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 junctions (P=0.004), suggesting formation by terminal deoxynucleotidyl transferase.
2 cell coreceptors CD4 and CD8, and the enzyme terminal deoxynucleotidyl transferase.
3 ressed the T-cell markers CD2, CD3, CD4, and terminal deoxynucleotidyl transferase.
4 us, and is surprisingly more proficient than terminal deoxynucleotidyl transferase.
5 d to the 3' end of the first-strand cDNAs by terminal deoxynucleotidyl transferase.
6 acute tubular necrosis scores and degrees of terminal deoxynucleotidyl transferase 2'-deoxyuridine, 5
8 transcriptase polymerase chain reaction and terminal deoxynucleotidyl transferase 2-deoxyuridine, 5-
10 (including laminin-5, MMPs, TGF beta, zyxin, terminal deoxynucleotidyl transferase, and angiogenesis-
13 ian DNA polymerase mu (pol mu) is related to terminal deoxynucleotidyl transferase, but its biologica
16 apoptosis in the spleen, as measured by the terminal deoxynucleotidyl transferase deoxyuridine triph
17 toxylin and eosin, periodic acid-Schiff) and terminal deoxynucleotidyl transferase dUTP nick end labe
19 ar endothelial growth factor A [VEGF-A], and terminal deoxynucleotidyl transferase dUTP nick end labe
20 cleotidyl transferase dUTP nick end labeling terminal deoxynucleotidyl transferase dutp nick end labe
21 taining, hematoxylin and eosin staining, and terminal deoxynucleotidyl transferase dUTP nick end labe
24 tly assessed for viability and apoptosis via terminal deoxynucleotidyl transferase dUTP nick end labe
25 hese behavioral changes were associated with terminal deoxynucleotidyl transferase dUTP nick end labe
26 ter apoptosis (caspase 3 activity and TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labe
27 umbra was associated with a lower density of terminal deoxynucleotidyl transferase dUTP nick end labe
28 ng in vivo lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labe
29 earance of DNA-fragmentation was detected by terminal deoxynucleotidyl transferase dUTP nick end labe
30 nd WST1 assays) and resistance to apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labe
31 O concentrations >1% (v/v), using annexin V, terminal deoxynucleotidyl transferase dUTP nick end labe
32 of stromal keratocytes (CD34), of apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labe
33 -linked immunosorbent assays and in liver by terminal deoxynucleotidyl transferase dUTP nick end labe
35 (lactate dehydrogenase leakage), apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labe
36 easured by lactate dehydrogenase release and terminal deoxynucleotidyl transferase dUTP nick end labe
38 ly, dying cells did not stain positively for terminal deoxynucleotidyl transferase dUTP nick end labe
39 se F(N) recombinants exhibited a decrease in terminal deoxynucleotidyl transferase dUTP nick end labe
40 erase activity, chromatin fragmentation, and terminal deoxynucleotidyl transferase dUTP nick end labe
41 t risk (15+/-4% versus 36+/-8%; P=0.004) and terminal deoxynucleotidyl transferase dUTP nick end labe
42 and von Willibrand factor (vWF) staining and terminal deoxynucleotidyl transferase dUTP nick end labe
44 optotic cellular events as evidenced by both terminal deoxynucleotidyl transferase dUTP nick-end labe
46 ooth muscle cells and endothelial cells were terminal deoxynucleotidyl transferase dUTP nick-end labe
48 d photoreceptor degeneration was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labe
49 However, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labe
50 ly detectable by cleaved caspase-3 staining, terminal deoxynucleotidyl transferase dUTP nick-end labe
51 after rupture of Bruch's membrane, there was terminal deoxynucleotidyl transferase dUTP nick-end labe
52 eased caspase-3 activation and appearance of terminal deoxynucleotidyl transferase dUTP nick-end labe
53 ed, and apoptotic cells were identified with terminal deoxynucleotidyl transferase dUTP nick-end labe
54 totic HEK-P2X(7) cells as ascertained by the terminal deoxynucleotidyl transferase dUTP nick-end labe
55 hatidylethanolamine, decreased the number of terminal deoxynucleotidyl transferase dUTP nick-end labe
57 accumulation attenuated HIRI as measured by terminal deoxynucleotidyl transferase dUTP nick-end labe
58 the percentage of cell death, as measured by terminal deoxynucleotidyl transferase dUTP nick-end labe
60 -3 and an increase in caspase-3 activity and terminal deoxynucleotidyl transferase dUTP nick-end labe
63 tection of DNA breaks than the commonly used terminal deoxynucleotidyl transferase dUTP nick-end labe
