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Cellosaurus AG08466 (CVCL_L272)

[Text version]
Cell line name AG08466
Synonyms AG8466
Accession CVCL_L272
Resource Identification Initiative To cite this cell line use: AG08466 (RRID:CVCL_L272)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
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)
Originate from same individual CVCL_L273 ! AG08467
CVCL_L271 ! AG08671
Sex of cell Female
Age at sampling 8Y5M
Category Finite cell line
Publications

PubMed=8246632; DOI=10.1016/0047-6374(93)90046-T
Giro M.G., Davidson J.M.
Familial co-segregation of the elastin phenotype in skin fibroblasts from Hutchinson-Gilford progeria.
Mech. Ageing Dev. 70:163-176(1993)

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=15130666; DOI=10.1016/j.exger.2004.02.002
Bridger J.M., Kill I.R.
Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis.
Exp. Gerontol. 39:717-724(2004)

Cross-references
Cell line collections (Providers) Coriell; AG08466
Cell line databases/resources CLO; CLO_0034143
Encyclopedic resources Wikidata; Q54742017
Entry history
Entry creation06-May-2013
Last entry update29-Jun-2023
Version number13