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1 , and a significant proportion were terminal deoxynucleotidyl transferase (TdT) -mediated deoxyuridin
2 g (V[D]J) recombination, the enzyme terminal deoxynucleotidyl transferase (Tdt) adds random nucleotid
3 B cell progenitors fail to express terminal deoxynucleotidyl transferase (TdT) and for other reasons
4 is based on exonuclease I (Exo I), terminal deoxynucleotidyl transferase (TdT) and methylene blue.
6 X family members such as Pol mu and terminal deoxynucleotidyl transferase (TdT) are important compone
7 rtoires due to the delayed onset of terminal deoxynucleotidyl transferase (TdT) expression in ontogen
8 ons by patterned UV light activates Terminal deoxynucleotidyl Transferase (TdT) for spatially-selecti
9 hat mice expressing a transgene for terminal deoxynucleotidyl transferase (TdT) have nucleotide inser
10 the template-independent polymerase terminal deoxynucleotidyl transferase (TdT) in kinetically contro
11 mplate independent polymerases, and terminal deoxynucleotidyl transferase (TdT) in particular, have b
14 -OH of an RNA molecule, followed by terminal deoxynucleotidyl transferase (TdT) to catalyze the seque
15 6C(-) Thy-1(-)CD43(+) CD16/32(Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in murine bo
16 rrow (BM) chimeras, made with adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) don
18 le stranded DNA (ssDNA) chain using terminal deoxynucleotidyl transferase (TdT), a template-independe
20 ovium, we also sought expression of terminal deoxynucleotidyl transferase (TdT), which is normally ex
21 d (N) nucleotides is carried out by terminal deoxynucleotidyl transferase (TdT), whose only known phy
22 h HA were examined for apoptosis in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP biotin
23 ive to WT animals, as documented by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
24 y, we compared these tests with the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
34 The short splice variant of mouse terminal deoxynucleotidyl transferase (TdTS) catalyzes the additi
35 ular necrosis scores and degrees of terminal deoxynucleotidyl transferase 2'-deoxyuridine, 5'-triphos
37 ptase polymerase chain reaction and terminal deoxynucleotidyl transferase 2-deoxyuridine, 5-triphosph
42 Apoptotic cells were detected by terminal deoxynucleotidyl transferase catalyzed labeling of DNA f
43 s in the spleen, as measured by the terminal deoxynucleotidyl transferase deoxyuridine triphosphate n
44 hematoxylin and eosin staining, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
46 vioral changes were associated with terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
47 f DNA-fragmentation was detected by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
48 rations >1% (v/v), using annexin V, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
49 mmunosorbent assays and in liver by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
51 cells did not stain positively for terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
52 illibrand factor (vWF) staining and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
53 transferase dUTP nick end labeling terminal deoxynucleotidyl transferase dutp nick end labeling [TUN
54 l keratocytes (CD34), of apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling [TUN
55 ssays) and resistance to apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling and
56 ecombinants exhibited a decrease in terminal deoxynucleotidyl transferase dUTP nick end labeling and
57 nd eosin, periodic acid-Schiff) and terminal deoxynucleotidyl transferase dUTP nick end labeling assa
58 o lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labeling assa
59 y lactate dehydrogenase release and terminal deoxynucleotidyl transferase dUTP nick end labeling of t
61 Here, using biochemical techniques, terminal deoxynucleotidyl transferase dUTP nick end labeling stai
62 sed for viability and apoptosis via terminal deoxynucleotidyl transferase dUTP nick end labeling stai
63 elial growth factor A [VEGF-A], and terminal deoxynucleotidyl transferase dUTP nick end labeling term
65 ivity, chromatin fragmentation, and terminal deoxynucleotidyl transferase dUTP nick end labeling), an
66 5+/-4% versus 36+/-8%; P=0.004) and terminal deoxynucleotidyl transferase dUTP nick end labeling-posi
67 osis (caspase 3 activity and TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labeling])-po
68 dehydrogenase leakage), apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labelingc cel
69 associated with a lower density of terminal deoxynucleotidyl transferase dUTP nick end labelling (TU
71 ellular events as evidenced by both terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
74 ceptor degeneration was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
75 ture of Bruch's membrane, there was terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
76 poptotic cells were identified with terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
77 tion attenuated HIRI as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
79 able by cleaved caspase-3 staining, terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
80 Hepatic apoptosis was detected by a terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
81 f DNA breaks than the commonly used terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
82 pithelial apoptosis was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
83 le cells and endothelial cells were terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
84 hanolamine, decreased the number of terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
85 Caspase-3 cleavage/activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
87 serum alanine transaminase levels, terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
88 -P2X(7) cells as ascertained by the terminal deoxynucleotidyl transferase dUTP nick-end labeling tech
89 ntage of cell death, as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling, was
90 r, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
91 pase-3 activation and appearance of terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
92 increase in caspase-3 activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
93 xt day and analyzed by means of the terminal deoxynucleotidyl transferase dUTP-biotin nick-end-labeli
94 ye and retinas were analyzed by the terminal-deoxynucleotidyl transferase dUTP-linked nick end labeli
95 mistry, immunoblot analysis and the terminal-deoxynucleotidyl transferase dUTP-linked nick-end labeli
97 ced apoptosis, as determined by the terminal deoxynucleotidyl transferase mediated deoxyuridine triph
98 he decreased frequency of TUNEL(+) (terminal deoxynucleotidyl transferase mediated deoxyuridine triph
99 nsities were measured with Ki67 and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
100 romo-deoxyuridine incorporation and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
101 eling by propidium iodide staining; terminal deoxynucleotidyl transferase mediated dUTP nick end labe
102 se 3 activity and fluorescent-based terminal deoxynucleotidyl transferase mediated nick end labelling
105 anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling) analysis
106 caspase-3 immunohistochemistry, and terminal deoxynucleotidyl transferase UTP nick-end labeling (TUNE
