ID   GM08398
AC   CVCL_7481
SY   GM8398; GM08398C
DR   CLO; CLO_0010526
DR   BioSample; SAMN00798056
DR   Coriell; GM08398
DR   GEO; GSM88313
DR   GEO; GSM88314
DR   GEO; GSM88315
DR   GEO; GSM88295
DR   GEO; GSM88296
DR   GEO; GSM88297
DR   GEO; GSM1316986
DR   GEO; GSM1317025
DR   GEO; GSM3124634
DR   Wikidata; Q54843196
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   PubMed=15268757;
RX   PubMed=16126733;
RX   PubMed=30567591;
RX   PubMed=33038742;
CC   Population: Caucasian.
CC   Omics: miRNA expression profiling.
CC   Omics: Transcriptome analysis by microarray.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Derived from site: In situ; Groin, skin; UBERON=UBERON_8410021.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   8Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 29-06-23; Version: 17
//
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=15268757; DOI=10.1111/j.1474-9728.2004.00105.x;
RA   Csoka A.B., English S.B., Simkevich C.P., Ginzinger D.G., Butte A.J.,
RA   Schatten G.P., Rothman F.G., Sedivy J.M.;
RT   "Genome-scale expression profiling of Hutchinson-Gilford progeria
RT   syndrome reveals widespread transcriptional misregulation leading to
RT   mesodermal/mesenchymal defects and accelerated atherosclerosis.";
RL   Aging Cell 3:235-243(2004).
//
RX   PubMed=16126733; DOI=10.1093/hmg/ddi326;
RA   Glynn M.W., Glover T.W.;
RT   "Incomplete processing of mutant lamin A in Hutchinson-Gilford
RT   progeria leads to nuclear abnormalities, which are reversed by
RT   farnesyltransferase inhibition.";
RL   Hum. Mol. Genet. 14:2959-2969(2005).
//
RX   PubMed=30567591; DOI=10.1186/s13059-018-1599-6;
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=33038742; DOI=10.1016/j.scr.2020.102011;
RA   Xu X.-G., Pradhan M., Xu M., Cheng Y.-S., Beers J.K., Linask K.L.,
RA   Lin Y.-S., Zheng W., Zou J.-H.;
RT   "Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D,
RT   TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy
RT   individuals.";
RL   Stem Cell Res. 49:102011-102011(2020).
//