Works by Hanauer, André

Results: 26

Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin–Lowry syndrome.

Published in:

Nucleic Acids Research, 2004, v. 32, n. 3, p. 1214, doi. 10.1093/nar/gkh272

By:

Zeniou, Maria;
Gattoni, Renata;
Hanauer, André;
Stévenin, James

Publication type:

Article

Erratum to: Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome.

Published in:

2011

By:

Mehmood, Tahir;
Schneider, Anne;
Sibille, Jérémie;
Marques Pereira, Patricia;
Pannetier, Solange;
Ammar, Mohamed;
Dembele, Doulaye;
Thibault-Carpentier, Christelle;
Rouach, Nathalie;
Hanauer, André

Publication type:

Correction Notice

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome.

Published in:

Human Genetics, 2011, v. 129, n. 3, p. 255, doi. 10.1007/s00439-010-0918-0

By:

Mehmood, Tahir;
Schneider, Anne;
Sibillec, Jérémie;
Marques Pereira, Patricia;
Pannetier, Solange;
Ammar, Mohamed Raafet;
Dembele, Doulaye;
Thibault-Carpentier, Christelle;
Rouach, Nathalie;
Hanauer, André

Publication type:

Article

The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient.

Published in:

Human Genetics, 2007, v. 122, n. 5, p. 541, doi. 10.1007/s00439-007-0424-1

By:

Marques Pereira, Patricia;
Heron, Delphine;
Hanauer, André

Publication type:

Article

Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.

Published in:

Human Genetics, 2006, v. 118, n. 5, p. 578, doi. 10.1007/s00439-005-0072-2

By:

Hagens, Olivier;
Dubos, Aline;
Abidi, Fatima;
Barbi, Gotthold;
Van Zutven, Laura;
Hoeltzenbein, Maria;
Tommerup, Niels;
Moraine, Claude;
Fryns, Jean-Pierre;
Chelly, Jamel;
van Bokhoven, Hans;
Gécz, Jozef;
Dollfus, Hélène;
Ropers, Hans-Hilger;
Schwartz, Charles E.;
de Cassia Stocco dos Santos, Rita;
Kalscheuer, Vera;
Hanauer, André

Publication type:

Article

RSK2 Signaling in Medial Habenula Contributes to Acute Morphine Analgesia.

Published in:

Neuropsychopharmacology, 2012, v. 37, n. 5, p. 1288, doi. 10.1038/npp.2011.316

By:

Darcq, Emmanuel;
Befort, Katia;
Koebel, Pascale;
Pannetier, Solange;
Mahoney, Megan K;
Gaveriaux-Ruff, Claire;
Hanauer, André;
Kieffer, Brigitte L

Publication type:

Article

Activation of RSK by UV-light: phosphorylation dynamics and involvement of the MAPK pathway.

Published in:

Oncogene, 2000, v. 19, n. 37, p. 4221

By:

Mérienne, Karine;
Jacquot, Sylvie;
Zeniou, Maria;
Pannetier, Solange;
Sassone-Corsi, Paolo;
Hanauer, André

Publication type:

Article

Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations.

Published in:

Clinical Genetics, 1990, v. 38, n. 6, p. 434, doi. 10.1111/j.1399-0004.1990.tb03609.x

By:

Salle, Corinne;
Wu, Qingyu;
Baas, Marie-Jeanne;
Hanauer, André;
Ruan, Changgeng;
Cazenave, Jean-Pierre

Publication type:

Article

The Coffin-Lowry Syndrome-Associated Protein RSK2 Regulates Neurite Outgrowth through Phosphorylation of Phospholipase DI (PLD1) and Synthesis of Phosphatidic Acid.

Published in:

Journal of Neuroscience, 2013, v. 33, n. 50, p. 19470, doi. 10.1523/JNEUROSCI.2283-13.2013

By:

Ammar, Mohamed-Raafet;
Humeau, Yann;
Hanauer, André;
Nieswandt, Bernard;
Bader, Marie-France;
Vitale, Nicolas

Publication type:

Article

A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 13, doi. 10.1038/8719

By:

Merienne, Karine;
Jacquot, Sylvie;
Pannetier, Solange;
Zeniou, Maria;
Bankier, Agnes;
Gecz, Jozef;
Mandel, Jean-Louis;
Mulley, John;
Sassone-Corsi, Paolo;
Hanauer, André

Publication type:

Article

Structural and Functional Basis for p38-MK2-Activated Rsk Signaling in Toll-Like Receptor-Stimulated Dendritic Cells.

Published in:

Molecular & Cellular Biology, 2015, v. 35, n. 1, p. 132, doi. 10.1128/MCB.00773-14

By:

Zaru, Rossana;
Edgar, Alexander J.;
Hanauer, André;
Watts, Colin

Publication type:

Article

Mutations in the X-linked RSK2 gene ( RPS6KA3) in patients with Coffin-Lowry syndrome.

Published in:

Human Mutation, 2001, v. 17, n. 2, p. 103, doi. 10.1002/1098-1004(200102)17:2<103::AID-HUMU2>3.0.CO;2-N

By:

Delaunoy, Jean-Pierre;
Abidi, Fatima;
Zeniou, Maria;
Jacquot, Sylvie;
Merienne, Karine;
Pannetier, Solange;
Schmitt, Michèle;
Schwartz, Charles E.;
Hanauer, André

Publication type:

Article

Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2.

