ライフサイエンスコーパス: dUTP

1 dUTP is a close structural congener of dTTP and can be r

2 dUTP nick end labeling (TUNEL) staining also revealed on

3 in immunoprecipitation assay using biotin-16-dUTP and terminal deoxynucleotide transferase showed tha

4 nucleotide analogues (dGTP-PC-Bodipy-FL-510, dUTP-PC-R6G, dATP-PC-ROX, and dCTP-PC-Bodipy-650) (PC, p

5 An oligo-dT adapter incorporating a dUTP-containing PCR primer primes first-strand cDNA synt

6 , single-step closed-system assay and uses a dUTP/uracil DNA glycosidase anti-PCR contamination contr

7 oring of patients treated by drugs affecting dUTP balance.

8 AHP dUTP is a versatile clickable nucleotide with potentiall

9 ally undemanding azide analogue of dTTP (AHP dUTP) with an alkyl chain and ethynyl attachment to the

10 cleavable fluorescent nucleotide, 3'-O-allyl-dUTP-PC-Bodipy-FL-510 (PC-Bodipy, photocleavable 4,4-dif

11 Maneuvers to alter dUTP levels appear to alter the toxicity of thymidine de

12 Although dUTP is a normal intermediate in DNA synthesis, its accu

13 ach dNTP against the other dNTPs, rNTPs, and dUTP evidenced the strong performance of the assay.

14 ode a fusion of thymidylate kinase (tmk) and dUTP diphosphatase (dut).

15 ng the levels of non-canonical dNTPs such as dUTP.

16 nscriptase (RT) does not distinguish between dUTP and dTTP.

17 e transcriptase discriminates poorly between dUTP and dTTP, and accordingly, viral DNA products becom

18 deoxynucleotidyl transferase-mediated biotin-dUTP nick-end labeling (TUNEL), observations that are in

19 Terminal deoxynucleotidyl transferase biotin-dUTP nick end labeling (TUNEL) assay was performed to de

20 optosis was quantified by transferase biotin-dUTP nick end labeling analysis.

21 terminal deoxynucleotidyl transferase biotin-dUTP nick end labeling, immunoblot analysis and quantita

22 ed mucosal injury, TUNEL (transferase biotin-dUTP nick end-labeling)-positive cells, neutrophil infil

23 ucleotidyl transferase-mediated biotinylated dUTP nick end labeling)-staining labeled dying cells.

24 type 1 dUTPases, Stl binding is inhibited by dUTP.

25 -MS/MS study revealed that the non-canonical dUTP concentration (2.9 mum) is approximately 60 times h

26 resented demonstrates that the non-canonical dUTP was abundant relative to TTP, and efficiently incor

27 or TTP over dUTP, implying that the cellular dUTP/TTP ratio determines the frequency of HIV-1 RT-medi

28 veloped a model system in which the cellular dUTP:dTTP ratio can be pharmacologically increased to fa

29 The double-stranded cDNA-containing dUTP serves as a universal template for the specific amp

30 rified and non-target transcripts containing dUTP degraded by Uracil DNA glycosylase, leaving only th

31 genomic DNAs with fluorescently labeled Cy3-dUTP and potentially be useful for diagnostic applicatio

32 tage of terminal deoxynucleotidyltransferase dUTP nick end label (TUNEL)-positive macrophages in the

33 osis by terminal deoxynucleotidyltransferase dUTP nick end-labeling (TUNEL) in myocardial samples fro

34 ins and terminal deoxynucleotidyltransferase dUTP nick end-labeling staining.

35 ing and terminal deoxynucleotidyltransferase dUTP nick-end labeling assay.

36 rescent terminal deoxynucleotidyltransferase dUTP-biotin nick end labeling (TUNEL) assay revealed tha

37 e) for their natural substrates (8-oxo-dGTP, dUTP, dITP, 2-oxo-dATP), which allows them to select the

38 ng dGTP/dATP, dGTP/dCTP, dGTP/dTTP, and dGTP/dUTP.

