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New Zebrafish Models for Mitochondrial Diseases

datacite.subject.fosCiências Médicas
dc.contributor.authorNogueira, Célia
dc.contributor.authorLaranjeira, Mateus
dc.contributor.authorPinho, Brígida
dc.contributor.authorMarchese, Maria
dc.contributor.authorPereira, Cristina
dc.contributor.authorAzevedo, L.
dc.contributor.authorOliveira, J.
dc.contributor.authorSantorelli, Filippo
dc.contributor.authorVilarinho, Laura
dc.date.accessioned2026-03-03T15:51:25Z
dc.date.available2026-03-03T15:51:25Z
dc.date.issued2025-03
dc.description.abstractIntroduction: Mitochondrial diseases (MD) are rare disorders with clinical and genetic heterogeneity and no effective therapies. Next Generation Sequencing has advanced MD diagnosis, although the interpretation of variants of unknown significance (VUS) remains a challenge (1). Functional validation is crucial for determining VUS pathogenicity, and zebrafish has emerged as a valuable organism to model MD, due to its conserved physiology and genetic similarity to humans. This project aims to functionally characterize four previously identified VUS in ACAD9 and TSFM using zebrafish as an in vivo model.eng
dc.description.sponsorshipThis Research Project (2023.12019.PEX) is supported by FCT, as well as the PhD student grant (2023.00457.BDANA)
dc.identifier.urihttp://hdl.handle.net/10400.18/11045
dc.language.isoeng
dc.peerreviewedn/a
dc.relation2023.12019.PEX
dc.relation.hasversionhttps://www.spdm.org.pt/media/6798/v41l_resumo_spdm2025_c.pdf
dc.rights.uriN/A
dc.subjectMitochondrial Diseases
dc.subjectDoenças Genéticas
dc.subjectRare Disorders
dc.subjectNext Generation Sequencing
dc.subjectMD Diagnosis
dc.titleNew Zebrafish Models for Mitochondrial Diseaseseng
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferenceDate2025-03
oaire.citation.conferencePlaceLisboa, Portugal
oaire.citation.title21st International Symposium da Sociedade Portuguesa de Doenças Metabólicas (SPDM), 27, 28 march 2025
oaire.versionhttp://purl.org/coar/version/c_be7fb7dd8ff6fe43

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