Differential overexpression of SERPINA3 in human prion diseases

Prion diseases are fatal neurodegenerative disorders with sporadic, genetic or acquired etiologies. The molecular alterations leading to the onset and the spreading of these diseases are still unknown. In a previous work we identified a five-gene signature able to distinguish intracranially BSE-infe...

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Detalles Bibliográficos
Autores principales: Vanni, S., Moda, F., Zattoni, M., Bistaffa, E., De Cecco, E., Rossi, M., Giaccone, G., Tagliavini, F., Haïk, S., Deslys, J. P., Zanusso, G., Ironside, J. W., Ferrer, I., Kovacs, G. G., Legname, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688139/
https://www.ncbi.nlm.nih.gov/pubmed/29142239
http://dx.doi.org/10.1038/s41598-017-15778-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688139/
https://www.ncbi.nlm.nih.gov/pubmed/29142239
http://dx.doi.org/10.1038/s41598-017-15778-8

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