An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2 , a Gene Involved in Prader-Willi Syndrome and Autism
Meziane, Hamid, Schaller, Fabienne, Bauer, Sylvian, Villard, Claude, Matarazzo, Valery, Riet, Fabrice, Guillon, Gilles, Lafitte, Daniel, Desarmenien, Michel G, Tauber, Maithé, Muscatelli, Françoise
Published in Biological psychiatry (1969) (15.07.2015)
Published in Biological psychiatry (1969) (15.07.2015)
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The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome
Jimenez-Armijo, Alexandra, Morkmued, Supawich, Ahumada, José Tomás, Kharouf, Naji, de Feraudy, Yvan, Gogl, Gergo, Riet, Fabrice, Niederreither, Karen, Laporte, Jocelyn, Birling, Marie Christine, Selloum, Mohammed, Herault, Yann, Hernandez, Magali, Bloch-Zupan, Agnès
Published in Scientific reports (03.01.2024)
Published in Scientific reports (03.01.2024)
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AAV‐delivered diacylglycerol kinase DGKk achieves long‐term rescue of fragile X syndrome mouse model
Habbas, Karima, Cakil, Oktay, Zámbó, Boglárka, Tabet, Ricardos, Riet, Fabrice, Dembele, Doulaye, Mandel, Jean‐Louis, Hocquemiller, Michaël, Laufer, Ralph, Piguet, Françoise, Moine, Hervé
Published in EMBO molecular medicine (09.05.2022)
Published in EMBO molecular medicine (09.05.2022)
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Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study
Mandillo, Silvia, Tucci, Valter, Holter, Sabine M, Meziane, Hamid, Banchaabouchi, Mumna Al, Kallnik, Magdalena, Lad, Heena V, Nolan, Patrick M, Ouagazzal, Abdel-Mouttalib, Coghill, Emma L, Gale, Karin, Golini, Elisabetta, Jacquot, Sylvie, Krezel, Wojtek, Parker, Andy, Riet, Fabrice, Schneider, Ilka, Marazziti, Daniela, Auwerx, Johan, Brown, Steve D. M, Chambon, Pierre, Rosenthal, Nadia, Tocchini-Valentini, Glauco, Wurst, Wolfgang
Published in Physiological genomics (01.08.2008)
Published in Physiological genomics (01.08.2008)
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The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cord
Meziane, Hamid, Fraulob, Valérie, Riet, Fabrice, Krezel, Wojciech, Selloum, Mohammed, Geffarth, Michaela, Acampora, Dario, Hérault, Yann, Simeone, Antonio, Brand, Michael, Dollé, Pascal, Rhinn, Muriel
Published in PeerJ (San Francisco, CA) (29.08.2013)
Published in PeerJ (San Francisco, CA) (29.08.2013)
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Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases
Boivin, Manon, Deng, Jianwen, Pfister, Véronique, Grandgirard, Erwan, Oulad-Abdelghani, Mustapha, Morlet, Bastien, Ruffenach, Frank, Negroni, Luc, Koebel, Pascale, Jacob, Hugues, Riet, Fabrice, Dijkstra, Anke A., McFadden, Kathryn, Clayton, Wiley A., Hong, Daojun, Miyahara, Hiroaki, Iwasaki, Yasushi, Sone, Jun, Wang, Zhaoxia, Charlet-Berguerand, Nicolas
Published in Neuron (Cambridge, Mass.) (02.06.2021)
Published in Neuron (Cambridge, Mass.) (02.06.2021)
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Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome
Iacono, Giovanni, Dubos, Aline, Méziane, Hamid, Benevento, Marco, Habibi, Ehsan, Mandoli, Amit, Riet, Fabrice, Selloum, Mohammed, Feil, Robert, Zhou, Huiqing, Kleefstra, Tjitske, Kasri, Nael Nadif, van Bokhoven, Hans, Herault, Yann, Stunnenberg, Hendrik G
Published in Nucleic acids research (01.06.2018)
Published in Nucleic acids research (01.06.2018)
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Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability
Meziane, Hamid, Khelfaoui, Malik, Morello, Noemi, Hiba, Bassem, Calcagno, Eleonora, Reibel-Foisset, Sophie, Selloum, Mohammed, Chelly, Jamel, Humeau, Yann, Riet, Fabrice, Zanni, Ginevra, Herault, Yann, Bienvenu, Thierry, Giustetto, Maurizio, Billuart, Pierre
Published in Human molecular genetics (01.06.2016)
