Increasing mtDNA levels as therapy for mitochondrial optic neuropathies-Reference-Cited by-同舟云学术

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Increasing mtDNA levels as therapy for mitochondrial optic neuropathies

Published:2018-03 Issue:3 Volume:23 Page:493-498
ISSN:1359-6446
Container-title:Drug Discovery Today
language:en
Short-container-title:Drug Discovery Today

Author:

Ruiz-Pesini Eduardo,Emperador Sonia,López-Gallardo Ester,Hernández-Ainsa Carmen,Montoya Julio

Funder

Instituto de Salud Carlos III

Departamento de Ciencia, Tecnología y Universidad del Gobierno de Aragón

FEDER Funding Program from the European Union

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology

Reference49 articles.

1. The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head;Barron;Br. J. Ophthalmol.,2004

2. 20 years of human mtDNA pathologic point mutations: carefully reading the pathogenicity criteria;Montoya;Biochim. Biophys. Acta,2009

3. A neurodegenerative perspective on mitochondrial optic neuropathies;Yu-Wai-Man;Acta Neuropathol.,2016

4. Measurement of systemic mitochondrial function in advanced primary open-angle glaucoma and Leber hereditary optic neuropathy;Van Bergen;PLoS One,2015

5. Leber hereditary optic neuropathy: exemplar of an mtDNA disease;Wallace;Handb. Exp. Pharmacol.,2017

Cited by 13 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. Mitochondrial DNA D-loop variants correlate with a primary open-angle glaucoma subgroup;Frontiers in Ophthalmology;2024-01-17

2. Low mitochondrial DNA copy number in buffy coat DNA of primary open-angle glaucoma patients;Experimental Eye Research;2023-07

3. Mitochondrial dysfunction in glaucomatous degeneration;International Journal of Ophthalmology;2023-05-18

4. MYOC/p.G367R mutation induces cell dysfunction of the trabecular meshwork and retina via impairment of the protein degradation mechanism;2022-11-10

5. Solutions to a Radical Problem: Overview of Current and Future Treatment Strategies in Leber’s Hereditary Opic Neuropathy;International Journal of Molecular Sciences;2022-10-30

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