ID   N-3.10
AC   CVCL_VH18
DR   Wikidata; Q54907278
RX   PubMed=25798938;
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
CC   Cell type: Mononuclear cell; CL=CL_0000842.
ST   Source(s): PubMed=25798938
ST   Amelogenin: X,Y
ST   D13S317: 8,12
ST   D18S51: 13,18
ST   D21S11: 28,30
ST   D3S1358: 14,15
ST   D5S818: 11
ST   D7S820: 8,9
ST   D8S1179: 12,15
ST   FGA: 21,23
ST   vWA: 16,18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_VH15 ! MDS-3.1
OI   CVCL_VH16 ! MDS-3.4
OI   CVCL_VH17 ! MDS-3.5
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).
//