Cellosaurus cell line XP1PO (CVCL

Cellosaurus XP1PO (CVCL_F506)

Cross-references
Cell line name	XP1PO
Synonyms	GM05424; GM 5424; GM5424
Accession	CVCL_F506
Resource Identification Initiative	To cite this cell line use: XP1PO (RRID:CVCL_F506)
Comments	Population: Caucasian. 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)
Sex of cell	Male
Age at sampling	2Y
Category	Finite cell line
Publications	PubMed=7163956; DOI=10.1007/BF01543020 James Edward Cleaver; Rapid complementation method for classifying excision repair-defective xeroderma pigmentosum cell strains. Somatic Cell Genet. 8:801-810(1982) PubMed=2570806; DOI=10.1111/1523-1747.ep12284030 Hae-Ryong Chang, Kanji Ishizaki, Masao S. Sasaki, Junya Toguchida, Mitsuo Kato, Yusuke Nakamura, Susumu Kawamura, Takahiko Moriguchi, Mituo Ikenaga; Somatic mosaicism for DNA repair capacity in fibroblasts derived from a group A xeroderma pigmentosum patient. J. Invest. Dermatol. 93:460-465(1989) CLPUB00447 Richard A. Mulivor, Sharon F. Suchy; 1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992. (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992) PubMed=1372108; DOI=10.1016/0921-8777(92)90072-b Robert T. Johnson, Shoshana Squires; The XPD complementation group. Insights into xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy. Mutat. Res. 273:97-118(1992)
Cell line collections (Providers)	Coriell; GM05424 JCRB; KURB1069 JCRB; KURB1070
Cell line databases/resources	CLO; CLO_0024796
Encyclopedic resources	Wikidata; Q54839016
Entry history
Entry creation	11-Feb-2013
Last entry update	29-Jun-2023
Version number	13