ID   GM00288
AC   CVCL_L938
SY   GM0288; GM-288; GM 288; GM288; GM00288A; GM0288A; GM00095; GM0095; C288
DR   CLO; CLO_0025524
DR   Coriell; GM00095
DR   Coriell; GM00288
DR   Wikidata; Q54836131
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=3863481;
RX   PubMed=6220707;
RX   PubMed=7299037;
RX   PubMed=29125828;
CC   Population: Caucasian.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Discontinued: Coriell; GM00095; true.
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   64Y
CA   Finite cell line
DT   Created: 06-05-13; Last updated: 29-06-23; Version: 15
//
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   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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   CelloPub=CLPUB00720;
RA   Greene A.E., Mulivor R.A.;
RT   "1986/1987 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 13th edition. October 1986.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (1986).
//
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=3863481;
RA   Goldman D., Goldin L.R., Rathnagiri P., O'Brien S.J., Egeland J.A.,
RA   Merril C.R.;
RT   "Twenty-seven protein polymorphisms by two-dimensional electrophoresis
RT   of serum, erythrocytes, and fibroblasts in two pedigrees.";
RL   Am. J. Hum. Genet. 37:898-911(1985).
//
RX   PubMed=6220707; DOI=10.1016/0006-291x(83)90361-3;
RA   Chua C.C., Geiman D.E., Ladda R.L.;
RT   "Detection of an Mr 200,000 glycoprotein in the culture medium of skin
RT   fibroblasts from patients with Huntington disease.";
RL   Biochem. Biophys. Res. Commun. 111:690-699(1983).
//
RX   PubMed=7299037; DOI=10.1016/0165-022X(81)90016-6;
RA   Sorbi S., Blass J.P.;
RT   "Spectrophotometric measurement of pyruvate dehydrogenase complex
RT   activity in cultured human fibroblasts.";
RL   J. Biochem. Biophys. Methods 5:169-176(1981).
//
RX   PubMed=29125828; DOI=10.1242/dmm.030536;
RA   Napierala J.S., Li Y.-J., Lu Y., Lin K., Hauser L.A., Lynch D.R.,
RA   Napierala M.;
RT   "Comprehensive analysis of gene expression patterns in Friedreich's
RT   ataxia fibroblasts by RNA sequencing reveals altered levels of protein
RT   synthesis factors and solute carriers.";
RL   Dis. Model. Mech. 10:1353-1369(2017).
//