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Neuropathology and Applied Neurobiology|November 30, 2013
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementiaTammaryn Lashley, Jonathan D Rohrer, Colin Mahoney, et al.Brain : a Journal of Neurology|January 18, 2006
Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutationsAndrew F Hill, Susan Joiner, Jonathan A Beck, et al.Elife|August 7, 2024
Syntaxin-6 delays prion protein fibril formation and prolongs the presence of toxic aggregation intermediatesDaljit Sangar, Elizabeth Hill, Kezia Jack, et al.The Journal of General Virology|February 22, 2005
An enzyme-detergent method for effective prion decontamination of surgical steelGraham S Jackson, Edward McKintosh, Eckhard Flechsig, et al.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.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.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.Pageof 36