Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue

Secondary mitochondrial dysfunction is a feature in a wide variety of human protein aggregate diseases caused by mutations in different proteins, both in the central nervous system and in striated muscle. The functional relationship between the expression of a mutated protein and mitochondrial dysfu...

Descripción completa

Detalles Bibliográficos
Autores principales: Winter, Lilli, Wittig, Ilka, Peeva, Viktoriya, Eggers, Britta, Heidler, Juliana, Chevessier, Frederic, Kley, Rudolf A., Barkovits, Katalin, Strecker, Valentina, Berwanger, Carolin, Herrmann, Harald, Marcus, Katrin, Kornblum, Cornelia, Kunz, Wolfram S., Schröder, Rolf, Clemen, Christoph S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992032/
https://www.ncbi.nlm.nih.gov/pubmed/27393313
http://dx.doi.org/10.1007/s00401-016-1592-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992032/
https://www.ncbi.nlm.nih.gov/pubmed/27393313
http://dx.doi.org/10.1007/s00401-016-1592-7

Ejemplares similares