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Cellosaurus MICCNi002-B (CVCL_UM16)

[Text version]
Cell line name MICCNi002-B
Synonyms ADHD Stem Cell Study_subject 5, hiPSC_03 affected sibling, clone A16
Accession CVCL_UM16
Resource Identification Initiative To cite this cell line use: MICCNi002-B (RRID:CVCL_UM16)
Comments From: Monash Institute of Cognitive and Clinical Neurosciences, Monash University; Victoria; Australia.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Attention deficit hyperactivity disorder (NCIt: C97160)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UM15 ! MICCNi002-A
Sex of cell Male
Age at sampling 16Y
Category Induced pluripotent stem cell
Publications

PubMed=30622032; DOI=10.1016/j.scr.2018.11.014
Tong J., Lee K.M., Liu X.-D., Nefzger C.M., Vijayakumar P., Hawi Z., Pang K.C., Parish C.L., Polo J.M., Bellgrove M.A.
Generation of four iPSC lines from peripheral blood mononuclear cells (PBMCs) of an attention deficit hyperactivity disorder (ADHD) individual and a healthy sibling in an Australia-Caucasian family.
Stem Cell Res. 34:101353-101353(2019)

Cross-references
Cell line databases/resources hPSCreg; MICCNi002-B
Biological sample resources BioSamples; SAMEA4984143
Encyclopedic resources Wikidata; Q95989696
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number5