Alexander G. Bassuk

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Tang PH, Chemudupati T, Wert KJ, et al. (2020) Phenotypic variance in Calpain-5 retinal degeneration. American Journal of Ophthalmology Case Reports. 18: 100627
Velez G, Sun YJ, Khan S, et al. (2020) Structural Insights into the Unique Activation Mechanisms of a Non-classical Calpain and Its Disease-Causing Variants. Cell Reports. 30: 881-892.e5
Oh JK, Lima de Carvalho JR, Sun YJ, et al. (2019) Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa. Orphanet Journal of Rare Diseases. 14: 295
Zhang L, Cui X, Han Y, et al. (2019) Hypoxic drive caused Type 3 neovascularization in a preclinical model of exudative age-related macular degeneration. Human Molecular Genetics
Wert KJ, Koch SF, Velez G, et al. (2019) CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials. Human Mutation
Chang YJ, Xu CL, Cui X, et al. (2019) CRISPR Base Editing in Induced Pluripotent Stem Cells. Methods in Molecular Biology (Clifton, N.J.)
Abe K, Cox A, Takamatsu N, et al. (2019) Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans. Proceedings of the National Academy of Sciences of the United States of America
Velez G, Yang J, Li AS, et al. (2019) Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy. Scientific Reports. 9: 7608
Wert KJ, Bakall B, Bassuk AG, et al. (2019) Insights into Retinal Development Using Live Imaging in Female Carriers of Choroideremia. Ophthalmic Surgery, Lasers & Imaging Retina. 50: e158-e162
Sancho-Pelluz J, Cui X, Lee W, et al. (2019) Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho mutation. Cellular and Molecular Life Sciences : Cmls