Published in Human molecular genetics (01.06.2016)
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Journal Article
Behavioral Testing Design for Evaluation of Cognitive Disabilities
Riet, Fabrice, Mittelhaeuser, Christophe, Lux, Aline, Bour, Raphael, Selloum, Mohammed, Sorg, Tania, Herault, Yann, Meziane, Hamid
Published in Current protocols (01.02.2022)
Published in Current protocols (01.02.2022)
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Journal Article
A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterations
Dubos, Aline, Meziane, Hamid, Iacono, Giovanni, Curie, Aurore, Riet, Fabrice, Martin, Christelle, Loaëc, Nadège, Birling, Marie-Christine, Selloum, Mohammed, Normand, Elisabeth, Pavlovic, Guillaume, Sorg, Tania, Stunnenberg, Henk G, Chelly, Jamel, Humeau, Yann, Friocourt, Gaëlle, Hérault, Yann
Published in Human molecular genetics (15.06.2018)
Published in Human molecular genetics (15.06.2018)
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Journal Article
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain
Garrett, Lillian, Trümbach, Dietrich, Lee, Donghyung, Mandillo, Silvia, Samaco, Rodney, Flenniken, Ann M., Stewart, Michelle, Aguilar-Pimental, Juan A., Amarie, Oana V., Becker, Lore, Calzada-Wack, Julia, Da Silva-Buttkus, Patricia, Dragano, Nathalia, Kraiger, Markus, Lengger, Christoph, Leuchtenberger, Stefanie, Marschall, Susan, Oestereicher, Manuela A., Rathkolb, Birgit, Sanz-Moreno, Adrián, Seisenberger, Claudia, Spielmann, Nadine, Stoeger, Claudia, Kumar, Vivek, Keskivali, Piia, King, Ruairidh, Haselimashhadi, Hamed, Bezginov, Alexandr, Norris, Clare, Taylor, Sarah, Pimm, Dale, Kelsey, Lois, Berberovic, Zorana, Qu, Dawei, D'Souza, Abigail, Bradaschia, Vivian, Eskandarian, Mohammed, Shang, Xueyuan, Duffin, Kyle, Roberton, Kyle, Xu, Catherine, Baguinat, Gloria, Laurin, Valerie, Lan, Qing, Sleep, Gillian, Lintott, Lauri, Gertsenstein, Marina, Tondat, Sandra, Cruz, Maribelle, Miller, David, Sorg, Tania, Riet, Fabrice, Tolentino, Heather, Tolentino, Todd, Schuchbauer, Mike, Hockenbury, Nichole, Beeman, Karrie, Pedroia, Sheryl, Salazar, Jason, Heffner, Mollie, Hsu, Joanne, Fletcher, Colin, Vanzanten, Maya, Golini, Elisabetta, Seavitt, John R., Lanza, Denise G., Lorenzo, Isabel, Gaspero, Angelina, Rios, Amanda, White, Jacqueline K., McKerlie, Colin, Nutter, Lauryl M.J., Vukobradovic, Igor, Veeraragavan, Surabi, Yuva, Lisa, Heaney, Jason D., Dickinson, Mary E., Meziane, Hamid, Hérault, Yann, Wells, Sara, Lloyd, K.C. Kent, Bower, Lynette, Lanoue, Louise, Clary, Dave, Zimprich, Annemarie, Gailus-Durner, Valerie, Fuchs, Helmut, Brown, Steve D.M., Chesler, Elissa J., Wurst, Wolfgang, Hrabě de Angelis, Martin, Hölter, Sabine M.
Published in Neuroscience Applied (2024)
Published in Neuroscience Applied (2024)
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Journal Article
AAV-delivery of diacylglycerol kinase kappa achieves long-term rescue of Fmr1-KO mouse model deficits of fragile X syndrome
Habbas, Karima, Oktay Cakil, Zambo, Boglarka, Tabet, Ricardos, Fabrice, Fabrice, Dembele, Doulaye, Mandel, Jean-Louis, Hocquemiller, Michael, Laufer, Ralph, Piguet, Francoise, Moine, Herve
Published in bioRxiv (14.04.2021)
Published in bioRxiv (14.04.2021)
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Rere-dependent Retinoic Acid signaling controls brain asymmetry and handedness
Rebagliati, Michael, Vihais-Neto, Goncalo, Petiet, Alexandra, Lange, Merlin, Michaut, Arthur, Plassat, Jean-Luc, Vermot, Julien, Riet, Fabrice, Noblet, Vincent, Brasse, David, Laquerriere, Patrice, Cussigh, Delphine, Dray, Nicolas, Bedu, Sebastien, Mohamed Sayed Gomaa, Simons, Claire, Meziane, Hamid, Lehericy, Stephane, Bally-Cuif, Laure, Pourquie, Olivier
Published in bioRxiv (15.03.2019)
Published in bioRxiv (15.03.2019)
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