ID   TD70-c4
AC   CVCL_RI90
DR   SKIP; SKIP001263
DR   Wikidata; Q54971918
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_RI89 ! TD70-c2
OI   CVCL_RI91 ! TD70-c5
SX   Male
AG   9Y3M
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).
//