[[abstract]]To get a clue to understand how mutations in the XPD gene result in different skin cancer susceptibilities in patients with xeroderma pigmentosum (XP) or trichothiodystrophy (TTD), a thorough understanding of their nucleotide excision repair (NER) defects is essential. Here, we extensively characterize the possible causes of NER defects in XP-D and in TTD fibroblasts. The 3 XP-D cell strains examined were similarly deficient in repairing UV-induced cyclobutane pyrimidine dimers (CPDs) and (6-4) photoproducts (6-4PPs) from genomic DNA. The severity of NER defects correlated with their UV sensitivities. Possible alterations of TFIIH (which consists of 10 subunits including XPD) were then examined. All XP-D cell strains were normal...
International audienceTrichothiodystrophy (TTD) is a rare, autosomal recessive disorder characterize...
Trichothiodystrophy (TTD) is a rare autosomal premature-ageing and neuroectodermal disease. The pho-...
SummaryXeroderma pigmentosum (XP) complementation group D is a heterogeneous group, containing patie...
International audienceDefects in nucleotide excision repair have been shown to be associated with th...
International audienceTo understand the heterogeneity in genetic predisposition to skin cancer in di...
Most trichothiodystrophy (TTD) patients present mutations in the xeroderma pigmentosum D (XPD) gene,...
Most trichothiodystrophy (TTD) patients present mutations in the xeroderma pigmentosum D (XPD) gene,...
Patients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) are highly pr...
To understand the relationship between DNA repair, apoptosis, transcription, and cancer-proneness, w...
textabstractPatients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) a...
International audienceThe human XPB DNA helicase is a subunit of the DNA repair/basal transcription ...
The xeroderma pigmentosum group D (XPD) protein is a subunit of transcription factor TFIIH with DNA ...
Patients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) are hig...
Trichothiodystrophy (TTD) is a rare autosomal recessive disease characterized by brittle hair with r...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder characterized by brittle hair, ment...
International audienceTrichothiodystrophy (TTD) is a rare, autosomal recessive disorder characterize...
Trichothiodystrophy (TTD) is a rare autosomal premature-ageing and neuroectodermal disease. The pho-...
SummaryXeroderma pigmentosum (XP) complementation group D is a heterogeneous group, containing patie...
International audienceDefects in nucleotide excision repair have been shown to be associated with th...
International audienceTo understand the heterogeneity in genetic predisposition to skin cancer in di...
Most trichothiodystrophy (TTD) patients present mutations in the xeroderma pigmentosum D (XPD) gene,...
Most trichothiodystrophy (TTD) patients present mutations in the xeroderma pigmentosum D (XPD) gene,...
Patients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) are highly pr...
To understand the relationship between DNA repair, apoptosis, transcription, and cancer-proneness, w...
textabstractPatients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) a...
International audienceThe human XPB DNA helicase is a subunit of the DNA repair/basal transcription ...
The xeroderma pigmentosum group D (XPD) protein is a subunit of transcription factor TFIIH with DNA ...
Patients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) are hig...
Trichothiodystrophy (TTD) is a rare autosomal recessive disease characterized by brittle hair with r...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder characterized by brittle hair, ment...
International audienceTrichothiodystrophy (TTD) is a rare, autosomal recessive disorder characterize...
Trichothiodystrophy (TTD) is a rare autosomal premature-ageing and neuroectodermal disease. The pho-...
SummaryXeroderma pigmentosum (XP) complementation group D is a heterogeneous group, containing patie...