Cargando…
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations
PURPOSE: To investigate the mechanism underlying the synergic interaction between Leber's hereditary optic neuropathy (LHON)-associated ND1 and mitochondrial tyrosyl-tRNA synthetase (YARS2) mutations. METHODS: Molecular dynamics simulation and differential scanning fluorimetry were used to eval...
Autores principales: | Jin, Xiaofen, Zhang, Juanjuan, Yi, Qiuzi, Meng, Feilong, Yu, Jialing, Ji, Yanchun, Mo, Jun Q., Tong, Yi, Jiang, Pingping, Guan, Min-Xin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237128/ https://www.ncbi.nlm.nih.gov/pubmed/34156427 http://dx.doi.org/10.1167/iovs.62.7.22 |
Ejemplares similares
-
Leber's Hereditary Optic Neuropathy Plus Causing Recurrent Myelopathy due to an MT-DN1 Mutation at G3635A
por: Lackey, Elijah, et al.
Publicado: (2022) -
Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy
por: Zhang, Juanjuan, et al.
Publicado: (2021) -
Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy
por: Bi, Rui, et al.
Publicado: (2012) -
A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy
por: Pandya, Bhadra U., et al.
Publicado: (2023) -
A Novel Homozygous Missense Mutation in the YARS Gene: Expanding the Phenotype of YARS Multisystem Disease
por: Zeiad, Rawah K H M, et al.
Publicado: (2021)