ID   GENEA029
AC   CVCL_9038
SY   SIVF029; 438; GENEAe014-A
DR   BioSamples; SAMEA104012532
DR   hPSCreg; GENEAe014-A
DR   ISCR; 1191
DR   Wikidata; Q54835595
RX   PubMed=24745836;
RX   PubMed=25316320;
WW   https://web.archive.org/web/20180912205435/http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
CC   From: Genea Biocells, Ltd; Sydney; Australia.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-60.
CC   Omics: Array-based CGH.
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 29-06-23; Version: 13
//
RX   PubMed=24745836; DOI=10.1016/j.rbmo.2014.02.001;
RA   Bradley C.K., Peura T.T., Dumevska B., Jovasevic A., Chami O.,
RA   Schmidt U., Jansen R.P.S., Stojanov T.;
RT   "Cell lines from morphologically abnormal discarded IVF embryos are
RT   typically euploid and unaccompanied by intrachromosomal
RT   aberrations.";
RL   Reprod. BioMed. Online 28:780-788(2014).
//
RX   PubMed=25316320; DOI=10.1021/pr500649m;
RA   McQuade L.R., Balachandran A., Scott H.A., Khaira S., Baker M.S.,
RA   Schmidt U.;
RT   "Proteomics of Huntington's disease-affected human embryonic stem
RT   cells reveals an evolving pathology involving mitochondrial
RT   dysfunction and metabolic disturbances.";
RL   J. Proteome Res. 13:5648-5659(2014).
//