XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C

Known as: XPCC, XP, Group C, Xeroderma Pigmentosum III 
An autosomal recessive inherited disorder caused by mutations in the XPC gene. This disease is characterized by increased sensitivity to sunlight… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2017
0102019762017

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2010
2010
Xeroderma pigmentosum (XP) is a group of rare inherited human neurocutaneous diseases, and the group C (XPC) is the major group… (More)
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2008
2008
Xeroderma pigmentousum group C protein (XPC) is involved in the first step of nucleotide excision repair, with multiple… (More)
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2006
2006
XPC is a 940-residue multidomain protein critical for the sensing of aberrant DNA and initiation of global genome nucleotide… (More)
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Highly Cited
2005
Highly Cited
2005
Xeroderma pigmentosum group C (XPC) protein plays a key role in DNA damage recognition in global genome nucleotide excision… (More)
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Highly Cited
2005
Highly Cited
2005
Previous studies point to the XPC-hHR23B complex as the principal initiator of global genome nucleotide excision repair (NER… (More)
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Highly Cited
2005
Highly Cited
2005
The xeroderma pigmentosum group C (XPC) protein complex plays a key role in recognizing DNA damage throughout the genome for… (More)
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2003
2003
The cyclobutane thymine dimer is the major DNA lesion induced in human skin by sunlight and is a primary cause of skin cancer… (More)
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Highly Cited
2002
Highly Cited
2002
DNA repair capacity (DRC) plays an important role in genetic susceptibility to cancer. Polymorphisms of a number of DNA repair… (More)
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Highly Cited
1998
Highly Cited
1998
The XPC-HR23B complex is specifically involved in global genome but not transcription-coupled nucleotide excision repair (NER… (More)
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Highly Cited
1994
Highly Cited
1994
The RNA polymerase II general transcription factor TFIIH is composed of several polypeptides. The observation that the largest… (More)
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