Thompson, Debra A.

Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

Bainbridge, J. W. B., Mehat, M. S., Sundaram, V., Robbie, S. J., Barker, S. E., Ripamonti, C., Georgiadis, A., Mowat, F. M., Beattie, S. G., Gardner, P. J., et al. (2015) · New England Journal of Medicine

Retinal Development and DisordersVirus-based gene therapy research

Cited by 743

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

Gal, A., Li, Y., Thompson, D. A., Weir, J., Orth, U., Jacobson, S. G., Apfelstedt-Sylla, E., & Vollrath, D. (2000) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 679

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

Gu, S.-M., Thompson, D. A., Srikumari, C. R. S., Lorenz, B., Finckh, U., Nicoletti, A., Murthy, K. R., Rathmann, M., Kumaramanickavel, G., Denton, M. J., et al. (1997) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 663

Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

Janecke, A. R., Thompson, D. A., Utermann, G., Becker, C., Hübner, C. A., Schmid, E., McHenry, C. L., Nair, A. R., Rüschendorf, F., Heckenlively, J., et al. (2004) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 246

Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy

Thompson, D. A., Li, Y., McHenry, C. L., Carlson, T. J., Ding, X., Sieving, P. A., Apfelstedt-Sylla, E., & Gal, A. (2001) · Nature Genetics

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 185

Deletion of autophagy inducer RB1CC1 results in degeneration of the retinal pigment epithelium

Yao, J., Jia, L., Khan, N., Lin, C., Mitter, S. K., Boulton, M. E., Dunaief, J. L., Klionsky, D. J., Guan, J.-L., Thompson, D. A., et al. (2015) · Autophagy

Retinal Diseases and TreatmentsAutophagy in Disease and Therapy

Cited by 130

Circadian and noncircadian modulation of autophagy in photoreceptors and retinal pigment epithelium

Yao, J., Jia, L., Shelby, S. J., Ganios, A. M., Feathers, K., Thompson, D. A., & Zacks, D. N. (2014) · Investigative Opthalmology & Visual Science

Autophagy in Disease and TherapyRetinal Development and Disorders

Cited by 68

Rdh12 activity and effects on retinoid processing in the murine retina

Chrispell, J. D., Feathers, K. L., Kane, M. A., Kim, C. Y., Brooks, M., Khanna, R., Kurth, I., Hübner, C. A., Gal, A., Mears, A. J., et al. (2009) · Journal of Biological Chemistry

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 56

Genetic defects in vitamin A metabolism of the retinal pigment epithelium

Thompson, D. A., & Gal, A. (2003) · Developments in Ophthalmology

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 47

MERTK interactions with SH2-domain proteins in the retinal pigment epithelium

Shelby, S. J., Colwill, K., Dhe-Paganon, S., Pawson, T., & Thompson, D. A. (2013) · PLoS ONE

Retinal Diseases and TreatmentsRetinal Development and Disorders

Cited by 35