Uncovering and dissecting the genotoxicity of self-inactivating lentiviral vectors in vivo
about
PSMA-specific CAR-engineered T cells eradicate disseminated prostate cancer in preclinical modelsDevelopment of an inducible caspase-9 safety switch for pluripotent stem cell-based therapiesOptimization of mucosal responses after intramuscular immunization with integrase defective lentiviral vectorDelivery of full-length factor VIII using a piggyBac transposon vector to correct a mouse model of hemophilia A.Lentiviral vector-based insertional mutagenesis identifies genes involved in the resistance to targeted anticancer therapies.Towards a Safer, More Randomized Lentiviral Vector Integration Profile Exploring Artificial LEDGF Chimeras.Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy.Genetic treatment of a molecular disorder: gene therapy approaches to sickle cell disease.Gene Therapy of the β-Hemoglobinopathies by Lentiviral Transfer of the β(A(T87Q))-Globin Gene.A comparison of foamy and lentiviral vector genotoxicity in SCID-repopulating cells shows foamy vectors are less prone to clonal dominance.Dimethyloxaloylglycine increases bone repair capacity of adipose-derived stem cells in the treatment of osteonecrosis of the femoral head.Pervasive supply of therapeutic lysosomal enzymes in the CNS of normal and Krabbe-affected non-human primates by intracerebral lentiviral gene therapyLentiviral hematopoietic stem cell gene therapy in inherited metabolic disorders.Integration site and clonal expansion in human chronic retroviral infection and gene therapy.Alpharetroviral vectors: from a cancer-causing agent to a useful tool for human gene therapy.Cartilage tissue engineering: recent advances and perspectives from gene regulation/therapy.CRISPR genome engineering and viral gene delivery: a case of mutual attraction.Recent trends in the gene therapy of β-thalassemia.Gene therapy and peripheral nerve repair: a perspective.Evidence for the in vivo safety of insulated foamy viral vectorsSafe and Effective Gene Therapy for Murine Wiskott-Aldrich Syndrome Using an Insulated Lentiviral VectorViral vectors for therapy of neurologic diseases.Viral Vectors: The Road to Reducing Genotoxicity.Insulated Foamy Viral Vectors.A minimal ubiquitous chromatin opening element (UCOE) effectively prevents silencing of juxtaposed heterologous promoters by epigenetic remodeling in multipotent and pluripotent stem cells.Retroviral vector interactions with hematopoietic cells.Gene delivery to rat and human Schwann cells and nerve segments: a comparison of AAV 1-9 and lentiviral vectors.HIV-1-mediated insertional activation of STAT5B and BACH2 trigger viral reservoir in T regulatory cells.Tightly regulated 'all-in-one' lentiviral vectors for protection of human hematopoietic cells from anticancer chemotherapy.Long-Term Restoration of Thymidine Phosphorylase Function and Nucleoside Homeostasis Using Hematopoietic Gene Therapy in a Murine Model of Mitochondrial Neurogastrointestinal Encephalomyopathy.Genome Editing of the Blood: Opportunities and ChallengesHighly efficient retinal gene delivery with helper-dependent adenoviral vectors.CCR5 Gene Editing of Resting CD4(+) T Cells by Transient ZFN Expression From HIV Envelope Pseudotyped Nonintegrating Lentivirus Confers HIV-1 Resistance in Humanized MiceVISPA: a computational pipeline for the identification and analysis of genomic vector integration sites.Hematopoietic Stem Cell Gene Therapy: Progress and Lessons Learned.Analyzing the Genotoxicity of Retroviral Vectors in Hematopoietic Cell Gene Therapy.Retroviral and Lentiviral Safety Analysis of Gene-Modified T Cell Products and Infused HIV and Oncology Patients.Improved calvarial bone repair by hASCs engineered with Cre/loxP-based baculovirus conferring prolonged BMP-2 and MiR-148b co-expression.Targeted in vivo knock-in of human alpha-1-antitrypsin cDNA using adenoviral delivery of CRISPR/Cas9.Clinical use of lentiviral vectors.
P2860
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P2860
Uncovering and dissecting the genotoxicity of self-inactivating lentiviral vectors in vivo
description
2014 nî lūn-bûn
@nan
2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@ast
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@en
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@nl
type
label
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@ast
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@en
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@nl
prefLabel
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@ast
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@en
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
Uncovering and dissecting the ...... ing lentiviral vectors in vivo
@en
P2093
Alessandro Nonis
Alexandre Artus
Caroline Duros
Chiara Brombin
Clelia Di Serio
Cynthia Bartholomae
Fabrizio Benedicenti
Francesca Sanvito
Lucia Sergi Sergi
Manfred Schmidt
P2860
P304
P3181
P356
10.1038/MT.2014.3
P407
P50
P577
2014-04-01T00:00:00Z