ID   DS2-iPS
AC   CVCL_ZA03
SY   DS-iPS clone 11; C11
DR   GEO; GSM1053964
DR   GEO; GSM1053965
DR   GEO; GSM1053966
DR   GEO; GSM1053991
DR   GEO; GSM1053992
DR   GEO; GSM1053993
DR   Wikidata; Q98125923
RX   PubMed=23225669;
CC   Population: Caucasian.
CC   Omics: Transcriptome analysis by microarray.
CC   Derived from site: In situ; Foreskin, skin; UBERON=UBERON_0001471.
CC   Cell type: Fibroblast of foreskin; CL=CL_1001608.
DI   NCIt; C2993; Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_2430 ! Detroit 532
SX   Male
AG   2M
CA   Induced pluripotent stem cell
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
//
RX   PubMed=23225669; DOI=10.1002/stem.1297;
RA   Briggs J.A., Sun J., Shepherd J., Ovchinnikov D.A., Chung T.-L.,
RA   Nayler S.P., Kao L.-P., Morrow C.A., Thakar N.Y., Soo S.-Y., Peura T.T.,
RA   Grimmond S.M., Wolvetang E.J.;
RT   "Integration-free induced pluripotent stem cells model genetic and
RT   neural developmental features of Down syndrome etiology.";
RL   Stem Cells 31:467-478(2013).
//