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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… 
2016
2016
The system described in this article has been developed within the project FANCI (Face and body Analysis Natural Computer… 
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…