ID   AG08466
AC   CVCL_L272
SY   AG8466
DR   CLO; CLO_0034143
DR   Coriell; AG08466
DR   Wikidata; Q54742017
RX   CelloPub=CLPUB00597;
RX   PubMed=8246632;
RX   PubMed=15130666;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C34951; Progeria
DI   ORDO; Orphanet_740; Hutchinson-Gilford progeria syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_L273 ! AG08467
OI   CVCL_L271 ! AG08671
SX   Female
AG   8Y5M
CA   Finite cell line
DT   Created: 06-05-13; Last updated: 29-06-23; Version: 13
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RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda (1994).
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RX   PubMed=8246632; DOI=10.1016/0047-6374(93)90046-T;
RA   Giro M.G., Davidson J.M.;
RT   "Familial co-segregation of the elastin phenotype in skin fibroblasts
RT   from Hutchinson-Gilford progeria.";
RL   Mech. Ageing Dev. 70:163-176(1993).
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RX   PubMed=15130666; DOI=10.1016/j.exger.2004.02.002;
RA   Bridger J.M., Kill I.R.;
RT   "Aging of Hutchinson-Gilford progeria syndrome fibroblasts is
RT   characterised by hyperproliferation and increased apoptosis.";
RL   Exp. Gerontol. 39:717-724(2004).
//