Phosphatidylserine improves axonal transport by inhibition of HDAC and has potential in treatment of neurodegenerative diseases

Familial dysautonomia (FD) is a rare children neurodegenerative disease caused due to a point mutation in the IKBKAP gene that results in decreased IKK complex-associated protein (IKAP) protein production. The disease affects mostly the dorsal root ganglion (DRG) and the sympathetic ganglion. Recent...

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Detalles Bibliográficos
Autores principales: Naftelberg, Shiran, Ast, Gil, Perlson, Eran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Invited Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436341/
https://www.ncbi.nlm.nih.gov/pubmed/28553323
http://dx.doi.org/10.4103/1673-5374.205082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436341/
https://www.ncbi.nlm.nih.gov/pubmed/28553323
http://dx.doi.org/10.4103/1673-5374.205082

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