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The EMBO Journal|May 15, 1994
The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factorL Schaeffer, V Moncollin, R Roy, et al.
Carcinogenesis|June 1, 1993
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophyM Stefanini, P Lagomarsini, S Giliani, et al.
Carcinogenesis|March 1, 1992
Striking differences in cellular catalase activity between two DNA repair-deficient diseases: xeroderma pigmentosum and trichothiodystrophyM Vuillaume, L Daya-Grosjean, P Vincens, et al.
The Journal of Investigative Dermatology|December 18, 2002
Germline and somatic mutations of the INK4a-ARF gene in a xeroderma pigmentosum group C patientN Soufir, M Ribojad, T Magnaldo, et al.
Oncogene|October 20, 2000
Role of the cAMP and MAPK pathways in the transformation of mouse 3T3 fibroblasts by a TSHR gene constitutively activated by point mutationJ A Du Villard, R Wicker, P Crespo, et al.
Molecular Carcinogenesis|January 20, 1998
Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genesN Dumaz, A Duthu, J C Ehrhart, et al.
Carcinogenesis|August 1, 1993
Decrease in catalase activity and loss of the 11p chromosome arm in the course of SV40 transformation of human fibroblastsF Hoffschir, M Vuillaume, L Sabatier, et al.
American Journal of Human Genetics|February 1, 1997
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophyG Weeda, E Eveno, I Donker, et al.
Oncogene|September 25, 2007
High expression of DNA repair pathways is associated with metastasis in melanoma patientsA Kauffmann, F Rosselli, V Lazar, et al.
Biochemical and Biophysical Research Communications|December 14, 1990
Mutagenic properties of a unique abasic site in mammalian cellsA Gentil, G Renault, C Madzak, et al.
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