ライフサイエンスコーパス: screening method

1 ntropy can be designed via a high-throughput screening method.

2 esults in order to be used as a quantitative screening method.

3 vaccine effectiveness was assessed using the screening method.

4 medical significance to this high-throughput screening method.

5 c assay as a new approach in high-throughput screening method.

6 small interfering RNA-based synthetic lethal screening method.

7 es, identified by using a simple plate-based screening method.

8 s was estimated with the use of the indirect screening method.

9 ed high-throughput synthesis and biochemical screening method.

10 e role for laxative-free CTC as an alternate screening method.

11 enzymatic hydrolysis using a high-throughput screening method.

12 become the building blocks for a new on-site screening method.

13 sed as test cases to benchmark our detergent screening method.

14 luate the effectiveness of this quantitative screening method.

15 n times may preclude its adoption as a rapid screening method.

16 ss the proposed method may be used as a fast screening method.

17 s a high-throughput BBB penetration oriented screening method.

18 e use of low-throughput chromatography-based screening methods.

19 velopment of improved functional metagenomic screening methods.

20 used to complement classical analysis and as screening methods.

21 s on animals; hence requiring new predictive screening methods.

22 ing intervals across the different available screening methods.

23 tes is hampered by a lack of reverse genetic screening methods.

24 are identifiable through existing amblyopia screening methods.

25 and mass spectrometry-based high-throughput screening methods.

26 traits difficult to analyze by other genetic screening methods.

27 implementable alternative to direct on-line screening methods.

28 assays are commonly used in high-throughput screening methods.

29 ated the performance characteristics of both screening methods.

30 subtypes with greater efficacy than isolated screening methods.

31 response, is a new approach to develop such screening methods.

32 ompared to wild type, thereby validating the screening methods.

33 age while qAG1-2 and qAG7-4 were specific to screening methods.

34 counselling, genetic risk testing, and other screening methods.

35 assembly as well as to afford rapid in vivo screening methods.

36 infusion mass spectrometry (MS)-based glycan screening method acquires data on a millisecond time sca

37 Modern high-throughput screening methods allow researchers to generate large da

38 eract with phototropins by using an in vitro screening method (AlphaScreen) to profile interactions a

39 he population was phenotyped under different screening methods (anaerobic screenhouse, anaerobic tray

40 a powerful functional and chemical genomics screening method and provide guidelines for designing ef

41 difficulties is unclear and the appropriate screening method and subsequent management is the subjec

42 Using both the biosensor based screening method and the in vitro biological assay, the

43 o better understand the relationship between screening methods and clinical outcome.

44 el interactions and recently developed toxin screening methods and practical applications of engineer

45 estigated the utility of several noninvasive screening methods and the propagation of new treatments

46 ectiveness of 2 population-based skin cancer screening methods and to assess their budget effect and

47 ectiveness of 2 population-based skin cancer screening methods and to assess their budget effect and

48 ecal coliforms, but flagged up by the MinION screening method, and confirmed by a qPCR assay.

49 We discuss established and emerging screening methods, and potential strategies to address c

50 Conventional screening methods are based on different technologies, m

51 More sensitive screening methods are detecting smaller and smaller lesi

52 Screening methods are effective but have limitations.

53 Such comprehensive screening methods are essential to define the concerted

54 Current screening methods are largely imaging based, but a more

55 enzymes by engineering approaches, suitable screening methods are necessary.

56 More efficient, quantitative high-throughput screening methods are needed to guide the optimization o

57 ry, flexible, sensitive, and high-throughput screening methods are required.

58 impaired in resource-poor countries, because screening methods are technologically and financially in

59 Screening methods are the first step in the control of a

60 Rapid and inexpensive screening methods are utilized when molecular methods ar

61 In this study, we develop a microfluidic screening method as a useful tool in the prediction and,

62 yet there are no reliable noninvasive early screening methods available.

63 ere analyzed initially by an anticancer drug-screening method based on a sulforhodamine B assay.

