ID   N-2.A11
AC   CVCL_VH23
DR   Wikidata; Q54907276
RX   PubMed=25798938;
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
CC   Cell type: Mononuclear cell; CL=CL_0000842.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_VH19 ! MDS-2.13
OI   CVCL_VH20 ! MDS-2.A3
OI   CVCL_VH22 ! N-2.8
OI   CVCL_VH21 ! N-2.12
OI   CVCL_VH24 ! N-2.A2
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 29-06-23; Version: 6
//
RX   PubMed=25798938; DOI=10.1038/nbt.3178; PMCID=PMC4464949;
RA   Kotini A.G., Chang C.-J., Boussaad I., Delrow J.J., Dolezal E.K.,
RA   Nagulapally A.B., Perna F., Fishbein G.A., Klimek V.M., Hawkins R.D.,
RA   Huangfu D.-W., Murry C.E., Graubert T.A., Nimer S.D., Papapetrou E.P.;
RT   "Functional analysis of a chromosomal deletion associated with
RT   myelodysplastic syndromes using isogenic human induced pluripotent
RT   stem cells.";
RL   Nat. Biotechnol. 33:646-655(2015).
//