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1                                              TdT addition of digoxigenin labeled nucleotides to 3' OH
2                                              TdT adds nontemplated N nucleotides to the junctions of
3                                              TdT and an Ig heavy chain transgene were detected within
4                                              TdT expression suggests the presence of immature B cells
5                                              TdT expression was found in several samples, but did not
6                                              TdT is a DNA polymerase that plays a major role in gener
7                                              TdT is a nuclear enzyme that catalyzes the addition of r
8                                              TdT staining indicated that following 2-MeOE2-mediated i
9                                              TdT's ability to incorporate fluorescent dNTPs into a ss
10                                              TdT(+) cells found within the tonsillar fibrous scaffold
11                                              TdT-mediated dUTP nick end labeling assay at 48 h indica
12                                              TdT-mediated dUTP nick-end labeling (TUNEL) assay was us
13                                              TdT-mediated nick end-label (TUNEL) staining showed apop
14                                              TdT-mediated synthesis may be a useful approach for crea
15 and included most RAG-1+ ELP and many RAG-1- TdT+ ELP.
16 ecombinase-activating gene-1 (RAG-1), RAG-2, TdT, Ig mu, lambda 5, and VpreB.
17 18 sequences from adult MRL/lpr- and C57BL/6 TdT-deficient B cell precursors and found only two examp
18 ins no TATA sequence, but instead contains a TdT-like initiator element (Inr) at nucleotides -3 to +5
19 d selection and suggest the possibility of a TdT-deficient precursor population in the adult BM.
20 was demonstrated in 5H7-treated PBMC using a TdT-mediated end-labeling (TUNEL) technique.
21 ha 1-->3 dextran [DEX]) by challenging adult TdT-sufficient (TdT(+/+)) and TdT-deficient (TdT(-/-)) g
22 Reconstitution of irradiated mice with adult TdT(+/+) BM reveals that the MZ can replenish N(-) B cel
23 sults suggest that Ku80 is required to allow TdT access to RAG post-cleavage complexes, providing sup
24        The ability of mu transgenes to alter TdT expression in cell lines also suggests that signalin
25 consistent with TdT-mediated N-addition, and TdT RNA is expressed exclusively at the pro-B cell stage
26 d contained transcripts of T early alpha and TdT, and 15 of 19 infant samples contained mRNA for RAG-
27  enhancer, and the 5' regions of the B29 and TdT loci.
28                CD3, RAG-1, Ikaros, CD10, and TdT transcripts were detected in the starting CD34+Lin-D
29 is was determined by both flow cytometry and TdT-dUTP terminal nick-end labeling analysis.
30 -associated defects with more 53BP1 foci and TdT-mediated dNTP nick end labeling-positive cells over
31          Histologic, immunocytochemical, and TdT-dUTP terminal nick-end labeling (TUNEL) analyses wer
32                     Immunohistochemistry and TdT-mediated biotin-dUTP nick end labeling (TUNEL) were
33 g in mammalian cells: pol mu, pol kappa, and TdT.
34               The interaction between Ku and TdT is also observed in pre-T cells with endogenously ex
35 K1) cells, as evidenced by DNA laddering and TdT-mediated dUTP nick end-labeling assay.
36 ciated DNA fragmentation, DNA laddering, and TdT-mediated dUTP nick end labeling (TUNEL).
37 l) X family members (pol mu, pol lambda, and TdT, but not pol beta) contribute to junctional addition
38 avy chain minilocus pHC1 transgenic mice and TdT-deficient mice.
39 wed evidence of apoptosis (by morphology and TdT-mediated dUTP nick end labeling [TUNEL] assay).
40 on regions of the BRCT domains of pol mu and TdT support the conclusion that they participate in NHEJ
41 in reaction (PCR) was used to detect RAG and TdT transcripts from unselected and B cell-enriched syno
42 (+) T cells, coinciding with Rag1, Rag2, and TdT expression and the accumulation of V(beta)-DJ(beta)
43 tivity and the expression of RAG1, RAG2, and TdT in B-ALL patients.
44 um bromide-acridine orange nuclear stain and TdT-mediated dUTP nick-end labeling (TUNEL).
