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1 ressed the T-cell markers CD2, CD3, CD4, and terminal deoxynucleotidyl transferase.
2 us, and is surprisingly more proficient than terminal deoxynucleotidyl transferase.
3 d to the 3' end of the first-strand cDNAs by terminal deoxynucleotidyl transferase.
4 junctions (P=0.004), suggesting formation by terminal deoxynucleotidyl transferase.
5 cell coreceptors CD4 and CD8, and the enzyme terminal deoxynucleotidyl transferase.
6 transcriptase polymerase chain reaction and terminal deoxynucleotidyl transferase 2-deoxyuridine, 5-
8 (including laminin-5, MMPs, TGF beta, zyxin, terminal deoxynucleotidyl transferase, and angiogenesis-
9 positive dUTP nick end-labeling mediated by terminal deoxynucleotidyl transferase, associated with a
12 ian DNA polymerase mu (pol mu) is related to terminal deoxynucleotidyl transferase, but its biologica
15 apoptosis in the spleen, as measured by the terminal deoxynucleotidyl transferase deoxyuridine triph
17 ng in vivo lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labe
19 taining, hematoxylin and eosin staining, and terminal deoxynucleotidyl transferase dUTP nick end labe
20 earance of DNA-fragmentation was detected by terminal deoxynucleotidyl transferase dUTP nick end labe
21 nd WST1 assays) and resistance to apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labe
22 O concentrations >1% (v/v), using annexin V, terminal deoxynucleotidyl transferase dUTP nick end labe
23 of stromal keratocytes (CD34), of apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labe
24 -linked immunosorbent assays and in liver by terminal deoxynucleotidyl transferase dUTP nick end labe
26 (lactate dehydrogenase leakage), apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labe
27 easured by lactate dehydrogenase release and terminal deoxynucleotidyl transferase dUTP nick end labe
29 ly, dying cells did not stain positively for terminal deoxynucleotidyl transferase dUTP nick end labe
30 se F(N) recombinants exhibited a decrease in terminal deoxynucleotidyl transferase dUTP nick end labe
31 erase activity, chromatin fragmentation, and terminal deoxynucleotidyl transferase dUTP nick end labe
32 t risk (15+/-4% versus 36+/-8%; P=0.004) and terminal deoxynucleotidyl transferase dUTP nick end labe
33 and von Willibrand factor (vWF) staining and terminal deoxynucleotidyl transferase dUTP nick end labe
34 tly assessed for viability and apoptosis via terminal deoxynucleotidyl transferase dUTP nick end labe
35 hese behavioral changes were associated with terminal deoxynucleotidyl transferase dUTP nick end labe
36 ter apoptosis (caspase 3 activity and TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labe
37 However, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labe
38 ly detectable by cleaved caspase-3 staining, terminal deoxynucleotidyl transferase dUTP nick-end labe
39 after rupture of Bruch's membrane, there was terminal deoxynucleotidyl transferase dUTP nick-end labe
40 eased caspase-3 activation and appearance of terminal deoxynucleotidyl transferase dUTP nick-end labe
41 ed, and apoptotic cells were identified with terminal deoxynucleotidyl transferase dUTP nick-end labe
42 totic HEK-P2X(7) cells as ascertained by the terminal deoxynucleotidyl transferase dUTP nick-end labe
44 -3 and an increase in caspase-3 activity and terminal deoxynucleotidyl transferase dUTP nick-end labe
48 d plasma membrane permeability and blebbing, terminal deoxynucleotidyl transferase dUTP nick-end labe
51 accumulation attenuated HIRI as measured by terminal deoxynucleotidyl transferase dUTP nick-end labe
52 the percentage of cell death, as measured by terminal deoxynucleotidyl transferase dUTP nick-end labe
56 ooth muscle cells and endothelial cells were terminal deoxynucleotidyl transferase dUTP nick-end labe
58 d photoreceptor degeneration was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labe
59 ed the next day and analyzed by means of the terminal deoxynucleotidyl transferase dUTP-biotin nick-e
60 the rat eye and retinas were analyzed by the terminal-deoxynucleotidyl transferase dUTP-linked nick e
61 ohistochemistry, immunoblot analysis and the terminal-deoxynucleotidyl transferase dUTP-linked nick-e
64 hown by the decreased frequency of TUNEL(+) (terminal deoxynucleotidyl transferase mediated deoxyurid
65 ased on bromo-deoxyuridine incorporation and terminal deoxynucleotidyl transferase mediated dUTP nick
66 clear labeling by propidium iodide staining; terminal deoxynucleotidyl transferase mediated dUTP nick
