Follow
Laura Westergard
Title
Cited by
Cited by
Year
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
5542007
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
1062011
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
632011
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
502011
Extracellular environment modulates the formation and propagation of particular amyloid structures
L Westergard, HL True
Molecular microbiology 92 (4), 698-715, 2014
292014
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
242014
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
The system can't perform the operation now. Try again later.
Articles 1–9