Related references
Note: Only part of the references are listed.Efficient Delivery and Nuclear Uptake Is Not Sufficient to Detect Gene Editing in CD34+Cells Directed by a Ribonucleoprotein Complex
Shirin R. Modarai et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2018)
Efficient, footprint-free human iPSC genome editing by consolidation of Cas9/CRISPR and piggyBac technologies
Gang Wang et al.
NATURE PROTOCOLS (2017)
Programmable base editing of A.T to G.C in genomic DNA without DNA cleavage
Nicole M. Gaudelli et al.
NATURE (2017)
Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing
Hao Yin et al.
NATURE BIOTECHNOLOGY (2017)
Marker-free coselection for CRISPR-driven genome editing in human cells
Daniel Agudelo et al.
NATURE METHODS (2017)
Lentivirus pre-packed with Cas9 protein for safer gene editing
J. G. Choi et al.
GENE THERAPY (2016)
Highly Efficient Mouse Genome Editing by CRISPR Ribonucleoprotein Electroporation of Zygotes
Sean Chen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2016)
Programmed Self-Assembly of an Active P22-Cas9 Nanocarrier System
Shefah Qazi et al.
MOLECULAR PHARMACEUTICS (2016)
Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo
Hao Yin et al.
NATURE BIOTECHNOLOGY (2016)
Reprogramming metabolic pathways in vivo with CRISPR/Cas9 genome editing to treat hereditary tyrosinaemia
Francis P. Pankowicz et al.
NATURE COMMUNICATIONS (2016)
Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System
Bernd Zetsche et al.
CELL (2015)
A localized nucleolar DNA damage response facilitates recruitment of the homology-directed repair machinery independent of cell cycle stage
Marjolein van Sluis et al.
GENES & DEVELOPMENT (2015)
Highly efficient Cas9-mediated transcriptional programming
Alejandro Chavez et al.
NATURE METHODS (2015)
Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells
Emmanuelle Massourides et al.
SKELETAL MUSCLE (2015)
HTSeq-a Python framework to work with high-throughput sequencing data
Simon Anders et al.
BIOINFORMATICS (2015)
GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
Shengdar Q. Tsai et al.
NATURE BIOTECHNOLOGY (2015)
An optimized kit-free method for making strand-specific deep sequencing libraries from RNA fragments
Erin E. Heyer et al.
NUCLEIC ACIDS RESEARCH (2015)
Baboon envelope pseudotyped LVs outperform VSV-G-LVs for gene transfer into early-cytokine-stimulated and resting HSCs
Anais Girard-Gagnepain et al.
BLOOD (2014)
Mystery solved: VSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptor
Fouzia Amirache et al.
BLOOD (2014)
Staufen1 senses overall transcript secondary structure to regulate translation
Emiliano P. Ricci et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2014)
Easy quantitative assessment of genome editing by sequence trace decomposition
Eva K. Brinkman et al.
NUCLEIC ACIDS RESEARCH (2014)
CRISPRseek: A Bioconductor Package to Identify Target-Specific Guide RNAs for CRISPR-Cas9 Genome-Editing Systems
Lihua J. Zhu et al.
PLOS ONE (2014)
Ribosomal DNA copy number is coupled with gene expression variation and mitochondrial abundance in humans
John G. Gibbons et al.
NATURE COMMUNICATIONS (2014)
Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System
Baohui Chen et al.
CELL (2013)
High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells
Yanfang Fu et al.
NATURE BIOTECHNOLOGY (2013)
A Long Noncoding RNA Mediates Both Activation and Repression of Immune Response Genes
Susan Carpenter et al.
SCIENCE (2013)
A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
Martin Jinek et al.
SCIENCE (2012)
Safe harbours for the integration of new DNA in the human genome
Michel Sadelain et al.
NATURE REVIEWS CANCER (2012)
Protein Transfer Into Human Cells by VSV-G-induced Nanovesicles
Philippe-Emmanuel Mangeot et al.
MOLECULAR THERAPY (2011)
Protein delivery using engineered virus-like particles
Stanislaw J. Kaczmarczyk et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Redirecting Lentiviral Vectors Pseudotyped with Sindbis Virus-Derived Envelope Proteins to DC-SIGN by Modification of N-Linked Glycans of Envelope Proteins
Kouki Morizono et al.
JOURNAL OF VIROLOGY (2010)
Protein transduction from retroviral Gag precursors
Christine Voelkel et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Stable transduction of quiescent T cells without induction of cycle progression by a novel lentiviral vector pseudotyped with measles virus glycoproteins
Cecilia Frecha et al.
BLOOD (2008)
gamma-H2AX in recognition and signaling of DNA double-strand breaks in the context of chromatin
Andrea Kinner et al.
NUCLEIC ACIDS RESEARCH (2008)
Robust expansion of human hepatocytes in Fah-/-/Rag2-/-/Il2rg-/- mice
Hisaya Azuma et al.
NATURE BIOTECHNOLOGY (2007)
Selective and nonselective packaging of cellular RNAs in retrovirus particles
Samuel J. Rulli et al.
JOURNAL OF VIROLOGY (2007)
Targeted retroviral vectors displaying a cleavage site-engineered hemagglutinin (HA) through HA-protease interactions
Judit Szecsi et al.
MOLECULAR THERAPY (2006)
Selective expression of the Cre recombinase in late-stage thymocytes using the distal promoter of the Lck gene
DJ Zhang et al.
JOURNAL OF IMMUNOLOGY (2005)
Lentiviral vector retargeting to P-glycoprotein on metastatic melanoma through intravenous injection
K Morizono et al.
NATURE MEDICINE (2005)
CD81 is required for hepatitis C virus glycoprotein-mediated viral infection
J Zhang et al.
JOURNAL OF VIROLOGY (2004)
VSV-G envelope glycoprotein forms complexes with plasmid DNA and MLV retrovirus-like particles in cell-free conditions and enhances DNA transfection
T Okimoto et al.
MOLECULAR THERAPY (2001)
Share Paper
