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1 nsferase-mediated deoxyuridine 5-triphospate nick end labeling).
2 l deoxynucleotidyl transferase-mediated dUTP nick end labeling).
3 by the terminal deoxynucleotidyl transferase nick end-labeling).
4 nal deoxyribonucleotide transferase-mediated nick-end labeling).
5 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling).
6 otidyl transferase-mediated biotinylated UTP nick end labeling.
7 al deoxynucleotidyltransferase-mediated dUTP nick end labeling.
8 l deoxynucleotidyl transferase-mediated dUTP nick end labeling analyses indicated a greater number of
9 l transferase 2-deoxyuridine, 5-triphosphate nick end-labeling analyses support UPR activation and UP
11 oxyribonucleotidyl transferase-mediated dUTP nick end labeling analysis shows that there is no increa
14 al deoxynucleotide transferase-mediated dUTP nick-end labeling analysis showed significantly decrease
15 se-mediated deoxyuridine triphosphate-biotin nick-end labeling analysis, respectively, in biopsies fr
16 l deoxynucleotidyl transferase-mediated dUTP nick-end-labeling analysis reveals greater abundance of
17 al deoxynucleotidyltransferase-mediated dUTP nick end labeling and a marked depletion of oligodendroc
18 ed apoptosis using terminal transferase dUTP nick end labeling and active caspase-3 staining in liver
19 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and annexin binding, in cardiac myocyt
21 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and caspase 3 and Bax expression in Aq
23 s (terminal nucleotidyl transferase-mediated nick end labeling and caspase-3) were observed in the is
24 deoxynucledotidyl transferase-mediated dUTP nick end labeling and CD31 to assess apoptotic index and
25 n terminal deoxynucleotidyl transferase dUTP nick end labeling and cleaved caspase-3 positive cells.
26 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and hallmarks of apoptosis including c
27 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and trypan blue exclusion assays, as w
29 rminal deoxynucleotidyl transferase-mediated nick-end labeling and Annexin V assays) in response to c
30 -alpha-induced apoptosis was detected by DNA nick-end labeling and by measuring histone associated DN
31 istological analyses including terminal dUTP nick-end labeling and caspase 3 immunocytochemical stain
33 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling and caspase-3, indicating that TXNIP i
34 d markers including TdT-mediated dUTP biotin nick-end labeling and cleaved caspase 3 immunofluorescen
36 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling and in situ oligo ligation methods.
38 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling and quantified by both caspase-3 activ
39 nd terminal nucleotidyl transferase-mediated nick end labeling) and decreased HSP70 mRNA and protein
40 rminal deoxynucleotidyl transferase-mediated nick-end labeling) and HMGR and COX-2 protein expression
41 d terminal deoxynucleotidyl transferase dUTP nick end labeling), and diminished Akt phosphorylation.
43 l deoxynucleotidyl transferase-mediated dUTP nick end labeling, and caspase-3 activation also increas
44 al deoxynucleotidyltransferase-mediated dUTP nick end labeling, and functional assessment of ventricu
45 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling, and propidium iodide staining assays,
46 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling, and Rad51) at the leptotene/zygotene
48 al deoxynucleotide transferase-mediated dUTP nick end-labeling, and single-cell gel electrophoresis (
49 oxyribonucleotidyl transferase-mediated dUTP nick-end labeling, and CD31 immunohistochemistry, respec
50 rated by immunohistochemistry, terminal dUTP nick-end labeling, and DNA agarose gel electrophoresis.