67 c cell densities were measured with Ki67 and terminal deoxynucleotidyl transferase mediated dUTP nick
68 by caspase 3 activity and fluorescent-based terminal deoxynucleotidyl transferase mediated nick end
70 were positive for cleaved caspase-3 and for terminal deoxynucleotidyl transferase-mediated biotin-dU
71 cture using electron microscopy, and in situ terminal deoxynucleotidyl transferase-mediated biotin-dU
72 and apoptosis were evidenced by increases in terminal deoxynucleotidyl transferase-mediated biotinyla
73 after ouabain injection, maximal numbers of terminal deoxynucleotidyl transferase-mediated biotinyla
75 d spinal cord ventral horn were positive for terminal deoxynucleotidyl transferase-mediated biotinyla
76 te viability was assessed by O4 staining and terminal deoxynucleotidyl transferase-mediated biotinyla
78 epidermal growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinyla
82 We found that deltaV1-1 reduced numbers of terminal deoxynucleotidyl transferase-mediated biotinyla
83 hese same brain areas developed infarcts and terminal deoxynucleotidyl transferase-mediated biotinyla
84 The mRNA from individual active caspase 3(+)/terminal deoxynucleotidyl transferase-mediated biotinyla
85 death, there was a 55.6% reduction in TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
86 nuclei (NeuN)-immunoreactive cells are also terminal deoxynucleotidyl transferase-mediated biotinyla
87 ly expressed in neurons and colocalized with terminal deoxynucleotidyl transferase-mediated biotinyla
92 urogenesis induced by KA were explored using terminal deoxynucleotidyl transferase-mediated biotinyla
93 and induces neuronal apoptosis, detected by terminal deoxynucleotidyl transferase-mediated biotinyla
94 t, there is little cell death, as assayed by terminal deoxynucleotidyl transferase-mediated biotinyla
95 nd the cleavage product appeared at 48 hr in terminal deoxynucleotidyl transferase-mediated biotinyla
97 immunoreactivity for single-stranded DNA and terminal deoxynucleotidyl transferase-mediated biotinyla
98 lls from each parental genotype while TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
99 idence of caspase-cleaved tau, but no TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
100 as determined by active caspase-3 and TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
101 ing flow cytometry, electron microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyurid
102 -tubulin III immunocytochemical staining and terminal deoxynucleotidyl transferase-mediated deoxyurid
103 ssessed using bromodeoxyuridine staining and terminal deoxynucleotidyl transferase-mediated deoxyurid
104 using gamma-counting, cleaved caspase-3, and terminal deoxynucleotidyl transferase-mediated deoxyurid
105 sis was quantitated by nuclear morphology or terminal deoxynucleotidyl transferase-mediated deoxyurid
106 HO-1 and a 2-fold reduction in the number of terminal deoxynucleotidyl transferase-mediated deoxyurid
107 ific techniques (hematoxylin-eosin staining, terminal deoxynucleotidyl transferase-mediated deoxyurid
108 activity, the expression of Fas ligand, and terminal deoxynucleotidyl transferase-mediated deoxyurid
109 tiapoptotic effect of MT, as determined by a terminal deoxynucleotidyl transferase-mediated deoxyurid
110 en (p<0.05), bromodeoxyuridine (p<0.05), and terminal deoxynucleotidyl transferase-mediated deoxyurid
111 dies or histology, immunohistochemistry, and terminal deoxynucleotidyl transferase-mediated deoxyurid
113 omal DNA degradation that can be detected by terminal deoxynucleotidyl transferase-mediated deoxyurid
114 fter oncotic necrosis and leads to pervasive terminal deoxynucleotidyl transferase-mediated deoxyurid
115 , S100-positive cells, ganglion cells, and a terminal deoxynucleotidyl transferase-mediated deoxyurid
117 orescence-activated cell sorter analysis and terminal deoxynucleotidyl transferase-mediated deoxyurid
118 orphology, DNA fragmentation, and apoptosis (terminal deoxynucleotidyl transferase-mediated deoxyurid
120 diamidino-2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferase-mediated deoxyurid
121 ping and sensory-deprived rat olfactory bulb terminal deoxynucleotidyl transferase-mediated deoxyurid
122 ndent methods: light microscopy, fluorescent terminal deoxynucleotidyl transferase-mediated deoxyurid
124 pase-3, caspase-9, and positive staining for terminal deoxynucleotidyl transferase-mediated deoxyurid
