Zobrazeno 1 - 7
of 7
pro vyhledávání: '"PrPSc, scrapie prion protein"'
Autor:
Mara Rigamonti, Roberto Chiesa, Ihssane Bouybayoune, Elena Restelli, Ilaria Bertani, Luca Porcu, Stefano Zordan, Antonio Masone, Giada Lavigna, Jacopo Lucchetti, Luca Imeri, Marco Gobbi
Publikováno v:
Neurobiology of Disease, Vol 158, Iss, Pp 105455-(2021)
Neurobiology of Disease
Neurobiology of Disease
Fatal familial insomnia (FFI) is a dominantly inherited prion disease linked to the D178N mutation in the gene encoding the prion protein (PrP). Symptoms, including insomnia, memory loss and motor abnormalities, appear around 50 years of age, leading
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::947f6abf69c24f0e3ded57cf103446a5
http://www.sciencedirect.com/science/article/pii/S0969996121002047
http://www.sciencedirect.com/science/article/pii/S0969996121002047
Publikováno v:
The Journal of Biological Chemistry
Prion diseases are a group of neurodegenerative disorders that infect animals and humans with proteinaceous particles called prions. Prions consist of scrapie prion protein (PrPSc), a misfolded version of the cellular prion protein (PrPC). During dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1920b1e24b134eac206b29073995b75d
https://doi.org/10.1016/j.jbc.2021.100359
https://doi.org/10.1016/j.jbc.2021.100359
Doppel and PrPC co-immunoprecipitate in detergent-resistant membrane domains of epithelial FRT cells
Autor:
Chiara Zurzolo, Maddalena Costanzo, Alessandro Negro, Vincenza Campana, Daniela Sarnataro, M. Catia Sorgato, Anna Caputo
Publikováno v:
Biochemical Journal
Biochemical Journal, 2010, 425 (2), pp.341-51. ⟨10.1042/BJ20091050⟩
Biochemical Journal, Portland Press, 2010, 425 (2), pp.341-51. ⟨10.1042/BJ20091050⟩
Biochemical Journal, 2010, 425 (2), pp.341-51. ⟨10.1042/BJ20091050⟩
Biochemical Journal, Portland Press, 2010, 425 (2), pp.341-51. ⟨10.1042/BJ20091050⟩
International audience; Dpl (doppel) is a paralogue of the PrPC (cellular prion protein), whose misfolded conformer (the scrapie prion protein, PrPSc) is responsible for the onset of TSEs (transmissible spongiform encephalopathies) or prion diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b535cf11e1441f046e7235fd030d365
https://doi.org/10.1042/bj20091050
https://doi.org/10.1042/bj20091050
Akademický článek
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Akademický článek
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Autor:
Komatsu J; a Department of Neurology and Neurobiology of Aging ; Kanazawa University Graduate School of Medical Sciences ; Kanazawa , Japan., Sakai K, Hamaguchi T, Sugiyama Y, Iwasa K, Yamada M
Publikováno v:
Prion [Prion] 2014; Vol. 8 (5), pp. 336-8.
Autor:
Hammond M; a Department of Immunology, Genetics and Pathology; Science for Life Laboratory ; Uppsala University ; Uppsala , Sweden., Wik L, Deslys JP, Comoy E, Linné T, Landegren U, Kamali-Moghaddam M
Publikováno v:
Prion [Prion] 2014; Vol. 8 (3), pp. 261-5.