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Cellosaurus XP14BR.2 (CVCL_F629)

[Text version]
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
Chavanne F., Broughton B.C., Pietra D., Nardo T., Browitt A., Lehmann A.R., Stefanini M.
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
Arlett C.F., Plowman P.N., Rogers P.B., Parris C.N., Abbaszadeh F., Green M.H.L., McMillan T.J., Bush C., Foray N., Lehmann A.R.
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
Arlett C.F., Green M.H.L., Rogers P.B., Lehmann A.R., Plowman P.N.
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