51 al deoxynucleotidyltransferase-mediated dUTP nick-end labeling, and DNA laddering, which were associa
53 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling, and Ki-67 immunoreactivity were evalu
54 oxyribonucleotidyl transferase-mediated dUTP nick end labeling- and caspase 3-stained cells at 6 and
56 optosis by terminal transferase-mediated DNA nick end labeling assay and measured expression of apopt
57 rminal deoxynucleotidyl transferase-mediated nick end labeling assay and mitochondrial membrane poten
58 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling assay following treatment of HTLV-1-tr
59 otidyl transferase-mediated biotinylated UTP nick end labeling assay revealed substantial deteriorati
60 d terminal deoxynucleotidyl transferase dUTP nick end labeling assay was used to assess alveolar cell
61 ansferase-mediated dUTP-tetramethylrhodamine nick end labeling assay, demonstrating the importance of
62 oxyribonucleotidyl transferase-mediated dUTP nick end labeling assay, was preceded by loss of mitocho
66 nucleotidyl transferase-mediated dUTP-biotin nick end-labeling assay demonstrated that BopC is requir
67 y terminal deoxynucleotidyl transferase dUTP nick-end labeling assay and activated caspase-3 staining
68 EAU, by using the terminal transferase dUTP nick-end labeling assay and polymerase chain reaction.
69 cell apoptosis [by transferase-mediated dUTP nick-end labeling assay and Western blotting for poly(AD
70 rminal deoxynucleotidyl transferase-mediated nick-end labeling assay confirmed that HCT116(p53+/+) ce
71 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay was performed, and intestinal in
73 , terminal deoxynucleotidyl transferase dUTP nick-end labeling assay, and electron microscopy in C1qa
74 nal deoxynucleotide tranferase-mediated dUTP nick-end labeling assay, and ex vivo via Western analysi
75 l deoxynucleotidyl-transferase-mediated dUTP nick-end labeling assay, we showed that the expression o
82 l cell death was determined by terminal dUTP nick-end labeling assay; BRB function by quantifying ext
83 l deoxynucleotidyl transferase-mediated dUTP nick-end-labeling assay showed no significant apoptosis
84 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling) assay determined that contact with th
85 (Terminal deoxynucleotidyl transferase dUTP nick end labeling) assay indicated that apoptosis was tr
87 l deoxynucleotidyl transferase-mediated dUTP nick end labeling assays on tissue sections revealed tha
89 is and terminal deoxynucleotidyl transferase nick-end labeling assays were performed on Raf small int
91 tidyl transferase (TdT)-mediated dUTP-biotin nick end labeling) assays demonstrate that gammaH2AX for
92 al deoxynucleotidyltransferase-mediated dUTP nick end labeling, caspase 3 cleavage, and re-localizati
94 l deoxynucleotidyl transferase-mediated dUTP nick end labeling) demonstrated that lack of p53 is init
98 otidyl transferase-mediated biotinylated UTP nick end labeling, hallmarks of apoptosis, were seen in
100 nal deoxynucleotidyl transferase biotin-dUTP nick end labeling, immunoblot analysis and quantitation
103 d Ki-67 and low positivity for terminal dUTP nick-end labeling indicated robust cell proliferation an
107 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling of DNA double-strand breakage, indicat
108 d terminal deoxynucleotidyl transferase dUTP nick end labeling of targeted doxorubicin micelles in Bc
109 l deoxynucleotidyl transferase mediated dUTP nick end labeling, or TUNEL, staining, respectively, and
110 otidyl transferase-mediated biotinylated UTP nick end labeling positive, and they can be mitotically
111 al deoxynucleotidyltransferase-mediated dUTP nick-end labeling positive CM (-44%, P<0.01), increased
112 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling positive nuclei and DNA fragmentation)
113 rminal deoxynucleotidyl transferase-mediated nick-end labeling positive) to apoptosis induction by IF
114 e terminal deoxynucleotidyl transferase dUTP nick-end labeling positive, suggesting remodeling involv
116 cosal injury, TUNEL (transferase biotin-dUTP nick end-labeling)-positive cells, neutrophil infiltrati
117 e number of TUNEL (transferase-mediated dUTP nick-end labeling)-positive capillary cells and acellula
118 erminal deoxynucleotidyltransferase-mediated nick end labeling-positive (P < 0.005-0.001), and cleave
119 l deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive apoptotic cells (8.3% +/- 1.4
121 e in the number of transferase-mediated dUTP nick end labeling-positive cells and a decrease in a bon
122 l deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive cells and expression of apopt
123 e-mediated deoxyuridine triphosphate in situ nick end labeling-positive cells compared with the MSC(L
124 s with more 53BP1 foci and TdT-mediated dNTP nick end labeling-positive cells over their corrected co
125 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling-positive cells were present in the cor
126 otidyl transferase-mediated biotinylated UTP nick end labeling-positive cells within 24-48 hr of HI.
