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Cellosaurus GM00526 (CVCL_X075)

[Text version]
Cell line name GM00526
Synonyms GM-526; GM-0526; GM 526
Accession CVCL_X075
Resource Identification Initiative To cite this cell line use: GM00526 (RRID:CVCL_X075)
Comments Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Disease Trisomy 13 (NCIt: C36529)
Trisomy 13 (ORDO: Orphanet_3378)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling <1M
Category Finite cell line
Publications

PubMed=7329430; DOI=10.1016/0027-5107(81)90059-2
Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.
Abnormalities of human chromosome 13 and in vitro radiosensitivity; a study of 19 fibroblast strains.
Mutat. Res. 84:157-167(1981)

PubMed=6661932; DOI=10.1159/000131990
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
Chromosome maps of cell lines with specific monosomic or trisomic portions of the genome in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 36:652-658(1983)

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; GM00526
Cell line databases/resources CLO; CLO_0026043
Encyclopedic resources Wikidata; Q54836291
Entry history
Entry creation17-Jul-2014
Last entry update29-Jun-2023
Version number11