ライフサイエンスコーパス: correct for

1 caused by optically dense structures can be corrected for.

2 ated with normal tissue can be estimated and corrected for.

3 ities and vacancies must be investigated and corrected for.

4 P-values for each setting were Bonferroni corrected for 404 tests.

5 ally available variable focal length lens to correct for a wide range of defocus commonly found in pa

6 nisms obtained by different force fields and correct for a wide range of stationary and dynamical obs

7 After correcting for a ~1 per thousand increase in Delta(13) C

8 when used as a standalone parameter or when corrected for additional independent predictors of trans

9 Significance was lost when corrected for age and sex (P = .073).

10 d risk of CVD events (P = 0.048), even after correcting for age (P = 0.037).

11 < 0.01), a relationship that persisted after correcting for age and BMI (r = -0.147, P < 0.01).

12 After correcting for age and sex, we identified 34 bacterial t

13 onance imaging measures and clinical scores, correcting for age, gender, spinal cord cross-sectional

14 ET) with [(11)C]raclopride (P<0.0001), while correcting for age, sex, BMI, education, smoking status,

15 ositive predictive value (PPV) or challenge, corrected for ancestry by principal components.

16 tions with striatal D2R were diminished when correcting for ancestry.

17 any argument dependent on effect sizes must correct for attenuation due to instrument reliabilities.

18 Pearson correlation coefficients (r), corrected for attenuation from within-person variation i

19 ges were reconstructed: non-TOF and TOF both corrected for attenuation using reference CT-based atten

20 axillary lymph nodes on each examination and corrected for background (18)F-fluciclovine avidity.

21 ral asymptomatic carotid arteries, which was corrected for background activity, resulting in a maximu

22 nd extrapolated to parent phthalate intakes, corrected for background and hood air exposures.

23 Determining and correcting for background contributions of Re and Os fro

24 water amounts and its isotopic values, after correcting for background.

25 Corrected for baseline differences, the mean IBDQ score

26 When correcting for baseline differences between the Afliberc

27 nfiltrate and/or scar size at 3 months after correcting for baseline values (95% CI, -1.33 to -0.32 m

28 from different studies after diagnosing and correcting for batch effects and retaining the biologica

29 r GRS_51 in the entire cohort and was (after correcting for bias) 9% for GRS_8 and GRS_12 and 7% for

30 ssed variations in absolute and adjusted GS (corrected for body surface area) between 1 and 12 months

31 st measurement by calculating using ICP, and correcting for, both translational and rotational misali

32 tely 2 x 10(-5), 8 x 10(-6), and 3 x 10(-7) [corrected] for C. jejuni, Salmonella spp., and enterovir

33 In our empirical data, SVA did not fully correct for cell-type effects, its performance was somew

34 ic effects of the differentiation process by correcting for cell type composition boosted the SZ sign

35 Once diversity was corrected for changes in food resource availability, its

36 major crisis in earth history; and third, to correct for clustering of extinctions when using the rar

37 In contrast, comparable analyses correcting for CNV size showed no enrichment of rare CNV

38 al-aperture (NA) benchtop microscope that is corrected for color distortions and chromatic aberration

39 e high-quality SIM data while accounting and correcting for common artifacts.

40 e interval, 1.11-4.67; P=0.02) in blood when corrected for confounders.

41 than a negative control outcome to partially correct for confounding.

42 After correcting for confounding, a one-unit increase in the A

43 We then simulated 3 scenarios correcting for contamination in the PLCO control arm usi

44 nt was change in baseline NCC concentrations corrected for copper in tetrathiomolybdate-copper-albumi

45 his pattern of declining nectar volume after correcting for correlations with flower size, number, an

46 ttenuation of annihilation photons, when not corrected for, could lead to photopenic areas on the PET

47 aw could potentially be used to overcome and correct for data heterogeneity and/or to select the most

48 We corrected for demographics, cell composition, and multip

49 Correcting for demography with traditional methods may l

50 noise suppression up to -2.4 dB (-3.6 dB if corrected for detection losses) and bandwidths less, sim

51 Propensity score matching was used to correct for differences in baseline characteristics.

52 Adaptive window sizes are used to correct for differences in signal coverage in near-bait

53 Propensity matching was corrected for differences between cohorts.

54 erences in HRQL between countries, even when corrected for differences in perceived disease severity.

