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Cellosaurus XP3MA (CVCL_ZQ76)

[Text version]
Cell line name XP3MA
Synonyms Xeroderma Pigmentosum 3 MAnnheim
Accession CVCL_ZQ76
Resource Identification Initiative To cite this cell line use: XP3MA (RRID:CVCL_ZQ76)
Comments Caution: Said to originate from a female patient in PubMed=2054785 and from a male patient in PubMed=7165374.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group C (NCIt: C114770)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 12Y
Category Finite cell line
Publications

PubMed=7165374; DOI=10.1007/BF00403726
Fischer E., Thielmann H.W., Neundorfer B., Rentsch F.J., Edler L., Jung E.G.
Xeroderma pigmentosum patients from Germany: clinical symptoms and DNA repair characteristics.
Arch. Dermatol. Res. 274:229-247(1982)

PubMed=2175267; DOI=10.1016/0014-4827(90)90012-Y
Klein B., Pastink A., Odijk H., Westerveld A., van der Eb A.J.
Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts.
Exp. Cell Res. 191:256-262(1990)

PubMed=2054785
Thielmann H.W., Popanda O., Edler L., Jung E.G.
Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany.
Cancer Res. 51:3456-3470(1991)

Cross-references
Cell line collections (Providers) JCRB; KURB1107
Encyclopedic resources Wikidata; Q98135776
Entry history
Entry creation02-Jul-2020
Last entry update29-Jun-2023
Version number5