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...
Hlavní autor: | Peddle, CF |
---|---|
Další autoři: | MacLaren, RE |
Médium: | Diplomová práce |
Jazyk: | English |
Vydáno: |
2021
|
Témata: |
Podobné jednotky
-
Rhodopsin mutations are scarcely implicated in autosomal recessive retinitis pigmentosa: A preliminary study of Egyptian retinitis pigmentosa patients
Autor: Reem Mebed, a další
Vydáno: (2015-10-01) -
AAV-CRISPR/Cas9 Gene Editing Preserves Long-Term Vision in the P23H Rat Model of Autosomal Dominant Retinitis Pigmentosa
Autor: Saba Shahin, a další
Vydáno: (2022-04-01) -
Herencia de la retinosis pigmentaria en la provincia Camagüey Inheritance of retinitis pigmentosa in the province of Camagüey
Autor: Elisa Dyce Gordon, a další
Vydáno: (1999-06-01) -
Whole exome sequencing reveals novel EYS mutations in Chinese patients with autosomal recessive retinitis pigmentosa
Autor: Xiaoqiang Xiao, a další
Vydáno: (2019-01-01) -
Genetic dissection of non-syndromic retinitis pigmentosa
Autor: Aarti Bhardwaj, a další
Vydáno: (2022-01-01)