ライフサイエンスコーパス: DCP

1 DCP also significantly reduced attack rates relative to

2 DCP inhibitory effects were attributed to induction of a

3 DCP is typically caused by non-progressive lesions to th

4 DCP potentiated monocyte antimycobacterial activity by i

5 DCP treatment of infected monocytes resulted in a signif

6 DCPs ensure thereby that only mutated sequences associat

7 DCPs prevent reassociation of denatured DNA strands: the

8 7 vs 0.513 (P = .004) and 0.560 (P = .0005); DCP, 0.357 vs 0.682 (P = .016) and 0.672 (P = .0005).

9 sophila caspase, named Drosophila caspase-1 (DCP-1), was identified and found to be structurally and

10 oropicrin (CP), and 1,1-dichloropropane (1,1-DCP) after a short period of heating.

11 tic acids (HAAs), 1,1-dichloropropanone (1,1-DCP), trichloroacetaldehyde (TCAL), haloacetonitriles (H

12 the best scFv bound tightly to the UO(2)(2+)-DCP complex (K(d), 19.6 nM).

13 en cells of rabbits immunized with UO(2)(2+)-DCP conjugated to keyhole limpet hemocyanin.

14 ehalogenimonas strain is responsible for 1,2-DCP conversion in the culture.

15 d a sediment-free culture dechlorinating 1,2-DCP in the absence of methanogenesis.

16 valuable approach for monitoring in situ 1,2-DCP reductive dechlorination by Dehalogenimonas strains.

17 scribed to encode a corrinoid-containing 1,2-DCP reductive dehalogenase was detected.

18 cally dechlorinated 1,2-dichloropropane (1,2-DCP) to propene.

19 ic fractionation (epsilonC(bulk)) of the 1,2-DCP-to-propene reaction was -15.0 +/- 0.7 per thousand u

20 copies in the culture and consumption of 1,2-DCP.

21 population, while concentrations of BPA, 24-DCP, and parabens were similar.

22 s and three parabens: 2,4-dichlorophenol (24-DCP), 2,5-dichlorophenol (25-DCP), benzophenone-3 (BP-3)

23 Urinary concentrations of TCS, BP-3, and 25-DCP were higher than among women of reproductive age in

24 BP-3 had the highest (0.62), followed by 25-DCP (0.49) and TCS (0.47).

25 hlorophenol (24-DCP), 2,5-dichlorophenol (25-DCP), benzophenone-3 (BP-3), bisphenol A (BPA), triclosa

26 2,3-DCP was dechlorinated to 3-CP, and, because cultures usi

27 higher for 2,5-DCP (6.1-12.9 mug/L) than 2,4-DCP (0.8-1.0 mug/L) throughout 2003-2010.

28 ed contact time of 0.55 min, over 90% of 2,4-DCP (initially 20 muM) and 90% of adsorbable organic chl

29 6-trichlorophenol (TCP) and 2,4,5-TCP to 2,4-DCP and 3,4-DCP, respectively, and dechlorinated 2,3,6-T

30 form for the comprehensive evaluation of 2,4-DCP and posed a great potential to simplify environmenta

31 JNA converted 2,3,4-TCP to 3,4-DCP and 2,4-DCP by ortho and meta dechlorination, respectively.

32 dical oxidation by achieving much higher 2,4-DCP degradation capacity and avoiding the formation of h

33 hlorine (AOCl) can be removed at the PDS/2,4-DCP molar ratio of 1 and 4, respectively.

34 step, followed by a rapid reaction with 2,4-DCP present in the solution.

35 ully applied to evaluate the toxicity of 2,4-DCP to HepG2 cells.

36 ummed environmental phenols (2,5-DCP and 2,4-DCP) were inversely associated with age of menarche [haz

37 n, benzophenone-3, total phthalates, and 2,4-DCP) were not significantly associated with age of menar

38 2,4-Dichlorophenol (2,4-DCP), 2,5-dichlorophenol (2,5-DCP), and their precursors

39 sess the toxicity of 2,4-dichlorophenol (2,4-DCP), a priority pollutant and has potential risk to pub

40 presence of H2O2 and 2,4-dichlorophenol (2,4-DCP), is characterised via the individualised quantifica

41 ng a model compound, 2,4-dichlorophenol (2,4-DCP).

