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1 - 2 of 2 results found for FKBP9.

  1. Towards understanding selective neuronal vulnerability: establishing an in-vitro model...

    Prion diseases are fatal neurodegenerative diseases that affect humans and animals. Prion strains, conformational variants of misfolded prion proteins, are thought to be associated with distinct clinical and pathological phenotypes. Why prion

    http://iris.ucl.ac.uk/iris/publication/1621284/1

  2. In vitro screen of prion disease susceptibility genes using the scrapie cell assay.

    Prion diseases (transmissible spongiform encephalopathies) are fatal neurodegenerative diseases, including Creutzfeldt-Jakob disease in humans, scrapie in sheep and bovine spongiform encephalopathy in cattle. While genome-wide association studies in

    http://iris.ucl.ac.uk/iris/publication/947161/2

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