A new model for fatty acid hydroxylase-associated neurodegeneration reveals mitochondrial and autophagy abnormalities.

Mandik, Frida; Kanana, Yuliia; Rody, Jost; Misera, Sophie; Wilken, Bernd; Laabs von Holt, Björn-Hergen; Klein, Christine; Vos, Melissa

Mandik, Frida; Kanana, Yuliia; Rody, Jost; Misera, Sophie; Wilken, Bernd; Laabs von Holt, Björn-Hergen; Klein, Christine; Vos, Melissa.

Afiliación

Mandik F; Institute of Neurogenetics, University of Luebeck, UKSH, Luebeck, Germany.
Kanana Y; Institute of Neurogenetics, University of Luebeck, UKSH, Luebeck, Germany.
Rody J; Institute of Neurogenetics, University of Luebeck, UKSH, Luebeck, Germany.
Misera S; Institute of Neurogenetics, University of Luebeck, UKSH, Luebeck, Germany.
Wilken B; Department of Neuropediatrics, Klinikum Kassel, Kassel, Germany.
Laabs von Holt BH; Institut für Medizinische Biometrie und Statistik, University of Luebeck, Luebeck, Germany.
Klein C; Institute of Neurogenetics, University of Luebeck, UKSH, Luebeck, Germany.
Vos M; Institute of Neurogenetics, University of Luebeck, UKSH, Luebeck, Germany.

Front Cell Dev Biol ; 10: 1000553, 2022.

Article en En | MEDLINE | ID: mdl-36589738

Palabras clave

Drosophila melanogaster; FA2H; autophagy; fatty acid hydroxylase-associated neurodegeneration; mitochondria

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Front Cell Dev Biol Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Suiza

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