42 inked to POD activity in the presence of 2,4-DCP.

43 bled a high electrocatalytic activity to 2,4-DCP.

44 tive concentrations of the same ([H2O2]/[2,4-DCP]/[Chl]=1:3:0.02) is crucial to explaining inhibition

45 JNA converted 2,3,4-TCP to 3,4-DCP and 2,4-DCP by ortho and meta dechlorination, respec

46 henol (TCP) and 2,4,5-TCP to 2,4-DCP and 3,4-DCP, respectively, and dechlorinated 2,3,6-TCP to 3-chlo

47 Chromosomal loci associated with 49 DCPs were confirmed by linkage analysis and tests of gen

48 ) urinary concentrations were higher for 2,5-DCP (6.1-12.9 mug/L) than 2,4-DCP (0.8-1.0 mug/L) throug

49 5-DCP) and summed environmental phenols (2,5-DCP and 2,4-DCP) were inversely associated with age of m

50 icity, we found that 2,5-dichlorophenol (2,5-DCP) and summed environmental phenols (2,5-DCP and 2,4-D

51 orophenol (2,4-DCP), 2,5-dichlorophenol (2,5-DCP), and their precursors are widely used in industry a

52 findings suggest an association between 2,5-DCP, a potential EDC, and earlier age of menarche in the

53 ted 2,3,6-TCP to 3-chlorophenol (CP) via 2,5-DCP.

54 on of a calibrated infrared pyrometer into a DCP instrument is shown to enhance the measurement capab

55 ROC curve indicated that a DCP value of 125 mAU/mL yielded the best sensitivity (89

56 quantities of beta-amyloid peptide (Abeta), DCP-LA and DHA-CP6 reduced the intracellular and secrete

57 Effective densities determined by absolute DCP for the silica particles ranged from 2.02 to 2.34 g/

58 diameter determinations provided by absolute DCP was confirmed using silica particles with nominal di

59 Advantages of absolute DCP determinations for size and density analysis relativ

60 erization of colloidal silica using absolute DCP suggests applicability of the technique to a variety

61 to 2,9-dicarboxyl-1,10-phenanthroline-acid (DCP), were produced using genetic material obtained from

62 t Reaper and Grim, but not HID, can activate DCP-1 in vivo.

63 milarly, the PKC epsilon-specific activator, DCP-LA, effectively prevents synaptic loss, amyloid plaq

64 Although active DCP-1 protein cleaves full-length DCP-1 and full-length

65 they complement AFP; and what factors affect DCP, AFP-L3%, or AFP levels.

66 AFP, DCP, and AFP-L3% levels were measured blinded to clinica

67 The SCP (P = .012) and DCP (P = .013) vessel density and perfusion density (P =

68 orrelated with SCP (r = -0.88, P = .012) and DCP capillary densities (r = -0.79, P = .048).

69 d telangiectasias in both SCP (P = .021) and DCP (P = .042).

70 ducted to compare the performance of AFP and DCP.

71 he binding curves obtained with 8A11-Cy5 and DCP-UO22+ species changed from sigmoidal to hyperbolic a

72 drICE and DCP-1 have similar yet different enzymatic specificities

73 y which can cleave p35, lamin DmO, drICE and DCP-1 in vitro, and which can trigger chromatin condensa

74 tor caspases, including Drosophila drICE and DCP-1, suggests that in vivo activation of these group I

75 The ICP and DCP VD were not significantly lower in the glaucoma grou

76 n-specific immunotherapy (EPIT) with OVA and DCP also protected sensitized mice from anaphylaxis and

77 tration in both normal control (NC) rats and DCP rats, but the sensitivity of FSK on HCN channels was

78 CP (P < .0001 and P = .02, respectively) and DCP (P < .0001 and P = .0004, respectively) compared to

79 SCP, 29 (21.5%) were visible in both SCP and DCP; and 21 (15.6%) were not visible on OCTA.

80 mproved when an appropriate adjuvant such as DCP is used.

81 eyes (28.8%) revealed capillary dilations at DCP, 15 of which were in stages 1 and 2.

