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Cellosaurus XP67TMA (CVCL_1F33)

[Text version]
Cell line name XP67TMA
Synonyms Xeroderma Pigmentosum Turkey MAlatya 67; GM14867
Accession CVCL_1F33
Resource Identification Initiative To cite this cell line use: XP67TMA (RRID:CVCL_1F33)
Comments Population: Turkish.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
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 Male
Age at sampling 7Y
Category Finite cell line
Publications

PubMed=11511294; DOI=10.1046/j.1523-1747.2001.01424.x
Gozukara E.M., Khan S.G., Metin A., Emmert S., Busch D.B., Shahlavi T., Coleman D.M., Miller M., Chinsomboon N., Stefanini M., Kraemer K.H.
A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: molecular genetic evidence for a common ancestor.
J. Invest. Dermatol. 117:197-204(2001)

PubMed=16081512; DOI=10.1093/carcin/bgi204
Khan S.G., Oh K.-S., Shahlavi T., Ueda T., Busch D.B., Inui H., Emmert S., Imoto K., Muniz-Medina V., Baker C.C., DiGiovanna J.J., Schmidt D., Khadavi A., Metin A., Gozukara E.M., Slor H., Sarasin A., Kraemer K.H.
Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.
Carcinogenesis 27:84-94(2006)

PubMed=18809580; DOI=10.1128/mcb.00781-08
Bernardes de Jesus B.M., Bjoras M., Coin F., Egly J.-M.
Dissection of the molecular defects caused by pathogenic mutations in the DNA repair factor XPC.
Mol. Cell. Biol. 28:7225-7235(2008)

Cross-references
Cell line collections (Providers) Coriell; GM14867
Cell line databases/resources CLO; CLO_0031923
Encyclopedic resources Wikidata; Q54847483
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number13