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Cellosaurus TTD1BR (CVCL_W046)

Cell line name TTD1BR
Synonyms TrichoThioDystrophy 1 BRighton
Accession CVCL_W046
Resource Identification Initiative To cite this cell line use: TTD1BR (RRID:CVCL_W046)
Comments Misspelling: TTD1BR3; PubMed=7671243.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Trichothiodystrophy 3, photosensitive (NCIt: C173099)
Trichothiodystrophy (ORDO: Orphanet_33364)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZP45 (TTD1BRSV)
Originate from same individual CVCL_2555 ! TTD1BR LCL
Sex of cell Male
Age at sampling 16Y
Category Finite cell line
STR profile Source(s): PubMed=11416159

Markers:
AmelogeninX,Y
D8S117911,14
D18S5113,21
D21S1130,31
FGA20,21
TH019.3
vWA17,18

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Publications

PubMed=1372096; DOI=10.1016/0921-8777(92)90074-d
Arlett C.F., Harcourt S.A., Cole J., Green M.H.L., Anstey A.V.
A comparison of the response of unstimulated and stimulated T-lymphocytes and fibroblasts from normal, xeroderma pigmentosum and trichothiodystrophy donors to the lethal action of UV-C.
Mutat. Res. 273:127-135(1992)

PubMed=8213812
Stefanini M., Vermeulen W., Weeda G., Giliani S., Nardo T., Mezzina M., Sarasin A., Harper J.I., Arlett C.F., Hoeijmakers J.H.J., Lehmann A.R.
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy.
Am. J. Hum. Genet. 53:817-821(1993)

PubMed=7671243
Eveno E., Bourre F., Quilliet X., Chevallier-Lagente O., Roza L., Eker A.P.M., Kleijer W.J., Nikaido O., Stefanini M., Hoeijmakers J.H.J., Bootsma D., Cleaver J.E., Sarasin A., Mezzina M.
Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.
Cancer Res. 55:4325-4332(1995)

PubMed=11416159; DOI=10.1073/pnas.121616198
Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.
Short tandem repeat profiling provides an international reference standard for human cell lines.
Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)

PubMed=15220921; DOI=10.1038/ng1387
Giglia-Mari G., Coin F., Ranish J.A., Hoogstraten D., Theil A.F., Wijgers N., Jaspers N.G.J., Raams A., Argentini M., van der Spek P.J., Botta E., Stefanini M., Egly J.-M., Aebersold R., Hoeijmakers J.H.J., Vermeulen W.
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A.
Nat. Genet. 36:714-719(2004)

Cross-references
Encyclopedic resources Wikidata; Q54973259
Entry history
Entry creation16-Apr-2014
Last entry update30-Jan-2024
Version number14