Associated Papers
Efficient induction of motor neuron disease in transgenic G93A SOD1 mice by prion-like seeding.
Xu G et al.
Prion, 2026
Contribution of A-to-I RNA editing, M6A RNA Methylation, and Alternative Splicing to physiological brain aging and neurodegenerative diseases.
Tassinari V et al.
Mechanisms of Ageing and Development, 2023
cGAS and DDX41-STING mediated intrinsic immunity spreads intercellularly to promote neuroinflammation in SOD1 ALS model.
Tan HY et al.
Iscience, 2022
The Role of VCP Mutations in the Spectrum of Amyotrophic Lateral Sclerosis-Frontotemporal Dementia.
Scarian E et al.
Frontiers in Neurology, 2022
Variation in the vulnerability of mice expressing human superoxide dismutase 1 to prion-like seeding: a study of the influence of primary amino acid sequence.
Ayers JI et al.
Acta Neuropathologica Communications, 2021
Are Astrocytes the Predominant Cell Type for Activation of Nrf2 in Aging and Neurodegeneration?
Liddell JR
Antioxidants (basel, Switzerland), 2017
Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS.
Ayers JI et al.
Acta Neuropathologica, 2016
Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathways.
Ayers JI et al.
Acta Neuropathologica, 2016
Genetic rodent models of amyotrophic lateral sclerosis.
Van Den Bosch L
Journal of Biomedicine & Biotechnology, 2011
Genetics of amyotrophic lateral sclerosis.
Siddique T et al.
Human Molecular Genetics, 1996
Superoxide dismutase and neurofilament transgenic models of amyotrophic lateral sclerosis.
Morrison BM et al.
The Journal of Experimental Zoology, 0
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