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Gene delivery to pulmonary mucosa
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Engineering lentiviral vectors for gene therapy and DC-vaccine
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Engineering lentiviral vectors for gene delivery
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Lentiviral vaccine engineering towards enhanced safety and efficiency
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Engineering immunotoxin and viral vectors for cancer therapy
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Targeting BCL-2 family proteins and plasminogen activator inhibitor-1 in turmor cell apoptosis
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Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy
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Comparative analysis of scFv and non-scFv based chimeric antigen receptors (CARs) against B cell maturation antigen (BCMA)
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Generation and characterization of humanized anti-CD19 chimeric antigen receptor T (CAR-T) cells for the treatment of hematologic malignancies
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Study of dendritic cell-specific lentivector vaccine system
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Microsoft Word - $ASQ117615_supp_undefined_04B12AF4-0287-11E1-A6A4-3DFF9D1A67F9.docx
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Dissecting the heterogeneity of mouse hematopoietic stem cells in vivo
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Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine
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Targeting lentivector gene delivery to hematopoietic stem and progenitor cells in vivo
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Generation of human ESC reporter-lines to isolate hippocampal precursors and study hippocampal development
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The mechanisms of somatic cell reprogramming
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Identification of molecular mechanism for cell-fate decision in liver; &, SARS-CoV replicon inhibitor high throughput drug screening
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Engineering viral vectors for gene and cell targeting
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Characterizing ZFX-mediated gene regulation to reveal possible candidates for clinical intervention
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Study of dendritic cell targeting by engineered lentivectors
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Using engineered exosomes and gene-editing to target latent HIV
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c-JUN mediated alteration of SLC2A2 expression in hepatoma cell line HepG2
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Role of integrin α4 in drug resistant acute lymphoblastic leukemia
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Stable cell lines expressing elastin-like polypeptide fusions with epidermal growth factor receptor modulate gene expression in a heat dependent manner
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