64 Employing a sequential screening method based on antibiotic sensitivity, RFLP p

65 A screening method based on fusion between SEA and coiled-

66 tudy reports on the development of a suspect screening method based on industrial compounds with bioa

67 lunteers were analyzed for OMPs by a suspect screening method based on mixed-mode solid-phase extract

68 Here, we report the use of a screening method based on the Gutzeit methodology to det

69 A rapid screening method based on traveling-wave ion-mobility sp

70 A non-targeted screening method based on ultrasound-assisted extraction

71 Through the use of computational screening methods based on periodic density functional t

72 In this study, we use screening methods based on wide scope solvent extraction

73 regression was used to assess the effect of screening method, breast density, patient age, and cance

74 Hence, these methods are useful for screening methods, but due to their low specificity and

75 we developed an efficient combinatorial drug screening method called the Feedback System Control (FSC

76 Fragment-based screening methods can be used to discover novel active s

77 Current screening methods can only be used to disrupt a gene or

78 rk presents a sensitive and easily performed screening method capable of detecting AZAs at concentrat

79 ction immunoassay provides an easy and rapid screening method capable of detecting simultaneously in

80 We developed an automated, time-resolved screening method capable of rapidly phenotyping channelr

81 High throughput screening methods combined with literature curation are

82 An screening method, comprised of straightforward sample tr

83 non-invasive, inexpensive, easily accessible screening method could be useful in both clinical and re

84 This screening method could be widely used to detect numerous

85 An FT-IR screening method coupled to data analysis using chemomet

86 Epigenome-wide screening methods cover an increasing number of CpG site

87 In this work, a screening method covering 116 human and veterinary drugs

88 ased immunoassay is suitable to be used as a screening method, detecting saxitoxin from 260 to 2360 m

89 Current blood bank screening methods do not identify infected donors, and B

90 asive cervical carcinoma was similar between screening methods during the first 2.5 years of follow-u

91 no-, micro- and mesoscales to random library screening methods (e.g. phage display), in vitro cellula

92 logy who are not identified with traditional screening methods (eg, CIA-positive, rapid plasma regain

93 here were differences in the microbiological screening methods employed, the individual clinical risk

94 ing at age 40 versus 50 years with different screening methods (film, digital) and screening interval

95 High-concentration biophysical screening methods followed by high-throughput crystallog

96 he methods and to identify the most suitable screening method, followed by bulk segregant analysis (B

97 otential of SERS application as a diagnostic screening method, following further validation and optim

98 lemented with ceftriaxone or cefotaxime as a screening method for accurately detecting and quantifyin

99 ital breast tomosynthesis (DBT) as a primary screening method for breast cancer.

100 se which might be useful to develop a better screening method for breast cancer.

101 We have developed an on-line screening method for CB1 and CB2 ligands, where cellular

102 ved the biosensor capability to be used as a screening method for detection of carbamate drugs in was

103 before CONDOR can replace pDUS as a reliable screening method for detection of eHAT.

104 s discovered using a glycan microarray-based screening method for detection of substrate specificitie

105 actice-based retrospective study evaluated a screening method for diabetes mellitus (DM) in patients

106 graphy as an easy, rapid and non-destructive screening method for evaluating large population trials

107 stem that could be used as a high throughput screening method for finding new alpha-synuclein anti-ag

108 e challenge test (OGCT) is a widely accepted screening method for gestational diabetes mellitus (GDM)

109 llary zone electrophoresis-mass spectrometry screening method for Hb proteoforms including sequence v

110 broadly applicable high-throughput operando screening method for heterogeneous catalysts.

111 copy could offer a rapid and high-throughput screening method for identification of Leptospermum hone

112 This profile could provide a zero-cost screening method for identification of mecC-positive MRS

113 chodilators provides an efficient cell-based screening method for identifying potent dilators from am

114 s test an easy-to-use, rapid, and convenient screening method for in-house control of OTA in wineries

115 A simple screening method for isolation and determination of the

116 Ultrasound can be used as a screening method for malrotation eliminating the need fo

117 onsidered suitable for health authorities as screening method for MCs and to optimize frequency of sa

118 gh Resolution Melting (HRM) application as a screening method for must and wine authenticity.

