ID   TS2-iPS-C7
AC   CVCL_UG59
DR   Wikidata; Q98133623
RX   PubMed=21949351;
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C26900; Turner syndrome
DI   ORDO; Orphanet_881; Turner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_X241 ! GM01176
SX   Female
AG   8Y
CA   Induced pluripotent stem cell
DT   Created: 13-11-18; Last updated: 02-05-24; Version: 7
//
RX   PubMed=21949351; DOI=10.1093/hmg/ddr435;
RA   Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S.,
RA   Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J.,
RA   Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D.,
RA   Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y.,
RA   Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.;
RT   "Modeling abnormal early development with induced pluripotent stem
RT   cells from aneuploid syndromes.";
RL   Hum. Mol. Genet. 21:32-45(2012).
//