Ozel, A Bilge; Moroi, Sayoko E; Reed, David M et al. (2014) Genome-wide association study and meta-analysis of intraocular pressure. Hum Genet 133:41-57
|
Thompson, Debra A; Khan, Naheed W; Othman, Mohammad I et al. (2012) Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15. PLoS One 7:e35865
|
Lu, Ying; He, Shirley; Jia, Lin et al. (2010) Two mouse models for recoverin-associated autoimmune retinopathy. Mol Vis 16:1936-48
|
Pang, Ji-Jing; Alexander, John; Lei, Bo et al. (2010) Achromatopsia as a potential candidate for gene therapy. Adv Exp Med Biol 664:639-46
|
Pang, J; Boye, S E; Lei, B et al. (2010) Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency. Gene Ther 17:815-26
|
Lu, Ying; Jia, Lin; He, Shirley et al. (2009) Melanoma-associated retinopathy: a paraneoplastic autoimmune complication. Arch Ophthalmol 127:1572-80
|
Chang, Bo; Grau, Tanja; Dangel, Susann et al. (2009) A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Proc Natl Acad Sci U S A 106:19581-6
|
Anderson, Michael G; Hawes, Norman L; Trantow, Colleen M et al. (2008) Iris phenotypes and pigment dispersion caused by genes influencing pigmentation. Pigment Cell Melanoma Res 21:565-78
|
Pang, Ji-Jing; Boye, Sanford L; Kumar, Ashok et al. (2008) AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation. Invest Ophthalmol Vis Sci 49:4278-83
|
Chang, Bo; Mandal, Md Nawajes A; Chavali, Venkata R M et al. (2008) Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene. Hum Mol Genet 17:3929-41
|
Showing the most recent 10 out of 62 publications