Magnetic separation and antibiotics selection enable enrichment of cells with ZFN/TALEN-induced mutations.
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Enhancing Targeted Genomic DNA Editing in Chicken Cells Using the CRISPR/Cas9 SystemSimple and efficient methods for enrichment and isolation of endonuclease modified cellsThe cell proliferation antigen Ki-67 organises heterochromatinGene disruption by cell-penetrating peptide-mediated delivery of Cas9 protein and guide RNA.Production of CMAH Knockout Preimplantation Embryos Derived From Immortalized Porcine Cells Via TALE Nucleases.Targeted inversion and reversion of the blood coagulation factor 8 gene in human iPS cells using TALENsProduction of Mutated Porcine Embryos Using Zinc Finger Nucleases and a Reporter-based Cell Enrichment SystemHepatitis C virus entry is impaired by claudin-1 downregulation in diacylglycerol acyltransferase-1-deficient cells.Simultaneous screening and validation of effective zinc finger nucleases in yeastTALEN-based knockout library for human microRNAs.Generation of CCR5-defective CD34 cells from ZFN-driven stop codon-integrated mesenchymal stem cell clones.Rh D blood group conversion using transcription activator-like effector nucleases.Efficient PRNP deletion in bovine genome using gene-editing technologies in bovine cells.Re-evaluation of the roles of DROSHA, Export in 5, and DICER in microRNA biogenesis.Efficient Genome Editing in Chicken DF-1 Cells Using the CRISPR/Cas9 SystemHeroes of peer review: Hyongbum (Henry) KimA guide to genome engineering with programmable nucleases.Precision genome editing: a small revolution for glycobiology.Recent developments and clinical studies utilizing engineered zinc finger nuclease technology.An efficient method to enrich for knock-out and knock-in cellular clones using the CRISPR/Cas9 system.A stable but reversible integrated surrogate reporter for assaying CRISPR/Cas9-stimulated homology-directed repair.Genome editing using FACS enrichment of nuclease-expressing cells and indel detection by amplicon analysis.Generation of Human Embryonic Stem Cell Line Expressing zsGreen in Cholinergic Neurons Using CRISPR/Cas9 System.Enhanced gene disruption by programmable nucleases delivered by a minicircle vector.Synthetically modified guide RNA and donor DNA are a versatile platform for CRISPR-Cas9 engineeringFAST-id system for enrichment of cells with TALEN-induced mutations and large deletions.Apancreatic pigs cloned using Pdx1-disrupted fibroblasts created via TALEN-mediated mutagenesis.Knockout of miR-221 and miR-222 reveals common and specific targets for paralogous miRNAs.
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P2860
Magnetic separation and antibiotics selection enable enrichment of cells with ZFN/TALEN-induced mutations.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@ast
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@en
type
label
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@ast
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@en
prefLabel
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@ast
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@en
P2093
P2860
P1433
P1476
Magnetic separation and antibi ...... h ZFN/TALEN-induced mutations.
@en
P2093
Choong-il Lee
Gabbine Wee
Hyojin Kim
Jin-Soo Kim
Myung-Sun Kim
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P304
P356
10.1371/JOURNAL.PONE.0056476
P407
P50
P577
2013-02-18T00:00:00Z