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Biochimica Et Biophysica Acta|April 25, 2007
The cellular prion protein (PrP(C)): its physiological function and role in diseaseLaura Westergard, Heather M Christensen, David A HarrisThe Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 30, 2011
A nine amino acid domain is essential for mutant prion protein toxicityLaura Westergard, Jessie A Turnbaugh, David A HarrisThe Journal of Biological Chemistry|October 26, 2011
A naturally occurring C-terminal fragment of the prion protein (PrP) delays disease and acts as a dominant-negative inhibitor of PrPSc formationLaura Westergard, Jessie A Turnbaugh, David A HarrisMolecular Neurodegeneration|August 23, 2008
Prion protein lacks robust cytoprotective activity in cultured cellsHeather M Christensen, David A HarrisJournal of Neurochemistry|December 3, 2008
A deleted prion protein that is neurotoxic in vivo is localized normally in cultured cellsHeather M Christensen, David A HarrisPlos One|October 8, 2011
The N-terminal, polybasic region is critical for prion protein neuroprotective activityJessie A Turnbaugh, Laura Westergard, Ursula Unterberger, et al.Molecular Microbiology|March 18, 2014
Extracellular environment modulates the formation and propagation of particular amyloid structuresLaura Westergard, Heather L TrueMolecular Microbiology|March 29, 2014
Wild yeast harbour a variety of distinct amyloid structures with strong prion-inducing capabilitiesLaura Westergard, Heather L TrueThe EMBO Journal|January 25, 2007
Neonatal lethality in transgenic mice expressing prion protein with a deletion of residues 105-125Aimin Li, Heather M Christensen, Leanne R Stewart, et al.The American Journal of Pathology|May 18, 2010
A highly toxic cellular prion protein induces a novel, nonapoptotic form of neuronal deathHeather M Christensen, Krikor Dikranian, Aimin Li, et al.Pageof 14