ID   WISCi005-B
DR   BioSamples; SAMEA104388691
DR   hPSCreg; WISCi005-B
DR   WiCell; uwwc1-ds4
DR   Wikidata; Q54994098
RX   PubMed=23716668;
CC   From: University of Wisconsin; Madison; USA.
CC   Population: Caucasian.
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: 12
RX   PubMed=23716668; DOI=10.1073/pnas.1216575110;
RA   Weick J.P., Held D.L., Bonadurer G.F. III, Doers M.E., Liu Y.,
RA   Maguire C., Clark A., Knackert J.A., Molinarolo K., Musser M.T., Yao L.,
RA   Yin Y.-N., Lu J.-F., Zhang X.-Q., Zhang S.-C., Bhattacharyya A.;
RT   "Deficits in human trisomy 21 iPSCs and neurons.";
RL   Proc. Natl. Acad. Sci. U.S.A. 110:9962-9967(2013).