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The Journal of Biological Chemistry|November 18, 2015
Proteolytic Processing of Neuregulin 1 Type III by Three Intramembrane-cleaving ProteasesDaniel Fleck, Matthias Voss, Ben Brankatschk, et al.Autophagy|September 24, 2024
Poly-GP accumulation due to C9orf72 loss of function induces motor neuron apoptosis through autophagy and mitophagy defectsHortense de Calbiac, Solène Renault, Grégoire Haouy, et al.EMBO Molecular Medicine|April 30, 2020
Synaptic dysfunction induced by glycine-alanine dipeptides in C9orf72-ALS/FTD is rescued by SV2 replenishmentBrigid K Jensen, Martin H Schuldi, Kevin McAvoy, et al.The EMBO Journal|September 28, 2011
microRNA-34c is a novel target to treat dementiasAthanasios Zovoilis, Hope Y Agbemenyah, Roberto C Agis-Balboa, et al.Acta Neuropathologica|February 6, 2013
hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutationsKohji Mori, Sven Lammich, Ian R A Mackenzie, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 3, 2013
Dual cleavage of neuregulin 1 type III by BACE1 and ADAM17 liberates its EGF-like domain and allows paracrine signalingDaniel Fleck, Frauke van Bebber, Alessio Colombo, et al.Acta Neuropathologica Communications|August 5, 2018
Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriersPetra Frick, Chantal Sellier, Ian R A Mackenzie, et al.Brain : a Journal of Neurology|May 29, 2014
Sequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansionsJohnathan Cooper-Knock, Matthew J Walsh, Adrian Higginbottom, et al.Proceedings of the National Academy of Sciences of the United States of America|February 9, 2012
MicroRNA-132 dysregulation in schizophrenia has implications for both neurodevelopment and adult brain functionBrooke H Miller, Zane Zeier, Li Xi, et al.Life Science Alliance|July 1, 2022
Multi-omics profiling identifies a deregulated FUS-MAP1B axis in ALS/FTD-associated UBQLN2 mutantsLaura Strohm, Zehan Hu, Yongwon Suk, et al.Pageof 11