ライフサイエンスコーパス: sensitive assay

1 B cells every 3 months with a novel, highly sensitive assay.

2 value of -0.2 obtained from data with a less sensitive assay.

3 ripheral leukocytes was detected by a highly sensitive assay.

4 tect any WHx protein in the cells by using a sensitive assay.

5 in addition to the O157 serotype by using a sensitive assay.

6 both a standard and a pre-commercial highly sensitive assay.

7 rus (HBV) infections are highly specific and sensitive assays.

8 tectable in normal aging epithelium by using sensitive assays.

9 urable viral suppression, as defined by very sensitive assays.

10 tent low-level viremia is detected with more sensitive assays.

11 ions of immunoreagents resulting in the most sensitive assays.

12 arily due to a lack of appropriate tools and sensitive assays.

13 Aquaporin 4 antibodies were tested using 2 sensitive assays.

14 In the most sensitive assays, 9 of 11 volunteers and 5 of 8 Ty21a co

15 In addition, such a highly sensitive assay allows discrimination of drug-induced re

16 This highly sensitive assay allows us to determine the endogenous le

17 levels of virus can be detected in plasma by sensitive assays and transient episodes of viremia, or H

18 etic resonance imaging (MRI), cTnT by highly sensitive assay, and NT-proBNP analysis (n = 2,413).

19 en for 31 days) on serum CRP, using a highly-sensitive assay, and on serum platelet-cyclo-oxygenase (

20 often detectable in community dwellers when sensitive assays are applied.

21 Highly sensitive assays are critical for early detection of cha

22 Sensitive assays are needed for detection of residual hu

23 ower than plasma levels, accurate and highly sensitive assays are needed for saliva measurements.

24 pecially from small clinical samples, highly sensitive assays are required.

25 which confirms the importance of using this sensitive assay as an initial screen in vaccine protocol

26 rior HF who had cTnT measured using a highly sensitive assay at baseline (1989-1990) and repeated aft

27 The ATPase activity is characterised using a sensitive assay based on a chemically modified form of t

28 Using a sensitive assay based on betagamma complex stimulation o

29 Receptor binding was measured initially by a sensitive assay based on coexpression of receptor and RB

30 A sensitive assay based on competition between cis-and tra

31 We developed a sensitive assay based on self-assembling radiolabeled te

32 A sensitive assay based on single lipid tracking experimen

33 mass spectrometry has produced accurate and sensitive assays, but chromatographic separations requir

34 This rapid and sensitive assay can be used to identify enterotoxigenic

35 The most sensitive assay can detect as few as two copies of HPV D

36 This sensitive assay can measure rates of DNA methylation dow

37 ing the local particle concentration, highly sensitive assays can be performed efficiently and rapidl

38 be the modification and development of three sensitive assays capable of detecting nanogram quantitie

39 MethyLight is a highly sensitive assay, capable of detecting methylated alleles

40 This nanopore-based methylation sensitive assay circumvents the need for bisulfite conve

41 Using the most sensitive assay combination, we measured TCS concentrati

42 A highly sensitive assay combining immunomagnetic enrichment with

43 Using a novel high-sensitive assay, cTnI levels could be determined in near

44 Overall, the results suggest that more sensitive assays (e.g., ELISPOT, ELISA analysis of cytok

45 We report a rapid, specific, and sensitive assay employing isothermal DNA amplification u

46 Using two sensitive assays (enzyme-linked immunospot assay and int

47 Using this sensitive assay, Escherichia coli tail-specific protease

48 spread from cell to cell, even though highly sensitive assays fail to detect infectious virus progeny

49 Using a sensitive assay for activated Ras, we show here that act

50 exchange has been developed into a rapid and sensitive assay for both SHMT and H4PteGlun and the one-

51 A sensitive assay for competitive binding of dinucleosome

52 -4-methylcoumarin (AzMC), serves as a highly sensitive assay for cystathionine beta-synthase activity

53 dy design and analysis, the Morris maze is a sensitive assay for detecting AD-relevant impairments ac

54 Significantly, a label-free sensitive assay for detecting carcinoembryonic antigen (

55 A sensitive assay for detecting double-stranded (ds) DNA i

56 erefore, may be used as part of a robust and sensitive assay for detecting not only purified, but als

57 To develop a highly sensitive assay for detecting the cellular immune respon

58 We describe a sensitive assay for detection of active hyaluronan synth

59 RT-QuIC, like IHC analysis, is a relatively sensitive assay for detection of CWD prions in RAMALT bi

60 s a primer for PCR represents a specific and sensitive assay for detection of H. pylori in highly con

61 nPCR was the most sensitive assay for detection of malaria in pregnancy, f

62 of these volatiles because of the lack of a sensitive assay for DMAPP in plant tissues.

