Self-Complementary Adeno-Associated Virus Vectors Improve Transduction Efficiency of Corneal Endothelial Cells

Capsid Mutated Adeno-Associated Virus Delivered to the Anterior Chamber Results in Efficient Transduction of Trabecular Meshwork in Mouse and Rat

(2015) Barbara Bogner et al.   PLoS One

Corneal Transduction by Intra-Stromal Injection of AAV Vectors In Vivo in the Mouse and Ex Vivo in Human Explants

(2012) Claire Hippert et al.   PLoS One

Experimental gene transfer to the corneal endothelium

(2011) D. Kampik et al.   EXPERIMENTAL EYE RESEARCH

Anti-apoptotic gene therapy prolongs survival of corneal endothelial cells during storage

(2011) T A Fuchsluger et al.   GENE THERAPY

AAV serotype influences gene transfer in corneal stroma in vivo

(2010) Ajay Sharma et al.   EXPERIMENTAL EYE RESEARCH

Corneal Endothelial Cells Are Protected from Apoptosis by Gene Therapy

(2010) Thomas A. Fuchsluger et al.   HUMAN GENE THERAPY

Recent advances in ocular gene therapy

(2009) Daniel C Chung et al.   CURRENT OPINION IN OPHTHALMOLOGY

Gene Therapy Using Adeno-Associated Virus Vectors

(2008) S. Daya et al.   CLINICAL MICROBIOLOGY REVIEWS

Recombinant Self-Complementary Adeno-Associated Virus Serotype Vector-Mediated Hematopoietic Stem Cell Transduction and Lineage-Restricted, Long-Term Transgene Expression in a Murine Serial Bone Marrow Transplantation Model

(2008) Njeri Maina et al.   HUMAN GENE THERAPY

Self-complementary AAV Vectors; Advances and Applications

(2008) Douglas M McCarty   MOLECULAR THERAPY

Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis

(2008) Albert M. Maguire et al.   NEW ENGLAND JOURNAL OF MEDICINE