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Cellosaurus WS79-c3 (CVCL_RJ02)

[Text version]
Cell line name WS79-c3
Accession CVCL_RJ02
Resource Identification Initiative To cite this cell line use: WS79-c3 (RRID:CVCL_RJ02)
Comments 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_RJ01 ! WS79-c2
CVCL_RJ03 ! WS79-c5
Sex of cell Male
Age at sampling 13Y6M
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; SKIP001246
Encyclopedic resources Wikidata; Q54994439
Entry history
Entry creation05-Mar-2018
Last entry update29-Jun-2023
Version number6