63 gamma-H2AX nuclear foci, considered the most sensitive assay for DNA DSBs.

64 Here we present a sensitive assay for DNA transesterification in which cat

65 In conclusion, a sensitive assay for exposure to tri-o-cresyl phosphate w

66 Furthermore, using a sensitive assay for glucose 6-P in hydrolysates of glyco

67 In this study, using an extremely sensitive assay for hCG, 10% of clinical pregnancies wer

68 tation of a homogeneous, miniaturizable, and sensitive assay for histone methylation-dependent intera

69 In addition, development of a highly sensitive assay for I in human plasma at low picogram pe

70 ther tests of species-typical behavior, is a sensitive assay for identifying previously unknown behav

71 We have used a sensitive assay for MAP kinase activity to investigate t

72 A convenient, sensitive assay for measurement of in vivo missense tran

73 system based on vitamin B12 auxotrophy as a sensitive assay for metabolite exchange between marine p

74 we report a simple, inexpensive, and highly sensitive assay for MMP activity.

75 We have developed a highly sensitive assay for monitoring the metastatic disseminat

76 ere we report the development of a rapid and sensitive assay for NRD convertase, based on the utiliza

77 Tg.AC transgenic mice provide a sensitive assay for oncogenic agents and a convenient al

78 ressed PIP(2)-dependent Kir2.1 channels as a sensitive assay for PLC activity, we show that simple gl

79 Sensory fMRI can provide a sensitive assay for probing the nature and function of S

80 omplementation provides a rapid, simple, and sensitive assay for protein interactions and for detecti

81 use of the strategy allowed us to develop a sensitive assay for proteins with three appealing featur

82 A sensitive assay for quantitating DNA damage within indiv

83 paper substrate provides a new, simple, and sensitive assay for rapid detection of blood group for p

84 ing highly resistant to BG, but the use of a sensitive assay for reaction of BG with AGT indicated th

85 This specific, sensitive assay for SEB on the portable fiber-optic bios

86 vs 97% at week 96, P = .002), despite a more sensitive assay for seminal plasma than for cervical wic

87 treatments with goserelin and exemestane, a sensitive assay for serum estradiol was checked and retu

88 This protocol was evaluated using a sensitive assay for spontaneous branch migration, and wa

89 varies across these conditions, providing a sensitive assay for TARP/AMPAR stoichiometry.

90 We have developed a sensitive assay for the AMP-activated protein kinase kin

91 A new, sensitive assay for the deformylase has been developed b

92 AMPLICOR CMV Test could provide a rapid and sensitive assay for the detection of CMV in plasma and C

93 Here we present a rapid, simple and sensitive assay for the detection of epidermal growth fa

94 Here we describe a sensitive assay for the determination of plasma homocyst

95 Here I describe a new sensitive assay for the determination of protein N-linke

96 tern blot assay still appears to be the more sensitive assay for the diagnosis of HIV-1 infection in

97 There is major need for a more sensitive assay for the diagnosis of pneumococcal commun

98 li cells are limited by the lack of a rapid, sensitive assay for the DNA damage that results.

99 his process, we developed a quantitative and sensitive assay for the induction of erythroid cells fro

100 the elements of H(3)PO(4) (98 Da) provides a sensitive assay for the presence of phosphopeptides.

101 f centromere dynamics in G1 yeast cells as a sensitive assay for the regulation of single k-MT dynami

102 We implemented a novel, extremely sensitive assay for the release and transfer of anterogr

103 The new reagents provide the most sensitive assay for the three lysosomal enzymes reported

104 f these heme adducts, we sought to develop a sensitive assay for their detection and quantitation.

105 cles coated with our aptamers as a rapid and sensitive assay for these compounds.

106 formation of VA2 muscle precursor cells as a sensitive assay for these genetic interaction studies.

107 othrombin F-1 x 2 concentrations, and a less sensitive assay for under-gamma-carboxylated prothrombin

108 nhancement in fluorescence, thus providing a sensitive assay for use in vitro and in vivo.

109 r reliable high-throughput, rapid and highly sensitive assays for a simultaneous detection of several

110 The development of highly sensitive assays for biochemical detection of PrP(Sc) in

111 Sensitive assays for coagulation activation have provide

112 tion provides a new platform of low cost and sensitive assays for cotinine detection.

