C17orf70 wt Allele

Known as: FLJ30151, FLJ22175, FAAP100 
Human C17orf70 wild-type allele is located in the vicinity of 17q25.3 and is approximately 13 kb in length. This allele, which encodes Fanconi anemia… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2007-2017
012320072017

Papers overview

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2017
2017
Monoubiquitination and deubiquitination of FANCD2:FANCI heterodimer is central to DNA repair in a pathway that is defective in… (More)
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2017
2017
Activation of the main DNA interstrand crosslink repair pathway in higher eukaryotes requires mono-ubiquitination of FANCI and… (More)
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2014
2014
Fanconi anaemia (FA) is a cancer predisposition syndrome characterized by cellular sensitivity to DNA interstrand crosslinkers… (More)
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2012
2012
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure (BMF), clonal proliferation of hematopoietic stem… (More)
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2009
2009
Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer susceptibility… (More)
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Review
2009
Review
2009
Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer susceptibility… (More)
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Review
2009
Review
2009
The Fanconi anemia (FA) molecular network consists of 15 "FANC" proteins, of which 13 are associated with mutations in patients… (More)
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2008
2008
volume 15 number 11 november 2008 nature structural & molecular biology that monoubiquitinates the Fanconi anemia ID complex… (More)
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Highly Cited
2007
Highly Cited
2007
The Fanconi anemia (FA) core complex plays a central role in the DNA damage response network involving breast cancer… (More)
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