Formalin RT-QuIC assay detects prion-seeding activity in formalin-fixed brain samples from sporadic Creutzfeldt–Jakob disease patients

[1]  M. Yamada,et al.  Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation , 2018, Prion.

[2]  S. Murayama,et al.  Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients , 2016, EBioMedicine.

[3]  Mari Yoshida,et al.  Rapid and Quantitative Assay of Amyloid-Seeding Activity in Human Brains Affected with Prion Diseases , 2015, PloS one.

[4]  R. Henry,et al.  White matter involvement in sporadic Creutzfeldt-Jakob disease , 2014, Brain : a journal of neurology.

[5]  Steven J Collins,et al.  Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion , 2011, Nature Medicine.

[6]  Brent Race,et al.  Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays , 2010, PLoS pathogens.

[7]  Y. Kuroiwa,et al.  Prospective 10-year surveillance of human prion diseases in Japan. , 2010, Brain : a journal of neurology.

[8]  S. Prusiner,et al.  A γ-secretase inhibitor and quinacrine reduce prions and prevent dendritic degeneration in murine brains , 2008, Proceedings of the National Academy of Sciences.

[9]  B. Caughey,et al.  Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking , 2008, Nature Methods.

[10]  B. Permanne,et al.  Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding , 2001, Nature.

[11]  P Brown,et al.  Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects , 1999, Annals of neurology.

[12]  F. Cohen,et al.  Prion Protein Biology , 1998, Cell.

[13]  D. Taylor,et al.  The effect of formic acid on BSE and scrapie infectivity in fixed and unfixed brain-tissue. , 1997, Veterinary microbiology.

[14]  H. Kretzschmar,et al.  Immunhistological evaluation of Creutzfeldt-Jakob disease with reference to the type PrPres deposition. , 1996, Clinical neuropathology.

[15]  J Q Trojanowski,et al.  Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease , 1996, Annals of neurology.

[16]  R. Meyermann,et al.  Reactive microgIia in Creutzfeldt‐Jakob disease , 1995, Neuropathology and applied neurobiology.

[17]  D. Taylor Survival of mouse-passaged bovine spongiform encephalopathy agent after exposure to paraformaldehyde-lysine-periodate and formic acid. , 1995, Veterinary microbiology.

[18]  P. Brown,et al.  A simple and effective method for inactivating virus infectivity in formalin‐fixed tissue samples from patients with Creutzfeldt‐Jakob disease , 1990, Neurology.

[19]  C. Sigurdson,et al.  [Prion diseases?]. , 1985, Deutsche medizinische Wochenschrift.