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1 i-functional maturase protein that is also a DNA endonuclease.
2 ndromic repeat (CRISPR)/Cas-based RNA-guided DNA endonucleases.
3 break at defined locations by site-specific DNA endonucleases.
4 neering of universal programmable RNA-guided DNA endonucleases.
5 phosphate for bottom-strand cleavage at the DNA endonuclease active site and then reposition the 3'
6 ode reverse transcriptase, RNA maturase, and DNA endonuclease activities for site-specific DNA insert
7 -encoded reverse transcriptase, maturase and DNA endonuclease activities for site-specific insertion
9 oded reverse transcriptase and site-specific DNA endonuclease activities required for this process.
14 We also demonstrate that the single-stranded DNA endonuclease activity of this T. thermophilus domain
15 eA inhibits this mechanism of HGT in cis via DNA endonuclease activity that is localized to the perip
16 vatives displays DNA-binding specificity and DNA endonuclease activity that is similar to that of the
17 oded reverse transcriptase uses a C-terminal DNA endonuclease activity to cleave the opposite strand
23 ossesses manganese-dependent single-stranded DNA endonuclease and 3' to 5' exonuclease activities.
24 purified from yeast, it is a single-stranded DNA endonuclease and a DNA-dependent ATPase, suggesting
25 of the Affymetrix p53 chip and the Surveyor DNA endonuclease and denaturing high-performance liquid
26 I-Ssp6803I represents a novel intron-encoded DNA endonuclease and is the first example of a chromosom
29 we show that the Streptococcus pyogenes Cas9 DNA endonuclease and single guide RNAs (sgRNAs) produced
30 in and excised intron RNA have site-specific DNA endonuclease and target DNA-primed reverse transcrip
31 , and is a member of the LAGLIDADG family of DNA endonucleases, but appears to have lost DNA cleavage
32 n from Aspergillus nidulans encodes a homing DNA endonuclease called I-AniI which also functions as a
35 eases (LHEs) are a family of highly specific DNA endonucleases capable of recognizing target sequence
37 nd breaks (DSBs) generated by the RNA-guided DNA endonuclease Cas9 determine how gene function is alt
39 ted (Cas) systems employ the dual RNA-guided DNA endonuclease Cas9 to defend against invading phages
41 ne systems in bacteria use a dual RNA-guided DNA endonuclease, Cas9, to cleave foreign DNA at specifi
43 1, redox effector-1), a key redox sensor and DNA endonuclease critical for oxidative DNA damage repai
44 that encode proteins lacking the C-terminal DNA endonuclease domain and for group II intron retrotra
45 ype and mutant LtrA proteins showed that the DNA endonuclease domain contains a single tightly bound
46 A UV-cross-linking assay showed that these DNA endonuclease domain mutations do not block DNA prime
48 ified features of the DNA-binding region and DNA endonuclease domain that are conserved in LtrA and r
49 at contributes to DNA binding, followed by a DNA endonuclease domain that contains conserved sequence
50 the intron-encoded protein uses a C-terminal DNA endonuclease domain to cleave the opposite strand an
51 the intron-encoded protein uses a C-terminal DNA endonuclease domain to cleave the opposite strand an
53 ins have reverse transcriptase, maturase and DNA endonuclease domains characteristic of canonical gro
55 LAGLIDADG and HNH families of site-specific DNA endonucleases encoded by viruses, bacteriophages as
56 Homing endonucleases are highly specific DNA endonucleases, encoded within mobile introns or inte
61 e GAL1 promoter joined to PvuII, a bacterial DNA endonuclease gene, are toxic to yeast cells even und
66 reveals the general utility of site-specific DNA endonucleases in producing targeted homologous recom
67 rved sequence motifs characteristic of H-N-H DNA endonucleases, interspersed with two pairs of conser
69 ERCC1-XPF heterodimer, a structure-specific DNA endonuclease, is best known for its function in the
70 trons, the Bastille intron encodes a nicking DNA endonuclease of the H-N-H family, I-BasI, with a cle
71 group J protein (FACJ, BRIP1)-deficient, or DNA endonuclease RBBP8 (CtIP)-compromised cells, whereas
72 we characterized the C-terminal DNA-binding/DNA endonuclease region of the LtrA protein encoded by t
75 independent ICL repair mechanism, in which a DNA endonuclease(s) unhooks an ICL from the leading stra
76 re converted to double-strand breaks using a DNA endonuclease (Surveyor) and oligonucleotide tails ar
78 The td intron of bacteriophage T4 encodes a DNA endonuclease that initiates intron homing to cognate
79 nd Slx4 are subunits of a structure-specific DNA endonuclease that is found in Saccharomyces cerevisi
80 ity) and then with the excised intron form a DNA endonuclease that mediates intron mobility by target
81 associated with the excised intron to form a DNA endonuclease that mediates intron mobility by target
82 ith the excised intron, form a site-specific DNA endonuclease that promotes intron mobility by revers
83 se activity, telomerase is associated with a DNA endonuclease that removes nucleotides from a primer
84 ) the putative HEG encodes a double-stranded DNA endonuclease that specifically cleaves intron-free h
86 SPR-associated protein Cas9 is an RNA-guided DNA endonuclease that uses RNA-DNA complementarity to id
87 Homing endonucleases are sequence-tolerant DNA endonucleases that act as mobile genetic elements.
88 on splicing (maturases) or are site-specific DNA endonucleases that function in intron mobility (a pr
89 member of a new family of structure-specific DNA endonucleases that interact with the replication cla
93 which employs Surveyor, a mismatch-specific DNA endonuclease, to remove errors from synthetic genes.
95 uI and I-BasI are two highly similar nicking DNA endonucleases, which are each encoded by a group I i
96 from Streptococcus pyogenes is an RNA-guided DNA endonuclease with widespread utility for genome modi
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