ID   CHB-5
AC   CVCL_A816
SY   CHB05
DR   NIHhESC; NIHhESC-10-0005
DR   Wikidata; Q54811751
RX   PubMed=18223642;
RX   PubMed=28445466;
CC   From: Children's Hospital Boston; Boston; USA.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-10-0005.
CC   Omics: Genomics; Whole exome sequencing.
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: 15
//
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=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).
//