing the whole-body bacterial flora of An. gambi

274 By analyzing the whole-exome sequences of 4,264 schizoph

275 methylcytosine reader Mbd1 and modifier Tet1 by analyzing their dynamic subcellular localization and

276 ance of these microparticles in food systems by analyzing their release profile under simulated gastr

277 By analyzing these substates at millisecond resolution,

278 during a vaccinia virus-induced host shutoff by analyzing total and actively translating mRNAs in a g

279 erns of all of the GalNAc-Ts in colon cancer by analyzing transcriptomic data.

280 By analyzing truncation mutants, we identified that the

281 The method was successfully verified by analyzing two certified reference materials (BCR-482

282 The method was further tested by analyzing two Norwegian human milk samples where arse

283 licability of our technique was demonstrated by analyzing tyramine in spiked serum and milk.

284 By analyzing UK National Health Service drug prescriptio

285 The system was evaluated by analyzing under- and overloaded aminopyrenetrisulfona

286 d as potential biomarkers for bladder cancer by analyzing urine glycoproteins from bladder cancer pat

287 ing procedure and illustrate the methodology by analyzing uterine fibroid gene expression data.

288 explore the role of coding variation in LAS by analyzing variants on the HumanExome BeadChip in a to

289 Finally, by analyzing very small amounts of tissues ( approximate

290 o dilute natural DOM samples was illustrated by analyzing water samples collected from northern peatl

291 sible to test directly for natural selection by analyzing whether genetic variants associated with va

292 By analyzing whole blood transcriptomes of 922 individua

293 (T/F) viruses in six HIV-1-infected subjects by analyzing whole genome sequences.

294 VHs) in patients with Parkinson disease (PD) by analyzing whole-brain resting-state functional connec

295 Here, by analyzing whole-exome sequencing data of metastatic b

296 By analyzing whole-genome bisulfite sequencing data in a

297 ally, we illustrate our proposed methodology by analyzing whole-genome genotyping data from a lung fu

298 By analyzing word lists covering nearly two-thirds of th

299 past research and offer theoretical insights by analyzing World Values Survey data from residents of

300 ked the biological relevance of this finding by analyzing WT plants under high-light stress condition