FANCONI ANEMIA, COMPLEMENTATION GROUP N

Known as: FANCN 
 

Topic mentions per year

Topic mentions per year

2007-2015
02420072015

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2013
2013
BACKGROUND The PALB2 gene, also known as FANCN, forms a bond and co-localizes with BRCA2 in DNA repair. Germline mutations in… (More)
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2011
2011
Inherited BRCA1 mutations confer elevated cancer risk. Recent studies have identified genes that encode proteins that interact… (More)
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2011
2011
Fanconi anemia (FA) associated genes [FANCA, -B, -C, FANCD1(BRCA2), -D2, -E, -F, -G, -I, -L, -M, FANCN (PALB2), FANCJ(BRIP1) and… (More)
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2009
2009
Fanconi anemia (FA) is characterized by cellular hypersensitivity to DNA crosslinking agents, but how the Fanconi pathway… (More)
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2009
2009
Fanconi anemia is a cancer-prone inherited bone marrow failure and cancer susceptibility syndrome with at least 13… (More)
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2009
2009
Fanconi Anemia (FA) is a rare recessive syndrome characterized by cellular hypersensitivity to DNA-cross-linking agents. To date… (More)
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2008
2008
The partner and localizer of BRCA2 (PALB2) gene was recently identified as a BRCA2-interacting protein and subsequently shown to… (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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2008
2008
F irst described by Guido Fanconi in 1927, Fanconi anemia (FA) is now one of the best defined inherited bone marrow failure… (More)
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2007
2007
B ack-to-back publications in the February issue of Nature Genetics reveal the identity of the gene underlying the thirteenth… (More)
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