Dysregulated mitophagy and mitochondrial transport in severe inherited optic atrophy due to OPA1 mutations
Hlavní autoři: | Poulton, J, Liao, C, Ashley, N, Morten, K, Phadwal, K, Williams, A, Feamley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Macleod, L, Downes, S, Zeviani, M, Simon, A, Votruba, M |
---|---|
Médium: | Conference item |
Vydáno: |
2012
|
Podobné jednotky
-
Dysregulated mitophagy and mitochondrial transport in severe dominant optic atrophy due to OPA1 mutations
Autor: Liao, C, a další
Vydáno: (2012) -
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations.
Autor: Liao, C, a další
Vydáno: (2016) -
Validating the RedMIT/GFP-LC3 mouse model by studying mitophagy in autosomal dominant optic atrophy due to the OPA1Q285STOP mutation
Autor: Diot, A, a další
Vydáno: (2018) -
A Perspective on Accelerated Aging Caused by the Genetic Deficiency of the Metabolic Protein, OPA1
Autor: Irina Erchova, a další
Vydáno: (2021-04-01) -
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology
Autor: Juan Manuel Chao de la Barca, a další
Vydáno: (2016-06-01)