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Cellosaurus CiRA00111-ES-H19 (CVCL_VM73)

[Text version]
Cell line name CiRA00111-ES-H19
Synonyms DMD-iPSC #1 ESH19; HPS0385
Accession CVCL_VM73
Resource Identification Initiative To cite this cell line use: CiRA00111-ES-H19 (RRID:CVCL_VM73)
Comments From: Center for iPS Cell Research and Application, Kyoto University; Kyoto; Japan.
Population: Japanese.
Characteristics: Using TALEN a 18 bp deletion was introduced spanning the splicing acceptor site of DMD exon 45 thus restoring the reading frame.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_VM71 (CiRA00111)
Sex of cell Male
Age at sampling 1-9Y
Category Induced pluripotent stem cell
Publications

PubMed=25434822; DOI=10.1016/j.stemcr.2014.10.013; PMCID=PMC4297888
Li H.-M.L.-S., Fujimoto N., Sasakawa N., Shirai S., Ohkame T., Sakuma T., Tanaka M., Amano N., Watanabe A., Sakurai H., Yamamoto T., Yamanaka S., Hotta A.
Precise correction of the dystrophin gene in Duchenne muscular dystrophy patient induced pluripotent stem cells by TALEN and CRISPR-Cas9.
Stem Cell Reports 4:143-154(2015)

Cross-references
Cell line collections (Providers) RCB; HPS0385
Encyclopedic resources Wikidata; Q93453762
Entry history
Entry creation07-Sep-2018
Last entry update29-Jun-2023
Version number8