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Cellosaurus BRCi017-A (CVCL_C0HI)

[Text version]
Cell line name BRCi017-A
Synonyms HiPS-GM05876
Accession CVCL_C0HI
Resource Identification Initiative To cite this cell line use: BRCi017-A (RRID:CVCL_C0HI)
Comments From: RIKEN BioResource Research Center; Kyoto; Japan.
Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Disease 22q11.2 deletion syndrome (NCIt: C2989)
22q11.2 deletion syndrome (ORDO: Orphanet_567)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_2Y97 (GM05876)
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=35292424; DOI=10.1016/j.scr.2022.102744
Shimizu T., Matsuo-Takasaki M., Luijkx D., Takami M., Arai Y., Noguchi M., Nakamura Y., Hayata T., Saito M.K., Hayashi Y.
Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion.
Stem Cell Res. 61:102744-102744(2022)

Cross-references
Cell line databases/resources hPSCreg; BRCi017-A
Encyclopedic resources Wikidata; Q112929344
Entry history
Entry creation23-Jun-2022
Last entry update10-Sep-2024
Version number5