Brain glucose metabolism as a neuronal substrate of the abnormal behavioral response to stress in the mdx mouse, a model of Duchenne muscular dystrophy von Goutal, Sébastien, Lancien, Marion, Rivier, François, Tournier, Nicolas, Vaillend, Cyrille

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Delayed postnatal brain development and ontogenesis of behavior and cognition in a mouse model of intellectual disability von Gonzalez, Laurine, Sébrié, Catherine, Laroche, Serge, Vaillend, Cyrille, Poirier, Roseline

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Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers von Goyenvalle, Aurélie, Griffith, Graziella, Babbs, Arran, Andaloussi, Samir El, Ezzat, Kariem, Avril, Aurélie, Dugovic, Branislav, Chaussenot, Rémi, Ferry, Arnaud, Voit, Thomas, Amthor, Helge, Bühr, Claudia, Schürch, Stefan, Wood, Matthew J A, Davies, Kay E, Vaillend, Cyrille, Leumann, Christian, Garcia, Luis

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Dp71-Dystrophin Deficiency Alters Prefrontal Cortex Excitation-Inhibition Balance and Executive Functions von Chaussenot, Rémi, Amar, Muriel, Fossier, Philippe, Vaillend, Cyrille

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Palmitic acid conjugation enhances potency of tricyclo-DNA splice switching oligonucleotides von Relizani, Karima, Echevarría, Lucía, Zarrouki, Faouzi, Gastaldi, Cécile, Dambrune, Chloe, Aupy, Philippine, Haeberli, Adrian, Komisarski, Marek, Tensorer, Thomas, Larcher, Thibaut, Svinartchouk, Fedor, Vaillend, Cyrille, Garcia, Luis, Goyenvalle, Aurélie

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Dp71 contribution to the molecular scaffold anchoring aquaporine‐4 channels in brain macroglial cells von Belmaati Cherkaoui, Mehdi, Vacca, Ophélie, Izabelle, Charlotte, Boulay, Anne‐Cécile, Boulogne, Claire, Gillet, Cynthia, Barnier, Jean‐Vianney, Rendon, Alvaro, Cohen‐Salmon, Martine, Vaillend, Cyrille

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Social and emotional alterations in mice lacking the short dystrophin-gene product, Dp71 von Miranda, Rubén, Ceschi, Léa, Le Verger, Delphine, Nagapin, Flora, Edeline, Jean-Marc, Chaussenot, Rémi, Vaillend, Cyrille

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Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophy von Saoudi, Amel, Zarrouki, Faouzi, Sebrié, Catherine, Izabelle, Charlotte, Goyenvalle, Aurélie, Vaillend, Cyrille

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Efficacy and Safety Profile of Tricyclo-DNA Antisense Oligonucleotides in Duchenne Muscular Dystrophy Mouse Model von Relizani, Karima, Griffith, Graziella, Echevarría, Lucía, Zarrouki, Faouzi, Facchinetti, Patricia, Vaillend, Cyrille, Leumann, Christian, Garcia, Luis, Goyenvalle, Aurélie

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The intellectual disability PAK3 R67C mutation impacts cognitive functions and adult hippocampal neurogenesis von Castillon, Charlotte, Gonzalez, Laurine, Domenichini, Florence, Guyon, Sandrine, Da Silva, Kevin, Durand, Christelle, Lestaevel, Philippe, Vaillend, Cyrille, Laroche, Serge, Barnier, Jean-Vianney, Poirier, Roseline

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Cognitive dysfunction in the dystrophin-deficient mouse model of Duchenne muscular dystrophy: A reappraisal from sensory to executive processes von Chaussenot, Rémi, Edeline, Jean-Marc, Le Bec, Benoit, El Massioui, Nicole, Laroche, Serge, Vaillend, Cyrille

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What is the ocular phenotype associated with a single exon 78 deletion in Duchenne muscular dystrophy? von Brignol, Tuy Nga, Mornet, Dominique, Montañez, Cecilia, Ventura, Dora Fix, Vaillend, Cyrille, Rendón, Alvaro

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Endolysosomal TPCs regulate social behavior by controlling oxytocin secretion von Martucci, Lora L, Launay, Jean-Marie, Kawakami, Natsuko, Sicard, Cécile, Desvignes, Nathalie, Dakouane-Giudicelli, Mbarka, Spix, Barbara, Têtu, Maude, Gilmaire, Franck-Olivier, Paulcan, Sloane, Callebert, Jacques, Vaillend, Cyrille, Bracher, Franz, Grimm, Christian, Fossier, Philippe, de la Porte, Sabine, Sakamoto, Hirotaka, Morris, John, Galione, Antony, Granon, Sylvie, Cancela, José-Manuel

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Impact of distinct dystrophin gene mutations on behavioral phenotypes of Duchenne muscular dystrophy von Saoudi, Amel, Mitsogiannis, Manuela D, Zarrouki, Faouzi, Fergus, Claire, Stojek, Erwina, Talavera, Silvia, Moore-Frederick, Dervla, Kelly, Vincent P, Goyenvalle, Aurélie, Montanaro, Federica, Muntoni, Francesco, Prenderville, Jack A, Sokolowska, Ewa, Vaillend, Cyrille

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Dystrophin Dp71 Isoforms Are Differentially Expressed in the Mouse Brain and Retina: Report of New Alternative Splicing and a Novel Nomenclature for Dp71 Isoforms von Aragón, Jorge, González-Reyes, Mayram, Romo-Yáñez, José, Vacca, Ophélie, Aguilar-González, Guadalupe, Rendón, Alvaro, Vaillend, Cyrille, Montañez, Cecilia

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Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy von Barboni, Mirella Telles Salgueiro, Liber, André Maurício Passos, Joachimsthaler, Anneka, Saoudi, Amel, Goyenvalle, Aurélie, Rendon, Alvaro, Roger, Jérome E., Ventura, Dora Fix, Kremers, Jan, Vaillend, Cyrille

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Partial restoration of brain dystrophin by tricyclo-DNA antisense oligonucleotides alleviates emotional deficits in mdx52 mice von Saoudi, Amel, Barberat, Sacha, le Coz, Olivier, Vacca, Ophélie, Doisy Caquant, Mathilde, Tensorer, Thomas, Sliwinski, Eric, Garcia, Luis, Muntoni, Francesco, Vaillend, Cyrille, Goyenvalle, Aurélie

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A multiscale analysis in CD38−/− mice unveils major prefrontal cortex dysfunctions von Martucci, Lora L., Amar, Muriel, Chaussenot, Remi, Benet, Gabriel, Bauer, Oscar, De Zélicourt, Antoine, Nosjean, Anne, Launay, Jean‐Marie, Callebert, Jacques, Sebrié, Catherine, Galione, Antony, Edeline, Jean‐Marc, De La Porte, Sabine, Fossier, Philippe, Granon, Sylvie, Vaillend, Cyrille, Cancela, José‐Manuel

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Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71 von Miranda, Rubén, Nudel, Uri, Laroche, Serge, Vaillend, Cyrille

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AAV-Mediated Restoration of Dystrophin-Dp71 in the Brain of Dp71-Null Mice: Molecular, Cellular and Behavioral Outcomes von Vacca, Ophélie, Zarrouki, Faouzi, Izabelle, Charlotte, Belmaati Cherkaoui, Mehdi, Rendon, Alvaro, Dalkara, Deniz, Vaillend, Cyrille

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