ライフサイエンスコーパス: ASV

1 ASV pol X binds the dsDNA with a site-size of n=10(+/-2)

2 ASV with CPE gave a 20x decrease (4.0 ppb) in the detect

3 ASV-ASV co-occurrence within hosts, independent of phylo

4 ASV-SECM can thus be used to detect and study induced di

5 ASVs positively correlated with yield were predominantly

6 ASVs were assigned to 17 known phyla and 213 known gener

7 2.03 +/- 9.70 vs. 12.52 +/- 7.43; p = 0.005; ASV: 12.84 +/- 10.48 vs. 13.76 +/- 8.69; p < 0.0001).

8 Comparison of the HIV-1, ASV and PFV CCD structures highlighted both conserved as

9 ividual ciliate species resulted in up to 11 ASVs per species, while SWARM produced up to 19 OTUs per

10 The avian sarcoma virus 16 (ASV 16) is a retrovirus that induces hemangiosarcomas in

11 mplicon Sequencing Variants (ASVs): ASV 191, ASV 44, and ASV 75, were identified as significantly mor

12 ) in ASV versus stable or decreasing (</=2%) ASV.

13 ersity of Perkinsea within soil samples (269 ASVs), challenging the previous assumption that this gro

14 e CRF2 receptor antagonist antisauvagine-30 (ASV-30).

15 (500 ng or 1 mug/side) or antisauvagine-30 (ASV-30; 500 ng/side) into the VTA.

16 ert in the genome of avian sarcoma virus 31 (ASV 31) and functions as the oncogenic determinant of th

17 e phylum level and Streptococcus (2340 [36%] ASVs) at the genus level.

18 a notable proportion of Perkinsea ASVs (428 ASVs) could correspond to putative new organisms, encomp

19 limited range of alginate-enriched taxa (82 ASVs).

20 rrectly classified strictures using either 9 ASVs (amplicon sequence variants), 4 serum chemistry tes

21 ns across regions, while most high-abundance ASVs were only identified in specific regions.

22 Several low abundance ASVs exhibited cosmopolitan distributions across regions

23 he vertical patterns of the 50 most abundant ASVs revealed niche partitioning of LP phylotypes in the

24 with moderate-to-severe sleep apnea, adding ASV to OMT did not improve 6-month cardiovascular outcom

25 nd in the present study to be active against ASV IN as well as HIV-1 IN.

26 titatively the transduction efficiency of an ASV vector in naturally arrested mouse hippocampal neuro

27 l fragment of Chmp6 inhibited both HIV-1 and ASV Gag release in a dominant negative manner.

28 integration site selection of the HIV-1 and ASV integrases in opposite ways.

29 encing Variants (ASVs): ASV 191, ASV 44, and ASV 75, were identified as significantly more abundant i

30 sequence variants (ASVs) and that clade and ASV composition can change over the course of blooms.

31 Among 9,572 patients, SD and ASV were significantly lower with atorvastatin 80 mg/day

32 ate stable interactions between HMG-I(Y) and ASV IN or between HMG-I(Y) and HIV-1 IN.

33 oast into SDB in terms of dominant clade and ASVs.

34 (3) 1.8 vs 4.5 cm(3) 7.8; P < .001), ENV(AP)/ASV% (0.9% 1.5 vs 1.7% 2.2; P = .003), and ENV(DP)/ASV%

35 AUC, 0.74), ENV(AP) (AUC, 0.71), and ENV(AP)/ASV% (AUC, 0.69) in indicating persistent endoleak.

36 NV(DP) in aneurysm sac volume (ASV) (ENV(AP)/ASV%, ENV(DP)/ASV%, respectively) were measured on first

37 present initial evidence that this apparent ASV switch is a physiological response rather than a cha

38 ccuracy and identified 19 disease-associated ASVs and five healthy-associated ASVs that were consiste

39 we tested whether the 19 disease-associated ASVs met the assumption of a pathogen and identified two

40 -associated ASVs and five healthy-associated ASVs that were consistently differentially abundant acro

41 ith (n = 3) or without (n = 13) asunaprevir (ASV; PI).