39 ed DNA is directly labelled with digoxigenin-dUTP near the sites of its initiation in a cell-free sys

40 ng the Cap finder approach, another distinct dUTP containing adapter is added to the 3' end of the ne

41 ays efficient dUTP incorporation in the dNTP/dUTP pools found in macrophages but not in T cells.

42 unodeficiency virus, also displays efficient dUTP incorporation in the dNTP/dUTP pools found in macro

43 the virus-infected cells contained elevated dUTP levels, reverse transcription was found to proceed

44 can be pharmacologically increased to favor dUTP incorporation, allowing dissection of this innate i

45 nucleotidyl transferase-mediated fluorescein-dUTP nick-end labeling (TUNEL) assay.

46 ort that the virus also encodes a functional dUTP triphosphatase, means that PBCV-1 is the first viru

47 estriction factor in cells that contain high dUTP.

48 hough monocyte-derived macrophages have high dUTP levels, these cells have low hUNG activity, which m

49 utants of Escherichia coli fail to hydrolyze dUTP and thus incorporate uracil into their DNA, sufferi

50 to cleave the dUTP analogue alpha,beta-imido-dUTP, containing the imido linkage usually regarded to b

51 rates that HIV-1 RT efficiently incorporates dUTP in the macrophage nucleotide pools but not in the T

52 Second-strand synthesis incorporating dUTP is achieved by PCR, using dUTP-containing primers c

53 es first-strand cDNA synthesis incorporating dUTP.

54 g reverse transcription and does not involve dUTP incorporation, indicating it results from bRT-catal

55 these cells have high dUTPase activity (low dUTP), and only modest levels of hUNG activity.

56 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling (TUNEL), and was not seen in norm

57 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling and a marked depletion of oligode

58 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling were analyzed.

59 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling, caspase 3 cleavage, and re-local

60 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling-positive myonuclei, and activated

61 ptosis (deoxynucleotidyltransferase-mediated dUTP nick end labeling-positive).

62 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling-positivity) and oxidative stress

63 erminal deoxynucleotidyltransferase-mediated dUTP nick end-labeling staining following TNF-alpha.

64 erminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling positive CM (-44%, P<0.01), incre

65 erminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling staining).

66 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) and fluorescence-a

67 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay suggested th

68 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay, compared to

69 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assays, and transm

70 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assays.

71 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining character

72 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining of intest

73 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining with GFP.

74 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining, but not

75 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining, indicati

76 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining.

77 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive cells in

78 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive myocytes

79 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling and caspase 3 and Bax expr

80 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling and trypan blue exclusion

81 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling assay following treatment

82 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling of DNA double-strand break

83 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling staining of lung tissue sa

84 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling) assay determined that con

85 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling, and Rad51) at the leptote

86 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling-positive cells were presen

87 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling-positive parasites followi

88 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end-labeling method in vivo.

89 erminal deoxynucleotidyltransferase-mediated dUTP-tetramethylrhodamine nick end labeling assay, demon

90 etermines the frequency of HIV-1 RT-mediated dUTP incorporation.

91 deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling (TUNEL) assays revealed th

92 deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling) assays demonstrate that g

93 with standard markers including TdT-mediated dUTP biotin nick-end labeling and cleaved caspase 3 immu

94 excised from treated animals by TdT-mediated dUTP nick end labeling assay.

95 (Ki67) and increased apoptosis (TdT-mediated dUTP nick end labeling; TUNEL).

96 nts of apoptosis as measured by TdT-mediated dUTP nick end labelling (TUNEL).

97 e of cornification, assessed as TdT-mediated dUTP nick end-labeling-positive cells in stratum granulo

98 tivation and DNA fragmentation (TdT-mediated dUTP nick-end labeling [TUNEL]).

99 irth (BrdU labeling) and death (Tdt-mediated dUTP-biotin nick end labeling) to investigate the specif

100 ne transferase (ALT), necrosis, TdT-mediated dUTP-digoxigenin nick-end labeling (TUNEL) staining, cas

101 terminal deoxynucleotide tranferase-mediated dUTP nick-end labeling assay, and ex vivo via Western an

102 terminal deoxynucleotide tranferase-mediated dUTP nick-end labeling staining and immunohistochemistry

103 rminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) assay and caspase-3 activ

104 rminal deoxynucleotidyl transferase mediated dUTP nick end labeling assays.

