Efficient genome editing in the mouse brain by local delivery of engineered Cas9 ribonucleoprotein complexes.
about
Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery.CRISPR/Cas9 system: a powerful technology for in vivo and ex vivo gene therapy.Models for discovery of targeted therapy in genetic epileptic encephalopathies.The Promise and Challenge of In Vivo Delivery for Genome Therapeutics.Immunity to CRISPR Cas9 and Cas12a therapeutics.A thermostable Cas9 with increased lifetime in human plasma.Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR.Engineering the Delivery System for CRISPR-Based Genome Editing.Evolution and Clinical Translation of Drug Delivery Nanomaterials.In vivo genome editing in animals using AAV-CRISPR system: applications to translational research of human disease.The prospects of CRISPR-based genome engineering in the treatment of neurodegenerative disorders.Somatic genome editing with the RCAS-TVA-CRISPR-Cas9 system for precision tumor modeling.CRISPR RNAs trigger innate immune responses in human cells.Applications of CRISPR/Cas9 in the Mammalian Central Nervous System.Chemically Modified Cpf1-CRISPR RNAs Mediate Efficient Genome Editing in Mammalian Cells.Receptor-Mediated Delivery of CRISPR-Cas9 Endonuclease for Cell Type Specific Gene Editing.Genome engineering for CNS injury and disease.Neuroepigenetic Editing.Somatic mutations in neurons during aging and neurodegeneration.Application of the CRISPR/Cas9 System to Drug Resistance in Breast Cancer.Autism spectrum disorder: prospects for treatment using gene therapy.Covalent linkage of the DNA repair template to the CRISPR-Cas9 nuclease enhances homology-directed repair.Unraveling of Central Nervous System Disease Mechanisms Using CRISPR Genome Manipulation.In vivo methods for acute modulation of gene expression in the central nervous systemThe synthetic histone-binding regulator protein PcTF activates interferon genes in breast cancer cellsIn vitro-transcribed guide RNAs trigger an innate immune response via the RIG-I pathwayNext-Generation Modeling of Human CancersA peptide delivery system sneaks CRISPR into cellsTRIAMF: A New Method for Delivery of Cas9 Ribonucleoprotein Complex to Human Hematopoietic Stem CellsCRISPR-delivery particles targeting nuclear receptor-interacting protein 1 () in adipose cells to enhance energy expenditure
P2860
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P2860
Efficient genome editing in the mouse brain by local delivery of engineered Cas9 ribonucleoprotein complexes.
description
2017 nî lūn-bûn
@nan
2017 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@ast
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@en
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@nl
type
label
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@ast
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@en
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@nl
prefLabel
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@ast
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@en
Efficient genome editing in th ...... 9 ribonucleoprotein complexes.
@nl
P2093
P2860
P356
P1433
P1476
Efficient genome editing in th ...... s9 ribonucleoprotein complexes
@en
P2093
Anirvan Ghosh
Ashwin A Banfal
Brett T Staahl
Claire Coulon-Bainier
Cole Urnes
Gabriela Acevedo Munares
Jennifer K Sabo
Madhurima Benekareddy
Stephen N Floor
P2860
P2888
P304
P356
10.1038/NBT.3806
P577
2017-02-13T00:00:00Z