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.contributor.funder | 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.date.accessioned | 2022-09-20T06:08:52Z | |
dc.date.available | 2022-09-20T06:08:52Z | |
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. | es_ES |
dc.description.version | Yes | es_ES |
dc.identifier.citation | Marí-Beffa M, Mesa-Román AB, Duran I. Zebrafish Models for Human Skeletal Disorders. Front Genet. 2021 Aug 5;12:675331 | es_ES |
dc.identifier.doi | 10.3389/fgene.2021.675331 | es_ES |
dc.identifier.essn | 1664-8021 | |
dc.identifier.pmc | PMC8418114 | |
dc.identifier.pmid | 34490030 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10668/4068 | |
dc.journal.title | Frontiers in Genetics | |
dc.language.iso | en | |
dc.page.number | 17 p. | |
dc.publisher | Frontiers | es_ES |
dc.relation.publisherversion | https://www.frontiersin.org/articles/10.3389/fgene.2021.675331/full | es_ES |
dc.rights | Atribución 4.0 Internacional | * |
dc.rights.accessRights | Acceso abierto | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | Skeletal dysplasia | es_ES |
dc.subject | Osteogenesis imperfecta | es_ES |
dc.subject | Osteoporosis | es_ES |
dc.subject | Skeletal ciliopathies | es_ES |
dc.subject | Dwarfisms | es_ES |
dc.subject | Dysostosis | es_ES |
dc.subject | Osteopetrosis | es_ES |
dc.subject | Zebrafish models | es_ES |
dc.subject | Acrocefalosindactilia | es_ES |
dc.subject | Dentinogénesis imperfecta | es_ES |
dc.subject | Ciliopatías | es_ES |
dc.subject | Disostosis | es_ES |
dc.subject | Pez cebra | es_ES |
dc.subject | Modelos animales | es_ES |
dc.subject.mesh | Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans | es_ES |
dc.subject.mesh | Medical Subject Headings::Persons::Persons::Age Groups::Adult | es_ES |
dc.subject.mesh | Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Exome | es_ES |
dc.subject.mesh | Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Genetic Association Studies::Genome-Wide Association Study | es_ES |
dc.subject.mesh | Medical Subject Headings::Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Rare Diseases | es_ES |
dc.subject.mesh | Medical Subject Headings::Anatomy::Cells::Connective Tissue Cells::Macrophages::Osteoclasts | es_ES |
dc.subject.mesh | Medical Subject Headings::Diseases::Musculoskeletal Diseases::Bone Diseases::Bone Diseases, Developmental::Osteochondrodysplasias::Osteosclerosis::Osteopetrosis | es_ES |
dc.subject.mesh | Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Phenotype | es_ES |
dc.subject.mesh | Medical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Dwarfism::Achondroplasia | es_ES |
dc.subject.mesh | Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype | es_ES |
dc.subject.mesh | Medical Subject Headings::Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics | es_ES |
dc.subject.mesh | Medical Subject Headings::Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genomics | es_ES |
dc.subject.mesh | Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Fishes::Cypriniformes::Cyprinidae::Zebrafish | es_ES |
dc.title | Zebrafish Models for Human Skeletal Disorders | es_ES |
dc.type | review article | |
dc.type.hasVersion | VoR | |
dspace.entity.type | Publication |
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