105 rminal deoxynucleotidyl transferase mediated dUTP nick end labeling, or TUNEL, staining, respectively

106 ase (terminal uridylyl transferase) mediated dUTP-dependent U-insertion/U-deletion cycle may be a pos

107 In addition, transferase-mediated dUTP (deoxyuridine triphosphate) nick end labeling (TUNE

108 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay and caspase-3 activ

109 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, and Western blo

110 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL)-positive nuclei, only 6 a

111 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling analyses indicated a greater numb

112 al deoxyribonucleotidyl transferase-mediated dUTP nick end labeling analysis shows that there is no i

113 minal deoxynucledotidyl transferase-mediated dUTP nick end labeling and CD31 to assess apoptotic inde

114 al deoxyribonucleotidyl transferase-mediated dUTP nick end labeling assay, was preceded by loss of mi

115 al deoxyribonucleotidyl transferase-mediated dUTP nick end labeling assay.

116 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling assays on tissue sections reveale

117 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling imaging.

118 al deoxyribonucleotidyl transferase-mediated dUTP nick end labeling staining was done to quantify apo

119 al deoxyribonucleotidyl transferase-mediated dUTP nick end labeling staining, was increased in cells

120 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling staining.

121 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling staining].

122 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling).

123 al deoxyribonucleotidyl transferase-mediated dUTP nick end labeling- and caspase 3-stained cells at 6

124 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive apoptotic cells (8.3% +/

125 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive apoptotic cells.

126 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive cells and expression of

127 els of active caspase-3/transferase-mediated dUTP nick end-labeling (TUNEL) apoptotic markers and enh

128 rminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay.

129 minal deoxy-nucleotidyl transferase-mediated dUTP nick end-labeling staining and caspase-3 activity a

130 rminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling staining.

131 erminal deoxynucleotide transferase-mediated dUTP nick end-labeling, and single-cell gel electrophore

132 rminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling-positive cells.

133 rminal deoxynucleotidyl transferase-mediated dUTP nick end-labelling (TUNEL) assay.

134 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) and an 11-fold increase i

135 , terminal deoxyribosyl transferase-mediated dUTP nick-end labeling (TUNEL) assay, and real-time RT-P

136 rminal deoxynucleotidyl-transferase-mediated dUTP nick-end labeling (TUNEL) assay.

137 erminal deoxynucleotide transferase-mediated dUTP nick-end labeling (TUNEL) assay; (2) frequencies of

138 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) for fixed tissues and acr

139 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) staining for intratumoral

140 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)-positive cells, NASH, and

141 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL).

142 ion, induced apoptosis (transferase-mediated dUTP nick-end labeling [TUNEL]) and decreased proliferat

143 palmitate on apoptosis (transferase-mediated dUTP nick-end labeling [TUNEL]), mitochondrial death pat

144 erminal deoxynucleotide transferase-mediated dUTP nick-end labeling analysis showed significantly dec

145 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and caspase-3, indicating that TX

146 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and DNA fragment enzyme-linked im

147 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and GC count.

148 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and in situ oligo ligation method

149 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and quantified by both caspase-3

150 beta-cell apoptosis [by transferase-mediated dUTP nick-end labeling assay and Western blotting for po

151 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay was performed, and intestin

152 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay) (P<0.05).

153 rminal deoxynucleotidyl-transferase-mediated dUTP nick-end labeling assay, we showed that the express

154 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay.

155 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay.

156 erminal deoxynucleotide transferase-mediated dUTP nick-end labeling methods.

157 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling positive nuclei and DNA fragmenta

158 droxydeoxyguanosine and transferase-mediated dUTP nick-end labeling positivity and also prevented ace

159 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling positivity, superoxide, and nitri

160 erminal deoxynucleotide transferase-mediated dUTP nick-end labeling reaction) and involve disruption

161 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling stain) activity was biphasic.

