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。Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors
A. A. Rahim et al.
GENE THERAPY (2009)
Targeted Gene Modification in Mouse ES Cells Using Integrase-Defective Lentiviral Vectors
Yuka Okada et al.
GENESIS (2009)
The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy
Eugenio Montini et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Hybrid Lentivirus-transposon Vectors With a Random Integration Profile in Human Cells
Nicklas H. Staunstrup et al.
MOLECULAR THERAPY (2009)
Sleeping Beauty Transposition From Nonintegrating Lentivirus
Conrad A. Vink et al.
MOLECULAR THERAPY (2009)
Conditionally replicating lentiviral-hybrid episomal vectors for suicide gene therapy
J. Vargas et al.
ANTIVIRAL RESEARCH (2008)
Transient gene expression mediated by integrase-defective retroviral vectors
Seung Shin Yu et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)
Genomic insertion of lentiviral DNA circles directed by the yeast Flp recombinase
Brian Moldt et al.
BMC BIOTECHNOLOGY (2008)
Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients
Steven J. Howe et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1
Salima Hacein-Bey-Abina et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Minicircle-DNA production by site specific recombination and protein-DNA interaction chromatography
Peter Mayrhofer et al.
JOURNAL OF GENE MEDICINE (2008)
Rational vector design for efficient non-viral gene delivery: Challenges facing the use of plasmid DNA
Juergen Mairhofer et al.
MOLECULAR BIOTECHNOLOGY (2008)
Rapid Open-Source engineering of customized zinc-finger nucleases for highly efficient gene modification
Morgan L. Maeder et al.
MOLECULAR CELL (2008)
The MDS1-EVI1 gene complex as a retrovirus integration site: Impact on behavior of hematopoietic cells and implications for gene therapy
Jean-Yves Metais et al.
MOLECULAR THERAPY (2008)
A Large U3 Deletion Causes Increased In Vivo Expression From a Nonintegrating Lentiviral Vector
Matthew Bayer et al.
MOLECULAR THERAPY (2008)
Protective Antiviral Immunity Conferred by a Nonintegrative Lentiviral Vector-Based Vaccine
Frederic Coutant et al.
PLOS ONE (2008)
Targeted genome modifications using integrase-deficient lentiviral vectors
Tatjana I. Cornu et al.
MOLECULAR THERAPY (2007)
Gene editing in human stem cells using zinc finger nucleases and integrase-defective lentiviral vector delivery
Angelo Lombardo et al.
NATURE BIOTECHNOLOGY (2007)
Stable gene transfer to muscle using non-integrating lentiviral vectors
Luis Apolonia et al.
MOLECULAR THERAPY (2007)
Successful immunization with a single injection of non-integrating lentiviral vector
Donatella R. M. Negri et al.
MOLECULAR THERAPY (2007)
HIV integration site selection: Analysis by massively parallel pyrosequencing reveals association with epigenetic modifications
Gary P. Wang et al.
GENOME RESEARCH (2007)
RNA interference: A tool for querying nervous system function and an emerging therapy
Beverly L. Davidson et al.
NEURON (2007)
Gene silencing by small regulatory RNAs in mammalian cells
Michaela Scherr et al.
CELL CYCLE (2007)
Purification of retroviral vectors for clinical application: Biological implications and technological challenges
Teresa Rodrigues et al.
JOURNAL OF BIOTECHNOLOGY (2007)
Lentiviral vectors with a defective integrase allow efficient and sustained transgene expression in vitro and in vivo
Stephanie Philippe et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Integration site choice of a feline immunodeficiency virus vector
Yubin Kang et al.
JOURNAL OF VIROLOGY (2006)
CCR5: no longer a 'good for nothing' gene - chemokine control of West Nile virus infection
Jean K. Lim et al.
TRENDS IN IMMUNOLOGY (2006)
Transient gene expression by nonintegrating lentiviral vectors
Sarah J. Nightingale et al.
MOLECULAR THERAPY (2006)
Effective gene therapy with nonintegrating lentiviral vectors
RJ Yáñez-Muñoz et al.
NATURE MEDICINE (2006)
Retrovirus vectors: Toward the plentivirus?
Christopher Baum et al.
MOLECULAR THERAPY (2006)
Expressing short hairpin RNAs in vivo
Ola Snove et al.
NATURE METHODS (2006)
Gene Therapy Progress and Prospects: Development of improved lentiviral and retroviral vectors - design, biosafety, and production
PL Sinn et al.
GENE THERAPY (2005)
Genetic analyses of DNA-binding mutants in the catalytic core domain of human immunodeficiency virus type I integrase
R Lu et al.
JOURNAL OF VIROLOGY (2005)
Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo
ZY Chen et al.
GENE THERAPY (2004)
Novel integrase-defective lentiviral episomal vectors for gene transfer
J Vargas et al.
HUMAN GENE THERAPY (2004)
Unintegrated lentivirus DNA persistence and accessibility to expression in nondividing cells: Analysis with class I integrase mutants
DT Saenz et al.
JOURNAL OF VIROLOGY (2004)
Toolbox for retrovectorologists
JC Pagès et al.
JOURNAL OF GENE MEDICINE (2004)
Retroviral DNA integration: ASLV, HIV, and MLV show distinct target site preferences
RS Mitchell et al.
PLOS BIOLOGY (2004)
Inhibition of influenza virus production in virus-infected mice by RNA interference
Q Ge et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Evidence for gene expression by unintegrated human immunodeficiency virus type 1 DNA species
A Brussel et al.
JOURNAL OF VIROLOGY (2004)
Retroviral vectors:: new applications for an old tool
J Barquinero et al.
GENE THERAPY (2004)
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1
S Hacein-Bey-Abina et al.
SCIENCE (2003)
Transcription start regions in the human genome are favored targets for MLV integration
XL Wu et al.
SCIENCE (2003)
A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency
S Hacein-Bey-Abina et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)
Comparison of wild-type and class I integrase mutant-FIV vectors in retina demonstrates sustained expression of integrated transgenes in retinal pigment epithelium
N Loewen et al.
JOURNAL OF GENE MEDICINE (2003)
HIV-1 integration in the human genome favors active genes and local hotspots
ARW Schröder et al.
CELL (2002)
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy
S Hacein-Bey-Abina et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
Human immunodeficiency virus cDNA metabolism: Notable stability of two-long terminal repeat circles
SL Butler et al.
JOURNAL OF VIROLOGY (2002)
Intrinsic stability of episomal circles formed during human immunodeficiency virus type 1 replication
TC Pierson et al.
JOURNAL OF VIROLOGY (2002)
Systematic determination of the packaging limit of lentiviral vectors
M Kumar et al.
HUMAN GENE THERAPY (2001)
Human immunodeficiency virus type 1 replication in the absence of integrase-mediated DNA recombination: Definition of permissive and nonpermissive T-Cell lines
N Nakajima et al.
JOURNAL OF VIROLOGY (2001)
HIV integrase, a brief overview from chemistry to therapeutics
R Craigie
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Role of the non-homologous DNA end joining pathway in the early steps of retroviral infection
L Li et al.
EMBO JOURNAL (2001)
Repair of gaps in retroviral DNA integration intermediates
KE Yoder et al.
JOURNAL OF VIROLOGY (2000)
分享论文
