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P Spargo

Showing results (11-20 of 19) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 3, 2023
SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in <i>SOD1</i> amyotrophic lateral sclerosisThomas P Spargo, Sarah Opie-Martin, Guy P Hunt, et al.
Nucleic Acids Research|May 24, 2022
GEOexplorer: a webserver for gene expression analysis and visualisationGuy P Hunt, Luigi Grassi, Rafael Henkin, et al.
Brain Communications|January 16, 2025
Lipid-mediated resolution of inflammation and survival in amyotrophic lateral sclerosisOzlem Yildiz, Guy P Hunt, Johannes Schroth, et al.
Frontiers in Molecular Neuroscience|September 22, 2022
A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene <i>CFAP410</i> correlates with differential isoform expressionJack N G Marshall, Alexander Fröhlich, Li Li, et al.
Computational and Structural Biotechnology Journal|November 13, 2023
Molecular dynamics analysis of superoxide dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progressionMunishikha Kalia, Mattia Miotto, Deborah Ness, et al.
Cell Reports|March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's diseaseThomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Annals of Clinical and Translational Neurology|May 22, 2024
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALSHeather Marriott, Thomas P Spargo, Ahmad Al Khleifat, et al.
Nature Communications|July 2, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 3, 2023
SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in <i>SOD1</i> amyotrophic lateral sclerosisThomas P Spargo, Sarah Opie-Martin, Guy P Hunt, et al.
Nucleic Acids Research|May 24, 2022
GEOexplorer: a webserver for gene expression analysis and visualisationGuy P Hunt, Luigi Grassi, Rafael Henkin, et al.
Brain Communications|January 16, 2025
Lipid-mediated resolution of inflammation and survival in amyotrophic lateral sclerosisOzlem Yildiz, Guy P Hunt, Johannes Schroth, et al.
Frontiers in Molecular Neuroscience|September 22, 2022
A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene <i>CFAP410</i> correlates with differential isoform expressionJack N G Marshall, Alexander Fröhlich, Li Li, et al.
Computational and Structural Biotechnology Journal|November 13, 2023
Molecular dynamics analysis of superoxide dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progressionMunishikha Kalia, Mattia Miotto, Deborah Ness, et al.
Cell Reports|March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's diseaseThomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Annals of Clinical and Translational Neurology|May 22, 2024
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALSHeather Marriott, Thomas P Spargo, Ahmad Al Khleifat, et al.
Nature Communications|July 2, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Pageof 2