42 of a clinical HCV-NS3 inhibitor asunaprevir (ASV).

43 inating Amplicon Sequencing Variants (ASVs): ASV 191, ASV 44, and ASV 75, were identified as signific

44 Most Atribacteria ASVs belonged to JS-1-Genus 1 and clustered with other s

45 o the ISS (102 fungal OTUs and 102 bacterial ASVs).

46 e diverse (465 fungal OTUs and 237 bacterial ASVs) compared to the ISS (102 fungal OTUs and 102 bacte

47 ange in community diversity but 36 bacterial ASVs significantly changed in relative abundance.

48 s demonstrated that a small set of bacterial ASVs can accurately classify periodontally healthy sampl

49 luenced the co-occurrence of many beneficial ASVs, as well as a few potentially harmful ones.

50 nts were not significantly different between ASV and control.

51 These bioindicator ASVs were additionally recovered in near-coral seawater

52 against both IN proteins was shown to block ASV IN DNA binding and end fraying, with similar dose re

53 ttle effect on HIV-1 Gag release but blocked ASV Gag release.

54 transcription factors HNF3 and GATA4 blocked ASV DNA integration in extended nucleosome arrays, local

55 rcoma virus genome, precise deletion of both ASV dr1 elements results in a very low level of virus re

56 each 1-SD increase in LDL-C variability (by ASV) increased the risk of any coronary event by 16% (ha

57 ogen and identified two pathogenic candidate ASVs-ASV25 Cysteiniphilum litorale and ASV8 Vibrio sp. t

58 ns between the salamander genera and certain ASVs, with mostly members of the family Burkholderiaceae

59 HIV-1 IN conferred partial ability to cleave ASV substrates with a concomitant loss in the ability to

60 For conducting ASV on-line with ICPMS, the DIHEN was found to be more a

61 The presence of some cosmopolitan ASVs across regions argues against dispersal limitation

62 (Hg-GC) electrodes were compared for the CPE-ASV.

63 ated with different groups of cyanobacterial ASVs including time-lagged predator-prey relationships.

64 with cirrhosis; 1 had previously failed DCV-ASV plus Peg-IFN and RBV).

65 Unexpectedly, bacterial diversity (ASV, Faith PD and Shannon) was higher among zoo gorillas

66 at the tuber elongation stage, and dominant ASVs identified as Sphingomonas, Rhodanobacter, Sphingob

67 a and Penicillium sp. were the most dominant ASVs detected in the air in rank order.

68 The dominant ASVs at the pier were found further offshore and in the

69 icola, Glarea and Lecanora were the dominant ASVs present.

70 0.9% 1.5 vs 1.7% 2.2; P = .003), and ENV(DP)/ASV% (1.6% 2.2 vs 3.7% 3.6; P < .001) were smaller in gr

71 .78) was superior to the accuracy of ENV(DP)/ASV% (AUC, 0.76), ENV(DP-AP) (AUC, 0.74), ENV(AP) (AUC,

72 rysm sac volume (ASV) (ENV(AP)/ASV%, ENV(DP)/ASV%, respectively) were measured on first postoperative

73 to the analysis in complex matrices, duplex ASV-QDs-based determination of bovine casein and bovine

74 The ECVDEP was also normalized as the ECV/ASV ratio.

75 th prokaryotes and eukaryotes, and eukaryote ASV richness was significantly higher in camelid latrine

76 oanalytical tools cannot efficiently examine ASV and PTM events simultaneously, which limits understa

77 mid acceptor, purified bacterially expressed ASV integrase (IN), and human high-mobility-group protei

78 The final ASVs dataset consisted of seven genera: Coxiella, Anapla

79 bgingival versus saliva models also had five ASVs.

80 l versus subgingival model consisted of five ASVs.

81 ngth 16S rRNA amplicon sequence variants (FL-ASVs) and are used to expand the MiDAS 4 database for ba

82 with the pH vs activity profile observed for ASV IN.

83 ults are consistent with a possible role for ASV IN in nuclear targeting.

