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.contributor.funderThis 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.date.accessioned2022-09-20T06:08:52Z
dc.date.available2022-09-20T06:08:52Z
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.es_ES
dc.description.versionYeses_ES
dc.identifier.citationMarí-Beffa M, Mesa-Román AB, Duran I. Zebrafish Models for Human Skeletal Disorders. Front Genet. 2021 Aug 5;12:675331es_ES
dc.identifier.doi10.3389/fgene.2021.675331es_ES
dc.identifier.essn1664-8021
dc.identifier.pmcPMC8418114
dc.identifier.pmid34490030es_ES
dc.identifier.urihttp://hdl.handle.net/10668/4068
dc.journal.titleFrontiers in Genetics
dc.language.isoen
dc.page.number17 p.
dc.publisherFrontierses_ES
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fgene.2021.675331/fulles_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.accessRightsAcceso abiertoes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSkeletal dysplasiaes_ES
dc.subjectOsteogenesis imperfectaes_ES
dc.subjectOsteoporosises_ES
dc.subjectSkeletal ciliopathieses_ES
dc.subjectDwarfismses_ES
dc.subjectDysostosises_ES
dc.subjectOsteopetrosises_ES
dc.subjectZebrafish modelses_ES
dc.subjectAcrocefalosindactiliaes_ES
dc.subjectDentinogénesis imperfectaes_ES
dc.subjectCiliopatíases_ES
dc.subjectDisostosises_ES
dc.subjectPez cebraes_ES
dc.subjectModelos animaleses_ES
dc.subject.meshMedical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humanses_ES
dc.subject.meshMedical Subject Headings::Persons::Persons::Age Groups::Adultes_ES
dc.subject.meshMedical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Exomees_ES
dc.subject.meshMedical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Genetic Association Studies::Genome-Wide Association Studyes_ES
dc.subject.meshMedical Subject Headings::Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Rare Diseaseses_ES
dc.subject.meshMedical Subject Headings::Anatomy::Cells::Connective Tissue Cells::Macrophages::Osteoclastses_ES
dc.subject.meshMedical Subject Headings::Diseases::Musculoskeletal Diseases::Bone Diseases::Bone Diseases, Developmental::Osteochondrodysplasias::Osteosclerosis::Osteopetrosises_ES
dc.subject.meshMedical Subject Headings::Phenomena and Processes::Genetic Phenomena::Phenotypees_ES
dc.subject.meshMedical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Dwarfism::Achondroplasiaes_ES
dc.subject.meshMedical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotypees_ES
dc.subject.meshMedical Subject Headings::Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Geneticses_ES
dc.subject.meshMedical Subject Headings::Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genomicses_ES
dc.subject.meshMedical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Fishes::Cypriniformes::Cyprinidae::Zebrafishes_ES
dc.titleZebrafish Models for Human Skeletal Disorderses_ES
dc.typereview article
dc.type.hasVersionVoR
dspace.entity.typePublication

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