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Molecular Neurodegeneration|July 17, 2013
Overcoming barriers and thresholds - signaling of oligomeric Aβ through the prion protein to FynHansen Wang, Carl He Ren, C Geeth Gunawardana, et al.Plos Computational Biology|March 12, 2021
Aggregation of Aβ40/42 chains in the presence of cyclic neuropeptides investigated by molecular dynamics simulationsMin Wu, Lyudmyla Dorosh, Gerold Schmitt-Ulms, et al.Plos One|September 29, 2009
Evolutionary descent of prion genes from the ZIP family of metal ion transportersGerold Schmitt-Ulms, Sepehr Ehsani, Joel C Watts, et al.Plos One|August 20, 2015
The Prion Protein Controls Polysialylation of Neural Cell Adhesion Molecule 1 during Cellular MorphogenesisMohadeseh Mehrabian, Dylan Brethour, Hansen Wang, et al.Arxiv|January 29, 2025
A unified model for the origins of spongiform degeneration and other neuropathological features in prion diseasesGerold Schmitt-Ulms, Xinzhu Wang, Joel Watts, et al.Plos One|May 29, 2019
The human brain somatostatin interactome: SST binds selectively to P-type family ATPasesMichael Solarski, Declan Williams, Mohadeseh Mehrabian, et al.Journal of Proteome Research|August 13, 2009
Peptide separations by on-line MudPIT compared to isoelectric focusing in an off-gel format: application to a membrane-enriched fraction from C2C12 mouse skeletal muscle cellsSarah Elschenbroich, Vladimir Ignatchenko, Parveen Sharma, et al.Plos One|September 24, 2024
Update on a brain-penetrant cardiac glycoside that can lower cellular prion protein levels in human and guinea pig paradigmsShehab Eid, Wenda Zhao, Declan Williams, et al.Analytical Chemistry|November 21, 2009
Method for the affinity purification of covalently linked peptides following cyanogen bromide cleavage of proteinsTujin Shi, Rasanjala Weerasekera, Chen Yan, et al.Plos One|June 22, 2016
Prion Protein Deficiency Causes Diverse Proteome Shifts in Cell Models That Escape Detection in Brain TissueMohadeseh Mehrabian, Dylan Brethour, Declan Williams, et al.Pageof 9