119 d be used in a manner similar to the testing/screening method for neural tube defects and common chro

120 It also may serve as the basis for a simple screening method for new enzyme inhibitors for disease t

121 We developed a screening method for orphan receptor ligands, in which c

122 erein, provides an optimized high-throughput screening method for other binary or ternary alloys as f

123 The sandwich ELISA can be a viable screening method for OVTXs detection in monitoring progr

124 od nowadays, a sensitive, accurate and rapid screening method for potential food allergens has become

125 posed method can be recommended as a routine screening method for quantitation of sulfonamides in mil

126 s great potential as a qualitative molecular screening method for resource-limited settings when comb

127 In the present contribution, an automated screening method for studying ligand interactions of sel

128 We have also developed a temperature-based screening method for synthetic paralysis that can be use

129 ent a fast, sensitive, reliable and low-cost screening method for the authentication of processed com

130 essed the performance of pulse oximetry as a screening method for the detection of critical congenita

131 Currently there is a need for a rapid screening method for the detection of veterinary drugs i

132 We invented a high-throughput screening method for the examination of radioprotective

133 development of a high resolution melt (HRM) screening method for the identification of eight common

134 The aim of this study was to develop a screening method for the identification of novel modulat

135 A novel, fast, and sensitive screening method for the identification of the two most

136 This paper proposed a new screening method for the simultaneous detection of five

137 ed with the patch-clamp, an equally powerful screening method for the transport of uncharged compound

138 ort routine clinical breast examination as a screening method for women at average risk.

139 Screening methods for anal squamous intraepithelial lesi

140 The research on fast screening methods for antibodies against zoonotic pathog

141 significant opportunity to develop practical screening methods for complex formulations.

142 Moreover, screening methods for cutaneous therapeutics require acc

143 Consequently, screening methods for duplication of FAD3 orthologues in

144 hallenge that would benefit from advances in screening methods for early detection that are rapid and

145 development of cost-effective toxicological screening methods for engineered nanomaterials.

146 The method was adapted for high-throughput screening methods for enzymology and drug discovery.

147 nsity of the pre-frying oil are suggested as screening methods for estimating the MCPD-E and G-E cont

148 High-throughput screening methods for fatty acid (FA) determination are

149 We consider 7 single-step and modular screening methods for identifying G-E interaction at a g

150 rams, yet the lack of robust high-throughput screening methods for large libraries of enzyme variants

151 ere is a need for facile and high-throughput screening methods for monitoring programs.

152 e, sensitive, quantitative, and mobile rapid screening methods for pathogenic organisms are not yet r

153 As current screening methods for selecting surgical trainees are re

154 Advances in high-throughput drug screening methods for small molecules, developments in d

155 common cancer detected in women and current screening methods for the disease are not sensitive.

156 Here we develop high-content phenotypic screening methods for the systematic identification of m

157 Improved screening methods for women with dense breasts are neede

158 Here, we describe an arrayed CRISPR screening method, Genome engineering-based Interrogation

159 The EDTA-CBDE screening method had an overall PPA and NPA of 100% and

160 A simple high-throughput solid-phase screening method has also been developed to identify PAL

161 In the present study, a rapid screening method has been developed for the direct surfa

162 With regard to diagnosis, a new screening method has been developed that allows predicti

163 A rapid screening method has been developed to determine binding

164 re for the first time, a new, easy and rapid screening method has been used to investigate the DNA da

165 s progress in high-throughput small molecule-screening methods has facilitated the rapid expansion of

166 However, the performance of different screening methods has not been studied.

167 These findings suggest that both Etest screening methods have excellent NPV, but positive resul

168 Advances in cancer screening methods have opened avenues for incidental fin

169 In the field of epigenetics, such screening methods have suffered from a lack of tools sen

170 o discover such molecules by high-throughput screening methods have utilized, as a read-out, a single

171 industry-standard preclinical cardiotoxicity screening methods, identify the effects of well-characte

172 Noncathartic CT colonography is an effective screening method in first-degree relatives of patients w

173 atologists, LDS is an acceptable alternative screening method in health care systems with limited bud

174 s the utility of our straightforward genetic screening method in identifying new drug combinations to

175 sive; hence, it is suggested to be used as a screening method in the field for preselection of rice w

176 Herein, we develop a competitive screening method in which G-quadruplex DNA linked magnet

177 We deployed a variety of screening methods in an effort to discover binders of Pr

178 ndoscopy and colonoscopy are the recommended screening methods in these patients, especially in the t

179 Lung Health Check appointments offering LDCT screening.Methods: In a two-arm, blinded, between-subjec

180 generation sequencing (NGS) and other mutant screening methods including T7 endonuclease 1 (T7E1), CR

181 Using high-throughput screening methods, including computational docking studi

182 We recommend colonoscopy as the preferred screening method, initiation of screening at age 40 year

183 ed for favorable harm-benefit ratios vary by screening method, interval, and outcome measure.

