コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 (P=0.004), suggesting formation by terminal deoxynucleotidyl transferase.
2 ceptors CD4 and CD8, and the enzyme terminal deoxynucleotidyl transferase.
3 e T-cell markers CD2, CD3, CD4, and terminal deoxynucleotidyl transferase.
4 s surprisingly more proficient than terminal deoxynucleotidyl transferase.
5 3' end of the first-strand cDNAs by terminal deoxynucleotidyl transferase.
6 ular necrosis scores and degrees of terminal deoxynucleotidyl transferase 2'-deoxyuridine, 5'-triphos
8 ptase polymerase chain reaction and terminal deoxynucleotidyl transferase 2-deoxyuridine, 5-triphosph
10 g laminin-5, MMPs, TGF beta, zyxin, terminal deoxynucleotidyl transferase, and angiogenesis-related p
13 olymerase mu (pol mu) is related to terminal deoxynucleotidyl transferase, but its biological role is
14 Apoptotic cells were detected by terminal deoxynucleotidyl transferase catalyzed labeling of DNA f
16 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
19 vioral changes were associated with terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
20 f DNA-fragmentation was detected by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
21 rations >1% (v/v), using annexin V, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
22 mmunosorbent assays and in liver by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
24 cells did not stain positively for terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
25 illibrand factor (vWF) staining and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
26 transferase dUTP nick end labeling terminal deoxynucleotidyl transferase dutp nick end labeling [TUN
27 l keratocytes (CD34), of apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling [TUN
28 ssays) and resistance to apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling and
29 ecombinants exhibited a decrease in terminal deoxynucleotidyl transferase dUTP nick end labeling and
30 nd eosin, periodic acid-Schiff) and terminal deoxynucleotidyl transferase dUTP nick end labeling assa
31 o lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labeling assa
32 y lactate dehydrogenase release and terminal deoxynucleotidyl transferase dUTP nick end labeling of t
34 Here, using biochemical techniques, terminal deoxynucleotidyl transferase dUTP nick end labeling stai
35 sed for viability and apoptosis via terminal deoxynucleotidyl transferase dUTP nick end labeling stai
36 elial growth factor A [VEGF-A], and terminal deoxynucleotidyl transferase dUTP nick end labeling term
38 ivity, chromatin fragmentation, and terminal deoxynucleotidyl transferase dUTP nick end labeling), an
39 5+/-4% versus 36+/-8%; P=0.004) and terminal deoxynucleotidyl transferase dUTP nick end labeling-posi
40 osis (caspase 3 activity and TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labeling])-po
41 dehydrogenase leakage), apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labelingc cel
42 associated with a lower density of terminal deoxynucleotidyl transferase dUTP nick end labelling (TU
44 ellular events as evidenced by both terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
47 ceptor degeneration was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
48 ture of Bruch's membrane, there was terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
49 poptotic cells were identified with terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
50 tion attenuated HIRI as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
52 able by cleaved caspase-3 staining, terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
53 Hepatic apoptosis was detected by a terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
54 f DNA breaks than the commonly used terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
55 pithelial apoptosis was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
56 le cells and endothelial cells were terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
57 hanolamine, decreased the number of terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
58 Caspase-3 cleavage/activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
60 serum alanine transaminase levels, terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
61 -P2X(7) cells as ascertained by the terminal deoxynucleotidyl transferase dUTP nick-end labeling tech
62 ntage of cell death, as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling, was
63 r, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
64 pase-3 activation and appearance of terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
65 increase in caspase-3 activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
66 xt day and analyzed by means of the terminal deoxynucleotidyl transferase dUTP-biotin nick-end-labeli
67 ye and retinas were analyzed by the terminal-deoxynucleotidyl transferase dUTP-linked nick end labeli
68 mistry, immunoblot analysis and the terminal-deoxynucleotidyl transferase dUTP-linked nick-end labeli
70 ced apoptosis, as determined by the terminal deoxynucleotidyl transferase mediated deoxyuridine triph
71 he decreased frequency of TUNEL(+) (terminal deoxynucleotidyl transferase mediated deoxyuridine triph
72 nsities were measured with Ki67 and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
73 romo-deoxyuridine incorporation and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
74 eling by propidium iodide staining; terminal deoxynucleotidyl transferase mediated dUTP nick end labe
75 se 3 activity and fluorescent-based terminal deoxynucleotidyl transferase mediated nick end labelling
76 Apoptosis was evaluated by in situ terminal deoxynucleotidyl-transferase mediated dUTP nick end labe
77 itive for cleaved caspase-3 and for terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
78 ng electron microscopy, and in situ terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
79 each parental genotype while TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated dUTP
80 caspase-cleaved tau, but no TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
81 ined by active caspase-3 and TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
82 osis were evidenced by increases in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
83 abain injection, maximal numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
85 cord ventral horn were positive for terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
86 ity was assessed by O4 staining and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
88 l growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
91 Purkinje cell loss was analyzed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
92 d that deltaV1-1 reduced numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
93 brain areas developed infarcts and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
94 from individual active caspase 3(+)/terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
95 ere was a 55.6% reduction in TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
96 NeuN)-immunoreactive cells are also terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
97 sed in neurons and colocalized with terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
