In the past decade, manipulation of PrP genes by transgenesis in mice has provided important insights into mechanisms of prion propagation and the molecular basis of prion strains and species barriers. Despite these advances, our understanding of these unique pathogens is far from complete. This review focuses on PrP gene knockout and gene replacement studies, PrP structure and function, and transgenic models of human and animal prion diseases. Transgenic approaches will doubtless remain the cornerstone of investigations into the prion diseases in the coming years, which will include mechanistic studies of prion pathogenesis and prion transmission barriers. Transgenic models will also be important tools for the evaluation of potential therapeutic agents for prion diseases.
机构:
Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
机构:
Carlos III Inst Hlth, Queen Sofia Fdn Alzheimer Ctr, CIEN Fdn, Alzheimer Dis Res Unit, Madrid, Spain
Network Ctr Biomed Res Neurodegenerat Dis CIBERNE, Madrid, SpainUniv Med Sch, Dept Neurol, Gottingen, Germany
Calero, Olga
Stehmann, Christiane
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Univ Melbourne, Florey Inst, Australian Natl Creutzfeldt Jakob Dis Registry, Melbourne, Vic, AustraliaUniv Med Sch, Dept Neurol, Gottingen, Germany
Stehmann, Christiane
Sarros, Shannon
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Univ Melbourne, Florey Inst, Australian Natl Creutzfeldt Jakob Dis Registry, Melbourne, Vic, AustraliaUniv Med Sch, Dept Neurol, Gottingen, Germany
Sarros, Shannon
Ladogana, Anna
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Ist Super Sanita, Dept Neurosci, Rome, ItalyUniv Med Sch, Dept Neurol, Gottingen, Germany
Ladogana, Anna
Poleggi, Anna
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Ist Super Sanita, Dept Neurosci, Rome, ItalyUniv Med Sch, Dept Neurol, Gottingen, Germany