Budd A. Tucker

Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration

Restoration of Aqueous Humor Outflow Following Transplantation of iPSC-Derived Trabecular Meshwork Cells in a Transgenic Mouse Model of Glaucoma

Preparation and evaluation of human choroid extracellular matrix scaffolds for the study of cell replacement strategies

Transplantation of iPSC-derived TM cells rescues glaucoma phenotypes in vivo

Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis

Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular Degeneration

Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trial

Concise Review: Patient-Specific Stem Cells to Interrogate Inherited Eye Disease

ABCB5 is a limbal stem cell gene required for corneal development and repair

CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype

Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseases

Mechanical properties of murine and porcine ocular tissues in compression

Stem cells for investigation and treatment of inherited retinal disease

Enhanced Differentiation and Delivery of Mouse Retinal Progenitor Cells Using a Micropatterned Biodegradable Thin-Film Polycaprolactone Scaffold

Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to CEP290 Mutation: Determining the Timing and Expectation of Therapy

Photoreceptor Cells With Profound Structural Deficits Can Support Useful Vision in Mice

Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa

Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease

Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease

Use of a Synthetic Xeno-Free Culture Substrate for Induced Pluripotent Stem Cell Induction and Retinal Differentiation

Collaborative Research: RECODE: Microfluidic and genetic technologies to direct and select retinal cell types from human induced pluripotent stem cell-derived retinal organoids