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F Prelli

Showing results (41-50 of 53) with videos related to

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Blood|August 1, 1970
Heavy chain disease of the gamma (gamma M) type: report of the first caseF A Forte, F Prelli, W J Yount, et al.
The EMBO Journal|March 1, 1991
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58F Tagliavini, F Prelli, J Ghiso, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitroF Tagliavini, F Prelli, L Verga, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 1, 1992
H chain V region sequences of three human monoclonal IgM with anti-myelin-associated glycoprotein activityH Ayadi, E Mihaesco, N Congy, et al.
Journal of Neuropathology and Experimental Neurology|November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)P Piccardo, C Seiler, S R Dlouhy, et al.
Cell|November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant alleleF Tagliavini, F Prelli, M Porro, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Neuroscience|April 15, 2008
High titers of mucosal and systemic anti-PrP antibodies abrogate oral prion infection in mucosal-vaccinated miceF Goñi, F Prelli, F Schreiber, et al.
Brain Research|October 25, 1988
Beta-protein deposition: a pathogenetic link between Alzheimer's disease and cerebral amyloid angiopathiesF Coria, F Prelli, E M Castaño, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Blood|August 1, 1970
Heavy chain disease of the gamma (gamma M) type: report of the first caseF A Forte, F Prelli, W J Yount, et al.
The EMBO Journal|March 1, 1991
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58F Tagliavini, F Prelli, J Ghiso, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitroF Tagliavini, F Prelli, L Verga, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 1, 1992
H chain V region sequences of three human monoclonal IgM with anti-myelin-associated glycoprotein activityH Ayadi, E Mihaesco, N Congy, et al.
Journal of Neuropathology and Experimental Neurology|November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)P Piccardo, C Seiler, S R Dlouhy, et al.
Cell|November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant alleleF Tagliavini, F Prelli, M Porro, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Neuroscience|April 15, 2008
High titers of mucosal and systemic anti-PrP antibodies abrogate oral prion infection in mucosal-vaccinated miceF Goñi, F Prelli, F Schreiber, et al.
Brain Research|October 25, 1988
Beta-protein deposition: a pathogenetic link between Alzheimer's disease and cerebral amyloid angiopathiesF Coria, F Prelli, E M Castaño, et al.
Pageof 6