Cellosaurus cell line pWS88-c18 (CVCL

Cellosaurus pWS88-c18 (CVCL_RI79)

Cross-references
Cell line name	pWS88-c18
Accession	CVCL_RI79
Resource Identification Initiative	To cite this cell line use: pWS88-c18 (RRID:CVCL_RI79)
Comments	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_RI76 ! pWS88-c1 CVCL_RI77 ! pWS88-c2 CVCL_RI78 ! pWS88-c15
Sex of cell	Male
Age at sampling	14Y9M
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; SKIP001252
Encyclopedic resources	Wikidata; Q54948741
Entry history
Entry creation	05-Mar-2018
Last entry update	29-Jun-2023
Version number	7