82 These findings, especially at DCP, may improve our understanding about the pathogenesi

83 Two of the authors (DCP and REvdR) belong to the Coloured population, with o

84 rance and rehabilitation differences between DCP-eligible vs -ineligible patients and among stratifie

85 ented work provides the missing link between DCP dispersive models and FETD and/or SETD based algorit

86 a Drosophila embryo cDNA library that block DCP-1 caspase-dependent yeast cell death.

87 Both DCP and AFP levels increased progressively from G1 to G4

88 Both DCP and AFP were tested using enzyme immunoassay methods

89 s increased progressively from G1 to G4, but DCP values had less overlap among the groups than AFP.

90 dence interval [CI]: 0.77-0.84), followed by DCP (0.72, 95% CI: 0.68-0.77) and AFP-L3% (0.66, 95% CI:

91 ression but are independent of regulation by DCP-66.

92 Des-gamma-carboxyprothrombin (DCP) has been reported to be more sensitive and specific

93 Two very similar Drosophila caspases, DCP-1 and drICE, have been previously identified.

94 ertebrates and possesses two known caspases, DCP-1 and drICE.

95 onds of exposure to diethyl chlorophosphate (DCP) vapor.

96 nd 25:12.5:2.5 mole ratio of surfactant:Chol:DCP was the optimum formulation in the encapsulation of

97 -2',2'-dimethyldihydropyrano[2,3-f]chromone (DCP, 4) were designed and synthesized.

98 In conclusion, DCP was more sensitive and specific than AFP for differe

99 Dynamic cystocolpoproctography (DCP) has evolved from a method of evaluating the anorect

100 r weak contractility of Diabetic cystopathy (DCP) and to study the possible mechanism of regulating t

101 abnormalities at superficial (SCP) and deep (DCP) capillary plexuses and choriocapillaris (CC) in pat

102 We detected DCPs in at least 81% of participants.

103 7 for 4-Cl-Ph-O-dG and 2,6-dichloro-Ph-O-dG (DCP-O-dG), respectively.

104 ted pentachlorophenol to 3,5-dichlorophenol (DCP) via removal of the ortho and para chlorines in all

105 ary concentrations of these dichlorophenols (DCPs) have been measured as part of four National Health

106 we tested the efficacy of dichlorphenamide (DCP; Daranide), a potent carbonic anhydrase inhibitor, i

107 simetrically detects diethylchlorophosphate (DCP), a model organophosphorous cholinesterase inhibitor

108 djuvant potential of diphenylcyclopropenone (DCP), a strong contact sensitizer, which is currently us

109 al. show that DIAP1 polyubiquitinates DRONC, DCP-1, and drICE, leading to their nondegradative inacti

110 rence (in terms of the end point) for either DCP or placebo, and 11 of these preferred DCP.

111 2-Ethyl DCP (8) exhibited the best anti-HIV activity in both ass

112 coding an Ex-1 binding transcription factor, DCP-66, using a yeast one-hybrid screen.

113 ncreased the affinity of the native 8A11 for DCP-UO22+ by 3-fold.

114 sed the affinity of the primary antibody for DCP-UO22+ by 4-fold.

115 r operating characteristic curve (AUROC) for DCP was 0.99 and was significantly larger than that of A

116 ow cutoff was 43% and 94%, respectively, for DCP and 47% and 75%, respectively, for AFP.

117 less tightly (K(d), 23.5 muM) to metal-free DCP.

118 Hence, DCP acts as an immunoregulatory compound enhancing the a

119 us (DCP), and all-plexus retina (SVC + ICP + DCP).

120 tigen in the absence of protein G, and (iii) DCP-UO22+ and protein G oppose each other's binding to t

121 In DCP, two major movement disorders, dystonia and choreoat

122 n HCN channels was clearly down-regulated in DCP rats.

123 dentified predictors and evaluated trends in DCP concentrations according to race/ethnicity, age, sex

124 thione S-transferase-DIAP1 directly inhibits DCP-1 caspase activity but that it had minimal effect on

125 ugh active DCP-1 protein cleaves full-length DCP-1 and full-length drICE in vitro, GMR-DeltaN-dcp-1 d

126 spite the advances in other imaging methods, DCP has remained a practical, cost-effective procedure f

127 d in the detection of early HCC, but neither DCP nor AFP is optimal.