45 llenging adult TdT-sufficient (TdT(+/+)) and TdT-deficient (TdT(-/-)) gene-targeted mice, limited to
46        Using tetramer staining, TdT(-/-) and TdT(+/+) NOD mice showed similar frequencies of the diab
47  deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) donor cells, demonstrate preferential repertoir
48  usage and CDR3 length between wild-type and TdT-/- mice.
49 s from neonatal liver and both wild-type and TdT-deficient adult bone marrow.
50 precursors in the liver and spleen of WT and TdT-transgenic mice but not in TdT(-/-) mice.
51 dition, analysis for evidence for apoptosis (TdT-dUTP terminal nick-end label [TUNEL] staining) and p
52 roliferation (Ki67) and increased apoptosis (TdT-mediated dUTP nick end labeling; TUNEL).
53 0 and involucrin), and markers of apoptosis (TdT-mediated dUTP nick end labeling (TUNEL) and anti-cas
54 n density along with pyknotic and apoptotic (TdT-mediated deoxyuridine triphosphate nick end-labeled)
55 c-Kit(-)Sca-1(high) bone marrow fraction are TdT(-), are RAG2(low), and do not display evidence for o
56 itiated a wave of cornification, assessed as TdT-mediated dUTP nick end-labeling-positive cells in st
57  majority of fluorescent nucleotides used as TdT substrates contain tethered fluorophores attached to
58             We report an association between TdT and a 55-kDa protein in lymphoid cells.
59 de evidence for a direct interaction between TdT and Ku proteins.
60 e is required for HSI and that N addition by TdT is a more effective mechanism in the induction of a
61            Although N-nucleotide addition by TdT plays a critical role in the generation of a diverse
62 s were found when the cells were analyzed by TdT-mediated dUTP nick end labeling (TUNEL).
63 ent dye-chromatin fragmentation assay and by TdT-dUTP terminal nick-end labeling (TUNEL) assay.
64  tumor cells excised from treated animals by TdT-mediated dUTP nick end labeling assay.
65  to TGF-beta1 were examined for apoptosis by TdT-mediated end-labeling and annexin staining.
66 ry, 70% of medial SMCs appeared apoptotic by TdT-mediated dUTP nick end labeling (TUNEL) analysis and
67                Cell viability was assayed by TdT-dUTP terminal nick-end labeling (TUNEL) in conjuncti
68 the nuclei of membrane-compromised cells, by TdT-dUTP terminal nick-end labeling (TUNEL) of apoptotic
69 ed zone was analyzed for keratocyte death by TdT-dUTP terminal nick-end label (TUNEL) staining and tr
70 chemically [DNA fragmentation as detected by TdT-mediated dUTP Nick-End Labeling (TUNEL) assay].
71                   Apoptosis was evaluated by TdT-mediated dUTP nick end labeling immunohistochemistry
72 nation signal sequences may be influenced by TdT expression.
73 ncreased amounts of apoptosis as measured by TdT-mediated dUTP nick end labelling (TUNEL).
74 se in apoptosis (assessed morphologically by TdT-mediated dUTP nick- end labeling staining) is preced
75                     Thus, the role played by TdT may be more extensive than previously thought.
76 matching of the second apparent D segment by TdT-introduced N nucleotides.
77 eavage reaction can be efficiently tailed by TdT, suggesting that the RAG proteins disassemble from t
78                                In both cases TdT added nucleotides efficiently to the cleaved DNA end
79 e complementary determining region 3 (CDR3) (TdT(-/-)) and mice with altered Ab repertoires due to re
80                               In these cells TdT protein is abundant at the time of recombination, lo
81 ciated with the RAG proteins after cleavage, TdT might be targeted for N region addition through inte
82    Thus, although differing in V(H) content, TdT-deficient mice appear to represent a good, although
83                                 In contrast, TdT was 3-fold upregulated in immature B cells of adults
84 TdT-sufficient (TdT(+/+)) and TdT-deficient (TdT(-/-)) gene-targeted mice, limited to the use of a si
85 ded by terminal deoxynucleotidyltransferase (TdT) activity and is not derived from DIR recombination.
