Xeroderma pigmentosum, group A

Known as: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A, XP1, Xeroderma Pigmentosum Group A 
 
National Institutes of Health

Papers overview

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2012
2012
Xeroderma pigmentosum group A (XPA) is a hereditary dermatological disease in which hypersensitivity to ultraviolet radiation and… (More)
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2009
2009
In response to DNA damage, eukaryotic cells activate a series of DNA damage-dependent pathways that serve to arrest cell cycle… (More)
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Highly Cited
2008
Highly Cited
2008
Cellular accumulation of DNA damage has been widely implicated in cellular senescence, aging, and premature aging. In Hutchinson… (More)
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2008
2008
Mutations in the RECQL4 helicase gene have been linked to Rothmund-Thomson syndrome, which is characterized by genome instability… (More)
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2008
2008
We have reported that xeroderma pigmentosum group A (Xpa) gene-knockout mice [Xpa (-/-) mice] are deficient in nucleotide… (More)
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2005
2005
Xeroderma pigmentosum group A (XPA) and Cockayne syndrome (CS) are caused by a genetic defect of nucleotide excision repair… (More)
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2004
2004
Xeroderma pigmentosum group A (XPA) is a hereditary disorder characterized by cutaneous symptoms and progressive… (More)
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Highly Cited
2001
Highly Cited
2001
The multiprotein factor composed of XPA and replication protein A (RPA) is an essential subunit of the mammalian nucleotide… (More)
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1996
1996
Xeroderma pigmentosum group A (XPA) gene-deficient mice were developed by gene targeting in mouse embryonic stem cells. To… (More)
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Highly Cited
1995
Highly Cited
1995
XERODERMA pigmentosum (XP) is an autosomal recessive disorder characterized by a high frequency of skin cancer on sun-exposed… (More)
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