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Adrian M Isaacs

Showing results (31-40 of 96) with videos related to

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Molecular and Cellular Neurosciences|October 3, 2002
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathyAdrian M Isaacs, Alexander Jeans, Peter L Oliver, 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.
Journal of Neurology|March 10, 2011
A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromesJonathan D Rohrer, Jason D Warren, David Reiman, et al.
Brain : a Journal of Neurology|August 10, 2010
Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathologyClement T Loy, Elizabeth McCusker, Jillian J Kril, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2010
The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Janice Holton, et al.
Acta Neuropathologica Communications|April 20, 2017
Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degenerationSarah Mizielinska, Charlotte E Ridler, Rubika Balendra, et al.
Wellcome Open Research|October 25, 2017
The integration site of the <i>APP</i> transgene in the J20 mouse model of Alzheimer's diseaseJustin L Tosh, Matthew Rickman, Ellie Rhymes, et al.
Acta Neuropathologica Communications|August 29, 2023
Repeat length of C9orf72-associated glycine-alanine polypeptides affects their toxicityJavier Morón-Oset, Lilly Katharina Sophie Fischer, Nathalie Jauré, et al.
Brain : a Journal of Neurology|November 30, 2018
Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdownEmma L Clayton, Carmelo Milioto, Bhavana Muralidharan, et al.
Dementia and Geriatric Cognitive Disorders|February 10, 2009
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutationJonathan D Rohrer, R Laila Ahsan, Adrian M Isaacs, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Molecular and Cellular Neurosciences|October 3, 2002
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathyAdrian M Isaacs, Alexander Jeans, Peter L Oliver, 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.
Journal of Neurology|March 10, 2011
A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromesJonathan D Rohrer, Jason D Warren, David Reiman, et al.
Brain : a Journal of Neurology|August 10, 2010
Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathologyClement T Loy, Elizabeth McCusker, Jillian J Kril, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2010
The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Janice Holton, et al.
Acta Neuropathologica Communications|April 20, 2017
Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degenerationSarah Mizielinska, Charlotte E Ridler, Rubika Balendra, et al.
Wellcome Open Research|October 25, 2017
The integration site of the <i>APP</i> transgene in the J20 mouse model of Alzheimer's diseaseJustin L Tosh, Matthew Rickman, Ellie Rhymes, et al.
Acta Neuropathologica Communications|August 29, 2023
Repeat length of C9orf72-associated glycine-alanine polypeptides affects their toxicityJavier Morón-Oset, Lilly Katharina Sophie Fischer, Nathalie Jauré, et al.
Brain : a Journal of Neurology|November 30, 2018
Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdownEmma L Clayton, Carmelo Milioto, Bhavana Muralidharan, et al.
Dementia and Geriatric Cognitive Disorders|February 10, 2009
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutationJonathan D Rohrer, R Laila Ahsan, Adrian M Isaacs, et al.
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