ID   MCI7885
AC   CVCL_A9E9
DR   Wikidata; Q102114507
RX   PubMed=7822435;
RX   PubMed=23847654;
CC   Population: Japanese.
CC   Derived from site: In situ; Abdomen, skin; UBERON=UBERON_0001416.
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)
SX   Female
AG   51Y
CA   Finite cell line
DT   Created: 29-10-20; Last updated: 29-06-23; Version: 5
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RX   PubMed=7822435; DOI=10.1002/jcp.1041620213;
RA   Oshima J., Campisi J., Tannock T.C.A., Martin G.M.;
RT   "Regulation of c-fos expression in senescing Werner syndrome
RT   fibroblasts differs from that observed in senescing fibroblasts from
RT   normal donors.";
RL   J. Cell. Physiol. 162:277-283(1995).
//
RX   PubMed=23847654; DOI=10.3389/fgene.2013.00129; PMCID=PMC3701863;
RA   Saha B., Zitnik G., Johnson S., Nguyen Q., Risques R.A., Martin G.M.,
RA   Oshima J.;
RT   "DNA damage accumulation and TRF2 degradation in atypical Werner
RT   syndrome fibroblasts with LMNA mutations.";
RL   Front. Genet. 4:129.1-129.12(2013).
//