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Cellosaurus XPKMSF (CVCL_U764)

[Text version]
Cell line name XPKMSF
Synonyms XPKM
Accession CVCL_U764
Resource Identification Initiative To cite this cell line use: XPKMSF (RRID:CVCL_U764)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group A (NCIt: C3965)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Category Finite cell line
Publications

PubMed=4811796; DOI=10.7326/0003-4819-80-2-221
Robbins J.H., Kraemer K.H., Lutzner M.A., Festoff B.W., Coon H.G.
Xeroderma pigmentosum. An inherited disease with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair.
Ann. Intern. Med. 80:221-248(1974)

Cross-references
Cell line collections (Providers) ATCC; CRL-1203 - Discontinued
Encyclopedic resources Wikidata; Q54995019
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number8