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Cellosaurus MCRIi012-A (CVCL_WN61)

[Text version]

Cell line name MCRIi012-A
Synonyms ASD2-6.4
Accession CVCL_WN61
Resource Identification Initiative To cite this cell line use: MCRIi012-A (RRID:CVCL_WN61)
Comments From: Murdoch Children's Research Institute; Melbourne; Australia.
Population: Caucasian.
Derived from sampling site: Peripheral blood.
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 62Y
Category Induced pluripotent stem cell

PubMed=31415975; DOI=10.1016/j.scr.2019.101516
Bozaoglu K., Gao Y., Stanley E., 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; MCRIi012-A
Other Wikidata; Q95987010
Entry history
Entry creation24-May-2019
Last entry update02-Jul-2020
Version number4