ID   AG12795
AC   CVCL_U316
DR   CLO; CLO_0022890
DR   Coriell; AG12795
DR   GEO; GSM476006
DR   Wikidata; Q54744466
RX   CelloPub=CLPUB00597;
RX   PubMed=10655550;
RX   PubMed=16339323;
RX   PubMed=19966276;
CC   Population: Japanese.
CC   Omics: Transcriptome analysis by microarray.
CC   Derived from site: In situ; Thigh, skin; UBERON=UBERON_0004262.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_U312 ! AG05231
SX   Male
AG   19Y
CA   Finite cell line
DT   Created: 03-02-14; Last updated: 29-06-23; Version: 12
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RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994).
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RX   PubMed=10655550; DOI=10.1093/hmg/9.3.403;
RA   Ouellette M.M., McDaniel L.D., Wright W.E., Shay J.W., Schultz R.A.;
RT   "The establishment of telomerase-immortalized cell lines representing
RT   human chromosome instability syndromes.";
RL   Hum. Mol. Genet. 9:403-411(2000).
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RX   PubMed=16339323; DOI=10.1093/gerona/60.11.1386;
RA   Davis T., Baird D.M., Haughton M.F., Jones C.J., Kipling D.;
RT   "Prevention of accelerated cell aging in Werner syndrome using a p38
RT   mitogen-activated protein kinase inhibitor.";
RL   J. Gerontol., A, Biol. Sci. Med. Sci. 60:1386-1393(2005).
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RX   PubMed=19966276; DOI=10.1093/nar/gkp1103; PMCID=PMC2831322;
RA   Johnson J.E., Cao K., Ryvkin P., Wang L.-S., Johnson F.B.;
RT   "Altered gene expression in the Werner and Bloom syndromes is
RT   associated with sequences having G-quadruplex forming potential.";
RL   Nucleic Acids Res. 38:1114-1122(2010).
//