ANT1 overexpression models: Some similarities with facioscapulohumeral muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder characterized by progressive muscle weakness. Adenine nucleotide translocator 1 (ANT1), the only 4q35 gene involved in mitochondrial function, is strongly expressed in FSHD skeletal muscle biopsies. However, its role in...

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Detalles Bibliográficos
Autores principales: Arbogast, Sandrine, Kotzur, Heinrich, Frank, Corinna, Compagnone, Nathalie, Sutra, Thibault, Pillard, Fabien, Pietri, Sylvia, Hmada, Nisrine, Moussa, Daouda Moustapha Abba, Bride, Jamie, Françonnet, Sarah, Mercier, Jacques, Cristol, Jean-Paul, Dabauvalle, Marie-Christine, Laoudj-Chenivesse, Dalila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434167/
https://www.ncbi.nlm.nih.gov/pubmed/36030628
http://dx.doi.org/10.1016/j.redox.2022.102450

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434167/
https://www.ncbi.nlm.nih.gov/pubmed/36030628
http://dx.doi.org/10.1016/j.redox.2022.102450

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