Variation in the Biochemical/Biophysical Properties of Mutant Superoxide Dismutase 1 Enzymes and the Rate of Disease Progression in Familial Amyotrophic Lateral Sclerosis KindredsTamara Ratovitski, David Borchelt, JJ Strain et al.|Human Molecular Genetics|1999Cited by 184
Superoxide dismutase 1 encoding mutations linked to ALS adopts a spectrum of misfolded statesMercedes Prudencio, David Borchelt|Molecular Neurodegeneration|2011Cited by 68
Disease-associated Mutations at Copper Ligand Histidine Residues of Superoxide Dismutase 1 Diminish the Binding of Copper and Compromise Dimer StabilityJiou Wang, David Borchelt|Journal of Biological Chemistry|2006Cited by 54
Transgenic mice expressing caspase-6-derived N-terminal fragments of mutant huntingtin develop neurologic abnormalities with predominant cytoplasmic inclusion pathology composed largely of a smaller proteolytic derivativeAndrew T.N. Tebbenkamp, David Borchelt|Human Molecular Genetics|2011Cited by 41
Collusion of α-Synuclein and Aβ aggravating co-morbidities in a novel prion-type mouse modelGrace M. Lloyd, David Borchelt|Molecular Neurodegeneration|2021Cited by 24