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Generation and characterization of fully human anti-CD19 chimeric antigen receptor T (CAR-T) cells for the treatment of hematologic malignancies
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Engineering lentiviral vectors for gene delivery
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Dissertation_Xiaolu_Han 20170416 final draft
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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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Reprogramming exosomes for immunotherapy of acute myeloid leukemia
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Engineered control of the CAR-T-tumor synapse using customized DNA linkers
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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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Optimization of nanomedicine based drug delivery systems for the treatment of solid tumors
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Control of endogenous gene expression in the mouse
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Engineering chimeric antigen receptor (CAR) -modified T cells for enhanced cancer immunotherapy
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Self-secretion of checkpoint blockade enhances antitumor immunity by murine chimeric antigen receptor-engineered T cells
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Engineering therapeutics for the improved antitumor efficacy of chimeric antigen receptor T cell therapy
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Generation and characterization of anti-CD138 chimeric antigen receptor T (CAR-T) cells for the treatment of hematologic malignancies
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Application of elastin-like polypeptides to therapeutics in leukemia
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Engineering chimeric antigen receptor-directed immune cells for enhanced antitumor efficacy in solid tumors
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Mechanistic model of chimeric antigen receptor T cell activation
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Engineered CAR-T cells for treatment of solid cancers
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Phosphorylation kinetics of T-cell receptor signaling domain in vitro
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Novel design and combinatory therapy to enhance chimeric antigen receptor engineered T cells (CAR-T) efficacy against solid tumor
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Combination therapy for solid tumor
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Targeting lentivector gene delivery to hematopoietic stem and progenitor cells in vivo
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