Inhibition of 53BP1 favors homology-dependent DNA repair and increases CRISPR–Cas9 genome-editing efficiency
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Inhibition of 53BP1 favors homology-dependent DNA repair and increases CRISPR–Cas9 genome-editing efficiency
Authors
Keywords
-
Journal
NATURE BIOTECHNOLOGY
Volume 36, Issue 1, Pages 95-102
Publisher
Springer Nature
Online
2017-11-28
DOI
10.1038/nbt.4021
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The control of DNA repair by the cell cycle
- (2017) Nicole Hustedt et al. NATURE CELL BIOLOGY
- Marker-free coselection for CRISPR-driven genome editing in human cells
- (2017) Daniel Agudelo et al. NATURE METHODS
- Noncanonical views of homology-directed DNA repair
- (2016) Priyanka Verma et al. GENES & DEVELOPMENT
- Origins of Programmable Nucleases for Genome Engineering
- (2016) Srinivasan Chandrasegaran et al. JOURNAL OF MOLECULAR BIOLOGY
- Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA
- (2016) Christopher D Richardson et al. NATURE BIOTECHNOLOGY
- Two Distinct Pathways Support Gene Correction by Single-Stranded Donors at DNA Nicks
- (2016) Luther Davis et al. Cell Reports
- High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities
- (2015) Traver Hart et al. CELL
- A mechanism for the suppression of homologous recombination in G1 cells
- (2015) Alexandre Orthwein et al. NATURE
- Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
- (2015) Takeshi Maruyama et al. NATURE BIOTECHNOLOGY
- Homology-driven genome editing in hematopoietic stem and progenitor cells using ZFN mRNA and AAV6 donors
- (2015) Jianbin Wang et al. NATURE BIOTECHNOLOGY
- Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells
- (2015) Van Trung Chu et al. NATURE BIOTECHNOLOGY
- Therapeutic genome editing: prospects and challenges
- (2015) David Benjamin Turitz Cox et al. NATURE MEDICINE
- Nuclear domain ‘knock-in’ screen for the evaluation and identification of small molecule enhancers of CRISPR-based genome editing
- (2015) Jordan Pinder et al. NUCLEIC ACIDS RESEARCH
- 53BP1 promotes microhomology-mediated end-joining in G1-phase cells
- (2015) Xiahui Xiong et al. NUCLEIC ACIDS RESEARCH
- Microhomology-Mediated End Joining: A Back-up Survival Mechanism or Dedicated Pathway?
- (2015) Agnel Sfeir et al. TRENDS IN BIOCHEMICAL SCIENCES
- Genome editing at the crossroads of delivery, specificity, and fidelity
- (2015) Ignazio Maggio et al. TRENDS IN BIOTECHNOLOGY
- Improved vectors and genome-wide libraries for CRISPR screening
- (2014) Neville E Sanjana et al. NATURE METHODS
- The new frontier of genome engineering with CRISPR-Cas9
- (2014) J. A. Doudna et al. SCIENCE
- RIF1 Counteracts BRCA1-mediated End Resection during DNA Repair
- (2013) Lin Feng et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- A Cell Cycle-Dependent Regulatory Circuit Composed of 53BP1-RIF1 and BRCA1-CtIP Controls DNA Repair Pathway Choice
- (2013) Cristina Escribano-Díaz et al. MOLECULAR CELL
- 53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark
- (2013) Amélie Fradet-Turcotte et al. NATURE
- Double-strand break repair: 53BP1 comes into focus
- (2013) Stephanie Panier et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- A Strategy for Modulation of Enzymes in the Ubiquitin System
- (2013) A. Ernst et al. SCIENCE
- An Inhibitor of Nonhomologous End-Joining Abrogates Double-Strand Break Repair and Impedes Cancer Progression
- (2012) Mrinal Srivastava et al. CELL
- Targeted gene addition to a predetermined site in the human genome using a ZFN-based nicking enzyme
- (2012) J. Wang et al. GENOME RESEARCH
- Ring Finger Nuclear Factor RNF168 Is Important for Defects in Homologous Recombination Caused by Loss of the Breast Cancer Susceptibility Factor BRCA1
- (2012) Meilen C. Muñoz et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The MMS22L-TONSL Complex Mediates Recovery from Replication Stress and Homologous Recombination
- (2010) Lara O'Donnell et al. MOLECULAR CELL
- Ubiquitin-binding domains — from structures to functions
- (2009) Ivan Dikic et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Establishment of HIV-1 resistance in CD4+ T cells by genome editing using zinc-finger nucleases
- (2008) Elena E Perez et al. NATURE BIOTECHNOLOGY
- Alternative-NHEJ Is a Mechanistically Distinct Pathway of Mammalian Chromosome Break Repair
- (2008) Nicole Bennardo et al. PLoS Genetics
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search