Related references
Note: Only part of the references are listed.Advances with using CRISPR/Cas-mediated gene editing to treat infections with hepatitis B virus and hepatitis C virus
Buhle Moyo et al.
VIRUS RESEARCH (2018)
CRISPR-Cas9 system-driven site-specific selection pressure on Herpes simplex virus genomes
Zhihua Li et al.
VIRUS RESEARCH (2018)
CRISPR/Cas9-The ultimate weapon to battle infectious diseases?
M. Doerflinger et al.
CELLULAR MICROBIOLOGY (2017)
New CRISPR-Cas systems from uncultivated microbes
David Burstein et al.
NATURE (2017)
Exploring the potential of genome editing CRISPR-Cas9 technology
Vijai Singh et al.
GENE (2017)
In Vivo Excision of HIV-1 Provirus by saCas9 and Multiplex Single-Guide RNAs in Animal Models
Chaoran Yin et al.
MOLECULAR THERAPY (2017)
In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni
Eunji Kim et al.
NATURE COMMUNICATIONS (2017)
Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice
Wenhan Yu et al.
NATURE COMMUNICATIONS (2017)
Reversal of Phenotypic Abnormalities by CRISPR/Cas9-Mediated Gene Correction in Huntington Disease Patient-Derived Induced Pluripotent Stem Cells
Xiaohong Xu et al.
STEM CELL REPORTS (2017)
Cas9, Cpf1 and C2c1/2/3-What's next?
Shota Nakade et al.
BIOENGINEERED (2017)
Detection of on-target and off-target mutations generated by CRISPR/Cas9 and other sequence-specific nucleases
Julia Zischewski et al.
BIOTECHNOLOGY ADVANCES (2017)
Novel AIDS therapies based on gene editing
Kamel Khalili et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2017)
Gene Editing With CRISPR/Cas9 RNA-Directed Nuclease
Thomas Doetschman et al.
CIRCULATION RESEARCH (2017)
CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes
Alexis C. Komor et al.
CELL (2017)
Inhibition of CRISPR-Cas9 with Bacteriophage Proteins
Benjamin J. Rauch et al.
CELL (2017)
Rationally engineered Cas9 nucleases with improved specificity
Ian M. Slaymaker et al.
SCIENCE (2016)
Functional screening of guide RNAs targeting the regulatory and structural HIV-1 viral genome for a cure of AIDS
Chaoran Yin et al.
AIDS (2016)
Current status of potential applications of repurposed Cas9 for structural and functional genomics of plants
Kunal Seth et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2016)
Structure and Engineering of Francisella novicida Cas9
Hisato Hirano et al.
CELL (2016)
Biology and Applications of CRISPR Systems: Harnessing Nature's Toolbox for Genome Engineering
Addison V. Wright et al.
CELL (2016)
Off-target effects of engineered nucleases
Jiing-Kuan Yee
FEBS JOURNAL (2016)
Using CRISPR/Cas to study gene function and model disease in vivo
Darjus F. Tschaharganeh et al.
FEBS JOURNAL (2016)
Excision of HIV-1 DNA by gene editing: a proof-of-concept in vivo study
R. Kaminski et al.
GENE THERAPY (2016)
Delivery methods for site-specific nucleases: Achieving the full potential of therapeutic gene editing
Jia Liu et al.
JOURNAL OF CONTROLLED RELEASE (2016)
Methods for Optimizing CRISPR-Cas9 Genome Editing Specificity
Josh Tycko et al.
MOLECULAR CELL (2016)
CRISPR-Cas9 Can Inhibit HIV-1 Replication but NHEJ Repair Facilitates Virus Escape
Gang Wang et al.
MOLECULAR THERAPY (2016)
CRISPR gene editing tested in a person
David Cyranoski
NATURE (2016)
CRISPR/Cas9 β-globin gene targeting in human haematopoietic stem cells
Daniel P. Dever et al.
NATURE (2016)
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
Alexis C. Komor et al.
NATURE (2016)
High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects
Benjamin P. Kleinstiver et al.
NATURE (2016)
Defining and improving the genome-wide specificities of CRISPR-Cas9 nucleases
Shengdar Q. Tsai et al.
NATURE REVIEWS GENETICS (2016)
Gene Editing for Treatment of Neurological Infections
Martyn K. White et al.
NEUROTHERAPEUTICS (2016)
Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles
Ming Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems
Keiji Nishida et al.
SCIENCE (2016)
Diverse evolutionary roots and mechanistic variations of the CRISPR-Cas systems
Prarthana Mohanraju et al.
SCIENCE (2016)
C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector
Omar O. Abudayyeh et al.
SCIENCE (2016)
Genome-Editing Technologies: Principles and Applications
Thomas Gaj et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2016)
CRISPR-dCas9 mediated TET1 targeting for selective DNA demethylation at BRCA1 promoter
Samrat Roy Choudhury et al.
ONCOTARGET (2016)
CRISPR/Cas9 and cancer targets: future possibilities and present challenges
Martyn K. White et al.
