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FANCONI ANEMIA, COMPLEMENTATION GROUP I

Known as: FANCI 
Fanconi anemia caused by mutations in the FANCI gene, encoding Fanconi anemia group I protein.
National Institutes of Health

Papers overview

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2020
2020
Monoubiquitinated FANCI and FANCD2 constitute the ID complex, which forms a sliding clamp on DNA. 
2017
2017
Fanconi anemia (FA), a cancer predisposition syndrome, exhibit hallmark feature of radial chromosome formation and hyper… 
2015
2015
New model of the FA pathway activation. Non-phosphorylated, non-ubiquitinated FANCI plays a critical role in recruitment of the… 
2014
2014
Hypoxia induces genomic instability through replication stress and dysregulation of vital DNA repair pathways. The Fanconi anemia… 
2014
2014
, 1698 (2009); 326 Science et al. Puck Knipscheer Interstrand Cross-Link Repair The Fanconi Anemia Pathway Promotes Replication… 
2013
2013
In this issue of Blood , Kim and colleagues demonstrate that the Fanconi anemia protein FANCP/SLX4 is multifunctional by… 
2008
2008
Cette invention se rapporte a des procedes et des compositions utilises dans le traitement du cancer. En particulier, l'invention…