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Human Molecular Genetics|August 1, 2007
Formation and progression of sub-retinal pigment epithelium deposits in Efemp1 mutation knock-in mice: a model for the early pathogenic course of macular degenerationLihua Y Marmorstein, Precious J McLaughlin, Neal S Peachey, et al.Translational Vision Science & Technology|June 6, 2015
Nonantibestrophin Anti-RPE Antibodies in Paraneoplastic Exudative Polymorphous Vitelliform MaculopathyLauren A Dalvin, Adiv A Johnson, Jose S Pulido, et al.Ophthalmic Genetics|September 18, 2018
A novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotypeFukutaro Mano, Stephen A LoBue, Timothy W Olsen, et al.Investigative Ophthalmology & Visual Science|June 17, 2017
Mutant Fibulin-3 Causes Proteoglycan Accumulation and Impaired Diffusion Across Bruch's MembraneAstrid Zayas-Santiago, Samuel D Cross, James B Stanton, et al.Investigative Ophthalmology & Visual Science|July 29, 2003
Expression and localization of bestrophin during normal mouse developmentBenjamin Bakall, Lihua Y Marmorstein, George Hoppe, et al.Investigative Ophthalmology & Visual Science|November 24, 2005
Tubby-like protein 1 (TULP1) interacts with F-actin in photoreceptor cellsQuansheng Xi, Gayle J T Pauer, Alan D Marmorstein, et al.Biochimica Et Biophysica Acta|April 8, 2006
Hydrodynamic properties of porcine bestrophin-1 in Triton X-100J Brett Stanton, Andrew F X Goldberg, George Hoppe, et al.Regenerative Medicine|December 16, 2017
Disease modeling studies using induced pluripotent stem cells: are we using enough controls?Adiv A Johnson, Cynthia Andrews-Pfannkoch, Timothy J Nelson, et al.Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|April 25, 2023
Carbonic Anhydrase Inhibitor Modulation of Intraocular Pressure Is Independent of Soluble Adenylyl CyclaseShakarr V Wiggins, Ryan Schreiner, Jacob Ferreira, et al.American Journal of Ophthalmology Case Reports|March 6, 2018
Retinitis pigmentosa associated with a mutation in BEST1Lauren A Dalvin, Jackson E Abou Chehade, John Chiang, et al.Pageof 7