66 ed the next day and analyzed by means of the terminal deoxynucleotidyl transferase dUTP-biotin nick-e
67 the rat eye and retinas were analyzed by the terminal-deoxynucleotidyl transferase dUTP-linked nick e
68 ohistochemistry, immunoblot analysis and the terminal-deoxynucleotidyl transferase dUTP-linked nick-e
70 and induced apoptosis, as determined by the terminal deoxynucleotidyl transferase mediated deoxyurid
71 hown by the decreased frequency of TUNEL(+) (terminal deoxynucleotidyl transferase mediated deoxyurid
72 c cell densities were measured with Ki67 and terminal deoxynucleotidyl transferase mediated dUTP nick
73 ased on bromo-deoxyuridine incorporation and terminal deoxynucleotidyl transferase mediated dUTP nick
74 clear labeling by propidium iodide staining; terminal deoxynucleotidyl transferase mediated dUTP nick
75 by caspase 3 activity and fluorescent-based terminal deoxynucleotidyl transferase mediated nick end
77 were positive for cleaved caspase-3 and for terminal deoxynucleotidyl transferase-mediated biotin-dU
78 cture using electron microscopy, and in situ terminal deoxynucleotidyl transferase-mediated biotin-dU
79 idence of caspase-cleaved tau, but no TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
80 as determined by active caspase-3 and TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
81 and apoptosis were evidenced by increases in terminal deoxynucleotidyl transferase-mediated biotinyla
82 after ouabain injection, maximal numbers of terminal deoxynucleotidyl transferase-mediated biotinyla
84 d spinal cord ventral horn were positive for terminal deoxynucleotidyl transferase-mediated biotinyla
85 te viability was assessed by O4 staining and terminal deoxynucleotidyl transferase-mediated biotinyla
87 epidermal growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinyla
91 We found that deltaV1-1 reduced numbers of terminal deoxynucleotidyl transferase-mediated biotinyla
92 hese same brain areas developed infarcts and terminal deoxynucleotidyl transferase-mediated biotinyla
93 The mRNA from individual active caspase 3(+)/terminal deoxynucleotidyl transferase-mediated biotinyla
94 death, there was a 55.6% reduction in TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
95 nuclei (NeuN)-immunoreactive cells are also terminal deoxynucleotidyl transferase-mediated biotinyla
96 ly expressed in neurons and colocalized with terminal deoxynucleotidyl transferase-mediated biotinyla
101 urogenesis induced by KA were explored using terminal deoxynucleotidyl transferase-mediated biotinyla
102 and induces neuronal apoptosis, detected by terminal deoxynucleotidyl transferase-mediated biotinyla
103 t, there is little cell death, as assayed by terminal deoxynucleotidyl transferase-mediated biotinyla
104 nd the cleavage product appeared at 48 hr in terminal deoxynucleotidyl transferase-mediated biotinyla
106 immunoreactivity for single-stranded DNA and terminal deoxynucleotidyl transferase-mediated biotinyla
107 lls from each parental genotype while TUNEL (terminal deoxynucleotidyl transferase-mediated biotinyla
108 sphorylated histone H3, activated caspase-3, terminal deoxynucleotidyl transferase-mediated deoxyurid
109 re assessed by Ki67 immunohistochemistry and terminal deoxynucleotidyl transferase-mediated deoxyurid
110 ing flow cytometry, electron microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyurid
111 -tubulin III immunocytochemical staining and terminal deoxynucleotidyl transferase-mediated deoxyurid
112 ssessed using bromodeoxyuridine staining and terminal deoxynucleotidyl transferase-mediated deoxyurid
113 sis was quantitated by nuclear morphology or terminal deoxynucleotidyl transferase-mediated deoxyurid
114 HO-1 and a 2-fold reduction in the number of terminal deoxynucleotidyl transferase-mediated deoxyurid
115 ific techniques (hematoxylin-eosin staining, terminal deoxynucleotidyl transferase-mediated deoxyurid
116 activity, the expression of Fas ligand, and terminal deoxynucleotidyl transferase-mediated deoxyurid
117 tiapoptotic effect of MT, as determined by a terminal deoxynucleotidyl transferase-mediated deoxyurid
118 en (p<0.05), bromodeoxyuridine (p<0.05), and terminal deoxynucleotidyl transferase-mediated deoxyurid
119 dies or histology, immunohistochemistry, and terminal deoxynucleotidyl transferase-mediated deoxyurid
121 omal DNA degradation that can be detected by terminal deoxynucleotidyl transferase-mediated deoxyurid
122 fter oncotic necrosis and leads to pervasive terminal deoxynucleotidyl transferase-mediated deoxyurid
