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Cellosaurus KSCBi007-A (CVCL_WR19)

[Text version]
Cell line name KSCBi007-A
Synonyms KNIH-PWS001i-A
Accession CVCL_WR19
Resource Identification Initiative To cite this cell line use: KSCBi007-A (RRID:CVCL_WR19)
Comments From: National Institute of Health, Korea-National Stem Cell Bank (KSCB); Cheongwon-gun; South Korea.
Population: Asian.
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 Female
Age at sampling 5M
Category Induced pluripotent stem cell
Publications

PubMed=31756696; DOI=10.1016/j.scr.2019.101647
Kim B.-Y., Lee J.-S., Kim Y.-O., Park M.-H., Koo S.K.
Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain maternal uniparental disomy (UPD).
Stem Cell Res. 41:101647-101647(2019)

Cross-references
Cell line databases/resources hPSCreg; KSCBi007-A
SKIP; SKIP005590
Biological sample resources BioSamples; SAMEA5727775
Encyclopedic resources Wikidata; Q95980261
Entry history
Entry creation05-Jul-2019
Last entry update29-Jun-2023
Version number9