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Non-viral and viral hematopoietic progenitor cell gene therapy
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Engineering viral vectors for gene and cell targeting
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Improving adeno-associated viral vector for hematopoietic stem cells gene therapy
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Effects of a GSK-3 inhibitor on retroviral-mediated gene transfer to human CD34+ hematopoietic progenitor cells
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Development of lentiviral vector mediated gene transfer techniques as tools to overexpress/knockdown P2X4 receptors in vitro
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Engineering lentiviral vectors for gene therapy and DC-vaccine
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Gene delivery to pulmonary mucosa
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Gene therapy for the prevention and treatment of leukemia
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Viral and cellular N⁶-methyladenosine and N⁶,2'-O-dimethyladenosine epitranscriptomes in the Kaposi’s sarcoma‐associated herpesvirus life cycle
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Engineering lentiviral vectors for gene delivery
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Stem cell and gene transfer-based approaches to generate insulin-producing cells
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Engineering nanoparticles for gene therapy and cancer therapy
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Non-stable viral and stable non-viral gene transfer to hematopoietic stem cells
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Photo-assisted gene therapy using light-responsive catanionic vesicles
Cell and gene therapy in the murine model of adenosine deaminase deficiency
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Viral, archaeal and bacterial colonization of native marine rock substrata
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Study of dendritic cell-specific lentivector vaccine system
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Antibody discovery and structural studies of the viral oncogene ORF74
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Packaging and delivery of plasmids by bacterial extracellular vesicles
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Engineering lentiviral vectors for gene delivery and immunization
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Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine
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System biology approaches to cancer and diabetes metabolism
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Development of a novel non-viral gene delivery vehicle:  Construction and functional testing of a targeted fusion protein
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Modulation of KIF3A function by herpes simplex virus-1 US3 kinase in viral immune evasion
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Immune responses by glia during neurotropic coronavirus induced encephalomyelitis
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