86    The terminal deoxynucleotidyltransferase (TdT) gene represents an attractive model for the analysi
87 t gene terminal deoxynucleotidyltransferase (TdT) was decreased by phosphorylation of two amino acids
88 ng terminal deoxyribonucleotidyltransferase (TdT), which adds N nucleotides to V-D and D-J junctions
89 iversity that was introduced by differential TdT activities, and somatic hypermutation.
90 ns with shorter CDR3(H) were both diminished TdT activity in the DJ(H) junction and the preferential
91 ted the role of the lymphoid-specific enzyme TdT in generating B cell clones responsive to alpha-1,3
92 ded during V(D)J recombination by the enzyme TdT).
93 on of N-region additions added by the enzyme TdT.
94  such as common lymphoid progenitors express TdT and relatively high levels of RAG2, and are enriched
95 PCR analysis showed that the cells expressed TdT, lambda5, and RAG-1 genes, but that their Ig genes w
96 , like their c-kitLo counterparts, expressed TdT, proliferated in response to interleukin (IL)-7, and
97 sion of PAX5 and 72.8% of the MCCs expressed TdT.
98 ed two bone marrow (BM) subsets enriched for TdT+ cells on the brink of CD45R acquisition.
99 n and protein-DNA interactions important for TdT function in vivo.
100      This region, although not important for TdT polymerization activity, contains a BRCA1 C-terminal
101 -OH group at the nick remains obstructed for TdT-catalyzed N nucleotide addition.
102 ted at postnatal day (P) 7 and processed for TdT-dUTP terminal nick-end labeling (TUNEL) staining, an
103  apoptosis in the retina, were processed for TdT-dUTP terminal nick-end labeling (TUNEL) to determine
104 -terminal (BRCT) domain, is not required for TdT activity, although the BRCT domain clearly contribut
105 correlate well with in vitro selectivity for TdT.
106  2'-deoxynucleotides that are substrates for TdT in lymphoid precursors.
107 se-3 (CC3) activation and DNA fragmentation (TdT-mediated dUTP nick-end labeling [TUNEL]).
108 e to sort fractions B-F B lineage cells from TdT-deficient BALB/c adult BM.
109                            We have generated TdT-deficient MRL/lpr, Fas-deficient (MRL-Fas(lpr)) mice
110                            We have generated TdT-deficient nonobese diabetic (NOD) and MRL-Fas(lpr) m
111                              Four gonococcal TdTs facilitate utilization of iron or iron chelates fro
112 erentiation of pre-pro-B cells (B220+, HSA-, TdT- or TdT+, c[mu-]) from adult rat, mouse, and human B
113 DSBs in Cos-7 cells transfected with a human TdT expression construct resulted in the appearance of d
114                 Evidence for potential human TdT (hTdT) isoforms derived from hTdT genomic sequences
115 ecific J558 idiotype (Id) is not detected in TdT(-/-) mice when compared with wild-type (WT) BALB/c m
116 s demonstrating a reduced response to DEX in TdT(-/-) mice with a WT D(H) locus, we concluded that in
117         Complementation of TdT expression in TdT(-/-) mice by early forced expression of the short sp
118 vage of DEVD-AMC and blocked the increase in TdT-mediated dUTP nick end labeling (TUNEL) positivity.
119 een of WT and TdT-transgenic mice but not in TdT(-/-) mice.
120  more severely impaired HSI were observed in TdT(-/-) mice compared to those in Delta D-iD mice, whil
121                            We report that in TdT-/- mice, total T(CD8+) responses to influenza and va
122            The pattern of V(H)DJ(H) usage in TdT-deficient BM largely matched that of TdT-sufficient
123 rminants are reduced to background values in TdT-/- mice while responses to three immunodominant dete
124 numbers than with standard markers including TdT-mediated dUTP biotin nick-end labeling and cleaved c
125 educed levels of DNA synthesis and increased TdT-mediated dUTP nick-end labeling staining.
