Cellosaurus cell line AG10548 (CVCL

Cellosaurus AG10548 (CVCL_L628)

Cross-references
Cell line name	AG10548
Synonyms	C8803
Accession	CVCL_L628
Resource Identification Initiative	To cite this cell line use: AG10548 (RRID:CVCL_L628)
Comments	Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427. Cell type: Fibroblast of skin; CL=CL_0002620.
Disease	Progeria (NCIt: C34951) Hutchinson-Gilford progeria syndrome (ORDO: Orphanet_740)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	8Y4M
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=10741968; DOI=10.1126/science.287.5462.2486 Danith H. Ly, David J. Lockhart, Richard Alan Lerner, Peter G. Schultz; Mitotic misregulation and human aging. Science 287:2486-2492(2000) PubMed=12714972; DOI=10.1038/nature01629; PMCID=PMC10540076 Maria Eriksson, W. Ted Brown, Leslie Beth Gordon, Michael W. Glynn, Joel Singer, Laura Scott, Michael R. Erdos, Christiane M. Robbins, Tracy Y. Moses, Peter Berglund, Amalia Dutra ...Show all 17 authors... , Evgenia Pak, Sandra Durkin, Antonei Benjamin Csoka, Michael Boehnke, Thomas W. Glover, Francis Sellers Collins; Show fewer authors Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 423:293-298(2003)
Cell line collections (Providers)	Coriell; AG10548 - Discontinued
Encyclopedic resources	Wikidata; Q54743352
Entry history
Entry creation	06-May-2013
Last entry update	29-Jun-2023
Version number	9