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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
20 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and caspase 3 and Bax expression in Aq
21 s (terminal nucleotidyl transferase-mediated nick end labeling and caspase-3) were observed in the is
22 deoxynucledotidyl transferase-mediated dUTP nick end labeling and CD31 to assess apoptotic index and
23 n terminal deoxynucleotidyl transferase dUTP nick end labeling and cleaved caspase-3 positive cells.
24 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and hallmarks of apoptosis including c
25 transferase 2'-Deoxyuridine, 5'-Triphosphate nick end labeling and p65 staining was used to examine f
26 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling and trypan blue exclusion assays, as w
28 rminal deoxynucleotidyl transferase-mediated nick-end labeling and Annexin V assays) in response to c
29 -alpha-induced apoptosis was detected by DNA nick-end labeling and by measuring histone associated DN
30 istological analyses including terminal dUTP nick-end labeling and caspase 3 immunocytochemical stain
32 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling and caspase-3, indicating that TXNIP i
33 d markers including TdT-mediated dUTP biotin nick-end labeling and cleaved caspase 3 immunofluorescen
34 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling and DNA fragment enzyme-linked immunos
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 d terminal deoxynucleotidyl transferase dUTP nick end labeling assay, Kim1 mRNA assessment, and Weste
63 oxyribonucleotidyl transferase-mediated dUTP nick end labeling assay, was preceded by loss of mitocho
68 nucleotidyl transferase-mediated dUTP-biotin nick end-labeling assay demonstrated that BopC is requir
69 y terminal deoxynucleotidyl transferase dUTP nick-end labeling assay and activated caspase-3 staining
70 EAU, by using the terminal transferase dUTP nick-end labeling assay and polymerase chain reaction.
71 cell apoptosis [by transferase-mediated dUTP nick-end labeling assay and Western blotting for poly(AD
72 rminal deoxynucleotidyl transferase-mediated nick-end labeling assay confirmed that HCT116(p53+/+) ce
73 d terminal deoxynucleotidyl transferase dUTP nick-end labeling assay or methods based on monitoring o
74 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay was performed, and intestinal in
76 , terminal deoxynucleotidyl transferase dUTP nick-end labeling assay, and electron microscopy in C1qa
77 nal deoxynucleotide tranferase-mediated dUTP nick-end labeling assay, and ex vivo via Western analysi
78 l deoxynucleotidyl-transferase-mediated dUTP nick-end labeling assay, we showed that the expression o
85 l cell death was determined by terminal dUTP nick-end labeling assay; BRB function by quantifying ext
86 l deoxynucleotidyl transferase-mediated dUTP nick-end-labeling assay showed no significant apoptosis
87 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling) assay determined that contact with th
88 (Terminal deoxynucleotidyl transferase dUTP nick end labeling) assay indicated that apoptosis was tr
90 l deoxynucleotidyl transferase-mediated dUTP nick end labeling assays on tissue sections revealed tha
92 is and terminal deoxynucleotidyl transferase nick-end labeling assays were performed on Raf small int
94 tidyl transferase (TdT)-mediated dUTP-biotin nick end labeling) assays demonstrate that gammaH2AX for
95 al deoxynucleotidyltransferase-mediated dUTP nick end labeling, caspase 3 cleavage, and re-localizati
97 l deoxynucleotidyl transferase-mediated dUTP nick end labeling) demonstrated that lack of p53 is init
100 otidyl transferase-mediated biotinylated UTP nick end labeling, hallmarks of apoptosis, were seen in
102 nal deoxynucleotidyl transferase biotin-dUTP nick end labeling, immunoblot analysis and quantitation
105 d Ki-67 and low positivity for terminal dUTP nick-end labeling indicated robust cell proliferation an
109 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling of DNA double-strand breakage, indicat
110 d terminal deoxynucleotidyl transferase dUTP nick end labeling of targeted doxorubicin micelles in Bc
111 l deoxynucleotidyl transferase mediated dUTP nick end labeling, or TUNEL, staining, respectively, and
112 otidyl transferase-mediated biotinylated UTP nick end labeling positive, and they can be mitotically
113 f terminal deoxynucleotidyl transferase dUTP nick-end labeling positive cells in the hippocampus, and
114 al deoxynucleotidyltransferase-mediated dUTP nick-end labeling positive CM (-44%, P<0.01), increased
115 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling positive nuclei and DNA fragmentation)
116 rminal deoxynucleotidyl transferase-mediated nick-end labeling positive) to apoptosis induction by IF
117 e terminal deoxynucleotidyl transferase dUTP nick-end labeling positive, suggesting remodeling involv
119 cosal injury, TUNEL (transferase biotin-dUTP nick end-labeling)-positive cells, neutrophil infiltrati
120 e number of TUNEL (transferase-mediated dUTP nick-end labeling)-positive capillary cells and acellula
121 l deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive apoptotic cells (8.3% +/- 1.4
123 e in the number of transferase-mediated dUTP nick end labeling-positive cells and a decrease in a bon
124 l deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive cells and expression of apopt
125 e-mediated deoxyuridine triphosphate in situ nick end labeling-positive cells compared with the MSC(L
126 s with more 53BP1 foci and TdT-mediated dNTP nick end labeling-positive cells over their corrected co
127 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling-positive cells were present in the cor
128 otidyl transferase-mediated biotinylated UTP nick end labeling-positive cells within 24-48 hr of HI.
