Search Results - Hany Goubran‐Botros

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  1. 1
    Mast Cell-Derived Exosomes Induce Phenotypic and Functional Maturation of Dendritic Cells and Elicit Specific Immune Responses In Vivo

    Mast Cell-Derived Exosomes Induce Phenotypic and Functional Maturation of Dendritic Cells and Elicit Specific Immune Responses In Vivo by Dimitris Skokos, Hany Goubran Botros, Christian E. Demeure, Joëlle Morin, Roger Péronet, Gerd Birkenmeier, Sarah Boudaly, Salaheddine Mécheri

    Published 2003
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  2. 2
    Crystal Structure of the Allergen Equ c 1

    Crystal Structure of the Allergen Equ c 1 by Marie‐Bernard Lascombe, Christophe Grégoire, Pascal Poncet, Gisele Tavares, Isabelle Rosinski‐Chupin, J. Rabillon, Hany Goubran‐Botros, J C Mazié, Bernard David, Pedro M. Alzari

    Published 2000
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  3. 3
    The serotonin-N-acetylserotonin–melatonin pathway as a biomarker for autism spectrum disorders

    The serotonin-N-acetylserotonin–melatonin pathway as a biomarker for autism spectrum disorders by C. Pagan, Richard Delorme, Jacques Callebert, Hany Goubran‐Botros, Frédérique Amsellem, Xavier Drouot, Carole Boudebesse, Katia Le Dudal, N Ngo-Nguyen, H. Laouamri, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron, J.M. Launay

    Published 2014
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  4. 4
    Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders

    Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders by Cécile Pagan, Hany Goubran‐Botros, Richard Delorme, Marion Benabou, Nathalie Lemière, Kerren Murray, Frédérique Amsellem, Jacques Callebert, Pauline Chaste, Stéphane Jamain, Fabien Fauchereau, Guillaume Huguet, Erik Maronde, Marion Leboyer, Jean‐Marie Launay, Thomas Bourgeron

    Published 2017
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  5. 5
    Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations

    Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations by Laura Gouder, Aline Vitrac, Hany Goubran‐Botros, Anne Danckaert, Jean-Yves Tinévez, Gwenaëlle André-Leroux, Ekaterina Atanasova, Nathalie Lemière, Anne Biton, Claire S. Leblond, Aurélie Poulet, Anne Boland, Jean‐François Deleuze, Alexandra Benchoua, Richard Delorme, Thomas Bourgeron, Isabelle Cloëz-Tayarani

    Published 2019
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  6. 6
    Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

    Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder by Bruno Étain, Anne Dumaine, Frank Bellivier, Cécile Pagan, Laetitia Francelle, Hany Goubran‐Botros, Sarah Moreno, Jasmine Deshommes, Khaled Moustafa, Katia Le Dudal, Flavie Mathieu, Chantal Henry, Jean‐Pierre Kahn, Jean‐Marie Launay, Thomas W. Mühleisen, Sven Cichon, Thomas Bourgeron, Marion Leboyer, Stéphane Jamain

    Published 2012
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  7. 7
    Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population

    Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population by Pauline Chaste, Nathalie Clément, Oriane Mercati, Jean‐Luc Guillaume, Richard Delorme, Hany Goubran Botros, Cécile Pagan, Samuel Périvier, Isabelle Scheid, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, Carina Gillberg, Emilie Serrano, Nathalie Lemière, Jean Marie Launay, Marie Christine Mouren-Siméoni, Marion Leboyer, Christopher Gillberg, Ralf Jockers, Thomas Bourgeron

    Published 2010
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  8. 8
    Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

    Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders by Christelle M. Durand, Catalina Betancur, Tobias M. Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Råstam, I. Carina Gillberg, Henrik Anckarsäter, Eili Sponheim, Hany Goubran‐Botros, Richard Delorme, Nadia Chabane, Marie‐Christine Mouren‐Siméoni, P. De Mas, Éric Bieth, Bernadette Rogé, Delphine Héron, Lydie Bürglen, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron

    Published 2006
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  9. 9
    Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders

    Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders by Pauline Chaste, Nathalie Clément, Hany Goubran Botros, Jean‐Luc Guillaume, Marina Konyukh, Cécile Pagan, Isabelle Scheid, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, I. Carina Gillberg, Jonas Melke, Richard Delorme, Claire S. Leblond, Roberto Toro, Guillaume Huguet, Fabien Fauchereau, Christelle M. Durand, Lydia Boudarène, Emilie Serrano, Nathalie Lemière, Jean Marie Launay, Marion Leboyer, Ralf Jockers, Christopher Gillberg, Thomas Bourgeron

    Published 2011
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  10. 10
    A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

    A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability by Anne‐Laure Mosca‐Boidron, Lucie Gueneau, Guillaume Huguet, Alice Goldenberg, Céline Henry, Nadège Gigot, Emilie Pallesi‐Pocachard, Antonio Falace, Laurence Duplomb, Julien Thévenon, Yannis Duffourd, Judith St‐Onge, Pascal Chambon, Jean‐Baptiste Rivière, Christel Thauvin‐Robinet, Patrick Callier, Nathalie Marle, Muriel Payet, Clémence Ragon, Hany Goubran Botros, Julien Buratti, Sophie Caldérari, Guillaume Dumas, Richard Delorme, Nathalie Lagarde, Jean‐Michel Pinoit, Antoine Rosier, Alice Masurel‐Paulet, Carlos Cardoso, Francine Mugneret, Pascale Saugier‐Veber, Dominique Campion, Laurence Faivre, Thomas Bourgeron

    Published 2015
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