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Cellosaurus AG06299 (CVCL_L606)

[Text version]
Cell line name AG06299
Accession CVCL_L606
Resource Identification Initiative To cite this cell line use: AG06299 (RRID:CVCL_L606)
Comments Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A4FR (N2-iPS-1)CVCL_A4FS (N2-iPS-2)
Sex of cell Female
Age at sampling 34Y11M
Category Finite cell line
Publications

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

PubMed=12714972; DOI=10.1038/nature01629
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; AG06299
Cell line databases/resources CLO; CLO_0035511
Encyclopedic resources Wikidata; Q54740301
Entry history
Entry creation06-May-2013
Last entry update29-Jun-2023
Version number9