162 erminal deoxynucleotide transferase-mediated dUTP nick-end labeling stain.

163 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling staining and cleaved caspase 3 ex

164 erminal deoxynucleotide transferase-mediated dUTP nick-end labeling staining, caspase-3 activity, and

165 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling staining.

166 ed the number of TUNEL (transferase-mediated dUTP nick-end labeling)-positive capillary cells and ace

167 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling).

168 al deoxyribonucleotidyl transferase-mediated dUTP nick-end labeling, and CD31 immunohistochemistry, r

169 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling, and immunohistochemistry.

170 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling, and Ki-67 immunoreactivity were

171 crease in the number of transferase-mediated dUTP nick-end labeling-positive capillary cells, acellul

172 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells in FECD samples.

173 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells were also increase

174 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells, TNF-alpha release

175 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive endothelial cells and pe

176 lded reduced apoptosis (transferase-mediated dUTP nick-end labeling-positive insulin-positive cells;

177 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive microvascular cell numbe

178 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive, and exhibited elevated

179 rminal deoxynucleotidyl-transferase-mediated dUTP nick-end staining, respectively.

180 rminal deoxynucleotidyl transferase-mediated dUTP nick-end-labeling analysis reveals greater abundanc

181 rminal deoxynucleotidyl transferase-mediated dUTP nick-end-labeling assay showed no significant apopt

182 rminal deoxynucleotidyl transferase-mediated dUTP nickend labeling assay.

183 rminal deoxynucleotidyl transferase-mediated dUTP-biotin end labeling staining of the increased conce

184 rminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling assay and Hoechst staining

185 rminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling assay demonstrated that Bo

186 rminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling-positive cells.

187 feeding also increased transferase-mediated dUTP-biotin nick-end labeling-positive cells, caspase-3

188 rminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin nick end labeling (TUNEL) were evaluate

189 rminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin nick end labeling (TUNEL), and caspase-

190 A series of 5-(2-nitrobenzyloxy)methyl-dUTP analogs (dU.I-dU.V) were synthesized based on our p

191 (S)-alpha-tert-Butyl-2-nitrobenzyloxy]methyl-dUTP (dU.V) was identified as an efficient reversible te

192 single uracil opposite an adenine (to mimic dUTP misincorporation during DNA synthesis) or a guanine

193 ion experiment comparing the use of modified dUTP derivatives with TTP for selecting aptamers to a pr

194 Six new 5-position modified dUTP derivatives connected by a unique amide linkage wer

195 tandard conditions using any of the modified dUTP derivatives studied.

196 Several of these modified dUTPs were then used in an in vitro selection experiment

197 sence of high concentrations of noncanonical dUTP, apolipoprotein B mRNA-editing, enzyme-catalytic, p

198 We have designed a nonsubstrate dUTP analogue with a methylene bridge connecting the alp

199 uggest that Ndk prevents the accumulation of dUTP in vivo.

200 n macrophages, whereas the concentrations of dUTP and TTP in dividing human primary lymphocytes are v

201 the presence of increasing concentrations of dUTP or by infecting with virus that contains the cytosi

202 corporated into DNA through the existence of dUTP in the nucleotide pool.

203 dUTPases catalyze the hydrolysis of dUTP into dUMP and pyrophosphate to maintain the proper

204 rolase (dUTPase) catalyzes the hydrolysis of dUTP to dUMP and PPi.

205 we study the dUTPase-catalyzed hydrolysis of dUTP, an incorrect DNA building block, to elaborate the

206 oxic U*A pairs arising from incorporation of dUTP in DNA, and for increasing immunoglobulin gene dive

207 f which is linked to direct incorporation of dUTP in place of dTTP.

208 dUTP to dTTP and subsequent incorporation of dUTP into DNA.

