Katz, Martin L.

Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog

Narfstro¨m, K., Katz, M. L., Bragadottir, R., Seeliger, M., Boulanger, A., Redmond, T. M., Caro, L., Lai, C.-M., & Rakoczy, P. E. (2003) · Investigative Opthalmology & Visual Science

Retinal Development and DisordersVirus-based gene therapy research

Cited by 252

AAV gene transfer delays disease onset in a TPP1-deficient canine model of the late infantile form of Batten disease

Katz, M. L., Tecedor, L., Chen, Y., Williamson, B. G., Lysenko, E., Wininger, F. A., Young, W. M., Johnson, G. C., Whiting, R. E. H., Coates, J. R., et al. (2015) · Science Translational Medicine

Lysosomal Storage Disorders ResearchVirus-based gene therapy research

Cited by 134

What is lipofuscin? Defining characteristics and differentiation from other autofluorescent lysosomal storage bodies

Katz, M. L., & Robison, W. G. (2002) · Archives of Gerontology and Geriatrics

Autophagy in Disease and TherapyLysosomal Storage Disorders Research

Cited by 122

Enzyme replacement therapy attenuates disease progression in a canine model of late‐infantile neuronal ceroid lipofuscinosis (CLN 2 disease)

Katz, M. L., Coates, J. R., Sibigtroth, C. M., Taylor, J. D., Carpentier, M., Young, W. M., Wininger, F. A., Kennedy, D., Vuillemenot, B. R., & O'Neill, C. A. (2014) · Journal of Neuroscience Research

Lysosomal Storage Disorders ResearchMetabolism and Genetic Disorders

Cited by 100

Lipofuscin autofluorescence: evidence for vitamin A involvement in the retina

Katz, M. L., Eldred, G. E., & Robison, W. G. (1987) · Mechanisms of Ageing and Development

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 88