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Cellosaurus XP14BR.2 (CVCL_F629)

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Cell line name XP14BR.2
Synonyms Xeroderma Pigmentosum 14 BRighton 2; GM16092
Accession CVCL_F629
Resource Identification Initiative To cite this cell line use: XP14BR.2 (RRID:CVCL_F629)
Comments Population: Pakistani.
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)
Hierarchy Children:
CVCL_F630 (XP14BRneo17)
Originate from same individual CVCL_ZN23 ! XP14BR.1
Sex of cell Female
Age at sampling 14-15Y
Category Finite cell line
Publications

PubMed=10766188
Franz Chavanne, Bernard C. Broughton, Daniela Pietra, Tiziana Nardo, Alison Browitt, Alan Robert Lehmann, Miria Stefanini;
Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels.
Cancer Res. 60:1974-1982(2000)

PubMed=16714754; DOI=10.1259/bjr/83726649
Colin Francis Arlett, Piers N. Plowman, Paul Bryan Rogers, Christopher N. Parris, Fatemeh Abbaszadeh, Michael H.L. Green, Trevor J. McMillan, Cyd Bush, Nicolas Foray, Alan Robert Lehmann;
Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum.
Br. J. Radiol. 79:510-517(2006)

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

Cross-references
Cell line collections (Providers) Coriell; GM16092
Cell line databases/resources CLO; CLO_0018856
Encyclopedic resources Wikidata; Q54848316
Entry history
Entry creation11-Feb-2013
Last entry update19-Dec-2024
Version number12