Dyka, Frank M.

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model

Akil, O., Dyka, F., Calvet, C., Emptoz, A., Lahlou, G., Nouaille, S., Boutet de Monvel, J., Hardelin, J.-P., Hauswirth, W. W., Avan, P., et al. (2019) · Proceedings of the National Academy of Sciences

Hearing, Cochlea, Tinnitus, GeneticsVirus-based gene therapy research

Cited by 300

Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors

Kay, C. N., Ryals, R. C., Aslanidi, G. V., Min, S. H., Ruan, Q., Sun, J., Dyka, F. M., Kasuga, D., Ayala, A. E., Van Vliet, K., et al. (2013) · PLoS ONE

Virus-based gene therapy researchRetinal Development and Disorders

Cited by 168

Dual Adeno-Associated Virus Vectors Result in Efficient In Vitro and In Vivo Expression of an Oversized Gene, MYO7A

Dyka, F. M., Boye, S. L., Chiodo, V. A., Hauswirth, W. W., & Boye, S. E. (2014) · Human Gene Therapy Methods

Virus-based gene therapy researchRetinal Development and Disorders

Cited by 128

Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus

Lopes, V. S., Boye, S. E., Louie, C. M., Boye, S., Dyka, F., Chiodo, V, Fofo, H., Hauswirth, W. W., & Williams, D. S. (2013) · Gene Therapy

Virus-based gene therapy researchRetinal Development and Disorders

Cited by 112

Dual ABCA4 -AAV Vector Treatment Reduces Pathogenic Retinal A2E Accumulation in a Mouse Model of Autosomal Recessive Stargardt Disease

Dyka, F. M., Molday, L. L., Chiodo, V. A., Molday, R. S., & Hauswirth, W. W. (2019) · Human Gene Therapy

Retinal Development and DisordersVirus-based gene therapy research

Cited by 56