123 , S100-positive cells, ganglion cells, and a terminal deoxynucleotidyl transferase-mediated deoxyurid
125 orescence-activated cell sorter analysis and terminal deoxynucleotidyl transferase-mediated deoxyurid
126 orphology, DNA fragmentation, and apoptosis (terminal deoxynucleotidyl transferase-mediated deoxyurid
127 diamidino-2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferase-mediated deoxyurid
128 using gamma-counting, cleaved caspase-3, and terminal deoxynucleotidyl transferase-mediated deoxyurid
130 pase-3, caspase-9, and positive staining for terminal deoxynucleotidyl transferase-mediated deoxyurid
131 orylated focal adhesion kinase and increased terminal deoxynucleotidyl transferase-mediated deoxyurid
132 istochemistry, laser-capture microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyurid
133 is was found at 4 h by DNA fragmentation and terminal deoxynucleotidyl transferase-mediated dUPT nick
134 endothelial cells (BAECs), as determined by terminal deoxynucleotidyl transferase-mediated dUTP biot
135 Similarly, the number of diabetes-enhanced terminal deoxynucleotidyl transferase-mediated dUTP nick
136 nst glucose-induced apoptosis as measured by terminal deoxynucleotidyl transferase-mediated dUTP nick
137 with less hepatic cell death as assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick
138 P<0.002) and less contraction band necrosis, terminal deoxynucleotidyl transferase-mediated dUTP nick
139 ce, BDL mice displayed a 13-fold increase in terminal deoxynucleotidyl transferase-mediated dUTP nick
140 Diabetes-increased activated caspase-3- and terminal deoxynucleotidyl transferase-mediated dUTP nick
141 erent neurons in heart failure, we performed terminal deoxynucleotidyl transferase-mediated dUTP nick
142 s to label apoptotic cells in Drosophila are terminal deoxynucleotidyl transferase-mediated dUTP nick
143 rypan blue uptake, and apoptotic cell death (terminal deoxynucleotidyl transferase-mediated dUTP nick
144 polymerase cleavage, Annexin V staining, and terminal deoxynucleotidyl transferase-mediated dUTP nick
145 Immunostaining for Ki-67 and cyclin D1 and terminal deoxynucleotidyl transferase-mediated dUTP nick
147 ic markers in the diaphragm (e.g., number of terminal deoxynucleotidyl transferase-mediated dUTP nick
150 treatment, cardiac apoptosis was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick
151 uced the frequency of intrahepatic apoptotic terminal deoxynucleotidyl transferase-mediated dUTP nick
152 ed increased intratumoral apoptotic index by terminal deoxynucleotidyl transferase-mediated dUTP nick
154 2 activity, as well as apoptosis detected by terminal deoxynucleotidyl transferase-mediated dUTP nick
155 to induction of apoptosis as revealed by the terminal deoxynucleotidyl transferase-mediated dUTP nick
156 Apoptosis within the retina was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick
157 e then analyzed for apoptotic nuclei using a terminal deoxynucleotidyl transferase-mediated dUTP nick
159 xy-6-nitro)benzene sulfonic acid) and TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
160 n as demonstrated by positive staining using terminal deoxynucleotidyl transferase-mediated dUTP nick
161 Apoptosis indicated by nuclear changes, terminal deoxynucleotidyl transferase-mediated dUTP nick
162 ificantly less apoptosis as measured by both terminal deoxynucleotidyl transferase-mediated dUTP nick
163 decreased retinal apoptosis as shown by the terminal deoxynucleotidyl transferase-mediated dUTP nick
166 excitation of piriform cortex, on apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick
167 n by 5-bromo-2'-dUTP incorporation assay and terminal deoxynucleotidyl transferase-mediated dUTP nick
168 V fluorescent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick
169 cytometry analysis, immunocytochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick
170 haloperidol and reduced haloperidol induced terminal deoxynucleotidyl transferase-mediated dUTP nick
171 was also observed with the use of either the terminal deoxynucleotidyl transferase-mediated dUTP nick
173 ng the wild type protein had very low TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
174 within 48-72 h, marked by nuclear blebbing, terminal deoxynucleotidyl transferase-mediated dUTP nick
175 apoptotic cell death occurred as detected by terminal deoxynucleotidyl transferase-mediated dUTP nick
176 ining of occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick
