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F Tagliavini

Showing results (81-90 of 133) with videos related to

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Annals of Neurology|August 12, 2000
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutationG Puoti, G Rossi, G Giaccone, et al.
Brain Pathology (Zurich, Switzerland)|February 11, 2000
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion proteinG Giaccone, B Canciani, G Puoti, et al.
The American Journal of Pathology|November 12, 1998
Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissuesA Jiménez-Huete, P M Lievens, R Vidal, et al.
Leukemia|November 13, 2010
Multiple forms of PKR present in the nuclei of acute leukemia cells represent an active kinase that is responsive to stressW L Blalock, A Bavelloni, M Piazzi, et al.
Neurobiology of Disease|January 1, 1997
A neurotoxic and gliotrophic fragment of the prion protein increases plasma membrane microviscosityM Salmona, G Forloni, L Diomede, et al.
Neurobiology of Aging|June 15, 2007
Tauopathy in human and experimental variant Creutzfeldt-Jakob diseaseG Giaccone, M Mangieri, R Capobianco, et al.
The American Journal of Pathology|May 11, 1999
A betaPP peptide carboxyl-terminal to Abeta is neurotoxicG Marcon, G Giaccone, B Canciani, et al.
Neurology|August 10, 2000
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP geneG Rossi, G Giaccone, L Giampaolo, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 19, 2000
Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126S Thellung, T Florio, A Corsaro, 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.
Pageof 14

Showing results (81-90 of 133) with videos related to

Sort By:
Pageof 14
Annals of Neurology|August 12, 2000
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutationG Puoti, G Rossi, G Giaccone, et al.
Brain Pathology (Zurich, Switzerland)|February 11, 2000
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion proteinG Giaccone, B Canciani, G Puoti, et al.
The American Journal of Pathology|November 12, 1998
Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissuesA Jiménez-Huete, P M Lievens, R Vidal, et al.
Leukemia|November 13, 2010
Multiple forms of PKR present in the nuclei of acute leukemia cells represent an active kinase that is responsive to stressW L Blalock, A Bavelloni, M Piazzi, et al.
Neurobiology of Disease|January 1, 1997
A neurotoxic and gliotrophic fragment of the prion protein increases plasma membrane microviscosityM Salmona, G Forloni, L Diomede, et al.
Neurobiology of Aging|June 15, 2007
Tauopathy in human and experimental variant Creutzfeldt-Jakob diseaseG Giaccone, M Mangieri, R Capobianco, et al.
The American Journal of Pathology|May 11, 1999
A betaPP peptide carboxyl-terminal to Abeta is neurotoxicG Marcon, G Giaccone, B Canciani, et al.
Neurology|August 10, 2000
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP geneG Rossi, G Giaccone, L Giampaolo, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 19, 2000
Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126S Thellung, T Florio, A Corsaro, 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.
Pageof 14