Related references
Note: Only part of the references are listed.Transcriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors
Julian Grunewald et al.
NATURE (2019)
Analysis and minimization of cellular RNA editing by DNA adenine base editors
Holly A. Rees et al.
SCIENCE ADVANCES (2019)
Off-target RNA mutation induced by DNA base editing and its elimination by mutagenesis
Changyang Zhou et al.
NATURE (2019)
Repair of double-strand breaks induced by CRISPR-Cas9 leads to large deletions and complex rearrangements
Michael Kosicki et al.
NATURE BIOTECHNOLOGY (2018)
Improving cytidine and adenine base editors by expression optimization and ancestral reconstruction
Luke W. Koblan et al.
NATURE BIOTECHNOLOGY (2018)
Optimized base editors enable efficient editing in cells, organoids and mice
Maria Paz Zafra et al.
NATURE BIOTECHNOLOGY (2018)
p53 inhibits CRISPR-Cas9 engineering in human pluripotent stem cells
Robert J. Ihry et al.
NATURE MEDICINE (2018)
CRISPR-Cas9 genome editing induces a p53-mediated DNA damage response
Emma Haapaniemi et al.
NATURE MEDICINE (2018)
Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression
Benjamin J. Schmiedel et al.
CELL (2018)
CRISPR-SKIP: programmable gene splicing with single base editors
Michael Gapinske et al.
GENOME BIOLOGY (2018)
EditR: A Method to Quantify Base Editing from Sanger Sequencing
Mitchell G. Kluesner et al.
CRISPR JOURNAL (2018)
Multiplex Genome Editing to Generate Universal CAR T Cells Resistant to PD1 Inhibition
Jiangtao Ren et al.
CLINICAL CANCER RESEARCH (2017)
CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons
Pierre Billon et al.
MOLECULAR CELL (2017)
Targeting a CAR to the TRAC locus with CRISPR/Cas9 enhances tumour rejection
Justin Eyquem et al.
NATURE (2017)
Programmable base editing of A.T to G.C in genomic DNA without DNA cleavage
Nicole M. Gaudelli et al.
NATURE (2017)
Increasing the genome-targeting scope and precision of base editing with engineered Cas9-cytidine deaminase fusions
Y. Bill Kim et al.
NATURE BIOTECHNOLOGY (2017)
CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations
Cem Kuscu et al.
NATURE METHODS (2017)
Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells
Waseem Qasim et al.
SCIENCE TRANSLATIONAL MEDICINE (2017)
CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline
Xuning Wang et al.
BIOINFORMATICS (2017)
Enhanced base editing by co-expression of free uracil DNA glycosylase inhibitor
Lijie Wang et al.
CELL RESEARCH (2017)
RNA mis-splicing in disease
Marina M. Scotti et al.
NATURE REVIEWS GENETICS (2016)
Structure and Engineering of Francisella novicida Cas9
Hisato Hirano et al.
CELL (2016)
Evaluation of TCR Gene Editing Achieved by TALENs, CRISPR/Cas9, and megaTAL Nucleases
Mark J. Osborn et al.
MOLECULAR THERAPY (2016)
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
Alexis C. Komor et al.
NATURE (2016)
Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells
Ayal Hendel et al.
NATURE BIOTECHNOLOGY (2015)
Oxygen and glucose deprivation induces widespread alterations in mRNA translation within 20 minutes
Dmitry E. Andreev et al.
GENOME BIOLOGY (2015)
GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
Shengdar Q. Tsai et al.
NATURE BIOTECHNOLOGY (2015)
A highly compact epitope-based marker/suicide gene for easier and safer T-cell therapy
Brian Philip et al.
BLOOD (2014)
Vector Integration and Tumorigenesis
Christof von Kalle et al.
HUMAN GENE THERAPY (2014)
Evidence of efficient stop codon readthrough in four mammalian genes
Gary Loughran et al.
NUCLEIC ACIDS RESEARCH (2014)
Easy quantitative assessment of genome editing by sequence trace decomposition
Eva K. Brinkman et al.
NUCLEIC ACIDS RESEARCH (2014)
Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity
F. Ann Ran et al.
CELL (2013)
The who's who of T-cell differentiation: Human memory T-cell subsets
Yolanda D. Mahnke et al.
EUROPEAN JOURNAL OF IMMUNOLOGY (2013)
B-cell depletion and remissions of malignancy along with cytokine-associated toxicity in a clinical trial of anti-CD19 chimeric-antigen-receptor-transduced T cells
James N. Kochenderfer et al.
BLOOD (2012)
Extensive Degradation of RNA Precursors by the Exosome in Wild-Type Cells
Rajani Kanth Gudipati et al.
MOLECULAR CELL (2012)
Playing the End Game: DNA Double-Strand Break Repair Pathway Choice
J. Ross Chapman et al.
MOLECULAR CELL (2012)
Editing T cell specificity towards leukemia by zinc finger nucleases and lentiviral gene transfer
Elena Provasi et al.
NATURE MEDICINE (2012)
Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells
Neil V. Morgan et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
A Pre-mRNA Degradation Pathway that Selectively Targets Intron-Containing Genes Requires the Nuclear Poly(A)-Binding Protein
Caroline Lemieux et al.
MOLECULAR CELL (2011)
Chimeric Antigen Receptor-Modified T Cells in Chronic Lymphoid Leukemia
David L. Porter et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Widespread impact of nonsense-mediated mRNA decay on the yeast intronome
Shakir Sayani et al.
MOLECULAR CELL (2008)
Silencing and variegation of gammaretrovirus and lentivirus vectors
J Ellis
HUMAN GENE THERAPY (2005)
DNA double-strand breaks: signaling, repair and the cancer connection
KK Khanna et al.
NATURE GENETICS (2001)