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1 hat could be radiolabeled by dideoxy ATP and terminal transferase.
2 mode of DNA synthesis, acting in effect as a terminal transferase.
3 lymerase, CCA-adding enzyme, and nonspecific terminal transferase.
4 en all available 3' DNA ends were labeled by terminal transferase.
9 eases, and enzymes with template-independent terminal transferase activity such as Taq polymerase.
14 oscillating between three different modes of terminal transferase activity: non-templated extension,
15 deoxyribonucleoside 5'-triphosphates) and by terminal transferase addition of a fluorescently labeled
16 of s-ODN in situ with digoxigenin-dUTP using terminal transferase and detection using anti-digoxigeni
18 ce of Polmu which has a critical role during terminal transferase and end-joining activities: it acts
19 ctivities, including gap-filling polymerase, terminal transferase, and primase, and is also a 3' to 5
20 independent nucleotide addition by mammalian terminal transferase, blocks exonucleolytic proofreading
21 nce for apoptosis was examined using in situ terminal transferase d-UTP nick-end labeling (TUNEL) sta
22 method is adapted from reverse transcription-terminal transferase-dependent PCR (RT-TDPCR) to include
25 e investigated the analysis of RNA by use of terminal transferase-dependent PCR (TDPCR), a procedure
26 informative was UV photofootprinting, using terminal transferase-dependent PCR and nonradioactive de
27 BC cleavage and ligation-mediated PCR or the terminal transferase-dependent PCR method, we have deter
29 BP-induced DNA adducts along the cII gene by terminal transferase-dependent PCR showed the formation
33 and/or irradiated with UVA as determined by terminal transferase-dependent polymerase chain reaction
35 voking hair-cell death, as judged by lack of terminal transferase dUTP nick end labeling (TUNEL) labe
36 is hypothesis, we quantified apoptosis using terminal transferase dUTP nick end labeling and active c
37 ermined the incidence of apoptosis by either terminal transferase dUTP nick end labeling or annexin-V
38 ats on capillary cell apoptosis (detected by terminal transferase dUTP nick-end labeling [TUNEL]) and
39 in wild-type animals with EAU, by using the terminal transferase dUTP nick-end labeling assay and po
41 ing for BrdU incorporation and cell death by terminal transferase dUTP-nick end labeling (TUNEL), 3'-
42 mentation in dying cells was monitored using terminal transferase-dUTP nick-end labeling (TUNEL).
44 al assembly of silent chromatin at the mouse terminal transferase gene (Dntt), which is silenced and
46 es of cytoplasmic polyadenylation machinery, terminal transferase-like enzymes, and the viral polymer
49 ch stains pyknotic nuclei intensely, or with terminal transferase-mediated deoxyuridine triphosphate
51 Brains from these rats were processed by the terminal transferase-mediated deoxyuridine triphosphate-
52 ugmented p75 immunoreactivity at a time when terminal transferase-mediated deoxyuridine trophosphate
55 poptosis was verified by ultrastructural and terminal transferase-mediated dUTP nick end labeling ana
59 trated a strong synergism as verified by the terminal transferase-mediated dUTP nick-end labeling (TU
61 -beta1 was examined by DNA fragmentation and terminal transferase-mediated dUTP-biotin end labeling a
63 vo and in isolated hepatocytes determined by terminal transferase-mediated dUTP-digoxigenin nick end-
65 ation by electron microscopy, and by in situ terminal transferase-mediated nick end labeling of fragm
66 natal day 22, animals were analyzed by using terminal transferase-mediated nick-end labeling to ident
67 o, as evidenced by acridine orange staining, terminal transferase nick end translation (TUNEL), and D
72 NA polymerase (RdRp) was reported to possess terminal transferase (TNTase) activity, the ability to a
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