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Cellosaurus CS7SE hTERT (CVCL_ZU52)

[Text version]
Cell line name CS7SE hTERT
Synonyms GM01428T
Accession CVCL_ZU52
Resource Identification Initiative To cite this cell line use: CS7SE hTERT (RRID:CVCL_ZU52)
Comments Population: African American.
Genetic integration: Method=Transfection/transduction; Gene=HGNC; 11730; TERT.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Cockayne syndrome type B (NCIt: C135726)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_L469 (CS7SE)
Sex of cell Female
Age at sampling 8Y
Category Telomerase immortalized cell line
Publications

PubMed=27543334; DOI=10.1073/pnas.1610020113; PMCID=PMC5018765
Reid-Bayliss K.S., Arron S.T., Loeb L.A., Bezrookove V., Cleaver J.E.
Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency.
Proc. Natl. Acad. Sci. U.S.A. 113:10151-10156(2016)

Cross-references
Encyclopedic resources Wikidata; Q98125770
Entry history
Entry creation02-Jul-2020
Last entry update10-Sep-2024
Version number6