55 Fluorescence amplitudes, corrected for differences in radiative rates, are used t

56 a receptor blocking study in monkeys, after correcting for differences in plasma protein binding.

57 and K(+)) for analyte and internal standard corrected for different ionization efficiencies showing

58 s, experienced night-migratory songbirds can correct for east-west displacements to unknown locations

59 Each genetic test was corrected for effects of variants on the other two lipid

60 er, Glenwood, Ill) reader, and readings were corrected for energy and scatter response.

61 passive sampler measurements that need to be corrected for equilibrium, typically by extrapolation of

62 oth generates the movement and can optimally correct for errors that arise within a movement.

63 to generate a Bell state with 78% fidelity (corrected for errors in state preparation and measuremen

64 ng Sparse Reduced Rank Regression (sRRR) and correcting for ethnicity and age at birth and imaging.

65 ent studies based on dose-response functions corrected for exposure misclassification are required to

66 endered seizure free and controls, even when corrected for extent of mesial temporal lobe resection.

67 n-theoretic representation of epigenomes and corrects for external covariate factors to better isolat

68 By correcting for extrinsic noise, we estimate an upper bou

69 pectroscopy experiments by highlighting, and correcting for, factors that complicate their interpreta

70 P values were corrected for false discovery rate.

71 tter volume at a significance level p <= .05 corrected for family-wise error across the whole brain a

72 g emotional face processing (cluster-level P corrected for familywise error = .006) in relatives comp

73 la-anterior cingulate cortex connectivity (P corrected for familywise error =.37 and .11, respectivel

74 imary sensory areas (all r > 0.58; P < 0.05, corrected for familywise error).

75 rection across the two eyes where one eye is corrected for far vision and the other eye is corrected

76 s the first transcriptome-wide quantifier to correct for fragment GC-content bias, which, as we demon

77 The [11C]PBR28 distribution volume (VT) corrected for free fraction (fP) was measured in patient

78 s using 10,000 replicates of these data sets corrected for gene size and allowed the calculation of a

79 ufficiency / cutoff value), which internally corrected for geographic region, trimester, and assay ty

80 However, after correcting for global amyloid burden, few of the negativ

81 Regression analysis, corrected for head mass, showed increased concentrations

82 phoid fever and iNTS disease incidences were corrected for health-care-seeking behaviour and recruitm

83 AI, corrected for heart rate, increased more rapidly with ag

84 more than threefold at constant recall while correcting for highly nonlinear chromatographic effects.

85 margin was not associated with outcome when corrected for hole size, and combined phacovitrectomy su

86 SlopeTree corrects for horizontal gene transfer, for composition v

87 methyl-tryptophan or synthetic tryptophan to correct for hydrolytic losses of tryptophan overestimate

88 protocol, and we compute data analytics that correct for imperfect detection.

89 After correcting for imperfect detection, we found that local

90 ding was measured using arterial sampling to correct for individual differences in radioligand metabo

91 ls, whereas the two-variance-component model corrects for inflation.

92 regresses protein dynamics to RNA dynamics, corrected for initial protein concentration.

93 es of GCIPL alone (cohorts 1 and 2) or GCIPL corrected for intrathecal B-cell frequencies (cohort 1)

94 However, such methods cannot correct for irreversible processes such as energy relaxa

95 work flow includes novel evaluation routines correcting for isotope interference of naturally distrib

96 We quantified this misclassification and corrected for it in a case-control study of children in

97 We describe techniques to correct for known issues associated with long autonomous

98 given level of granularity, at the same time correcting for known dependencies among events.

