ID   TD63-c1
AC   CVCL_RI86
DR   SKIP; SKIP001259
DR   Wikidata; Q54971914
RX   PubMed=27509850;
CC   Omics: Transcriptomics; Microarray.
CC   Omics: Transcriptomics; RNAseq.
CC   Omics: Variations; SNP array analysis.
CC   Derived from site: In situ; Tooth, dental pulp; UBERON=UBERON_0001754.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_RI87 ! TD63-c3
OI   CVCL_RI88 ! TD63-c6
SX   Female
AG   19Y8M
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 10-04-25; Version: 6
//
RX   PubMed=27509850; DOI=10.1038/nature19067; PMCID=PMC4995142;
RA   Chailangkarn T., Trujillo C.A., Freitas B.C., Hrvoj-Mihic B.,
RA   Herai R.H., Yu D.X., Brown T.T., Marchetto M.C.N., Bardy C., McHenry L.,
RA   Stefanacci L., Jarvinen A.M., Searcy Y.M., DeWitt M., Wong W., Lai P.,
RA   Ard M.C., Hanson K.L., Romero S., Jacobs B., Dale A.M., Dai L.,
RA   Korenberg J.R., Gage F.H., Bellugi U., Halgren E., Semendeferi K.,
RA   Muotri A.R.;
RT   "A human neurodevelopmental model for Williams syndrome.";
RL   Nature 536:338-343(2016).
//