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TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE

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

Papers overview

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2014
2014
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
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
Biomedical imaging techniques can provide a vast amount of anatomical information, enabling diagnosis and the monitoring of… Expand
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2013
2013
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
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
With the objective of tuning the lipophilicity of ligands and maintaining the neutrality and stability of Gd(III) chelate, we… Expand
2006
2006
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
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
Trichothiodystrophy (TTD) is a rare, autosomal recessive disorder characterized by sulfur-deficient brittle hair and nails… Expand
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1993
1993
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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