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pro vyhledávání: '"Emma G Maytham"'
Autor:
Sarah E Lloyd, Emma G Maytham, Hirva Pota, Julia Grizenkova, Eleni Molou, James Uphill, Holger Hummerich, Jerome Whitfield, Michael P Alpers, Simon Mead, John Collinge
Publikováno v:
PLoS Genetics, Vol 5, Iss 2, p e1000383 (2009)
Prion diseases are fatal transmissible neurodegenerative disorders, which include Scrapie, Bovine Spongiform Encephalopathy (BSE), Creutzfeldt-Jakob Disease (CJD), and kuru. They are characterised by a prolonged clinically silent incubation period, v
Externí odkaz:
https://doaj.org/article/ea236d7807b243039970fe21131ee691
Publikováno v:
Neurogenetics
Prion disease incubation time in mice is determined by many factors including genetic background. The prion gene itself plays a major role in incubation time; however, other genes are also known to be important. Whilst quantitative trait loci (QTL) s
Autor:
Holger Hummerich, Hirva Pota, Sarah E. Lloyd, Jerome Whitfield, John Collinge, Simon Mead, Julia Grizenkova, Emma G. Maytham, Eleni Molou, Michael P. Alpers, James Uphill
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 5, Iss 2, p e1000383 (2009)
PLoS Genetics, Vol 5, Iss 2, p e1000383 (2009)
Prion diseases are fatal transmissible neurodegenerative disorders, which include Scrapie, Bovine Spongiform Encephalopathy (BSE), Creutzfeldt-Jakob Disease (CJD), and kuru. They are characterised by a prolonged clinically silent incubation period, v
Autor:
Jackie Linehan, John Collinge, Sarah E. Lloyd, Marie O'Shea, Sebastian Brandner, Emma G. Maytham
The genetic basis of prion disease incubation time is principally determined by polymorphisms in the prion protein gene, Prnp. However, it is now known that other genetic factors are important. Several quantitative trait loci (QTL) have been identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4f517ed58c358a8887fb836897ef47
https://europepmc.org/articles/PMC2535705/
https://europepmc.org/articles/PMC2535705/