High Efficiency Gene Correction in Hematopoietic Cells by Donor-Template-Free CRISPR/Cas9 Genome Editing-Reference-Cited by-同舟云学术

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High Efficiency Gene Correction in Hematopoietic Cells by Donor-Template-Free CRISPR/Cas9 Genome Editing

Published:2018-03 Issue: Volume:10 Page:1-8
ISSN:2162-2531
Container-title:Molecular Therapy - Nucleic Acids
language:en
Short-container-title:Molecular Therapy - Nucleic Acids

Author:

Sürün Duran,Schwäble Joachim,Tomasovic Ana,Ehling Roy,Stein Stefan,Kurrle Nina,von Melchner Harald,Schnütgen Frank

Funder

Deutsche Forschungsgemeinschaft

Bundesministerium für Bildung und Forschung

NGFNplus-DiGtoPconsortium

Loewe Center for Cell and Gene Therapy

Publisher

Elsevier BV

Subject

Drug Discovery,Molecular Medicine

Reference39 articles.

1. Gene therapy for primary immunodeficiencies: looking ahead, toward gene correction;Pessach;J. Allergy Clin. Immunol.,2011

2. Clinical applications of gene therapy for primary immunodeficiencies;Cicalese;Hum. Gene Ther.,2015

3. Ex vivo gene transfer and correction for cell-based therapies;Naldini;Nat. Rev. Genet.,2011

4. A conditional knockout resource for the genome-wide study of mouse gene function;Skarnes;Nature,2011

5. Highly efficient endogenous human gene correction using designed zinc-finger nucleases;Urnov;Nature,2005

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1. Targeted knock-in of NCF1 cDNA into the NCF2 locus leads to myeloid phenotypic correction of p47 -deficient chronic granulomatous disease;Molecular Therapy - Nucleic Acids;2024-09

2. Application of Transgenic Technology in Identification for Gene Function on Grasses;Phyton;2024

3. PCR-Based Strategy for Introducing CRISPR/Cas9 Machinery into Hematopoietic Cell Lines;Cancers;2023-08-25

4. Precise excision of HTLV-1 provirus with a designer-recombinase;Molecular Therapy;2023-07

5. CRISPR medicine for blood disorders: Progress and challenges in delivery;Frontiers in Genome Editing;2023-01-06

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