129 otidyl transferase-mediated biotinylated UTP nick end labeling-positive cells, indicating decreased a
130 otidyl transferase-mediated biotinylated UTP nick end labeling-positive matrices and p53 at the outer
131 rminal deoxynucleotidyl transferase-mediated nick end labeling-positive myocytes or loss of JC-1 fluo
132 al deoxynucleotidyltransferase-mediated dUTP nick end labeling-positive myonuclei, and activated casp
133 d terminal deoxynucleotidyl transferase dUTP nick end labeling-positive nuclei (4+/-3% versus 10+/-1%
134 otidyl transferase-mediated biotinylated UTP nick end labeling-positive nuclei increased dramatically
135 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling-positive parasites following heat trea
136 ssociated with higher numbers of dUTP-biotin nick end labeling-positive renal tubule cells, suggestin
137 rminal deoxynucleotidyl transferase-mediated nick end labeling-positive staining in mammary tumor cel
139 cornification, assessed as TdT-mediated dUTP nick end-labeling-positive cells in stratum granulosum a
142 e in the number of transferase-mediated dUTP nick-end labeling-positive capillary cells, acellular ca
143 rminal deoxynucleotidyl transferase-mediated nick-end labeling-positive cells and by increased bindin
144 mpanied by enhanced numbers of terminal dUTP nick-end labeling-positive cells at days 4, 6, and 10.
146 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells were also increased in
147 o increased transferase-mediated dUTP-biotin nick-end labeling-positive cells, caspase-3 activity, an
148 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells, TNF-alpha release, and
152 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive endothelial cells and pericyt
153 n terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive enterocyte nuclei in the Myo1
154 reduced apoptosis (transferase-mediated dUTP nick-end labeling-positive insulin-positive cells; P < 0
155 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive microvascular cell numbers we
156 ansferase-mediated deoxyuridine triphosphate nick-end labeling-positive nuclei and accumulation of cy
157 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive, and exhibited elevated level
158 [terminal deoxynucleotidyl transferase dUTP nick end labeling])-positive cells) of NPIs compared wit
159 deoxyguanosine and transferase-mediated dUTP nick-end labeling positivity and also prevented acellula
160 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling positivity, superoxide, and nitric oxi
161 al deoxynucleotidyltransferase-mediated dUTP nick end labeling-positivity) and oxidative stress (loss
162 nal deoxyribonucleotide transferase-mediated nick-end labeling) ratio of ductal cells increased with
163 al deoxynucleotide transferase-mediated dUTP nick-end labeling reaction) and involve disruption of th
166 a terminal deoxynucleotidyl transferase dUTP nick end labeling staining and caspase-3 activation.
167 by terminal deoxynucleotide transferase dUTP nick end labeling staining and cleaved caspase-3 express
168 o terminal deoxynucleotidyl transferase dUTP nick end labeling staining for apoptotic DNA fragmentati
170 transferase 2'-deoxyuridine, 5'-triphosphate nick end labeling staining versus kidneys treated with c
171 oxyribonucleotidyl transferase-mediated dUTP nick end labeling staining was done to quantify apoptoti
172 rminal deoxynucleotidyl transferase-mediated nick end labeling staining within the colonic epithelium
173 , terminal deoxynucleotidyl transferase dUTP nick end labeling staining, and immunohistochemistry in
174 oxyribonucleotidyl transferase-mediated dUTP nick end labeling staining, was increased in cells overe
178 deoxy-nucleotidyl transferase-mediated dUTP nick end-labeling staining and caspase-3 activity after
180 effects, as evidenced by less terminal dUTP nick end-labeling staining, a lower incidence of DNA lad
184 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling staining and cleaved caspase 3 express
186 nal deoxynucleotide tranferase-mediated dUTP nick-end labeling staining and immunohistochemistry.
188 nucleotidyl transferase-mediated biotin-dUTP nick-end labeling staining to quantitate myocyte apoptos
189 Terminal deoxynucleotidyl transferase dUTP nick-end labeling staining was used for the identificati
190 d terminal deoxynucleotidyl transferase dUTP nick-end labeling staining were tested for apoptosis.
