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Cellosaurus PWS iPS del 1-8 (CVCL_U530)

[Text version]
Cell line name PWS iPS del 1-8
Accession CVCL_U530
Resource Identification Initiative To cite this cell line use: PWS iPS del 1-8 (RRID:CVCL_U530)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Prader-Willi syndrome (NCIt: C75463)
Prader-Willi syndrome (ORDO: Orphanet_739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_5I47 (WG1534)
Sex of cell Female
Category Induced pluripotent stem cell
Publications

PubMed=20876107; DOI=10.1073/pnas.1004487107; PMCID=PMC2955112
Chamberlain S.J., Chen I.P.-F., Ng K.Y., Bourgois-Rocha F., Lemtiri-Chlieh F., Levine E.S., Lalande M.E.
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.
Proc. Natl. Acad. Sci. U.S.A. 107:17668-17673(2010)

Cross-references
Encyclopedic resources Wikidata; Q54948730
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number10