ID   GENEA019
AC   CVCL_9028
SY   Genea019; GENEA-019; SIVF019; SIV019; GENEAe020-A
DR   BioSamples; SAMEA104013010
DR   hPSCreg; GENEAe020-A
DR   SKIP; SKIP002919
DR   Wikidata; Q54835581
RX   PubMed=20649476;
RX   PubMed=25316320;
RX   PubMed=27217344;
RX   PubMed=27346002;
RX   PubMed=35805069;
WW   Info; NIHhESC; -; https://grants.nih.gov/stem_cells/registry/not_approved.htm
WW   Provider; Genea; -; 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: NIH Human Embryonic Stem Cell Registry; not approved.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-62.
CC   Omics: Proteomics.
CC   Omics: Variations; Array-based CGH.
CC   Donor information: Embryo is sibling to that giving rise to GENEA020 (Cellosaurus=CVCL_9029).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): PubMed=27346002
ST   Amelogenin: X
ST   CSF1PO: 10,11
ST   D13S317: 11,12
ST   D16S539: 11
ST   D18S51: 12,18
ST   D19S433: 13,14
ST   D21S11: 29,30
ST   D2S1338: 18,23
ST   D3S1358: 15
ST   D5S818: 11,12
ST   D7S820: 7,8
ST   D8S1179: 12,13
ST   FGA: 22,23
ST   TH01: 9.3,10
ST   TPOX: 11
ST   vWA: 17
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 10-04-25; Version: 20
//
RX   PubMed=27346002; DOI=10.1016/j.scr.2016.02.008;
RA   Dumevska, Biljana
RA   Peura, Teija Tuulikki
RA   McKernan, Robert
RA   Goel, Divya
RA   Schmidt, Uli
RT   "Derivation of human embryonic stem cell line Genea019.";
RL   Stem Cell Res. 16:397-400(2016).
//
RX   PubMed=20649476; DOI=10.1089/scd.2010.0120;
RA   Bradley, Cara K.
RA   Scott, Heather A.
RA   Chami, Omar
RA   Peura, Teija Tuulikki
RA   Dumevska, Biljana
RA   Schmidt, Uli
RA   Stojanov, Tomas
RT   "Derivation of Huntington's disease-affected human embryonic stem cell
RT   lines.";
RL   Stem Cells Dev. 20:495-502(2011).
//
RX   PubMed=35805069; DOI=10.3390/cells11131984; PMCID=PMC9265327;
RA   Molina-Ruiz, Francisco Jose
RA   Introna, Clelia
RA   Bombau, Georgina
RA   Galofre, Mireia
RA   Canals, Josep Maria
RT   "Standardization of cell culture conditions and routine genomic
RT   screening under a quality management system leads to reduced genomic
RT   instability in hPSCs.";
RL   Cells 11:1984.1-1984.25(2022).
//
RX   PubMed=25316320; DOI=10.1021/pr500649m;
RA   McQuade, Leon R.
RA   Balachandran, Anushree
RA   Scott, Heather A.
RA   Khaira, Simer
RA   Baker, Mark Scott
RA   Schmidt, Uli
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).
//
RX   PubMed=27217344; DOI=10.5966/sctm.2015-0224; PMCID=PMC4996435;
RA   Caron, Leslie
RA   Kher, Devaki
RA   Lee, Kian Leong
RA   McKernan, Robert
RA   Dumevska, Biljana
RA   Hidalgo, Alejandro
RA   Li, Jia
RA   Yang, Henry He
RA   Main, Heather
RA   Ferri, Giulia
RA   Petek, Lisa M.
RA   Poellinger, Lorenz
RA   Miller, Daniel Guthrie
RA   Gabellini, Davide
RA   Schmidt, Uli
RT   "A human pluripotent stem cell model of facioscapulohumeral muscular
RT   dystrophy-affected skeletal muscles.";
RL   Stem Cells Transl. Med. 5:1145-1161(2016).
//