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Zebrafish Models for Human Skeletal Disorders

In 2019, the Nosology Committee of the International Skeletal Dysplasia Society provided an updated version of the Nosology and Classification of Genetic Skeletal Disorders. This is a reference list of recognized diseases in humans and their causal genes published to help clinician diagnosis and sci...

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Autores principales: Marí-Beffa, Manuel, Mesa-Román, Ana B., Duran, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418114/
https://www.ncbi.nlm.nih.gov/pubmed/34490030
http://dx.doi.org/10.3389/fgene.2021.675331
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author Marí-Beffa, Manuel
Mesa-Román, Ana B.
Duran, Ivan
author_facet Marí-Beffa, Manuel
Mesa-Román, Ana B.
Duran, Ivan
author_sort Marí-Beffa, Manuel
collection PubMed
description In 2019, the Nosology Committee of the International Skeletal Dysplasia Society provided an updated version of the Nosology and Classification of Genetic Skeletal Disorders. This is a reference list of recognized diseases in humans and their causal genes published to help clinician diagnosis and scientific research advances. Complementary to mammalian models, zebrafish has emerged as an interesting species to evaluate chemical treatments against these human skeletal disorders. Due to its versatility and the low cost of experiments, more than 80 models are currently available. In this article, we review the state-of-art of this “aquarium to bedside” approach describing the models according to the list provided by the Nosology Committee. With this, we intend to stimulate research in the appropriate direction to efficiently meet the actual needs of clinicians under the scope of the Nosology Committee.
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spelling pubmed-84181142021-09-05 Zebrafish Models for Human Skeletal Disorders Marí-Beffa, Manuel Mesa-Román, Ana B. Duran, Ivan Front Genet Genetics In 2019, the Nosology Committee of the International Skeletal Dysplasia Society provided an updated version of the Nosology and Classification of Genetic Skeletal Disorders. This is a reference list of recognized diseases in humans and their causal genes published to help clinician diagnosis and scientific research advances. Complementary to mammalian models, zebrafish has emerged as an interesting species to evaluate chemical treatments against these human skeletal disorders. Due to its versatility and the low cost of experiments, more than 80 models are currently available. In this article, we review the state-of-art of this “aquarium to bedside” approach describing the models according to the list provided by the Nosology Committee. With this, we intend to stimulate research in the appropriate direction to efficiently meet the actual needs of clinicians under the scope of the Nosology Committee. Frontiers Media S.A. 2021-08-05 /pmc/articles/PMC8418114/ /pubmed/34490030 http://dx.doi.org/10.3389/fgene.2021.675331 Text en Copyright © 2021 Marí-Beffa, Mesa-Román and Duran. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Marí-Beffa, Manuel
Mesa-Román, Ana B.
Duran, Ivan
Zebrafish Models for Human Skeletal Disorders
title Zebrafish Models for Human Skeletal Disorders
title_full Zebrafish Models for Human Skeletal Disorders
title_fullStr Zebrafish Models for Human Skeletal Disorders
title_full_unstemmed Zebrafish Models for Human Skeletal Disorders
title_short Zebrafish Models for Human Skeletal Disorders
title_sort zebrafish models for human skeletal disorders
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418114/
https://www.ncbi.nlm.nih.gov/pubmed/34490030
http://dx.doi.org/10.3389/fgene.2021.675331
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