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Immune response to green fluorescent protein : implications for gene therapy

Gene therapy, 1999-07, Vol.6 (7), p.1305-1312

1999

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A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency

The New England journal of medicine, 2014-10, Vol.371 (15), p.1407-1417

2014

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Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vector

Gene therapy, 2010-10, Vol.17 (10), p.1244-1252

2010

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The woodchuck hepatitis virus post-transcriptional regulatory element reduces readthrough transcription from retroviral vectors

Gene therapy, 2007-09, Vol.14 (17), p.1298-1304

2007

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Time Course of Bioluminescent Signal in Orthotopic and Heterotopic Brain Tumors in Nude Mice

BioTechniques, 2003-06, Vol.34 (6), p.1184-1188

2003

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Lack of Expression from a Retroviral Vector After Transduction of Murine Hematopoietic Stem Cells is Associated with Methylation in vivo

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (7), p.2567-2571

1994

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HIV-1-derived lentiviral vectors and fetal route of administration on transgene biodistribution and expression in rhesus monkeys

Gene therapy, 2005-05, Vol.12 (10), p.821-830

2005

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Gene therapy for genetic haematological disorders and immunodeficiencies

Journal of internal medicine, 2001-04, Vol.249 (4), p.379-390

Kohn, D. B.

2001

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The enhanced green fluorescent protein (eGFP) is minimally immunogenic in C57BL/6 mice

Gene therapy, 2001-12, Vol.8 (23), p.1813-1814

2001

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Improved Expression in Hematopoietic and Lymphoid Cells in Mice After Transplantation of Bone Marrow Transduced With a Modified Retroviral Vector

Blood, 1999-11, Vol.94 (10), p.3349-3357

1999

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Tissue-specific restriction of cyclophilin A-independent HIV-1- and SIV-derived lentiviral vectors

Gene therapy, 2008-08, Vol.15 (15), p.1079-1089

2008

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A clinical trial of retroviral-mediated transfer of a rev-responsive element decoy gene into CD34+ cells from the bone marrow of human immunodeficiency virus-1-infected children

Blood, 1999-07, Vol.94 (1), p.368-371

1999

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Lentiviral vectors with amplified β cell-specific gene expression

Gene therapy, 2009-08, Vol.16 (8), p.998-1008

2009

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Transduction of Pluripotent Human Hematopoietic Stem Cells Demonstrated by Clonal Analysis after Engraftment in Immune-Deficient Mice

Proceedings of the National Academy of Sciences - PNAS, 1996-03, Vol.93 (6), p.2414-2419

1996

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Occurrence of leukaemia following gene therapy of X-linked SCID

Nature reviews. Cancer, 2003-07, Vol.3 (7), p.477-488

2003

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Analysis of Optimal Conditions for Retroviral-Mediated Transduction of Primitive Human Hematopoietic Cells

Blood, 1995-07, Vol.86 (1), p.101-110

1995

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Comparison of Gene Transfer Efficiencies and Gene Expression Levels Achieved with Equine Infectious Anemia Virus- and Human Immunodeficiency Virus Type 1-Derived Lentivirus Vectors

Journal of Virology, 2002-02, Vol.76 (3), p.1510-1515

2002

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Gene therapy for childhood immunological diseases

Bone marrow transplantation (Basingstoke), 2008-01, Vol.41 (2), p.199-205

Kohn, D B

2008

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Sustained human hematopoiesis in immunodeficient mice by cotransplantation of marrow stroma expressing human interleukin-3 : analysis of gene transduction of long-lived progenitors

Blood, 1994-05, Vol.83 (10), p.3041-3051

1994

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Gene therapy to inhibit xenoantibody production using lentiviral vectors in non-human primates

Gene therapy, 2007-01, Vol.14 (1), p.49-57

2007

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Lentiviral vectors for efficient delivery of CD80 and granulocyte-macrophage– colony-stimulating factor in human acute lymphoblastic leukemia and acute myeloid leukemia cells to induce antileukemic immune responses

