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Briefings in Bioinformatics|November 9, 2014
Case study: using sequence homology to identify putative phosphorylation sites in an evolutionarily distant species (honeybee)Brett Trost, Scott Napper, Anthony KusalikClinical & Developmental Immunology|November 15, 2013
Evidence for prion-like mechanisms in several neurodegenerative diseases: potential implications for immunotherapyKristen Marciniuk, Ryan Taschuk, Scott NapperBioinformatics (Oxford, England)|March 10, 2015
EpIC: a rational pipeline for epitope immunogenicity characterizationKristen Marciniuk, Brett Trost, Scott NapperPlos One|April 6, 2016
Computational Analysis of the Predicted Evolutionary Conservation of Human Phosphorylation SitesBrett Trost, Anthony Kusalik, Scott NapperPhysical Chemistry Chemical Physics : PCCP|March 2, 2011
A theory for the anisotropic and inhomogeneous dielectric properties of proteinsWill C Guest, Neil R Cashman, Steven S PlotkinJournal of Toxicology and Environmental Health. Part A|January 11, 2011
Toward a mechanism of prion misfolding and structural models of PrP(Sc): current knowledge and future directionsWill C Guest, Steven S Plotkin, Neil R CashmanBiochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|May 11, 2010
Electrostatics in the stability and misfolding of the prion protein: salt bridges, self energy, and solvationWill C Guest, Neil R Cashman, Steven S PlotkinNeurobiology of Disease|February 22, 2015
From molecule to molecule and cell to cell: prion-like mechanisms in amyotrophic lateral sclerosisLeslie I Grad, Sarah M Fernando, Neil R CashmanExpert Review of Molecular Diagnostics|July 11, 2006
Current and future molecular diagnostics for prion diseasesMarty T Lehto, Harry E Peery, Neil R CashmanBiochemistry|August 16, 2008
Structural investigation of a phosphorylation-catalyzed, isoaspartate-free, protein succinimide: crystallographic structure of post-succinimide His15Asp histidine-containing proteinScott Napper, Lata Prasad, Louis T J DelbaerePageof 2,838