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Cellosaurus AG12795 (CVCL_U316)

[Text version]
Cell line name AG12795
Accession CVCL_U316
Resource Identification Initiative To cite this cell line use: AG12795 (RRID:CVCL_U316)
Comments Population: Japanese.
Omics: Transcriptome analysis by microarray.
Derived from site: In situ; Thigh, skin; UBERON=UBERON_0004262.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Werner syndrome (NCIt: C3447)
Werner syndrome (ORDO: Orphanet_902)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZS70 (hTERT-WRN2)
Originate from same individual CVCL_U312 ! AG05231
Sex of cell Male
Age at sampling 19Y
Category Finite cell line
Publications

CLPUB00597
National Institute on Aging
1994 catalog of cell lines. NIA Aging Cell Repository.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994)

PubMed=10655550; DOI=10.1093/hmg/9.3.403
Ouellette M.M., McDaniel L.D., Wright W.E., Shay J.W., Schultz R.A.
The establishment of telomerase-immortalized cell lines representing human chromosome instability syndromes.
Hum. Mol. Genet. 9:403-411(2000)

PubMed=16339323; DOI=10.1093/gerona/60.11.1386
Davis T., Baird D.M., Haughton M.F., Jones C.J., Kipling D.
Prevention of accelerated cell aging in Werner syndrome using a p38 mitogen-activated protein kinase inhibitor.
J. Gerontol., A, Biol. Sci. Med. Sci. 60:1386-1393(2005)

PubMed=19966276; DOI=10.1093/nar/gkp1103; PMCID=PMC2831322
Johnson J.E., Cao K., Ryvkin P., Wang L.-S., Johnson F.B.
Altered gene expression in the Werner and Bloom syndromes is associated with sequences having G-quadruplex forming potential.
Nucleic Acids Res. 38:1114-1122(2010)

Cross-references
Cell line collections (Providers) Coriell; AG12795
Cell line databases/resources CLO; CLO_0022890
Encyclopedic resources Wikidata; Q54744466
Gene expression databases GEO; GSM476006
Entry history
Entry creation03-Feb-2014
Last entry update29-Jun-2023
Version number12