ID   GM00201
AC   CVCL_V460
SY   GM-201; GM-0201; GM 201; GM201; GM00201A; GM 0201A
DR   CLO; CLO_0025659
DR   Coriell; GM00201
DR   Wikidata; Q54836088
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   Patent=US5773219;
RX   PubMed=1132251;
RX   PubMed=6293786;
RX   PubMed=6661932;
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   13Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 15
//
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   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   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=1132251; DOI=10.1159/000130323;
RA   de la Chapelle A., Miller R.C., Greene A.E., Coriell L.L.;
RT   "A (1;17) translocation, balanced, plus trisomy 21, 47 chromosomes.
RT   Repository identification No. GM-201.";
RL   Cytogenet. Cell Genet. 14:82-83(1975).
//
RX   PubMed=6293786; DOI=10.1002/cyto.990030302;
RA   Lebo R.V.;
RT   "Chromosome sorting and DNA sequence localization.";
RL   Cytometry 3:145-154(1982).
//
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).
//