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Journal of Molecular Neuroscience : MN|May 24, 2011
Novel types of frontotemporal lobar degeneration: beyond tau and TDP-43Ian R A Mackenzie, Manuela Neumann, Nigel J Cairns, et al.
Acta Neuropathologica Communications|February 14, 2019
Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUSLauren M Gittings, Sandrine C Foti, Bridget C Benson, et al.
Acta Neuropathologica|October 31, 2013
C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA fociSarah Mizielinska, Tammaryn Lashley, Frances E Norona, et al.
Developmental Cell|June 25, 2026
The ALS- and FTD-associated proteins annexin A11 and CHMP2B act sequentially in plasma membrane repairCatherine M Heffner, Georgina P Starling, Lorian C Straker, et al.
Scientific Reports|December 25, 2012
C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexesPietro Fratta, Sarah Mizielinska, Andrew J Nicoll, et al.
Life Science Alliance|June 12, 2023
Toxicity of C9orf72-associated dipeptide repeat peptides is modified by commonly used protein tagsJavier Morón-Oset, Lilly Ks Fischer, Mireia Carcolé, et al.
Neuroimage|January 20, 2009
Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriersSimon F Eskildsen, Lasse R Østergaard, Anders B Rodell, et al.
Nature Communications|December 13, 2023
The ALS/FTD-related C9orf72 hexanucleotide repeat expansion forms RNA condensates through multimolecular G-quadruplexesFederica Raguseo, Yiran Wang, Jessica Li, et al.
The Lancet. Neurology|February 22, 2025
Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeuticsSarah Mizielinska, Guillaume M Hautbergue, Tania F Gendron, et al.
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