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Cellosaurus ISTEMi002-A (CVCL_C6Q3)

[Text version]
Cell line name ISTEMi002-A
Accession CVCL_C6Q3
Resource Identification Initiative To cite this cell line use: ISTEMi002-A (RRID:CVCL_C6Q3)
Comments From: Institut from Stem cell Therapy and Exploration of Monogenic diseases; Corbeil-Essonnes; France.
Population: Arab.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Glycogen storage disease type III (NCIt: C84736)
Glycogen storage disease due to glycogen debranching enzyme deficiency (ORDO: Orphanet_366)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_1F14 (GM03390)
Sex of cell Male
Age at sampling 1Y4M
Category Induced pluripotent stem cell
Publications

PubMed=37769385; DOI=10.1016/j.scr.2023.103214
Rossiaud L., Pellier E., Benabides M., Nissan X., Ronzitti G., Hoch L.
Generation of three induced pluripotent stem cell lines from patients with glycogen storage disease type III.
Stem Cell Res. 72:103214-103214(2023)

Cross-references
Cell line databases/resources hPSCreg; ISTEMi002-A
Biological sample resources BioSamples; SAMEA112700911
Encyclopedic resources Wikidata; Q117704556
Entry history
Entry creation21-Mar-2023
Last entry update30-Jan-2024
Version number4