ID   UHOMe001-A
AC   CVCL_C391
SY   HD90; HD90/FE07-142-L1; HD90/D18/FE07-142-L1; HD90/D18E7; D18
DR   hPSCreg; UHOMe001-A
DR   SKIP; SKIP002299
DR   Wikidata; Q54990169
RX   DOI=10.1016/S1472-6483(10)62372-3;
RX   PubMed=19128516;
WW   https://www.agence-biomedecine.fr/IMG/pdf/chu_montpellier_hd90.pdf
CC   From: University Hospital of Montpellier; Montpellier; France.
CC   Registration: French Agence de la Biomedecine; FE07-142-L1.
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C3105; Von Hippel-Lindau syndrome
DI   ORDO; Orphanet_892; Von Hippel-Lindau disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 22-10-12; Last updated: 29-06-23; Version: 13
//
RX   DOI=10.1016/S1472-6483(10)62372-3;
RA   Pellestor F., Monzo C., Nadal L., De Vos J., Hamamah S.;
RT   "Acquisition of a trisomy 20 in the human embryonic stem cell line
RT   HD90.";
RL   Reprod. BioMed. Online 20 Suppl. 1:S41-S41(2011).
//
RX   PubMed=19128516; DOI=10.1186/1471-2164-10-10;
RA   Assou S., Cerecedo D., Tondeur S., Pantesco V., Hovatta O., Klein B.,
RA   Hamamah S., De Vos J.;
RT   "A gene expression signature shared by human mature oocytes and
RT   embryonic stem cells.";
RL   BMC Genomics 10:10.1-10.15(2009).
//