Development of all-in-one CRISPR/Cas9 and CRISPRi AAV constructs to treat autosomal dominant retinitis pigmentosa
<p>Dominant mutations in RHO (rhodopsin) are the most common cause of autosomal dominant retinitis pigmentosa (RHO-adRP). RHO-adRP causes progressive loss of rod cells, followed by cone cells, leading to blindness. This disease is a candidate for CRISPR gene editing, as reduction of mutant rho...
Κύριος συγγραφέας: | Peddle, CF |
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Άλλοι συγγραφείς: | MacLaren, RE |
Μορφή: | Thesis |
Γλώσσα: | English |
Έκδοση: |
2021
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Θέματα: |
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Rhodopsin mutations are scarcely implicated in autosomal recessive retinitis pigmentosa: A preliminary study of Egyptian retinitis pigmentosa patients
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Έκδοση: (2015-10-01) -
AAV-CRISPR/Cas9 Gene Editing Preserves Long-Term Vision in the P23H Rat Model of Autosomal Dominant Retinitis Pigmentosa
ανά: Saba Shahin, κ.ά.
Έκδοση: (2022-04-01) -
Herencia de la retinosis pigmentaria en la provincia Camagüey Inheritance of retinitis pigmentosa in the province of Camagüey
ανά: Elisa Dyce Gordon, κ.ά.
Έκδοση: (1999-06-01) -
Whole exome sequencing reveals novel EYS mutations in Chinese patients with autosomal recessive retinitis pigmentosa
ανά: Xiaoqiang Xiao, κ.ά.
Έκδοση: (2019-01-01) -
Genetic dissection of non-syndromic retinitis pigmentosa
ανά: Aarti Bhardwaj, κ.ά.
Έκδοση: (2022-01-01)