177 initiation factor 2 alpha), and cell death [terminal deoxynucleotidyl transferase-mediated dUTP nick
178 rtex, an area that also showed more positive terminal deoxynucleotidyl transferase-mediated dUTP nick
181 DAPI (4', 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
183 ic grafts by hematoxylin and eosin staining, terminal deoxynucleotidyl transferase-mediated dUTP nick
184 ced tumor size, reduced Ki-67, and increased terminal deoxynucleotidyl transferase-mediated dUTP nick
185 Histologic damage, cytokine expression, terminal deoxynucleotidyl transferase-mediated dUTP nick
186 leavage, caspase-activated DNase levels, and terminal deoxynucleotidyl transferase-mediated dUTP nick
187 Apoptosis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick
188 xyuridine [BrdU]) and cell death (caspase-3, terminal deoxynucleotidyl transferase-mediated dUTP nick
189 treatment resulted in a marked reduction in terminal deoxynucleotidyl transferase-mediated dUTP nick
190 lactosidase, sclerostin immunochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick
191 both settings its expression correlated with terminal deoxynucleotidyl transferase-mediated dUTP nick
192 the endothelial markers CD31 and VEGFR-2 and terminal deoxynucleotidyl transferase-mediated dUTP nick
193 c A((2)A)AR(-/-) mice had significantly more terminal deoxynucleotidyl transferase-mediated dUTP nick
195 tely 3-fold) and HA expression but increased terminal deoxynucleotidyl transferase-mediated dUTP nick
196 c release by Western blot, and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP nick
197 er rates of apoptosis, as measured by TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick
199 topathy corneas, whereas it colocalized with terminal deoxynucleotidyl transferase-mediated dUTP nick
200 10 Gy significantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick
201 ed Boyden chamber assay), and antiapoptotic (terminal deoxynucleotidyl transferase-mediated dUTP nick
202 hed from the culture plate over time, became terminal deoxynucleotidyl transferase-mediated dUTP nick
203 rse transcription polymerase chain reaction, terminal deoxynucleotidyl transferase-mediated dUTP nick
204 by poly(ADP-ribose) polymerase cleavage and terminal deoxynucleotidyl transferase-mediated dUTP nick
205 aminotransferase (ALT), caspase-3 activity, terminal deoxynucleotidyl transferase-mediated dUTP nick
206 EM011 caused DNA degradation as evident by terminal deoxynucleotidyl transferase-mediated dUTP-biot
207 of a lactate dehydrogenase release assay and terminal deoxynucleotidyl transferase-mediated dUTP-biot
208 ities of caspases 3 and 8, and the number of terminal deoxynucleotidyl transferase-mediated dUTP-biot
210 optosis in vitro at 72 hours (P < 0.05), and terminal deoxynucleotidyl transferase-mediated dUTP-biot
211 tosis of LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biot
213 ity and cell death were investigated by MTT, terminal deoxynucleotidyl transferase-mediated dUTP-digo
214 ryosectioned, and evaluated for apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-digo
215 ity to active (Ac)-caspase-3, -8, and -9 and terminal deoxynucleotidyl transferase-mediated dUTP-digo
216 er, as determined by Hoechst 33342 staining, terminal deoxynucleotidyl transferase-mediated dUTP-FITC
217 s were stained for interleukin (IL)-12 or by terminal deoxynucleotidyl transferase-mediated dUTP-nick
218 P<0.005) and protected against diabetes, and terminal deoxynucleotidyl transferase-mediated nick end
219 nd induced tumor cell apoptosis (assessed by terminal deoxynucleotidyl transferase-mediated nick end
221 e attenuated levels of apoptosis observed by terminal deoxynucleotidyl transferase-mediated nick end
223 proliferation, and a significant increase in terminal deoxynucleotidyl transferase-mediated nick end
224 hown by fluorescence-activated cell sorting, terminal deoxynucleotidyl transferase-mediated nick end
225 e PDT as indicated by caspase-3 activity and terminal deoxynucleotidyl transferase-mediated nick end
226 o DU145) using flow cytometric Annexin V and terminal deoxynucleotidyl transferase-mediated nick end
227 construct did not involve apoptosis because terminal deoxynucleotidyl transferase-mediated nick end
228 hesizing SK-RC-45 line stimulated the TUNEL (terminal deoxynucleotidyl transferase-mediated nick end
230 o DNA, as revealed by caspase activation and terminal deoxynucleotidyl transferase-mediated nick end
231 as 5-fluorouracil (5-FU), induced apoptosis (terminal deoxynucleotidyl transferase-mediated nick end
