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Neurobiology of Aging|February 17, 2009
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degenerationSara Rollinson, Patrizia Rizzu, Stephen Sikkink, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 8, 2005
Protein conformation significantly influences immune responses to prion proteinAzadeh Khalili-Shirazi, Sonia Quaratino, Marco Londei, et al.Journal of Huntington'S Disease|October 30, 2025
Emotion recognition in people with Huntington's disease: A comprehensive systematic reviewNicolò Zarotti, Alice Storey, Sarah Lloyd, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 1, 2026
Evidence for progressive neurodegeneration in iatrogenic cerebral amyloid angiopathyLarysa Panteleienko, Gargi Banerjee, Dermot Mallon, et al.Child Development|July 28, 2009
Social perception in infancy: a near infrared spectroscopy studySarah Lloyd-Fox, Anna Blasi, Agnes Volein, et al.Neuroimage|January 5, 2010
Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutationsJonathan D Rohrer, Gerard R Ridgway, Marc Modat, et al.The Biochemical Journal|August 24, 2006
Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4Mark A Wells, Clare Jelinska, Laszlo L P Hosszu, et al.Neuron|February 3, 2007
Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected miceGiovanna R Mallucci, Melanie D White, Michael Farmer, et al.The Biochemical Journal|July 11, 2006
A reassessment of copper(II) binding in the full-length prion proteinMark A Wells, Graham S Jackson, Samantha Jones, et al.Scientific Reports|January 25, 2019
Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitroCassandra Terry, Robert L Harniman, Jessica Sells, et al.Pageof 43