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Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B

Articolo
Data di Pubblicazione:
2019
Abstract:
We report the generation of three isogenic iPSC clones (UNIBSi007-A, UNIBSi007-B, and UNIBSi007-C) obtained from fibroblasts of a patient with Aicardi Goutières Syndrome (AGS) carrying a homozygous mutation in RNaseH2B. Cells were transduced using a Sendai virus based system, delivering the human OCT4, SOX2, c-MYC and KLF4 transcription factors. The resulting transgene-free iPSC lines retained the disease-causing DNA mutation, showed normal karyotype, expressed pluripotent markers and could differentiate in vitro toward cells of the three embryonic germ layers.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Autoimmune Diseases of the Nervous System; Base Sequence; Cell Culture Techniques; Cell Line; Child; Female; Fibroblasts; Humans; Induced Pluripotent Stem Cells; Mutation; Nervous System Malformations; Reproducibility of Results; Ribonuclease H
Elenco autori:
Ferraro, R. M.; Masneri, S.; Lanzi, G.; Barisani, C.; Piovani, G.; Savio, G.; Cattalini, M.; Galli, J.; Cereda, C.; Muzi-Falconi, M.; Orcesi, S.; Fazzi, E.; Giliani, S.
Autori di Ateneo:
ORCESI SIMONA
Link alla scheda completa:
https://iris.unipv.it/handle/11571/1361055
Pubblicato in:
STEM CELL RESEARCH
Journal
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https://www.sciencedirect.com/science/article/pii/S1873506119302508?via=ihub
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