ID   AG00991
AC   CVCL_V551
AS   CVCL_CV50
SY   AG-991; AG 991; AG991; AG0991A; GM00991; GM-991; GM 991; GM991; L.D.
DR   Coriell; AG00991
DR   Coriell; GM00991
DR   Wikidata; Q54609424
RX   CelloPub=CLPUB00387;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=4412878;
RX   PubMed=7253718;
RX   PubMed=7471105;
CC   Discontinued: Coriell; AG00991; probable.
CC   Discontinued: Coriell; GM00991; probable.
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)
SX   Male
AG   4Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 11
//
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   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=4412878; DOI=10.1016/S0006-291X(74)80058-6;
RA   Regan J.D., Setlow R.B.;
RT   "DNA repair in human progeroid cells.";
RL   Biochem. Biophys. Res. Commun. 59:858-864(1974).
//
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).
//
RX   PubMed=7471105;
RA   Weichselbaum R.R., Nove J., Little J.B.;
RT   "X-ray sensitivity of fifty-three human diploid fibroblast cell
RT   strains from patients with characterized genetic disorders.";
RL   Cancer Res. 40:920-925(1980).
//