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TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE

Known as: TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A, TTD3, TTDA 
 
National Institutes of Health

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Related topics

2 relations
GTF2H5 geneGTF2H5 wt Allele

Papers overview

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2014
2014
Sequential and ordered assembly of a large DNA repair complex on undamaged chromatin
The nucleotide excision repair preincision complex assembles on chromatin even in the absence of DNA damage through the… Expand
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2014
2014
Peptide-based MRI contrast agent and near-infrared fluorescent probe for intratumoral legumain detection.
Recent studies suggest that intratumoral legumain promotes tumorigenesis. To monitor legumain activity in tumors, we developed a… Expand
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Review
2013
Review
2013
Environmentally responsive MRI contrast agents.
Biomedical imaging techniques can provide a vast amount of anatomical information, enabling diagnosis and the monitoring of… Expand
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2013
2013
Disruption of TTDA Results in Complete Nucleotide Excision Repair Deficiency and Embryonic Lethality
The ten-subunit transcription factor IIH (TFIIH) plays a crucial role in transcription and nucleotide excision repair (NER… Expand
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2013
2013
In vivo interactions of TTDA mutant proteins within TFIIH
Summary Trichothiodystrophy group A (TTD-A) patients carry a mutation in the transcription factor II H (TFIIH) subunit TTDA… Expand
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2007
2007
Synthesis, complexation and water exchange properties of Gd(III)-TTDA-mono and bis(amide) derivatives and their binding affinity to human serum albumin.
With the objective of tuning the lipophilicity of ligands and maintaining the neutrality and stability of Gd(III) chelate, we… Expand
2006
2006
Functional identification of ygiP as a positive regulator of the ttdA-ttdB-ygjE operon.
Functional characterization of unknown genes is currently a major task in biology. The search for gene function involves a… Expand
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Highly Cited
2004
Highly Cited
2004
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A
DNA repair-deficient trichothiodystrophy (TTD) results from mutations in the XPD and XPB subunits of the DNA repair and… Expand
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Highly Cited
1997
Highly Cited
1997
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
Trichothiodystrophy (TTD) is a rare, autosomal recessive disorder characterized by sulfur-deficient brittle hair and nails… Expand
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1993
1993
Identification of the L-tartrate dehydratase genes (ttdA and ttdB) of Escherichia coli and evolutionary relationship with the class I fumarase genes.
The genes encoding an oxygen-labile stereospecific L-tartrate dehydratase (L-Ttd, EC 4.2.1.32) have been identified as the orfZ1… Expand
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