ONCOTARGET (2016)
CRISPR/Cas9-Derived Mutations Both Inhibit HIV-1 Replication and Accelerate Viral Escape
Zhen Wang et al.
CELL REPORTS (2016)
Gene Editing Approaches against Viral Infections and Strategy to Prevent Occurrence of Viral Escape
Martyn K. White et al.
PLOS PATHOGENS (2016)
CRISPR/Cas9-Mediated Genome Editing of Herpesviruses Limits Productive and Latent Infections
Ferdy R. van Diemen et al.
PLOS PATHOGENS (2016)
CRISPR-Cas9 System as a Versatile Tool for Genome Engineering in Human Cells
Xuelian Wang et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2016)
Targeted HIV-1 Latency Reversal Using CRISPR/Cas9-Derived Transcriptional Activator Systems
Julia K. Bialek et al.
PLOS ONE (2016)
Elimination of HIV-1 Genomes from Human T-lymphoid Cells by CRISPR/Cas9 Gene Editing
Rafal Kaminski et al.
SCIENTIFIC REPORTS (2016)
Inhibition of HSV-1 Replication by Gene Editing Strategy
Pamela C. Roehm et al.
SCIENTIFIC REPORTS (2016)
Negative Feedback Regulation of HIV-1 by Gene Editing Strategy
Rafal Kaminski et al.
SCIENTIFIC REPORTS (2016)
Inhibition of JCPyV infection mediated by targeted viral genome editing using CRISPR/Cas9
Yi-ying Chou et al.
SCIENTIFIC REPORTS (2016)
Persistence and Pathogenesis of the Neurotropic Polyomavirus JC
Hassen S. Wollebo et al.
ANNALS OF NEUROLOGY (2015)
Viral Vectors for Gene Therapy: Translational and Clinical Outlook
Melissa A. Kotterman et al.
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, VOL 17 (2015)
Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System
Bernd Zetsche et al.
CELL (2015)
Recent developments and clinical studies utilizing engineered zinc finger nuclease technology
Young-Il Jo et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2015)
Rapid and highly efficient mammalian cell engineering via Cas9 protein transfection
Xiquan Liang et al.
JOURNAL OF BIOTECHNOLOGY (2015)
Genome editing strategies: potential tools for eradicating HIV-1/AIDS
Kamel Khalili et al.
JOURNAL OF NEUROVIROLOGY (2015)
Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems
Sergey Shmakov et al.
MOLECULAR CELL (2015)
Engineered CRISPR-Cas9 nucleases with altered PAM specificities
Benjamin P. Kleinstiver et al.
NATURE (2015)
In vivo genome editing using Staphylococcus aureus Cas9
F. Ann Ran et al.
NATURE (2015)
Small molecule-triggered Cas9 protein with improved genome-editing specificity
Kevin M. Davis et al.
NATURE CHEMICAL BIOLOGY (2015)
High-throughput functional genomics using CRISPR-Cas9
Ophir Shalem et al.
NATURE REVIEWS GENETICS (2015)
Cas9-mediated targeting of viral RNA in eukaryotic cells
Aryn A. Price et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Use of the CRISPR/Cas9 system as an intracellular defense against HIV-1 infection in human cells
Hsin-Kai Liao et al.
NATURE COMMUNICATIONS (2015)
Genome editing of CXCR4 by CRISPR/cas9 confers cells resistant to HIV-1 infection
Panpan Hou et al.
SCIENTIFIC REPORTS (2015)
CRISPR/gRNA-directed synergistic activation mediator (SAM) induces specific, persistent and robust reactivation of the HIV-1 latent reservoirs
Yonggang Zhang et al.
SCIENTIFIC REPORTS (2015)
Off-target Effects in CRISPR/Cas9-mediated Genome Engineering
Xiao-Hui Zhang et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2015)
CRISPR/Cas9 System as an Agent for Eliminating Polyomavirus JC Infection
Hassen S. Wollebo et al.
PLOS ONE (2015)
Rapid characterization of CRISPR-Cas9 protospacer adjacent motif sequence elements
Tautvydas Karvelis et al.
GENOME BIOLOGY (2015)
TALEN-mediated genome editing: prospects and perspectives
David A. Wright et al.
BIOCHEMICAL JOURNAL (2014)
CRISPR/Cas9-mediated genome engineering: An adeno-associated viral (AAV) vector toolbox
Elena Senis et al.
BIOTECHNOLOGY JOURNAL (2014)
Programmable RNA recognition and cleavage by CRISPR/Cas9
Mitchell R. O'Connell et al.
NATURE (2014)
Seamless modification of wild-type induced pluripotent stem cells to the natural CCR5Δ32 mutation confers resistance to HIV infection
Lin Ye et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (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)
Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System
Baohui Chen et al.
CELL (2013)
Harnessing the CRISPR/Cas9 system to disrupt latent HIV-1 provirus
Hirotaka Ebina et al.
SCIENTIFIC REPORTS (2013)
A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
Martin Jinek et al.
SCIENCE (2012)
Topics in herpesvirus genomics and evolution
DJ McGeoch et al.
VIRUS RESEARCH (2006)
Share Paper
