Works by Pannetier, Solange

Results: 14

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

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

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

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

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

Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP).

Published in:

Human Molecular Genetics, 1997, v. 6, n. 4, p. 539, doi. 10.1093/hmg/6.4.539

By:

Rowe, Peter S. N.;
Oudet, Claudine L.;
Francis, Fiona;
Sinding, Christiane;
Pannetier, Solange;
Econs, Mike J.;
Strom, Tim M.;
Meitinger, Thomas;
Garabedian, Michele;
David, Albert;
Macher, Marie-Alice;
Questiaux, Elisabeth;
Popowska, Ewa;
Pronicka, Ewa;
Read, Andrew P.;
Mokrzycki, Agnes;
Glorieux, Francis H.;
Drezner, Marc K.;
Hanauer, Andre;
Lehrach, Hans

Publication type:

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

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

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