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Cellosaurus 18T-iPSC (CVCL_VK55)

[Text version]
Cell line name 18T-iPSC
Accession CVCL_VK55
Resource Identification Initiative To cite this cell line use: 18T-iPSC (RRID:CVCL_VK55)
Comments From: Key Laboratory for Rare Disease Research of Shandong Province; Jinan; China.
Omics: Transcriptomics; RNAseq.
Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Disease Trisomy 18 (NCIt: C36626)
Trisomy 18 (ORDO: Orphanet_3380)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Fetus
Category Induced pluripotent stem cell
Publications

PubMed=29862150; DOI=10.5582/irdr.218.01038; PMCID=PMC5982630
Xing K.-X., Cui Y.-Z., Luan J., Zhou X.-Y., Shi L., Han J.-X.
Establishment of a human trisomy 18 induced pluripotent stem cell line from amniotic fluid cells.
Intractable Rare Dis. Res. 7:94-99(2018)

Cross-references
Encyclopedic resources Wikidata; Q93300538
Entry history
Entry creation07-Sep-2018
Last entry update10-Apr-2025
Version number6