ID   WG1534
AC   CVCL_5I47
SY   PWSdel1; PWS-1
DR   Wikidata; Q54993885
RX   PubMed=20876107;
RX   PubMed=24816254;
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
CA   Finite cell line
DT   Created: 14-12-15; Last updated: 29-06-23; Version: 8
//
RX   PubMed=20876107; DOI=10.1073/pnas.1004487107; PMCID=PMC2955112;
RA   Chamberlain S.J., Chen I.P.-F., Ng K.Y., Bourgois-Rocha F.,
RA   Lemtiri-Chlieh F., Levine E.S., Lalande M.E.;
RT   "Induced pluripotent stem cell models of the genomic imprinting
RT   disorders Angelman and Prader-Willi syndromes.";
RL   Proc. Natl. Acad. Sci. U.S.A. 107:17668-17673(2010).
//
RX   PubMed=24816254; DOI=10.1038/ng.2968;
RA   Stelzer Y., Sagi I., Yanuka O., Eiges R., Benvenisty N.;
RT   "The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an
RT   induced pluripotent stem cell model of Prader-Willi syndrome.";
RL   Nat. Genet. 46:551-557(2014).
//