The m.11778 A > G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metabolic interplay between mitochondrial oxidative phosphorylation and glycolysis-Reference-Cited by-同舟云学术

The m.11778 A > G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metabolic interplay between mitochondrial oxidative phosphorylation and glycolysis

Published:2019-05 Issue: Volume:46 Page:187-194
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Uittenbogaard Martine,Brantner Christine A.,Fang ZiShui,Wong Lee-Jun,Gropman Andrea,Chiaramello Anne

Funder

National Institute of Neurological Disorders and Stroke

National Institute of Child Health and Development

National Center for Advancing Translational Sciences

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference40 articles.

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5. Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte cultures;Bourgeron;J. Biol. Chem.,1993

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2. Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber’s Hereditary Optic Neuropathy (LHON) Subjects;International Journal of Molecular Sciences;2023-08-08

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5. Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber's Hereditary Optic Neuropathy Patients;Frontiers in Molecular Neuroscience;2022-07-13