Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Tagliavini

Showing results (111-120 of 133) with videos related to

Pageof 14
Sort By:
Neurology|November 12, 2003
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP geneV Pietrini, G Puoti, L Limido, et al.
Neuropathology and Applied Neurobiology|January 23, 2008
Atypical tauopathy with massive involvement of the white matterG Giaccone, G Marcon, M Mangieri, et al.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2002
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizuresM Takao, B Ghetti, J R Murrell, et al.
Journal of Molecular Biology|July 25, 2000
Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitroF Tagliavini, G Forloni, L Colombo, et al.
The Biochemical Journal|August 5, 1999
Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126M Salmona, P Malesani, L De Gioia, et al.
The American Journal of Pathology|June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Neurochemistry International|March 29, 2002
Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion proteinA Corsaro, S Thellung, C Russo, et al.
Neurology|April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotypeP Piscopo, G Marcon, M R Piras, et al.
Lancet (London, England)|February 16, 2000
Reversion of prion protein conformational changes by synthetic beta-sheet breaker peptidesC Soto, R J Kascsak, G P Saborío, et al.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
Neurology|November 12, 2003
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP geneV Pietrini, G Puoti, L Limido, et al.
Neuropathology and Applied Neurobiology|January 23, 2008
Atypical tauopathy with massive involvement of the white matterG Giaccone, G Marcon, M Mangieri, et al.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2002
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizuresM Takao, B Ghetti, J R Murrell, et al.
Journal of Molecular Biology|July 25, 2000
Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitroF Tagliavini, G Forloni, L Colombo, et al.
The Biochemical Journal|August 5, 1999
Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126M Salmona, P Malesani, L De Gioia, et al.
The American Journal of Pathology|June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Neurochemistry International|March 29, 2002
Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion proteinA Corsaro, S Thellung, C Russo, et al.
Neurology|April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotypeP Piscopo, G Marcon, M R Piras, et al.
Lancet (London, England)|February 16, 2000
Reversion of prion protein conformational changes by synthetic beta-sheet breaker peptidesC Soto, R J Kascsak, G P Saborío, et al.
Pageof 14