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R A Mackenzie

Showing results (131-140 of 155) with videos related to

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Acta Neuropathologica|February 20, 2016
Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUSMarc Suárez-Calvet, Manuela Neumann, Thomas Arzberger, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Neurology|November 4, 2009
The heritability and genetics of frontotemporal lobar degenerationJ D Rohrer, R Guerreiro, J Vandrovcova, et al.
Molecular Neurodegeneration|April 24, 2025
Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal healthJolien Perneel, Miranda Lastra Osua, Sara Alidadiani, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15Stephan Tetter, Nikhil R Varghese, Alexey G Murzin, et al.
Nature Neuroscience|June 1, 2021
Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathwayYen-Chen Lin, Meenakshi Sundaram Kumar, Nandini Ramesh, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
Annals of Neurology|May 1, 2007
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsIan R A Mackenzie, Eileen H Bigio, Paul G Ince, et al.
Cell|March 5, 2022
Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseasesAndrew Chang, Xinyu Xiang, Jing Wang, et al.
Acta Neuropathologica|November 19, 2008
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendationsIan R A Mackenzie, Manuela Neumann, Eileen H Bigio, et al.
Pageof 16

Showing results (131-140 of 155) with videos related to

Sort By:
Pageof 16
Acta Neuropathologica|February 20, 2016
Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUSMarc Suárez-Calvet, Manuela Neumann, Thomas Arzberger, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Neurology|November 4, 2009
The heritability and genetics of frontotemporal lobar degenerationJ D Rohrer, R Guerreiro, J Vandrovcova, et al.
Molecular Neurodegeneration|April 24, 2025
Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal healthJolien Perneel, Miranda Lastra Osua, Sara Alidadiani, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15Stephan Tetter, Nikhil R Varghese, Alexey G Murzin, et al.
Nature Neuroscience|June 1, 2021
Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathwayYen-Chen Lin, Meenakshi Sundaram Kumar, Nandini Ramesh, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
Annals of Neurology|May 1, 2007
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsIan R A Mackenzie, Eileen H Bigio, Paul G Ince, et al.
Cell|March 5, 2022
Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseasesAndrew Chang, Xinyu Xiang, Jing Wang, et al.
Acta Neuropathologica|November 19, 2008
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendationsIan R A Mackenzie, Manuela Neumann, Eileen H Bigio, et al.
Pageof 16