99 admitted during normal working hours, after correcting for known independent predictors of outcome a

100 and with lower mortality up to 1 year, after correcting for known independent predictors of outcome,

101 icant change in average SNP allele frequency corrected for latitude.

102 SUV corrected for lean body mass (SUL and SULpeak) were obta

103 change in maximum standardized uptake values corrected for lean body mass (SUL(max)) on (18)F-FDG PET

104 ted to the daily average UVB light intensity corrected for light screening incorporating water absorb

105 numbers of the two chromosome haplotypes and corrects for local allele-specific coverage biases.

106 al confidence estimates for interactions and corrects for major sources of bias including differentia

107 hydrocarbons detected in sediment extracts (corrected for mass loss relative to C30 hopane) proceeds

108 With use of SIL-IS to correct for matrix effects, LC-MS/MS offers unprecedente

109 Therefore, it simultaneously corrects for matrix effects and for fluctuations due to

110 l and mean tumoral standardized uptake value corrected for mean background activity in the contralate

111 CT image contrast was measured and corrected for measured concentrations and presence of ch

112 ch, and existing methods may not effectively correct for measurement error.

113 After correcting for measurement errors, we found that associa

114 consistent with intrinsic binding affinity (corrected for membrane interaction).

115 luding a variation of the 2T4k model without correcting for metabolite fractions in plasma (2T4k-WP).

116 the palaeoelevation of the fossil locality, corrected for Miocene global temperature difference, is

117 After correcting for misclassification, VE ranged from 57% (95

118 We hypothesize that such changes correct for mismatches in the membrane topogenic signals

119 Incidence rates were corrected for missing serotype data and changes in surve

120 biased machine learning prediction model and corrected for model-selection bias.

121 s connectivity predicts drug analgesia after correcting for modeled placebo-related analgesia.

122 rating a monolithic metasurface lens doublet corrected for monochromatic aberrations, and an image se

123 treatment based on single electron states is correct for most materials this approach can fail specta

124 In normal circumstances motor adaptation corrects for movements' inaccuracies and as such, it is

125 ANOVA with Bonferroni P value adjustment to correct for multiple comparisons.

126 number of independent SNPs was calculated to correct for multiple testing.

127 nearby variants and the permutation test to correct for multiple testing.

128 d on group-specific linear regression models corrected for multiple comparisons for both athletes and

129 onnaire adjusted for confounding factors and corrected for multiple comparisons while minimizing reca

130 isher z transformation were used, which were corrected for multiple comparisons with the Bonferroni m

131 llar WM pathways (P < .05, family-wise error corrected for multiple comparisons) and cervical cord (P

132 a alone, and this was significant (P < 0.05, corrected for multiple comparisons) in 13/22 language ta

133 p-by-midbrain D2/D3 BPnd interaction, P<0.05 corrected for multiple comparisons).

134 ssessed using general linear model (P < 0.05 corrected for multiple comparisons).

135 ital cortex, cerebellum and thalamus (P<0.05 corrected for multiple comparisons).

136 tructures within the parietal lobe (P < .05, corrected for multiple comparisons).

137 he hippocampus and anterior insula (P < .05, corrected for multiple comparisons).

138 ative temporal changes of hs-cTnT (p < 0.01, corrected for multiple comparisons).

139 n analysis of covariance family-wise cluster corrected for multiple comparisons, with a threshold P v

140 ults were considered significant at p < 0.05 corrected for multiple comparisons.

141 uency were assessed with a Fisher exact test corrected for multiple comparisons.

142 All P values were corrected for multiple hypothesis testing by controlling

143 ive a significance level that was Bonferroni corrected for multiple subcortical region comparisons (p

144 standard univariate individual gene analysis corrected for multiple testing as well as a standard a G

145 P values were corrected for multiple testing using false discovery rat

146 -associated single-nucleotide polymorphisms, corrected for multiple testing).

