ID   GM02912
AC   CVCL_7367
SY   GM2912; GM02912A; GM 2912A; GM2912A
DR   CLO; CLO_0012806
DR   BioSample; SAMN00808167
DR   Coriell; GM02912
DR   Wikidata; Q54837749
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   Patent=US5773219;
RX   PubMed=3863481;
RX   PubMed=8643543;
RX   PubMed=29762696;
CC   Population: Caucasian.
CC   Misspelling: GMO2912; PubMed=29762696.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   26Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 29-06-23; Version: 13
//
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   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=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=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=29762696; DOI=10.1093/nar/gky395;
RA   Bruun G.H., Bang J.M.V., Christensen L.L., Broner S., Petersen U.S.S.,
RA   Guerra B., Gronning A.G.B., Doktor T.K., Andresen B.S.;
RT   "Blocking of an intronic splicing silencer completely rescues IKBKAP
RT   exon 20 splicing in familial dysautonomia patient cells.";
RL   Nucleic Acids Res. 46:7938-7952(2018).
//