126                         Template-independent TdT promotes diversity during NHEJ-dependent repair of V
127 vely disrupt Ikaros binding to an integrated TdT promoter had no effect on promoter function in a CD4
128 eviously shown that newborn mice, which lack TdT due to the late onset of its expression, do not cont
129  tendency to select rearrangements with less TdT activity and shorter D segments.
130                                       Lin(-) TdT(+) early pro-B cells are shown here to be CD27(+) AA
131 rkers was exploited to isolate viable Lin(-) TdT(+) cells from murine bone marrow.
132 rther analysis demonstrated CD24 on most Lin-TdT+ cells and all CD45R+CD19-DX5-Ly-6C- cells.
133           Most lineage marker-negative (Lin-)TdT+ cells from murine marrow lack CD34 but display c-ki
134 itors that were Lin(-)IL-7R alpha(+)c-kit(lo)TdT(+) (lineage marker(-), interleukin receptor 7 alpha(
135 itis and increased life span in MRL-Fas(lpr) TdT(-/-) mice.
136  in the IgH CDR3 regions of the MRL-Fas(lpr) TdT(-/-) mice.
137  tested 21 MCCs for the expression of MCPyV, TdT, PAX5, IgG, IgM, IgA, kappa, and lambda by immunohis
138         To test this hypothesis, we measured TdT's ability to add nucleotides to endonuclease-induced
139                              In normal mice, TdT is sharply down-regulated at the early pre-B stage i
140 ts (where H is heavy chain) in the minilocus TdT-/- mice use small portions of DIR2 located throughou
141   Furthermore, we show that DNA-PK modulates TdT activity in vitro by limiting both the length and co
142 expression was elevated in AD cases and most TdT-labeled nuclei also showed strong NT immunoreactivit
143  a structure-function analysis of the murine TdT protein to determine the roles of individual structu
144  hours, alanine transferase (ALT), necrosis, TdT-mediated dUTP-digoxigenin nick-end labeling (TUNEL)
145 and decreased pancreatic infiltration in NOD TdT(-/-) mice, and reduced glomerulonephritis and increa
146 e in CD4(+)CD25(+) regulatory T cells in NOD TdT(-/-) mice.
147                            In the absence of TdT and with a defined set of human D gene segments, it
148  region 3 sequences formed in the absence of TdT are more uniform due to the use of short sequence ho
149 -Fas(lpr) mice are shorter in the absence of TdT, and there is a paucity of arginines in the IgH CDR3
150              Additionally, in the absence of TdT, D-limited mice failed to produce a DEX response.
151 d B-1a cell IgM developing in the absence of TdT, increased in 7- to 24-mo-old mice as compared with
152                            In the absence of TdT, the pseudo-VH gene segment present in the minilocus
153 antial N-addition despite initial absence of TdT.
154 minilocus mice in the presence or absence of TdT.
155                                The action of TdT on mouse TCR genes accounts for approximately 90% of
156                          Thus, the action of TdT produces an adult repertoire that is both different
157 ensive postneonatally due to the activity of TdT, which adds nontemplated N nucleotides to Ig and TCR
158 uclear localization or enzymatic activity of TdT.
159                  The physical association of TdT with Ku suggests a possible mechanism by which TdT i
160                           As coexpression of TdT and PAX5 under physiologic circumstances is restrict
161                           Complementation of TdT expression in TdT(-/-) mice by early forced expressi
162 tural alterations, 2) enzymatic detection of TdT-positive DNA degradation, and 3) automated cytometri
163     The second helix-hairpin-helix domain of TdT, but not the first, is required for activity.
164 Ikaros to the upstream regulatory element of TdT.
165 ntial for 1) up-regulating the expression of TdT and IL-7R alpha, 2) initiating the production of cmu
166                                Expression of TdT and the lymphoid-associated genes Ig beta and RAG-1,
167                       Further, expression of TdT, a molecule that is normally down-regulated by a fun
168 e N-nucleotide addition by the short form of TdT, but did not increase nucleotide deletion from codin
169 activity and function of the long isoform of TdT (TdTL) have not been determined.
