Generation and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24

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dc.contributor.authorRamovs, Veronika
dc.contributor.authorFuentes, Ignacia
dc.contributor.authorFreund, Christian
dc.contributor.authorMikkers, Harald
dc.contributor.authorMummery, Christine L.
dc.contributor.authorRaymond, Karine
dc.date.accessioned2022-04-04T21:26:44Z
dc.date.available2022-04-04T21:26:44Z
dc.date.issued2021
dc.description.abstractFibroblasts from two patients carrying a heterozygous mutation in the translation initiation codon (c.2 T > G) of the kelch-like protein 24 (KLHL24) gene were used to generate human induced pluripotent stem cells (hiPSCs), using non-integrating Sendai virus to deliver reprogramming factors. CRISPR-Cas9 editing was used for genetic correction of the mutation in the patient-hiPSCs. The top-predicted off-target sites were not altered. Patient and isogenic hiPSCs showed typical morphology, expressed pluripotency-associated markers, had the capacity for in vitro differentiation into the three germ layers and displayed a normal karyotype. These isogenic pairs will enable in vitro modelling of KLHL24-associated heart and skin conditions.es
dc.description.versionVersión Publicadaes
dc.identifier.citationVeronika Ramovs, Ignacia Fuentes, Christian Freund, Harald Mikkers, Christine L. Mummery, Karine Raymond, Generation and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24, Stem Cell Research, Volume 57, 2021, 102582, ISSN 1873-5061, https://doi.org/10.1016/j.scr.2021.102582.es
dc.identifier.urihttps://doi.org/10.1016/j.scr.2021.102582es
dc.identifier.urihttp://hdl.handle.net/11447/5925
dc.language.isoenes
dc.subjectStem cellses
dc.titleGeneration and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24es
dc.typeArticlees
dcterms.sourceStem Cell Researches

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