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Cellosaurus TTD1GL (CVCL_ZU59)

[Text version]
Cell line name TTD1GL
Synonyms TrichoThioDystrophy 1 GLascow; P1
Accession CVCL_ZU59
Resource Identification Initiative To cite this cell line use: TTD1GL (RRID:CVCL_ZU59)
Comments Population: Caucasian; Scottish.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Trichothiodystrophy (NCIt: C4924)
Trichothiodystrophy (ORDO: Orphanet_33364)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 4Y
Category Finite cell line
Publications

PubMed=6492094; DOI=10.1136/jmg.21.4.286; PMCID=PMC1049299
King M.D., Gummer C.L., Stephenson J.B.P.
Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases.
J. Med. Genet. 21:286-289(1984)

PubMed=2458832
Lehmann A.R., Arlett C.F., Broughton B.C., Harcourt S.A., Steingrimsdottir H., Stefanini M., Taylor A.M.R., Natarajan A.T., Green S., King M.D., MacKie R.M., Stephenson J.B.P., Tolmie J.L.
Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.
Cancer Res. 48:6090-6096(1988)

Cross-references
Encyclopedic resources Wikidata; Q98133657
Entry history
Entry creation02-Jul-2020
Last entry update29-Jun-2023
Version number5