ERCC6 protein, human

Known as: Cockayne Syndrome B Repair Protein, Cockayne Syndrome Protein CSB, ATP-Dependent Helicase ERCC6 
DNA excision repair protein ERCC-6 (1493 aa, ~168 kDa) is encoded by the human ERCC6 gene. This protein plays a role in transcription-coupled DNA… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2017
051019922017

Papers overview

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2012
2012
UV-sensitive syndrome (UVSS) is an autosomal recessive disorder characterized by photosensitivity and deficiency in transcription… (More)
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2009
2009
Laryngeal cancer is known to be associated with smoking and high alcohol consumption. Nucleotide excision repair (NER) plays a… (More)
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2006
2006
Cockayne syndrome (CS) is an inherited neurodevelopmental disorder with progeroid features. Although the genes responsible for CS… (More)
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2006
2006
OBJECTIVES Nucleotide excision repair enzymes remove bulky damage caused by environmental agents, including carcinogenic… (More)
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2006
2006
This study investigates age-related macular degeneration (AMD) genetic risk factors through identification of a functional single… (More)
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Highly Cited
1997
Highly Cited
1997
Cockayne's syndrome (CS) is a disease characterized by developmental and growth defects, sunlight sensitivity, and a defect in… (More)
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Highly Cited
1997
Highly Cited
1997
Transcription is coupled to repair in Escherichia coli and in humans. Proteins encoded by the mfd gene in E. coli and by the… (More)
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Highly Cited
1995
Highly Cited
1995
The ATR-X syndrome is an X-linked disorder comprising severe psychomotor retardation, characteristic facial features, genital… (More)
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Highly Cited
1994
Highly Cited
1994
Transcription-coupled repair (TCR) is a universal sub-pathway of the nucleotide excision repair (NER) system that is limited to… (More)
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Highly Cited
1992
Highly Cited
1992
Cells from patients with the UV-sensitive nucleotide excision repair disorder Cockayne's syndrome (CS) have a specific defect in… (More)
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