84 Additionally, four ASVs (Algicola, Cohaesibacter, Thalassobius and Vibrio)

85 ion of the LTR termini, the amino acids from ASV IN were substituted into the structurally equivalent

86 behaviour of sucrose has been discussed from ASV and ASIC parameters, as these parameters, which are

87 behaviour of sucrose has been discussed from ASV and ASIC parameters.

88 However, viral reporter gene expression from ASV-based vectors was substantially higher in the Daxx-n

89 Thirty-eight fungal ASVs could only be assigned to higher taxonomic levels,

90 Of the total fungal ASVs detected, 29 were only present in the air sample an

91 the proteolytic degradation of GFP[AAV], GFP[ASV], and GFP[LVA], which are popular variants of GFP wi

92 Specific bacteria, including Gilliamella ASVs, were positively associated with infection, indicat

93 There were 77 salivary ASVs and 39 gut ASVs differentially abundant in self-reported periodonta

94 followed by IL10 rs6667202, and that of gut ASVs was NPY rs2521364.

95 CI, 1.16-1.67 and no CKD: HR per 1-SD higher ASV, 1.13; 95% CI, 1.01-1.27), among placebo and spirono

96 .10-1.33) and creatinine (HR per 1-SD higher ASV, 1.13; 95% CI, 1.04-1.22) were independently associa

97 composite events (sodium: HR per 1-SD higher ASV, 1.14; 95% CI, 1.01-1.30 and potassium: HR per 1-SD

98 1.01-1.30 and potassium: HR per 1-SD higher ASV, 1.21; 95% CI, 1.02-1.44).

99 .03-1.65 and placebo arm: HR per 1-SD higher ASV, 1.27; 95% CI, 1.04-1.56).

100 e (CKD) at baseline (CKD: HR per 1-SD higher ASV, 1.39; 95% CI, 1.16-1.67 and no CKD: HR per 1-SD hig

101 Specific clade II ASVs became relatively more abundant towards the back of

102 Isolates matching clade II ASVs from SDB show pigment composition that is better ad

103 was determined as interval increase (>2%) in ASV versus stable or decreasing (</=2%) ASV.

104 s in relative abundance and small changes in ASV community composition among sites.

105 These results suggest the dr1 elements in ASV act to selectively inhibit src splicing and that bot

106 Daxx was not required for early events in ASV replication, including integration, as Daxx-null cel

107 endoleaks, there was an interval increase in ASV.

108 surements in indicating interval increase in ASV.

109 s can substitute for Nedd4 family members in ASV Gag release.

110 the chromosomal features that may influence ASV integration and support the idea that distinct, viru

111 ore domain of avian sarcoma virus integrase (ASV IN) have provided the most detailed picture so far o

112 ore domain of avian sarcoma virus integrase (ASV IN) were solved at 1.9- to 2.0-A resolution at two p

113 tal sequence reads which were clustered into ASVs by sample year.

114 is included 323 proteoforms for the 14.1 kDa ASV alone.

115 d, and stearic acid at C78 of the 17.125 kDa ASV.

116 , the EPD time required to achieve a maximum ASV signal increases with decreasing Au NP concentration

117 cterization workflow resolved four known MBP ASVs and hundreds of differentially modified states from

118 merican Society for Virology Annual Meeting (ASV), the International Herpesvirus Workshop (IHW), the

119 Using a modified ASV encoding a murine leukemia virus amphotropic env gen

120 CAT-HF (Cardiovascular Improvements With MV-ASV Therapy in Heart Failure) trial investigated whether

121 In the structures of native ASV IN at pH 6.0 and below, as well as in all structures

122 ted at low pH for the crystals of the native ASV IN core domain.

123 The putative yield-negative ASVs detected in Gangneung may have been influenced by d

124 Notably, ASVs that were observed in the surface layer comprised ~

125 We also identified two novel ASVs from an alternative transcriptional start site (ATS

126 observed as pregnancy progressed (p(observed ASV) = 0.006, LMM).

127 ffusion phenomena may relate to the observed ASV-SECM behavior.