128 In this study, we tested the ability of DCP to mediate inhibition of intracellular mycobacteria

129 The antimicrobial activity of DCP was comparable to that of pyrazinamide (PZA), one of

130 d Participants: A longitudinal assessment of DCP implementation and Medicaid expansion/open enrollmen

131 stic regressions to estimate associations of DCP concentrations above the 95th percentile with housin

132 conjugate with saturating concentrations of DCP-UO22+ decreased the affinity of the conjugate for pr

133 oacetate) reversed the inhibitory effects of DCP on intracellular mycobacterial growth.

134 ate, (ii) binding of the first equivalent of DCP-UO22+ to the antibody promotes the binding of the se

135 e energy binding model in which (i) 2 mol of DCP-UO22+ and 1 mol of protein G bind to each mole of th

136 ICCs-DM is important in the pathogenesis of DCP.

137 this study were to determine performance of DCP and AFP-L3% for the diagnosis of early HCC; whether

138 ace/ethnicity were significant predictors of DCP urinary concentrations above the 95th percentile.

139 tudying the wideband plasmonic properties of DCP media.

140 Prospective studies to evaluate the role of DCP in early HCC are underway.

141 The sensitivity and specificity of DCP at month 0 was 74% and 86%, respectively, at a cutof

142 The sensitivity and specificity of DCP were 96.8% and 98.3% respectively, based on a Receiv

143 target for the pharmacological treatment of DCP.

144 In conclusion, the utility of DCP for the diagnosis of HCC among Nigerian patients was

145 cuss the limitations and clinical utility of DCP.

146 survey cycle with urinary concentrations of DCPs during NHANES 2003-2010.

147 Only DCP vessel density significantly correlated with the sta

148 ary nonperfusion at the superficial (SCP) or DCP, we used the spectral-domain optical coherence tomog

149 temporary and permanent dual-chamber pacing (DCP) were evaluated in symptomatic pediatric patients wi

150 Dyskinetic cerebral palsy (DCP) is the second most common type of cerebral palsy af

151 nges in the drying/crystallization patterns (DCP) of an array of microdroplets containing solutions o

152 Dipterinyl calcium pentahydrate (DCP), a calcium-complexed pterin compound, has previousl

153 cribe the technique they use when performing DCP, define the radiographic criteria used for diagnosis

154 Permanent DCP is an effective therapy for selected pediatric patie

155 Permanent DCP pacing can reduce left ventricular outflow tract (LV

156 derwent surgical implantation of a permanent DCP system.

157 exed with 2,9-dicarboxy-1,10-phenanthroline (DCP-UO22+).

158 iated with differential chemical phenotypes (DCPs), defined as greater than or equal to fivefold diff

159 of cholesterol (Chol) and dicetyl phosphate (DCP) as well as different concentration of alpha-tocophe

160 Disc centrifuge photosedimentometry (DCP) with fluids of different densities is used to simul

161 A specific activator of PKCepsilon, DCP-LA, slowed CBF after maximal PKCepsilon activation.

162 ere assessed with the Direct Current Plasma (DCP) technique and its distribution assessed with Morin

163 lary plexus (SCP) and deep capillary plexus (DCP) in the central macula in all 6 patients were compar

164 the level of SCP and deep capillary plexus (DCP) on OCTA.

165 pillary plexus (ICP), deep capillary plexus (DCP), and all-plexus retina (SVC + ICP + DCP).

166 chemia of the retinal deep capillary plexus (DCP).

167 perficial (SCP) and deep capillary plexuses (DCP).

168 tectures comprised of Drude-Critical Points (DCP) media (e.g., gold and silver) is proposed and valid

169 ighted average equivalent exposure of 10 ppb DCP effects an irreversible change in smartphone readout

170 er DCP or placebo, and 11 of these preferred DCP.

171 egy relying on the use of DNA clutch probes (DCPs) that render specific sequences of ctDNA accessible

172 e pre-mRNA, the downstream cleavage product (DCP) is degraded by the 5'-3' exonuclease activity of CP

173 g cleavage, the downstream cleavage product (DCP) is rapidly degraded in vitro by a nuclease that als

174 we show three orthologs of P body proteins, DCP-2, CAR-1 and CGH-1, and two markers of stress granul

175 ein (AFP) and des-gamma-carboxy prothrombin (DCP) in the early diagnosis of HCC.

