Correction of a genetic disease in mouse via use of CRISPR-Cas9.
about
CRISPR/Cas9-mediated gene editing in human tripronuclear zygotesSpermatogonial stem cell autotransplantation and germline genomic editing: a future cure for spermatogenic failure and prevention of transmission of genomic diseasesCRISPR/Cas9: Implications for Modeling and Therapy of Neurodegenerative DiseasesCustomizing the genome as therapy for the β-hemoglobinopathiesThe Rise of CRISPR/Cas for Genome Editing in Stem CellsGenome-editing Technologies for Gene and Cell TherapyGenome Editing and Its Applications in Model OrganismsNeuroprotective therapies in glaucoma: II. Genetic nanotechnology toolsOligonucleotide-directed mutagenesis for precision gene editingMinimizing off-Target Mutagenesis Risks Caused by Programmable NucleasesBreaking bad: The mutagenic effect of DNA repairAdvances in CRISPR-Cas9 genome engineering: lessons learned from RNA interferenceRNA-guided CRISPR-Cas technologies for genome-scale investigation of disease processesCRISPR-Cas9 delivery to hard-to-transfect cells via membrane deformationSurvival and Evolution of CRISPR-Cas System in Prokaryotes and Its ApplicationsThe CRISPR system can correct or modify the expression of genes responsible for hereditary diseasesTherapeutic genome editing: prospects and challengesBacterial CRISPR/Cas DNA endonucleases: A revolutionary technology that could dramatically impact viral research and treatmentDevelopment and applications of CRISPR-Cas9 for genome engineering.CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx MiceCRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.Decoding the complex genetic causes of heart diseases using systems biologyEfficient gene disruption in diverse strains of Toxoplasma gondii using CRISPR/CAS9.Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivoA class of circadian long non-coding RNAs mark enhancers modulating long-range circadian gene regulation.Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells.Allele-specific genome editing and correction of disease-associated phenotypes in rats using the CRISPR-Cas platformCharacterization of genomic deletion efficiency mediated by clustered regularly interspaced palindromic repeats (CRISPR)/Cas9 nuclease system in mammalian cells.Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype.The potential of the combination of CRISPR/Cas9 and pluripotent stem cells to provide human organs from chimaeric pigs.CRISPR/Cas9 in allergic and immunologic diseases.Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells.Seamless gene correction of β-thalassemia mutations in patient-specific iPSCs using CRISPR/Cas9 and piggyBac.Protospacer adjacent motif (PAM)-distal sequences engage CRISPR Cas9 DNA target cleavage.A CRISPR view of development.CRISPR-mediated direct mutation of cancer genes in the mouse liverTALEN and CRISPR/Cas Genome Editing Systems: Tools of Discovery.CRISPR-based technologies: prokaryotic defense weapons repurposedPrevention of muscular dystrophy in mice by CRISPR/Cas9-mediated editing of germline DNAA mouse geneticist's practical guide to CRISPR applications.
P2860
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P2860
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
description
2013 nî lūn-bûn
@nan
2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@ast
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@en
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@nl
type
label
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@ast
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@en
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@nl
prefLabel
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@ast
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@en
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@nl
P2093
P1433
P1476
Correction of a genetic disease in mouse via use of CRISPR-Cas9.
@en
P2093
Dangsheng Li
Jinsong Li
Meizhu Bai
Shiming Bao
Yinghua Wang
Zhiqiang Yan
P304
P356
10.1016/J.STEM.2013.10.016
P407
P577
2013-12-01T00:00:00Z