ID   AG03593
AC   CVCL_A2MC
SY   AG 3593; AG3593
DR   Coriell; AG03593
DR   Wikidata; Q105506210
RX   CelloPub=CLPUB00387;
RX   PubMed=7176709;
RX   PubMed=7253718;
CC   Discontinued: Coriell; AG03593; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   28Y
CA   Finite cell line
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 5
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.A.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 7th edition. October 1980.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//
RX   PubMed=7176709; DOI=10.1016/0047-6374(82)90061-6;
RA   Tollefsbol T.O., Zaun M.R., Gracy R.W.;
RT   "Increased lability of triosephosphate isomerase in progeria and
RT   Werner's syndrome fibroblasts.";
RL   Mech. Ageing Dev. 20:93-101(1982).
//
RX   PubMed=7253718; DOI=10.1016/0047-6374(81)90027-0;
RA   Das N.K., Murphy D.G.;
RT   "The National Institute on Aging repository cell cultures.";
RL   Mech. Ageing Dev. 16:1-17(1981).
//