Search Results - "Ehinger, Yann"

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  1. 1

    Brain-specific inhibition of mTORC1 eliminates side effects resulting from mTORC1 blockade in the periphery and reduces alcohol intake in mice by Ehinger, Yann, Zhang, Ziyang, Phamluong, Khanhky, Soneja, Drishti, Shokat, Kevan M., Ron, Dorit

    Published in Nature communications (27-07-2021)
    “…Alcohol Use Disorder (AUD) affects a large portion of the population. Unfortunately, efficacious medications to treat the disease are limited. Studies in…”
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  2. 2

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

    Published in Neurobiology of disease (01-02-2021)
    “…Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2)…”
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  3. 3

    mTORC1 in the orbitofrontal cortex promotes habitual alcohol seeking by Morisot, Nadege, Phamluong, Khanhky, Ehinger, Yann, Berger, Anthony L, Moffat, Jeffrey J, Ron, Dorit

    Published in eLife (11-12-2019)
    “…The mechanistic target of rapamycin complex 1 (mTORC1) plays an important role in dendritic translation and in learning and memory. We previously showed that…”
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  4. 4

    cAMP-Fyn signaling in the dorsomedial striatum direct pathway drives excessive alcohol use by Ehinger, Yann, Morisot, Nadege, Phamluong, Khanhky, Sakhai, Samuel A, Soneja, Drishti, Adrover, Martin F, Alvarez, Veronica A, Ron, Dorit

    Published in Neuropsychopharmacology (New York, N.Y.) (01-01-2021)
    “…Fyn kinase in the dorsomedial striatum (DMS) of rodents plays a central role in mechanisms underlying excessive alcohol intake. The DMS is comprised of medium…”
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    A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome by Matagne, Valerie, Ehinger, Yann, Saidi, Lydia, Borges-Correia, Ana, Barkats, Martine, Bartoli, Marc, Villard, Laurent, Roux, Jean-Christophe

    Published in Neurobiology of disease (01-03-2017)
    “…Abstract Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (…”
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  7. 7

    Rett syndrome from bench to bedside: recent advances [version 1; peer review: 2 approved] by Ehinger, Yann, Matagne, Valerie, Villard, Laurent, Roux, Jean-Christophe

    Published in F1000 research (2018)
    “…Rett Syndrome is a severe neurological disorder mainly due to de novo mutations in the methyl-CpG-binding protein 2 gene ( MECP2). Mecp2 is known to play a…”
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  8. 8

    Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome by Ehinger, Yann, Matagne, Valerie, Cunin, Valérie, Borloz, Emilie, Seve, Michel, Bourgoin-Voillard, Sandrine, Borges-Correia, Ana, Villard, Laurent, Roux, Jean-Christophe

    “…Mutations in the X-linked gene are responsible for Rett syndrome (RTT), a severe neurological disorder. MECP2 is a transcriptional modulator that finely…”
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  9. 9

    Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice by Ehinger, Yann, Bruyère, Julie, Panayotis, Nicolas, Abada, Yah‐Se, Borloz, Emilie, Matagne, Valérie, Scaramuzzino, Chiara, Vitet, Hélène, Delatour, Benoit, Saidi, Lydia, Villard, Laurent, Saudou, Frédéric, Roux, Jean‐Christophe

    Published in EMBO molecular medicine (07-02-2020)
    “…Mutations in the X‐linked MECP2 gene are responsible for Rett syndrome (RTT), a severe neurological disorder for which there is no treatment. Several studies…”
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  10. 10

    Ultrasound-Mediated Blood-Brain Barrier Opening Improves Whole Brain Gene Delivery in Mice by Felix, Marie-Solenne, Borloz, Emilie, Metwally, Khaled, Dauba, Ambre, Larrat, Benoit, Matagne, Valerie, Ehinger, Yann, Villard, Laurent, Novell, Anthony, Mensah, Serge, Roux, Jean-Christophe

    Published in Pharmaceutics (12-08-2021)
    “…Gene therapy represents a powerful therapeutic tool to treat diseased tissues and provide a durable and effective correction. The central nervous system (CNS)…”
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    State‐of‐the‐art therapies for Rett syndrome by Panayotis, Nicolas, Ehinger, Yann, Felix, Marie Solenne, Roux, Jean‐Christophe

    Published in Developmental medicine and child neurology (01-02-2023)
    “…Rett syndrome (RTT) is an X‐linked neurogenetic disorder caused by mutations of the MECP2 (methyl‐CpG‐binding protein 2) gene. Over two decades of work…”
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    Identification of Novel BDNF-Specific Corticostriatal Circuitries by Ehinger, Yann, Soneja, Drishti, Phamluong, Khanhky, Salvi, Alexandra, Ron, Dorit

    Published in eNeuro (01-05-2023)
    “…Brain-derived neurotrophic factor (BDNF) is released from axon terminals originating in the cerebral cortex onto striatal neurons. Here, we characterized BDNF…”
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    Differential correlation of serum BDNF and microRNA content in rats with rapid or late onset of heavy alcohol use by Ehinger, Yann, Phamluong, Khanhky, Darevesky, David, Welman, Melanie, Moffat, Jeffrey J., Sakhai, Samuel A., Whiteley, Ellanor L., Berger, Anthony L., Laguesse, Sophie, Farokhnia, Mehdi, Leggio, Lorenzo, Lordkipanidzé, Marie, Ron, Dorit

    Published in Addiction biology (01-03-2021)
    “…Heavy alcohol use reduces the levels of the brain‐derived neurotrophic factor (BDNF) in the prefrontal cortex of rodents through the upregulation of microRNAs…”
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