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Efficient gene delivery with calcium -alginate nanoparticles
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Development of a novel gene delivery system: Construction and testing of retrovirus-adenovirus
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Viewing the picture we paint
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Cell and gene therapy in the murine model of adenosine deaminase deficiency
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Microsoft Word - PC_Thesis_USC_3.doc
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Manipulation of RGCs response using different stimulation strategies for retinal prosthesis
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Improving adeno-associated viral vector for hematopoietic stem cells gene therapy
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Enhancing the anti-HIV potency of eCD4-Ig by unnatural amino acid mutagenesis
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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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0725-1st revision
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Microsoft Word - 4-Dissertation_Shanxi Feng.doc
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Engineering lentiviral vectors for gene delivery
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Using engineered exosomes and gene-editing to target latent HIV
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Searching for mitogenic factors from the epicardium: PDGFA, Igf2 and more
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Gene delivery to pulmonary mucosa
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Production and purification of recombinant mouse cathepsin S
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PhD Dissertation_TMHSU_FINAL V1
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Characterization of the STARS (STochastic gene Activation with Regulated Sparseness) mouse line
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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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Dissecting the entry mechanism of targeting lentiviral vectors in living cells and developing quantum dot labeling of viruses for single virus tracking
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Control of endogenous gene expression in the mouse
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Engineering viral vectors for gene and cell targeting
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Nanomaterials for bio-imaging and therapeutics
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Photo-assisted gene therapy using light-responsive catanionic vesicles
Engineering nanoparticles for gene therapy and cancer therapy
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