128 Observed ASVs showed a quadratic pattern with age (peak at 30 yea

129 ned for alpha diversity (Q = 0.002, Observed ASVs; Q = 0.04 Shannon Index), but not beta diversity, w

130 s in alpha diversity indices (e.g., observed ASVs and chao1, P < 0.001), and increased abundance of p

131 e based on the algorithm DADA2 for obtaining ASVs against a pipeline based on the algorithm SWARM for

132 nce of ASV and its removal in the absence of ASV creates a practically reversible chemical switch.

133 roup analysis suggested a positive effect of ASV in patients with HF with preserved ejection fraction

134 nals and identifying differential effects of ASV in patients with HF with preserved ejection fraction

135 d efficient accumulation of nuclear forms of ASV DNA in gamma-irradiation-arrested cells.

136 Translational fusion of ASV Gag with an L domain deletion (Deltap2b) to proteins

137 rming that nuclear import and integration of ASV DNA can occur in the absence of mitosis.

138 mitosis in nuclear import and integration of ASV DNA.

139 cells revealed that the expression levels of ASV target genes were similar to the median level for al

140 integration, underscoring the preference of ASV for compacted chromatin.

141 display of anti-CD19 scFv in the presence of ASV and its removal in the absence of ASV creates a prac

142 To identify the region of ASV IN that specifies nuclear localization, various subd

143 on is necessary for efficient replication of ASV in culture.

144 tacts with the LTRs and that substitution of ASV IN amino acids at many of the analogous positions in

145 oding genes) appear to be favored targets of ASV integration.

146 erved in the surface layer comprised ~20% of ASVs and ~60% of sequences in each of the deeper (includ

147 Notably, 79.4% of ASVs matched soil bacteria from the same location, sugge

148 Other examples of ASVs associated with VS were Collinsella aerofaciens, pr

149 urrent, but we did observe more oligotrophic ASVs and clades along with depth variation in Synechococ

150 Ag in the AuAg alloy following AGR based on ASV is 17.8 +/- 0.6% for 4.1 nm diameter Au NPs, 87.2 +/

151 ool of Vps37C (ESCRT-I) had little effect on ASV but blocked HIV-1 Gag release.

152 lear import mechanism for the oncoretrovirus ASV and suggest that this mechanism can operate in both

153 One ASV (classified as Sutterella wadsworthensis) was associ

154 y of the chimeras to 3 ' process U5 HIV-1 or ASV duplex oligos was determined.

155 Relatively few other ASV were detected, but included two variant Rhabdochlamy

156 ealed that a notable proportion of Perkinsea ASVs (428 ASVs) could correspond to putative new organis

157 dom forest machine learning models on pooled ASV counts for the genus data were highly predictive of

158 bial signatures and highlight the predictive ASVs as promising biomarkers for characterizing oral nic

159 We found no evidence for preferred ASV integration sites over the length of genes and immed

160 oising and taxa binning/parsing of prevalent ASVs at the single nucleotide level of resolution.

161 sequencing study with protists we recommend ASVs as replacement for OTUs, best in combination with S

162 nd end fraying, with similar dose responses; ASV IN substitutions that reduced DNA binding also reduc

163 There were 77 salivary ASVs and 39 gut ASVs differentially abundant in self-rep

164 ociated with the greatest number of salivary ASVs was VDR 2228570 followed by IL10 rs6667202, and tha

165 Select ASVs group phylogenetically and show similar seasonal an

166 In group B, 46 patients (72%) showed ASV enlargement and 44 patients (69%) underwent endoleak

167 Relative abundance of a single ASV within the family Ruminococcaceae was the only diffe

168 In addition, a single ASV-SECM image is shown to produce unique concentration

169 sequence variants (ASVs), as well as single ASVs from Coprobacter, Parabacteroides, Paraprevotella,

170 Specific ASVs from Escherichia, Fusobacterium, Granulicatella, Tr

171 growth aged from 6 to 9 mo, but no specific ASVs differed in relative abundance.

172 stinal permeability at 9 mo, but no specific ASVs differed in relative abundance.

