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Matthieu Moisse

Showing results (41-50 of 66) with videos related to

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Science Advances|April 10, 2021
<i>C9orf72</i>-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motilityLaura Fumagalli, Florence L Young, Steven Boeynaems, et al.
Cell Reports|February 28, 2019
Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral SclerosisJohnathan Cooper-Knock, Tobias Moll, Tennore Ramesh, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 22, 2022
CRISPR/Cas9 screen in human iPSC-derived cortical neurons identifies NEK6 as a novel disease modifier of C9orf72 poly(PR) toxicityWenting Guo, Haibo Wang, Arun Kumar Tharkeshwar, et al.
International Journal of Cancer|June 24, 2015
Genetic variants in VEGF pathway genes in neoadjuvant breast cancer patients receiving bevacizumab: Results from the randomized phase III GeparQuinto studyAlexander Hein, Diether Lambrechts, Gunter von Minckwitz, et al.
Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Annals of Neurology|January 3, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease SeverityMatthieu Moisse, Ramona A J Zwamborn, Joke van Vugt, et al.
Brain : a Journal of Neurology|April 12, 2023
Genetic variability in sporadic amyotrophic lateral sclerosisSien Hilde Van Daele, Matthieu Moisse, Joke J F A van Vugt, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 14, 2017
Reconsidering the causality of TIA1 mutations in ALSRick A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Brain Communications|September 21, 2020
<i>ATXN1</i> repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalizationGijs H P Tazelaar, Steven Boeynaems, Mathias De Decker, et al.
Nature Neuroscience|April 1, 2022
Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALSChen Eitan, Aviad Siany, Elad Barkan, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Science Advances|April 10, 2021
<i>C9orf72</i>-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motilityLaura Fumagalli, Florence L Young, Steven Boeynaems, et al.
Cell Reports|February 28, 2019
Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral SclerosisJohnathan Cooper-Knock, Tobias Moll, Tennore Ramesh, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 22, 2022
CRISPR/Cas9 screen in human iPSC-derived cortical neurons identifies NEK6 as a novel disease modifier of C9orf72 poly(PR) toxicityWenting Guo, Haibo Wang, Arun Kumar Tharkeshwar, et al.
International Journal of Cancer|June 24, 2015
Genetic variants in VEGF pathway genes in neoadjuvant breast cancer patients receiving bevacizumab: Results from the randomized phase III GeparQuinto studyAlexander Hein, Diether Lambrechts, Gunter von Minckwitz, et al.
Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Annals of Neurology|January 3, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease SeverityMatthieu Moisse, Ramona A J Zwamborn, Joke van Vugt, et al.
Brain : a Journal of Neurology|April 12, 2023
Genetic variability in sporadic amyotrophic lateral sclerosisSien Hilde Van Daele, Matthieu Moisse, Joke J F A van Vugt, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 14, 2017
Reconsidering the causality of TIA1 mutations in ALSRick A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Brain Communications|September 21, 2020
<i>ATXN1</i> repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalizationGijs H P Tazelaar, Steven Boeynaems, Mathias De Decker, et al.
Nature Neuroscience|April 1, 2022
Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALSChen Eitan, Aviad Siany, Elad Barkan, et al.
Pageof 7