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Cellosaurus WS17-c1 (CVCL_RI92)

[Text version]
Cell line name WS17-c1
Accession CVCL_RI92
Resource Identification Initiative To cite this cell line use: WS17-c1 (RRID:CVCL_RI92)
Comments Omics: Variations; SNP array analysis.
Derived from site: In situ; Tooth, dental pulp; UBERON=UBERON_0001754.
Disease Williams syndrome (NCIt: C85232)
Williams syndrome (ORDO: Orphanet_904)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_RI93 ! WS17-c2
CVCL_RI94 ! WS17-c4
Sex of cell Male
Age at sampling 9Y8M
Category Induced pluripotent stem cell
Publications

PubMed=27509850; DOI=10.1038/nature19067; PMCID=PMC4995142
Chailangkarn T., Trujillo C.A., Freitas B.C., Hrvoj-Mihic B., Herai R.H., Yu D.X., Brown T.T., Marchetto M.C.N., Bardy C., McHenry L., Stefanacci L., Jarvinen A.M., Searcy Y.M., DeWitt M., Wong W., Lai P., Ard M.C., Hanson K.L., Romero S., Jacobs B., Dale A.M., Dai L., Korenberg J.R., Gage F.H., Bellugi U., Halgren E., Semendeferi K., Muotri A.R.
A human neurodevelopmental model for Williams syndrome.
Nature 536:338-343(2016)

Cross-references
Cell line databases/resources SKIP; SKIP001237
Encyclopedic resources Wikidata; Q54994421
Entry history
Entry creation05-Mar-2018
Last entry update10-Apr-2025
Version number7