Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ilaria Mirabile"'
Autor:
Gabrielle Rees, Manuel Salto‐Tellez, Jessica L Lee, Karin Oien, Clare Verrill, Alex Freeman, Ilaria Mirabile, Nicholas P West, on behalf of the National Cancer Research Institute (NCRI) Cellular‐Molecular Pathology (CM‐Path) clinical trials working group
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 5, Iss 2, Pp 100-107 (2019)
Abstract Clinical trials rely on multidisciplinary teams for successful delivery. Pathologists should be involved in clinical trial design from the outset to ensure that protocols are optimised to deliver maximum data collection and translational res
Externí odkaz:
https://doaj.org/article/d3437ca3b5c44b2dbc3578c2cb723bbf
Publikováno v:
Neuropathology and Applied Neurobiology. 41:613-630
While prion infection ultimately involves the entire brain, it has long been thought that the abrupt clinical onset and rapid neurological decline in laboratory rodents relates to involvement of specific critical neuroanatomical target areas. The sev
Publikováno v:
Neuropathology and Applied Neurobiology
Aims While prion infection ultimately involves the entire brain, it has long been thought that the abrupt clinical onset and rapid neurological decline in laboratory rodents relates to involvement of specific critical neuroanatomical target areas. Th
Autor:
Chiara Zurzolo, Philippe Casanova, Ilaria Mirabile, Giuseppe Legname, Vincenza Campana, Lorena Zentilin, Mauro Giacca, Agata Kranjc, Stanley B. Prusiner
Publikováno v:
Biochemical Journal
Biochemical Journal, Portland Press, 2009, 418 (3), pp.507-515. ⟨10.1042/BJ20081541⟩
Biochemical Journal, 2009, 418 (3), pp.507-515. ⟨10.1042/BJ20081541⟩
Biochemical Journal, Portland Press, 2009, 418 (3), pp.507-515. ⟨10.1042/BJ20081541⟩
Biochemical Journal, 2009, 418 (3), pp.507-515. ⟨10.1042/BJ20081541⟩
International audience; Prions are infectious proteins responsible for a group of fatal neurodegenerative diseases called transmissible spongiform encephalopathies (TSEs), or prion diseases. In mammals, prions reproduce themselves by recruiting the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c2895af749db0719856f1e78249c0d2
https://hdl.handle.net/11368/2493573
https://hdl.handle.net/11368/2493573
Autor:
Sebastian Brandner, Ilaria Mirabile, Michael Farmer, John Collinge, Giovanna R. Mallucci, Melanie D. White
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 105(29)
Prion diseases are fatal neurodegenerative conditions for which there is no effective treatment. Prion propagation involves the conversion of cellular prion protein, PrP C , to its conformational isomer, PrP Sc , which accumulates in disease. Here, w
Autor:
Vincenza Campana, Lorena Zentilin, Ilaria Mirabile, Agata Kranjc, Philippe Casanova, Mauro Giacca, Stanley B. Prusiner, Giuseppe Legname, Chiara Zurzolo
Publikováno v:
Biochemical Journal; Mar2009, Vol. 418 Issue 3, p507-515, 9p
Autor:
Peter Rudge, M Groves, Sebastian Brandner, Ana Lukic, Jessica Lowe, Jacqueline M. Linehan, Ronald Druyeh, Lilla Reiniger, Ilaria Mirabile, Simon Mead, John Collinge, Jonathan D. F. Wadsworth
Publikováno v:
Acta Neuropathologica Communications
Background Sporadic, inherited and acquired prion diseases show distinct histological patterns of abnormal prion protein (PrP) deposits. Many of the inherited prion diseases show striking histological patterns, which often associate with specific mut