ID   GM00509
AC   CVCL_L952
SY   GM-509; GM-0509; GM 509; GM00509A; GM 509 A; GM00250; GM-250; GM250
DR   CLO; CLO_0025940
DR   Coriell; GM00250
DR   Coriell; GM00509
DR   Wikidata; Q54836277
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1183234;
RX   PubMed=6617268;
RX   PubMed=6661932;
RX   PubMed=7329430;
RX   PubMed=7471105;
CC   Population: African American.
CC   Karyotypic information: 46,XX,del(13)(pter->q14) (Coriell=GM00509).
CC   Discontinued: Coriell; GM00250; true.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   1Y
CA   Finite cell line
DT   Created: 06-05-13; Last updated: 29-06-23; Version: 13
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
RX   PubMed=1183234; DOI=10.1159/000130500;
RA   Aronson M.M., Zackai E.H., Mellman W.J., Miller R.C., Greene A.E.,
RA   Coriell L.L.;
RT   "A (13) terminal deletion, 46 chromosomes. Repository identification
RT   No. GM-250.";
RL   Cytogenet. Cell Genet. 15:57-58(1975).
//
RX   PubMed=6617268; DOI=10.1159/000131883;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Breakpoint map of chromosomal inversion and deletion cell cultures in
RT   the NIGMS Human Genetic Mutant Cell Repository.";
RL   Cytogenet. Cell Genet. 35:298-302(1983).
//
RX   PubMed=6661932; DOI=10.1159/000131990;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Chromosome maps of cell lines with specific monosomic or trisomic
RT   portions of the genome in the NIGMS Human Genetic Mutant Cell
RT   Repository.";
RL   Cytogenet. Cell Genet. 36:652-658(1983).
//
RX   PubMed=7329430; DOI=10.1016/0027-5107(81)90059-2;
RA   Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.;
RT   "Abnormalities of human chromosome 13 and in vitro radiosensitivity; a
RT   study of 19 fibroblast strains.";
RL   Mutat. Res. 84:157-167(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).
//