127 otidyl transferase-mediated biotinylated UTP nick end labeling-positive cells, indicating decreased a
128 otidyl transferase-mediated biotinylated UTP nick end labeling-positive matrices and p53 at the outer
129 rminal deoxynucleotidyl transferase-mediated nick end labeling-positive myocytes or loss of JC-1 fluo
130 al deoxynucleotidyltransferase-mediated dUTP nick end labeling-positive myonuclei, and activated casp
131 d terminal deoxynucleotidyl transferase dUTP nick end labeling-positive nuclei (4+/-3% versus 10+/-1%
132 otidyl transferase-mediated biotinylated UTP nick end labeling-positive nuclei increased dramatically
133 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling-positive parasites following heat trea
134 ssociated with higher numbers of dUTP-biotin nick end labeling-positive renal tubule cells, suggestin
135 rminal deoxynucleotidyl transferase-mediated nick end labeling-positive staining in mammary tumor cel
137 cornification, assessed as TdT-mediated dUTP nick end-labeling-positive cells in stratum granulosum a
140 e in the number of transferase-mediated dUTP nick-end labeling-positive capillary cells, acellular ca
141 rminal deoxynucleotidyl transferase-mediated nick-end labeling-positive cells and by increased bindin
142 mpanied by enhanced numbers of terminal dUTP nick-end labeling-positive cells at days 4, 6, and 10.
144 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells were also increased in
145 o increased transferase-mediated dUTP-biotin nick-end labeling-positive cells, caspase-3 activity, an
146 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells, TNF-alpha release, and
150 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive endothelial cells and pericyt
151 n terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive enterocyte nuclei in the Myo1
152 reduced apoptosis (transferase-mediated dUTP nick-end labeling-positive insulin-positive cells; P < 0
153 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive microvascular cell numbers we
154 ansferase-mediated deoxyuridine triphosphate nick-end labeling-positive nuclei and accumulation of cy
155 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive, and exhibited elevated level
156 [terminal deoxynucleotidyl transferase dUTP nick end labeling])-positive cells) of NPIs compared wit
157 ncreased terminal deoxy uridine triphosphate nick end labeling positivity was observed in centrin mut
158 deoxyguanosine and transferase-mediated dUTP nick-end labeling positivity and also prevented acellula
159 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling positivity, superoxide, and nitric oxi
160 al deoxynucleotidyltransferase-mediated dUTP nick end labeling-positivity) and oxidative stress (loss
161 nal deoxyribonucleotide transferase-mediated nick-end labeling) ratio of ductal cells increased with
162 al deoxynucleotide transferase-mediated dUTP nick-end labeling reaction) and involve disruption of th
165 a terminal deoxynucleotidyl transferase dUTP nick end labeling staining and caspase-3 activation.
166 by terminal deoxynucleotide transferase dUTP nick end labeling staining and cleaved caspase-3 express
167 o terminal deoxynucleotidyl transferase dUTP nick end labeling staining for apoptotic DNA fragmentati
169 oxyribonucleotidyl transferase-mediated dUTP nick end labeling staining was done to quantify apoptoti
170 rminal deoxynucleotidyl transferase-mediated nick end labeling staining within the colonic epithelium
171 oxyribonucleotidyl transferase-mediated dUTP nick end labeling staining, was increased in cells overe
175 deoxy-nucleotidyl transferase-mediated dUTP nick end-labeling staining and caspase-3 activity after
177 effects, as evidenced by less terminal dUTP nick end-labeling staining, a lower incidence of DNA lad
182 nal deoxynucleotide tranferase-mediated dUTP nick-end labeling staining and immunohistochemistry.
