1. Digitum: Repositorio Institucional de la Universidad de Murcia
  2. Revistas y Congresos
  3. Revistas
  4. Histology and histopathology
  5. Vol.36, nº7 (2021)
Por favor, use este identificador para citar o enlazar este ítem: https://doi.org/10.14670/HH-18-307

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dc.contributor.authorZhang, Xiao-Hui-
dc.contributor.authorJin, Zi-Bing-
dc.date.accessioned2023-01-19T09:13:15Z-
dc.date.available2023-01-19T09:13:15Z-
dc.date.issued2021-
dc.identifier.citationHistology and Histopathology Vol. 36, nº7 (2021)es
dc.identifier.issn0213-3911-
dc.identifier.issn1699-5848-
dc.identifier.urihttp://hdl.handle.net/10201/127527-
dc.description.abstractInduced pluripotent stem cells (iPSCs), reprogrammed from human somatic cells, hold the capacity to differentiate into most human body cells. iPSCs can be differentiated into retinal organoids, a three-dimensional structured retina containing various retinal cells. Patient-specific retinal organoids provide a powerful disease model to recapitulate the disease to study the pathogenesis of inherited retinal dystrophies, to screen or discover new drugs, and most importantly to supply an unlimited cell source for retinal regenerationes
dc.formatapplication/pdfes
dc.format.extent6es
dc.languageenges
dc.publisherUniversidad de Murcia, Departamento de Biologia Celular e Histiologiaes
dc.relationSin financiación externa a la Universidades
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectInduced pluripotent stem cellses
dc.subjectRetinal organoidses
dc.subjectInherited retinal dystrophyes
dc.subjectGene editinges
dc.subjectDisease modelinges
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncologíaes
dc.titlePatient iPSC-derived retinal organoids: Observable retinal diseases in-a-dishes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.14670/HH-18-307-
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