147 We corrected for multiple testing, yielding a significance

148 at included age, BMI, and sex as covariates, corrected for multiple testing.

149 al connectivity to happy faces (all P-values corrected for multiple tests) than offspring of non-bipo

150 teralized network including insula (P < 0.05 corrected for multiple voxel-wise comparisons within the

151 ed with posterior thalamic atrophy (P < 0.05 corrected for multiple voxel-wise comparisons within the

152 san remained statistically significant after correcting for multiple comparisons (mean concentration

153 This significance disappeared after correcting for multiple comparisons using Bonferroni ana

154 these associations remained significant when correcting for multiple comparisons, suggesting that fur

155 significantly associated with CVD risk after correcting for multiple comparisons.Although the MedDiet

156 e exome-wide significant associations (after correcting for multiple hypothesis testing) in single va

157 white populations in either tumor type after correcting for multiple hypothesis testing.

158 paper, we propose an efficient approach for correcting for multiple testing and assess eGene p value

159 ons that were predictive beyond chance after correcting for multiple testing genome wide.

160 After correcting for multiple testing, we observed significant

161 Diet + nuts group remained significant after correcting for multiple testing.

162 gulates intracellular glucose metabolism and corrects for multiple damaging effects of high glucose,

163 ue among all variants in cis with a gene and corrects for multiple testing to obtain a gene-level p v

164 ed over many years with regard to whether to correct for multiplicity and, if so, how it should be do

165 these approaches presupposes that we should correct for multiplicity, which is not universally accep

166 e of the methods that have been proposed for correcting for multiplicity, including single-step proce

167 dystrophy (LGMD2I, n = 11), before and after correcting for muscle fat infiltration.

168 orrected for far vision and the other eye is corrected for near vision.

169 d and excited states of the cost function to correct for noise.

170 ET analysis software packages either fail to correct for non-specific interactions due to genomic pro

171 Results were further from the null when correcting for nonadherence: 1) among the strata with an

172 This simulation showed that after correcting for noncompliance and contamination, there is

173 aluated 5 alternative approaches designed to correct for nonresponse bias under different attrition m

174 ated alternative approaches to assessing and correcting for nonresponse bias in a longitudinal survey

175 unknown how the visual system calibrates and corrects for normal variability in image quality between

176 idence interval: 0.27-0.74; P = 0.002), when corrected for number of tumors, bilobar disease, and int

177 Even when correcting for obesity, poverty and race, ambient temper

178 After images were enhanced, segmented, and corrected for ocular magnification, juxtapapillary choro

179 Adaptive optics can correct for optical aberrations.

180 g diabetes, hyperglycemia, and hypoglycemia, corrected for other factors, was analyzed using a genera

181 ratio LAVI, 4.27 [2.35-7.74], P<0.001) after correcting for other clinical variables.

182 Correcting for other variables had a minimal impact on t

183 L), analysed with a Poisson regression model corrected for overdispersion with Pearson chi(2) that in

184 wer anxiety in upper cranial persisted after correcting for pain and dystonia severity.

185 left atrium and, in the case of (62)Cu-ETS, corrected for partial decomposition of the agent by bloo

186 The absorbed doses were corrected for partial-volume effect based on phantom mea

187 model with age, smoking, and body mass index corrected for, PCB serum concentrations at baseline were

188 The remaining raw reads are used to correct for PCR resampling and sequencing errors.

189 Correcting for per-unit withdrawal time, the mean dyspla

190 re of the motors needs to be considered when correcting for photobleaching.

191 he downstream use of admixture parameters to correct for population structure in association studies.

192 Correcting for population structure in these studies can

193 ss large LD regions of the genome while also correcting for population structure.