184 A mass spectrometry screening method is available to detect the addition of

185 This screening method is based on measurements of immunoglobu

186 The screening method is demonstrated for both ammonia lyases

187 es of a few selected muteins proved that the screening method is efficient and accurate in predicting

188 A rapid, sensitive, and specific screening method is needed for in-field or bedside testi

189 ating on the market, a rapid transgenic food screening method is needed to protect consumer rights.

190 d on UV-VIS spectroscopy and chemometrics, a screening method is proposed to quickly screening some c

191 The most readily available supplemental screening method is ultrasonography, but little is known

192 This screening method is using a database of over 600 metabol

193 The development of improved breast cancer screening methods is hindered by a lack of cancer-specif

194 Current screening methods lack sensitivity, specificity, and hav

195 e of pesticides in soil, a multiple-compound screening method (log Kow 1.7-5.5) was developed based o

196 We compared the performance of two Etest screening methods (macromethod [MAC] and glycopeptide re

197 Using this screening method, mature leaves from fully developed pla

198 Here, we developed a screening method named "Tiling CRISPR" to identify lncRN

199 n we have combined an underutilized fragment screening method, native state mass spectrometry, togeth

200 We propose that our screening method not only enables elucidation of new ChR

201 Therefore, an alternative screening method, not directly based on the structure bu

202 A limitation of the conventional biomarker-screening method of enzyme-linked immunosorbent assay (E

203 We have developed a screening method of identifying the 'master regulator' t

204 a promising and viable approach for a green screening method of phenolic compounds in EVOO, by means

205 Using the orthogonal fragment screening methods of native state mass spectrometry and

206 ul tool to assess the performance of virtual screening methods on NRs, to assist the understanding of

207 The analysis of screening methods, optimization strategies, and molecula

208 A screening method optimized to discover cytotoxic compoun

209 Thus, a complete recessive carrier screening method or diagnostic test should detect CNV al

210 Topics such as target class, screening methods, physicochemical properties, and ligan

211 the recommended age of screening initiation, screening method, preparation, and the interval for repe

212 This protocol covers the docking and virtual screening methods provided by the AutoDock suite of prog

213 rlap score (xLOS), a 3D ligand-based virtual screening method recently developed in our group, to sel

214 ded to identify the biological processes and screening methods relevant for other common diseases.

215 Existing screening methods require prolonged monitoring and are l

216 es offer these advantages, the validation of screening methods requiring the application of multivari

217 This study demonstrates the success of the screening method resulting in a powerful lysin with pote

218 Virtual screening methods seek some active-enriched fraction of

219 Screening methods should be simple, quick, inexpensive a

220 By utilizing this double-layer screening method, six positive mutants were obtained fro

221 ddition to Z(2) topological insulators, this screening method successfully identified many semimetals

222 f death from colorectal cancer indicate that screening methods such as colonoscopy have a positive im

223 The future implementation of early screening methods such as exhaled breath condensate anal

224 ogether with two proven and popular fragment screening methods, surface plasmon resonance and X-ray c

225 Since traditional screening methods target only a limited number of marker

226 We report a high-throughput screening method that allows diverse genotypes and corre

227 nknown modulators of Foxp3 and demonstrate a screening method that can be broadly applied to discover

228 provides a sensitive, rapid, and noninvasive screening method that can be used for imaging and quanti

229 Here, we present a screening method that comprehensively explores the param

230 des a rapid, sensitive, and easily performed screening method that could be multiplexed for the simul

231 Here, we developed a screening method that joins both bait and prey as a conv

232 Here, we report a screening method that probes over 3,000,000 combinations

233 veloped a broadly applicable high-throughput screening method that simultaneously identifies multiple

234 We present a novel screening method that utilized 144 additive conditions t

235 thus a need for inexpensive and non-invasive screening methods that are able to accurately estimate b

236 evelopment has been aided by high throughput screening methods that detect compound effects on a sing

237 Screening methods that use traditional genomic, transcri

238 ntially following the introduction of breast-screening methods, the clinical significance of early de

239 he review focused on resting ABI as the sole screening method; the diagnostic performance of ABI test

240 ass spectrometry as a complementary fragment screening method to accelerate drug discovery.

