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dc.contributor.authorGarreta, Elena
dc.contributor.authorSánchez, Sonia
dc.contributor.authorLajara Blesa, Jerónimo
dc.contributor.authorMontserrat, Núria
dc.contributor.authorIzpisua Belmonte, Juan Carlos
dc.date.accessioned2024-02-07T15:17:28Z
dc.date.available2024-02-07T15:17:28Z
dc.date.issued2018
dc.identifier.urihttp://hdl.handle.net/10952/7241
dc.description.abstractPurpose of Review The goal of this paper is to highlight the major challenges in the translation of human pluripotent stem cells into a clinical setting. Recent Findings Innate features from human induced pluripotent stem cells (hiPSCs) positioned these patient-specific cells as an unprecedented cell source for regenerative medicine applications. Immunogenicity of differentiated iPSCs requires more research towards the definition of common criteria for the evaluation of innate and host immune responses as well as in the generation of standardized protocols for iPSC generation and differentiation. The coming years will resolve ongoing clinical trials using both human embryonic stem cells (hESCs) and hiPSCs providing exciting information for the optimization of potential clinical applications of stem cell therapies. Summary Rapid advances in the field of iPSCs generated high expectations in the field of regenerative medicine. Understanding therapeutic applications of iPSCs certainly needs further investigation on autologous/allogenic iPSC transplantation.es
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectHuman embryonic stem cellses
dc.subjectInduced pluripotent stem cellses
dc.subjectImmunogenicityes
dc.titleRoadblocks in the Path of iPSC to the Clinices
dc.typearticlees
dc.rights.accessRightsopenAccesses
dc.journal.titleCurrent Transplantation Reportses
dc.volume.number5es
dc.description.disciplineMedicinaes
dc.identifier.doi10.1007/s40472-018-0177-xes


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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