170                          The long isoform of TdT was found to reduce N-nucleotide addition by the sho
171 c mutation are compensated by early onset of TdT activity and other mechanisms that contribute to CDR
172 % CD19(+) B cells with normal percentages of TdT(+)VpreB(+)CD19(-) B cell precursors.
173  demonstrates that the N-terminal portion of TdT, including the BRCA-1 C-terminal (BRCT) domain, is n
174  cell lines results in a marked reduction of TdT expression.
175 riments reveal that the N-terminal region of TdT (131 amino acids) is essential for interaction with
176 ggested that the entire C-terminal region of TdT is necessary for N-nucleotide addition in vivo.
177 eported structure of the catalytic region of TdT.
178               Consequently, up-regulation of TdT and IL-7R alpha expression requires signaling throug
179 chains, together with the down-regulation of TdT transcription in pre-B cells (prior to light chain p
180 production results in the down-regulation of TdT.
181 cin results in transcriptional repression of TdT expression.
182  in TdT-deficient BM largely matched that of TdT-sufficient adult cells.
183 ed expression of the short splice variant of TdT-restored WT proportions of J558 Id+ clones and also
184 , we examined the effect of mu production on TdT gene expression in B lineage subsets from normal mic
185 ion of pre-pro-B cells (B220+, HSA-, TdT- or TdT+, c[mu-]) from adult rat, mouse, and human BM.
186 nd P berghei iRBCs with apoptotic parasites (TdT(+)) exhibited minimal platelet binding (<5%), which
187                               In particular, TdT-mediated nucleotide insertions varied depending on a
188 hoid (B220(+)CD19(+)CD43(+)sIgM(-), PAX5(+), TdT(+), IgH rearranged)/myeloid (CD11b/Mac1(+), c-fms(+)
189  these differences reflect limited perinatal TdT activity versus differences in the fetal/adult envir
190 lt of the action of a unique DNA polymerase, TdT.
191  and PAX-5, and were uniformly TdT-positive (TdT+).
192  Such regulated access would help to prevent TdT from acting at other types of broken ends and degrad
193                            Although purified TdT can act at free DNA ends, its ability to add nucleot
194  on-chip labeling method, we also quantified TdT mediated signal amplification on the surface by immo
195 e of Ku80, indicating that Ku80 may regulate TdT's activity at DNA ends in vivo.
196 chain (mu) protein might negatively regulate TdT expression.
197 of Ikaros as well as its ability to regulate TdT expression during thymocyte differentiation.
198 nd the failure of pro-B cells to up-regulate TdT and the IL-7R alpha (but not the common gamma-chain)
199  consisting of 35.4% and 7.4%, respectively, TdT+ cells, generated B-lineage cells in overnight cultu
200 were similar to Lin- c-Kit(high) L-selectin+ TdT+ RAG-1- progenitors present in the marrow, suggestin
201 ) (DQ52, DSP, or DST) gene segment sequence, TdT activity, or both to produce D99, all three D-limite
202 monstrated by morphological changes, in situ TdT labeling and internucleosomal laddering.
203 osis-associated DNA strand breaks by in situ TdT labeling showed that a significant number of flavopi
204                                  The in situ TdT-mediated biotin-dUTP nick end labeling (TUNEL) metho
205 tor for occupancy of the lymphocyte-specific TdT promoter.
206 ed for degeneration-induced silver staining, TdT-mediated dUTP-digoxigenin nick end-labeling (TUNEL)
207                     Using tetramer staining, TdT(-/-) and TdT(+/+) NOD mice showed similar frequencie
208  [DEX]) by challenging adult TdT-sufficient (TdT(+/+)) and TdT-deficient (TdT(-/-)) gene-targeted mic
209 ndolyl diketo acids that specifically target TdT and behave as nucleotide-competitive inhibitors.
210                         The TUNEL technique (TdT-mediated dUTP nick-end labeling) was used to detect
211              These findings demonstrate that TdT plays a critical role in the magnitude and breadth o
212            In this report, we establish that TdT forms a stable complex with DNA-PK.
213 n addition to the G preference, we find that TdT adds strings of purines or strings of pyrimidines at
214                    The current model is that TdT adds N regions during V(D)J recombination by random
215         Based on these data, we propose that TdT does not add to recombination junctions through rand
216 orded to the newborn, may be the reason that TdT expression is delayed in ontogeny.
