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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.Brain Pathology (Zurich, Switzerland)|June 15, 2004
Early-onset dementia with Lewy bodiesMasaki Takao, Bernardino Ghetti, Hirotaka Yoshida, et al.Proceedings of Spie--The International Society for Optical Engineering|September 2, 2024
Spatiospectral image processing workflow considerations for advanced MR spectroscopy of the brainLeon Y Cai, Stephanie N Del Tufo, Laura Barquero, et al.Nature Structural & Molecular Biology|March 30, 2024
Cryo-EM structures of amyloid-β and tau filaments in Down syndromeAnllely Fernandez, Md Rejaul Hoq, Grace I Hallinan, et al.Acta Neuropathologica|June 23, 2023
Mutation ∆K281 in MAPT causes Pick's diseaseManuel Schweighauser, Holly J Garringer, Therése Klingstedt, et al.Scientific Reports|February 21, 2018
Molecular subtypes of Alzheimer's diseaseGiuseppe Di Fede, Marcella Catania, Emanuela Maderna, 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.Acta Neuropathologica|July 27, 2000
Senile dementia associated with amyloid beta protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-epsilon4 alleleR Vidal, M Calero, P Piccardo, et al.Plos Pathogens|April 19, 2024
Sensitive detection of pathological seeds of α-synuclein, tau and prion protein on solid surfacesChristina D Orrú, Bradley R Groveman, Andrew G Hughson, et al.Nature|May 29, 2020
Structures of α-synuclein filaments from multiple system atrophyManuel Schweighauser, Yang Shi, Airi Tarutani, et al.Pageof 98