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Caring for a bright future, the establishment and introduction of mouse models of hereditary ophthalmic diseases

 Last Update: 2022-09-14
 Source: Internet
 Author: User

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In 2017, Luxturna, the first gene therapy for the treatment of hereditary retinal dystrophy, was approved by the FDA to target inherited Retinal Diseases (IRDs)

Vision "stolen" by time – a mouse model of neovascular macular degeneration (AMD).

Figure 1 Schematic diagram of hVEGF overexpressed mouse (TG) construction strategy

Figure 2 FFA (fundus fluorescence angiography) results

Saeye Bio Ophthalmic Gene Therapy Solutions

I sincerely hope that with the efforts of all parties, more gene therapy methods will enter clinical trials to help people with congenital blindness see the dawn

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