Related references
Note: Only part of the references are listed.A Versatile Tool for the Quantification of CRISPR/Cas9-Induced Genome Editing Events in Human Hematopoietic Cell Lines and Hematopoietic Stem/Progenitor Cells
Rajeswari Jayavaradhan et al.
JOURNAL OF MOLECULAR BIOLOGY (2019)
Inhibition of 53BP1 favors homology-dependent DNA repair and increases CRISPR-Cas9 genome-editing efficiency
Marella D. Canny et al.
NATURE BIOTECHNOLOGY (2018)
CRISPR/Cas9 genome editing in human hematopoietic stem cells
Rasmus O. Bak et al.
NATURE PROTOCOLS (2018)
New roles for RAD52 in DNA repair
Chaoyou Xue et al.
CELL RESEARCH (2018)
Enhancing CRISPR/Cas9-mediated homology-directed repair in mammalian cells by expressing Saccharomyces cerevisiae Rad52
Simin Shao et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2017)
Multiplexed genetic engineering of human hematopoietic stem and progenitor cells using CRISPR/Cas9 and AAV6
Rasmus O Bak et al.
eLife (2017)
Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR-Cas9 genome editing
Bruna S. Paulsen et al.
NATURE BIOMEDICAL ENGINEERING (2017)
Highly Efficient Genome Editing of Murine and Human Hematopoietic Progenitor Cells by CRISPR/Cas9
Michael C. Gundry et al.
CELL REPORTS (2016)
Post-translational Regulation of Cas9 during G1 Enhances Homology-Directed Repair
Tony Gutschner et al.
CELL REPORTS (2016)
A Cas9 Variant for Efficient Generation of Indel-Free Knockin or Gene-Corrected Human Pluripotent Stem Cells
Sara E. Howden et al.
STEM CELL REPORTS (2016)
Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
Takeshi Maruyama et al.
NATURE BIOTECHNOLOGY (2015)
Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells
Van Trung Chu et al.
NATURE BIOTECHNOLOGY (2015)
Off-Target Assessment of CRISPR-Cas9 Guiding RNAs in Human iPS and Mouse ES Cells
E-Pien Tan et al.
GENESIS (2015)
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity
Michael Y. Zhang et al.
HAEMATOLOGICA (2015)
Bcl2 overexpression rescues the hematopoietic stem cell defects in Ku70-deficient mice by restoration of quiescence
Yulan Qing et al.
BLOOD (2014)
The clinical impact of deficiency in DNA non-homologous end-joining
Lisa Woodbine et al.
DNA REPAIR (2014)
Highly efficient RNA-guided genome editing in human cells via delivery of purified Cas9 ribonucleoproteins
Sojung Kim et al.
GENOME RESEARCH (2014)
Fusion of catalytically inactive Cas9 to Fokl nuclease improves the specificity of genome modification
John P. Guilinger et al.
NATURE BIOTECHNOLOGY (2014)
Double-strand break repair: 53BP1 comes into focus
Stephanie Panier et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2014)
Easy quantitative assessment of genome editing by sequence trace decomposition
Eva K. Brinkman et al.
NUCLEIC ACIDS RESEARCH (2014)
53BP1: pro choice in DNA repair
Michal Zimmerman et al.
TRENDS IN CELL BIOLOGY (2014)
Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery
Steven Lin et al.
ELIFE (2014)
AAV2 production with optimized N/P ratio and PEI-mediated transfection results in low toxicity and high titer for in vitro and in vivo applications
Xinping Huang et al.
JOURNAL OF VIROLOGICAL METHODS (2013)
A Cell Cycle-Dependent Regulatory Circuit Composed of 53BP1-RIF1 and BRCA1-CtIP Controls DNA Repair Pathway Choice
Cristina Escribano-Diaz et al.
MOLECULAR CELL (2013)
Genome engineering using the CRISPR-Cas9 system
F. Ann Ran et al.
NATURE PROTOCOLS (2013)
RNA-Guided Human Genome Engineering via Cas9
Prashant Mali et al.
SCIENCE (2013)
Treatment of canine leukocyte adhesion deficiency by foamy virus vectors expressing CD18 from a PGK promoter
T. R. Bauer et al.
GENE THERAPY (2011)
Congenital bone marrow failure in DNA-PKcs mutant mice associated with deficiencies in DNA repair
Shichuan Zhang et al.
JOURNAL OF CELL BIOLOGY (2011)
AAV-mediated gene targeting methods for human cells
Iram F. Khan et al.
NATURE PROTOCOLS (2011)
Overlap extension PCR cloning: a simple and reliable way to create recombinant plasmids
Anton V. Bryksin et al.
BIOTECHNIQUES (2010)
53BP1 regulates DNA resection and the choice between classical and alternative end joining during class switch recombination
Anne Bothmer et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2010)
An Oligomerized 53BP1 Tudor Domain Suffices for Recognition of DNA Double-Strand Breaks
Omar Zgheib et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
Comparison of nonhomologous end joining and homologous recombination in human cells
Zhiyong Mao et al.
DNA REPAIR (2008)
Alternative-NHEJ Is a Mechanistically Distinct Pathway of Mammalian Chromosome Break Repair
Nicole Bennardo et al.
PLOS GENETICS (2008)
Successful treatment of canine leukocyte adhesion deficiency by foamy virus vectors
Thomas R. Bauer et al.
NATURE MEDICINE (2008)
DNA repair is limiting for haematopoietic stem cells during ageing
Anastasia Nijnik et al.
NATURE (2007)
Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age
Derrick J. Rossi et al.
NATURE (2007)
Human Rif1, ortholog of a yeast telomeric protein, is regulated by ATM and 53BP1 and functions in the S-phase checkpoint
J Silverman et al.
GENES & DEVELOPMENT (2004)
Targeted transgene insertion into human chromosomes by adeno-associated virus vectors
R Hirata et al.
NATURE BIOTECHNOLOGY (2002)
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency
M O'Driscoll et al.
MOLECULAR CELL (2001)
Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis
DM McCarty et al.
GENE THERAPY (2001)