194 However, after correcting for possible confounders such as body mass in

195 The purpose of this study is to quantify and correct for potential selection bias in observed NIHSS d

196 s were analyzed by using regression analysis corrected for potential differences in laboratory equipm

197 Cox regression survival analysis, corrected for potential modifiers, including cardiovascu

198 ee diagnostic groups (glaucoma, OHT and GLD) correcting for potential confounding factors, IOP and ag

199 iate phenotypes and correlated observations, correcting for potential population stratification and u

200 When obesity prevalence was corrected for poverty and race the significant effect of

201 The effect on obesity prevalence corrected for poverty, race education and temperature wa

202 Toric IOLs may correct for preexisting corneal astigmatism at the time

203 tcome of death/disability at 18 to 24 months corrected for prematurity; however, this outcome has not

204 ter originating from that region, even after correcting for prenatal EPDS.

205 The area was corrected for projection distortion.

206 57 for IGF1 to 872 for IGF2R, although when corrected for protein length the rate ranged from 0.22 t

207 e's 'trim and fill' were used to examine and correct for publication bias.

208 We also tested and corrected for publication bias by 3 funnel plot-based me

209 Bayesian techniques were used to correct for purported nondifferential misclassification

210 Percentage injected doses (%IDs) corrected for radioactive decay in all dosimetry-evaluab

211 g data between contiguous acquisition steps, corrected for radiotracer decay and injected dose, and f

212 For each region of interest, correcting for regional grey matter density, age, educat

213 t) to conduct a genome-wide association test correcting for relatedness, and then used an adjusted lo

214 productive lifespan), and social group size, correcting for research effort.

215 We present a new method to partially correct for residual confounding: When confounding is pr

216 Correcting for respective confounders is thus necessary

217 Correcting for risk factors, LV mass index, aortic valve

218 stable carbon isotopes and element ratios to correct for rock-derived POC.

219 ic mutations, and establish a method termed 'CORRECT' for scarless genome editing.

220 n in observational studies but many have not corrected for selection bias or independent predictors o

221 only used RNA-seq normalization methods only correct for sequencing depth.

222 usly estimates the transcript abundances and corrects for sequencing bias through an EM algorithm.

223 Serum calcium was measured at baseline and corrected for serum albumin.

224 Serum calcium was corrected for serum albumin.

225 The inability to correct for signal mixing represents a major limitation

226 t explain significant variation in FRB after correcting for soil fertility.

227 ed based on CBS-QB3 calculated free energies corrected for solvation using COSMO-RS.

228 -311+G(d,p) and the core system with CBS-QB3 corrected for solvation using COSMO-RS.

229 Biotransformation rate constants corrected for sorption and abiotic processes were estima

230 How cells correct for stochasticity to coordinate the chromosome r

231 ough methods developed for human studies can correct for strain structure(3,4), this risks considerab

232 We developed calibration equations that correct for subject-specific error in reporting that can

233 Here we implement methods to correct for such biases and use computer simulation to e

234 ments of the corresponding metabolites to be corrected for such matrix effects.

235 biased, and propose an analytical method for correcting for such bias.

236 ied proteins, highlighting the importance of correcting for such interactions.

237 ments and associated somatosensory inputs to correct for systematic real-time changes to auditory fee

238 Dynamic MR data were corrected for T1 relaxation and RF excitation and modele

239 We correct for TBV effects with a novel allometric method h

240 variants, and the necessity to statistically correct for testing millions of genetic variants.

241 ese methods are on average approximately 40% correct for the 100 strongest predicted contacts in each

242 ous findings (using the suppression ratio to correct for the baseline difference) produced a systemat

243 provided for association analysis that also correct for the clonal population structure of bacteria.

244 sian statistical approach called BaalChIP to correct for the effect of background allele frequency on

245 Usually, reconstructions do not, however, correct for the effect of intrinsic developmental change

246 without the availability of a sound model to correct for the intraparticle effect on the observed edd

247 methyl-tryptophan or synthetic tryptophan to correct for the losses of protein-bound tryptophan in fo

248 Here we propose an approach to correct for the matrix effect in LC-MS with electrospray

249 s to speech acoustical outputs that serve to correct for the perturbation.

