Debra A. Thompson
Department of Ophthalmology and Visual Sciences
University of Michigan Medical School
Ann Arbor 48105
and Unidad de Genética Médica y Diagnóstico Prenatal
Spain
Name/email consistency: high
- Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle. Thompson, D.A., Janecke, A.R., Lange, J., Feathers, K.L., Hübner, C.A., McHenry, C.L., Stockton, D.W., Rammesmayer, G., Lupski, J.R., Antinolo, G., Ayuso, C., Baiget, M., Gouras, P., Heckenlively, J.R., den Hollander, A., Jacobson, S.G., Lewis, R.A., Sieving, P.A., Wissinger, B., Yzer, S., Zrenner, E., Utermann, G., Gal, A. Hum. Mol. Genet. (2005)
- Vitamin A metabolism in the retinal pigment epithelium: genes, mutations, and diseases. Thompson, D.A., Gal, A. Prog. Retin. Eye. Res (2003)
- 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. Nat. Genet. (2001)
- Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration. Thompson, D.A., Gyürüs, P., Fleischer, L.L., Bingham, E.L., McHenry, C.L., Apfelstedt-Sylla, E., Zrenner, E., Lorenz, B., Richards, J.E., Jacobson, S.G., Sieving, P.A., Gal, A. Invest. Ophthalmol. Vis. Sci. (2000)
- Localization of receptors for luteinizing hormone/chorionic gonadotropin in neural retina. Thompson, D.A., Othman, M.I., Lei, Z., Li, X., Huang, Z.H., Eadie, D.M., Rao, C.V. Life Sci. (1998)
- Characterization of the human type 2 neuropeptide Y receptor gene (NPY2R) and localization to the chromosome 4q region containing the type 1 neuropeptide Y receptor gene. Ammar, D.A., Eadie, D.M., Wong, D.J., Ma, Y.Y., Kolakowski, L.F., Yang-Feng, T.L., Thompson, D.A. Genomics (1996)
