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Cellosaurus MCRIi012-A (CVCL_WN61)

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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 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 62Y
Category Induced pluripotent stem cell
Publications

PubMed=31415975; DOI=10.1016/j.scr.2019.101516
Kiymet Bozaoglu, Yu-Jing Gao, Edouard G. Stanley, Miriam Fanjul-Fernandez, Natasha J. Brown, Kate Pope, Cherie C. Green, Katerina Vlahos, Koula Sourris, Melanie Bahlo, Martin Delatycki ...Show all 13 authors... , Ingrid Eileen Scheffer, Paul J. Lockhart; Show fewer authors
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; MCRIi012-A
Encyclopedic resources Wikidata; Q95987010
Entry history
Entry creation24-May-2019
Last entry update29-Jun-2023
Version number6