209 this study was to assess the involvement of dUTP binding and dUTPase activity in derepression by Dut

210 by oxaliplatin promoted increased levels of dUTP that was enhanced by subsequent addition of fluorop

211 d macrophages (MDMs) contains high levels of dUTP, which is incorporated into HIV-1 DNA during revers

212 ndk and genes involved in the metabolism of dUTP, a potentially mutagenic precursor of thymidine bio

213 ues yielded after either misincorporation of dUTP during replication or deamination of cytosine.

214 -alpha was associated with higher numbers of dUTP-biotin nick end labeling-positive renal tubule cell

215 state and steady state kinetic parameters of dUTP incorporation reveals minimal selectivity of HIV-1

216 ter release was inhibited in the presence of dUTP or dUMP.

217 ne depletion is a sharp rise in the ratio of dUTP to dTTP and subsequent incorporation of dUTP into D

218 nfect host cells that contain high ratios of dUTP:dTTP.

219 of thymidylate synthase and increased use of dUTP in place of TTP during DNA replication, with subseq

220 the Duts derepress the SaPI cycle depends on dUTP and involves both motifs V and VI, as we have previ

221 minimal selectivity of HIV-1 RT for TTP over dUTP, implying that the cellular dUTP/TTP ratio determin

222 ession of CaTMPK, but not of hTMPK, produced dUTP/5-FdUTP-mediated DNA toxicity in budding yeast (Sac

223 also has dCTP deaminase activity, producing dUTP.

224 L) technology, where a ruthenylated dUTP (Ru-dUTP) is employed as one of the dNTPs.

225 cence (ECL) technology, where a ruthenylated dUTP (Ru-dUTP) is employed as one of the dNTPs.

226 These are annealed to single-stranded dUTP-containing template plasmid and extended with T7 po

227 Terminal dUTP nick-end labeling staining revealed a 213% increase

228 ayer were studied by morphology and terminal dUTP nucleotide end labeling analyses, respectively.

229 an increase in positivity for both terminal dUTP nick-end labeling and Ki67.

230 etinal cell death was determined by terminal dUTP nick-end labeling assay; BRB function by quantifyin

231 By terminal dUTP nick-end labeling staining, widespread cell injury

232 mpared to controls as determined by terminal dUTP nick-end labeling-positive cells.

233 en and Ki-67 and low positivity for terminal dUTP nick-end labeling indicated robust cell proliferati

234 monstrated by immunohistochemistry, terminal dUTP nick-end labeling, and DNA agarose gel electrophore

235 topathologic analysis that included terminal dUTP nick end-labeling (TUNEL), capillary and cardiomyoc

236 accompanied by enhanced numbers of terminal dUTP nick-end labeling-positive cells at days 4, 6, and

237 ost fertilization (hpf) through the terminal dUTP transferase-mediated nick end-labeling (TUNEL) assa

238 tivated Caspases 3 and 9 and TUNEL (terminal dUTP nick end labeling) assay.

239 in the retina were quantified using terminal dUTP nick-end labeling (TUNEL) and active caspase-3 (CM-

240 ereas apoptosis was quantified with terminal dUTP nick end labeling (TUNEL) and fluorescence microsco

241 hows the capability of dUTPase to cleave the dUTP analogue alpha,beta-imido-dUTP, containing the imid

242 od's performance and ease, we identified the dUTP second-strand marking and the Illumina RNA ligation

243 ent with the proposed alternative model, the dUTP inhibits rather than inducing the process, as we ha

244 th primer extension product, with all of the dUTP derivatives tested giving yields similar to those o

245 ity to efficiently incorporate each of these dUTP derivatives during PCR.

246 UNEL (terminal deoxyneucleotidyl transferase dUTP nick end labeling) expression in xenografts.

247 ated by terminal deoxynucleotide transferase dUTP nick end labeling staining and cleaved caspase-3 ex

248 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and phospho-histone H3 (P

249 ted by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and used to estimate the

250 ng and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay.

251 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays and ultrastructura

252 ly for terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) or activated-caspase 3, s

253 ver by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining in situ.

