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Cellosaurus XP165MA (CVCL_4T40)

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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
Annika Schafer, Steffen Schubert, Alexei Gratchev, Christina Seebode, Antje Apel, Petra Laspe, Lars Hofmann, Andreas Ohlenbusch, Toshio Mori, Nobuhiko Kobayashi, Anke Schurer ...Show all 13 authors... , Michael P. Schon, Steffen Emmert; Show fewer authors
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