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Cellosaurus CPG18 (CVCL_B3RU)

[Text version]
Cell line name CPG18
Accession CVCL_B3RU
Resource Identification Initiative To cite this cell line use: CPG18 (RRID:CVCL_B3RU)
Comments 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 Children:
CVCL_B3RR (ICGi032-A)
Sex of cell Male
Age at sampling 9Y
Category Transformed cell line
Publications

PubMed=33426406; DOI=10.1016/j.ncrna.2020.11.006
Dolskiy A.A., Yarushkin A.A., Grishchenko I.V., Lemskaya N.A., Pindyurin A.V., Boldyreva L.V., Pustylnyak V.O., Yudkin D.V.
miRNA expression and interaction with the 3'UTR of FMR1 in FRAXopathy pathogenesis.
Noncoding RNA Res. 6:1-7(2021)

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
Encyclopedic resources Wikidata; Q110432742
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4