Home  |  Contact

Cellosaurus HPS2296 (CVCL_YS53)

[Text version]

Cell line name HPS2296
Synonyms BRCi020-A
Accession CVCL_YS53
Resource Identification Initiative To cite this cell line use: HPS2296 (RRID:CVCL_YS53)
Comments Population: Japanese.
Derived from sampling site: Peripheral blood.
Disease 22q11.2 deletion syndrome (NCIt: C2989)
22q11.2 deletion syndrome (ORDO: Orphanet_567)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_YS54 ! HPS2297
CVCL_YS55 ! HPS2298
CVCL_YS56 ! HPS2299
CVCL_YS57 ! HPS2300
Sex of cell Male
Age at sampling <10Y
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 collections RCB; HPS2296
Cell line databases/resources hPSCreg; BRCi020-A
Encyclopedic resources Wikidata; Q94220064
Entry history
Entry creation12-Mar-2020
Last entry update23-Jun-2022
Version number3