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Cellosaurus GM00368 (CVCL_W056)

[Text version]
Cell line name GM00368
Synonyms GM-368; GM 368; GM0368; GM00368A; C17
Accession CVCL_W056
Resource Identification Initiative To cite this cell line use: GM00368 (RRID:CVCL_W056)
Comments Population: African American.
Doubling time: 30.7 +- 1.6 hours (PubMed=1214005).
Derived from site: In situ; Forearm, skin; UBERON=UBERON_0003399.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Fanconi anemia (NCIt: C62505)
Fanconi anemia (ORDO: Orphanet_84)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 8Y
Category Finite cell line
Publications

PubMed=1214005; DOI=10.1002/jcp.1040870211
Elmore E., Swift M.
Growth of cultured cells from patients with Fanconi anemia.
J. Cell. Physiol. 87:229-233(1975)

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=2878433; DOI=10.1098/rspb.1986.0070
Huschtscha L.I., Thompson K.V.A., Holliday R.
The susceptibility of Werner's syndrome and other human skin fibroblasts to SV40-induced transformation and immortalization.
Proc. R. Soc. Lond. B. Biol. Sci. 229:1-12(1986)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)

Cross-references
Cell line collections (Providers) Coriell; GM00368
Cell line databases/resources CLO; CLO_0025551
Encyclopedic resources Wikidata; Q54836186
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number14