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Handbook of Clinical Neurology|June 12, 2018
Prion-like mechanisms in amyotrophic lateral sclerosisJacob I Ayers, Neil R Cashman
Trends in Neurosciences|May 1, 2020
Proteome Homeostasis Dysfunction: A Unifying Principle in ALS PathogenesisJustin J Yerbury, Natalie E Farrawell, Luke McAlary
Proceedings of the National Academy of Sciences of the United States of America|September 21, 2011
Intermolecular transmission of superoxide dismutase 1 misfolding in living cellsLeslie I Grad, Will C Guest, Anat Yanai, et al.
Molecular Neurodegeneration|March 28, 2020
Cerebrovascular amyloid Angiopathy in bioengineered vessels is reduced by high-density lipoprotein particles enriched in Apolipoprotein EJerome Robert, Emily B Button, Emma M Martin, et al.
Protein Science : a Publication of the Protein Society|June 25, 2004
The effects of nonnative interactions on protein folding rates: theory and simulationCecilia Clementi, Steven S Plotkin
Journal of Molecular Biology|January 8, 2013
Mechanical probes of SOD1 predict systematic trends in metal and dimer affinity of ALS-associated mutantsAtanu Das, Steven S Plotkin
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2013
SOD1 exhibits allosteric frustration to facilitate metal binding affinityAtanu Das, Steven S Plotkin
Immunotherapy|July 20, 2010
Immunotherapy for prion diseases: opportunities and obstaclesLi Li, Scott Napper, Neil R Cashman
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