Cellosaurus logo
expasy logo

Cellosaurus TTD2VI (CVCL_XG00)

[Text][XML][JSON]
Cell line name TTD2VI
Synonyms TTD 2VI; TrichoThioDystrophy 2 VIllejuif
Accession CVCL_XG00
Resource Identification Initiative To cite this cell line use: TTD2VI (RRID:CVCL_XG00)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Trichothiodystrophy 1, photosensitive (NCIt: C156433)
Trichothiodystrophy (ORDO: Orphanet_33364)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_XG01 (TTD2VILas)
Sex of cell Female
Age at sampling 4Y
Category Finite cell line
Publications

PubMed=1281671; DOI=10.1111/j.1365-2133.1992.tb14845.x
Alain Sarasin, Claudine Blanchet-Bardon, Georges Renault, Alan Robert Lehmann, Colin Francis Arlett, Yves Dumez;
Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair.
Br. J. Dermatol. 127:485-491(1992)

PubMed=8392442; DOI=10.1093/carcin/14.7.1255
Catherine Madzak, Jacques Armier, Anne Stary, Leela Daya-Grosjean, Alain Sarasin;
UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum.
Carcinogenesis 14:1255-1260(1993)

PubMed=8055625; DOI=10.1093/carcin/15.8.1493
Mauro Mezzina, Eric Eveno, Odile Chevallier-Lagente, Annie Benoit, Madeleine Carreau, Wim Vermeulen, Jan Hendrik Jozef Hoeijmakers, Miria Stefanini, Alan Robert Lehmann, Christine A. Weber, Alain Sarasin;
Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
Carcinogenesis 15:1493-1498(1994)

PubMed=7671243
Eric Eveno, Francois Bourre, Xavier Quilliet, Odile Chevallier-Lagente, Len Roza, Andre P.M. Eker, Wim J. Kleijer, Osamu Nikaido, Miria Stefanini, Jan Hendrik Jozef Hoeijmakers, Dirk Bootsma ...Show all 14 authors... , James Edward Cleaver, Alain Sarasin, Mauro Mezzina; Show fewer authors
Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.
Cancer Res. 55:4325-4332(1995)

PubMed=8824772; DOI=10.1016/0300-9084(95)90011-x
Eric Eveno, Xavier Quilliet, Odile Chevallier-Lagente, Leela Daya-Grosjean, Anne Stary, Lin Zeng, Annie Benoit, Elena Savini, Giovanni Ciarrocchi, Patricia Kannouche, Bernard Salles ...Show all 13 authors... , Alain Sarasin, Mauro Mezzina; Show fewer authors
Stable SV40-transformation and characterisation of some DNA repair properties of fibroblasts from a trichothiodystrophy patient.
Biochimie 77:906-912(1995)

PubMed=9012405; PMCID=PMC1712398
Geert Weeda, Eric Eveno, Ingrid Donker, Wim Vermeulen, Odile Chevallier-Lagente, Alain Taieb, Anne Stary, Jan Hendrik Jozef Hoeijmakers, Mauro Mezzina, Alain Sarasin;
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
Am. J. Hum. Genet. 60:320-329(1997)

PubMed=15009740; DOI=10.1046/j.0022-202X.2004.22226.x
Yoko Nishiwaki, Nobuhiko Kobayashi, Kyoko Imoto, Taka-aki Iwamoto, Aya Yamamoto, Sachiko Katsumi, Toshihiko Shirai, Shigeki Sugiura, Yu Nakamura, Alain Sarasin, Sachiko Miyagawa, Toshio Mori;
Trichothiodystrophy fibroblasts are deficient in the repair of ultraviolet-induced cyclobutane pyrimidine dimers and (6-4)photoproducts.
J. Invest. Dermatol. 122:526-532(2004)

Cross-references
Encyclopedic resources Wikidata; Q98133664
Entry history
Entry creation06-Sep-2019
Last entry update29-Jun-2023
Version number7