Cellosaurus logo
expasy logo

Cellosaurus pWS88-c0 (CVCL_RI75)

[Text version]
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
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; SKIP001248
Encyclopedic resources Wikidata; Q54948738
Entry history
Entry creation05-Mar-2018
Last entry update29-Jun-2023
Version number7