Publication:
The Value of Mouse Models of Rare Diseases: A Spanish Experience.

dc.contributor.authorMurillo-Cuesta, Silvia
dc.contributor.authorArtuch, Rafael
dc.contributor.authorAsensio, Fernando
dc.contributor.authorde la Villa, Pedro
dc.contributor.authorDierssen, Mara
dc.contributor.authorEnriquez, Jose Antonio
dc.contributor.authorFillat, Cristina
dc.contributor.authorFourcade, Stéphane
dc.contributor.authorIbáñez, Borja
dc.contributor.authorMontoliu, Lluis
dc.contributor.authorOliver, Eduardo
dc.contributor.authorPujol, Aurora
dc.contributor.authorSalido, Eduardo
dc.contributor.authorVallejo, Mario
dc.contributor.authorVarela-Nieto, Isabel
dc.contributor.funderCentro de Investigación Biomedica en Red - CIBER
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderGovernment of Catalonia (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)
dc.contributor.funderFundación ProCNIC
dc.contributor.funderComunidad de Madrid (España)
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.date.accessioned2021-04-12T08:45:33Z
dc.date.available2021-04-12T08:45:33Z
dc.date.issued2020-10-14
dc.description.abstractAnimal models are invaluable for biomedical research, especially in the context of rare diseases, which have a very low prevalence and are often complex. Concretely mouse models provide key information on rare disease mechanisms and therapeutic strategies that cannot be obtained by using only alternative methods, and greatly contribute to accelerate the development of new therapeutic options for rare diseases. Despite this, the use of experimental animals remains controversial. The combination of respectful management, ethical laws and transparency regarding animal experimentation contributes to improve society's opinion about biomedical research and positively impacts on research quality, which eventually also benefits patients. Here we present examples of current advances in preclinical research in rare diseases using mouse models, together with our perspective on future directions and challenges.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work was supported by a grant from the Center for Biomedical Research on Rare Diseases (CIBERER) (ER18GDT761) to SM-C. Additional support came from: Multi Target and View FEDER/CM-B2017/BMD-3688 and MINECO/FEDER SAF2017-86107-R grants to SM-C and IV-N; CERCA Program/Generalitat de Catalunya, Autonomous Government of Catalonia (2017SGR1206), and CIBERER (ACCI18-27) to AP; Miguel Servet program CPII16/00016 (Instituto de Salud Carlos III co-funded by European Social Fund ESF) to SF; CNIC (ISCIII, Ministerio de Ciencia, Innovación y Universidades), Pro CNIC Foundation, Severo Ochoa Center of Excellence (SEV-2015-0505) to BI and EO; Generalitat de Catalunya (Grups consolidats 2017 SGR 926) to MD. EO was beneficiary of a grant from “Programa de Atracción de Talento” of Comunidad de Madrid (2017-T1/BMD-5185). SM-C holds a ISCiii CIBER postdoctoral researcher contract. The work at CRG was supported by grants from the Spanish Ministry of Science and Innovation to the EMBL partnership, the Centro de Excelencia Severo Ochoa and the CERCA Programme/Generalitat de Catalunya.es_ES
dc.format.page583932es_ES
dc.format.volume11es_ES
dc.identifier.citationFront Genet. 2020; 11:583932es_ES
dc.identifier.doi10.3389/fgene.2020.583932es_ES
dc.identifier.issn1664-8021es_ES
dc.identifier.journalFrontiers in geneticses_ES
dc.identifier.pubmedID33173540es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/12606
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/ER18GDT761es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/2017SGR1206es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/ACCI18-27es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/CPII16/00016es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/ SEV-2015-0505es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/2017-SGR-926es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/2017-T1/BMD-5185es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/SAF2017-86107-Res_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/CM-B2017/BMD-3688es_ES
dc.relation.publisherversionhttps://doi.org/10.3389/fgene.2020.583932es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Genética Funcional del Sistema de Fosforilación Oxidativaes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Laboratorio Traslacional para la Imagen y Terapia Cardiovasculares_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectOrphan diseaseses_ES
dc.subjectAnimal modelses_ES
dc.subjectPreclinical researches_ES
dc.subjectNovel therapieses_ES
dc.subjectEthicses_ES
dc.subjectTransparencyes_ES
dc.titleThe Value of Mouse Models of Rare Diseases: A Spanish Experience.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication3a0c79b2-8c86-491c-91f1-116d726c24b3
relation.isAuthorOfPublication2cac8bb6-2bff-4bf6-8209-bdbd21781786
relation.isAuthorOfPublication6ac0323c-934c-4156-8099-cbf453615d48
relation.isAuthorOfPublication.latestForDiscovery3a0c79b2-8c86-491c-91f1-116d726c24b3

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