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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 19, 2008
Amyloid pathology is associated with progressive monoaminergic neurodegeneration in a transgenic mouse model of Alzheimer's diseaseYing Liu, Mi-Jeong Yoo, Alena Savonenko, et al.
Biochemistry|February 21, 2009
Structural and biophysical properties of the pathogenic SOD1 variant H46R/H48QDuane D Winkler, Jonathan P Schuermann, Xiaohang Cao, et al.
Plos One|August 7, 2008
Messenger RNA oxidation occurs early in disease pathogenesis and promotes motor neuron degeneration in ALSYueming Chang, Qiongman Kong, Xiu Shan, et al.
The Journal of Biological Chemistry|February 17, 1995
Superoxide dismutase 1 subunits with mutations linked to familial amyotrophic lateral sclerosis do not affect wild-type subunit functionD R Borchelt, M Guarnieri, P C Wong, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 1, 2013
Reversible pathologic and cognitive phenotypes in an inducible model of Alzheimer-amyloidosisTatiana Melnikova, Susan Fromholt, HyunSu Kim, et al.
Human Molecular Genetics|November 16, 2001
Hyper-expression of human apolipoprotein E4 in astroglia and neurons does not enhance amyloid deposition in transgenic miceC Lesuisse, G Xu, J Anderson, et al.
The Journal of Comparative Neurology|February 16, 2016
Heterogeneity of Matrin 3 in the developing and aging murine central nervous systemSruti Rayaprolu, Simon D'Alton, Keith Crosby, et al.
Acta Neuropathologica Communications|April 8, 2020
Diversity in Aβ deposit morphology and secondary proteome insolubility across models of Alzheimer-type amyloidosisGuilian Xu, Susan E Fromholt, Paramita Chakrabarty, et al.
Acta Neuropathologica Communications|July 23, 2023
Carboxyl truncation of α-synuclein occurs early and is influenced by human APOE genotype in transgenic mouse models of α-synuclein pathogenesisGrace M Lloyd, Brooke Long, Stephan Quintin, et al.
Cell Cycle (Georgetown, Tex.)|December 25, 2007
N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's diseaseTamara Ratovitski, Masayuki Nakamura, James D'Ambola, et al.
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