4 Ergebnisse.

A conformational transition of the cellular prion protein (PrPC) into an aberrantly folded isoform designated scrapie prion protein (PrPSc) is the hallmark of a variety of neurodegenerative disorders collectively called prion diseases. They include Creutzfeldt-Jakob disease and Gerstmann-Stäussler-Scheinker syndrome in humans, scrapie in sheep, bovine spongiform encephalopathy (BSE) in cattle and chronic wasting disease (CWD) in free-ranging d...

Genetics of Prion Disease, by S. Lloyd, S. Mead and J. Collinge.- Atypical Prion Diseases in Humans and Animals, by M. A. Tranulis, S. L. Benestad, T. Baron and H. Kretzschmar.- Chronic Wasting Disease, by S. Gilch, N. Chitoor, Y. Taguchi, M. Stuart, J. E. Jewell and H. M. Schätzl.- Transgenic Mouse Models and Prion Strains, by G. C. Telling.- Neuroprotective and Neurotoxic Signaling by the Prion Protein, by U. K. Resenberger, K. F. Win...

Genetics of Prion Disease, by S. Lloyd, S. Mead and J. Collinge.- Atypical Prion Diseases in Humans and Animals, by M. A. Tranulis, S. L. Benestad, T. Baron and H. Kretzschmar.- Chronic Wasting Disease, by S. Gilch, N. Chitoor, Y. Taguchi, M. Stuart, J. E. Jewell and H. M. Schätzl.- Transgenic Mouse Models and Prion Strains, by G. C. Telling.- Neuroprotective and Neurotoxic Signaling by the Prion Protein, by U. K. Resenberger, K. F. Win...

Keine Beschreibung.