ID   GM03652
AC   CVCL_7397
SY   GM3652; GM3652A; GM03652C; C3652
DR   CLO; CLO_0015442
DR   BioSample; SAMN00808487
DR   Coriell; GM03652
DR   GEO; GSM2794409
DR   GEO; GSM3124681
DR   Wikidata; Q54838179
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   PubMed=2897722;
RX   PubMed=3863481;
RX   PubMed=7847674;
RX   PubMed=8247227;
RX   PubMed=26184184;
RX   PubMed=29125828;
RX   PubMed=30567591;
RX   PubMed=32291635;
RX   PubMed=35850241;
CC   Population: Caucasian.
CC   Omics: Lipidomics.
CC   Omics: Metabolomics.
CC   Omics: Transcriptomics; RNAseq.
CC   Misspelling: AG03652; PubMed=2897722; Note=In table 1.
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   24Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 10-04-25; Version: 16
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda; USA (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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda; USA (1986).
//
RX   PubMed=2897722; DOI=10.1002/tcm.1770080104;
RA   Nagasawa H., Burke M.J., Little F.F., McCone E.F., Chan G.L.,
RA   Little J.B.;
RT   "Multiple abnormalities in the ultraviolet light response of cultured
RT   fibroblasts derived from patients with the basal cell nevus syndrome.";
RL   Teratog. Carcinog. Mutagen. 8:25-33(1988).
//
RX   PubMed=3863481; PMCID=PMC1684690;
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=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=8247227; DOI=10.1016/0197-4580(93)90103-i;
RA   McCoy K.R., Mullins R.D., Newcomb T.G., Ng G.M., Pavlinkova G.,
RA   Polinsky R.J., Nee L.E., Sisken J.E.;
RT   "Serum- and bradykinin-induced calcium transients in familial
RT   Alzheimer's fibroblasts.";
RL   Neurobiol. Aging 14:447-455(1993).
//
RX   PubMed=26184184; DOI=10.3390/ijms160715985; PMCID=PMC4519934;
RA   Bowden N.A., Beveridge N.J., Ashton K.A., Baines K.J., Scott R.J.;
RT   "Understanding xeroderma pigmentosum complementation groups using gene
RT   expression profiling after UV-light exposure.";
RL   Int. J. Mol. Sci. 16:15985-15996(2015).
//
RX   PubMed=29125828; DOI=10.1242/dmm.030536; PMCID=PMC5719256;
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).
//
RX   PubMed=30567591; DOI=10.1186/s13059-018-1599-6; PMCID=PMC6300908;
RA   Fleischer J.G., Schulte R., Tsai H.H., Tyagi S., Ibarra A.,
RA   Shokhirev M.N., Huang L., Hetzer M.W., Navlakha S.;
RT   "Predicting age from the transcriptome of human dermal fibroblasts.";
RL   Genome Biol. 19:221.1-221.8(2018).
//
RX   PubMed=32291635; DOI=10.1007/s12035-020-01899-1; PMCID=PMC7253519;
RA   Misiorek J.O., Schreiber A.M., Urbanek-Trzeciak M.O., Hauser L.A.,
RA   Lynch D.R., Napierala J.S., Napierala M.;
RT   "A comprehensive transcriptome analysis identifies FXN and BDNF as
RT   novel targets of miRNAs in Friedreich's ataxia patients.";
RL   Mol. Neurobiol. 57:2639-2653(2020).
//
RX   PubMed=35850241; DOI=10.1016/j.jlr.2022.100255; PMCID=PMC9399481;
RA   Wang D.-Z., Ho E.S., Cotticelli M.G., Xu J.P.-N., Napierala J.S.,
RA   Hauser L.A., Napierala M., Himes B.E., Wilson R.B., Lynch D.R.,
RA   Mesaros C.;
RT   "Skin fibroblast metabolomic profiling reveals that lipid dysfunction
RT   predicts the severity of Friedreich's ataxia.";
RL   J. Lipid Res. 63:100255.1-100255.14(2022).
//