Lista de obras -

"RCL-Pooling Assay": A Simplified Method for the Detection of Replication-Competent Lentiviruses in Vector Batches Using Sequential Pooling.

artículo científico publicado en 2016

Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID

scientific article published on 13 September 2019

Concurrent measures of fusion and transduction efficiency of primary CD34+ cells with human immunodeficiency virus 1-based lentiviral vectors reveal different effects of transduction enhancers

artículo científico publicado en 2013

Delineation of the human hematolymphoid system: potential applications of defined cell populations in cellular therapy ⬇️

artículo científico publicado el 1 de junio de 1997

Engraftment and in vivo proliferation advantage of gene corrected mobilized CD34(+) cells from Fanconi anemia patients.

artículo científico

Engraftment of human hematopoietic precursor cells with secondary transfer potential in SCID-hu mice ⬇️

artículo científico publicado el 15 de octubre de 1994

Equal distribution of competitive long-term repopulating stem cells in the CD34+ and CD34- fractions of Thy-1lowLin-/lowSca-1+ bone marrow cells

artículo científico publicado el 1 de mayo de 1998

Gene therapy for Wiskott-Aldrich syndrome in a severely affected adult

artículo científico publicado en 2017

Gene therapy on the move

artículo científico publicado en 2013

Human T, B, natural killer, and dendritic cells arise from a common bone marrow progenitor cell subset ⬇️

artículo científico publicado el 1 de octubre de 1995

Improvement of De Novo Cholesterol Biosynthesis Efficiently Promotes the Production of Human Immunodeficiency Virus Type 1-Derived Lentiviral Vectors.

artículo científico publicado en 2017

Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome.

artículo científico publicado en 2013

Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCs.

artículo científico publicado en 2015

Lymphopoiesis in transgenic mice over-expressing Artemis

artículo científico publicado en 2015

Molecular Determinants of Vectofusin-1 and Its Derivatives for the Enhancement of Lentivirally Mediated Gene Transfer into Hematopoietic Stem/Progenitor Cells

artículo científico publicado en 2015

MyD88 Signaling in B Cells Regulates the Production of Th1-dependent Antibodies to AAV ⬇️

artículo científico publicado el 29 de mayo de 2012

Non-Clinical Efficacy and Safety Studies on G1XCGD, a Lentiviral Vector for Ex Vivo Gene Therapy of X-Linked Chronic Granulomatous Disease.

artículo científico publicado en 2018

Peptides derived from evolutionarily conserved domains in Beclin1 and Beclin2 enhance the entry of lentiviral vectors into human cells

artículo científico publicado en 2017

Phenotypic and functional analysis of T-cell precursors in the human fetal liver and thymus: CD7 expression in the early stages of T- and myeloid-cell development ⬇️

artículo científico publicado el 1 de diciembre de 1993

Precursors of CD3+CD4+CD8+ cells in the human thymus are defined by expression of CD34. Delineation of early events in human thymic development ⬇️

artículo científico publicado el 1 de agosto de 1993

Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia

scientific article published on 09 September 2019

Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene Transfer

artículo científico publicado en 2019

Toward a Scalable Purification Protocol of GaLV-TR-Pseudotyped Lentiviral Vectors

artículo científico publicado en 2019

Treatment of Uveitis by In Situ Administration of Ex Vivo-Activated Polyclonal Regulatory T Cells.

artículo científico publicado en 2016

Vectofusin-1 Improves Transduction of Primary Human Cells with Diverse Retroviral and Lentiviral Pseudotypes, Enabling Robust, Automated Closed-System Manufacturing

artículo científico publicado en 2019

Vectofusin-1, a Potent Peptidic Enhancer of Viral Gene Transfer forms pH-dependent α-Helical Nanofibrils, Concentrating Viral Particles.

artículo científico publicado en 2017

Vectofusin-1, a new viral entry enhancer, strongly promotes lentiviral transduction of human hematopoietic stem cells.

artículo científico publicado en 2013

Lista de obras de

"RCL-Pooling Assay": A Simplified Method for the Detection of Replication-Competent Lentiviruses in Vector Batches Using Sequential Pooling.

Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID

Concurrent measures of fusion and transduction efficiency of primary CD34+ cells with human immunodeficiency virus 1-based lentiviral vectors reveal different effects of transduction enhancers

Delineation of the human hematolymphoid system: potential applications of defined cell populations in cellular therapy ⬇️

Engraftment and in vivo proliferation advantage of gene corrected mobilized CD34(+) cells from Fanconi anemia patients.

Engraftment of human hematopoietic precursor cells with secondary transfer potential in SCID-hu mice ⬇️

Equal distribution of competitive long-term repopulating stem cells in the CD34+ and CD34- fractions of Thy-1lowLin-/lowSca-1+ bone marrow cells

Gene therapy for Wiskott-Aldrich syndrome in a severely affected adult

Gene therapy on the move

Human T, B, natural killer, and dendritic cells arise from a common bone marrow progenitor cell subset ⬇️

Improvement of De Novo Cholesterol Biosynthesis Efficiently Promotes the Production of Human Immunodeficiency Virus Type 1-Derived Lentiviral Vectors.

Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome.

Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCs.

Lymphopoiesis in transgenic mice over-expressing Artemis

Molecular Determinants of Vectofusin-1 and Its Derivatives for the Enhancement of Lentivirally Mediated Gene Transfer into Hematopoietic Stem/Progenitor Cells

MyD88 Signaling in B Cells Regulates the Production of Th1-dependent Antibodies to AAV ⬇️

Non-Clinical Efficacy and Safety Studies on G1XCGD, a Lentiviral Vector for Ex Vivo Gene Therapy of X-Linked Chronic Granulomatous Disease.

Peptides derived from evolutionarily conserved domains in Beclin1 and Beclin2 enhance the entry of lentiviral vectors into human cells

Phenotypic and functional analysis of T-cell precursors in the human fetal liver and thymus: CD7 expression in the early stages of T- and myeloid-cell development ⬇️

Precursors of CD3+CD4+CD8+ cells in the human thymus are defined by expression of CD34. Delineation of early events in human thymic development ⬇️

Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia

Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene Transfer

Toward a Scalable Purification Protocol of GaLV-TR-Pseudotyped Lentiviral Vectors

Treatment of Uveitis by In Situ Administration of Ex Vivo-Activated Polyclonal Regulatory T Cells.

Vectofusin-1 Improves Transduction of Primary Human Cells with Diverse Retroviral and Lentiviral Pseudotypes, Enabling Robust, Automated Closed-System Manufacturing

Vectofusin-1, a Potent Peptidic Enhancer of Viral Gene Transfer forms pH-dependent α-Helical Nanofibrils, Concentrating Viral Particles.

Vectofusin-1, a new viral entry enhancer, strongly promotes lentiviral transduction of human hematopoietic stem cells.