217 th a baculovirus expression system show that TdT can interact specifically with each of the Ku subuni
218                         These data show that TdT is essential for the generation of the predominant h
219 blasts, sorted postimmunization, showed that TdT(-/-) mice generate a lower frequency of the predomin
220                      These data suggest that TdT expression is initiated as c-kit downregulation begi
221  those in late term fetuses, suggesting that TdT is fully active at the onset of VDJ rearrangement; 2
222    Apoptotic cell death was evaluated by the TdT-mediated digoxigenin-dUTP nick-end labeling TUNEL as
223 the RNA by PaP acts as the initiator for the TdT-catalyzed polymerization of longer DNA strands from
224 hough the patterns of V(H)DJ(H) usage in the TdT-deficient B lineage cells paralleled that of wild-ty
225 cific for MCMV or for T cells or used in the TdT-dUTP terminal nick-end labeling (TUNEL) assay to det
226 e first expressed by late pre-B cells in the TdT-insufficient perinatal liver.
227                       The combination of the TdT assay and confocal microscopy demonstrated that 20 m
228 hymocytes, Ikaros acts as a repressor of the TdT gene.
229 ed using hematoxylin and eosin staining, the TdT-dUTP terminal nick-end labeling (TUNEL) assay, and T
230 eractions between Ikaros dimers bound to the TdT promoter and those bound to pericentromeric repeat s
231 ed DNA binding affinity of Ikaros toward the TdT promoter.
232             Cell death was assayed using the TdT-dUTP terminal nick-end labeling (TUNEL) assay.
233   DNA fragmentation was determined using the TdT-dUTP terminal nick-end labeling assay and by agarose
234  in situ apoptosis detection assay using the TdT-mediated dUTP nick end labeling method.
235 distinctive in vivo role correlates with the TdT-like ability of pol mu, but not pol lambda, to act w
236 ere detected and the majority (93%) of these TdT-labeled neurons lacked evidence of tangle formation.
237 ditions led us to evaluate the role of these TdTs in the acquisition of nutrients other than iron.
238                                        Thus, TdT deficiency ameliorates the severity of disease in bo
239 traordinary cases of FL, which progressed to TdT(+)CD20(-) precursor B-lymphoblastic lymphoma (B-LBL)
240 peting terminal deoxynucleotide transferase (TdT) activity unlike any other B-family DNA polymerase.
241  were terminal deoxynucleotidyl transferase (TdT) -mediated deoxyuridine triphosphate (dUTP)-rhodamin
242 nzyme terminal deoxynucleotidyl transferase (TdT) adds nontemplate-derived nucleotides (N regions) to
243 press terminal deoxynucleotidyl transferase (TdT) and for other reasons, they are likely to express a
244 f the terminal deoxynucleotidyl transferase (TdT) and the paired box gene 5 (PAX 5) has been consiste
245       Terminal deoxynucleotidyl transferase (TdT) catalyzes the addition of nucleotides at the juncti
246 et of terminal deoxynucleotidyl transferase (TdT) expression in ontogeny.
247 e for terminal deoxynucleotidyl transferase (TdT) have nucleotide insertions at S-S junctions, indica
248 erase terminal deoxynucleotidyl transferase (TdT) in order to assess occupancy of the reaction interm
249 , and terminal deoxynucleotidyl transferase (TdT) in particular, have been widely used in enzymatic l
250 on by terminal deoxynucleotidyl transferase (TdT) increase the diversity of antigen receptors.
251 y the terminal deoxynucleotidyl transferase (TdT) reaction.