173 The results found pointed out that both SW-ASV approaches were suitable and easy-to-use method to m

174 The results obtained by SW-ASV were compared with those obtained using Direct Mercu

175 square wave anodic stripping voltammetry (SW-ASV) conducted at both solid gold electrode (SGE) and a

176 square wave anodic stripping voltammetry (SW-ASV) with a solid gold electrode (SGE) and using a porta

177 The resultant hyphenated technique (ASV-DIHEN-ICPMS) is capable of analyzing select heavy me

178 was also found to be required for long-term ASV silencing maintenance and full viral DNA methylation

179 Taken together, these results indicate that ASV and HIV-1 Gag utilize different combinations of ESCR

180 The results indicate that ASV is able to transduce these differentiated neurons ef

181 Lastly, we observed that ASV can transduce postmitotic mouse neurons.

182 Here we report that ASV integrase (IN) expressed as a fusion to beta-galacto

183 The ASV values showed that arabitol remained sweet in the pr

184 ns cyanobacterial community structure at the ASV level than the abiotic environmental factors.

185 interest that can subsequently be run at the ASV level.

186 int did not differ significantly between the ASV and control groups (p = 0.92 Wilcoxon).

187 lk-modified with bismuth citrate; during the ASV measurements, the bismuth precursor is converted to

188 ased from 35.7/h to 2.1/h at 6 months in the ASV group versus 35.1/h to 19.0/h in the control group (

189 Analysis of the ASV 16 genome revealed that it encodes an oncogene that

190 The transduction efficiency of the ASV vector was found to be intermediate between the rela

191 Six months following the symposium, the ASV held an online panel discussion on the ongoing H5N1

192 These analyses showed that the ASV IN protein possesses a functional nuclear localizati

193 , consistent with qualitative changes to the ASV.

194 We have used the ASV and HIV-1 reconstituted systems to compare the mecha

195 mapping shows very close agreement with the ASV-determined compositions.

196 mining the weighted UniFrac distances of the ASVs and comparing them using permutational multivariate

197 tial distribution patterns, indicating these ASVs have adapted to SDB.

198 12 Streptomyces isolates representing these ASVs for phenotypic and genomic characterization.

199 (4.0 ppb) in the detection limit compared to ASV without CPE.

200 In contrast to ASV Gag, HIV-1 Gag containing an L domain inactivating m

201 DGT measured similar labile fractions to ASV, with detailed differences being consistent with a t

202 ate-to-severe sleep apnea were randomized to ASV plus optimized medical therapy (OMT) or OMT alone (c

203 insula samples, representing 57.91% of total ASVs.

204 equences from (13)C-SIP metagenomes to total ASVs showed at least 92 bacteria and archaea were signif

205 ng dimer" previously described for wild type ASV apoIN and resembles the inner, substrate binding dim

206 e mutant of Vps4 ATPase similar to wild type ASV Gag.

207 of the U5 ASV substrate closer to wild type ASV IN compared with chimeras with individual amino acid

208 Unlike wild type, ASV Gag/Deltap2b -ESCRT chimeras failed to co-immunoprec

209 s showed a specificity of cleavage of the U5 ASV substrate closer to wild type ASV IN compared with c

210 as induced in an interferon-like manner upon ASV infection.

211 Gut microbiome dysbiosis using ASV prevalence data may offer the diagnostic potential o

212 The results obtained using ASV are in good agreement with reference values using co

213 ability: SD, average successive variability (ASV), coefficient of variation, and variation independen

214 1-SD higher average successive variability [ASV], 1.21; 95% CI, 1.10-1.33) and creatinine (HR per 1-

215 S microbiome and amplicon sequence variant (ASV) approach was used to study the bacteria present in

216 ted 16S rRNA gene amplicon sequence variant (ASV) composition was observed, with 16S rRNA gene assemb

217 mic unit (OTU) or amplicon sequence variant (ASV) datasets to identify key taxonomic groups, diversit

218 t abundant fungal amplicon sequence variant (ASV) in the core microbiome.

