AAV Gene Therapy for Autosomal Dominant Optic Atrophy Caused by Mutation in the Opa1 Gene

被引:0
|
作者
Stupay, Rachel M. [1 ]
Cascone, Alyna [1 ]
Padegimas, Linas [2 ]
Wille, Paul T. [1 ]
Kevany, Brian M. [3 ]
机构
[1] Abeona Therapeut, Product Dev, Cleveland, OH USA
[2] Forge Biol, Grove City, OH USA
[3] Abeona Therapeut, Cleveland, OH USA
关键词
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
1478
引用
收藏
页码:696 / 697
页数:2
相关论文
共 50 条
  • [21] Mutation screenings of OPA1 in dominant optic atrophy.
    Murton, NJ
    Toomes, C
    Mackey, DA
    Inglehearn, CF
    Churchill, AJ
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2001, 42 (04) : S650 - S650
  • [22] Development of an Optimized AAV Gene Therapy for Autosomal Dominant Optic Atrophy
    Liu, Ting
    Rong, Yu
    Cheng, Chao
    Zhang, Xin
    Luk, Alvin
    Li, Qiutang
    Li, Bin
    MOLECULAR THERAPY, 2022, 30 (04) : 251 - 251
  • [23] Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy
    Votruba, M
    Thiselton, D
    Bhattacharya, SS
    BRITISH JOURNAL OF OPHTHALMOLOGY, 2003, 87 (01) : 48 - 53
  • [24] A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family
    Zhang, Liping
    Shi, Wei
    Song, Liming
    Zhang, Xiao
    Cheng, Lulu
    Wang, Yanfang
    Ge, Xianglian
    Li, Wei
    Zhang, Wei
    Min, Qingjie
    Jin, Zi-Bing
    Qu, Jia
    Gu, Feng
    SCIENTIFIC REPORTS, 2014, 4
  • [25] A splicing site OPA1 mutation associated with autosomal dominant optic atrophy in an Italian family
    Ranieri, M.
    Del Bo, R.
    Corti, S.
    Bordoni, A.
    Mancarella, G.
    Bresolin, N.
    Comi, G. P.
    JOURNAL OF NEUROLOGY, 2010, 257 : S205 - S205
  • [26] Mutation Screening of OPA1 in a cohort Chinese patients with Suspected Autosomal Dominant Optic Atrophy
    Xie, Yue
    Xiao, Ting
    Xu, Ke
    Zhang, Xiaohui
    Li, Yang
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2019, 60 (09)
  • [27] A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family
    Liping Zhang
    Wei Shi
    Liming Song
    Xiao Zhang
    Lulu Cheng
    Yanfang Wang
    Xianglian Ge
    Wei Li
    Wei Zhang
    Qingjie Min
    Zi-Bing Jin
    Jia Qu
    Feng Gu
    Scientific Reports, 4
  • [28] Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene
    Granse, L
    Bergstrand, I
    Thiselton, D
    Ponjavic, V
    Heijl, A
    Votruba, M
    Andréasson, S
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 : U446 - U446
  • [29] Peripapillary capillary network in dominant optic atrophy linked to OPA1 gene
    Rahhal-Ortuno, Miriam
    Avino-Martinez, Juan Aurelio
    Fernandez-Santodomingo, Alex Samir
    Aguilar-Gonzalez, Marina
    Placinta-Tat, Ioan Alexandru
    Espana-Gregori, Enrique
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2023, 33 (01) : NP19 - NP22
  • [30] Dominant (Kjer's) optic atrophy associated with mutations in OPA1 gene
    Kelifova, S.
    Honzik, T.
    Tesarova, M.
    Kousal, B.
    Liskova, P.
    Havrankova, P.
    Kolarova, H.
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2020, 83 (01) : 33 - 42