254 xin V, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), 3-(4,5-dimethylthiazol-2

255 d with terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)-positive soma and the eve

256 tosis (terminal deoxynucleotidyl transferase dUTP nick end labeling [TUNEL] assay), and of collagen t

257 tosis (terminal deoxynucleotidyl transferase dUTP nick end labeling and Annexin V assays).

258 ase in terminal deoxynucleotidyl transferase dUTP nick end labeling and cleaved caspase-3 positive ce

259 y, and terminal deoxynucleotidyl transferase dUTP nick end labeling assay was used to assess alveolar

260 f) and terminal deoxynucleotidyl transferase dUTP nick end labeling assay, Kim1 mRNA assessment, and

261 se and terminal deoxynucleotidyl transferase dUTP nick end labeling of targeted doxorubicin micelles

262 is via terminal deoxynucleotidyl transferase dUTP nick end labeling staining and caspase-3 activation

263 iques, terminal deoxynucleotidyl transferase dUTP nick end labeling staining, and immunohistochemistr

264 ], and terminal deoxynucleotidyl transferase dUTP nick end labeling terminal deoxynucleotidyl transfe

265 TUNEL (Terminal deoxynucleotidyl transferase dUTP nick end labeling) assay indicated that apoptosis w

266 n, and terminal deoxynucleotidyl transferase dUTP nick end labeling), and diminished Akt phosphorylat

267 4) and terminal deoxynucleotidyl transferase dUTP nick end labeling-positive nuclei (4+/-3% versus 10

268 TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labeling])-positive cells) of NPIs compare

269 tosis (terminal deoxynucleotidyl transferase dUTP nick end labelingc cells), and caspase-8 activity w

270 ity of terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL)-positive dying cells and

271 Terminal deoxynucleotidyl transferase dUTP nick end-labelling assay, SYTOX((R)) green uptake a

272 sed by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) and measurement of outer

273 y both terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) assay and immunohistochem

274 ntense terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) signals were found at E16

275 re was terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining in vascular cell

276 red by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining, circulating lev

277 Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) was performed 3 days afte

278 Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) was performed in retinal

279 sed by terminal deoxynucleotidyl transferase dUTP nick-end labeling assay and activated caspase-3 sta

280 y used terminal deoxynucleotidyl transferase dUTP nick-end labeling assay or methods based on monitor

281 ining, terminal deoxynucleotidyl transferase dUTP nick-end labeling assay, and electron microscopy in

282 ber of terminal deoxynucleotidyl transferase dUTP nick-end labeling positive cells in the hippocampus

283 s were terminal deoxynucleotidyl transferase dUTP nick-end labeling positive, suggesting remodeling i

284 Terminal deoxynucleotidyl transferase dUTP nick-end labeling staining was used for the identif

285 ty and terminal deoxynucleotidyl transferase dUTP nick-end labeling staining were tested for apoptosi

286 evels, terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, cytochrome c release, t

287 red by terminal deoxynucleotidyl transferase dUTP nick-end labeling, was significantly decreased in t

288 nce of terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive cells.

289 ty and terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive cells.

290 ase in terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive enterocyte nuclei in the

291 of the terminal deoxynucleotidyl transferase dUTP-biotin nick-end-labeling (TUNEL) assay.

292 nd the terminal-deoxynucleotidyl transferase dUTP-linked nick-end labeling (TUNEL) procedure determin

293 h, as judged by lack of terminal transferase dUTP nick end labeling (TUNEL) labeling or reactivity to

294 ntified apoptosis using terminal transferase dUTP nick end labeling and active caspase-3 staining in

295 with EAU, by using the terminal transferase dUTP nick-end labeling assay and polymerase chain reacti

296 erminal deoxynucleotidyl transferasemediated dUTP nick-end labeling (TUNEL) reaction, and histopathol

297 nsferase-mediated deoxyuridine triphosphate (dUTP) nick end-labeling (TUNEL) assay were conducted to

298 incorporating dUTP is achieved by PCR, using dUTP-containing primers complimentary to the adapter seq

299 analogously to eukaryotic G-proteins, using dUTP as a second messenger.

300 we show that the DNA polymerase can utilize dUTP as a substrate in vitro.