Related references
Note: Only part of the references are listed.A highly specific SpCas9 variant is identified by in vivo screening in yeast
Antonio Casini et al.
NATURE BIOTECHNOLOGY (2018)
Repair of double-strand breaks induced by CRISPR-Cas9 leads to large deletions and complex rearrangements (vol 36, pg 765, 2018)
Michael Kosicki et al.
NATURE BIOTECHNOLOGY (2018)
Biallelic insertion of a transcriptional terminator via the CRISPR/Cas9 system efficiently silences expression of protein-coding and non-coding RNA genes
Yangyang Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2017)
Enhanced proofreading governs CRISPR-Cas9 targeting accuracy
Janice S. Chen et al.
NATURE (2017)
Gene Editing in Human Lymphoid Cells: Role for Donor DNA, Type of Genomic Nuclease and Cell Selection Method
Anastasia Zotova et al.
VIRUSES-BASEL (2017)
Molecular switching system using glycosylphosphatidylinositol to select cells highly expressing recombinant proteins
Emmanuel Matabaro et al.
SCIENTIFIC REPORTS (2017)
CRISPR/Cas9 in Genome Editing and Beyond
Haifeng Wang et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85 (2016)
Targeting protein function: the expanding toolkit for conditional disruption
Amy E. Campbell et al.
BIOCHEMICAL JOURNAL (2016)
Anti-HIV-1 potency of the CRISPR/Cas9 system insufficient to fully inhibit viral replication
Shuhei Ueda et al.
MICROBIOLOGY AND IMMUNOLOGY (2016)
CRISPR-Cas9 Can Inhibit HIV-1 Replication but NHEJ Repair Facilitates Virus Escape
Gang Wang et al.
MOLECULAR THERAPY (2016)
High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects
Benjamin P. Kleinstiver et al.
NATURE (2016)
A dual molecular analogue tuner for dissecting protein function in mammalian cells
Ran Brosh et al.
NATURE COMMUNICATIONS (2016)
Rapid Protein Depletion in Human Cells by Auxin-Inducible Degron Tagging with Short Homology Donors
Toyoaki Natsume et al.
CELL REPORTS (2016)
CRISPR/Cas9-Derived Mutations Both Inhibit HIV-1 Replication and Accelerate Viral Escape
Zhen Wang et al.
CELL REPORTS (2016)
Elimination of HIV-1 Genomes from Human T-lymphoid Cells by CRISPR/Cas9 Gene Editing
Rafal Kaminski et al.
SCIENTIFIC REPORTS (2016)
Systematic quantification of HDR and NHEJ reveals effects of locus, nuclease, and cell type on genome-editing
Yuichiro Miyaoka et al.
SCIENTIFIC REPORTS (2016)
The CRISPR/Cas9 system inactivates latent HIV-1 proviral DNA
Weijun Zhu et al.
RETROVIROLOGY (2015)
Monoclonal antibody profiling of cell surface proteins associated with the viral biofilms on HTLV-1 transformed cells
A. Tarasevich et al.
ACTA VIROLOGICA (2015)
Identification and Characterization of Small Molecules That Inhibit Nonsense-Mediated RNA Decay and Suppress Nonsense p53 Mutations
Leenus Martin et al.
CANCER RESEARCH (2014)
Dimeric CRISPR RNA-guided Fokl nucleases for highly specific genome editing
Shengdar Q. Tsai et al.
NATURE BIOTECHNOLOGY (2014)
Fusion of catalytically inactive Cas9 to Fokl nuclease improves the specificity of genome modification
John P. Guilinger et al.
NATURE BIOTECHNOLOGY (2014)
RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection
Wenhui Hu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Optimized signal peptides for the development of high expressing CHO cell lines
Lars Kober et al.
BIOTECHNOLOGY AND BIOENGINEERING (2013)
Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity
F. Ann Ran et al.
CELL (2013)
The Elg1 Replication Factor C-like Complex Functions in PCNA Unloading during DNA Replication
Takashi Kubota et al.
MOLECULAR CELL (2013)
RNA-Guided Human Genome Engineering via Cas9
Prashant Mali et al.
SCIENCE (2013)
Multiplex Genome Engineering Using CRISPR/Cas Systems
Le Cong et al.
SCIENCE (2013)
An expanded tool kit for the auxin-inducible degron system in budding yeast
Magdalena Morawska et al.
YEAST (2013)
Voltage-dependant anion channels: Novel insights into isoform function through genetic models
Adithya Raghavan et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2012)
Inducible, reversible system for the rapid and complete degradation of proteins in mammalian cells
Andrew J. Holland et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Tracking genome engineering outcome at individual DNA breakpoints
Michael T. Certo et al.
NATURE METHODS (2011)
Enhancing the Secretion of Recombinant Proteins by Engineering N-Glycosylation Sites
Yan Liu et al.
BIOTECHNOLOGY PROGRESS (2009)
An auxin-based degron system for the rapid depletion of proteins in nonplant cells
Kohei Nishimura et al.
NATURE METHODS (2009)
Comparison of nonhomologous end joining and homologous recombination in human cells
Zhiyong Mao et al.
DNA REPAIR (2008)
Evaluation of a novel short polyadenylation signal as an alternative to the SV40 polyadenylation signal
Trevor J. McFarland et al.
PLASMID (2006)
Ku86 is essential in human somatic cells
G Li et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Comparative efficiencies of C-terminal signals of native glycophosphatidylinositol (GPI)-anchored proproteins in conferring GPI-anchoring
R Chen et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2002)
Analysis of the aphthovirus 2A/2B polyprotein 'cleavage' mechanism indicates not a proteolytic reaction, but a novel translational effect: a putative ribosomal 'skip'
MLL Donnelly et al.
JOURNAL OF GENERAL VIROLOGY (2001)
Share Paper
