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Cellosaurus KSCBi009-A (CVCL_WR21)

[Text version]
Cell line name KSCBi009-A
Synonyms KNIH-PWS003i-A
Accession CVCL_WR21
Resource Identification Initiative To cite this cell line use: KSCBi009-A (RRID:CVCL_WR21)
Comments From: National Institute of Health, Korea-National Stem Cell Bank (KSCB); Cheongwon-gun; South Korea.
Population: Korean.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Prader-Willi syndrome (NCIt: C75463)
Prader-Willi syndrome (ORDO: Orphanet_739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 13Y
Category Induced pluripotent stem cell
Publications

PubMed=32474395; DOI=10.1016/j.scr.2020.101847
Kim B.-Y., Lee J.-S., Kim Y.-O., Koo S.K., Park M.-H.
Generation of induced pluripotent stem cells (KSCBi009-A) from a patient with Prader-Willi syndrome (PWS) featuring deletion of the paternal chromosome region 15q11.2-q13.
Stem Cell Res. 46:101847-101847(2020)

Cross-references
Cell line databases/resources hPSCreg; KSCBi009-A
SKIP; SKIP005770
Biological sample resources BioSamples; SAMEA5727777
Encyclopedic resources Wikidata; Q95980263
Entry history
Entry creation05-Jul-2019
Last entry update29-Jun-2023
Version number6