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Plos One|January 28, 2014
A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defectsThomas Ricketts, Philip McGoldrick, Pietro Fratta, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 17, 2019
Uses for humanised mouse models in precision medicine for neurodegenerative diseaseRemya R Nair, Silvia Corrochano, Samanta Gasco, 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.Neurobiology of Aging|January 28, 2014
Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathyAndrea Cortese, Vincent Plagnol, Stefen Brady, et al.Acta Neuropathologica|July 18, 2021
HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicingAlexander Bampton, Ariana Gatt, Jack Humphrey, et al.Brain Communications|October 21, 2022
NOS1AP is a novel molecular target and critical factor in TDP-43 pathologySara Cappelli, Alida Spalloni, Fabian Feiguin, et al.Neuron|March 29, 2025
Seeded aggregation of TDP-43 induces its loss of function and reveals early pathological signaturesCarlo Scialò, Weijia Zhong, Somanath Jagannath, et al.Communications Biology|September 2, 2021
ALS-related FUS mutations alter axon growth in motoneurons and affect HuD/ELAVL4 and FMRP activityMaria Giovanna Garone, Nicol Birsa, Maria Rosito, et al.Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.Biorxiv : the Preprint Server for Biology|December 3, 2025
Sensitivity to TDP-43 loss and degradation resistance determine cryptic exon biomarker potentialAnna-Leigh Brown, Matteo Zanovello, Alla Mikheenko, et al.Pageof 12