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Neurobiology of Disease|May 8, 2014
Excitation/inhibition balance and learning are modified by Dyrk1a gene dosageBenoit Souchet, Fayçal Guedj, Ignasi Sahún, et al.
Plos Genetics|March 25, 2015
Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App regionVéronique Brault, Arnaud Duchon, Caroline Romestaing, et al.
Human Molecular Genetics|March 11, 2021
Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse modelsArnaud Duchon, Maria Del Mar Muniz Moreno, Sandra Martin Lorenzo, et al.
Disease Models & Mechanisms|August 18, 2018
Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1AThu Lan Nguyen, Arnaud Duchon, Antigoni Manousopoulou, et al.
Plos One|October 22, 2009
DYRK1A, a novel determinant of the methionine-homocysteine cycle in different mouse models overexpressing this Down-syndrome-associated kinaseChristophe Noll, Chris Planque, Clémentine Ripoll, et al.
Human Molecular Genetics|September 29, 2009
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndromePatricia Lopes Pereira, Laetitia Magnol, Ignasi Sahún, et al.
Scientific Reports|January 26, 2020
A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology TreatmentAnne-Cécile Guyot, Charlotte Leuxe, Clémence Disdier, et al.
Scientific Reports|July 5, 2020
Author Correction: A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology TreatmentAnne-Cécile Guyot, Charlotte Leuxe, Clémence Disdier, et al.
Molecular Nutrition & Food Research|September 17, 2013
Epigallocatechin-3-gallate, a DYRK1A inhibitor, rescues cognitive deficits in Down syndrome mouse models and in humansRafael De la Torre, Susana De Sola, Meritxell Pons, et al.
Nature Communications|May 16, 2019
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesisEkaterina L Ivanova, Johan G Gilet, Vadym Sulimenko, et al.
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