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The predictive value of models of neuromuscular disorders to potentiate clinical translation
Neuromuscular disorders (NMDs) are a heterogenous group of rare inherited diseases that compromise the function of peripheral nerves and/or muscles. With limited treatment options available, there is a growing need to design effective preclinical studies that can lead to greater success in clinical...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Company of Biologists Ltd
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366891/ https://www.ncbi.nlm.nih.gov/pubmed/35912512 http://dx.doi.org/10.1242/dmm.049788 |
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author | van Putten, Maaike |
author_facet | van Putten, Maaike |
author_sort | van Putten, Maaike |
collection | PubMed |
description | Neuromuscular disorders (NMDs) are a heterogenous group of rare inherited diseases that compromise the function of peripheral nerves and/or muscles. With limited treatment options available, there is a growing need to design effective preclinical studies that can lead to greater success in clinical trials for novel therapeutics. Here, I discuss recent advances in modelling NMDs to improve preclinical studies as well as two articles from this issue that work in parallel to enable a deeper understanding of a particularly rare NMD, known as X-linked myotubular myopathy. |
format | Online Article Text |
id | pubmed-9366891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-93668912022-08-11 The predictive value of models of neuromuscular disorders to potentiate clinical translation van Putten, Maaike Dis Model Mech Editorial Neuromuscular disorders (NMDs) are a heterogenous group of rare inherited diseases that compromise the function of peripheral nerves and/or muscles. With limited treatment options available, there is a growing need to design effective preclinical studies that can lead to greater success in clinical trials for novel therapeutics. Here, I discuss recent advances in modelling NMDs to improve preclinical studies as well as two articles from this issue that work in parallel to enable a deeper understanding of a particularly rare NMD, known as X-linked myotubular myopathy. The Company of Biologists Ltd 2022-08-01 /pmc/articles/PMC9366891/ /pubmed/35912512 http://dx.doi.org/10.1242/dmm.049788 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Editorial van Putten, Maaike The predictive value of models of neuromuscular disorders to potentiate clinical translation |
title | The predictive value of models of neuromuscular disorders to potentiate clinical translation |
title_full | The predictive value of models of neuromuscular disorders to potentiate clinical translation |
title_fullStr | The predictive value of models of neuromuscular disorders to potentiate clinical translation |
title_full_unstemmed | The predictive value of models of neuromuscular disorders to potentiate clinical translation |
title_short | The predictive value of models of neuromuscular disorders to potentiate clinical translation |
title_sort | predictive value of models of neuromuscular disorders to potentiate clinical translation |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366891/ https://www.ncbi.nlm.nih.gov/pubmed/35912512 http://dx.doi.org/10.1242/dmm.049788 |
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