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Cellosaurus GM09812 (CVCL_6G79)

[Text version]
Cell line name GM09812
Accession CVCL_6G79
Resource Identification Initiative To cite this cell line use: GM09812 (RRID:CVCL_6G79)
Comments Population: Jewish.
Cell type: Fibroblast; CL=CL_0000057.
Disease Seckel syndrome (NCIt: C125488)
Seckel syndrome (ORDO: Orphanet_808)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_6G78 ! GM09703
Sex of cell Female
Age at sampling 15Y
Category Finite cell line
Publications

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

PubMed=19896956; DOI=10.1016/j.mrfmmm.2009.10.013
Paul F. Wilson, Peter B. Nham, Salustra S. Urbin, John M. Hinz, Irene M. Jones, Lawrence H. Thompson;
Inter-individual variation in DNA double-strand break repair in human fibroblasts before and after exposure to low doses of ionizing radiation.
Mutat. Res. 683:91-97(2010)

Cross-references
Cell line collections (Providers) Coriell; GM09812
Cell line databases/resources CLO; CLO_0030457
Encyclopedic resources Wikidata; Q54844071
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number8