ID   CSES7
AC   CVCL_B818
SY   CSES07; Cedars Sinai Embryonic Stem cell 7
DR   GEO; GSM1246012
DR   NIHhESC; NIHhESC-11-0108
DR   Wikidata; Q54814636
RX   PubMed=18450823;
RX   PubMed=20224970;
RX   PubMed=20641042;
RX   PubMed=26070610;
RX   PubMed=28445466;
CC   From: Cedars-Sinai Medical Center; Los Angeles; USA.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-11-0108.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Transcriptomics; Microarray.
CC   Omics: Variations; SNP array analysis.
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: 10-04-25; Version: 17
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RX   PubMed=18450823; DOI=10.1634/stemcells.2008-0156;
RA   Lavon N., Narwani K., Golan-Lev T., Buehler N., Hill D.,
RA   Benvenisty N.;
RT   "Derivation of euploid human embryonic stem cells from aneuploid
RT   embryos.";
RL   Stem Cells 26:1874-1882(2008).
//
RX   PubMed=20224970; DOI=10.1007/s11626-010-9303-5; PMCID=PMC2855810;
RA   Narwani K., Biancotti J.C., Golan-Lev T., Buehler N., Hill D.,
RA   Shifman S., Benvenisty N., Lavon N.;
RT   "Human embryonic stem cells from aneuploid blastocysts identified by
RT   pre-implantation genetic screening.";
RL   In Vitro Cell. Dev. Biol. Anim. 46:309-316(2010).
//
RX   PubMed=20641042; DOI=10.1002/stem.483;
RA   Biancotti J.C., Narwani K., Buehler N., Mandefro B., Golan-Lev T.,
RA   Yanuka O., Clark A., Hill D., Benvenisty N., Lavon N.;
RT   "Human embryonic stem cells as models for aneuploid chromosomal
RT   syndromes.";
RL   Stem Cells 28:1530-1540(2010).
//
RX   PubMed=26070610; DOI=10.1016/j.stemcr.2015.05.006; PMCID=PMC4471824;
RA   Avior Y., Biancotti J.C., Benvenisty N.;
RT   "TeratoScore: assessing the differentiation potential of human
RT   pluripotent stem cells by quantitative expression analysis of
RT   teratomas.";
RL   Stem Cell Reports 4:967-974(2015).
//
RX   PubMed=28445466; DOI=10.1038/nature22312; PMCID=PMC5427175;
RA   Merkle F.T., Ghosh S., Kamitaki N., Mitchell J., Avior Y., Mello C.,
RA   Kashin S., Mekhoubad S., Ilic D., Charlton M., Saphier G.,
RA   Handsaker R.E., Genovese G., Bar S., Benvenisty N., McCarroll S.A.,
RA   Eggan K.C.;
RT   "Human pluripotent stem cells recurrently acquire and expand dominant
RT   negative p53 mutations.";
RL   Nature 545:229-233(2017).
//