176 Des-gamma carboxy-prothrombin (DCP) and lectin-bound AFP (AFP-L3%) are potential survei

177 Des-gamma carboxy-prothrombin (DCP) has been reported to be more sensitive and specific

178 including the Dependent Coverage Provision (DCP) and Medicaid expansion/open enrollment, and to cons

179 Several DCP analogues (4, 5, 7, 8, 13, and 17) exhibited extreme

180 Even more promisingly, some DCP analogues also showed activity against a multi-RT in

181 nd density analysis relative to standardized DCP measurements include the elimination of instrument s

182 negative surface charge than inactive strain DCP-Ps1.

183 d by metabolically active cultures of strain DCP-Ps1, which at similar values of SIcalcite, have a mo

184 The ability of Pseudomonas stutzeri strain DCP-Ps1 to drive CaCO3 biomineralization has been invest

185 and 4-methyl DCK (2), all newly synthesized DCP analogues (4-21) were screened for anti-HIV-1 activi

186 AFP was more sensitive than DCP and AFP-L3% for the diagnosis of early and very earl

187 We conclude that DCP is effective in the prevention of episodic weakness

188 These findings indicate that DCP induced mycobacterial killing via MIP-1beta- and nit

189 We now show that DCP-1 has a substrate specificity that is remarkably sim

190 aenorhabditis elegans CED-3, suggesting that DCP-1 is a death effector caspase.

191 The DCP and Chol improved the physicochemical properties of

192 FAZ area was enlarged at the DCP (P = .001).

193 clease, suggesting that CPSF-73 degrades the DCP both in vitro and in vivo.

194 characterize the activity that degrades the DCP.

195 ty is processive and continues degrading the DCP substrate even after complete removal of the U7-bind

196 FA (P = .016), exclusively localized in the DCP (P = .016).

197 g substantial protein-induced changes in the DCP as "1" and those that show no or small changes as "0

198 on OCTA; 76 (56.3%) were visible only in the DCP, 9 (6.7%) only in the SCP, 29 (21.5%) were visible i

199 HeLa cells indicate that degradation of the DCP does not depend on the Xrn2 5' exonuclease, suggesti

200 ASH antibodies, the 5'-3' degradation of the DCP is not affected.

201 to enhance the measurement capability of the DCP technique by correcting for the temperature dependen

202 tant in highlighting the contribution of the DCP to the oxygen requirements of the photoreceptors as

203 Before implementation of the DCP, 1 of 4 patients was uninsured.

204 ry plexus, PAMM is caused by ischemia of the DCP, and appears as hyper-reflective, band-like lesions

205 e-mRNA and the subsequent degradation of the DCP.

206 f capillary nonperfusion at the level of the DCP.

207 pillaries, and capillary nonperfusion of the DCP.

208 nges on SDOCT showed robust perfusion of the DCP.

209 nd altered patient outcomes in ways that the DCP alone was never intended to do.

210 V cross-linking studies demonstrate that the DCP and its 5'-truncated version specifically interact w

211 f value was 11 ng/mL and was inferior to the DCP value of 125 mAU/mL, the area under the ROC curves b

212 Adjusted GM concentrations of the DCPs among children (6-11 years of age) and adults > 60

213 g three genes that were linked to 96% of the DCPs.

214 When the microbeads are subjected to DCP vapor, the conversion of FLA into a phosphoramide ca

215 Exposure to DCPs and their precursors was prevalent in the general U

216 In the PSPP trial, DCP significantly reduced attack rates relative to place

217 Furthermore, urinary DCP concentrations have showed a downward trend since 20

218 ional case control study to evaluate whether DCP is more sensitive and specific than AFP for differen

219 Binding curves obtained with DCP-UO22+ and the bivalent (Fab)2 or the monovalent Fab

220 488 altered the binding curves obtained with DCP-UO22+ from hyperbolic to sigmoidal, the latter chara

221 n nanotube based chemidosimetric scheme with DCP limits of detection of 28 ppb.

222 Loss of zygotic DCP-1 function in Drosophila caused larval lethality and