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Cellosaurus HGADFN005 (CVCL_2A26)

[Text version]
Cell line name HGADFN005
Accession CVCL_2A26
Resource Identification Initiative To cite this cell line use: HGADFN005 (RRID:CVCL_2A26)
Comments Part of: Progeria Research Foundation cell lines.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
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 Female
Category Finite cell line
Publications

PubMed=12714972; DOI=10.1038/nature01629
Eriksson M., Brown W.T., Gordon L.B., Glynn M.W., Singer J., Scott L., Erdos M.R., Robbins C.M., Moses T.Y., Berglund P., Dutra A., Pak E., Durkin S., Csoka A.B., Boehnke M., Glover T.W., Collins F.S.
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Nature 423:293-298(2003)

Cross-references
Encyclopedic resources Wikidata; Q54885940
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number9