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Cellosaurus AG10548 (CVCL_L628)

[Text version]
Cell line name AG10548
Synonyms C8803
Accession CVCL_L628
Resource Identification Initiative To cite this cell line use: AG10548 (RRID:CVCL_L628)
Comments Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Progeria (NCIt: C34951)
Hutchinson-Gilford progeria syndrome (ORDO: Orphanet_740)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 8Y4M
Category Finite cell line
Publications

CLPUB00597
National Institute on Aging
1994 catalog of cell lines. NIA Aging Cell Repository.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994)

PubMed=10741968; DOI=10.1126/science.287.5462.2486
Ly D.H., Lockhart D.J., Lerner R.A., Schultz P.G.
Mitotic misregulation and human aging.
Science 287:2486-2492(2000)

PubMed=12714972; DOI=10.1038/nature01629; PMCID=PMC10540076
Eriksson M., Brown W.T., Gordon L.B., Glynn M.W., Singer J., Scott L., Erdos M.R., Robbins C.M., Moses T.Y., Berglund P., Dutra A., Pak E., Durkin S., Csoka A.B., Boehnke M., Glover T.W., Collins F.S.
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Nature 423:293-298(2003)

Cross-references
Cell line collections (Providers) Coriell; AG10548 - Discontinued
Encyclopedic resources Wikidata; Q54743352
Entry history
Entry creation06-May-2013
Last entry update29-Jun-2023
Version number9