102 s induced by KA were explored using terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
103 ces neuronal apoptosis, detected by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
104 is little cell death, as assayed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
105 eavage product appeared at 48 hr in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
107 ctivity for single-stranded DNA and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
108 ic effect of MT, as determined by a terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
109 aspase-9, and positive staining for terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
110 ed histone H3, activated caspase-3, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
111 ed by Ki67 immunohistochemistry and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
112 cytometry, electron microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
113 III immunocytochemical staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
114 sing bromodeoxyuridine staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
115 uantitated by nuclear morphology or terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
116 a 2-fold reduction in the number of terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
117 niques (hematoxylin-eosin staining, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
118 , the expression of Fas ligand, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
119 5), bromodeoxyuridine (p<0.05), and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
120 istology, immunohistochemistry, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
121 At 2 wk, hematoxylin-eosin and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
122 degradation that can be detected by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
123 tic necrosis and leads to pervasive terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
124 sitive cells, ganglion cells, and a terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
126 -activated cell sorter analysis and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
127 , DNA fragmentation, and apoptosis (terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
128 -2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
129 ma-counting, cleaved caspase-3, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
130 anol-induced apoptosis, assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
131 focal adhesion kinase and increased terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
132 stry, laser-capture microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
133 und at 4 h by DNA fragmentation and terminal deoxynucleotidyl transferase-mediated dUPT nick-end labe
134 ial cells (BAECs), as determined by terminal deoxynucleotidyl transferase-mediated dUTP biotin nick-e
135 , 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick and labe
136 e cleavage, Annexin V staining, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
137 taining for Ki-67 and cyclin D1 and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
139 , cardiac apoptosis was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
140 sed intratumoral apoptotic index by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
141 o)benzene sulfonic acid) and TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
142 tosis indicated by nuclear changes, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
144 n of piriform cortex, on apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
145 dol and reduced haloperidol induced terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
146 observed with the use of either the terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
147 ld type protein had very low TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
148 sis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
149 t resulted in a marked reduction in terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
150 ings its expression correlated with terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
151 ld) and HA expression but increased terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
152 of apoptosis, as measured by TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
153 nificantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
154 ADP-ribose) polymerase cleavage and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
155 rons in heart failure, we performed terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
156 frequency of intrahepatic apoptotic terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
157 alyzed for apoptotic nuclei using a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
158 omo-2'-dUTP incorporation assay and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
161 caspase-activated DNase levels, and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
162 ly, the number of diabetes-enhanced terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
163 se-induced apoptosis as measured by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
164 s hepatic cell death as assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
165 and less contraction band necrosis, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
166 ice displayed a 13-fold increase in terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
167 -increased activated caspase-3- and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
168 l apoptotic cells in Drosophila are terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
169 e uptake, and apoptotic cell death (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
170 s in the diaphragm (e.g., number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
171 ptosis was assessed with the use of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
172 y, as well as apoptosis detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
173 ion of apoptosis as revealed by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
174 s within the retina was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
176 nstrated by positive staining using terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
177 less apoptosis as measured by both terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
178 d retinal apoptosis as shown by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
180 scent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
181 analysis, immunocytochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
182 8-72 h, marked by nuclear blebbing, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
183 cell death occurred as detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
184 occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
185 on factor 2 alpha), and cell death [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
186 area that also showed more positive terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
189 by hematoxylin and eosin staining, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
190 size, reduced Ki-67, and increased terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
191 ologic damage, cytokine expression, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
192 [BrdU]) and cell death (caspase-3, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
