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Genetics and Molecular Biology|May 31, 2017
A never-ending story: the steadily growing family of the FA and FA-like genesAnna Gueiderikh, Filippo Rosselli, Januario B C Neto
Journal of Cell Science|July 13, 2014
Proteomic analysis reveals a FANCA-modulated neddylation pathway involved in CXCR5 membrane targeting and cell mobilityXavier Renaudin, Jean-Hugues Guervilly, Said Aoufouchi, et al.
Blood|December 7, 2007
Aberrant activation of stress-response pathways leads to TNF-alpha oversecretion in Fanconi anemiaDelphine Briot, Gaëtane Macé-Aimé, Frédéric Subra, et al.
Human Molecular Genetics|March 11, 2011
USP1 deubiquitinase maintains phosphorylated CHK1 by limiting its DDB1-dependent degradationJean-Hugues Guervilly, Emilie Renaud, Minoru Takata, et al.
The Journal of Experimental Medicine|May 7, 2014
Fanca deficiency reduces A/T transitions in somatic hypermutation and alters class switch recombination junctions in mouse B cellsThuy Vy Nguyen, Lydia Riou, Saïd Aoufouchi, et al.
Scientific Reports|November 21, 2019
Fanconi anemia proteins counteract the implementation of the oncogene-induced senescence programAnne Helbling-Leclerc, Françoise Dessarps-Freichey, Caroline Evrard, et al.
Nucleic Acids Research|August 24, 2007
Psoralen-induced DNA adducts are substrates for the base excision repair pathway in human cellsSophie Couvé-Privat, Gaëtane Macé, Filippo Rosselli, et al.
The Journal of Clinical Investigation|December 27, 2019
Microphthalmia transcription factor expression contributes to bone marrow failure in Fanconi anemiaAlessia Oppezzo, Julie Bourseguin, Emilie Renaud, et al.
The Journal of Biological Chemistry|March 5, 2009
The human oxidative DNA glycosylase NEIL1 excises psoralen-induced interstrand DNA cross-links in a three-stranded DNA structureSophie Couvé, Gaëtane Macé-Aimé, Filippo Rosselli, et al.
Blood|September 28, 2014
Defective endomitosis during megakaryopoiesis leads to thrombocytopenia in Fanca-/- micePatrycja Pawlikowska, Pierre Fouchet, William Vainchenker, et al.
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