107 is of heavily modified DNA, whereas terminal deoxynucleotidyl transferase was used for a single-nucle
108 receptor 7 alpha(+), c-kit(lo) and terminal deoxynucleotidyl transferase(+)) were selectively deplet
109 g laminin-5, MMPs, TGF beta, zyxin, terminal deoxynucleotidyl transferase, and angiogenesis-related p
110 olymerase mu (pol mu) is related to terminal deoxynucleotidyl transferase, but its biological role is
111 stained against a leukemic marker (terminal deoxynucleotidyl transferase, TdT), and we successfully
112 mplated (N) nucleotides inserted by terminal deoxynucleotidyl transferase, which resulted in a decrea
114 itive for cleaved caspase-3 and for terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
115 ng electron microscopy, and in situ terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
116 each parental genotype while TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated dUTP
117 caspase-cleaved tau, but no TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
118 ined by active caspase-3 and TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
119 osis were evidenced by increases in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
120 abain injection, maximal numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
122 cord ventral horn were positive for terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
123 ity was assessed by O4 staining and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
125 l growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
128 Purkinje cell loss was analyzed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
129 d that deltaV1-1 reduced numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
130 brain areas developed infarcts and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
131 from individual active caspase 3(+)/terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
132 ere was a 55.6% reduction in TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
133 NeuN)-immunoreactive cells are also terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
134 sed in neurons and colocalized with terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
139 s induced by KA were explored using terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
140 ces neuronal apoptosis, detected by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
141 is little cell death, as assayed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
142 eavage product appeared at 48 hr in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
144 ctivity for single-stranded DNA and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
145 ic effect of MT, as determined by a terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
146 aspase-9, and positive staining for terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
147 ed histone H3, activated caspase-3, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
148 ed by Ki67 immunohistochemistry and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
149 cytometry, electron microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
150 III immunocytochemical staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
151 sing bromodeoxyuridine staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
152 uantitated by nuclear morphology or terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
153 a 2-fold reduction in the number of terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
154 niques (hematoxylin-eosin staining, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
155 , the expression of Fas ligand, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
156 5), bromodeoxyuridine (p<0.05), and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
157 istology, immunohistochemistry, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
158 At 2 wk, hematoxylin-eosin and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
159 degradation that can be detected by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
160 tic necrosis and leads to pervasive terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
161 sitive cells, ganglion cells, and a terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
163 -activated cell sorter analysis and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
164 , DNA fragmentation, and apoptosis (terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
165 -2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
166 ma-counting, cleaved caspase-3, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
167 anol-induced apoptosis, assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
168 focal adhesion kinase and increased terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
169 stry, laser-capture microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
170 und at 4 h by DNA fragmentation and terminal deoxynucleotidyl transferase-mediated dUPT nick-end labe
171 ial cells (BAECs), as determined by terminal deoxynucleotidyl transferase-mediated dUTP biotin nick-e
172 , 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick and labe
173 e cleavage, Annexin V staining, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
174 taining for Ki-67 and cyclin D1 and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
176 , cardiac apoptosis was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
177 sed intratumoral apoptotic index by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
178 o)benzene sulfonic acid) and TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
179 tosis indicated by nuclear changes, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
181 n of piriform cortex, on apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
182 dol and reduced haloperidol induced terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
183 observed with the use of either the terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
184 ld type protein had very low TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
185 sis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
186 t resulted in a marked reduction in terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
187 ings its expression correlated with terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
188 ld) and HA expression but increased terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
189 of apoptosis, as measured by TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
190 nificantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
191 ADP-ribose) polymerase cleavage and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
192 rons in heart failure, we performed terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
193 frequency of intrahepatic apoptotic terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
194 alyzed for apoptotic nuclei using a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
195 omo-2'-dUTP incorporation assay and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
198 caspase-activated DNase levels, and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
199 nsferase (ALT), caspase-3 activity, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
200 ly, the number of diabetes-enhanced terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
