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1 e T-cell markers CD2, CD3, CD4, and terminal deoxynucleotidyl transferase.
2 s surprisingly more proficient than terminal deoxynucleotidyl transferase.
3 3' end of the first-strand cDNAs by terminal deoxynucleotidyl transferase.
4 (P=0.004), suggesting formation by terminal deoxynucleotidyl transferase.
5 ceptors CD4 and CD8, and the enzyme terminal deoxynucleotidyl transferase.
6 ptase polymerase chain reaction and terminal deoxynucleotidyl transferase 2-deoxyuridine, 5-triphosph
8 g laminin-5, MMPs, TGF beta, zyxin, terminal deoxynucleotidyl transferase, and angiogenesis-related p
9 dUTP nick end-labeling mediated by terminal deoxynucleotidyl transferase, associated with a robust i
12 olymerase mu (pol mu) is related to terminal deoxynucleotidyl transferase, but its biological role is
13 Apoptotic cells were detected by terminal deoxynucleotidyl transferase catalyzed labeling of DNA f
15 s in the spleen, as measured by the terminal deoxynucleotidyl transferase deoxyuridine triphosphate n
17 hematoxylin and eosin staining, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
18 f DNA-fragmentation was detected by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
19 rations >1% (v/v), using annexin V, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
20 mmunosorbent assays and in liver by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
22 cells did not stain positively for terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
23 illibrand factor (vWF) staining and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
24 vioral changes were associated with terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
25 l keratocytes (CD34), of apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling [TUN
26 ssays) and resistance to apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling and
27 ecombinants exhibited a decrease in terminal deoxynucleotidyl transferase dUTP nick end labeling and
28 o lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labeling assa
29 y lactate dehydrogenase release and terminal deoxynucleotidyl transferase dUTP nick end labeling of t
31 sed for viability and apoptosis via terminal deoxynucleotidyl transferase dUTP nick end labeling stai
33 ivity, chromatin fragmentation, and terminal deoxynucleotidyl transferase dUTP nick end labeling), an
34 5+/-4% versus 36+/-8%; P=0.004) and terminal deoxynucleotidyl transferase dUTP nick end labeling-posi
35 osis (caspase 3 activity and TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labeling])-po
36 dehydrogenase leakage), apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labelingc cel
37 ture of Bruch's membrane, there was terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
38 poptotic cells were identified with terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
40 1 month after MI, the frequency of terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
41 tion attenuated HIRI as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
45 ceptor degeneration was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
46 able by cleaved caspase-3 staining, terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
47 Hepatic apoptosis was detected by a terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
48 pithelial apoptosis was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
49 membrane permeability and blebbing, terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
50 le cells and endothelial cells were terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
51 Caspase-3 cleavage/activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
53 serum alanine transaminase levels, terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
54 -P2X(7) cells as ascertained by the terminal deoxynucleotidyl transferase dUTP nick-end labeling tech
55 ntage of cell death, as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling, was
56 r, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
57 pase-3 activation and appearance of terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
58 increase in caspase-3 activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
59 xt day and analyzed by means of the terminal deoxynucleotidyl transferase dUTP-biotin nick-end-labeli
60 ye and retinas were analyzed by the terminal-deoxynucleotidyl transferase dUTP-linked nick end labeli
61 mistry, immunoblot analysis and the terminal-deoxynucleotidyl transferase dUTP-linked nick-end labeli
62 Apoptosis was determined by the terminal deoxynucleotidyl- transferase-dUTP nick-end labeling ass
64 he decreased frequency of TUNEL(+) (terminal deoxynucleotidyl transferase mediated deoxyuridine triph
65 romo-deoxyuridine incorporation and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
66 eling by propidium iodide staining; terminal deoxynucleotidyl transferase mediated dUTP nick end labe
67 nsities were measured with Ki67 and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
68 se 3 activity and fluorescent-based terminal deoxynucleotidyl transferase mediated nick end labelling
69 Apoptosis was evaluated by in situ terminal deoxynucleotidyl-transferase mediated dUTP nick end labe
70 itive for cleaved caspase-3 and for terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
71 ng electron microscopy, and in situ terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
72 each parental genotype while TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated dUTP
73 osis were evidenced by increases in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
74 abain injection, maximal numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
76 cord ventral horn were positive for terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
77 ity was assessed by O4 staining and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
79 l growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
82 Purkinje cell loss was analyzed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
83 d that deltaV1-1 reduced numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
84 brain areas developed infarcts and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
85 from individual active caspase 3(+)/terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
86 ere was a 55.6% reduction in TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
87 NeuN)-immunoreactive cells are also terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
88 sed in neurons and colocalized with terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
93 s induced by KA were explored using terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
94 ces neuronal apoptosis, detected by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
95 is little cell death, as assayed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
96 eavage product appeared at 48 hr in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
98 ctivity for single-stranded DNA and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
99 caspase-cleaved tau, but no TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
100 ined by active caspase-3 and TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
