Search Results - "RYU, Byoung Y"
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Optimizing lentiviral vector transduction of hematopoietic stem cells for gene therapy
Published in Gene therapy (01-12-2020)“…Autologous gene therapy using lentiviral vectors (LVs) holds promise for treating monogenetic blood diseases. However, clinical applications can be limited by…”
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2
Genome editing of HBG1 and HBG2 to induce fetal hemoglobin
Published in Blood advances (12-11-2019)“…Induction of fetal hemoglobin (HbF) via clustered regularly interspaced short palindromic repeats/Cas9–mediated disruption of DNA regulatory elements that…”
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3
Preclinical proof of concept for VivoVec, a lentiviral-based platform for in vivo CAR T-cell engineering
Published in Journal for immunotherapy of cancer (01-03-2023)“…BackgroundChimeric antigen receptor (CAR) T-cell therapies have demonstrated transformational outcomes in the treatment of B-cell malignancies, but their…”
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4
Successful targeting and disruption of an integrated reporter lentivirus using the engineered homing endonuclease Y2 I-AniI
Published in PloS one (09-02-2011)“…Current antiviral therapy does not cure HIV-infected individuals because the virus establishes lifelong latent infection within long-lived memory T cells as…”
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An experimental system for the evaluation of retroviral vector design to diminish the risk for proto-oncogene activation
Published in Blood (15-02-2008)“…Pathogenic activation of the LMO2 proto-oncogene by an oncoretroviral vector insertion in a clinical trial for X-linked severe combined immunodeficiency…”
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Effective, safe, and sustained correction of murine XLA using a UCOE-BTK promoter-based lentiviral vector
Published in Molecular therapy. Methods & clinical development (12-03-2021)“…X-linked agammaglobulinemia (XLA) is an immune disorder caused by mutations in Bruton’s tyrosine kinase (BTK). BTK is expressed in B and myeloid cells, and its…”
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Targeted Entry via Somatostatin Receptors Using a Novel Modified Retrovirus Glycoprotein That Delivers Genes at Levels Comparable to Those of Wild-Type Viral Glycoproteins
Published in Journal of Virology (01-01-2012)“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Daedalus: a robust, turnkey platform for rapid production of decigram quantities of active recombinant proteins in human cell lines using novel lentiviral vectors
Published in Nucleic acids research (01-11-2011)“…A key challenge for the academic and biopharmaceutical communities is the rapid and scalable production of recombinant proteins for supporting downstream…”
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9
In vivo CAR T-cell generation in nonhuman primates using lentiviral vectors displaying a multidomain fusion ligand
Published in Blood (29-08-2024)“…•Lentiviral vectors displaying T-cell activation and costimulatory molecules (VivoVec) generate CAR T cells in vivo without lymphodepletion.•VivoVec…”
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10
Resveratrol trimer enhances gene delivery to hematopoietic stem cells by reducing antiviral restriction at endosomes
Published in Blood (17-10-2019)“…Therapeutic gene delivery to hematopoietic stem cells (HSCs) holds great potential as a life-saving treatment of monogenic, oncologic, and infectious diseases…”
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11
Coupling endonucleases with DNA end–processing enzymes to drive gene disruption
Published in Nature methods (01-10-2012)“…Coexpression of DNA end–processing enzymes with targeted nucleases improves the efficiency of gene disruption in mammalian cells. Targeted DNA double-strand…”
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Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndrome
Published in Blood (10-05-2012)“…The immunodeficiency disorder Wiskott-Aldrich syndrome (WAS) leads to life-threatening hematopoietic cell dysfunction. We used WAS protein (WASp)–deficient…”
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13
Tracking genome engineering outcome at individual DNA breakpoints
Published in Nature methods (01-08-2011)“…A fluorescent reporter, named traffic light, reads out whether repair of a DNA break occurs by nonhomologous end-joining or by homologous recombination. It…”
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B cell–specific lentiviral gene therapy leads to sustained B-cell functional recovery in a murine model of X-linked agammaglobulinemia
Published in Blood (18-03-2010)“…The immunodeficiency disorder, X-linked agammaglobulinemia (XLA), results from mutations in the gene encoding Bruton tyrosine kinase (Btk). Btk is required for…”
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15
Developmentally regulated expression of MEF2C limits the response to BCR engagement in transitional B cells
Published in European journal of immunology (01-05-2012)“…Transitional and naïve mature peripheral B cells respond very differently to B‐cell receptor (BCR) cross‐linking. While transitional B cells undergo apoptosis…”
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Development of B-lineage Predominant Lentiviral Vectors for Use in Genetic Therapies for B Cell Disorders
Published in Molecular therapy (01-03-2011)“…Sustained, targeted, high-level transgene expression in primary B lymphocytes may be useful for gene therapy in B cell disorders. We developed several…”
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17
Novel reporter systems for facile evaluation of I-SceI-mediated genome editing
Published in Nucleic acids research (01-01-2012)“…Two major limitations to achieve efficient homing endonuclease-stimulated gene correction using retroviral vectors are low frequency of gene targeting and…”
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18
The block to membrane fusion differs with the site of ligand insertion in modified retroviral envelope proteins
Published in Journal of general virology (01-04-2008)“…Department of Molecular Sciences, University of Tennessee Health Science Center, Memphis, TN, USA Correspondence Lorraine M. Albritton lalbritton{at}utmem.edu…”
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A chromatin insulator blocks interactions between globin regulatory elements and cellular promoters in erythroid cells
Published in Blood cells, molecules, & diseases (01-11-2007)“…Retroviral vectors have been developed for gene therapy of blood disorders because they achieve long-term expression of the transgene. However, interactions…”
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1059. The Influence of a Chromatin Insulator on Interactions between Globin Regulatory Elements and Cellular Promoters in Erythroid Cells
Published in Molecular therapy (01-05-2006)“…Integrating retroviral vectors have been developed for gene therapy of blood disorders because they achieve long term expression of the transgene. However,…”
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