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dc.contributor.authorPérez Campo, Flor María 
dc.contributor.authorRiancho Moral, José Antonio 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2017-01-05T09:40:06Z
dc.date.available2017-01-05T09:40:06Z
dc.date.issued2015
dc.identifier.issn1389-2029
dc.identifier.issn1875-5488
dc.identifier.urihttp://hdl.handle.net/10902/9923
dc.description.abstractHuman Mesenchymal Stem Cells (hMSCs) have emerged in the last few years as one of the most promising therapeutic cell sources and, in particular, as an important tool for regenerative medicine of skeletal tissues. Although they present a more restricted potency than Embryonic Stem (ES) cells, the use of hMCS in regenerative medicine avoids many of the drawbacks characteristic of ES cells or induced pluripotent stem cells. The challenge in using these cells lies into developing precise protocols for directing cellular differentiation to generate a specific cell lineage. In order to achieve this goal, it is of the upmost importance to be able to control de process of fate decision and lineage commitment. This process requires the coordinate regulation of different molecular layers at transcriptional, posttranscriptional and translational levels. At the transcriptional level, switching on and off different sets of genes is achieved not only through transcriptional regulators, but also through their interplay with epigenetic modifiers. It is now well known that epigenetic changes take place in an orderly way through development and are critical in the determination of lineage-specific differentiation. More importantly, alteration of these epigenetic changes would, in many cases, lead to disease generation and even tumour formation. Therefore, it is crucial to elucidate how epigenetic factors, through their interplay with transcriptional regulators, control lineage commitment in hMSCs.es_ES
dc.format.extent16 p.es_ES
dc.language.isoenges_ES
dc.publisherHilversum, Netherlands ; Boca Raton, FL : Bentham Science Publisherses_ES
dc.rightsAtribución-NoComercial 3.0 Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceCurr Genomics. 2015 Dec;16(6):368-83es_ES
dc.subject.otherEpigeneticses_ES
dc.subject.otherBonees_ES
dc.subject.otherOsteoporosises_ES
dc.subject.otherMesenchymal stem cellses_ES
dc.subject.otherHistone acetylationes_ES
dc.subject.otherHistone methylationes_ES
dc.subject.otherDNA methylationes_ES
dc.titleEpigenetic Mechanisms Regulating Mesenchymal Stem Cell Differentiationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.2174/1389202916666150817202559
dc.type.versionpublishedVersiones_ES


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Atribución-NoComercial 3.0 EspañaExcepto si se señala otra cosa, la licencia del ítem se describe como Atribución-NoComercial 3.0 España