ID   AG10548
AC   CVCL_L628
SY   C8803
DR   Coriell; AG10548
DR   Wikidata; Q54743352
RX   CelloPub=CLPUB00597;
RX   PubMed=10741968;
RX   PubMed=12714972;
CC   Discontinued: Coriell; AG10548; probable.
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
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)
SX   Male
AG   8Y4M
CA   Finite cell line
DT   Created: 06-05-13; Last updated: 29-06-23; Version: 9
//
RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994).
//
RX   PubMed=10741968; DOI=10.1126/science.287.5462.2486;
RA   Ly D.H., Lockhart D.J., Lerner R.A., Schultz P.G.;
RT   "Mitotic misregulation and human aging.";
RL   Science 287:2486-2492(2000).
//
RX   PubMed=12714972; DOI=10.1038/nature01629; PMCID=PMC10540076;
RA   Eriksson M., Brown W.T., Gordon L.B., Glynn M.W., Singer J., Scott L.,
RA   Erdos M.R., Robbins C.M., Moses T.Y., Berglund P., Dutra A., Pak E.,
RA   Durkin S., Csoka A.B., Boehnke M., Glover T.W., Collins F.S.;
RT   "Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford
RT   progeria syndrome.";
RL   Nature 423:293-298(2003).
//