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Cellosaurus MCRIi013-A (CVCL_WN62)

[Text version]
Cell line name MCRIi013-A
Synonyms ASD2-7.1
Accession CVCL_WN62
Resource Identification Initiative To cite this cell line use: MCRIi013-A (RRID:CVCL_WN62)
Comments From: Murdoch Children's Research Institute; Melbourne; Australia.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 26Y
Category Induced pluripotent stem cell

PubMed=31415975; DOI=10.1016/j.scr.2019.101516
Bozaoglu K., Gao Y.-J., Stanley E.G., Fanjul-Fernandez M., Brown N.J., Pope K., Green C.C., Vlahos K., Sourris K., Bahlo M., Delatycki M., Scheffer I.E., Lockhart P.J.
Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate autism spectrum disorder.
Stem Cell Res. 39:101516-101516(2019)

Cell line databases/resources hPSCreg; MCRIi013-A
Encyclopedic resources Wikidata; Q95987012
Entry history
Entry creation24-May-2019
Last entry update29-Jun-2023
Version number6