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Cellosaurus MICCNi002-B (CVCL_UM16)

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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
Janette Tong, Kyung Min Lee, Xiao-Dong Liu, Christian M. Nefzger, Parameswaran Vijayakumar, Ziarih Hawi, Ken C. Pang, Clare L. Parish, Jose M. Polo, Mark A. Bellgrove;
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