113 Accordingly, sensitive assays for detecting Bcr-Abl kinase activity c

114 vation during immune responses, we have used sensitive assays for detecting native IL-15 and IL-15Ral

115 Sensitive assays for DSB-dependent homologous recombinat

116 Sensitive assays for HBV DNA levels in serum have been d

117 More sensitive assays for human immunodeficiency virus type 1

118 Moreover, sensitive assays for KSHV ORF65-specific and ORF73-speci

119 Molecular tools are highly sensitive assays for Leishmania detection and may contri

120 direct range of Shh signalling, we developed sensitive assays for localizing Shh by attaching alkalin

121 The availability of sensitive assays for plasma HIV viral load and the trend

122 Sensitive assays for rapid quantitative analysis of hist

123 developed in the 1970s involving especially sensitive assays for RT as a surrogate marker for a retr

124 We describe a variety of sensitive assays for SFV isolation and detection which w

125 urine has several preanalytic drawbacks, and sensitive assays for the detection of uromodulin in bloo

126 The widespread use of sensitive assays for the detection of viral and cellular

127 ratio, allows for the development of highly sensitive assays for the determination of miRNA in a var

128 Widespread use of automated sensitive assays for thyroid hormones and thyroid-stimul

129 as a biothreat agent has made development of sensitive assays for toxin detection and potent antitoxi

130 The most sensitive assay from the screening studies [coating anti

131 ukocyte PCRs (L-PCR and L-AMP) were the most sensitive assays, had positive results an average of bet

132 A sensitive assay has been developed to quantitate fibrino

133 of CD4(+) T cells in vitro, but the lack of sensitive assays has limited its application for studyin

134 tion of very low troponin levels with highly sensitive assays has made feasible several potential new

135 ctrophoresis or dot blot hybridization, is a sensitive assay; however, at this time it cannot complet

136 We measured cardiac troponin T with a highly sensitive assay (hs-cTnT) at 2 time points, 6 years apar

137 of cardiac troponin T, measured by a highly sensitive assay (hs-cTnT), are strongly associated with

138 diomyocyte injury, were measured by a highly sensitive assay (hsTnT) in 4,431 ambulatory participants

139 The most sensitive assay identified was one utilizing antiserum n

140 Low-level increases in cTnI using a sensitive assay identify patients at higher risk of deat

141 I (cTnI) was measured by using a novel, high-sensitive assay in community dwellers aged 70 years from

142 troponin I (cTnI) using a current-generation sensitive assay in patients with suspected acute coronar

143 Measurement of estradiol level by sensitive assay in postmenopausal women identifies those

144 nant enzyme was characterized using a highly sensitive assay in the presence and absence of the propo

145 sured using both the standard and the highly sensitive assays in 3546 individuals aged 30 to 65 years

146 MI, and the incremental value of newer, more sensitive assays in identifying high-risk patients with

147 versity, and the influence of novel and more sensitive assays in the detection and analysis of signal

148 Recent modifications of this sensitive assay include elimination of radioactivity by

149 Novel algorithms with highly sensitive assays, incorporating baseline troponin values

150 We used a sensitive assay involving biotinylation to show that all

151 For these latter studies, we used a sensitive assay involving the infusion of highly purifie

152 The sensitive assay is based on the close to absolute electr

153 This sensitive assay is ideal for kinetic analysis of Tdp1 fu

154 pg/mL (61 pmol/L); postmenopausal range for sensitive assay is less than 15 pg/mL (< 50 pmol/L).

155 This is especially the case when a very sensitive assay is required to differentiate often highl

156 cal significance of low-level increases with sensitive assays is still debated.

157 These findings support the use of more sensitive assays, like NAT, in HIV screening of populati

158 This highly sensitive assay may be used to determine accurately less

159 These rapid sensitive assays may have potential use in clinical sett

160 between the various treatment groups, 2 more sensitive assays measuring antigen-specific interferon-g

161 Based on tetramer binding and two sensitive assays measuring interferon-gamma production a

162 A nonradioactive, sensitive assay method to evaluate the activity of prote

163 colon cancer, along with easier-to-use, more sensitive assay methods, may improve the detection, trea

164 inefficient process and therefore provides a sensitive assay of altered opioid receptor function and

165 ptic mechanisms of attention, we developed a sensitive assay of attentional modulation of neuronal co