125 orylated focal adhesion kinase and increased terminal deoxynucleotidyl transferase-mediated deoxyurid
126 istochemistry, laser-capture microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyurid
127 sphorylated histone H3, activated caspase-3, terminal deoxynucleotidyl transferase-mediated deoxyurid
128 re assessed by Ki67 immunohistochemistry and terminal deoxynucleotidyl transferase-mediated deoxyurid
130 y induction of apoptosis, assessed by TUNEL (terminal deoxynucleotidyl transferase-mediated dNTP-biot
131 is was found at 4 h by DNA fragmentation and terminal deoxynucleotidyl transferase-mediated dUPT nick
132 endothelial cells (BAECs), as determined by terminal deoxynucleotidyl transferase-mediated dUTP biot
133 ining of occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick
134 s to label apoptotic cells in Drosophila are terminal deoxynucleotidyl transferase-mediated dUTP nick
135 rypan blue uptake, and apoptotic cell death (terminal deoxynucleotidyl transferase-mediated dUTP nick
136 polymerase cleavage, Annexin V staining, and terminal deoxynucleotidyl transferase-mediated dUTP nick
137 Immunostaining for Ki-67 and cyclin D1 and terminal deoxynucleotidyl transferase-mediated dUTP nick
139 Histologic damage, cytokine expression, terminal deoxynucleotidyl transferase-mediated dUTP nick
140 ic markers in the diaphragm (e.g., number of terminal deoxynucleotidyl transferase-mediated dUTP nick
143 treatment, cardiac apoptosis was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick
144 uced the frequency of intrahepatic apoptotic terminal deoxynucleotidyl transferase-mediated dUTP nick
145 ed increased intratumoral apoptotic index by terminal deoxynucleotidyl transferase-mediated dUTP nick
147 2 activity, as well as apoptosis detected by terminal deoxynucleotidyl transferase-mediated dUTP nick
148 to induction of apoptosis as revealed by the terminal deoxynucleotidyl transferase-mediated dUTP nick
149 Apoptosis within the retina was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick
150 e then analyzed for apoptotic nuclei using a terminal deoxynucleotidyl transferase-mediated dUTP nick
151 leavage, caspase-activated DNase levels, and terminal deoxynucleotidyl transferase-mediated dUTP nick
153 xy-6-nitro)benzene sulfonic acid) and TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
154 n as demonstrated by positive staining using terminal deoxynucleotidyl transferase-mediated dUTP nick
155 Apoptosis indicated by nuclear changes, terminal deoxynucleotidyl transferase-mediated dUTP nick
156 ificantly less apoptosis as measured by both terminal deoxynucleotidyl transferase-mediated dUTP nick
159 Apoptosis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick
160 excitation of piriform cortex, on apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick
161 n by 5-bromo-2'-dUTP incorporation assay and terminal deoxynucleotidyl transferase-mediated dUTP nick
162 V fluorescent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick
163 cytometry analysis, immunocytochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick
164 haloperidol and reduced haloperidol induced terminal deoxynucleotidyl transferase-mediated dUTP nick
165 xyuridine [BrdU]) and cell death (caspase-3, terminal deoxynucleotidyl transferase-mediated dUTP nick
166 was also observed with the use of either the terminal deoxynucleotidyl transferase-mediated dUTP nick
168 ng the wild type protein had very low TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
169 within 48-72 h, marked by nuclear blebbing, terminal deoxynucleotidyl transferase-mediated dUTP nick
170 apoptotic cell death occurred as detected by terminal deoxynucleotidyl transferase-mediated dUTP nick
171 initiation factor 2 alpha), and cell death [terminal deoxynucleotidyl transferase-mediated dUTP nick
172 rtex, an area that also showed more positive terminal deoxynucleotidyl transferase-mediated dUTP nick
175 DAPI (4', 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
177 ic grafts by hematoxylin and eosin staining, terminal deoxynucleotidyl transferase-mediated dUTP nick
179 ) polymerase, ii) DNA ladder formation, iii) terminal deoxynucleotidyl transferase-mediated dUTP nick
180 treatment resulted in a marked reduction in terminal deoxynucleotidyl transferase-mediated dUTP nick
181 ated biotin-dATP nick translation (PANT) and terminal deoxynucleotidyl transferase-mediated dUTP nick
182 al ganglion cells as assessed by morphology, terminal deoxynucleotidyl transferase-mediated dUTP nick