184 nucleotidyl transferase-mediated biotin-dUTP nick-end labeling staining to quantitate myocyte apoptos
185 Terminal deoxynucleotidyl transferase dUTP nick-end labeling staining was used for the identificati
186 d terminal deoxynucleotidyl transferase dUTP nick-end labeling staining were tested for apoptosis.
188 ed with fragmented DNA by terminal deoxy-UTP nick-end labeling staining, activated caspase-3, and the
189 al deoxynucleotide transferase-mediated dUTP nick-end labeling staining, caspase-3 activity, and nucl
190 serum transaminases, bilirubin, triphosphate nick-end labeling staining, caspase-3 activity, oxidativ
191 , terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, cytochrome c release, the fo
195 l deoxynucleotidyl-transferase-mediated dUTP nick end labeling) staining revealed EGCG-dependent G(1)
196 al deoxynucleotidyltransferase-mediated dUTP nick-end labeling) staining were performed on adjacent t
198 ansferase-mediated deoxyuridine triphosphate nick end labeling) to determine whether tumor cells had
199 abeling) and death (Tdt-mediated dUTP-biotin nick end labeling) to investigate the specificity of Brd
200 aluated by the TdT-mediated digoxigenin-dUTP nick-end labeling TUNEL assay, and by DNA laddering anal
201 se-mediated dUTP (deoxyuridine triphosphate) nick end labeling (TUNEL) and active caspase-3 analyses
203 apoptosis was quantified with terminal dUTP nick end labeling (TUNEL) and fluorescence microscopy.
204 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) and fluorescence-activated cel
205 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and phospho-histone H3 (PH3) s
206 y terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and used to estimate the occur
207 l deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay and caspase-3 activation
208 l deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) assay and caspase-3 activities
209 inal deoxynucleotidyltransferase dUTP-biotin nick end labeling (TUNEL) assay revealed that 70% of THP
210 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay suggested that apoptosis
211 nal deoxynucleotidyl transferase biotin-dUTP nick end labeling (TUNEL) assay was performed to detect
212 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay, compared to T cells iso
215 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays and ultrastructural obs
216 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assays, and transmission elect
218 judged by lack of terminal transferase dUTP nick end labeling (TUNEL) labeling or reactivity to anti
219 r terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) or activated-caspase 3, sugges
220 nal-deoxynucleotidyl transferase dUTP-linked nick end labeling (TUNEL) procedure and by immunohistoch
221 otidyl transferase-mediated biotinylated UTP nick end labeling (TUNEL) reactivity and activation of c
222 rminal deoxynucleotidyl transferase-mediated nick end labeling (TUNEL) revealed a approximately 50-fo
224 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining characteristic of apo
226 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining of intestinal section
228 l deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, and Western blot for
229 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining, but not in neurons.
