ライフサイエンスコーパス: dUTP

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

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

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

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

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

6 oring of patients treated by drugs affecting dUTP balance.

7 AHP dUTP is a versatile clickable nucleotide with potentiall

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

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

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

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

12 eavable (PC) biotinylated nucleotide analog, dUTP-PC-Biotin, for DNA polymerase extension reaction to

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

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

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

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

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

18 deoxynucleotidyl transferase-mediated biotin-dUTP nick-end labeling staining to quantitate myocyte ap

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 lls resulted in a significant enhancement in dUTP pool expansion after TS inhibition.

52 in HT29 cells and that a further increase in dUTP levels has no additive effect.

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

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

55 es first-strand cDNA synthesis incorporating dUTP.

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

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

58 erminal deoxynucleotidyltransferase-mediated dUTP nick end labeling (TUNEL) staining, DNA fragmentati

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

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

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

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

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

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

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

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

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

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

69 erminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling, and DNA laddering, which were as

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 erminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling and hallmarks of apoptosis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 rminal deoxynucleotidyl transferase mediated dUTP nick end labeling assays.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 rminal deoxynucleotidyl transferase-mediated dUTP nick end labeling) demonstrated that lack of p53 is

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

145 rminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL), Ki-67, p53, bcl-2, and M

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

187 rminal deoxynucleotidyl transferase-mediated dUTP-biotin end labeling and activated caspase-3 immunoh

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

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

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

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

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

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

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

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

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

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

198 dified nucleotides, a C5-imidazolyl-modified dUTP and 3-(aminopropynyl)-7-deaza-dATP were used in pla

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 n of uracil DNA-glycosylase or by preventing dUTP production via inactivation of dCTP deaminase.

229 also has dCTP deaminase activity, producing dUTP.

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

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

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

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

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

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

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

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

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

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

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

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

242 ctive effects, as evidenced by less terminal dUTP nick end-labeling staining, a lower incidence of DN

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 ect to terminal deoxynucleotidyl transferase dUTP nick end labeling staining for apoptotic DNA fragme

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

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

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

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

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

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

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

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

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

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

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

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

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

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 apoptosis (detected by terminal transferase dUTP nick-end labeling [TUNEL]) and formation of acellul

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

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.

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