Donald B Kohn


Ontology type: schema:Person     


Person Info

NAME

Donald B

SURNAME

Kohn

Publications in SciGraph latest 50 shown

  • 2021-06-28 Normal IgH Repertoire Diversity in an Infant with ADA Deficiency After Gene Therapy in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-12-03 Correction to: Infections in Infants with SCID: Isolation, Infection Screening and Prophylaxis in PIDTC Centers in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-10-02 Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-09-02 Adenosine Deaminase (ADA)–Deficient Severe Combined Immune Deficiency (SCID) in the US Immunodeficiency Network (USIDNet) Registry in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2020-01-27 Lentiviral gene therapy for X-linked chronic granulomatous disease in NATURE MEDICINE
  • 2019-08-02 Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2019-02-12 Correction to: Differentiation of RPE cells from integration-free iPS cells and their cell biological characterization in STEM CELL RESEARCH & THERAPY
  • 2018-09-28 T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiency in GENOME MEDICINE
  • 2018-09-06 Superior lentiviral vectors designed for BSL-0 environment abolish vector mobilization. in GENE THERAPY
  • 2017-10-02 Differentiation of RPE cells from integration-free iPS cells and their cell biological characterization in STEM CELL RESEARCH & THERAPY
  • 2017-08-25 Adenosine Deaminase (ADA)-Deficient Severe Combined Immune Deficiency (SCID): Molecular Pathogenesis and Clinical Manifestations in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2017-04-03 Generation of mature T cells from human hematopoietic stem/progenitor cells in artificial thymic organoids in NATURE METHODS
  • 2017-02-14 How We Manage Adenosine Deaminase-Deficient Severe Combined Immune Deficiency (ADA SCID) in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2016-07-12 Analyzing CRISPR genome-editing experiments with CRISPResso in NATURE BIOTECHNOLOGY
  • 2016-04-07 Gene Therapy for the Treatment of Primary Immune Deficiencies in CURRENT ALLERGY AND ASTHMA REPORTS
  • 2015-12-18 Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency in ORPHANET JOURNAL OF RARE DISEASES
  • 2014-04-08 HIV eradication—from Berlin to Boston in NATURE BIOTECHNOLOGY
  • 2013-07-26 Generation and characterization of transgene-free human induced pluripotent stem cells and conversion to putative clinical-grade status in STEM CELL RESEARCH & THERAPY
  • 2013-07-02 The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901 in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2013-01-29 A CD19/Fc fusion protein for detection of anti-CD19 chimeric antigen receptors in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2010-07-02 Zinc finger nuclease-mediated CCR5 knockout hematopoietic stem cell transplantation controls HIV-1 in vivo in NATURE BIOTECHNOLOGY
  • 2010-05-20 Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vector in GENE THERAPY
  • 2009-05-14 Lentiviral Vectors with Amplified Beta Cell-Specific Gene Expression in GENE THERAPY
  • 2008-09-20 Long-Term Neurocognitive Function of Pediatric Patients with Severe Combined Immune Deficiency (SCID): Pre- and Post-Hematopoietic Stem Cell Transplant (HSCT) in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2008-04-03 Tissue-specific restriction of cyclophilin A-independent HIV-1- and SIV-derived lentiviral vectors in GENE THERAPY
  • 2007-12-07 Genetic therapies against HIV in NATURE BIOTECHNOLOGY
  • 2007-11-12 Gene therapy for childhood immunological diseases in BONE MARROW TRANSPLANTATION
  • 2007-06-28 The woodchuck hepatitis virus post-transcriptional regulatory element reduces readthrough transcription from retroviral vectors in GENE THERAPY
  • 2007-01 Lentiviral vectors ready for prime-time in NATURE BIOTECHNOLOGY
  • 2006-08-03 Gene therapy to inhibit xenoantibody production using lentiviral vectors in non-human primates in GENE THERAPY
  • 2005-05-06 Recombinant murine interleukin-12 elicits potent antileukemic immune responses in a murine model of philadelphia chromosome-positive acute lymphoblastic leukemia in CANCER GENE THERAPY
  • 2005-04-07 HIV-1-derived lentiviral vectors and fetal route of administration on transgene biodistribution and expression in rhesus monkeys in GENE THERAPY
  • 2003-11 Correction: Occurrence of leukaemia following gene therapy of X-linked SCID in NATURE REVIEWS CANCER
  • 2003-07 Occurrence of leukaemia following gene therapy of X-linked SCID in NATURE REVIEWS CANCER
  • 2003-03-17 Clonality analysis after retroviral-mediated gene transfer to CD34+ cells from the cord blood of ADA-deficient SCID neonates in NATURE MEDICINE
  • 2001-12 The enhanced green fluorescent protein (eGFP) is minimally immunogenic in C57BL/6 mice in GENE THERAPY
  • 2001-09 Hematopoietic stem cell transplantation for severe combined immune deficiency in CURRENT ALLERGY AND ASTHMA REPORTS
  • 2000-11 Gene Therapy for XSCID: The First Success of Gene Therapy in PEDIATRIC RESEARCH
  • 2000-02-17 Expression of human Wiskott–Aldrich syndrome protein in patients’ cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins in GENE THERAPY
  • 2000 Gene Therapy with Cord Blood Hematopoietic Stem Cells for Adenosine Deaminase Deficiency: An Update in TRANSPLANTATION IN HEMATOLOGY AND ONCOLOGY
  • 1999-07 Immune response to green fluorescent protein: implications for gene therapy in GENE THERAPY
  • 1998-07 T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates in NATURE MEDICINE
  • 1998-05-21 Gene transfer into human umbilical cord blood-derived CD34+ cells by particle-mediated gene transfer in GENE THERAPY
  • 1998-03 Immunotherapy against murine leukemia in LEUKEMIA
  • 1997-11 Retrovirus-mediated transfer of the human α- L-iduronidase cDNA into human hematopoietic progenitor cells leads to correction in trans of Hurler fibroblasts in GENE THERAPY
  • 1996 Gene Therapy for HIV-1 Infection in ANTIVIRAL CHEMOTHERAPY 4
  • 1996 Induction of Immunity Against Leukemia in ACUTE LEUKEMIAS V
  • 1995-10 Engraftment of gene–modified umbilical cord blood cells in neonates with adenosine deaminase deficiency in NATURE MEDICINE
  • 1995 Bone Marrow Transplantation for Metabolic Diseases in TECHNICAL AND BIOLOGICAL COMPONENTS OF MARROW TRANSPLANTATION
  • 1990 Bone marrow transplantation for immunodeficiency and genetic diseases in BONE MARROW TRANSPLANTATION
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