ID   HT149B
AC   CVCL_UD80
DR   Wikidata; Q94305139
RX   PubMed=28659158;
CC   From: NIH-NCATS-TRND Branch; Rockville; USA.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): PubMed=28659158
ST   Amelogenin: X
ST   CSF1PO: 10,12
ST   D13S317: 9,12
ST   D16S539: 11,13
ST   D18S51: 14,15
ST   D21S11: 28,29
ST   D3S1358: 14,16
ST   D5S818: 11,12
ST   D7S820: 10,12
ST   D8S1179: 13
ST   FGA: 21
ST   Penta D: 9,11
ST   Penta E: 11,13
ST   TH01: 6,7
ST   TPOX: 8
ST   vWA: 17
DI   NCIt; C61271; Wolman disease
DI   ORDO; Orphanet_75233; Wolman disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_8B12 ! GM11851
SX   Female
AG   4M
CA   Induced pluripotent stem cell
DT   Created: 13-11-18; Last updated: 29-06-23; Version: 8
//
RX   PubMed=28659158; DOI=10.1186/s13023-017-0670-9; PMCID=PMC5490176;
RA   Aguisanda, Francis
RA   Yeh, Charles D.
RA   Chen, Catherine Z.
RA   Li, Rong
RA   Beers, Jeanette K.
RA   Zou, Ji-Zhong
RA   Thorne, Natasha
RA   Zheng, Wei
RT   "Neural stem cells for disease modeling of Wolman disease and
RT   evaluation of therapeutics.";
RL   Orphanet J. Rare Dis. 12:120.1-120.13(2017).
//