Cellosaurus cell line pWS88-c1 (CVCL

Cross-references
Cell line name	pWS88-c1
Accession	CVCL_RI76
Resource Identification Initiative	To cite this cell line use: pWS88-c1 (RRID:CVCL_RI76)
Comments	Omics: Transcriptomics; Microarray. Omics: Transcriptomics; RNAseq. Omics: Variations; SNP array analysis. Donor information: Established from a patient that harbors a partial deletion in the WBS critical region. 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_RI75 ! pWS88-c0 CVCL_RI77 ! pWS88-c2 CVCL_RI78 ! pWS88-c15 CVCL_RI79 ! pWS88-c18
Sex of cell	Male
Age at sampling	14Y9M
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)
Cell line databases/resources	SKIP; SKIP001249
Encyclopedic resources	Wikidata; Q54948739
Entry history
Entry creation	05-Mar-2018
Last entry update	10-Apr-2025
Version number	8