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Cellosaurus XP3TA (CVCL_ZQ21)

[Text version]
Cell line name XP3TA
Synonyms Xeroderma Pigmentosum 3 Tel Aviv
Accession CVCL_ZQ21
Resource Identification Initiative To cite this cell line use: XP3TA (RRID:CVCL_ZQ21)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group D (NCIt: C3967)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=11121128; DOI=10.1046/j.1523-1747.2000.00190.x
Hanoch Slor, Sima Batko, Sikandar G. Khan, Tama Sobe, Steffen Emmert, Arash Khadavi, Azriel Frumkin, David B. Busch, Roberta B. Albert, Kenneth H. Kraemer;
Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life.
J. Invest. Dermatol. 115:974-980(2000)

PubMed=12060391; DOI=10.1046/j.1523-1747.2002.01782.x
Steffen Emmert, Hanoch Slor, David B. Busch, Sima Batko, Roberta B. Albert, Donna M. Coleman, Sikandar G. Khan, Bassam Abu-Libdeh, John Joseph DiGiovanna, Bari Bickel Cunningham, Myung-Moo Lee ...Show all 19 authors... , Jill Crollick, Hiroki Inui, Takahiro Ueda, Mohammad Hedayati, Lawrence Grossman, Tala Shahlavi, James Edward Cleaver, Kenneth H. Kraemer; Show fewer authors
Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
J. Invest. Dermatol. 118:972-982(2002)

Cross-references
Encyclopedic resources Wikidata; Q98135789
Entry history
Entry creation02-Jul-2020
Last entry update29-Jun-2023
Version number5