Xeroderma pigmentosum, group F

Known as: Xeroderma Pigmentosum, Complementation Group F, XP, GROUP F, Xeroderma Pigmentosum Vi 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2018
02419842018

Papers overview

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2010
2010
Xeroderma pigmentosum group F (XPF) has an essential role in the nucleotide excision repair pathway that removes a wide variety… (More)
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Highly Cited
2009
Highly Cited
2009
Many studies have detailed the repressive effects of DNA methylation on gene expression. However, the mechanisms that promote… (More)
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2009
2009
Many repair and recombination proteins play essential roles in telomere function and chromosome stability, notwithstanding the… (More)
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2008
2008
XPF-ERCC1, a structure-specific endonuclease, is involved in nucleotide excision repair, crosslink repair and homologous… (More)
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2007
2007
Resistance to camptothecin (CPT), a topoisomerase I (Top1) inhibitor, is frequently encountered in non-small cell lung cancer… (More)
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Highly Cited
2004
Highly Cited
2004
Xeroderma pigmentosum (XP) is a human genetic disease which is caused by defects in nucleotide excision repair. Since this repair… (More)
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2004
2004
The Rad1-Rad10 nuclease of yeast and its human counterpart ERCC1-XPF are indispensable for nucleotide excision repair, where they… (More)
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2003
2003
The events responsible for repair of DNA interstrand cross-links in mammalian cells, the proteins involved and their interactions… (More)
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2002
2002
XPF-ERCC1 is a structure-specific endonuclease involved in nucleotide excision repair, interstrand crosslink repair and… (More)
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2001
2001
ERCC1-XPF is a structure-specific nuclease with two subunits, ERCC1 and XPF. The enzyme cuts DNA at junctions where a single… (More)
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