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Cellosaurus XPCS2BA (CVCL_V272)

[Text version]
Cell line name XPCS2BA
Synonyms XP2BA; Xeroderma Pigmentosum/Cockayne Syndrome 2 BAsel; GM13026
Accession CVCL_V272
Resource Identification Initiative To cite this cell line use: XPCS2BA (RRID:CVCL_V272)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Xeroderma pigmentosum-Cockayne syndrome complex (NCIt: C156031)
Xeroderma pigmentosum-Cockayne syndrome complex (ORDO: Orphanet_220295)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZP38 (XPCS2BASV)
Sex of cell Male
Age at sampling 36Y
Category Finite cell line
Publications

PubMed=8408834; DOI=10.1016/0190-9622(93)70263-s
Rodney James Scott, Peter Itin, Wim J. Kleijer, Kristoph Kolb, Colin Francis Arlett, Hansjakob Muller;
Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair.
J. Am. Acad. Dermatol. 29:883-889(1993)

PubMed=9584159; DOI=10.1128/mcb.18.6.3182; PMCID=PMC108900
Vesna Rapic-Otrin, Isao Kuraoka, Tiziana Nardo, Mary McLenigan, Andre P.M. Eker, Miria Stefanini, Arthur S. Levine, Richard Dean Wood;
Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A.
Mol. Cell. Biol. 18:3182-3190(1998)

PubMed=10332046; DOI=10.1093/hmg/8.6.1125
Lydia Riou, Lin Zeng, Odile Chevallier-Lagente, Anne Stary, Osamu Nikaido, Alain Taieb, Geert Weeda, Mauro Mezzina, Alain Sarasin;
The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
Hum. Mol. Genet. 8:1125-1133(1999)

PubMed=16947863; DOI=10.1002/humu.20392
Kyu-Seon Oh, Sikandar G. Khan, Nicolaas G.J. Jaspers, Anja Raams, Takahiro Ueda, Alan R. Lehmann, Peter S. Friedmann, Steffen Emmert, Alexei Gratchev, Katherine Lachlan, Anneke Lucassan ...Show all 13 authors... , Carl C. Baker, Kenneth H. Kraemer; Show fewer authors
Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
Hum. Mutat. 27:1092-1103(2006)

PubMed=18079351; DOI=10.1259/bjr/27072321
Colin Francis Arlett, Michael H.L. Green, Paul Bryan Rogers, Alan R. Lehmann, Piers N. Plowman;
Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts.
Br. J. Radiol. 81:51-58(2008)

PubMed=26184184; DOI=10.3390/ijms160715985; PMCID=PMC4519934
Nikola A. Bowden, Natalie J. Beveridge, Katie A. Ashton, Katherine J. Baines, Rodney James Scott;
Understanding xeroderma pigmentosum complementation groups using gene expression profiling after UV-light exposure.
Int. J. Mol. Sci. 16:15985-15996(2015)

Cross-references
Cell line collections (Providers) Coriell; GM13026
Cell line databases/resources CLO; CLO_0013998
Biological sample resources BioSample; SAMN00802024
Encyclopedic resources Wikidata; Q54846269
Experimental variables resources EFO; EFO_0022698
Entry history
Entry creation16-Apr-2014
Last entry update19-Dec-2024
Version number16