Clarisse Fligor
Affiliations: | 2015-2020 | Biology | IUPUI, Indianapolis, IN, United States |
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| Huang KC, Gomes C, Shiga Y, et al. (2023) Autophagy disruption reduces mTORC1 activation leading to retinal ganglion cell neurodegeneration associated with glaucoma. Biorxiv : the Preprint Server For Biology |
| Gomes C, VanderWall KB, Pan Y, et al. (2022) Astrocytes modulate neurodegenerative phenotypes associated with glaucoma in OPTN(E50K) human stem cell-derived retinal ganglion cells. Stem Cell Reports |
| Fligor CM, Lavekar SS, Harkin J, et al. (2021) Extension of retinofugal projections in an assembled model of human pluripotent stem cell-derived organoids. Stem Cell Reports |
| Fligor CM, Huang KC, Lavekar SS, et al. (2020) Differentiation of retinal organoids from human pluripotent stem cells. Methods in Cell Biology. 159: 279-302 |
| VanderWall KB, Huang KC, Pan Y, et al. (2020) Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids. Stem Cell Reports |
| Wang Q, Zhuang PS, Huang H, et al. (2020) Mouse gamma-Synuclein Promoter-Mediated Gene Expression and Editing in Mammalian Retinal Ganglion Cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Ohlemacher SK, Langer KB, Fligor CM, et al. (2019) Advances in the Differentiation of Retinal Ganglion Cells from Human Pluripotent Stem Cells. Advances in Experimental Medicine and Biology. 1186: 121-140 |
| VanderWall KB, Vij R, Ohlemacher SK, et al. (2018) Astrocytes Regulate the Development and Maturation of Retinal Ganglion Cells Derived from Human Pluripotent Stem Cells. Stem Cell Reports |
| Fligor CM, Langer KB, Sridhar A, et al. (2018) Three-Dimensional Retinal Organoids Facilitate the Investigation of Retinal Ganglion Cell Development, Organization and Neurite Outgrowth from Human Pluripotent Stem Cells. Scientific Reports. 8: 14520 |
| Langer KB, Ohlemacher SK, Phillips MJ, et al. (2018) Retinal Ganglion Cell Diversity and Subtype Specification from Human Pluripotent Stem Cells. Stem Cell Reports |