232 n cancer cells were apoptotic as judged by a terminal deoxynucleotidyl transferase-mediated nick end
236 ning; creatine kinase release) or apoptosis (terminal deoxynucleotidyl transferase-mediated nick end
237 ogically, and apoptosis was evaluated by the terminal deoxynucleotidyl transferase-mediated nick end
238 protein, OX-42, gamma-aminobutyric acid, or terminal deoxynucleotidyl transferase-mediated nick end
239 from the mitochondria to the cytoplasm, and terminal deoxynucleotidyl transferase-mediated nick end
242 apoptosis was also noted in PiZ BDL mice by terminal deoxynucleotidyl transferase-mediated nick-end
243 apoptosis, as shown by increased numbers of terminal deoxynucleotidyl transferase-mediated nick-end
244 T1 AS) were employed in cells resistant (<5% terminal deoxynucleotidyl transferase-mediated nick-end
245 rs were harvested and assayed for apoptosis (terminal deoxynucleotidyl transferase-mediated nick-end
246 anine aminotransferase (ALT), pathology, and terminal deoxynucleotidyl transferase-mediated nick-end
247 eduction in the apoptosis rate was observed (terminal deoxynucleotidyl transferase-mediated nick-end
249 g with cytochrome c immunohistochemistry and terminal deoxynucleotidyl transferase-mediated uridine 5
251 p75(NTR) expression was induced primarily in terminal deoxynucleotidyl transferase-mediated UTP nick-
252 ed by proliferating cell nuclear antigen and terminal deoxynucleotidyl-transferase-mediated dUTP nick
253 ptosis in endothelial cells as determined by terminal deoxynucleotidyl-transferase-mediated dUTP nick
255 th these findings, flow cytometry and TUNEL (terminal deoxynucleotidyl-transferase-mediated dUTP nick
256 controls were studied by routine microscopy, terminal deoxynucleotidyl-transferase-mediated dUTP nick
257 nd in situ DNA fragmentation assessed by the terminal deoxynucleotidyl transferase nick end-labeling)
259 ti-B7.1, anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling)
260 92 total), and a significant proportion were terminal deoxynucleotidyl transferase (TdT) -mediated de
261 ty/joining (V[D]J) recombination, the enzyme terminal deoxynucleotidyl transferase (Tdt) adds random
262 l-derived B cell progenitors fail to express terminal deoxynucleotidyl transferase (TdT) and for othe
263 platform is based on exonuclease I (Exo I), terminal deoxynucleotidyl transferase (TdT) and methylen
265 se (Pol) X family members such as Pol mu and terminal deoxynucleotidyl transferase (TdT) are importan
266 dult repertoires due to the delayed onset of terminal deoxynucleotidyl transferase (TdT) expression i
267 Co(2+) ions by patterned UV light activates Terminal deoxynucleotidyl Transferase (TdT) for spatiall
268 we find that mice expressing a transgene for terminal deoxynucleotidyl transferase (TdT) have nucleot
269 arnesses the template-independent polymerase terminal deoxynucleotidyl transferase (TdT) in kinetical
273 at the 3'-OH of an RNA molecule, followed by terminal deoxynucleotidyl transferase (TdT) to catalyze
274 27(+) Ly-6C(-) Thy-1(-)CD43(+) CD16/32(Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in
275 d bone marrow (BM) chimeras, made with adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT
277 to a single stranded DNA (ssDNA) chain using terminal deoxynucleotidyl transferase (TdT), a template-
279 om RA synovium, we also sought expression of terminal deoxynucleotidyl transferase (TdT), which is no
280 ntemplated (N) nucleotides is carried out by terminal deoxynucleotidyl transferase (TdT), whose only
282 uts relative to WT animals, as documented by terminal deoxynucleotidyl transferase (TdT)-mediated dUT
284 eated with HA were examined for apoptosis in terminal deoxynucleotidyl transferase (TdT)-mediated dUT
285 this study, we compared these tests with the terminal deoxynucleotidyl transferase (TdT)-mediated dUT
293 s first converted to double-stranded-DNA via terminal-deoxynucleotidyl-transferase (TdT) prior to ini
294 oid (P <.10) or early hematopoietic markers (terminal deoxynucleotidyl transferase [TdT], CD34; P <.1
295 line was stained against a leukemic marker (terminal deoxynucleotidyl transferase, TdT), and we succ
297 cleaved caspase-3 immunohistochemistry, and terminal deoxynucleotidyl transferase UTP nick-end label
298 e synthesis of heavily modified DNA, whereas terminal deoxynucleotidyl transferase was used for a sin
299 terleukin receptor 7 alpha(+), c-kit(lo) and terminal deoxynucleotidyl transferase(+)) were selective
300 of nontemplated (N) nucleotides inserted by terminal deoxynucleotidyl transferase, which resulted in