Neuronal JNK pathway activation by IL-1 is mediated through IL1RAPL1, a protein required for development of cognitive functions

Por Pavlowsky, Alice, Zanchi, Alice, Pallotto, Marta, Giustetto, Maurizio, Chelly, Jamel, Sala, Carlo, Billuart, Pierre
Publicado em 2010

Pharmacological rescue of adult hippocampal neurogenesis in a mouse model of X-linked intellectual disability

Por Allegra, Manuela, Spalletti, Cristina, Vignoli, Beatrice, Azzimondi, Stefano, Busti, Irene, Billuart, Pierre, Canossa, Marco, Caleo, Matteo
Publicado no Neurobiol Dis (2017)

Autophosphorylation-independent and -dependent Functions of Focal Adhesion Kinase during Development

Por Corsi, Jean-Marc, Houbron, Christophe, Billuart, Pierre, Brunet, Isabelle, Bouvrée, Karine, Eichmann, Anne, Girault, Jean-Antoine, Enslen, Hervé
Publicado em 2009

Rho Kinase Inhibition Is Essential During In Vitro Neurogenesis and Promotes Phenotypic Rescue of Human Induced Pluripotent Stem Cell-Derived Neurons With Oligophrenin-1 Loss of Fu...

Por Compagnucci, Claudia, Barresi, Sabina, Petrini, Stefania, Billuart, Pierre, Piccini, Giorgia, Chiurazzi, Pietro, Alfieri, Paolo, Bertini, Enrico, Zanni, Ginevra
Publicado no Stem Cells Transl Med (2016)

Rapid reversal of impaired inhibitory and excitatory transmission but not spine dysgenesis in a mouse model of mental retardation

Por Powell, Andrew D, Gill, Kalbinder K, Saintot, Pierre-Philippe, Jiruska, Premysl, Chelly, Jamel, Billuart, Pierre, Jefferys, John G R
Publicado em 2012

Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation

Por Khelfaoui, Malik, Pavlowsky, Alice, Powell, Andrew D., Valnegri, Pamela, Cheong, Kenneth W., Blandin, Yann, Passafaro, Maria, Jefferys, John G.R., Chelly, Jamel, Billuart, Pierre
Publicado em 2009

Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas

Por Coste, Alix de La, Romagnolo, Béatrice, Billuart, Pierre, Renard, Claire-Angélique, Buendia, Marie-Annick, Soubrane, Olivier, Fabre, Monique, Chelly, Jamel, Beldjord, Cherif, Kahn, Axel, Perret, Christine
Publicado em 1998

Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes

Por Delépine, Chloé, Meziane, Hamid, Nectoux, Juliette, Opitz, Matthieu, Smith, Amos B., Ballatore, Carlo, Saillour, Yoann, Bennaceur-Griscelli, Annelise, Chang, Qiang, Williams, Emily Cunningham, Dahan, Maxime, Duboin, Aurélien, Billuart, Pierre, Herault, Yann, Bienvenu, Thierry
Publicado no Hum Mol Genet (2016)

Lack of the presynaptic RhoGAP protein oligophrenin1 leads to cognitive disabilities through dysregulation of the cAMP/PKA signalling pathway

Por Khelfaoui, Malik, Gambino, Frédéric, Houbaert, Xander, Ragazzon, Bruno, Müller, Christian, Carta, Mario, Lanore, Frédéric, