ID   GM02767
AC   CVCL_V469
SY   GM-2767; GM 2767; GM2767; GM02767C; GM 2767C
DR   CLO; CLO_0014806
DR   BioSample; SAMN00808092
DR   Coriell; GM02767
DR   GEO; GSM426281
DR   Wikidata; Q54837675
RX   CelloPub=CLPUB00447;
RX   Patent=US5773219;
RX   PubMed=291901;
RX   PubMed=6661932;
RX   PubMed=7299037;
RX   PubMed=8643543;
RX   PubMed=17668376;
RX   PubMed=19727395;
CC   Omics: Transcriptome analysis by microarray.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C2993; Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   14Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 18
//
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   Patent=US5773219;
RA   Sanford K.K., Parshad R., Robbins J.H.;
RT   "Process for detecting Alzheimer disease using cultured cells.";
RL   Patent number US5773219, 30-Jun-1998.
//
RX   PubMed=291901; DOI=10.1073/pnas.76.10.4817;
RA   Gupta S.L., Rubin B.Y., Holmes S.L.;
RT   "Interferon action: induction of specific proteins in mouse and human
RT   cells by homologous interferons.";
RL   Proc. Natl. Acad. Sci. U.S.A. 76:4817-4821(1979).
//
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=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=8643543; DOI=10.1073/pnas.93.10.5146;
RA   Parshad R., Sanford K.K., Price F.M., Melnick L.K., Nee L.E.,
RA   Schapiro M.B., Tarone R.E., Robbins J.H.;
RT   "Fluorescent light-induced chromatid breaks distinguish Alzheimer
RT   disease cells from normal cells in tissue culture.";
RL   Proc. Natl. Acad. Sci. U.S.A. 93:5146-5150(1996).
//
RX   PubMed=17668376; DOI=10.1086/519248;
RA   Prandini P., Deutsch S., Lyle R., Gagnebin M., Delucinge-Vivier C.,
RA   Delorenzi M., Gehrig C., Descombes P., Sherman S.L.,
RA   Dagna-Bricarelli F., Baldo C., Novelli A., Dallapiccola B.,
RA   Antonarakis S.E.;
RT   "Natural gene-expression variation in Down syndrome modulates the
RT   outcome of gene-dosage imbalance.";
RL   Am. J. Hum. Genet. 81:252-263(2007).
//
RX   PubMed=19727395; DOI=10.1371/journal.pone.0006888;
RA   Wadlow R.C., Wittner B.S., Finley S.A., Bergquist H., Upadhyay R.,
RA   Finn S.P., Loda M., Mahmood U., Ramaswamy S.;
RT   "Systems-level modeling of cancer-fibroblast interaction.";
RL   PLoS ONE 4:E6888-E6888(2009).
//