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Cellosaurus XP165MA (CVCL_4T40)

[Text version]
Cell line name XP165MA
Accession CVCL_4T40
Resource Identification Initiative To cite this cell line use: XP165MA (RRID:CVCL_4T40)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group G (NCIt: C3969)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=23370536; DOI=10.1038/jid.2013.54
Schafer A., Schubert S., Gratchev A., Seebode C., Apel A., Laspe P., Hofmann L., Ohlenbusch A., Mori T., Kobayashi N., Schurer A., Schon M.P., Emmert S.
Characterization of three XPG-defective patients identifies three missense mutations that impair repair and transcription.
J. Invest. Dermatol. 133:1841-1849(2013)

Cross-references
Encyclopedic resources Wikidata; Q54994889
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number6