183 DNA fragmentation, measured by the number of terminal deoxynucleotidyl transferase-mediated dUTP nick
184 ne administration resulted in an increase in terminal deoxynucleotidyl transferase-mediated dUTP nick
185 ng of osteocytes/periosteal osteoblasts with terminal deoxynucleotidyl transferase-mediated dUTP nick
186 ced tumor size, reduced Ki-67, and increased terminal deoxynucleotidyl transferase-mediated dUTP nick
187 both settings its expression correlated with terminal deoxynucleotidyl transferase-mediated dUTP nick
188 the endothelial markers CD31 and VEGFR-2 and terminal deoxynucleotidyl transferase-mediated dUTP nick
189 c A((2)A)AR(-/-) mice had significantly more terminal deoxynucleotidyl transferase-mediated dUTP nick
191 tely 3-fold) and HA expression but increased terminal deoxynucleotidyl transferase-mediated dUTP nick
192 c release by Western blot, and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP nick
193 er rates of apoptosis, as measured by TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
195 topathy corneas, whereas it colocalized with terminal deoxynucleotidyl transferase-mediated dUTP nick
196 10 Gy significantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick
197 ed Boyden chamber assay), and antiapoptotic (terminal deoxynucleotidyl transferase-mediated dUTP nick
198 hed from the culture plate over time, became terminal deoxynucleotidyl transferase-mediated dUTP nick
199 rse transcription polymerase chain reaction, terminal deoxynucleotidyl transferase-mediated dUTP nick
200 by poly(ADP-ribose) polymerase cleavage and terminal deoxynucleotidyl transferase-mediated dUTP nick
201 aminotransferase (ALT), caspase-3 activity, terminal deoxynucleotidyl transferase-mediated dUTP nick
202 Similarly, the number of diabetes-enhanced terminal deoxynucleotidyl transferase-mediated dUTP nick
203 nst glucose-induced apoptosis as measured by terminal deoxynucleotidyl transferase-mediated dUTP nick
204 P<0.002) and less contraction band necrosis, terminal deoxynucleotidyl transferase-mediated dUTP nick
205 ce, BDL mice displayed a 13-fold increase in terminal deoxynucleotidyl transferase-mediated dUTP nick
206 Diabetes-increased activated caspase-3- and terminal deoxynucleotidyl transferase-mediated dUTP nick
207 erent neurons in heart failure, we performed terminal deoxynucleotidyl transferase-mediated dUTP nick
208 tosis of LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biot
209 of a lactate dehydrogenase release assay and terminal deoxynucleotidyl transferase-mediated dUTP-biot
210 ities of caspases 3 and 8, and the number of terminal deoxynucleotidyl transferase-mediated dUTP-biot
212 optosis in vitro at 72 hours (P < 0.05), and terminal deoxynucleotidyl transferase-mediated dUTP-biot
215 EM011 caused DNA degradation as evident by terminal deoxynucleotidyl transferase-mediated dUTP-biot
216 ity and cell death were investigated by MTT, terminal deoxynucleotidyl transferase-mediated dUTP-digo
217 ryosectioned, and evaluated for apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-digo
218 ity to active (Ac)-caspase-3, -8, and -9 and terminal deoxynucleotidyl transferase-mediated dUTP-digo
219 er, as determined by Hoechst 33342 staining, terminal deoxynucleotidyl transferase-mediated dUTP-FITC
220 s were stained for interleukin (IL)-12 or by terminal deoxynucleotidyl transferase-mediated dUTP-nick
221 nd induced tumor cell apoptosis (assessed by terminal deoxynucleotidyl transferase-mediated nick end
223 e attenuated levels of apoptosis observed by terminal deoxynucleotidyl transferase-mediated nick end
225 proliferation, and a significant increase in terminal deoxynucleotidyl transferase-mediated nick end
226 hown by fluorescence-activated cell sorting, terminal deoxynucleotidyl transferase-mediated nick end
227 e PDT as indicated by caspase-3 activity and terminal deoxynucleotidyl transferase-mediated nick end
228 o DU145) using flow cytometric Annexin V and terminal deoxynucleotidyl transferase-mediated nick end
229 construct did not involve apoptosis because terminal deoxynucleotidyl transferase-mediated nick end
230 hesizing SK-RC-45 line stimulated the TUNEL (terminal deoxynucleotidyl transferase-mediated nick end
232 o DNA, as revealed by caspase activation and terminal deoxynucleotidyl transferase-mediated nick end
233 as 5-fluorouracil (5-FU), induced apoptosis (terminal deoxynucleotidyl transferase-mediated nick end
234 n cancer cells were apoptotic as judged by a terminal deoxynucleotidyl transferase-mediated nick end
