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Cellosaurus GM01865 (CVCL_DE31)

[Text version]
Cell line name GM01865
Synonyms GM-1865; GM1865
Accession CVCL_DE31
Resource Identification Initiative To cite this cell line use: GM01865 (RRID:CVCL_DE31)
Comments Cell type: Fibroblast; CL=CL_0000057.
Disease Cockayne syndrome (NCIt: C9460)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Sex ambiguous
Age at sampling 36Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977)

PubMed=7565859; DOI=10.1016/0921-8777(95)00015-C
Volpe J.P.G., Cleaver J.E.
Xeroderma pigmentosum variant cells are resistant to immortalization.
Mutat. Res. 337:111-117(1995)

Cross-references
Cell line collections (Providers) Coriell; GM01865 - Discontinued
Encyclopedic resources Wikidata; Q54837141
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number8