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Cellosaurus ICGi032-A (CVCL_B3RR)

[Text version]
Cell line name ICGi032-A
Accession CVCL_B3RR
Resource Identification Initiative To cite this cell line use: ICGi032-A (RRID:CVCL_B3RR)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Population: Caucasian.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Fragile X syndrome (NCIt: C84717)
Fragile X syndrome (ORDO: Orphanet_908)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_B3RU (CPG18)
Sex of cell Male
Age at sampling 9Y
Category Induced pluripotent stem cell
Publications

PubMed=34864218; DOI=10.1016/j.scr.2021.102615
Gridina M.M., Shitik E.M., Lemskaya N.A., Minina J.M., Grishchenko I.V., Dolskiy A.A., Shorina A.R., Maksimova Y.V., Yudkin D.V.
Derivation of iPS cell line (ICGi032-A) from a patient affected with fragile X syndrome.
Stem Cell Res. 57:102615-102615(2021)

Cross-references
Cell line databases/resources hPSCreg; ICGi032-A
Biological sample resources BioSamples; SAMEA9652840
Encyclopedic resources Wikidata; Q110432905
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4