238 ning; creatine kinase release) or apoptosis (terminal deoxynucleotidyl transferase-mediated nick end
239 ogically, and apoptosis was evaluated by the terminal deoxynucleotidyl transferase-mediated nick end
240 protein, OX-42, gamma-aminobutyric acid, or terminal deoxynucleotidyl transferase-mediated nick end
241 from the mitochondria to the cytoplasm, and terminal deoxynucleotidyl transferase-mediated nick end
242 apoptosis as measured by flow cytometry and terminal deoxynucleotidyl transferase-mediated nick end
244 rmined by histochemical double labeling with terminal deoxynucleotidyl transferase-mediated nick end
245 more, tumors were apoptotic as determined by terminal deoxynucleotidyl transferase-mediated nick end
247 P<0.005) and protected against diabetes, and terminal deoxynucleotidyl transferase-mediated nick end
249 apoptosis was also noted in PiZ BDL mice by terminal deoxynucleotidyl transferase-mediated nick-end
250 apoptosis, as shown by increased numbers of terminal deoxynucleotidyl transferase-mediated nick-end
251 T1 AS) were employed in cells resistant (<5% terminal deoxynucleotidyl transferase-mediated nick-end
252 rs were harvested and assayed for apoptosis (terminal deoxynucleotidyl transferase-mediated nick-end
253 anine aminotransferase (ALT), pathology, and terminal deoxynucleotidyl transferase-mediated nick-end
254 eduction in the apoptosis rate was observed (terminal deoxynucleotidyl transferase-mediated nick-end
257 g with cytochrome c immunohistochemistry and terminal deoxynucleotidyl transferase-mediated uridine 5
259 th cases was observed with the appearance of terminal deoxynucleotidyl transferase-mediated UTP end l
260 -stained, hematoxylin and eosin-stained, and terminal deoxynucleotidyl transferase-mediated UTP nick
261 p75(NTR) expression was induced primarily in terminal deoxynucleotidyl transferase-mediated UTP nick-
262 th these findings, flow cytometry and TUNEL (terminal deoxynucleotidyl-transferase-mediated dUTP nick
263 controls were studied by routine microscopy, terminal deoxynucleotidyl-transferase-mediated dUTP nick
264 ed by proliferating cell nuclear antigen and terminal deoxynucleotidyl-transferase-mediated dUTP nick
265 ptosis in endothelial cells as determined by terminal deoxynucleotidyl-transferase-mediated dUTP nick
267 nd in situ DNA fragmentation assessed by the terminal deoxynucleotidyl transferase nick end-labeling)
269 ti-B7.1, anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling)
270 92 total), and a significant proportion were terminal deoxynucleotidyl transferase (TdT) -mediated de
271 ty/joining (V[D]J) recombination, the enzyme terminal deoxynucleotidyl transferase (Tdt) adds random
272 l-derived B cell progenitors fail to express terminal deoxynucleotidyl transferase (TdT) and for othe
274 dult repertoires due to the delayed onset of terminal deoxynucleotidyl transferase (TdT) expression i
275 we find that mice expressing a transgene for terminal deoxynucleotidyl transferase (TdT) have nucleot
277 at the 3'-OH of an RNA molecule, followed by terminal deoxynucleotidyl transferase (TdT) to catalyze
278 27(+) Ly-6C(-) Thy-1(-)CD43(+) CD16/32(Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in
279 d bone marrow (BM) chimeras, made with adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT
281 to a single stranded DNA (ssDNA) chain using terminal deoxynucleotidyl transferase (TdT), a template-
283 om RA synovium, we also sought expression of terminal deoxynucleotidyl transferase (TdT), which is no
284 ntemplated (N) nucleotides is carried out by terminal deoxynucleotidyl transferase (TdT), whose only
287 uts relative to WT animals, as documented by terminal deoxynucleotidyl transferase (TdT)-mediated dUT
289 eated with HA were examined for apoptosis in terminal deoxynucleotidyl transferase (TdT)-mediated dUT
290 this study, we compared these tests with the terminal deoxynucleotidyl transferase (TdT)-mediated dUT
294 oid (P <.10) or early hematopoietic markers (terminal deoxynucleotidyl transferase [TdT], CD34; P <.1
297 cleaved caspase-3 immunohistochemistry, and terminal deoxynucleotidyl transferase UTP nick-end label
298 e synthesis of heavily modified DNA, whereas terminal deoxynucleotidyl transferase was used for a sin
299 terleukin receptor 7 alpha(+), c-kit(lo) and terminal deoxynucleotidyl transferase(+)) were selective
300 of nontemplated (N) nucleotides inserted by terminal deoxynucleotidyl transferase, which resulted in
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