ID   GM02987
AC   CVCL_7370
SY   GM2987; GM 2987; GM 2,987; GM2987A; GM02987C
DR   CLO; CLO_0012588
DR   BioSample; SAMN00808197
DR   Coriell; GM02987
DR   Wikidata; Q54837789
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   PubMed=2445735;
RX   PubMed=6458814;
RX   PubMed=6621576;
RX   PubMed=6726265;
RX   PubMed=6773986;
RX   PubMed=6782112;
RX   PubMed=7847674;
RX   PubMed=8823375;
RX   PubMed=9804340;
CC   Population: Caucasian.
CC   Doubling time: Slow growth (Coriell=GM02987).
CC   Karyotypic information: 46,XY [43]; 46,XY,t(7;9)(7pter->7q36::9q12->9qter;9pter->9q12::7q36->qter) [7] (Coriell=GM02987).
CC   Derived from site: In situ; Leg, skin; UBERON=UBERON_0001511.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   19Y
CA   Finite cell line
DT   Created: 04-04-12; 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   PubMed=2445735; DOI=10.1016/S0021-9258(18)47730-7;
RA   Lin P.-Y., Gruenstein E.;
RT   "Identification of a defective cAMP-stimulated Cl- channel in cystic
RT   fibrosis fibroblasts.";
RL   J. Biol. Chem. 262:15345-15347(1987).
//
RX   PubMed=6458814; DOI=10.1073/pnas.78.10.6451;
RA   Scudiero D.A., Meyer S.A., Clatterbuck B.E., Tarone R.E.,
RA   Robbins J.H.;
RT   "Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in
RT   fibroblasts from patients with Huntington disease, familial
RT   dysautonomia, and other primary neuronal degenerations.";
RL   Proc. Natl. Acad. Sci. U.S.A. 78:6451-6455(1981).
//
RX   PubMed=6621576; DOI=10.1016/0027-5107(83)90010-6;
RA   Tarone R.E., Scudiero D.A., Robbins J.H.;
RT   "Statistical methods for in vitro cell survival assays.";
RL   Mutat. Res. 111:79-96(1983).
//
RX   PubMed=6726265; DOI=10.1136/jnnp.47.4.391;
RA   Robbins J.H., Scudiero D.A., Otsuka F., Tarone R.E., Brumback R.A.,
RA   Wirtschafter J.D., Polinsky R.J., Barrett S.F., Moshell A.N.,
RA   Scarpinato R.G., Ganges M.B., Nee L.E., Meyer S.A., Clatterbuck B.E.;
RT   "Hypersensitivity to DNA-damaging agents in cultured cells from
RT   patients with Usher's syndrome and Duchenne muscular dystrophy.";
RL   J. Neurol. Neurosurg. Psych. 47:391-398(1984).
//
RX   PubMed=6773986; DOI=10.1172/JCI109804;
RA   Gelman B.B., Papa L., Davis M.H., Gruenstein E.;
RT   "Decreased lysosomal dipeptidyl aminopeptidase I activity in cultured
RT   human skin fibroblasts in Duchenne's muscular dystrophy.";
RL   J. Clin. Invest. 65:1398-1406(1980).
//
RX   PubMed=6782112; DOI=10.1083/jcb.88.2.329;
RA   Gelman B.B., Davis M.H., Morris R.E., Gruenstein E.;
RT   "Structural changes in lysosomes from cultured human fibroblasts in
RT   Duchenne's muscular dystrophy.";
RL   J. Cell Biol. 88:329-337(1981).
//
RX   PubMed=7847674; DOI=10.1111/j.1749-6632.1994.tb44413.x;
RA   Etcheberrigaray R., Gibson G.E., Alkon D.L.;
RT   "Molecular mechanisms of memory and the pathophysiology of Alzheimer's
RT   disease.";
RL   Ann. N. Y. Acad. Sci. 747:245-255(1994).
//
RX   PubMed=8823375; DOI=10.1111/1523-1747.ep12584287;
RA   Moriwaki S.-i., Stefanini M., Lehmann A.R., Hoeijmakers J.H.J.,
RA   Robbins J.H., Rapin I., Botta E., Tanganelli B., Vermeulen W.,
RA   Broughton B.C., Kraemer K.H.;
RT   "DNA repair and ultraviolet mutagenesis in cells from a new patient
RT   with xeroderma pigmentosum group G and Cockayne syndrome resemble
RT   xeroderma pigmentosum cells.";
RL   J. Invest. Dermatol. 107:647-653(1996).
//
RX   PubMed=9804340; DOI=10.1046/j.1523-1747.1998.00391.x;
RA   Khan S.G., Levy H.L., Legerski R.J., Quackenbush E., Reardon J.T.,
RA   Emmert S., Sancar A., Li L., Schneider T.D., Cleaver J.E.,
RA   Kraemer K.H.;
RT   "Xeroderma pigmentosum group C splice mutation associated with autism
RT   and hypoglycinemia.";
RL   J. Invest. Dermatol. 111:791-796(1998).
//