101 ic effect of MT, as determined by a terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
102 aspase-9, and positive staining for terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
103 cytometry, electron microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
104 III immunocytochemical staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
105 sing bromodeoxyuridine staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
106 ma-counting, cleaved caspase-3, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
107 uantitated by nuclear morphology or terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
108 a 2-fold reduction in the number of terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
109 niques (hematoxylin-eosin staining, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
110 , the expression of Fas ligand, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
111 5), bromodeoxyuridine (p<0.05), and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
112 istology, immunohistochemistry, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
113 At 2 wk, hematoxylin-eosin and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
114 degradation that can be detected by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
115 tic necrosis and leads to pervasive terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
116 sitive cells, ganglion cells, and a terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
118 -activated cell sorter analysis and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
119 , DNA fragmentation, and apoptosis (terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
120 anol-induced apoptosis, assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
121 -2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
122 sensory-deprived rat olfactory bulb terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
123 hods: light microscopy, fluorescent terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
125 focal adhesion kinase and increased terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
126 stry, laser-capture microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
127 ed histone H3, activated caspase-3, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
128 ed by Ki67 immunohistochemistry and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
130 on of apoptosis, assessed by TUNEL (terminal deoxynucleotidyl transferase-mediated dNTP-biotin nick e
131 und at 4 h by DNA fragmentation and terminal deoxynucleotidyl transferase-mediated dUPT nick-end labe
132 ial cells (BAECs), as determined by terminal deoxynucleotidyl transferase-mediated dUTP biotin nick-e
133 , 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick and labe
134 e cleavage, Annexin V staining, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
135 taining for Ki-67 and cyclin D1 and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
137 , cardiac apoptosis was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
138 sed intratumoral apoptotic index by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
139 o)benzene sulfonic acid) and TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
140 tosis indicated by nuclear changes, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
142 sis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
143 n of piriform cortex, on apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
144 dol and reduced haloperidol induced terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
145 observed with the use of either the terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
146 ld type protein had very low TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
147 ase, ii) DNA ladder formation, iii) terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
148 t resulted in a marked reduction in terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
149 in-dATP nick translation (PANT) and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
150 on cells as assessed by morphology, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
151 stration resulted in an increase in terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
152 ings its expression correlated with terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
153 ld) and HA expression but increased terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
154 of apoptosis, as measured by TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
155 nificantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
156 ADP-ribose) polymerase cleavage and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
157 frequency of intrahepatic apoptotic terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
158 alyzed for apoptotic nuclei using a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
159 caspase-activated DNase levels, and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
160 omo-2'-dUTP incorporation assay and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
164 rons in heart failure, we performed terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
165 occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
166 l apoptotic cells in Drosophila are terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
167 e uptake, and apoptotic cell death (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
168 ologic damage, cytokine expression, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
169 s in the diaphragm (e.g., number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
170 ptosis was assessed with the use of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
171 y, as well as apoptosis detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
172 ion of apoptosis as revealed by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
173 s within the retina was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
175 nstrated by positive staining using terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
176 less apoptosis as measured by both terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
178 scent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
179 analysis, immunocytochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
180 [BrdU]) and cell death (caspase-3, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
181 8-72 h, marked by nuclear blebbing, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
182 cell death occurred as detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
183 on factor 2 alpha), and cell death [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
184 area that also showed more positive terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
187 by hematoxylin and eosin staining, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
188 eocytes/periosteal osteoblasts with terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
189 size, reduced Ki-67, and increased terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
190 helial markers CD31 and VEGFR-2 and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
191 AR(-/-) mice had significantly more terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
193 e by Western blot, and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
