about
Integrase-Deficient Lentiviral Vector as an All-in-One Platform for Highly Efficient CRISPR/Cas9-Mediated Gene EditingCRISPR/Cas9-mediated targeted mutagenesis in upland cotton (Gossypium hirsutum L.).Non-viral delivery of genome-editing nucleases for gene therapy.Gene therapies that restore dystrophin expression for the treatment of Duchenne muscular dystrophy.In Vivo Delivery of CRISPR/Cas9 for Therapeutic Gene Editing: Progress and Challenges.Therapeutic gene editing: delivery and regulatory perspectivesGenome engineering: a new approach to gene therapy for neuromuscular disorders.Immunity to CRISPR Cas9 and Cas12a therapeutics.A Protocol for the Production of Integrase-deficient Lentiviral Vectors for CRISPR/Cas9-mediated Gene Knockout in Dividing Cells.Direct Cytosolic Delivery of CRISPR/Cas9-Ribonucleoprotein for Efficient Gene Editing.Boosting, Not Breaking: CRISPR Activators Treat Disease Models.Harnessing natural DNA modifying activities for editing of the genome and epigenome.RNA-guided transcriptional silencing in vivo with S. aureus CRISPR-Cas9 repressors.Targeted Delivery of CRISPR/Cas9-Mediated Cancer Gene Therapy via Liposome-Templated Hydrogel Nanoparticles.VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Engineering Delivery Vehicles for Genome Editing.
@en
type
label
Engineering Delivery Vehicles for Genome Editing.
@en
prefLabel
Engineering Delivery Vehicles for Genome Editing.
@en
P1476
Engineering Delivery Vehicles for Genome Editing
@en
P2093
Charles A Gersbach
P304
P356
10.1146/ANNUREV-CHEMBIOENG-080615-034711
P577
2016-04-21T00:00:00Z