Prion-like disorders and Transmissible Spongiform Encephalopathies: An overview of the mechanistic features that are shared by the various disease-related misfolded proteins.

Eraña, Hasier; Venegas, Vanesa; Moreno, Jorge; Castilla, Joaquín

Eraña, Hasier; Venegas, Vanesa; Moreno, Jorge; Castilla, Joaquín.

Affiliation

Eraña H; CIC bioGUNE, Parque Tecnológico de Bizkaia, 48160, Derio, Spain.
Venegas V; CIC bioGUNE, Parque Tecnológico de Bizkaia, 48160, Derio, Spain.
Moreno J; CIC bioGUNE, Parque Tecnológico de Bizkaia, 48160, Derio, Spain.
Castilla J; CIC bioGUNE, Parque Tecnológico de Bizkaia, 48160, Derio, Spain; IKERBASQUE, Basque Foundation for Science, Bilbao, 48011, Bizkaia, Spain. Electronic address: castilla@joaquincastilla.com.

Biochem Biophys Res Commun ; 483(4): 1125-1136, 2017 02 19.

Article in En | MEDLINE | ID: mdl-27590581

Subject(s)

Prion Diseases/metabolism; Alzheimer Disease/metabolism; Amyloidosis/metabolism; Amyotrophic Lateral Sclerosis/metabolism; Animals; Humans; Parkinson Disease/metabolism; Protein Folding

Key words

Alzheimer; Prion; Prion strain; Prion-like diseases; Protein misfolding disorders; Transmissible Spongiform Encephalopathy (TSE)

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prion Diseases Limits: Animals / Humans Language: En Journal: Biochem Biophys Res Commun Year: 2017 Document type: Article Affiliation country: Spain Country of publication: United States

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