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Cellosaurus INSRMi009-A (CVCL_A2XW)

[Text version]
Cell line name INSRMi009-A
Synonyms DMD_RaPer_PhyMedExp
Accession CVCL_A2XW
Resource Identification Initiative To cite this cell line use: INSRMi009-A (RRID:CVCL_A2XW)
Comments From: INSERM; Paris; France.
Omics: Array-based CGH.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex52del; Zygosity=Hemizygous (PubMed=33246213).
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 12Y
Category Induced pluripotent stem cell
Publications

PubMed=33246213; DOI=10.1016/j.scr.2020.102094
Souidi M., Amedro P., Meyer P., Desprat R., Lemaitre J.-M., Rivier F., Lacampagne A., Meli A.C.
Generation of three Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD_YoTaz_PhyMedEXp, DMD_RaPer_PhyMedEXp, DMD_OuMen_PhyMedEXp (INSRMi008-A, INSRMi009-A and INSRMi010-A).
Stem Cell Res. 49:102094-102094(2020)

Cross-references
Cell line databases/resources hPSCreg; INSRMi009-A
Encyclopedic resources Wikidata; Q105509671
Entry history
Entry creation12-Jan-2021
Last entry update19-Dec-2024
Version number5