检索结果 - Duchon, Arnaud

DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome 由 Duchon, Arnaud, Herault, Yann

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Modeling Chromosomes in Mouse to Explore the Function of Genes, Genomic Disorders, and Chromosomal Organization 由 Brault, Véronique, Pereira, Patricia, Duchon, Arnaud, Hérault, Yann

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Dosage of the Abcg1-U2af1 Region Modifies Locomotor and Cognitive Deficits Observed in the Tc1 Mouse Model of Down Syndrome 由 Marechal, Damien, Pereira, Patricia Lopes, Duchon, Arnaud, Herault, Yann

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Dyrk1a from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down Syndrome 由 Atas-Ozcan, Helin, Brault, Véronique, Duchon, Arnaud, Herault, Yann

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Inducing Segmental Aneuploid Mosaicism in the Mouse Through Targeted Asymmetric Sister Chromatid Event of Recombination 由 Duchon, Arnaud, Besson, Vanessa, Pereira, Patricia Lopes, Magnol, Laetitia, Hérault, Yann

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Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome 由 Duchon, Arnaud, Raveau, Matthieu, Chevalier, Claire, Nalesso, Valérie, Sharp, Andrew J., Herault, Yann

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Controlled Somatic and Germline Copy Number Variation in the Mouse Model 由 Hérault, Yann, Duchon, Arnaud, Maréchal, Damien, Raveau, Matthieu, Pereira, Patricia L., Dalloneau, Emilie, Brault, Véronique

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The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome 由 Duchon, Arnaud, Pothion, Stéphanie, Brault, Véronique, Sharp, Andrew J., Tybulewicz, Victor L.J., Fisher, Elizabeth M.C., Herault, Yann

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The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model 由 Raveau, Matthieu, Lignon, Jacques M., Nalesso, Valérie, Duchon, Arnaud, Groner, Yoram, Sharp, Andrew J., Dembele, Doulaye, Brault, Véronique, Hérault, Yann

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Deletion of the App-Runx1 region in mice models human partial monosomy 21 由 Arbogast, Thomas, Raveau, Matthieu, Chevalier, Claire, Nalesso, Valérie, Dembele, Doulaye, Jacobs, Hugues, Wendling, Olivia, Roux, Michel, Duchon, Arnaud, Herault, Yann

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Long‐lasting correction of in vivo LTP and cognitive deficits of mice modelling Down syndrome with an α5‐selective GABA(A) inverse agonist 由 Duchon, Arnaud, Gruart, Agnès, Albac, Christelle, Delatour, Benoît, Zorrilla de San Martin, Javier, Delgado‐García, José María, Hérault, Yann, Potier, Marie‐Claude

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Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models 由 Souchet, Benoit, Duchon, Arnaud, Gu, Yuchen, Dairou, Julien, Chevalier, Claire, Daubigney, Fabrice, Nalesso, Valérie, Créau, Nicole, Yu, Yuejin, Janel, Nathalie, Herault, Yann, Delabar, Jean Maurice

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Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region 由 Brault, Véronique, Duchon, Arnaud, Romestaing, Caroline, Sahun, Ignasi, Pothion, Stéphanie, Karout, Mona, Borel, Christelle, Dembele, Doulaye, Bizot, Jean-Charles, Messaddeq, Nadia, Sharp, Andrew J., Roussel, Damien, Antonarakis, Stylianos E, Dierssen, Mara, Hérault, Yann

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Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models 由 Duchon, Arnaud, del Mar Muniz Moreno, Maria, Martin Lorenzo, Sandra, Silva de Souza, Marcia Priscilla, Chevalier, Claire, Nalesso, Valérie, Meziane, Hamid, Loureiro de Sousa, Paulo, Noblet, Vincent, Armspach, Jean-Paul, Brault, Veronique, Herault, Yann

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DYRK1A, a Novel Determinant of the Methionine-Homocysteine Cycle in Different Mouse Models Overexpressing this Down-Syndrome-Associated Kinase 由 Noll, Christophe, Planque, Chris, Ripoll, Clémentine, Guedj, Fayçal, Diez, Anna, Ducros, Véronique, Belin, Nicole, Duchon, Arnaud, Paul, Jean-Louis, Badel, Anne, de Freminville, Bénédicte, Grattau, Yann, Bléhaut, Henri, Herault, Yann, Janel, Nathalie, Delabar, Jean-Maurice

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Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A 由 Nguyen, Thu Lan, Duchon, Arnaud, Manousopoulou, Antigoni, Loaëc, Nadège, Villiers, Benoît, Pani, Guillaume, Karatas, Meltem, Mechling, Anna E., Harsan, Laura-Adela, Limanton, Emmanuelle, Bazureau, Jean-Pierre, Carreaux, François, Garbis, Spiros D., Meijer, Laurent, Herault, Yann

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A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome 由 Pereira, Patricia Lopes, Magnol, Laetitia, Sahún, Ignasi, Brault, Véronique, Duchon, Arnaud, Prandini, Paola, Gruart, Agnès, Bizot, Jean-Charles, Chadefaux-Vekemans, Bernadette, Deutsch, Samuel, Trovero, Fabrice, Delgado-García, José María, Antonarakis, Stylianos E., Dierssen, Mara, Herault, Yann

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A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology Treatment 由 Guyot, Anne-Cécile, Leuxe, Charlotte, Disdier, Clémence, Oumata, Nassima, Costa, Narciso, Roux, Gwenaëlle Le, Fernandez-Varela, Paloma, Duchon, Arnaud, Charbonnier, Jean Baptiste, Herault, Yann, Pavoni, Serena, Galons, Hervé, Andriambeloson, Emile, Wagner, Stéphanie, Meijer, Laurent, Lund, Amie K., Mabondzo, Aloïse

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Author Correction: A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology Treatment 由 Guyot, Anne-Cécile, Leuxe, Charlotte, Disdier, Clémence, Oumata, Nassima, Costa, Narciso, Le Roux, Gwenaëlle, Varela, Paloma F., Duchon, Arnaud, Charbonnier, Jean Baptiste, Herault, Yann, Pavoni, Serena, Galons, Hervé, Andriambeloson, Emile, Wagner, Stéphanie, Meijer, Laurent, Lund, Amie K., Mabondzo, Aloïse

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TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis 由 Ivanova, Ekaterina L., Gilet, Johan G., Sulimenko, Vadym, Duchon, Arnaud, Rudolf, Gabrielle, Runge, Karen, Collins, Stephan C., Asselin, Laure, Broix, Loic, Drouot, Nathalie, Tilly, Peggy, Nusbaum, Patrick, Vincent, Alexandre, Magnant, William, Skory, Valerie, Birling, Marie-Christine, Pavlovic, Guillaume, Godin, Juliette D., Yalcin, Binnaz, Hérault, Yann, Dráber, Pavel, Chelly, Jamel, Hinckelmann, Maria-Victoria

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