195 orneas, whereas it colocalized with terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
196 chamber assay), and antiapoptotic (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
197 the culture plate over time, became terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
198 cription polymerase chain reaction, 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
207 entation, measured by the number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end-labe
208 Apoptosis was assessed by using terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
209 aused DNA degradation as evident by terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
210 LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
211 ate dehydrogenase release assay and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
212 caspases 3 and 8, and the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
213 n vitro at 72 hours (P < 0.05), and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
216 ell death were investigated by MTT, terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
217 ned, and evaluated for apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
218 tive (Ac)-caspase-3, -8, and -9 and terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
219 termined by Hoechst 33342 staining, terminal deoxynucleotidyl transferase-mediated dUTP-FITC nick end
220 ained for interleukin (IL)-12 or by terminal deoxynucleotidyl transferase-mediated dUTP-nick end labe
222 ted levels of apoptosis observed by terminal deoxynucleotidyl transferase-mediated nick end labeling
223 indicated by caspase-3 activity and terminal deoxynucleotidyl transferase-mediated nick end labeling
224 using flow cytometric Annexin V and terminal deoxynucleotidyl transferase-mediated nick end labeling
225 t did not involve apoptosis because terminal deoxynucleotidyl transferase-mediated nick end labeling
227 revealed by caspase activation and terminal deoxynucleotidyl transferase-mediated nick end labeling
228 rouracil (5-FU), induced apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
229 cells were apoptotic as judged by a terminal deoxynucleotidyl transferase-mediated nick end labeling
233 atine kinase release) or apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
234 and apoptosis was evaluated by the terminal deoxynucleotidyl transferase-mediated nick end labeling
235 OX-42, gamma-aminobutyric acid, or terminal deoxynucleotidyl transferase-mediated nick end labeling
236 s as measured by flow cytometry and terminal deoxynucleotidyl transferase-mediated nick end labeling
237 histochemical double labeling with terminal deoxynucleotidyl transferase-mediated nick end labeling
238 ors were apoptotic as determined by terminal deoxynucleotidyl transferase-mediated nick end labeling
240 and protected against diabetes, and terminal deoxynucleotidyl transferase-mediated nick end labeling
241 d tumor cell apoptosis (assessed by terminal deoxynucleotidyl transferase-mediated nick end labeling)
242 SK-RC-45 line stimulated the TUNEL (terminal deoxynucleotidyl transferase-mediated nick end labeling)
243 luorescence-activated cell sorting, terminal deoxynucleotidyl transferase-mediated nick end labeling,
246 tion, and a significant increase in terminal deoxynucleotidyl transferase-mediated nick end labeling-
247 mitochondria to the cytoplasm, and terminal deoxynucleotidyl transferase-mediated nick end labeling.
249 s was also noted in PiZ BDL mice by terminal deoxynucleotidyl transferase-mediated nick-end labeling
250 re employed in cells resistant (<5% terminal deoxynucleotidyl transferase-mediated nick-end labeling
251 notransferase (ALT), pathology, and terminal deoxynucleotidyl transferase-mediated nick-end labeling
252 in the apoptosis rate was observed (terminal deoxynucleotidyl transferase-mediated nick-end labeling
254 arvested and assayed for apoptosis (terminal deoxynucleotidyl transferase-mediated nick-end labeling)
255 s, as shown by increased numbers of terminal deoxynucleotidyl transferase-mediated nick-end labeling-
256 DNA fragmentation was evaluated by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
257 tochrome c immunohistochemistry and terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
258 Neuronal cell death was examined by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
259 was observed with the appearance of terminal deoxynucleotidyl transferase-mediated UTP end labeling r
260 hematoxylin and eosin-stained, and terminal deoxynucleotidyl transferase-mediated UTP nick end-label
261 expression was induced primarily in terminal deoxynucleotidyl transferase-mediated UTP nick-end label
262 findings, flow cytometry and TUNEL (terminal deoxynucleotidyl-transferase-mediated dUTP nick end labe
263 were studied by routine microscopy, terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
264 endothelial cells as determined by terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
266 liferating cell nuclear antigen and terminal deoxynucleotidyl-transferase-mediated dUTP nick-end stai
269 anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling) analysis
270 , and a significant proportion were terminal deoxynucleotidyl transferase (TdT) -mediated deoxyuridin
271 g (V[D]J) recombination, the enzyme terminal deoxynucleotidyl transferase (Tdt) adds random nucleotid
272 B cell progenitors fail to express terminal deoxynucleotidyl transferase (TdT) and for other reasons
274 rtoires due to the delayed onset of terminal deoxynucleotidyl transferase (TdT) expression in ontogen
275 hat mice expressing a transgene for terminal deoxynucleotidyl transferase (TdT) have nucleotide inser
276 mplate independent polymerases, and terminal deoxynucleotidyl transferase (TdT) in particular, have b
277 -OH of an RNA molecule, followed by terminal deoxynucleotidyl transferase (TdT) to catalyze the seque
278 6C(-) Thy-1(-)CD43(+) CD16/32(Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in murine bo
279 rrow (BM) chimeras, made with adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) don
281 le stranded DNA (ssDNA) chain using terminal deoxynucleotidyl transferase (TdT), a template-independe
283 ovium, we also sought expression of terminal deoxynucleotidyl transferase (TdT), which is normally ex
284 d (N) nucleotides is carried out by terminal deoxynucleotidyl transferase (TdT), whose only known phy
286 h HA were examined for apoptosis in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP biotin
287 ive to WT animals, as documented by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
288 y, we compared these tests with the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
296 The short splice variant of mouse terminal deoxynucleotidyl transferase (TdTS) catalyzes the additi
297 caspase-3 immunohistochemistry, and terminal deoxynucleotidyl transferase UTP nick-end labeling (TUNE
298 is of heavily modified DNA, whereas terminal deoxynucleotidyl transferase was used for a single-nucle
299 receptor 7 alpha(+), c-kit(lo) and terminal deoxynucleotidyl transferase(+)) were selectively deplet
300 mplated (N) nucleotides inserted by terminal deoxynucleotidyl transferase, which resulted in a decrea
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