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Cellosaurus 139-CUMC/UF (CVCL_IJ18)

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Cell line name 139-CUMC/UF
Accession CVCL_IJ18
Resource Identification Initiative To cite this cell line use: 139-CUMC/UF (RRID:CVCL_IJ18)
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)
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=27789403; DOI=10.1016/j.scr.2016.08.008; PMCID=PMC8202351
Lisa Cole Burnett, Charles A. LeDuc, Carlos R. Sulsona, Daniel J. Paull, Sanaa Eddiry, Brynn Levy, Jean-Pierre Salles, Maithe Tauber, Daniel J. Driscoll, Dietrich Meinrad Egli, Rudolph L. Leibel;
Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.
Stem Cell Res. 17:526-530(2016)

Cross-references
Encyclopedic resources Wikidata; Q54581757
Entry history
Entry creation01-Dec-2016
Last entry update29-Jun-2023
Version number8