Publications by authors named "Andre Hanauer"

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Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome.
Charlotte Castillon, Steeve Lunion, Nathalie Desvignes, André Hanauer, Serge Laroche

Neurobiol Dis· July 2018

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The PDK1-Rsk Signaling Pathway Controls Langerhans Cell Proliferation and Patterning.
Rossana Zaru, Stephen P Matthews, Alexander J Edgar, Alan R Prescott, Diego Gomez-Nicola, André Hanauer

J Immunol· November 2015

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PLD1 participates in BDNF-induced signalling in cortical neurons.
Mohamed Raafet Ammar, Tamou Thahouly, André Hanauer, David Stegner, Bernhard Nieswandt

Sci Rep· October 2015

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Structural and functional basis for p38-MK2-activated Rsk signaling in toll-like receptor-stimulated dendritic cells.
Rossana Zaru, Alexander J Edgar, André Hanauer, Colin Watts

Mol Cell Biol· January 2015

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RSK2 is a modulator of craniofacial development.
Virginie Laugel-Haushalter, Marie Paschaki, Pauline Marangoni, Coralie Pilgram, Arnaud Langer, André Hanauer

PLoS One· September 2014

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The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid.
Mohamed-Raafet Ammar, Yann Humeau, André Hanauer, Bernard Nieswandt, Marie-France Bader

J Neurosci· December 2013

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Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome.
Elise Morice, Séverine Farley, Roseline Poirier, Glenn Dallerac, Carine Chagneau, André Hanauer

Neurobiol Dis· October 2013

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Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin-Lowry syndrome.
Anne Schneider, Saskia M Maas, Raoul C M Hennekam, André Hanauer

Eur J Med Genet· March 2013

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Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2.
Tahir Mehmood, Anne Schneider, Solange Pannetier, André Hanauer

Int J Mol Sci· February 2013

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Anchored p90 ribosomal S6 kinase 3 is required for cardiac myocyte hypertrophy.
Jinliang Li, Michael D Kritzer, Jennifer J Carlisle Michel, Andrew Le, Hrishikesh Thakur, Andre Hanauer

Circ Res· January 2013

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Stimulus-induced drop episodes in Coffin-Lowry syndrome.
Jin S Hahn, André Hanauer

Eur J Med Genet· May 2012

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RSK2 signaling in medial habenula contributes to acute morphine analgesia.
Emmanuel Darcq, Katia Befort, Pascale Koebel, Solange Pannetier, Megan K Mahoney, André Hanauer

Neuropsychopharmacology· April 2012

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Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin-Lowry syndrome.
Anne Schneider, Tahir Mehmood, Solange Pannetier, André Hanauer

J Neurochem· November 2011

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RSK2 signaling in brain habenula contributes to place aversion learning.
Emmanuel Darcq, Pascale Koebel, Carolina Del Boca, Solange Pannetier, Anne-Sophie Kirstetter, André Hanauer

Learn Mem· September 2011

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Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome.
Tahir Mehmood, Anne Schneider, Jérémie Sibille, Patricia Marques Pereira, Solange Pannetier, André Hanauer

Hum Genet· March 2011

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Coffin-Lowry syndrome.
Patricia Marques Pereira, Anne Schneider, Solange Pannetier, Delphine Heron, André Hanauer

Eur J Hum Genet· June 2010

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P90 Ribosomal s6 kinase 2 negatively regulates axon growth in motoneurons.
Matthias Fischer, Patricia Marques Pereira, Bettina Holtmann, Christian M Simon, Andre Hanauer

Mol Cell Neurosci· October 2009

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Fibroblast growth factor receptor 3 associates with and tyrosine phosphorylates p90 RSK2, leading to RSK2 activation that mediates hematopoietic transformation.
Sumin Kang, Shannon Elf, Shaozhong Dong, Taro Hitosugi, Katherine Lythgoe, André Hanauer

Mol Cell Biol· April 2009

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Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome.
Patricia Marques Pereira, Michael Gruss, Katharina Braun, Nicolas Foos, Solange Pannetier, André Hanauer

J Neurochem· December 2008

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The Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1.
Maria Zeniou-Meyer, Yuanyuan Liu, Aurélie Béglé, Mary E Olanich, André Hanauer

Proc Natl Acad Sci U S A· June 2008

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Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation.
Aline Dubos, Solange Pannetier, André Hanauer

Am J Med Genet A· May 2008

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The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient.
Patricia Marques Pereira, Delphine Heron, André Hanauer

Hum Genet· December 2007

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Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.
Olivier Hagens, Aline Dubos, Fatima Abidi, Gotthold Barbi, Laura Van Zutven, André Hanauer

Hum Genet· January 2006

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Genetic background of HSH in three Polish families and a patient with an X;9 translocation.
Reetta Jalkanen, Ewa Pronicka, Henna Tyynismaa, Andre Hanauer, Roxanne Walder

Eur J Hum Genet· January 2006

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p90Rsk is not involved in cytostatic factor arrest in mouse oocytes.
Julien Dumont, Muriel Umbhauer, Pascale Rassinier, André Hanauer, Marie-Hélène Verlhac

J Cell Biol· April 2005

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