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dc.contributor.authorKarydas Stavros
dc.date.accessioned2016-05-09T08:25:51Z
dc.date.available2016-05-09T08:25:51Z
dc.date.issued2015
dc.identifier.otherB-11158
dc.identifier.urihttp://hdl.handle.net/10832/1465
dc.description.abstractScrapie is a fatal, neurodegenerative disease of sheep and goat, which belongs together with Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob disease of humans, to the group of Transmissible Spongiform Encephalopathies. TSEs, or prion diseases, affect the central nervous system of many mammals and are characterized by long, asymptomatic incubation periods. The name of TSE arises from the spongiform changes caused by Prions, acronym of Proteinaceous Infectious Particles, defined by the accumulation of an abnormal form of PrP (referred to as PrPSc) of a host membrane glycoprotein (prion protein or PrP) in the CNS.en
dc.subjectEurópai Unió
dc.subjectScrapie
dc.subjectJuhhu
dc.subjectKecskehu
dc.subjectBSE
dc.subjectGenetikahu
dc.subjectSheepen
dc.subjectGoaten
dc.subjectGeneticsen
dc.subjectÁllattenyésztési, Takarmányozási és Laborállat-tudományi Intézethu
dc.titleCyprus pilot project
dc.typeThesisen


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