192 ed with fragmented DNA by terminal deoxy-UTP nick-end labeling staining, activated caspase-3, and the
193 al deoxynucleotide transferase-mediated dUTP nick-end labeling staining, caspase-3 activity, and nucl
194 serum transaminases, bilirubin, triphosphate nick-end labeling staining, caspase-3 activity, oxidativ
195 , terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, cytochrome c release, the fo
199 al deoxynucleotidyltransferase-mediated dUTP nick-end labeling) staining were performed on adjacent t
201 d terminal deoxynucleotidyl transferase dUTP nick end labeling terminal deoxynucleotidyl transferase
202 ansferase-mediated deoxyuridine triphosphate nick end labeling) to determine whether tumor cells had
203 abeling) and death (Tdt-mediated dUTP-biotin nick end labeling) to investigate the specificity of Brd
204 se-mediated dUTP (deoxyuridine triphosphate) nick end labeling (TUNEL) and active caspase-3 analyses
206 apoptosis was quantified with terminal dUTP nick end labeling (TUNEL) and fluorescence microscopy.
207 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) and fluorescence-activated cel
208 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and phospho-histone H3 (PH3) s
209 y terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and used to estimate the occur
210 l deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay and caspase-3 activation
211 l deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) assay and caspase-3 activities
212 inal deoxynucleotidyltransferase dUTP-biotin nick end labeling (TUNEL) assay revealed that 70% of THP
213 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay suggested that apoptosis
214 nal deoxynucleotidyl transferase biotin-dUTP nick end labeling (TUNEL) assay was performed to detect
215 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay, compared to T cells iso
218 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays and ultrastructural obs
219 tidyl transferase (TdT)-mediated dUTP-biotin nick end labeling (TUNEL) assays revealed that S. suis i
220 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assays, and transmission elect
222 judged by lack of terminal transferase dUTP nick end labeling (TUNEL) labeling or reactivity to anti
223 r terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) or activated-caspase 3, sugges
224 otidyl transferase-mediated biotinylated UTP nick end labeling (TUNEL) reactivity and activation of c
225 rminal deoxynucleotidyl transferase-mediated nick end labeling (TUNEL) revealed a approximately 50-fo
227 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining characteristic of apo
229 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining of intestinal section
231 l deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, and Western blot for
232 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining, but not in neurons.
233 al deoxynucleotidyltransferase-mediated dUTP nick end labeling (TUNEL) staining, DNA fragmentation, c
234 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) staining, indicating that the
236 otidyl transferase-mediated dUTP-digoxigenin nick end labeling (TUNEL) were evaluated in cryosections
237 , terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), 3-(4,5-dimethylthiazol-2-yl)-
239 otidyl transferase-mediated biotinylated UTP nick end labeling (TUNEL), and Purkinje cells were TUNEL
240 al deoxynucleotidyltransferase-mediated dUTP nick end labeling (TUNEL), and was not seen in normal me
241 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive cells in several regi
242 otidyl transferase-mediated biotinylated UTP nick end labeling (TUNEL)-positive cells were detected i
243 ynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive myocytes were increas
244 l deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL)-positive nuclei, only 6 and 10
245 h terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)-positive soma and the eventual
247 f active caspase-3/transferase-mediated dUTP nick end-labeling (TUNEL) apoptotic markers and enhanced
248 rough the terminal dUTP transferase-mediated nick end-labeling (TUNEL) assay followed by counting the
249 se-mediated deoxyuridine triphosphate (dUTP) nick end-labeling (TUNEL) assay were conducted to detect
251 by terminal deoxynucleotidyltransferase dUTP nick end-labeling (TUNEL) in myocardial samples from fai
252 hologic analysis that included terminal dUTP nick end-labeling (TUNEL), capillary and cardiomyocyte d
253 ansferase-mediated deoxyuridine triphosphate nick end-labeling (TUNEL)-positive cells and mortality c
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 y terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) and measurement of outer nucle
260 h terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) assay and immunohistochemistry
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 al deoxynucleotidyl transferasemediated dUTP nick-end labeling (TUNEL) reaction, and histopathology.
269 e terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) signals were found at E16.5.
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
278 Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) was performed 3 days after sep
279 Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) was performed in retinal secti
280 ansferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL)(+) nuclei and caspase 3 immuno
281 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL), Ki-67, p53, bcl-2, and MMR we
282 nucleotidyl transferase-mediated biotin-dUTP nick-end labeling (TUNEL), observations that are indicat
283 l deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)-positive cells, NASH, and fibr
289 (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