252 wn by terminal deoxynucleotidyl transferase (TdT) staining, and upregulation of wt p53 expression, as
253 ed by terminal deoxynucleotidyl transferase (TdT) to catalyze the sequential addition of a mixture of
254 Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in murine bone marrow are functional lymph
255 adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) donor cells, demonstrate preferen
256       Terminal deoxynucleotidyl transferase (TdT), a polymerase that adds random nucleotides (N regio
257 using terminal deoxynucleotidyl transferase (TdT), a template-independent DNA polymerase that catalyz
258 essed terminal deoxynucleotidyl transferase (TdT), the ETS transcription factor Spi-B, the nuclear fa
259 on of terminal deoxynucleotidyl transferase (TdT), which is normally expressed only in B cell precurs
260 ut by terminal deoxynucleotidyl transferase (TdT), whose only known physiological role is to create d
261 py of terminal deoxynucleotidyl transferase (TdT)-labeled lens slices confirmed that DNA fragmentatio
262   The terminal deoxynucleotidyl transferase (TdT)-mediated deoxyuridine triphosphate (dUTP)-biotin ni
263       Terminal deoxynucleotidyl transferase (TdT)-mediated deoxyuridine triphosphate-biotin nick end
264 is in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP biotin nick-end labeling assays.
265 h the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) assay and a
266 ed by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling and caspase-3 stain
267 using Terminal deoxynucleotidyl Transferase (TdT)-mediated dUTP nick-end labeling (TUNEL) and DNA lad
268  with terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labeling (TUNEL) and flow cy
269  situ terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labeling (TUNEL) to describe
270 ge of terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labeling (TUNEL)-positive le
271 UNEL (terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling) assays demo
272  Many terminal deoxynucleotidyl transferase (TdT)-positive neurons were detected and the majority (93
273 ) and terminal deoxynucleotidyl transferase (TdT).
274 P) by terminal deoxynucleotidyl transferase (TdT).
275       Terminal deoxynucleotidyl transferase (TdT; EC 2.7.7.31) adds nucleotides to DNA ends generated
276        Terminal deoxynucletidyl transferase (TdT) is overexpressed in some cancer types, where it mig
277 e terminal deoxyribonucleotidyl transferase (TdT)-mediated dUTP Nick End Labeling (TUNEL) assay.
278                        Terminal transferase (TdT), when incubated with a purified(32)P-5"-end-labeled
279                        Terminal transferase (TdT)-mediated deoxyuridine triphosphate (d-UTP)-biotin n
280 kers (terminal deoxynucleotidyl transferase [TdT], CD34; P <.10).
281       Terminal deoxynucleotidyl transferase [TdT]-mediated dUTP nick end labelling analysis demonstra
282 y production of TonB-dependent transporters (TdTs)-outer membrane proteins that facilitate nutrient t
283  outer membrane TonB-dependent transporters (TdTs.) Survival within host epithelial cells is importan
284 cytic cells, as determined by in vivo TUNEL (TdT-mediated dUTP nick-end labeling) staining.
285          These findings suggest that the two TdT isoforms may act in concert to preserve the integrit
286  roles of the remaining four uncharacterized TdTs (TdfF, TdfG, TdfH, and TdfJ) remain elusive.
287 g beta, RAG-1, and PAX-5, and were uniformly TdT-positive (TdT+).
288                              However, unlike TdT, synthesis by pol mu in this context is primarily in
289 , in situ staining for apoptotic cells using TdT-mediated dUTP-digoxigenin nick-end labeling (TUNEL),
290                       With the goal of using TdT as an on-chip labeling method, we also quantified Td
291 hese mice during a stage in development when TdT is not expressed.
292 of Ag receptor genes, the mechanism by which TdT acts remains unclear.
293 th Ku suggests a possible mechanism by which TdT is recruited to the sites of DSBs such as V(D)J reco
294 appearance of discrete nuclear foci in which TdT and Ku colocalize.
295 nd studies of their substrate abilities with TdT.
296 ors was determined by cocrystallization with TdT, explaining why these compounds are competitive inhi
297 exhibit junctional diversity consistent with TdT-mediated N-addition, and TdT RNA is expressed exclus
298                           Dual labeling with TdT and an antibody against protein disulfide isomerase,
299 l death was analyzed by double labeling with TdT-dUTP terminal nick-end labeling and cone-specific an
300                         Partial overlap with TdT(+) cells suggested that distinctive early lymphocyte

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