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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/218527
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dc.contributor.authorBousquets Muñoz, Pablo-
dc.contributor.authorMolina, Òscar-
dc.contributor.authorVarela, Ignacio-
dc.contributor.authorÁlvarez-Eguiluz, Ángel-
dc.contributor.authorFernández-Mateos, Javier-
dc.contributor.authorGómez, Ana-
dc.contributor.authorSánchez, Elena G.-
dc.contributor.authorBalbín, Milagros-
dc.contributor.authorRuano, David-
dc.contributor.authorRamírez-Orellana, Manuel-
dc.contributor.authorPuente, Xose S.-
dc.contributor.authorMenéndez, Pablo-
dc.contributor.authorVelasco-Hernandez, Talia-
dc.date.accessioned2025-02-05T15:12:45Z-
dc.date.available2025-02-05T15:12:45Z-
dc.date.issued2024-05-17-
dc.identifier.issn0887-6924-
dc.identifier.urihttps://hdl.handle.net/2445/218527-
dc.description.abstractThis work demonstrated the prenatal origin of the translocation t(7;12) giving rise to the ETV6-NOM1 fusion protein, in a 5-month-old patient with acute myeloblastic leukemia using an umbilical cord blood (CB) sample from the patient stored at birth. Our findings revealed the presence of a specific t(7;12)/ETV6-NOM1 fusion in both CD34+ hematopoietic stem/progenitor cells and in the CD34-CD33+ myeloid cellular compartment isolated from the patient’s umbilical CB.-
dc.format.extent5 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Nature-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41375-024-02293-9-
dc.relation.ispartofLeukemia, 2024, vol. 38, p. 1808-1812-
dc.relation.urihttps://doi.org/10.1038/s41375-024-02293-9-
dc.rightscc by (c) Bousquets-Muñoz, P. et al., 2024-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.sourceArticles publicats en revistes (Ciències Fisiològiques)-
dc.subject.classificationLeucèmia mieloide-
dc.subject.classificationCromosomes humans-
dc.subject.classificationInfants-
dc.subject.otherMyeloid leukemia-
dc.subject.otherHuman chromosomes-
dc.subject.otherChildren-
dc.titleBacktracking NOM1::ETV6 fusion to neonatal pathogenesis of t(7;12) (q36;p13) infant AML.-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec752720-
dc.date.updated2025-02-05T15:12:45Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid38806630-
Appears in Collections:Articles publicats en revistes (Ciències Fisiològiques)

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