檢索結果 - Jean‐Christophe Roux

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  1. 1
    State‐of‐the‐art therapies for Rett syndrome

    State‐of‐the‐art therapies for Rett syndrome 由 Nicolas Panayotis, Yann Ehinger, Marie‐Solenne Félix, Jean‐Christophe Roux

    出版 2022
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  2. 2
    Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome

    Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome 由 Valérie Matagne, Emilie Borloz, Yann Ehinger, Lydia Saidi, Laurent Villard, Jean‐Christophe Roux

    出版 2020
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    Artigo
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  3. 3
    Perinatal exposure to nicotine causes deficits associated with a loss of nicotinic receptor function

    Perinatal exposure to nicotine causes deficits associated with a loss of nicotinic receptor function 由 Gary Cohen, Jean‐Christophe Roux, Régis Grailhe, Girvan Malcolm, Jean‐Pierre Changeux, Hugo Lagercrantz

    出版 2005
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  4. 4
    GABA and Glutamate Pathways Are Spatially and Developmentally Affected in the Brain of Mecp2-Deficient Mice

    GABA and Glutamate Pathways Are Spatially and Developmentally Affected in the Brain of Mecp2-Deficient Mice 由 Rita El-Khoury, Nicolas Panayotis, Valérie Matagne, Adeline Ghata, Laurent Villard, Jean‐Christophe Roux

    出版 2014
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    Artigo
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  5. 5
    Prenatal hypoxia impairs the postnatal development of neural and functional chemoafferent pathway in rat

    Prenatal hypoxia impairs the postnatal development of neural and functional chemoafferent pathway in rat 由 Julie Peyronnet, Jean‐Christophe Roux, Alain Géloën, Lieqi Tang, J. M. Pequignot, Hugo Lagercrantz, Y. Dalmaz

    出版 2000
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  6. 6
    A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome

    A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome 由 Valérie Matagne, Yann Ehinger, Lydia Saidi, Ana Borges-Correia, Martine Barkats, Marc Bartoli, Laurent Villard, Jean‐Christophe Roux

    出版 2016
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  7. 7
    Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus

    Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus 由 Pierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, Jean‐Christophe Roux, Imen Dorboz, Jean-Pierre Desvignes, Catherine Badens, Marc Delépine, Mark Lathrop, Pierre Cau, Nicolas Lévy, Nadine Girard, Pierre Sarda, Odile Boespflug‐Tanguy, Laurent Villard

    出版 2013
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  8. 8
    Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice

    Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice 由 Jean‐Charles Viemari, Jean‐Christophe Roux, Andrew K. Tryba, Véronique Saywell, H. Burnet, Fernando Peña‐Ortega, Sébastien Zanella, Michelle Bévengut, Magali Barthélémy-Requin, Laura B. K. Herzing, Anne Moncla, Josette Mancini, Jan‐Marino Ramirez, Laurent Villard, Gérard Hilaire

    出版 2005
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    Artigo
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  9. 9
    DNA methylation map of mouse and human brain identifies target genes in Alzheimer’s disease

    DNA methylation map of mouse and human brain identifies target genes in Alzheimer’s disease 由 José V. Sánchez‐Mut, Ester Aso, Nicolas Panayotis, Ira T. Lott, Mara Dierssen, Alberto Rábano, Rocío G. Urdinguio, Agustín F. Fernández, Aurora Astudillo, José I. Martı́n-Subero, Balázs Bálint, Mario F. Fraga, Antonio Gómez, Cécile Gurnot, Jean‐Christophe Roux, Jesús Ávila, Takao K. Hensch, Isidró Ferrer, Manel Esteller

    出版 2013
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