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Neurobiology of Aging|February 14, 2021
Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosisSandrine Chan Moi Fat, Emily P McCann, Kelly L Williams, et al.
Neuro-Degenerative Diseases|November 14, 2017
Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral SclerosisJennifer A Fifita, Katharine Y Zhang, Jasmin Galper, et al.
Molecular Brain|August 21, 2021
Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivoMaxinne Watchon, Luan Luu, Katherine J Robinson, et al.
Brain Pathology (Zurich, Switzerland)|December 20, 2023
Distribution of ubiquilin 2 and TDP-43 aggregates throughout the CNS in UBQLN2 p.T487I-linked amyotrophic lateral sclerosis and frontotemporal dementiaLaura R Nementzik, Kyrah M Thumbadoo, Helen C Murray, et al.
Biology Open|February 20, 2016
Genetic basis of hindlimb loss in a naturally occurring vertebrate modelEmily K Don, Tanya A de Jong-Curtain, Karen Doggett, et al.
Brain : a Journal of Neurology|July 15, 2005
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutationsKumaraswamy Sivakumar, Theodoros Kyriakides, Imke Puls, et al.
Scientific Reports|June 6, 2019
Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expressionIngrid S Tarr, Emily P McCann, Beben Benyamin, et al.
Brain : a Journal of Neurology|November 16, 2022
Novel gene-intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathyAnthony N Cutrupi, Ramesh K Narayanan, Gonzalo Perez-Siles, et al.
Plos Genetics|July 21, 2016
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3Megan H Brewer, Rabia Chaudhry, Jessica Qi, et al.
Zebrafish|October 10, 2018
Motor Neuron Abnormalities Correlate with Impaired Movement in Zebrafish that Express Mutant Superoxide Dismutase 1Katherine J Robinson, Kristy C Yuan, Emily K Don, et al.
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