Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
出版年份 2019 全文链接
标题
Stimulation of CRISPR-mediated homology-directed repair by an engineered RAD18 variant
作者
关键词
-
出版物
Nature Communications
Volume 10, Issue 1, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2019-07-30
DOI
10.1038/s41467-019-11105-z
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- H4K20me0 recognition by BRCA1–BARD1 directs homologous recombination to sister chromatids
- (2019) Kyosuke Nakamura et al. NATURE CELL BIOLOGY
- DNA Repair Network Analysis Reveals Shieldin as a Key Regulator of NHEJ and PARP Inhibitor Sensitivity
- (2018) Rajat Gupta et al. CELL
- Shieldin complex promotes DNA end-joining and counters homologous recombination in BRCA1-null cells
- (2018) Harveer Dev et al. NATURE CELL BIOLOGY
- CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway
- (2018) Chris D. Richardson et al. NATURE GENETICS
- Targeting repair pathways with small molecules increases precise genome editing in pluripotent stem cells
- (2018) Stephan Riesenberg et al. Nature Communications
- C-NHEJ without indels is robust and requires synergistic function of distinct XLF domains
- (2018) Ragini Bhargava et al. Nature Communications
- 53BP1 cooperation with the REV7–shieldin complex underpins DNA structure-specific NHEJ
- (2018) Hind Ghezraoui et al. NATURE
- The shieldin complex mediates 53BP1-dependent DNA repair
- (2018) Sylvie M. Noordermeer et al. NATURE
- 53BP1–RIF1–shieldin counteracts DSB resection through CST- and Polα-dependent fill-in
- (2018) Zachary Mirman et al. NATURE
- CRISPR-Cas guides the future of genetic engineering
- (2018) Gavin J. Knott et al. SCIENCE
- Systematic gene tagging using CRISPR/Cas9 in human stem cells to illuminate cell organization
- (2017) Brock Roberts et al. MOLECULAR BIOLOGY OF THE CELL
- Mechanisms of Ubiquitin-Nucleosome Recognition and Regulation of 53BP1 Chromatin Recruitment by RNF168/169 and RAD18
- (2017) Qi Hu et al. MOLECULAR CELL
- CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons
- (2017) Pierre Billon et al. MOLECULAR CELL
- Inhibition of 53BP1 favors homology-dependent DNA repair and increases CRISPR–Cas9 genome-editing efficiency
- (2017) Marella D Canny et al. NATURE BIOTECHNOLOGY
- Marker-free coselection for CRISPR-driven genome editing in human cells
- (2017) Daniel Agudelo et al. NATURE METHODS
- Inactivation of Pol θ and C-NHEJ eliminates off-target integration of exogenous DNA
- (2017) Alex N. Zelensky et al. Nature Communications
- Characterization of the interplay between DNA repair and CRISPR/Cas9-induced DNA lesions at an endogenous locus
- (2017) Anne Bothmer et al. Nature Communications
- Microhomology-mediated end joining: new players join the team
- (2017) Hailong Wang et al. Cell and Bioscience
- The RNF168 paralog RNF169 defines a new class of ubiquitylated histone reader involved in the response to DNA damage
- (2017) Julianne Kitevski-LeBlanc et al. eLife
- Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR–Cas9 genome editing
- (2017) Bruna S. Paulsen et al. Nature Biomedical Engineering
- Mechanism and regulation of DNA end resection in eukaryotes
- (2016) Lorraine S. Symington CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY
- The democratization of gene editing: Insights from site-specific cleavage and double-strand break repair
- (2016) Maria Jasin et al. DNA REPAIR
- 53BP1 Integrates DNA Repair and p53-Dependent Cell Fate Decisions via Distinct Mechanisms
- (2016) Raquel Cuella-Martin et al. MOLECULAR CELL
- Derivation and differentiation of haploid human embryonic stem cells
- (2016) Ido Sagi et al. NATURE
- Analyzing CRISPR genome-editing experiments with CRISPResso
- (2016) Luca Pinello et al. NATURE BIOTECHNOLOGY
- Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA
- (2016) Christopher D Richardson et al. NATURE BIOTECHNOLOGY
- Regulation of Single-Strand Annealing and its Role in Genome Maintenance
- (2016) Ragini Bhargava et al. TRENDS IN GENETICS
- Two Distinct Pathways Support Gene Correction by Single-Stranded Donors at DNA Nicks
- (2016) Luther Davis et al. Cell Reports
- Functions of Ubiquitin and SUMO in DNA Replication and Replication Stress
- (2016) Néstor García-Rodríguez et al. Frontiers in Genetics
- The BioPlex Network: A Systematic Exploration of the Human Interactome
- (2015) Edward L. Huttlin et al. CELL
- Small Molecules Enhance CRISPR Genome Editing in Pluripotent Stem Cells
- (2015) Chen Yu et al. Cell Stem Cell
- Mammalian polymerase θ promotes alternative NHEJ and suppresses recombination
- (2015) Pedro A. Mateos-Gomez 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
- 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
- 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
- Microhomology-Mediated End Joining: A Back-up Survival Mechanism or Dedicated Pathway?