193 helial markers CD31 and VEGFR-2 and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
194 AR(-/-) mice had significantly more terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
196 e by Western blot, and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
198 orneas, whereas it colocalized with terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
199 chamber assay), and antiapoptotic (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
200 the culture plate over time, became terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
201 cription polymerase chain reaction, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
202 nsferase (ALT), caspase-3 activity, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
205 se, sclerostin immunochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nickend label
206 aused DNA degradation as evident by terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
207 Apoptosis was assessed by using terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
208 ate dehydrogenase release assay and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
209 caspases 3 and 8, and the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
210 n vitro at 72 hours (P < 0.05), and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
211 LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
213 ell death were investigated by MTT, terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
214 ned, and evaluated for apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
215 tive (Ac)-caspase-3, -8, and -9 and terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
216 termined by Hoechst 33342 staining, terminal deoxynucleotidyl transferase-mediated dUTP-FITC nick end
217 ained for interleukin (IL)-12 or by terminal deoxynucleotidyl transferase-mediated dUTP-nick end labe
218 and protected against diabetes, and terminal deoxynucleotidyl transferase-mediated nick end labeling
220 ted levels of apoptosis observed by terminal deoxynucleotidyl transferase-mediated nick end labeling
221 indicated by caspase-3 activity and terminal deoxynucleotidyl transferase-mediated nick end labeling
222 using flow cytometric Annexin V and terminal deoxynucleotidyl transferase-mediated nick end labeling
223 t did not involve apoptosis because terminal deoxynucleotidyl transferase-mediated nick end labeling
225 revealed by caspase activation and terminal deoxynucleotidyl transferase-mediated nick end labeling
226 rouracil (5-FU), induced apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
227 cells were apoptotic as judged by a terminal deoxynucleotidyl transferase-mediated nick end labeling
231 atine kinase release) or apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
232 and apoptosis was evaluated by the terminal deoxynucleotidyl transferase-mediated nick end labeling
233 OX-42, gamma-aminobutyric acid, or terminal deoxynucleotidyl transferase-mediated nick end labeling
234 d tumor cell apoptosis (assessed by terminal deoxynucleotidyl transferase-mediated nick end labeling)
235 SK-RC-45 line stimulated the TUNEL (terminal deoxynucleotidyl transferase-mediated nick end labeling)
236 luorescence-activated cell sorting, terminal deoxynucleotidyl transferase-mediated nick end labeling,
238 tion, and a significant increase in terminal deoxynucleotidyl transferase-mediated nick end labeling-
239 mitochondria to the cytoplasm, and terminal deoxynucleotidyl transferase-mediated nick end labeling.
242 s was also noted in PiZ BDL mice by terminal deoxynucleotidyl transferase-mediated nick-end labeling
243 re employed in cells resistant (<5% terminal deoxynucleotidyl transferase-mediated nick-end labeling
244 notransferase (ALT), pathology, and terminal deoxynucleotidyl transferase-mediated nick-end labeling
245 in the apoptosis rate was observed (terminal deoxynucleotidyl transferase-mediated nick-end labeling
246 arvested and assayed for apoptosis (terminal deoxynucleotidyl transferase-mediated nick-end labeling)
247 s, as shown by increased numbers of terminal deoxynucleotidyl transferase-mediated nick-end labeling-
248 DNA fragmentation was evaluated by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
249 tochrome c immunohistochemistry and terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
250 Neuronal cell death was examined by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
251 expression was induced primarily in terminal deoxynucleotidyl transferase-mediated UTP nick-end label
252 findings, flow cytometry and TUNEL (terminal deoxynucleotidyl-transferase-mediated dUTP nick end labe
253 endothelial cells as determined by terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
255 were studied by routine microscopy, terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
256 liferating cell nuclear antigen and terminal deoxynucleotidyl-transferase-mediated dUTP nick-end stai
259 anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling) analysis
260 , and a significant proportion were terminal deoxynucleotidyl transferase (TdT) -mediated deoxyuridin
261 g (V[D]J) recombination, the enzyme terminal deoxynucleotidyl transferase (Tdt) adds random nucleotid
262 B cell progenitors fail to express terminal deoxynucleotidyl transferase (TdT) and for other reasons
263 is based on exonuclease I (Exo I), terminal deoxynucleotidyl transferase (TdT) and methylene blue.
265 X family members such as Pol mu and terminal deoxynucleotidyl transferase (TdT) are important compone
266 rtoires due to the delayed onset of terminal deoxynucleotidyl transferase (TdT) expression in ontogen
267 ons by patterned UV light activates Terminal deoxynucleotidyl Transferase (TdT) for spatially-selecti
268 hat mice expressing a transgene for terminal deoxynucleotidyl transferase (TdT) have nucleotide inser
269 the template-independent polymerase terminal deoxynucleotidyl transferase (TdT) in kinetically contro
270 mplate independent polymerases, and terminal deoxynucleotidyl transferase (TdT) in particular, have b
273 -OH of an RNA molecule, followed by terminal deoxynucleotidyl transferase (TdT) to catalyze the seque
274 6C(-) Thy-1(-)CD43(+) CD16/32(Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in murine bo
275 rrow (BM) chimeras, made with adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) don
277 le stranded DNA (ssDNA) chain using terminal deoxynucleotidyl transferase (TdT), a template-independe
279 ovium, we also sought expression of terminal deoxynucleotidyl transferase (TdT), which is normally ex
280 d (N) nucleotides is carried out by terminal deoxynucleotidyl transferase (TdT), whose only known phy
281 h HA were examined for apoptosis in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP biotin
282 ive to WT animals, as documented by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
283 y, we compared these tests with the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
293 onverted to double-stranded-DNA via terminal-deoxynucleotidyl-transferase (TdT) prior to initiation o
295 stained against a leukemic marker (terminal deoxynucleotidyl transferase, TdT), and we successfully
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