Resultados da pesquisa - Duchon, Arnaud
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Inducing Segmental Aneuploid Mosaicism in the Mouse Through Targeted Asymmetric Sister Chromatid Event of Recombination Por Duchon, Arnaud, Besson, Vanessa, Pereira, Patricia Lopes, Magnol, Laetitia, Hérault, Yann
Publicado em 2008Text -
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Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome Por Duchon, Arnaud, Raveau, Matthieu, Chevalier, Claire, Nalesso, Valérie, Sharp, Andrew J., Herault, Yann
Publicado em 2011Text -
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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 Por Duchon, Arnaud, Pothion, Stéphanie, Brault, Véronique, Sharp, Andrew J., Tybulewicz, Victor L.J., Fisher, Elizabeth M.C., Herault, Yann
Publicado em 2011Text -
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The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model Por Raveau, Matthieu, Lignon, Jacques M., Nalesso, Valérie, Duchon, Arnaud, Groner, Yoram, Sharp, Andrew J., Dembele, Doulaye, Brault, Véronique, Hérault, Yann
Publicado em 2012Text -
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Deletion of the App-Runx1 region in mice models human partial monosomy 21 Por Arbogast, Thomas, Raveau, Matthieu, Chevalier, Claire, Nalesso, Valérie, Dembele, Doulaye, Jacobs, Hugues, Wendling, Olivia, Roux, Michel, Duchon, Arnaud, Herault, Yann
Publicado em 2015Text -
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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 Por Duchon, Arnaud, Gruart, Agnès, Albac, Christelle, Delatour, Benoît, Zorrilla de San Martin, Javier, Delgado‐García, José María, Hérault, Yann, Potier, Marie‐Claude
Publicado em 2020Text -
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Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models Por 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
Publicado em 2019Text -
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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 Por 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
Publicado em 2015Text -
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Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models Por 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
Publicado em 2021Text -
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DYRK1A, a Novel Determinant of the Methionine-Homocysteine Cycle in Different Mouse Models Overexpressing this Down-Syndrome-Associated Kinase Por 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
Publicado em 2009Text -
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Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A Por 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
Publicado em 2018Text -
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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 Por 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
Publicado em 2009Text -
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A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology Treatment Por 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
Publicado em 2020Text -
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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 Por 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
Publicado em 2020Text -
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TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis Por 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
Publicado em 2019Text