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Cellosaurus HGMLBV078 (CVCL_2A22)

[Text version]
Cell line name HGMLBV078
Accession CVCL_2A22
Resource Identification Initiative To cite this cell line use: HGMLBV078 (RRID:CVCL_2A22)
Comments Part of: Progeria Research Foundation cell lines.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Category Transformed cell line
Publications

PubMed=12714972; DOI=10.1038/nature01629; PMCID=PMC10540076
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; Q54887304
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number9