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The Journal of Biological Chemistry|May 5, 2004
The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPCLaszlo L P Hosszu, Graham S Jackson, Clare R Trevitt, et al.Biochemistry|August 20, 2010
The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like formLaszlo L P Hosszu, M Howard Tattum, Samantha Jones, et al.Nature Communications|March 6, 2014
mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivoNeng-Wei Hu, Andrew J Nicoll, Dainan Zhang, et al.Journal of Molecular Biology|December 19, 2022
Prion Propagation is Dependent on Key Amino Acids in Charge Cluster 2 within the Prion ProteinSavroop Bhamra, Parineeta Arora, Szymon W Manka, et al.Brain Research|December 30, 2018
PrP-grafted antibodies bind certain amyloid β-protein aggregates, but do not prevent toxicityDavid Mengel, Wei Hong, Grant T Corbett, et al.Open Biology|November 17, 2017
Soluble Aβ aggregates can inhibit prion propagationClaire J Sarell, Emma Quarterman, Daniel C-M Yip, et al.Dementia and Geriatric Cognitive Disorders|June 5, 2004
Frontotemporal dementia linked to chromosome 3Jerry Brown, Susanne Gydesen, Peter Johannsen, et al.Prion|September 30, 2025
Development of a user guide to support administration of the MRC Prion Disease Rating Scale in research and clinical settings for prion diseasesRobert S Pulido, Chris Marshall, Anne V Smith, et al.Nature Reviews. Neurology|November 10, 2020
Genetic testing in dementia - utility and clinical strategiesCarolin A M Koriath, Joanna Kenny, Natalie S Ryan, et al.Neurobiology of Aging|August 16, 2016
Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutationJose Bras, Ruth Djaldetti, Ana Margarida Alves, et al.Pageof 36