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EMBO Molecular Medicine|November 9, 2017
G-quadruplex-binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivoRoberto Simone, Rubika Balendra, Thomas G Moens, et al.Journal of Neurology|March 10, 2011
A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromesJonathan D Rohrer, Jason D Warren, David Reiman, et al.Wellcome Open Research|October 25, 2017
The integration site of the APP transgene in the J20 mouse model of Alzheimer's diseaseJustin L Tosh, Matthew Rickman, Ellie Rhymes, et al.Acta Neuropathologica Communications|August 29, 2023
Repeat length of C9orf72-associated glycine-alanine polypeptides affects their toxicityJavier Morón-Oset, Lilly Katharina Sophie Fischer, Nathalie Jauré, et al.Brain : a Journal of Neurology|November 30, 2018
Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdownEmma L Clayton, Carmelo Milioto, Bhavana Muralidharan, et al.Neurobiology of Aging|April 17, 2013
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeatAshley R Jones, Ione Woollacott, Aleksey Shatunov, et al.Dementia and Geriatric Cognitive Disorders|February 10, 2009
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutationJonathan D Rohrer, R Laila Ahsan, Adrian M Isaacs, et al.Disease Models & Mechanisms|August 26, 2025
Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosisSevda Boyanova, Gareth Banks, Tatiana V Lipina, et al.Methods (San Diego, Calif.)|July 30, 2020
Sizing, stabilising, and cloning repeat-expansions for gene targeting constructsRemya R Nair, Charlotte Tibbit, David Thompson, et al.Molecular Neurodegeneration|May 4, 2023
Opinion: more mouse models and more translation needed for ALSElizabeth M C Fisher, Linda Greensmith, Andrea Malaspina, et al.Pageof 10