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Cellosaurus MDS-2.A3C (CVCL_VH26)

[Text version]
Cell line name MDS-2.A3C
Accession CVCL_VH26
Resource Identification Initiative To cite this cell line use: MDS-2.A3C (RRID:CVCL_VH26)
Comments Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
Cell type: Mononuclear cell; CL=CL_0000842.
Disease Myelodysplastic syndrome (NCIt: C3247)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_VH20 (MDS-2.A3)
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=25798938; DOI=10.1038/nbt.3178; PMCID=PMC4464949
Kotini A.G., Chang C.-J., Boussaad I., Delrow J.J., Dolezal E.K., Nagulapally A.B., Perna F., Fishbein G.A., Klimek V.M., Hawkins R.D., Huangfu D.-W., Murry C.E., Graubert T.A., Nimer S.D., Papapetrou E.P.
Functional analysis of a chromosomal deletion associated with myelodysplastic syndromes using isogenic human induced pluripotent stem cells.
Nat. Biotechnol. 33:646-655(2015)

Cross-references
Encyclopedic resources Wikidata; Q54904823
Gene expression databases GEO; GSM1594192
Entry history
Entry creation14-May-2018
Last entry update29-Jun-2023
Version number6