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B Ghetti

Showing results (201-210 of 227) with videos related to

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Journal of Neuropathology and Experimental Neurology|April 22, 2004
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide geneR Vidal, B Ghetti, M Takao, 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.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 1999
Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's diseaseK R Bales, T Verina, D J Cummins, et al.
European Journal of Neurology|August 21, 2012
Phenotypic variability in three families with valosin-containing protein mutationS Spina, A D Van Laar, J R Murrell, et al.
The Journal of Trauma and Acute Care Surgery|May 12, 2022
Integrating traffic safety data with area deprivation index: A method to better understand the causes of pediatric pedestrian versus automobile collisionsVíctor de Cos, Alexandra S Rooney, Alicia G Sykes, et al.
Journal of Neuropathology and Experimental Neurology|January 4, 2001
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsyM Takao, M D Benson, J R Murrell, et al.
The Journal of Surgical Research|May 19, 2022
Bike Helmet Usage in the Most Disadvantaged Neighborhoods: A Focused Area for Trauma PreventionOwen S Henry, Alexandra S Rooney, Megan V Heflinger, et al.
Nature Genetics|November 14, 1997
Lack of apolipoprotein E dramatically reduces amyloid beta-peptide depositionK R Bales, T Verina, R C Dodel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
The Journal of Biological Chemistry|November 23, 2000
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117VF Tagliavini, P M Lievens, C Tranchant, et al.
Pageof 23

Showing results (201-210 of 227) with videos related to

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Pageof 23
Journal of Neuropathology and Experimental Neurology|April 22, 2004
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide geneR Vidal, B Ghetti, M Takao, 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.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 1999
Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's diseaseK R Bales, T Verina, D J Cummins, et al.
European Journal of Neurology|August 21, 2012
Phenotypic variability in three families with valosin-containing protein mutationS Spina, A D Van Laar, J R Murrell, et al.
The Journal of Trauma and Acute Care Surgery|May 12, 2022
Integrating traffic safety data with area deprivation index: A method to better understand the causes of pediatric pedestrian versus automobile collisionsVíctor de Cos, Alexandra S Rooney, Alicia G Sykes, et al.
Journal of Neuropathology and Experimental Neurology|January 4, 2001
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsyM Takao, M D Benson, J R Murrell, et al.
The Journal of Surgical Research|May 19, 2022
Bike Helmet Usage in the Most Disadvantaged Neighborhoods: A Focused Area for Trauma PreventionOwen S Henry, Alexandra S Rooney, Megan V Heflinger, et al.
Nature Genetics|November 14, 1997
Lack of apolipoprotein E dramatically reduces amyloid beta-peptide depositionK R Bales, T Verina, R C Dodel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
The Journal of Biological Chemistry|November 23, 2000
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117VF Tagliavini, P M Lievens, C Tranchant, et al.
Pageof 23