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Cellosaurus XP13CA (CVCL_V266)

[Text version]
Cell line name XP13CA
Synonyms Xeroderma Pigmentosum 13 CAiro; AG03964; AG3964; GM03964; GM3964
Accession CVCL_V266
Resource Identification Initiative To cite this cell line use: XP13CA (RRID:CVCL_V266)
Comments Population: Egyptian.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
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 Male
Age at sampling 35Y
Category Finite cell line
Publications

PubMed=7252263; DOI=10.1111/1523-1747.ep12479271
Cleaver J.E., Zelle B., Hashem N., El-Hefnawi M.H., German J.L. III
Xeroderma pigmentosum patients from Egypt: II. Preliminary correlations of epidemiology, clinical symptoms and molecular biology.
J. Invest. Dermatol. 77:96-101(1981)

PubMed=7163956; DOI=10.1007/BF01543020
Cleaver J.E.
Rapid complementation method for classifying excision repair-defective xeroderma pigmentosum cell strains.
Somatic Cell Genet. 8:801-810(1982)

CLPUB00597
National Institute on Aging
1994 catalog of cell lines. NIA Aging Cell Repository.
(In) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda (1994)

PubMed=9671271; DOI=10.1002/(SICI)1098-1004(1998)12:2<103::AID-HUMU5>3.0.CO;2-6
States J.C., McDuffie E.R., Myrand S.P., McDowell M., Cleaver J.E.
Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein.
Hum. Mutat. 12:103-113(1998)

Cross-references
Cell line collections (Providers) Coriell; AG03964
Coriell; GM03964 - Discontinued
Cell line databases/resources CLO; CLO_0034763
Encyclopedic resources Wikidata; Q54609899
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number12