Torthaí cuardaigh - 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 de réir Nicolas Panayotis, Yann Ehinger, Marie‐Solenne Félix, Jean‐Christophe Roux

    Foilsithe / Cruthaithe 2022
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    Revisão
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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 de réir Valérie Matagne, Emilie Borloz, Yann Ehinger, Lydia Saidi, Laurent Villard, Jean‐Christophe Roux

    Foilsithe / Cruthaithe 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 de réir Gary Cohen, Jean‐Christophe Roux, Régis Grailhe, Girvan Malcolm, Jean‐Pierre Changeux, Hugo Lagercrantz

    Foilsithe / Cruthaithe 2005
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    Artigo
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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 de réir Rita El-Khoury, Nicolas Panayotis, Valérie Matagne, Adeline Ghata, Laurent Villard, Jean‐Christophe Roux

    Foilsithe / Cruthaithe 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 de réir Julie Peyronnet, Jean‐Christophe Roux, Alain Géloën, Lieqi Tang, J. M. Pequignot, Hugo Lagercrantz, Y. Dalmaz

    Foilsithe / Cruthaithe 2000
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    Artigo
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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 de réir Valérie Matagne, Yann Ehinger, Lydia Saidi, Ana Borges-Correia, Martine Barkats, Marc Bartoli, Laurent Villard, Jean‐Christophe Roux

    Foilsithe / Cruthaithe 2016
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  7. 7
    A knock‐in mouse model for <i>KCNQ2</i>‐related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment

    A knock‐in mouse model for <i>KCNQ2</i>‐related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment de réir Mathieu Milh, Pierre L. Roubertoux, Najoua Biba, Julie Chavany, Adeline Ghata, Camille Fulachier, Stephan C. Collins, Christel Wagner, Jean‐Christophe Roux, Binnaz Yalcin, Marie‐Solenne Félix, Florence Molinari, Pierre‐Pascal Lenck‐Santini, Laurent Villard

    Foilsithe / Cruthaithe 2020
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  8. 8
    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 de réir 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

    Foilsithe / Cruthaithe 2013
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    Artigo
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  9. 9
    Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice

    Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice de réir 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

    Foilsithe / Cruthaithe 2005
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  10. 10
    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 de réir 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

    Foilsithe / Cruthaithe 2013
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