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Cellosaurus XP81TO (CVCL_DE30)

[Text version]
Cell line name XP81TO
Synonyms Xeroderma Pigmentosum 81 TOkyo
Accession CVCL_DE30
Resource Identification Initiative To cite this cell line use: XP81TO (RRID:CVCL_DE30)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group E (NCIt: C114771)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=1376435; DOI=10.1016/0921-8777(92)90049-9
Keeney S.N., Wein H., Linn S.M.
Biochemical heterogeneity in xeroderma pigmentosum complementation group E.
Mutat. Res. 273:49-56(1992)

PubMed=12812979; DOI=10.1093/hmg/ddg174
Rapic-Otrin V., Navazza V., Nardo T., Botta E., McLenigan M., Bisi D.C., Levine A.S., Stefanini M.
True XP group E patients have a defective UV-damaged DNA binding protein complex and mutations in DDB2 which reveal the functional domains of its p48 product.
Hum. Mol. Genet. 12:1507-1522(2003)

Cross-references
Cell line collections (Providers) JCRB; KURB1085
Encyclopedic resources Wikidata; Q54994969
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number7