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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
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
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
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-
30 -associated defects with more 53BP1 foci and TdT-mediated dNTP nick end labeling-positive cells over
37 l) X family members (pol mu, pol lambda, and TdT, but not pol beta) contribute to junctional addition
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)
45 llenging adult TdT-sufficient (TdT(+/+)) and TdT-deficient (TdT(-/-)) gene-targeted mice, limited to
47 deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) donor cells, demonstrate preferential repertoir
51 dition, analysis for evidence for apoptosis (TdT-dUTP terminal nick-end label [TUNEL] staining) and p
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
60 e is required for HSI and that N addition by TdT is a more effective mechanism in the induction of a
66 ry, 70% of medial SMCs appeared apoptotic by TdT-mediated dUTP nick end labeling (TUNEL) analysis and
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
74 se in apoptosis (assessed morphologically by TdT-mediated dUTP nick- end labeling staining) is preced
77 eavage reaction can be efficiently tailed by TdT, suggesting that the RAG proteins disassemble from t
79 e complementary determining region 3 (CDR3) (TdT(-/-)) and mice with altered Ab repertoires due to re
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
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
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
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
100 This region, although not important for TdT polymerization activity, contains a BRCA1 C-terminal
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
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
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
118 vage of DEVD-AMC and blocked the increase in TdT-mediated dUTP nick end labeling (TUNEL) positivity.
120 more severely impaired HSI were observed in TdT(-/-) mice compared to those in Delta D-iD mice, whil
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
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
134 itors that were Lin(-)IL-7R alpha(+)c-kit(lo)TdT(+) (lineage marker(-), interleukin receptor 7 alpha(
137 tested 21 MCCs for the expression of MCPyV, TdT, PAX5, IgG, IgM, IgA, kappa, and lambda by immunohis
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
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
151 d B-1a cell IgM developing in the absence of TdT, increased in 7- to 24-mo-old mice as compared with
157 ensive postneonatally due to the activity of TdT, which adds nontemplated N nucleotides to Ig and TCR
162 tural alterations, 2) enzymatic detection of TdT-positive DNA degradation, and 3) automated cytometri
165 ntial for 1) up-regulating the expression of TdT and IL-7R alpha, 2) initiating the production of cmu
168 e N-nucleotide addition by the short form of TdT, but did not increase nucleotide deletion from codin
171 c mutation are compensated by early onset of TdT activity and other mechanisms that contribute to CDR
173 demonstrates that the N-terminal portion of TdT, including the BRCA-1 C-terminal (BRCT) domain, is n
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.
179 chains, together with the down-regulation of TdT transcription in pre-B cells (prior to light chain p
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
186 nd P berghei iRBCs with apoptotic parasites (TdT(+)) exhibited minimal platelet binding (<5%), which
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
192 Such regulated access would help to prevent TdT from acting at other types of broken ends and degrad
194 on-chip labeling method, we also quantified TdT mediated signal amplification on the surface by immo
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
203 osis-associated DNA strand breaks by in situ TdT labeling showed that a significant number of flavopi
206 ed for degeneration-induced silver staining, TdT-mediated dUTP-digoxigenin nick end-labeling (TUNEL)
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.
213 n addition to the G preference, we find that TdT adds strings of purines or strings of pyrimidines at
217 th a baculovirus expression system show that TdT can interact specifically with each of the Ku subuni
219 blasts, sorted postimmunization, showed that TdT(-/-) mice generate a lower frequency of the predomin
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
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
233 DNA fragmentation was determined using the TdT-dUTP terminal nick-end labeling assay and by agarose
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.
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
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
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
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
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
277 e terminal deoxyribonucleotidyl transferase (TdT)-mediated dUTP Nick End Labeling (TUNEL) assay.
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
289 , in situ staining for apoptotic cells using TdT-mediated dUTP-digoxigenin nick-end labeling (TUNEL),
293 th Ku suggests a possible mechanism by which TdT is recruited to the sites of DSBs such as V(D)J reco
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
299 l death was analyzed by double labeling with TdT-dUTP terminal nick-end labeling and cone-specific an
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