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Engineering lentiviral vectors for gene delivery
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Engineering lentiviral vectors for gene delivery and immunization
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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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Development of lentiviral vector mediated gene transfer techniques as tools to overexpress/knockdown P2X4 receptors in vitro
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Engineering viral vectors for gene and cell targeting
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Engineering lentiviral vectors for gene therapy and DC-vaccine
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Promoters and insulators: creating a safer integrating vector
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Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine
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Improving adeno-associated viral vector for hematopoietic stem cells gene therapy
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Non-viral and viral hematopoietic progenitor cell gene therapy
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Stem cell and gene transfer-based approaches to generate insulin-producing cells
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Engineering immunotoxin and viral vectors for cancer therapy
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Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells
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Creating a multiple micrornia expression vector to target GRP78, an ER chaperone and signaling regulator in cancer
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Lentiviral vaccine engineering towards enhanced safety and efficiency
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Leukemia cell vaccine generation using lentiviral vectors
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Development of novel adenovirus-retroelement vectors and their applications beyond gene therapy
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Development of a novel gene delivery system:  Construction and testing of retrovirus-adenovirus hybrid vectors
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Study of dendritic cell-specific lentivector vaccine system
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Studies on the relationship between the gibbon ape leukemia virus (GaLV) Env glycoprotein and HIV-1-based lentiviral vectors: Implications in enveloped vector assembly
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Study of dendritic cell targeting by engineered lentivectors
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A functional genomic approach based on shRNA-mediated gene silencing to delineate the role of NF-κB and cell death proteins in the survival and proliferation of KSHV associated primary effusion l...
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Cell and gene therapy in the murine model of adenosine deaminase deficiency
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Improving antitumor efficacy of chimeric antigen receptor-engineered immune cell therapy with synthetic biology and combination therapy approaches
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Gene delivery to pulmonary mucosa
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