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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.
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
Publications

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., 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)

Cross-references
Cell line databases/resources hPSCreg; MCRIi013-A
Entry history
Entry creation24-May-2019
Last entry updated06-Sep-2019
Version number2