Charcot–Marie–Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments

Mutations in the small heat shock protein HSPB1 (HSP27) are a cause of axonal Charcot–Marie–Tooth neuropathy (CMT2F) and distal hereditary motor neuropathy. To better understand the effect of mutations in HSPB1 on the neuronal cytoskeleton, we stably transduced neuronal cells with wild-type and muta...

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Detalles Bibliográficos
Autores principales: Holmgren, Anne, Bouhy, Delphine, De Winter, Vicky, Asselbergh, Bob, Timmermans, Jean-Pierre, Irobi, Joy, Timmerman, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2013
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963106/
https://www.ncbi.nlm.nih.gov/pubmed/23728742
http://dx.doi.org/10.1007/s00401-013-1133-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963106/
https://www.ncbi.nlm.nih.gov/pubmed/23728742
http://dx.doi.org/10.1007/s00401-013-1133-6

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