Publication:
Genetic Tools to Study Cardiovascular Biology.

dc.contributor.authorGarcia-Gonzalez, Irene
dc.contributor.authorMühleder, Severin
dc.contributor.authorFernandez-Chacon, Macarena
dc.contributor.authorBenedito, Rui
dc.contributor.funderUnión Europea. Comisión Europea. European Research Council (ERC)
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderFundación ProCNIC
dc.contributor.funderFundación La Caixa
dc.contributor.funderFWF Austrian Science Fund
dc.date.accessioned2020-10-27T11:53:45Z
dc.date.available2020-10-27T11:53:45Z
dc.date.issued2020-10
dc.description.abstractProgress in biomedical science is tightly associated with the improvement of methods and genetic tools to manipulate and analyze gene function in mice, the most widely used model organism in biomedical research. The joint effort of numerous individual laboratories and consortiums has contributed to the creation of a large genetic resource that enables scientists to image cells, probe signaling pathways activities, or modify a gene function in any desired cell type or time point, à la carte. However, as these tools significantly increase in number and become more sophisticated, it is more difficult to keep track of each tool's possibilities and understand their advantages and disadvantages. Knowing the best currently available genetic technology to answer a particular biological question is key to reach a higher standard in biomedical research. In this review, we list and discuss the main advantages and disadvantages of available mammalian genetic technology to analyze cardiovascular cell biology at higher cellular and molecular resolution. We start with the most simple and classical genetic approaches and end with the most advanced technology available to fluorescently label cells, conditionally target their genes, image their clonal expansion, and decode their lineages.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipRB is supported by the European Research Council (ERC-2014-StG-638028), the Centro Nacional de Investigaciones Cardiovasculares (CNIC), and the Ministerio de Ciencia y Innovación (MCIN: SAF2017-89299-P). The CNIC is supported by MCIN, the Pro CNIC Foundation and is a Severo Ochoa Center of Excellence (SEV-2015-0505). IG-G and MF-C were supported by PhD fellowships from Fundación La Caixa (CX-SO- 16-1 and CX_E-2015-01, respectively). SM was funded by the Austrian Science Fund (FWF) project J4358.es_ES
dc.format.page1084es_ES
dc.format.volume11es_ES
dc.identifier.citationFront Physiol. 2020; 11:1084es_ES
dc.identifier.doi10.3389/fphys.2020.01084es_ES
dc.identifier.issn1664-042X
dc.identifier.journalFrontiers in physiologyes_ES
dc.identifier.pubmedID33071802es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/11206
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SEV-2015-0505es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/638028es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2017-89299-Pes_ES
dc.relation.publisherversionhttps://doi.org/10.3389/fphys.2020.01084es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Genética Molecular de la Angiogénesises_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleGenetic Tools to Study Cardiovascular Biology.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationdf89c94e-79a2-458f-aeb4-bb76ebffd71a
relation.isAuthorOfPublication655524a2-7a61-4d4b-8334-2d5fdb9c2c96
relation.isAuthorOfPublication924c4677-29f1-4917-92d2-765d534c2242
relation.isAuthorOfPublication.latestForDiscoverydf89c94e-79a2-458f-aeb4-bb76ebffd71a

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