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Cellosaurus NSI001-A (CVCL_C0HK)

[Text version]
Cell line name NSI001-A
Synonyms iR14T21-A
Accession CVCL_C0HK
Resource Identification Initiative To cite this cell line use: NSI001-A (RRID:CVCL_C0HK)
Comments From: Stem Cell and Neurobiology Lab, National Centre for Cell Science; Pune; India.
Population: Indian.
Karyotypic information: 46,XX,rob(14;21) (PubMed=35381521).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Robertsonian translocation Down syndrome (NCIt: C188150)
Down syndrome (ORDO: Orphanet_870)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C0HL ! NSI001-B
CVCL_C0HM ! NSI001-C
Sex of cell Female
Age at sampling 1Y5M
Category Induced pluripotent stem cell
Publications

PubMed=35381521; DOI=10.1016/j.scr.2022.102771
Nehra S., Sharma V., Singh M., Singhal P., Singhal N.
Generation of integration free hiPSCs clones, NSi001-A, NSi001-B, and NSi001-C from peripheral blood mononuclear cells of an individual with Down syndrome having Robertsonian translocation.
Stem Cell Res. 61:102771-102771(2022)

Cross-references
Cell line databases/resources hPSCreg; NSI001-A
Biological sample resources BioSamples; SAMEA112442033
Encyclopedic resources Wikidata; Q112930225
Entry history
Entry creation23-Jun-2022
Last entry update30-Jan-2024
Version number5