- (2015) Agnel Sfeir et al. TRENDS IN BIOCHEMICAL SCIENCES
- Pharmacological inhibition of DNA-PK stimulates Cas9-mediated genome editing
- (2015) Francis Robert et al. Genome Medicine
- Development and Applications of CRISPR-Cas9 for Genome Engineering
- (2014) Patrick D. Hsu et al. CELL
- Two-way communications between ubiquitin-like modifiers and DNA
- (2014) Helle D Ulrich NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Rad18 and Rnf8 facilitate homologous recombination by two distinct mechanisms, promoting Rad51 focus formation and suppressing the toxic effect of nonhomologous end joining
- (2014) S Kobayashi et al. ONCOGENE
- Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response
- (2014) Alberto Ciccia et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Homology-directed repair of DNA nicks via pathways distinct from canonical double-strand break repair
- (2014) L. Davis et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A small ubiquitin binding domain inhibits ubiquitin-dependent protein recruitment to DNA repair foci
- (2013) Corey Helchowski et al. CELL CYCLE
- 53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark
- (2013) Amélie Fradet-Turcotte et al. NATURE
- 53BP1: pro choice in DNA repair
- (2013) Michal Zimmermann et al. TRENDS IN CELL BIOLOGY
- Repair of Strand Breaks by Homologous Recombination
- (2013) M. Jasin et al. Cold Spring Harbor Perspectives in Biology
- An Inhibitor of Nonhomologous End-Joining Abrogates Double-Strand Break Repair and Impedes Cancer Progression
- (2012) Mrinal Srivastava et al. CELL
- RNF8- and RNF168-dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sites
- (2012) Frédérick A Mallette et al. EMBO JOURNAL
- Tandem Protein Interaction Modules Organize the Ubiquitin-Dependent Response to DNA Double-Strand Breaks
- (2012) Stephanie Panier et al. MOLECULAR CELL
- The promise of induced pluripotent stem cells in research and therapy
- (2012) Daisy A. Robinton et al. NATURE
- 53BP1 Inhibits Homologous Recombination in Brca1-Deficient Cells by Blocking Resection of DNA Breaks
- (2010) Samuel F. Bunting et al. CELL
- 53BP1 regulates DNA resection and the choice between classical and alternative end joining during class switch recombination
- (2010) Anne Bothmer et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Defining the Human Deubiquitinating Enzyme Interaction Landscape
- (2009) Mathew E. Sowa et al. CELL
- The SIOD disorder protein SMARCAL1 is an RPA-interacting protein involved in replication fork restart
- (2009) A. Ciccia et al. GENES & DEVELOPMENT
- RAD18 transmits DNA damage signalling to elicit homologous recombination repair
- (2009) Jun Huang et al. NATURE CELL BIOLOGY
- Recognition of forked and single-stranded DNA structures by human RAD18 complexed with RAD6B protein triggers its recruitment to stalled replication forks
- (2008) Yuri Tsuji et al. GENES TO CELLS
- Human Wrnip1 Is Localized in Replication Factories in a Ubiquitin-binding Zinc Finger-dependent Manner
- (2008) Nicola Crosetto et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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