ID   MDS-3.1
AC   CVCL_VH15
DR   GEO; GSM1594194
DR   Wikidata; Q54904824
RX   PubMed=25798938;
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
CC   Cell type: Mononuclear cell of bone marrow; CL=CL_0010004.
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: 9
ST   D8S1179: 12,15
ST   FGA: 21,23
ST   vWA: 16,18
DI   NCIt; C3247; Myelodysplastic syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_VH16 ! MDS-3.4
OI   CVCL_VH17 ! MDS-3.5
OI   CVCL_VH18 ! N-3.10
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 10-04-25; Version: 7
//
RX   PubMed=25798938; DOI=10.1038/nbt.3178; PMCID=PMC4464949;
RA   Kotini, Andriana G.
RA   Chang, Chan-Jung
RA   Boussaad, Ibrahim
RA   Delrow, Jeffrey J.
RA   Dolezal, Emily K.
RA   Nagulapally, Abhinav B.
RA   Perna, Fabiana
RA   Fishbein, Gregory A.
RA   Klimek, Virginia Marie
RA   Hawkins, R. David
RA   Huangfu, Dan-Wei
RA   Murry, Charles E.
RA   Graubert, Timothy Aaron
RA   Nimer, Stephen D.
RA   Papapetrou, Eirini 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).
//