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Publications

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Filters: Keyword is Retinal Degeneration  [Clear All Filters]
2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa., Wu, Wen-Hsuan, Tsai Yi-Ting, Justus Sally, Lee Ting-Ting, Zhang Lijuan, Lin Chyuan-Sheng, Bassuk Alexander G., Mahajan Vinit B., and Tsang Stephen H. , Mol Ther, 2016 08, Volume 24, Issue 8, p.1388-94, (2016)
2015
Quantitative autofluorescence as a clinical tool for expedited differential diagnosis of retinal degeneration., Marsiglia, Marcela, Lee Winston, Mahajan Vinit B., Zernant Jana, Delori François C., Tsang Stephen H., and Sparrow Janet R. , JAMA Ophthalmol, 2015 Feb, Volume 133, Issue 2, p.219-20, (2015)
2012
Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration., Mahajan, Vinit B., Skeie Jessica M., Bassuk Alexander G., Fingert John H., Braun Terry A., Daggett Heather T., Folk James C., Sheffield Val C., and Stone Edwin M. , PLoS Genet, 2012, Volume 8, Issue 10, p.e1003001, (2012)
2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis., Ko, Audrey C., Brinton Jason P., Mahajan Vinit B., Zimmerman Bridget, Brinton Gregory S., Stone Edwin M., Folk James C., and Mullins Robert F. , Archives of ophthalmology, 2011 Apr, Volume 129, Issue 4, p.415-20, (2011)
2007
Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness., Tsang, Stephen H., Woodruff Michael L., Jun Lin, Mahajan Vinit, Yamashita Clyde K., Pedersen Robert, Lin Chyuan-Sheng, Goff Stephen P., Rosenberg Thomas, Larsen Michael, et al. , Human mutation, 2007 Mar, Volume 28, Issue 3, p.243-54, (2007)