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O Bugiani

Showing results (91-100 of 138) with videos related to

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The Journal of Biological Chemistry|March 18, 1994
Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinL De Gioia, C Selvaggini, E Ghibaudi, et al.
The Journal of Biological Chemistry|April 24, 2001
The stimulation of inducible nitric-oxide synthase by the prion protein fragment 106--126 in human microglia is tumor necrosis factor-alpha-dependent and involves p38 mitogen-activated protein kinaseC Fabrizi, V Silei, M Menegazzi, et al.
Journal of Neuroscience Research|November 18, 1998
Prion protein fragment 106-126 induces apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in the GH3 cell lineT Florio, S Thellung, C Amico, et al.
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|May 11, 1999
A betaPP peptide carboxyl-terminal to Abeta is neurotoxicG Marcon, G Giaccone, B Canciani, et al.
European Review for Medical and Pharmacological Sciences|July 3, 2026
Oxygen-ozone action on Isaac's syndrome: a case reportL Valdenassi, S Chirumbolo, M T Corsetti, et al.
European Neurology|January 1, 1978
Surface markers on lymphocytes from human cerebrospinal fluid. Predominance of T lymphocytes bearing receptors for the Fc segment of IgGP E Manconi, D Zaccheo, O Bugiani, 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.
Pageof 14

Showing results (91-100 of 138) with videos related to

Sort By:
Pageof 14
The Journal of Biological Chemistry|March 18, 1994
Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinL De Gioia, C Selvaggini, E Ghibaudi, et al.
The Journal of Biological Chemistry|April 24, 2001
The stimulation of inducible nitric-oxide synthase by the prion protein fragment 106--126 in human microglia is tumor necrosis factor-alpha-dependent and involves p38 mitogen-activated protein kinaseC Fabrizi, V Silei, M Menegazzi, et al.
Journal of Neuroscience Research|November 18, 1998
Prion protein fragment 106-126 induces apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in the GH3 cell lineT Florio, S Thellung, C Amico, et al.
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|May 11, 1999
A betaPP peptide carboxyl-terminal to Abeta is neurotoxicG Marcon, G Giaccone, B Canciani, et al.
European Review for Medical and Pharmacological Sciences|July 3, 2026
Oxygen-ozone action on Isaac's syndrome: a case reportL Valdenassi, S Chirumbolo, M T Corsetti, et al.
European Neurology|January 1, 1978
Surface markers on lymphocytes from human cerebrospinal fluid. Predominance of T lymphocytes bearing receptors for the Fc segment of IgGP E Manconi, D Zaccheo, O Bugiani, 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.
Pageof 14