166 We describe a sensitive assay of chromatin structure which is performe

167 Using a robust, sensitive assay of KIR binding and a representative pane

168 by hydrolysis of lipoyl-N-epsilon-lysine, a sensitive assay of lipoamidase activity was developed ba

169 We report a practical, nonradioactive, sensitive assay of MCD in crude tissue extract.

170 These approaches are based on the sensitive assay of molecular markers in stool, blood, an

171 Using an accurate and sensitive assay of parasite genotype, real-time quantita

172 ERG timing is a sensitive assay of retinal function, and our results ind

173 We have developed a highly sensitive assay of RNA interference (RNAi) in mammalian

174 A sensitive assay of the 2H-enrichment of water based on t

175 A highly sensitive assay of tRNA aminoacylation was developed tha

176 Salmonella) had immune responses in the most sensitive assay of urease-specific immunoglobulin produc

177 eport the development of a set of robust and sensitive assays of human SIX3 function in zebrafish and

178 eficiency virus (SIV) infection by using the sensitive assays of intracellular cytokine staining and

179 ant to promote the development of robust and sensitive assays of islet-reactive T-cells in patients w

180 ssayed by consensus sequencing and by a more sensitive assay (oligonucleotide ligation assay [OLA]) u

181 Here we present an inexpensive and sensitive assay platform for activity-based protease qua

182 essed in a label-free, quantifiable and very sensitive assay platform.

183 troponin detected by new-generation, highly sensitive assays predicts clinical outcomes among patien

184 Sensitive assay procedures were developed and employed t

185 We validated a highly specific and sensitive assay protocol that should be used as the stan

186 These robust and sensitive assays provide a toolkit for the identificatio

187 This rapid, simple, economical, and highly sensitive assay provides a practical alternative to dide

188 This simple and sensitive assay provides the basis for the development o

189 This sensitive assay quantifies specific bacteria in a sample

190 Thus, these new sensitive assays reveal a heretofore unappreciated, yet

191 INTERPRETATION: This new highly specific and sensitive assay showed asymptomatic infection with Ebola

192 Results of very sensitive assays showed that 6 of 31 monkeys had weak SI

193 HLA class I antibody development by a highly sensitive assay such as the PRA-STAT ELISA after LT can

194 iently applied in a reagent free manner, all sensitive assays such as these suffer, however, from pro

195 We examined this hypothesis using a highly sensitive assay system for detection of misfolded protei

196 ovides, along with gene fusion approaches, a sensitive assay system for signal sequences that utilize

197 ocyte and its meiotic spindle will provide a sensitive assay system for the study of reproductive tox

198 CR offers a relatively simple-to-perform and sensitive assay system.

199 pend on the development of more reliable and sensitive assay systems, possibly formatted for cytochem

200 However, more sensitive assay techniques are needed when compared to b

201 repeat blood donors using the sensitive/less sensitive assay testing strategy was 2.95 per 100000 per

202 ential of these techniques to provide a more sensitive assay than behavioral measures used alone.

203 We have developed a highly sensitive assay that accurately determines the number of

204 iated epitopes in class II MHC, we devised a sensitive assay that averted potential activation of B c

205 In this regard, a sensitive assay that can accurately and rapidly quantify

206 receptors and that the SPA was a simple and sensitive assay that could be readily adapted into a hig

207 Here we describe a sensitive assay that enables quantitative analysis of ga

208 We have developed a rapid and sensitive assay that enables quantitative immunodetectio

209 gen affinity of each oxidase, using a highly sensitive assay that exploits globin deoxygenation durin

210 ied by measuring phalloidin binding sites, a sensitive assay that had not been used previously for pl

211 A sensitive assay that is capable of detecting the interac

212 This experimental system is a very sensitive assay that lends itself to the dissection of p

213 Utilizing a new sensitive assay that measures the production of glucosam

214 Development of a sensitive assay that measures the rate of cellular inter

215 Second, a sensitive assay that quantitates UTP mass at low nanomol

216 have therefore focused on the development of sensitive assays that allow the specific detection of si

217 dialysis and by steady-state kinetics using sensitive assays that allowed initial rate calculations.

