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dc.contributor.authorAlés Palmer, María Luisa
dc.contributor.authorAndujar Vera, Francisco
dc.contributor.authorIglesias Baena, Iván
dc.contributor.authorMuñoz de Rueda, Paloma
dc.contributor.authorOcete Hita, Esther 
dc.date.accessioned2024-07-29T11:39:34Z
dc.date.available2024-07-29T11:39:34Z
dc.date.issued2024-06-11
dc.identifier.citationAlés Palmer, M.L. et. al. Biomedicines 2024, 12, 1288. [https://doi.org/10.3390/biomedicines12061288]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/93588
dc.description.abstractIdiosyncratic drug-induced liver injury (DILI) is a complex multifactorial disease in which the toxic potential of the drug, together with genetic and acquired factors and deficiencies in adaptive processes, which limit the extent of damage, may determine susceptibility and make individuals unique in their development of hepatotoxicity. In our study, we sequenced the exomes of 43 pediatric patients diagnosed with DILI to identify important gene variations associated with this pathology. The result showed the presence of two variations in the NAT2 gene: c.590G>A (p.Arg197Gln) and c.341T>C (p.Ile114Thr). These variations could be found separately or together in 41 of the 43 patients studied. The presence of these variations as a risk factor for DILI could confirm the importance of the acetylation pathway in drug metabolism.es_ES
dc.description.sponsorshipInstitute of Health Carlos III (PI17/01989)es_ES
dc.description.sponsorshipServicio Andaluz de Salud (F2-0071-2015 and F1-0008-2022)es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectDILIes_ES
dc.subjectwhole-exome sequencinges_ES
dc.subjectrisk factorses_ES
dc.titleN-acetyltransferase Gene Variants Involved in Pediatric Idiosyncratic Drug-Induced Liver Injuryes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/biomedicines12061288
dc.type.hasVersionVoRes_ES


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