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Cellosaurus AG13207 (CVCL_0Q99)

[Text version]
Cell line name AG13207
Accession CVCL_0Q99
Resource Identification Initiative To cite this cell line use: AG13207 (RRID:CVCL_0Q99)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Neonatal progeroid syndrome (NCIt: C121565)
Wiedemann-Rautenstrauch syndrome (ORDO: Orphanet_3455)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 1M
Category Finite cell line
Publications

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

PubMed=12768443; DOI=10.1007/s10038-003-0025-3
Cao H.-N., Hegele R.A.
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).
J. Hum. Genet. 48:271-274(2003)

Cross-references
Cell line collections (Providers) Coriell; AG13207
Cell line databases/resources CLO; CLO_0022093
Encyclopedic resources Wikidata; Q54744768
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number9