Publication:
Zebrafish Models for Human Skeletal Disorders

dc.contributor.authorMarí-Beffa, Manuel
dc.contributor.authorMesa-Román, Ana B.
dc.contributor.authorDuran, Ivan
dc.contributor.authoraffiliation[Marí-Beffa,M; Mesa-Román,AB; Duran,I] Department of Cell Biology, Genetics and Physiology, Faculty of Sciences, University of Málaga, IBIMA, Málaga, Spain. [Marí-Beffa,M; Duran,I] Networking Biomedical Research Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Andalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.
dc.date.accessioned2024-02-19T15:30:28Z
dc.date.available2024-02-19T15:30:28Z
dc.date.issued2021-08-05
dc.description.abstractIn 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.
dc.description.sponsorshipThis research is supported by grants PIGE-0178-2020, PID2020-117255RB-100, UMA18-FEDERJA-177, UMA18-FEDERJA-274, and CV20-81404 from Junta de Andalucía and the support of the Fundación AHUCE through a funding contract for OI research.
dc.identifier.doi10.3389/fgene.2021.675331
dc.identifier.e-issn1664-8021es_ES
dc.identifier.journalFrontiers in Geneticses_ES
dc.identifier.otherhttp://hdl.handle.net/10668/4068
dc.identifier.pubmedID34490030es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/18427
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fgene.2021.675331/fulles
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSkeletal dysplasia
dc.subjectOsteogenesis imperfecta
dc.subjectOsteoporosis
dc.subjectSkeletal ciliopathies
dc.subjectDwarfisms
dc.subjectDysostosis
dc.subjectOsteopetrosis
dc.subjectZebrafish models
dc.subjectAcrocefalosindactilia
dc.subjectDentinogénesis imperfecta
dc.subjectCiliopatías
dc.subjectDisostosis
dc.subjectPez cebra
dc.subjectModelos animales
dc.subject.meshHumans
dc.subject.meshAdult
dc.subject.meshExome
dc.subject.meshGenome-Wide Association Study
dc.subject.meshRare Diseases
dc.subject.meshOsteoclasts
dc.subject.meshOsteopetrosis
dc.subject.meshPhenotype
dc.subject.meshAchondroplasia
dc.subject.meshGenotype
dc.subject.meshGenetics
dc.subject.meshGenomics
dc.subject.meshZebrafish
dc.titleZebrafish Models for Human Skeletal Disorders
dc.typereview article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isPublisherOfPublication9f9fa5ea-093b-43d8-bf2c-5bd65d08a802
relation.isPublisherOfPublication.latestForDiscovery9f9fa5ea-093b-43d8-bf2c-5bd65d08a802

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