ID   WISCi005-C
AC   CVCL_EJ82
SY   UWWC1-DS2U; DS2U
DR   BioSamples; SAMEA104388690
DR   hPSCreg; WISCi005-C
DR   WiCell; uwwc1-ds2u
DR   Wikidata; Q54994099
RX   PubMed=23716668;
CC   From: University of Wisconsin; Madison; USA.
CC   Population: Caucasian.
CC   Karyotypic information: Lost the third copy of chromosome 21.
CC   Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): PubMed=23716668
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 11
ST   D16S539: 11,13
ST   D5S818: 10,12
ST   D7S820: 10,12
ST   TH01: 6,9
ST   TPOX: 8,10
ST   vWA: 15,17
DI   NCIt; C2993; Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_L780 ! AG05397
SX   Male
AG   1Y
CA   Induced pluripotent stem cell
DT   Created: 26-09-16; Last updated: 29-06-23; Version: 13
//
RX   PubMed=23716668; DOI=10.1073/pnas.1216575110; PMCID=PMC3683748;
RA   Weick, Jason P.
RA   Held, Dustie L.
RA   Bonadurer, George Fred 3rd
RA   Doers, Matthew E.
RA   Liu, Yan
RA   Maguire, Chelsie
RA   Clark, Aaron
RA   Knackert, Joshua A.
RA   Molinarolo, Katharine
RA   Musser, Michael T.
RA   Yao, Lin
RA   Yin, Ying-Nan
RA   Lu, Jian-Feng
RA   Zhang, Xiao-Qing
RA   Zhang, Su-Chun
RA   Bhattacharyya, Anita
RT   "Deficits in human trisomy 21 iPSCs and neurons.";
RL   Proc. Natl. Acad. Sci. U.S.A. 110:9962-9967(2013).
//