219 rference and runs amplicon sequence variant (ASV)-based amplicon sequencing analysis automatically an

220 nucleotide exact amplicon sequence variants (ASV) of the human gut microbiome were used to evaluate i

221 mber of observed Amplicon Sequence Variants (ASV) was positively associated with PWV and AIX.

222 showed multiple amplicon sequence variants (ASV) within the same bacterial family to be differential

223 ds from only 1-3 amplicon sequence variants (ASV), and most individuals were infected with an apparen

224 pression of two alternative splice variants (ASV), which differ in length and in the exon/intron rete

225 us Synechococcus amplicon sequence variants (ASVs) and that clade and ASV composition can change over

226 25 bioindicator amplicon sequence variants (ASVs) enriched in diseased corals.

227 insea, with 1568 Amplicon Sequence Variants (ASVs) identified across thousands of environmental sampl

228 ugants, we found amplicon sequence variants (ASVs) of genera whose origin was traced to soils (Bacill

229 Amplicon sequence variants (ASVs) offer a promising alternative that may supersede t

230 A total of 121 amplicon sequence variants (ASVs) presented with differential abundances between the

231 fied 29 distinct Amplicon Sequence Variants (ASVs) representing Tetracladium, with large differences

232 distinct fungal amplicon sequence variants (ASVs) representing the phyla Ascomycota, Basidiomycota,

233 diversity hosted amplicon sequence variants (ASVs) that were subsets of the overall community, though

234 Symbiodiniaceae amplicon sequence variants (ASVs) were found in all three compartments, and over hal

235 to thousands of amplicon sequence variants (ASVs) within ecotypes, many of which exhibited distinct

236 tionship between amplicon sequence variants (ASVs) within the Lachnospiraceae family and methylation

237 ected 171 fungal amplicon sequence variants (ASVs), 70 from the air and 142 from the snow.

238 4 Prevotellaceae amplicon sequence variants (ASVs), as well as single ASVs from Coprobacter, Parabact

239 a diversity, and amplicon sequence variants (ASVs), were investigated in a multivariate mixed model.

240 a as read out by amplicon sequence variants (ASVs).

241 sequencing using amplicon sequence variants (ASVs).

242 in 19,542 unique Amplicon Sequence Variants (ASVs).

243 ated bacterial amplicon sequencing variants (ASVs) from at least nine bacterial families with little

244 discriminating Amplicon Sequencing Variants (ASVs): ASV 191, ASV 44, and ASV 75, were identified as s

245 y with numerous alternative splice variants (ASVs) and post-translational modifications (PTMs) report

246 or suspected alternative splicing variants (ASVs) using PCR, primer extension and matrix-assisted la

247 60 [44%] of 6500 amplicon sequence variants [ASVs]) at the phylum level and Streptococcus (2340 [36%]

248 ersity (observed amplicon sequence variants [ASVs], Faith phylogenetic diversity, Shannon-Weiner Inde

249 ciated taxa (161 amplicon sequence variants; ASVs) belonging to Alteromonadaceae, Rhodobacteraceae, P

250 ventilation (MV) adaptive servo-ventilation (ASV) improved cardiovascular outcomes in hospitalized HF

251 e more as the American Society for Virology (ASV) hosted a satellite symposium on the subject in June

252 of catalysis with both avian sarcoma virus (ASV) and human immunodeficiency virus type 1 (HIV-1) IN

253 of integrase (IN) from avian sarcoma virus (ASV) and its active-site derivative containing an Asp64

254 epeat elements (dr1) of avian sarcoma virus (ASV) and leukosis virus have the properties of constitut

255 y virus type 1 (HIV-1), avian sarcoma virus (ASV) and their close orthologs from the Lentivirus and A

256 have demonstrated that avian sarcoma virus (ASV) can transduce cycle-arrested cells.

257 scribed a reconstituted avian sarcoma virus (ASV) concerted DNA integration system with specially des

258 a model system in which avian sarcoma virus (ASV) DNA is epigenetically repressed in mammalian cells,

259 es bind the L domain in avian sarcoma virus (ASV) Gag and facilitate viral particle release.

