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Cellosaurus BRCi018-A (CVCL_C0HJ)

[Text version]
Cell line name BRCi018-A
Synonyms HiPS-GM13325
Accession CVCL_C0HJ
Resource Identification Initiative To cite this cell line use: BRCi018-A (RRID:CVCL_C0HJ)
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_2Y99 (GM13325)
Sex of cell Female
Age at sampling 9D
Category Induced pluripotent stem cell
Publications

PubMed=35292424; DOI=10.1016/j.scr.2022.102744
Tomoya Shimizu, Mami Matsuo-Takasaki, Dorian Luijkx, Miho Takami, Yutaka Arai, Michiya Noguchi, Yukio Nakamura, Tadayoshi Hayata, Megumu K. Saito, Yohei Hayashi;
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; BRCi018-A
Encyclopedic resources Wikidata; Q112929345
Entry history
Entry creation23-Jun-2022
Last entry update10-Sep-2024
Version number5