The cellular prion protein (PrPC): its physiological function and role in disease L Westergard, HM Christensen, DA Harris Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1772 (6), 629-644, 2007 | 563 | 2007 |
A naturally occurring C-terminal fragment of the prion protein (PrP) delays disease and acts as a dominant-negative inhibitor of PrPSc formation L Westergard, JA Turnbaugh, DA Harris Journal of Biological Chemistry 286 (51), 44234-44242, 2011 | 107 | 2011 |
A nine amino acid domain is essential for mutant prion protein toxicity L Westergard, JA Turnbaugh, DA Harris Journal of Neuroscience 31 (39), 14005-14017, 2011 | 64 | 2011 |
The N-terminal, polybasic region is critical for prion protein neuroprotective activity JA Turnbaugh, L Westergard, U Unterberger, E Biasini, DA Harris PloS one 6 (9), e25675, 2011 | 50 | 2011 |
Extracellular environment modulates the formation and propagation of particular amyloid structures L Westergard, HL True Molecular microbiology 92 (4), 698-715, 2014 | 29 | 2014 |
Wild yeast harbour a variety of distinct amyloid structures with strong prion‐inducing capabilities L Westergard, HL True Molecular microbiology 92 (1), 183-193, 2014 | 23 | 2014 |
NEUROTOXIC AND NEUROPROTECTIVE ACTIVITIES OF THE PRION PROTEIN DA Harris, IH Solomon, JA Turnbaugh, T Massignan, L Westergard, ... JOURNAL OF NEUROCHEMISTRY 118, 177-177, 2011 | | 2011 |
The Polybasic N-terminal Region of the Prion Protein is Essential for its Neuroprotective Activity JA Turnbaugh, LC Westergard, DA Harris PRION 4 (3), 188-189, 2010 | | 2010 |
Prion Protein Domains Necessary for Mutant Toxicity and Scrapie Formation L Westergard | | 2009 |