Publication: Zebrafish Models for Human Skeletal Disorders
| dc.contributor.author | Marí-Beffa, Manuel | |
| dc.contributor.author | Mesa-Román, Ana B. | |
| dc.contributor.author | Duran, 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.accessioned | 2024-02-19T15:30:28Z | |
| dc.date.available | 2024-02-19T15:30:28Z | |
| dc.date.issued | 2021-08-05 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | This 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.doi | 10.3389/fgene.2021.675331 | |
| dc.identifier.e-issn | 1664-8021 | es_ES |
| dc.identifier.journal | Frontiers in Genetics | es_ES |
| dc.identifier.other | http://hdl.handle.net/10668/4068 | |
| dc.identifier.pubmedID | 34490030 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/18427 | |
| dc.language.iso | eng | |
| dc.publisher | Frontiers Media | |
| dc.relation.publisherversion | https://www.frontiersin.org/articles/10.3389/fgene.2021.675331/full | es |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Attribution 4.0 International | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | Skeletal dysplasia | |
| dc.subject | Osteogenesis imperfecta | |
| dc.subject | Osteoporosis | |
| dc.subject | Skeletal ciliopathies | |
| dc.subject | Dwarfisms | |
| dc.subject | Dysostosis | |
| dc.subject | Osteopetrosis | |
| dc.subject | Zebrafish models | |
| dc.subject | Acrocefalosindactilia | |
| dc.subject | Dentinogénesis imperfecta | |
| dc.subject | Ciliopatías | |
| dc.subject | Disostosis | |
| dc.subject | Pez cebra | |
| dc.subject | Modelos animales | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Exome | |
| dc.subject.mesh | Genome-Wide Association Study | |
| dc.subject.mesh | Rare Diseases | |
| dc.subject.mesh | Osteoclasts | |
| dc.subject.mesh | Osteopetrosis | |
| dc.subject.mesh | Phenotype | |
| dc.subject.mesh | Achondroplasia | |
| dc.subject.mesh | Genotype | |
| dc.subject.mesh | Genetics | |
| dc.subject.mesh | Genomics | |
| dc.subject.mesh | Zebrafish | |
| dc.title | Zebrafish Models for Human Skeletal Disorders | |
| dc.type | review article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication | |
| relation.isPublisherOfPublication | 9f9fa5ea-093b-43d8-bf2c-5bd65d08a802 | |
| relation.isPublisherOfPublication.latestForDiscovery | 9f9fa5ea-093b-43d8-bf2c-5bd65d08a802 |


