Hereditary optic neuropathies share a common mitochondrial coupling defect-Reference-Cited by-同舟云学术

Hereditary optic neuropathies share a common mitochondrial coupling defect

Published:2008-06 Issue:6 Volume:63 Page:794-798
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Chevrollier Arnaud,Guillet Virginie,Loiseau Dominique,Gueguen Naïg,Pou de Crescenzo Marie-Anne,Verny Christophe,Ferre Marc,Dollfus Hélène,Odent Sylvie,Milea Dan,Goizet Cyril,Amati-Bonneau Patrizia,Procaccio Vincent,Bonneau Dominique,Reynier Pascal

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

1. Optic atrophies in metabolic disorders;Huizing;Mol Genet Metab,2005

2. Mitochondrial optic neuropathies: how two genomes may kill the same cell type?;Carelli;Biosci Rep,2007

3. Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration;Carelli;Biochim Biophys Acta,2004

4. Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy;Kjer;Acta Ophthalmol (Copenh),1983

5. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat Genet,2000

Cited by 109 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene;International Journal of Molecular Sciences;2024-06-30

2. Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission;iScience;2024-05

3. OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts;Human Molecular Genetics;2024-01-27

4. Plasmodium falciparumOPA3‐like protein (PfOPA3) is essential for maintenance of mitochondrial homeostasis and parasite proliferation;The FASEB Journal;2023-10-11

5. OPA1 deficiency impairs oxidative metabolism in cycling cells, underlining a translational approach for degenerative diseases;Disease Models & Mechanisms;2023-09-01