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Nonviral strategies for gene therapy.
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Neurosurgical gene therapy for central nervous system diseases.
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microRNA-181a silencing by antisense oligonucleotides delivered by virus-like particles.
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Gene Therapy Approach with an Emphasis on Growth Factors: Theoretical and Clinical Outcomes in Neurodegenerative Diseases.
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Gene Therapy Tools for Brain Diseases.
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Poly(ethylenimine) conjugated bioreducible dendrimer for efficient gene delivery.
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Gene and cell therapy for muscle regeneration.
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Delivery systems for gene therapy.
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Effects of moisture content on the storage stability of dried lipoplex formulations.
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Rapid titration of adenoviral infectivity by flow cytometry in batch culture of infected HEK293 cells.
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Characterization of cationic liposome-mediated gene transfer in vivo by intravenous administration.
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Recombinant adeno-associated virus for muscle directed gene therapy.
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New cationic lipid formulations for gene transfer.
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