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J Cauchi

Showing results (41-50 of 47) with videos related to

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Iscience|January 14, 2020
Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN MutantMarie Antoine, Kristin L Patrick, Johann Soret, et al.
European Journal of Human Genetics : EJHG|January 8, 2021
Genetic analysis of ALS cases in the isolated island population of MaltaRebecca Borg, Maia Farrugia Wismayer, Karl Bonavia, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2023
An activator of voltage-gated K<sup>+</sup> channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1Ilenio Servettini, Giuseppe Talani, Alfredo Megaro, et al.
Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Nature Genetics|February 1, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Iscience|January 14, 2020
Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN MutantMarie Antoine, Kristin L Patrick, Johann Soret, et al.
European Journal of Human Genetics : EJHG|January 8, 2021
Genetic analysis of ALS cases in the isolated island population of MaltaRebecca Borg, Maia Farrugia Wismayer, Karl Bonavia, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2023
An activator of voltage-gated K<sup>+</sup> channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1Ilenio Servettini, Giuseppe Talani, Alfredo Megaro, et al.
Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Nature Genetics|February 1, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
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