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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
Lucille Rossiaud, Emilie Pellier, Manon Benabides, Xavier Nissan, Giuseppe Ronzitti, Lucile Hoch;
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