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Frontiers in Behavioral Neuroscience|July 5, 2016
DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down SyndromeArnaud Duchon, Yann HeraultPlos Genetics|July 15, 2006
Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organizationVéronique Brault, Patricia Pereira, Arnaud Duchon, et al.Genes|November 27, 2021
Dyrk1a from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down SyndromeHelin Atas-Ozcan, Véronique Brault, Arnaud Duchon, et al.Plos One|February 24, 2015
Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndromeDamien Marechal, Patricia Lopes Pereira, Arnaud Duchon, et al.Progress in Brain Research|May 1, 2012
The in vivo Down syndrome genomic library in mouseYann Herault, Arnaud Duchon, Emilie Velot, et al.Genetics|September 2, 2008
Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombinationArnaud Duchon, Vanessa Besson, Patricia Lopes Pereira, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndromeArnaud Duchon, Matthieu Raveau, Claire Chevalier, et al.Current Genomics|March 2, 2011
Controlled somatic and germline copy number variation in the mouse modelYann Hérault, Arnaud Duchon, Damien Maréchal, et al.Neuroscience Letters|February 10, 2025
Dendritic phenotype and proliferation potency in the hippocampal dentate gyrus of the Ts66Yah model of Down syndromeMarco Emili, Fiorenza Stagni, Sandra Guidi, et al.Life (Basel, Switzerland)|February 26, 2025
DYRK1A Up-Regulation Specifically Impairs a Presynaptic Form of Long-Term PotentiationAude-Marie Lepagnol-Bestel, Simon Haziza, Julia Viard, et al.Pageof 4