Cellosaurus cell line WS17-c2 (CVCL

Cross-references
Cell line name	WS17-c2
Accession	CVCL_RI93
Resource Identification Initiative	To cite this cell line use: WS17-c2 (RRID:CVCL_RI93)
Comments	Omics: Transcriptomics; RNAseq. 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_RI92 ! WS17-c1 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 Thanathom Chailangkarn, Cleber A. Trujillo, Beatriz C. Freitas, Branka Hrvoj-Mihic, Roberto Hirochi Herai, Diana X. Yu, Timothy T. Brown, Maria Carolina N. Marchetto, Cedric Bardy, Lauren McHenry, Lisa Stefanacci ...Show all 28 authors... , Anna M. Jarvinen, Yvonne M. Searcy, Michelle DeWitt, Wenny Wong, Philip Lai, M. Colin Ard, Kari L. Hanson, Sarah Romero, Bob Jacobs, Anders Martin Dale, Li Dai, Julie R. Korenberg, Fred Harrison Gage, Ursula Bellugi, Eric Halgren, Katerina Semendeferi, Alysson Renato Muotri; Show fewer authors A human neurodevelopmental model for Williams syndrome. Nature 536:338-343(2016)
Cell line databases/resources	SKIP; SKIP001236
Encyclopedic resources	Wikidata; Q54994422
Entry history
Entry creation	05-Mar-2018
Last entry update	10-Apr-2025
Version number	7