230 al deoxynucleotidyltransferase-mediated dUTP nick end labeling (TUNEL) staining, DNA fragmentation, c
231 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining, indicating that the
233 otidyl transferase-mediated dUTP-digoxigenin nick end labeling (TUNEL) were evaluated in cryosections
234 , terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), 3-(4,5-dimethylthiazol-2-yl)-
236 oxyribonucleotidyl transferase-mediated dUTP nick end labeling (TUNEL), and caspase-3 staining 1 to 1
237 otidyl transferase-mediated biotinylated UTP nick end labeling (TUNEL), and Purkinje cells were TUNEL
238 al deoxynucleotidyltransferase-mediated dUTP nick end labeling (TUNEL), and was not seen in normal me
239 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive cells in several regi
240 otidyl transferase-mediated biotinylated UTP nick end labeling (TUNEL)-positive cells were detected i
241 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive myocytes were increas
242 l deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL)-positive nuclei, only 6 and 10
243 h terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)-positive soma and the eventual
245 f active caspase-3/transferase-mediated dUTP nick end-labeling (TUNEL) apoptotic markers and enhanced
246 rough the terminal dUTP transferase-mediated nick end-labeling (TUNEL) assay followed by counting the
247 se-mediated deoxyuridine triphosphate (dUTP) nick end-labeling (TUNEL) assay were conducted to detect
249 nucleotidyl transferase-mediated dUTP-biotin nick end-labeling (TUNEL) evaluation of tumor sections r
250 by terminal deoxynucleotidyltransferase dUTP nick end-labeling (TUNEL) in myocardial samples from fai
251 hologic analysis that included terminal dUTP nick end-labeling (TUNEL), capillary and cardiomyocyte d
252 ansferase-mediated deoxyuridine triphosphate nick end-labeling (TUNEL)-positive cells and mortality c
253 al deoxynucleotidyltransferase-mediated dUTP nick end-labeling (TUNEL)-positive cells were approximat
254 rminal deoxynucleotidyl transferase-mediated nick-end labeling (TUNEL) also decreased from 21.4% and
255 nucleotidyl transferase-mediated dUTP biotin nick-end labeling (TUNEL) analysis and caspase-3 activit
256 e retina were quantified using terminal dUTP nick-end labeling (TUNEL) and active caspase-3 (CM-1) im
257 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) and an 11-fold increase in cas
258 rminal deoxynucleotidyl transferase-mediated nick-end labeling (TUNEL) and cleaved caspase-3 histolog
259 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) and double immunofluorescent l
260 y terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) and measurement of outer nucle
261 minal deoxyribosyl transferase-mediated dUTP nick-end labeling (TUNEL) assay, and real-time RT-PCR.
264 al deoxynucleotide transferase-mediated dUTP nick-end labeling (TUNEL) assay; (2) frequencies of Th s
265 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) for fixed tissues and acridine
267 nal-deoxynucleotidyl transferase dUTP-linked nick-end labeling (TUNEL) procedure determined the effec
268 e terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) signals were found at E16.5.
269 by terminal deoxynucleotidyltransferase dUTP nick-end labeling (TUNEL) staining and caspase 3 activat
270 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) staining for intratumoral apop
271 se-mediated deoxyuridine triphosphate-biotin nick-end labeling (TUNEL) staining in tumor biopsies (n
272 s terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining in vascular cells wit
273 nd terminal deoxynucleotidyl transferase UTP nick-end labeling (TUNEL) staining of histologic section
274 rminal deoxynucleotidyl transferase-mediated nick-end labeling (TUNEL) staining was minimal in mice f
275 LT), necrosis, TdT-mediated dUTP-digoxigenin nick-end labeling (TUNEL) staining, caspase-3 activation
276 y terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining, circulating levels o
277 Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) was performed 3 days after sep
278 Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) was performed in retinal secti
279 ansferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL)(+) nuclei and caspase 3 immuno
280 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL), Ki-67, p53, bcl-2, and MMR we
281 nucleotidyl transferase-mediated biotin-dUTP nick-end labeling (TUNEL), observations that are indicat
282 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)-positive cells, NASH, and fibr
289 otidyl transferase-mediated biotinylated UTP nick end labeling [TUNEL(-)] and active caspase 3(+)/TUN
290 (terminal deoxynucleotidyl transferase dUTP nick end labeling [TUNEL] assay), and of collagen type I
291 induced apoptosis (transferase-mediated dUTP nick-end labeling [TUNEL]) and decreased proliferation (
292 tosis (detected by terminal transferase dUTP nick-end labeling [TUNEL]) and formation of acellular ca
293 tate on apoptosis (transferase-mediated dUTP nick-end labeling [TUNEL]), mitochondrial death pathway
296 y terminal deoxynucleotidyl transferase dUTP nick-end labeling, was significantly decreased in the pr
298 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling were not detected in infected astrocyt
299 s (terminal nucleotidyl transferase-mediated nick end labeling) were done by immunohistochemistry and
300 llular apoptosis as assessed by terminal UTP nick-end labeling when compared to ConA-treated Wt mice
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