ライフサイエンスコーパス: terminal transferase

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.

5 nternal to Pol IV transcript ends and RDR2's terminal transferase activity collectively yield a code

6 We further find that Poltheta terminal transferase activity is most efficient on DNA c

7 hesis, NTA, template jumping, and the unique terminal transferase activity of Bombyx mori R2 non-long

8 Finally, the terminal transferase activity of DeltaC(21)-NS5B was fou

9 eated by RT were ragged, probably due to the terminal transferase activity of RT.

10 The terminal transferase activity of telomerase may account

11 at the 5'-end of RNA template influences the terminal transferase activity of the RT.

12 eases, and enzymes with template-independent terminal transferase activity such as Taq polymerase.

13 RDR2 terminal transferase activity, also demonstrated in vitr

14 mplate allow for a unique template-dependent terminal transferase activity.

15 , NTP substrate selection, and modulation of terminal transferase activity.

16 de novo initiation by NS5B rather than by a terminal transferase activity.

17 oscillating between three different modes of terminal transferase activity: non-templated extension,

18 deoxyribonucleoside 5'-triphosphates) and by terminal transferase addition of a fluorescently labeled

19 of s-ODN in situ with digoxigenin-dUTP using terminal transferase and detection using anti-digoxigeni

20 the cases for gap filling, largely affected terminal transferase and end-joining activities.

21 ce of Polmu which has a critical role during terminal transferase and end-joining activities: it acts

22 q), a multiplex indexing method based on TdT terminal transferase and T4 DNA ligase-mediated barcodin

23 ctivities, including gap-filling polymerase, terminal transferase, and primase, and is also a 3' to 5

24 independent nucleotide addition by mammalian terminal transferase, blocks exonucleolytic proofreading

25 nce for apoptosis was examined using in situ terminal transferase d-UTP nick-end labeling (TUNEL) sta

26 method is adapted from reverse transcription-terminal transferase-dependent PCR (RT-TDPCR) to include

27 enome and in the cII transgene determined by terminal transferase-dependent PCR (TD-PCR).

28 This terminal transferase-dependent PCR (TDPCR) method can ge

29 e investigated the analysis of RNA by use of terminal transferase-dependent PCR (TDPCR), a procedure

30 informative was UV photofootprinting, using terminal transferase-dependent PCR and nonradioactive de

31 BC cleavage and ligation-mediated PCR or the terminal transferase-dependent PCR method, we have deter

32 Mapping of DNA damages by terminal transferase-dependent PCR revealed preferential

33 BP-induced DNA adducts along the cII gene by terminal transferase-dependent PCR showed the formation

34 Mapping of DNA adducts by terminal transferase-dependent PCR showed the preferenti

35 e resolution using ligation-mediated PCR and terminal transferase-dependent PCR.

36 We used the terminal transferase-dependent polymerase chain reaction

37 and/or irradiated with UVA as determined by terminal transferase-dependent polymerase chain reaction

38 By terminal transferase dUTP nick end labeling (TUNEL) in c

39 voking hair-cell death, as judged by lack of terminal transferase dUTP nick end labeling (TUNEL) labe

40 is hypothesis, we quantified apoptosis using terminal transferase dUTP nick end labeling and active c

41 ermined the incidence of apoptosis by either terminal transferase dUTP nick end labeling or annexin-V

42 ats on capillary cell apoptosis (detected by terminal transferase dUTP nick-end labeling [TUNEL]) and

43 in wild-type animals with EAU, by using the terminal transferase dUTP nick-end labeling assay and po

44 Apoptosis was estimated by terminal transferase dUTP-biotin nick-end labeling (TUNE

45 ing for BrdU incorporation and cell death by terminal transferase dUTP-nick end labeling (TUNEL), 3'-

46 mentation in dying cells was monitored using terminal transferase-dUTP nick-end labeling (TUNEL).

47 Terminal transferase end-labeling analysis indicated tha

48 al assembly of silent chromatin at the mouse terminal transferase gene (Dntt), which is silenced and

49 erizes Poltheta as among the most proficient terminal transferases known.

50 es of cytoplasmic polyadenylation machinery, terminal transferase-like enzymes, and the viral polymer

51 The hearts were then harvested for the terminal transferase-mediated 2'-deoxyuridine, 5'-tripho

52 By using both the terminal transferase-mediated deoxyuridine nick-end labe

53 ch stains pyknotic nuclei intensely, or with terminal transferase-mediated deoxyuridine triphosphate

54 Terminal transferase-mediated deoxyuridine triphosphate

55 Brains from these rats were processed by the terminal transferase-mediated deoxyuridine triphosphate-

56 ugmented p75 immunoreactivity at a time when terminal transferase-mediated deoxyuridine trophosphate

57 We studied apoptosis by terminal transferase-mediated DNA nick end labeling assa

58 Internucleosomal DNA fragmentation and terminal transferase-mediated dUTP digoxigenin nick end

59 poptosis was verified by ultrastructural and terminal transferase-mediated dUTP nick end labeling ana

60 Using two different in situ techniques, terminal transferase-mediated dUTP nick end labeling and

61 Enhanced apoptosis was verified by the terminal transferase-mediated dUTP nick end labeling ass

62 In situ terminal transferase-mediated dUTP nick end-labeling (TU

63 trated a strong synergism as verified by the terminal transferase-mediated dUTP nick-end labeling (TU

64 Capillary cell apoptosis (by terminal transferase-mediated dUTP nick-end labeling) an

65 -beta1 was examined by DNA fragmentation and terminal transferase-mediated dUTP-biotin end labeling a

66 Using terminal transferase-mediated dUTP-digoxigenin nick end

67 vo and in isolated hepatocytes determined by terminal transferase-mediated dUTP-digoxigenin nick end-

68 Terminal transferase-mediated end-labeling and DNA ladde

69 ation by electron microscopy, and by in situ terminal transferase-mediated nick end labeling of fragm

70 natal day 22, animals were analyzed by using terminal transferase-mediated nick-end labeling to ident

71 and that telomerase was a specific telomere-terminal transferase necessary for the replication of ch

72 o, as evidenced by acridine orange staining, terminal transferase nick end translation (TUNEL), and D

73 The UVB-induced lesions detected by terminal transferase-PCR were almost exclusively mapped

74 e nuclease-resistant oligonucleotides and 3'-terminal transferase tailing.

75 Terminal transferase (TdT), when incubated with a purifi

76 Terminal transferase (TdT)-mediated deoxyuridine triphos

77 Human telomerase is a terminal transferase that adds TTAGGG units onto the tel

78 NA polymerase (RdRp) was reported to possess terminal transferase (TNTase) activity, the ability to a

79 Even as a terminal transferase, yeast telomerase retains a species