Published in:

International Journal of Molecular Sciences, 2013, v. 14, n. 2, p. 3358, doi. 10.3390/ijms14023358

By:

Mehmood, Tahir;
Schneider, Anne;
Pannetier, Solange;
Hanauer, André

Publication type:

Article

Coffin–Lowry syndrome.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 6, p. 627, doi. 10.1038/ejhg.2009.189

By:

Marques Pereira, Patricia;
Schneider, Anne;
Pannetier, Solange;
Heron, Delphine;
Hanauer, André

Publication type:

Article

Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin-Lowry syndrome.

Published in:

Journal of Neurochemistry, 2011, v. 119, n. 3, p. 447, doi. 10.1111/j.1471-4159.2011.07423.x

By:

Schneider, Anne;
Mehmood, Tahir;
Pannetier, Solange;
Hanauer, André

Publication type:

Article

PLD1 participates in BDNF-induced signalling in cortical neurons.

Published in:

Scientific Reports, 2015, p. 1, doi. 10.1038/srep14778

By:

Raafet Ammar, Mohamed;
Thahouly, Tamou;
Hanauer, André;
Stegner, David;
Nieswandt, Bernhard;
Vitale, Nicolas

Publication type:

Article

RSK2 Is a Modulator of Craniofacial Development.

Published in:

PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084343

By:

Laugel-Haushalter, Virginie;
Paschaki, Marie;
Marangoni, Pauline;
Pilgram, Coralie;
Langer, Arnaud;
Kuntz, Thibaut;
Demassue, Julie;
Morkmued, Supawich;
Choquet, Philippe;
Constantinesco, André;
Bornert, Fabien;
Schmittbuhl, Matthieu;
Pannetier, Solange;
Viriot, Laurent;
Hanauer, André;
Dollé, Pascal;
Bloch-Zupan, Agnès

Publication type:

Article

Glutamate Dehydrogenase in Cerebellar Mutant Mice: Gene Localization and Enzyme Activity in Different Tissues.

Published in:

Journal of Neurochemistry, 1990, v. 54, n. 1, p. 23, doi. 10.1111/j.1471-4159.1990.tb13278.x

By:

Miret-Duvaux, Odile;
Frederic, Florence;
Simon, Dominique;
Guenet, Jean-Louis;
Hanauer, André;
Delhaye-Bouchaud, Nicole;
Mariani, Jean

Publication type:

Article

Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin–Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 23, p. 2929, doi. 10.1093/hmg/11.23.2929

By:

Zeniou, Maria;
Ding, Thomas;
Trivier, Elisabeth;
Hanauer, André

Publication type:

Article

Two hot spots of recombination in the DMD gene correlate with the deletion prone regions.

Published in:

Human Molecular Genetics, 1992, v. 1, n. 8, p. 599

By:

Oudet, Claudine;
Hanauer, André;
Clemens, Paula;
Caskey, Thomas;
Mandel, Jean-Louis

Publication type:

Article

A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome.

Published in:

2002

By:

Touraine, Renaud-Laurian;
Zeniou, Maria;
Hanauer, André

Publication type:

journal article

Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 5, p. 615, doi. 10.1038/sj.ejhg.5200341

By:

Filisetti, Denis;
Ostermann, Georg;
von Bredow, Moritz;
Strom, Tim;
Filler, Guido;
Ehrich, Johen;
Pannetier, Solange;
Garnier, Jean-Marie;
Rowe, Peter;
Francis, Fiona;
Julienne, Annick;
Hanauer, André;
Econs, Michael J;
Oudet, Claudine

Publication type:

Article

Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS).

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 1, p. 20, doi. 10.1038/sj.ejhg.5200231

By:

Abidi, Fatima;
Jacquot, Sylvie;
Lassiter, Christopher;
Trivier, Elizabeth;
Hanauer, André;
Schwartz, Charles E

Publication type:

Article

Germline mosaicism in Coffin-Lowry syndrome.

Published in:

European Journal of Human Genetics, 1998, v. 6, n. 6, p. 578, doi. 10.1038/sj.ejhg.5200230

By:

Jacquot, Sylvie;
Merienne, Karine;
Pannetier, Solange;
Blumenfeld, Sandra;
Schinzel, Albert;
Hanauer, André

Publication type:

Article

Fibroblast Growth Factor Receptor 3 Associates with and Tyrosine Phosphorylates p90 RSK2, Leading to RSK2 Activation That Mediates Hematopoietic Transformation.

Published in:

Molecular & Cellular Biology, 2009, v. 29, n. 8, p. 2105, doi. 10.1128/MCB.00998-08

By:

Kang, Sumin;
Elf, Shannon;
Shaozhong Dong;
Hitosugi, Taro;
Lythgoe, Katherine;
Guo, Ailan;
Hong Ruan;
Lonial, Sagar;
Khoury, Hanna J.;
Williams, Ifor R.;
Lee, Benjamin H.;
Roesel, Johannes L.;
Gerard Karsenty;
Hanauer, André;
Taunton, Jack;
Boggon, Titus J.;
Ting-Lei Gu;
Jing Chen

Publication type:

Article

Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome.

Published in:

Journal of Neurochemistry, 2008, v. 107, n. 5, p. 1325, doi. 10.1111/j.1471-4159.2008.05703.x

By:

Marques Pereira, Patricia;
Gruss, Michael;
Braun, Katharina;
Foos, Nicolas;
Pannetier, Solange;
Hanauer, André

Publication type:

Article