Askew, Charles

A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear

Landegger, L. D., Pan, B., Askew, C., Wassmer, S. J., Gluck, S. D., Galvin, A., Taylor, R., Forge, A., Stankovic, K. M., Holt, J. R., et al. (2017) · Nature Biotechnology

Virus-based gene therapy researchHearing, Cochlea, Tinnitus, Genetics

Cited by 325

Customized blood-brain barrier shuttle peptide to increase AAV9 vector crossing the BBB and augment transduction in the brain

Zhang, X., Chai, Z., Lee Dobbins, A., Itano, M. S., Askew, C., Miao, Z., Niu, H., Samulski, R. J., & Li, C. (2022) · Biomaterials

Virus-based gene therapy researchBarrier Structure and Function Studies

Cited by 23

Superior human hepatocyte transduction with adeno-associated virus vector serotype 7

Shao, W., Pei, X., Cui, C., Askew, C., Dobbins, A., Chen, X., Abajas, Y. L., Gerber, D. A., Samulski, R. J., Nichols, T. C., et al. (2019) · Gene Therapy

Virus-based gene therapy researchHemophilia Treatment and Research

Cited by 22