ID   CHB-12
AC   CVCL_A823
SY   CHB12; BCHe006-A
DR   hPSCreg; BCHe006-A
DR   ISCR; 77
DR   NIHhESC; NIHhESC-10-0011
DR   SKIP; SKIP001989
DR   Wikidata; Q54811744
RX   PubMed=18223642;
RX   PubMed=28445466;
CC   From: Children's Hospital Boston; Boston; USA.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-10-0011.
CC   Omics: Deep exome analysis.
CC   Omics: 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: 29-06-23; Version: 14
//
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;
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).
//