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- Development of gene therapy for inner ear disease: Using bilateral vestibular hypofunction as a vehicle for translational research
- Basic concepts, current evidence, and future potential for gene therapy in managing cutaneous wounds
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- Genetically-manipulated adult stem cells as therapeutic agents and gene delivery vehicle for wound repair and regeneration
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- <i>In vivo</i>reprogramming of wound-resident cells generates skin with hair
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
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