Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Unknown (R35)
Project #
5R35AG008992-06
Application #
5204668
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
1996
Total Cost
Indirect Cost
Gambetti, Pierluigi; Kong, Qingzhong; Zou, Wenquan et al. (2003) Sporadic and familial CJD: classification and characterisation. Br Med Bull 66:213-39
Taratuto, Ana Lia; Piccardo, P; Reich, E G et al. (2002) Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology 58:362-7
Parchi, P; Capellari, S; Gambetti, P (2000) Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia. Microsc Res Tech 50:16-25
Capellari, S; Parchi, P; Russo, C M et al. (2000) Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain. Am J Pathol 157:613-22
Capellari, S; Zaidi, S I; Urig, C B et al. (1999) Prion protein glycosylation is sensitive to redox change. J Biol Chem 274:34846-50
Parchi, P; Giese, A; Capellari, S et al. (1999) Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46:224-33
Parchi, P; Capellari, S; Chin, S et al. (1999) A subtype of sporadic prion disease mimicking fatal familial insomnia. Neurology 52:1757-63
Zagorski, M G; Yang, J; Shao, H et al. (1999) Methodological and chemical factors affecting amyloid beta peptide amyloidogenicity. Methods Enzymol 309:189-204
Shao, H; Jao, S; Ma, K et al. (1999) Solution structures of micelle-bound amyloid beta-(1-40) and beta-(1-42) peptides of Alzheimer's disease. J Mol Biol 285:755-73
Worrall, B B; Herman, S T; Capellari, S et al. (1999) Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry 67:671-4

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