ID   CHB-8
AC   CVCL_A819
SY   CHB08; CHB8; BCHe002-A; PCBC08hse2012100902; SC12-039
DR   hPSCreg; BCHe002-A
DR   ISCR; 73
DR   NIHhESC; NIHhESC-10-0007
DR   SKIP; SKIP001985
DR   Wikidata; Q54811754
RX   PubMed=18223642;
RX   PubMed=27293150;
RX   PubMed=28445466;
CC   Part of: NHBLI Progenitor Cell Biology Consortium (PCBC) collection.
CC   From: Children's Hospital Boston; Boston; USA.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-10-0007.
CC   Omics: Deep exome analysis.
CC   Omics: DNA methylation analysis.
CC   Omics: SNP array analysis.
CC   Omics: Transcriptome analysis by RNAseq.
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: 16
//
RX   PubMed=18223642; DOI=10.1038/nbt1378;
RA   Lerou P.H., Yabuuchi A., Huo H.-G., Takeuchi A., Shea J., Cimini T.,
RA   Ince T.A., Ginsburg E., Racowsky C., Daley G.Q.;
RT   "Human embryonic stem cell derivation from poor-quality embryos.";
RL   Nat. Biotechnol. 26:212-214(2008).
//
RX   PubMed=27293150; DOI=10.1016/j.stemcr.2016.05.006;
RA   Salomonis N., Dexheimer P.J., Omberg L., Schroll R., Bush S., Huo J.,
RA   Schriml L.M., Sui S.H., Keddache M., Mayhew C.N., Shanmukhappa S.K.,
RA   Wells J.M., Daily K., Hubler S., Wang Y.-L., Zambidis E.T., Margolin A.A.,
RA   Hide W.A., Hatzopoulos A.K., Malik P., Cancelas J.A., Aronow B.J.,
RA   Lutzko C.;
RT   "Integrated genomic analysis of diverse induced pluripotent stem cells
RT   from the Progenitor Cell Biology Consortium.";
RL   Stem Cell Reports 7:110-125(2016).
//
RX   PubMed=28445466; DOI=10.1038/nature22312;
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).
//