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Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish

A hexanucleotide repeat expansion within the C9orf72 gene is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and its discovery has revolutionized our understanding of this devastating disease. Model systems are a valuable tool for studying ALS pathobiology and potential therapie...

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Detalles Bibliográficos
Autores principales: Fortier, Gabrielle, Butti, Zoé, Patten, Shunmoogum A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589578/
https://www.ncbi.nlm.nih.gov/pubmed/33096681
http://dx.doi.org/10.3390/biomedicines8100440
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author Fortier, Gabrielle
Butti, Zoé
Patten, Shunmoogum A.
author_facet Fortier, Gabrielle
Butti, Zoé
Patten, Shunmoogum A.
author_sort Fortier, Gabrielle
collection PubMed
description A hexanucleotide repeat expansion within the C9orf72 gene is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and its discovery has revolutionized our understanding of this devastating disease. Model systems are a valuable tool for studying ALS pathobiology and potential therapies. The zebrafish (Danio rerio) has particularly become a useful model organism to study neurological diseases, including ALS, due to high genetic and physiological homology to mammals, and sensitivity to various genetic and pharmacological manipulations. In this review we summarize the zebrafish models that have been used to study the pathology of C9orf72-related ALS. We discuss their value in providing mechanistic insights and their potential use for drug discovery.
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spelling pubmed-75895782020-10-29 Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish Fortier, Gabrielle Butti, Zoé Patten, Shunmoogum A. Biomedicines Review A hexanucleotide repeat expansion within the C9orf72 gene is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and its discovery has revolutionized our understanding of this devastating disease. Model systems are a valuable tool for studying ALS pathobiology and potential therapies. The zebrafish (Danio rerio) has particularly become a useful model organism to study neurological diseases, including ALS, due to high genetic and physiological homology to mammals, and sensitivity to various genetic and pharmacological manipulations. In this review we summarize the zebrafish models that have been used to study the pathology of C9orf72-related ALS. We discuss their value in providing mechanistic insights and their potential use for drug discovery. MDPI 2020-10-21 /pmc/articles/PMC7589578/ /pubmed/33096681 http://dx.doi.org/10.3390/biomedicines8100440 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fortier, Gabrielle
Butti, Zoé
Patten, Shunmoogum A.
Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish
title Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish
title_full Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish
title_fullStr Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish
title_full_unstemmed Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish
title_short Modelling C9orf72-Related Amyotrophic Lateral Sclerosis in Zebrafish
title_sort modelling c9orf72-related amyotrophic lateral sclerosis in zebrafish
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589578/
https://www.ncbi.nlm.nih.gov/pubmed/33096681
http://dx.doi.org/10.3390/biomedicines8100440
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