218 yed in this quantitation platform for highly sensitive assays that can detect as low as 16 pM Ebola V

219 European small ruminant populations, highly sensitive assays that can specifically detect BSE, even

220 etter investigate this process, we developed sensitive assays that use the fluorescein arsenical dye

221 We measured cTnI using a sensitive assay (TnI-Ultra, Siemens Healthcare Diagnosti

222 We developed an efficient and sensitive assay to compare active PKA levels based on bi

223 is, via clonogenic assay, was used as a more sensitive assay to confirm the interaction of the treatm

224 To accomplish this, a specific and sensitive assay to detect and serotype rhinovirus direct

225 We developed a rapid and sensitive assay to detect B. anthracis bacteremia using

226 ivity of PBP4, we developed a simple, highly sensitive assay to detect cellular pools of lipid-linked

227 We established a highly sensitive assay to determine frequencies of various cate

228 stepwise transcription approach and a highly sensitive assay to determine the dynamics of interaction

229 uated in susceptible strains, we developed a sensitive assay to directly quantitate sPLA2 activity in

230 D system with our previously reported highly sensitive assay to measure cre activity in vitro using a

231 It is very challenging to develop a highly sensitive assay to measure endogenous OT, including radi

232 ld further reduce this risk to <10%, using a sensitive assay to measure resistance.

233 We further report a new, highly sensitive assay to measure the activity of SepCysS under

234 Using a sensitive assay to measure the RAG1 activity level of 79

235 We have designed a novel, precise, and sensitive assay to measure unspliced (US) human immunode

236 ng and after radiotherapy that may provide a sensitive assay to monitor changes in radiation-induced

237 Here, we present a simple and sensitive assay to monitor mycoplasma contamination (myc

238 Here, we use a new, highly sensitive assay to redefine the relationship between mit

239 e application and further refinement of this sensitive assay to the replication of a T x T-containing

240 g observations and the recent development of sensitive assays to assess the in vivo levels of active

241 t this type of cell could be used to develop sensitive assays to detect herpesviruses.

242 urge the need for more rapid, accurate, and sensitive assays to detect potential allergens in food i

243 accine manufacturers are expected to develop sensitive assays to detect residual BSA.

244 one marrow aspiration and the lack of highly sensitive assays to detect residual disease present chal

245 electivity allowed us to apply our rapid and sensitive assays to detection of AA in vitamin C tablets

246 We have employed relatively simple and sensitive assays to determine the function of BRCA1 vari

247 evaluate this we used a complementary set of sensitive assays to explore the mtDNA rearrangements in

248 Sensitive assays to measure plasma and serum KIM-1 in mi

249 and in vivo, we have developed exceptionally sensitive assays to study the role of Escherichia coli t

250 A sensitive assay using biotinylated ubiquitin revealed ex

251 A sensitive assay using high-performance liquid chromatogr

252 r DNA than in plasma RNA, as determined by a sensitive assay using sufficient copies of virus, sugges

253 nsitivity in comparison to the previous most sensitive assay using the same mass spectrometry instrum

254 Sensitive assays using HLA class II multimers were used

255 interval [CI], 22.7%-27.4%) with the highly sensitive assay vs 0.7% (95% CI, 0.3%-1.1%) with the sta

256 cTnT detectable with a highly sensitive assay was associated with incident CHD, mortal

257 troponin T (cTnT) measured with a new highly sensitive assay was associated with incident coronary he

258 on-based cohort, cTnT detected with a highly sensitive assay was associated with structural heart dis

259 A more sensitive assay was therefore developed using multiple r

260 A highly sensitive assay was used to test the hypothesis that B c

261 In contrast, cTnI, measured using 2 sensitive assays, was persistently normal throughout the

262 Here we show, using a sensitive assay we developed, that the reduction of foli

263 id-induced microtubule depolymerization as a sensitive assay, we examined the characteristics of COC

264 Using a sensitive assay, we observed low levels of an unknown su

265 As a more sensitive assay, we used oligonucleotide microarrays to

266 Using sensitive assays, we found significant increases of hepa

267 Using highly sensitive assays, we have shown that B cell depletion is

268 hanges in cTnT levels measured with a highly sensitive assay were significantly associated with incid

269 D. magna was shown to be the most sensitive assay when carbon nanomaterials were present.

270 zation scheme could be easily adapted into a sensitive assay, where competition between tracer and ta

271 In particular, the need for a more sensitive assay will be emphasized.

272 during the "window period." Thus, the highly sensitive assay will be useful for early detection of HI

273 Such sensitive assays will facilitate distinguishing the rela

274 The development of more specific and sensitive assays will further illuminate the biology beh

275 solution melt (HRM) real-time PCR which is a sensitive assay with a rapid time-to-answer.

276 A simple and highly sensitive assay with optical amplification that uses the