250 We present a set of tools to identify and correct for the presence of pseudo beta-diversity in con

251 gical filament assemblies allows not only to correct for the rotational flexibility of the label but

252 nal age in these functions, one of which was corrected for the age of the father, and found that the

253 Logistic regression models that corrected for the clustering of patients in hospitals we

254 resonance spectra from native membranes are corrected for the contribution from the bilayer regions

255 However, previous studies have not properly corrected for the fact that some protein targets have mu

256 parameters between groups; the P values were corrected for the five comparisons by using the Bonferro

257 rs, the measured absorbance was successfully corrected for the fractional surface coverage of the pil

258 uld be due to chance (P = 0.1) if Bonferroni corrected for the multiplicity of hypotheses tested (n =

259 The incidence and period prevalences of IPF, corrected for the PPV, were 14.6 per 100,000 person-year

260 valence of IPF using the sensitive algorithm corrected for the PPV.

261 tive to that in ZnTPP-PDI, when the data are corrected for the statistics of having two electron acce

262 from two-dimensional (2D) leaf sections and corrected for the three-dimensional (3D) geometry of mes

263 The BHI was corrected for the water content of drinks and was calcul

264 After correcting for the effect of ethnolinguistic boundaries,

265 lds for reward receipt (RPS models 1 and 3), correcting for the familywise error rate (0.8%-1.9% vari

266 Correcting for the geographical component of genetic var

267 concentrations of steroidal estrogens after correcting for the in vitro potency of each compound.

268 By correcting for the known biases of the interactome, prox

269 Correcting for the known contributions of longitudinal d

270 als for asthma using logistic regression and correcting for the known sampling fractions from stage 1

271 using a Cox proportional hazard model, while correcting for the use of other lipid-lowering therapy,

272 rom protein-crowder potential of mean force, corrects for the penetrability of extended chains and is

273 orescent images that takes into account (and corrects for) the gross modifications in mitochondrial s

274 hich the activation density was too high and correct for them, in both live- and fixed-cell experimen

275 Importantly, induced expression of SLP-2 corrected for these mitochondrial alterations caused by

276 mass of Hg present in 7.4 cm(3) of air, and correcting for these blanks was not an important source

277 Correcting for these inaccuracies in normalization decre

278 is work, we perform a direct comparison that corrects for these experimental limitations and computat

279 expression based method that can be used to correct for this confounder in future studies.

280 study describes a computational approach to correct for this copy number effect, increasing the spec

281 To correct for this deficiency, we propose a new model that

282 t, we update our motor commands to partially correct for this error on the next trial.

283 We have designed a method that fully corrects for this source of error.

284 unts to a pooled reference, we evaluated and corrected for three sources of bias that explain most of

285 < .001) and putamen (P = .01) volumes (both corrected for total brain volume) in control individuals

286 healthy controls (P < 0.05 family-wise error corrected for total sodium concentration, P < 0.05 uncor

287 in a multivariate logistic regression model correcting for total CNV size.

288 o EGP was quantitated using deuterated water corrected for transaldolase exchange.

289 Adjusted Cox regression, corrected for treatment adjustments, showed that intensi

290 All analyses were corrected for TSPO rs6971 polymorphism (which is implica

291 c read counts, and integer copy number calls corrected for tumor purity, ploidy and clonal heterogene

292 10(6) counts per second at saturation, after correcting for uncorrelated photon background.

293 parallel these effects can be estimated and corrected for under certain smoothness assumptions on ce

294 reatinine concentration was also measured to correct for urine dilution.

295 Publication bias was corrected for using funnel plots, the Egger regression t

296 sewage-sourced enterococci and E. coli after correcting for UVB light screening, suggesting that alth

297 ty of internal standards that can adequately correct for variability in sample preparation and the MA

298 ivariable Cox proportional hazards analysis, corrected for variables with a known significant influen

299 Models that correct for vertical mixing are based on limited data.

300 n 1 kcal/mol in terms of electronic energies corrected for zero-point vibrations.