241 using our previously described differential screening method to analyse the proteome of blood-stage

242 The concept of using pulse oximetry as a screening method to detect undiagnosed critical congenit

243 this quantitative method is very useful as a screening method to determine gelatin from various sourc

244 d a polyacrylamide gel electrophoresis-based screening method to determine topological effects of het

245 light mass spectrometry (MALDI-TOF MS)-based screening method to discover natural products that modif

246 We used the screening method to estimate vaccine effectiveness (VE)

247 -energy searches, which provide an in silico screening method to evaluate candidate molecular buildin

248 an spectroscopy has been explored as a quick screening method to evaluate the presence of lactose and

249 ary, we developed an in vivo Drosophila RNAi screening method to identify flow-sensitive genes that r

250 study established a novel, simple and quick screening method to identify gRNA candidates for targeti

251 roblasts, thus validating the ability of the screening method to identify intracellular replication-d

252 yme-linked immunosorbent assay (ELISA)-based screening method to identify mutants from a transposon i

253 Here we developed a high throughput screening method to identify mutants of 6-phosphoglucona

254 Here we describe a screening method to identify mutations that have a criti

255 There is currently no rapid, unbiased screening method to identify new classes of covalent inh

256 Here, we establish a simple, high-throughput screening method to identify optimal detergent condition

257 holds potential to be further developed as a screening method to identify pathogen-specific recogniti

258 try (DSF) as an inexpensive, high throughput screening method to investigate the folding of silk prot

259 as a simple and generic biophysical fragment screening method to reproduce assessments from NMR-based

260 e first stage, we use a Bayesian independent screening method to select the most promising SNPs.

261 ht to investigate the ability of whole-exome screening methods to detect disease-causing variants in

262 Two screening methods to detect staphylococcal colonization

263 mportance of employing appropriate molecular screening methods to detect unintended alterations follo

264 emia, sample availability is very scarce and screening methods to diagnose the illness are not common

265 We applied high-content screening methods to monitor B-cell activation on the ce

266 hese observations support the development of screening methods to predict those at risk for VUE and t

267 High-quality screening methods to prioritize homes for monitoring and

268 cal production cell lines requires efficient screening methods to select the host cell line and final

269 Effective and feasible screening methods to triage suspicious patients to CT ar

270 Here, we describe a screening method using Drosophila to identify small mole

271 in high-throughput, we designed a novel mAb screening method using high-content imaging (HCI) and im

272 used to develop and optimize a HRMS suspect screening method using only the exact mass as a priori i

273 Here we present a genetic screening method using photo-highlighting for candidate

274 Here, we established an in vitro screening method using the rainbow trout gill cell line,

275 Here, we present novel screening methods using an electrochemical chip coupled

276 required to implement comprehensive suspect screening methods using high-resolution mass spectrometr

277 This represents a facile catalyst screening method, using replaceable glassy carbon disk e

278 Here, we describe a high-throughput screening method utilizing error-prone PCR and next-gene

279 ng tandem mass spectrometry (wide-SIM/MS(2)) screening method utilizing ultraperformance-LC nanoelect

280 An efficient screening method was developed for functionalized DNA-ta

281 In the current work, a nontargeted screening method was developed using a two-dimensional g

282 To cover a broader range, a new GMO screening method was developed, based on two real-time P

283 Ls showed an effect when survival across all screening methods was analyzed.

284 n this paper, an EU-validation procedure for screening methods was successfully applied to a multivar

285 Using a high-throughput screening method, we have identified several compounds t

286 Using our screening method, we have identified small molecules tha

287 Applying our screening method, we identified 51 lncRNAs that can posi

288 Using a differential whole-proteome screening method, we identified Plasmodium falciparum sc

289 Here, by using in silico drug-screening methods, we discovered that Celastrol, a penta

290 Using these orthogonal screening methods, we identified drugs that restored the

291 n value, sensitivity and specificity of this screening method were established through ROC analysis.

292 past 10 years, as cell-based high-throughput screening methods were applied, together with large chem

293 e allowed for the development of nontargeted screening methods, where data sets can be archived and r

294 The change in color offers a fast pre-screening method, whereas monitoring via SERS is used fo

295 This screening method will expedite the discovery of drug tar

296 ed for large-scale use, this high-throughput screening method will facilitate rapid screening of nano

297 his work, we demonstrate the validity of the screening method with the commercial laccase from the fu

298 We argue that combining multiple diagnostic screening methods with multivariate logistic regression

299 e combination of pharmacophore-based virtual screening methods with radioactive methylation assays pr

300 Nontargeted screening methods with ultrahigh-performance liquid chro