Blood, 2000-08, Vol.96 (4), p.1317-1326

2000

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Cells Expressing Human Glucocerebrosidase From a Retroviral Vector Repopulate Macrophages and Central Nervous System Microglia After Murine Bone Marrow Transplantation

Blood, 1994-05, Vol.83 (9), p.2737-2748

1994

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Gene therapy using hematopoietic stem cells : Sisyphus approaches the crest

Human gene therapy, 2000-06, Vol.11 (9), p.1259-1267

2000

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Long-term efficacy of enzyme replacement therapy for Adenosine deaminase (ADA)-deficient Severe Combined Immunodeficiency (SCID)

Clinical Immunology, 2005-11, Vol.117 (2), p.133-143

2005

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FLT3 ligand preserves the ability of human CD34+ progenitors to sustain long-term hematopoiesis in immune-deficient mice after ex vivo retroviral-mediated transduction

Blood, 1997-01, Vol.89 (2), p.446-456

1997

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Immune response to green fluorescent protein : implications for gene therapy

A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency

Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vector

The woodchuck hepatitis virus post-transcriptional regulatory element reduces readthrough transcription from retroviral vectors

Time Course of Bioluminescent Signal in Orthotopic and Heterotopic Brain Tumors in Nude Mice

Lack of Expression from a Retroviral Vector After Transduction of Murine Hematopoietic Stem Cells is Associated with Methylation in vivo

HIV-1-derived lentiviral vectors and fetal route of administration on transgene biodistribution and expression in rhesus monkeys

Gene therapy for genetic haematological disorders and immunodeficiencies

The enhanced green fluorescent protein (eGFP) is minimally immunogenic in C57BL/6 mice

Improved Expression in Hematopoietic and Lymphoid Cells in Mice After Transplantation of Bone Marrow Transduced With a Modified Retroviral Vector

Tissue-specific restriction of cyclophilin A-independent HIV-1- and SIV-derived lentiviral vectors

A clinical trial of retroviral-mediated transfer of a rev-responsive element decoy gene into CD34+ cells from the bone marrow of human immunodeficiency virus-1-infected children

Lentiviral vectors with amplified β cell-specific gene expression

Transduction of Pluripotent Human Hematopoietic Stem Cells Demonstrated by Clonal Analysis after Engraftment in Immune-Deficient Mice

Occurrence of leukaemia following gene therapy of X-linked SCID

Analysis of Optimal Conditions for Retroviral-Mediated Transduction of Primitive Human Hematopoietic Cells

Comparison of Gene Transfer Efficiencies and Gene Expression Levels Achieved with Equine Infectious Anemia Virus- and Human Immunodeficiency Virus Type 1-Derived Lentivirus Vectors

Gene therapy for childhood immunological diseases

Sustained human hematopoiesis in immunodeficient mice by cotransplantation of marrow stroma expressing human interleukin-3 : analysis of gene transduction of long-lived progenitors

Gene therapy to inhibit xenoantibody production using lentiviral vectors in non-human primates

Lentiviral vectors for efficient delivery of CD80 and granulocyte-macrophage– colony-stimulating factor in human acute lymphoblastic leukemia and acute myeloid leukemia cells to induce antileukemic immune responses

Cells Expressing Human Glucocerebrosidase From a Retroviral Vector Repopulate Macrophages and Central Nervous System Microglia After Murine Bone Marrow Transplantation

Gene therapy using hematopoietic stem cells : Sisyphus approaches the crest

Long-term efficacy of enzyme replacement therapy for Adenosine deaminase (ADA)-deficient Severe Combined Immunodeficiency (SCID)

FLT3 ligand preserves the ability of human CD34+ progenitors to sustain long-term hematopoiesis in immune-deficient mice after ex vivo retroviral-mediated transduction

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