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1 ough linked protein domains (e.g. TALENs and zinc-finger nucleases).
2 th activity on par with a homodimeric Zif268 zinc-finger nuclease.
3 we compared with the well-established 'QQR' zinc-finger nuclease.
4 integrating RNA destabilizing elements using zinc finger nucleases.
5 a cells by targeted mutation of exon 8 using zinc finger nucleases.
6 ogenous Ig loci were silenced using designer zinc finger nucleases.
7 on of alpha or beta TCR chains with designer zinc finger nucleases.
8 t HIV Rev protein M10, fusion inhibitors and zinc-finger nucleases.
9 ation can now be reliably accomplished using zinc-finger nucleases.
12 er other sequence-specific nucleases, namely zinc finger nucleases and meganucleases, lies in their e
13 to other customizable endonucleases, such as zinc finger nucleases and transcription activator-like e
14 efficiencies similar to those obtained using zinc finger nucleases and transcription activator-like e
15 Tev-LHEs are distinct from the FokI-derived zinc-finger nuclease and TAL effector nuclease platforms
17 ed the Plasmodium falciparum K13 locus using zinc-finger nucleases and measured ring-stage survival r
18 porter gene carried a recognition site for a zinc-finger nuclease, and protoplasts from each tobacco
23 codons and exerting control by microRNAs or zinc finger nucleases--are providing new ways of control
24 g DSBs (5' DSBs) in yeast using an optimized zinc finger nuclease at an efficiency that approached HO
28 double-strand break induced by the resulting zinc-finger nuclease can create specific sequence altera
30 n vivo applications and to determine whether zinc finger nucleases create undesired genomic instabili
34 assist selection of rare targeted clones and zinc finger nucleases engineered to specifically stimula
35 ial fingers can be used to create functional zinc finger nucleases for editing vertebrate genomes.
38 emonstrate that chromosome breaks created by zinc-finger nucleases greatly enhance the frequency of l
42 as an anticancer strategy, we disrupted, via zinc finger nucleases, MCT4 and BASIGIN genes in colon a
43 d mitochondrial DNA (mtDNA) damage and after zinc finger nuclease-mediated gene mutation correction,
48 as motor and behavioural function in a novel zinc-finger nuclease model of RTT utilizing both male an
50 strate that temporally optimized delivery of zinc finger nuclease mRNA via electroporation and adeno-
52 ns and in cells genetically engineered using zinc-finger nucleases, single-nucleotide changes occur f
53 ines made deficient in O-glycan extension by zinc finger nuclease targeting of a key gene in O-glycan
56 developed a novel Bace1(-/-) rat line using zinc-finger nuclease technology and compared Bace1(-/-)
58 from several breast cancer cell lines using Zinc-Finger Nuclease technology, which resulted in drast
61 are other potential biotechnologies, such as zinc finger nucleases, that could be also used for trans
68 ogies for facile manipulation of the genome (zinc finger nucleases, transcription activator-like effe
70 e mainstream genome editing tools, including zinc finger nucleases, transcription activator-like effe
72 t expression of sequence-specific nucleases (zinc-finger nucleases, transcription activator-like effe
79 o wild-type (MSTN(+/+) ) rats, rats in which zinc finger nucleases were used to genetically inactivat
80 ome of the Dahl Salt-sensitive (S) rat using zinc-finger nucleases, wherein the mutant rat had a 17 b
81 ccelerated site-specific DNA cleavage by the zinc-finger nuclease, without enhancing off-target cleav
82 ement therapies that addresses these issues: zinc finger nuclease (ZFN) -mediated site-specific integ
83 activator-like effector nuclease (TALEN) and zinc finger nuclease (ZFN) can be engineered into site-s
85 activator-like effector nuclease (TALEN) and zinc finger nuclease (ZFN) genome editing technology ena
87 we report that combining electroporation of zinc finger nuclease (ZFN) mRNA with donor template deli
90 FP respectively) by targeted integration via zinc finger nuclease (ZFN)--mediated homologous recombin
92 past two years, advances in transposon- and zinc finger nuclease (ZFN)-mediated gene knockout as wel
94 ate a method for ligand-mediated delivery of zinc finger nucleases (ZFN) proteins using transferrin r
96 ryonic stem cell (ESC)-based gene targeting, zinc-finger nuclease (ZFN) and transcription activator-l
102 no-associated virus (AAV) vector delivery of zinc finger nucleases (ZFNs) and corrective donor templa
103 vectors by using a combination of engineered zinc finger nucleases (ZFNs) and homing endonucleases.
105 ering sequence-specific nucleases, including zinc finger nucleases (ZFNs) and TAL effector nucleases
107 ablished a broadly applicable strategy using zinc finger nucleases (ZFNs) and transcription activator
113 ed double-strand break induced by engineered zinc finger nucleases (ZFNs) can stimulate integration o
116 on of genomic double-strand breaks (DSBs) by zinc finger nucleases (ZFNs) has been deployed for gene
121 The first truly targetable reagents were the zinc finger nucleases (ZFNs) showing that arbitrary DNA
122 off-target site for the extensively studied zinc finger nucleases (ZFNs) targeting C-C chemokine rec
123 stability in mammalian systems, we developed zinc finger nucleases (ZFNs) that recognize and cleave C
124 by the transient expression of CCR5-targeted zinc finger nucleases (ZFNs) to generate CCR5-negative c
126 ds for identifying the off-target effects of zinc finger nucleases (ZFNs) were described-one using an
130 dopsis genes through regulated expression of zinc finger nucleases (ZFNs)-enzymes engineered to creat
134 relies on cleavage of the target by designed zinc-finger nucleases (ZFNs) and production of a linear
138 of engineered site-directed nucleases, like zinc-finger nucleases (ZFNs) and transcription activator
147 ly, we and others have shown that customized zinc-finger nucleases (ZFNs) can introduce targeted fram
161 olution to this problem: the use of designed zinc-finger nucleases (ZFNs) that induce a double-strand
162 d genetic engineering of this parasite using zinc-finger nucleases (ZFNs) that produce a double-stran
165 -resistant genotype de novo using engineered zinc-finger nucleases (ZFNs) to disrupt endogenous CCR5.
168 gene-targeting approach in the monarch using zinc-finger nucleases (ZFNs), engineered nucleases that
169 s strains (including wild-type CC-125) using zinc-finger nucleases (ZFNs), genetically encoded CRISPR
171 uding homing endonucleases or meganucleases, zinc-finger nucleases (ZFNs), TAL effector nucleases (TA
174 ree classes of targetable cleavage reagents: zinc-finger nucleases (ZFNs), transcription activator-li
176 rgeting in mice using embryonic injection of zinc-finger nucleases (ZFNs), which generate site-specif
177 To stably modify this organism, we used zinc-finger nucleases (ZFNs), which take advantage of ho
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