相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Construction and characterization of adenoviral vectors for the delivery of TALENs into human cells
Maarten Holkers et al.
METHODS (2014)
Genome Engineering at the Dawn of the Golden Age
David J. Segal et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 14 (2013)
Enhanced Efficiency of Human Pluripotent Stem Cell Genome Editing through Replacing TALENs with CRISPRs
Qiurong Ding et al.
CELL STEM CELL (2013)
Histone Deacetylase Inhibition Activates Transgene Expression from Integration-Defective Lentiviral Vectors in Dividing and Non-Dividing Cells
Laetitia P. L. Pelascini et al.
HUMAN GENE THERAPY (2013)
Development of an AdEasy-based system to produce first- and second-generation adenoviral vectors with tropism for CAR- or CD46-positive cells
Josephine M. Janssen et al.
JOURNAL OF GENE MEDICINE (2013)
Targeted Gene Addition in Human Epithelial Stem Cells by Zinc-finger Nuclease-mediated Homologous Recombination
Andrea Coluccio et al.
MOLECULAR THERAPY (2013)
CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering
Prashant Mali et al.
NATURE BIOTECHNOLOGY (2013)
DNA targeting specificity of RNA-guided Cas9 nucleases
Patrick D. Hsu et al.
NATURE BIOTECHNOLOGY (2013)
High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity
Vikram Pattanayak et al.
NATURE BIOTECHNOLOGY (2013)
High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells
Yanfang Fu et al.
NATURE BIOTECHNOLOGY (2013)
Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cells
Maarten Holkers et al.
NUCLEIC ACIDS RESEARCH (2013)
CRISPR/Cas9 systems targeting β-globin and CCR5 genes have substantial off-target activity
Thomas J. Cradick et al.
NUCLEIC ACIDS RESEARCH (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)
ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering
Thomas Gaj et al.
TRENDS IN BIOTECHNOLOGY (2013)
RNA-dependent DNA endonuclease Cas9 of the CRISPR system: Holy Grail of genome editing?
Giedrius Gasiunas et al.
TRENDS IN MICROBIOLOGY (2013)
Harnessing the CRISPR/Cas9 system to disrupt latent HIV-1 provirus
Hirotaka Ebina et al.
SCIENTIFIC REPORTS (2013)
Histone Deacetylase Inhibition Rescues Gene Knockout Levels Achieved with Integrase-Defective Lentiviral Vectors Encoding Zinc-Finger Nucleases
Laetitia P. L. Pelascini et al.
HUMAN GENE THERAPY METHODS (2013)
Genetic cancer vaccines: current status and perspectives
Luigi Aurisicchio et al.
EXPERT OPINION ON BIOLOGICAL THERAPY (2012)
Retroviral Integrations in Gene Therapy Trials
Luca Biasco et al.
MOLECULAR THERAPY (2012)
RNA-guided genetic silencing systems in bacteria and archaea
Blake Wiedenheft et al.
NATURE (2012)
Cas9-crRNA ribonucleoprotein complex mediates specific DNA cleavage for adaptive immunity in bacteria
Giedrius Gasiunas et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
Martin Jinek et al.
SCIENCE (2012)
CRISPR-Cas Systems in Bacteria and Archaea: Versatile Small RNAs for Adaptive Defense and Regulation
Devaki Bhaya et al.
ANNUAL REVIEW OF GENETICS, VOL 45 (2011)
Transcription Factor Rational Design Improves Directed Differentiation of Human Mesenchymal Stem Cells Into Skeletal Myocytes
Manuel A. F. V. Goncalves et al.
MOLECULAR THERAPY (2011)
Surrogate reporters for enrichment of cells with nuclease-induced mutations
Hyojin Kim et al.
NATURE METHODS (2011)
Serum-free transient protein production system based on adenoviral vector and PER.C6 technology: High yield and preserved bioactivity
M. J. E. Havenga et al.
BIOTECHNOLOGY AND BIOENGINEERING (2008)
Establishment of HIV-1 resistance in CD4+ T cells by genome editing using zinc-finger nucleases
Elena E. Perez et al.
NATURE BIOTECHNOLOGY (2008)
Adenovirus:: from foe to friend
MAFV Gonçalves et al.
REVIEWS IN MEDICAL VIROLOGY (2006)
Transduction of myogenic cells by retargeted dual high-capacity hybrid viral vectors:: Robust dystrophin synthesis in Duchenne muscular dystrophy muscle cells
Manuel A. F. V. Goncalves et al.
MOLECULAR THERAPY (2006)
Endowing human adenovirus serotype 5 vectors with fiber domains of species B greatly enhances gene transfer into human mesenchymal stem cells
S Knaän-Shanzer et al.
STEM CELLS (2005)
Adenovirus vector-based vaccines for human immunodeficiency virus type 1
DH Barouch et al.
HUMAN GENE THERAPY (2005)
Stable transduction of large DNA by high-capactity adeno-associated virus/adenovirus hybrid vectors
MAFV Gonçalves et al.
VIROLOGY (2004)
Lentivector-mediated transfer of Bmi-1 and telomerase in muscle satellite cells yields a Duchenne myoblast cell line with long-term genotypic and phenotypic stability
C Cudré-Mauroux et al.
HUMAN GENE THERAPY (2003)
Replicative oncolytic adenoviruses in multimodal cancer regimens
DE Post et al.
HUMAN GENE THERAPY (2003)
Efficient gene transfer into human CD34(+) cells by a retargeted adenovirus vector
DM Shayakhmetov et al.
JOURNAL OF VIROLOGY (2000)
分享论文
