To investigate mitophagy in 5 patients with severe dominantly inherited optic atrophy (DOA), caused by depletion of OPA1 (a protein that is essential for mitochondrial fusion), compared with healthy controls.

Liao, C., Ashley, N., Diot, A., Morten, K., Phadwal, K., Williams, A., et al. (2017). Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations. NEUROLOGY, 88(2), 131-142 [10.1212/WNL.0000000000003491].

Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations

Campanella, Michelangelo;
2017-01-10

Abstract

To investigate mitophagy in 5 patients with severe dominantly inherited optic atrophy (DOA), caused by depletion of OPA1 (a protein that is essential for mitochondrial fusion), compared with healthy controls.
10-gen-2017
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/06 - ANATOMIA COMPARATA E CITOLOGIA
English
Con Impact Factor ISI
Antioxidants
Cognition Disorders
DNA Mutational Analysis
DNA, Mitochondrial
Family Health
Female
Fibroblasts
GTP Phosphohydrolases
Humans
Male
Membrane Potential, Mitochondrial
Mitochondrial Proteins
Mitophagy
Mutation
Optic Atrophy
Pedigree
Protein Kinases
RNA, Small Interfering
Transfection
Ubiquinone
Ubiquitin-Protein Ligases
Cells, Cultured
Liao, C., Ashley, N., Diot, A., Morten, K., Phadwal, K., Williams, A., et al. (2017). Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations. NEUROLOGY, 88(2), 131-142 [10.1212/WNL.0000000000003491].
Liao, C; Ashley, N; Diot, A; Morten, K; Phadwal, K; Williams, A; Fearnley, I; Rosser, L; Lowndes, J; Fratter, C; Ferguson, Djp; Vay, L; Quaghebeur, G;...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/264658
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