Katherine J. Wert, PhD
Affiliations: | Whitehead | Massachusetts Institute of Technology, Cambridge, MA, United States |
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"Katherine Wert"Mean distance: 19.27 (cluster 28) | S | N | B | C | P |
Parents
Sign in to add mentor| Stephen H. Tsang | grad student | 2013 | Columbia | |
| (Gene Therapy Provides Long-term Visual Function in a Pre-clinical Model of Retinitis Pigmentosa.) | ||||
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Publications
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| Yee T, Wert KJ. (2023) Human retina-in-a-dish: Unlocking the potential to study mechanisms of inherited retinal disease. Molecular Therapy. Methods & Clinical Development. 30: 573-575 |
| Kong Y, Liu PK, Li Y, et al. (2023) HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy. Embo Molecular Medicine. e16525 |
| Rowe AA, Chen X, Nettesheim ER, et al. (2022) Long-term progression of retinal degeneration in a preclinical model of CLN7 Batten disease as a baseline for testing clinical therapeutics. Ebiomedicine. 85: 104314 |
| Yee T, Wert KJ. (2022) Base and Prime Editing in the Retina-From Preclinical Research toward Human Clinical Trials. International Journal of Molecular Sciences. 23 |
| Rowe AA, Patel PD, Gordillo R, et al. (2021) Replenishment of TCA cycle intermediates provides photoreceptor resilience against neurodegeneration during progression of retinitis pigmentosa. Jci Insight |
| Tang PH, Chemudupati T, Wert KJ, et al. (2020) Phenotypic variance in Calpain-5 retinal degeneration. American Journal of Ophthalmology Case Reports. 18: 100627 |
| Wert KJ, Velez G, Kanchustambham VL, et al. (2020) Metabolite therapy guided by liquid biopsy proteomics delays retinal neurodegeneration. Ebiomedicine. 52: 102636 |
| Wert KJ, Koch SF, Velez G, et al. (2019) CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials. Human Mutation |
| 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 |
| Wert KJ, Mahajan VB. (2019) In Vivo Expression of Mutant Calpains in the Eye Using Lentivirus. Methods in Molecular Biology (Clifton, N.J.). 1915: 233-247 |