LC3, an autophagosome marker, is expressed on oligodendrocytes in Nasu-Hakola disease brains

BACKGROUND: Nasu-Hakola disease (NHD) is a rare autosomal recessive disorder characterized by sclerosing leukoencephalopathy and multifocal bone cysts, caused by a loss-of-function mutation of either DAP12 or TREM2. TREM2 and DAP12 constitute a receptor/adaptor signaling complex expressed exclusivel...

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Detalles Bibliográficos
Autores principales: Satoh, Jun-ichi, Motohashi, Nobutaka, Kino, Yoshihiro, Ishida, Tsuyoshi, Yagishita, Saburo, Jinnai, Kenji, Arai, Nobutaka, Nakamagoe, Kiyotaka, Tamaoka, Akira, Saito, Yuko, Arima, Kunimasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022378/
https://www.ncbi.nlm.nih.gov/pubmed/24886140
http://dx.doi.org/10.1186/1750-1172-9-68

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022378/
https://www.ncbi.nlm.nih.gov/pubmed/24886140
http://dx.doi.org/10.1186/1750-1172-9-68

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