260 everse transcription in avian sarcoma virus (ASV) initiates from the 3' end of a tRNA(Trp) primer, wh

261 arcoma virus (SIV), and avian sarcoma virus (ASV) INs predicted which of these residues were unique.

262 d as an interactor with avian sarcoma virus (ASV) integrase (IN) in a yeast two-hybrid screen.

263 nd shape of full-length avian sarcoma virus (ASV) integrase (IN) monomers and dimers in solution usin

264 al region of the 286-aa avian sarcoma virus (ASV) integrase (IN) protein has been shown previously to

265 ontrast, integration by avian sarcoma virus (ASV) integrase was more efficient after compaction by ei

266 port the mapping of 226 avian sarcoma virus (ASV) integration sites in the human genome.

267 he process by which the avian sarcoma virus (ASV) preintegration complex gains access to target chrom

268 reviously described for avian sarcoma virus (ASV) that was stimulated by the presence of HMG-1.

269 n of an oncoretrovirus, avian sarcoma virus (ASV), suggesting an active import mechanism for the inte

270 silencing of integrated avian sarcoma virus (ASV)-based vector DNAs in human HeLa cells.

271 the simple retrovirus, avian sarcoma virus (ASV).

272 simultaneous anodic stripping voltammetric (ASV) determination of Pb(II) and Cd(II) at the bismuth n

273 determined by anodic stripping voltammetry (ASV) after transferring the gold microelectrode in an aq

274 ontrast, while anodic stripping voltammetry (ASV) also revealed five peaks, peak identification was n

275 Anodic Stripping Voltammetry (ASV) and Scanning Transmission Electron Microscopy with

276 ter to perform anodic stripping voltammetry (ASV) at a thin mercury film followed by subsequent ICPMS

277 nce (SPR) with anodic stripping voltammetry (ASV) capability has been demonstrated for detecting heav

278 Au measured by anodic stripping voltammetry (ASV) is indicative of the NP/NC size.

279 tures, and (3) anodic stripping voltammetry (ASV) of Au in 0.010 M KBr plus 0.1 M KClO(4).

280 For anodic stripping voltammetry (ASV) of Pb, our sensor shows 21 nM (4.4 ppb) limit of de

281 Anodic stripping voltammetry (ASV) performed at Hg/Pt UMEs displayed a linear response

282 ying fast-scan anodic stripping voltammetry (ASV) to provide sensitive and selective imaging of multi

283 Using anodic stripping voltammetry (ASV) with a pre-concentration time of 6 min, we achieved

284 roscopy (AAS), anodic stripping voltammetry (ASV), and DGT.

285 n required for anodic stripping voltammetry (ASV), so cathodic stripping voltammetry (CSV) has been s

286 ed directly by anodic stripping voltammetry (ASV).

287 metal ions by anodic stripping voltammetry (ASV).

288 metal ions by anodic stripping voltammetry (ASV).

289 oelectrode and anodic stripping voltammetry (ASV).

290 um (Cd(2+)) by anodic stripping voltammetry (ASV).

291 ENV(AP) and ENV(DP) in aneurysm sac volume (ASV) (ENV(AP)/ASV%, ENV(DP)/ASV%, respectively) were mea

292 lar volume ( (v)), apparent specific volume (ASV), compressibility ( (k)(0)) etc.

293 n determined from apparent specific volumes (ASV) data at 20-45 degrees C and 0.04-0.89 mol kg(-1).Th

294 lumes, V2,varphi, apparent specific volumes, ASV, apparent molar isentropic compressibilities, Ks,2,v

295 AMMI, WAASBY/ASV, and YSI all identified broadly stable genotypes; G3

296 hich also produced the highest yields, while ASVs negatively correlated with yield were associated wi

297 tone deacetylases (HDACs) can associate with ASV DNA soon after infection and may act to repress vira

298 rated HNO3/30% H2O2 mixture, compatible with ASV and the iridium electrode.

299 Pre-treatment with ASV-30 blocked these effects.

300 While complexes containing HMG-I(Y), ASV IN, and donor DNA can be detected in gel shift exper