Cellosaurus cell line pWS88-c0 (CVCL

Cellosaurus pWS88-c0 (CVCL_RI75)

Cross-references
Cell line name	pWS88-c0
Accession	CVCL_RI75
Resource Identification Initiative	To cite this cell line use: pWS88-c0 (RRID:CVCL_RI75)
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_RI76 ! pWS88-c1 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 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; SKIP001248
Encyclopedic resources	Wikidata; Q54948738
Entry history
Entry creation	05-Mar-2018
Last entry update	29-Jun-2023
Version number	7