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Adrian M Isaacs

Showing results (51-60 of 96) with videos related to

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Science Advances|August 22, 2025
An alternative cytoplasmic SFPQ isoform with reduced phase separation potential is up-regulated in ALSJacob Neeves, Marija Petrić Howe, Oliver J Ziff, et al.
The Lancet. Neurology|February 2, 2015
C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosisJonathan D Rohrer, Adrian M Isaacs, Sarah Mizielinska, et al.
Neuropathology and Applied Neurobiology|April 23, 2014
Adult polyglucosan body disease with GBE1 haploinsufficiency and concomitant frontotemporal lobar degenerationEsther N Bit-Ivan, Kyung-Hwa Lee, Darren Gitelman, et al.
Plos Genetics|September 21, 2023
A monocarboxylate transporter rescues frontotemporal dementia and Alzheimer's disease modelsDongwei Xu, Alec Vincent, Andrés González-Gutiérrez, et al.
Acta Neurologica Scandinavica|January 8, 2022
Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survivalPeter Roos, Peter Johannsen, Suzanne G Lindquist, et al.
Life Science Alliance|July 12, 2023
Transcriptome-wide RNA binding analysis of C9orf72 poly(PR) dipeptidesRubika Balendra, Igor Ruiz de Los Mozos, Hana M Odeh, et al.
Acta Neuropathologica|September 12, 2015
Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathologyEmma L Clayton, Sarah Mizielinska, James R Edgar, et al.
Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology|February 28, 2012
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic miceShabnam Ghazi-Noori, Kristina E Froud, Sarah Mizielinska, et al.
Frontiers in Neuroscience|September 20, 2021
Dysregulation in Subcellular Localization of Myelin Basic Protein mRNA Does Not Result in Altered Myelination in Amyotrophic Lateral SclerosisSamantha K Barton, Jenna M Gregory, Bhuvaneish T Selvaraj, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Science Advances|August 22, 2025
An alternative cytoplasmic SFPQ isoform with reduced phase separation potential is up-regulated in ALSJacob Neeves, Marija Petrić Howe, Oliver J Ziff, et al.
The Lancet. Neurology|February 2, 2015
C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosisJonathan D Rohrer, Adrian M Isaacs, Sarah Mizielinska, et al.
Neuropathology and Applied Neurobiology|April 23, 2014
Adult polyglucosan body disease with GBE1 haploinsufficiency and concomitant frontotemporal lobar degenerationEsther N Bit-Ivan, Kyung-Hwa Lee, Darren Gitelman, et al.
Plos Genetics|September 21, 2023
A monocarboxylate transporter rescues frontotemporal dementia and Alzheimer's disease modelsDongwei Xu, Alec Vincent, Andrés González-Gutiérrez, et al.
Acta Neurologica Scandinavica|January 8, 2022
Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survivalPeter Roos, Peter Johannsen, Suzanne G Lindquist, et al.
Life Science Alliance|July 12, 2023
Transcriptome-wide RNA binding analysis of C9orf72 poly(PR) dipeptidesRubika Balendra, Igor Ruiz de Los Mozos, Hana M Odeh, et al.
Acta Neuropathologica|September 12, 2015
Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathologyEmma L Clayton, Sarah Mizielinska, James R Edgar, et al.
Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology|February 28, 2012
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic miceShabnam Ghazi-Noori, Kristina E Froud, Sarah Mizielinska, et al.
Frontiers in Neuroscience|September 20, 2021
Dysregulation in Subcellular Localization of Myelin Basic Protein mRNA Does Not Result in Altered Myelination in Amyotrophic Lateral SclerosisSamantha K Barton, Jenna M Gregory, Bhuvaneish T Selvaraj, et al.
Pageof 10