201 se-induced apoptosis as measured by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
202 and less contraction band necrosis, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
203 ice displayed a 13-fold increase in terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
204 -increased activated caspase-3- and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
205 s hepatic cell death as assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
206 l apoptotic cells in Drosophila are terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
207 e uptake, and apoptotic cell death (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
208 s in the diaphragm (e.g., number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
209 ptosis was assessed with the use of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
210 y, as well as apoptosis detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
211 ion of apoptosis as revealed by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
212 s within the retina was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
214 nstrated by positive staining using terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
215 d retinal apoptosis as shown by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
216 less apoptosis as measured by both terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
218 scent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
219 analysis, immunocytochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
220 8-72 h, marked by nuclear blebbing, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
221 cell death occurred as detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
222 on factor 2 alpha), and cell death [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
223 area that also showed more positive terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
224 occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
226 size, reduced Ki-67, and increased terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
227 ologic damage, cytokine expression, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
228 [BrdU]) and cell death (caspase-3, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
229 helial markers CD31 and VEGFR-2 and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
230 AR(-/-) mice had significantly more terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
232 e by Western blot, and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
234 orneas, whereas it colocalized with terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
235 chamber assay), and antiapoptotic (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
236 the culture plate over time, became terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
237 cription polymerase chain reaction, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
240 se, sclerostin immunochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nickend label
241 aused DNA degradation as evident by terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
242 Apoptosis was assessed by using terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
243 ate dehydrogenase release assay and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
244 caspases 3 and 8, and the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
245 n vitro at 72 hours (P < 0.05), and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
247 LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
248 ell death were investigated by MTT, terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
249 ned, and evaluated for apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
250 tive (Ac)-caspase-3, -8, and -9 and terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
251 termined by Hoechst 33342 staining, terminal deoxynucleotidyl transferase-mediated dUTP-FITC nick end
252 ained for interleukin (IL)-12 or by terminal deoxynucleotidyl transferase-mediated dUTP-nick end labe
253 and protected against diabetes, and terminal deoxynucleotidyl transferase-mediated nick end labeling
255 ted levels of apoptosis observed by terminal deoxynucleotidyl transferase-mediated nick end labeling
256 indicated by caspase-3 activity and terminal deoxynucleotidyl transferase-mediated nick end labeling
257 using flow cytometric Annexin V and terminal deoxynucleotidyl transferase-mediated nick end labeling
258 t did not involve apoptosis because terminal deoxynucleotidyl transferase-mediated nick end labeling
260 revealed by caspase activation and terminal deoxynucleotidyl transferase-mediated nick end labeling
261 rouracil (5-FU), induced apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
262 cells were apoptotic as judged by a terminal deoxynucleotidyl transferase-mediated nick end labeling
266 atine kinase release) or apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
267 and apoptosis was evaluated by the terminal deoxynucleotidyl transferase-mediated nick end labeling
268 OX-42, gamma-aminobutyric acid, or terminal deoxynucleotidyl transferase-mediated nick end labeling
269 d tumor cell apoptosis (assessed by terminal deoxynucleotidyl transferase-mediated nick end labeling)
270 SK-RC-45 line stimulated the TUNEL (terminal deoxynucleotidyl transferase-mediated nick end labeling)
271 luorescence-activated cell sorting, terminal deoxynucleotidyl transferase-mediated nick end labeling,
273 tion, and a significant increase in terminal deoxynucleotidyl transferase-mediated nick end labeling-
274 mitochondria to the cytoplasm, and terminal deoxynucleotidyl transferase-mediated nick end labeling.
277 s was also noted in PiZ BDL mice by terminal deoxynucleotidyl transferase-mediated nick-end labeling
278 re employed in cells resistant (<5% terminal deoxynucleotidyl transferase-mediated nick-end labeling
279 notransferase (ALT), pathology, and terminal deoxynucleotidyl transferase-mediated nick-end labeling
280 in the apoptosis rate was observed (terminal deoxynucleotidyl transferase-mediated nick-end labeling
281 arvested and assayed for apoptosis (terminal deoxynucleotidyl transferase-mediated nick-end labeling)
282 s, as shown by increased numbers of terminal deoxynucleotidyl transferase-mediated nick-end labeling-
283 DNA fragmentation was evaluated by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
284 tochrome c immunohistochemistry and terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
285 Neuronal cell death was examined by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
286 expression was induced primarily in terminal deoxynucleotidyl transferase-mediated UTP nick-end label
292 onverted to double-stranded-DNA via terminal-deoxynucleotidyl-transferase (TdT) prior to initiation o
293 Apoptosis was evaluated by in situ terminal deoxynucleotidyl-transferase mediated dUTP nick end labe
294 findings, flow cytometry and TUNEL (terminal deoxynucleotidyl-transferase-mediated dUTP nick end labe
295 endothelial cells as determined by terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
297 were studied by routine microscopy, terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
298 liferating cell nuclear antigen and terminal deoxynucleotidyl-transferase-mediated dUTP nick-end stai
299 y (IHC), degree of apoptosis by the terminal deoxynucleotidyl transferasemediated dUTP nick-end label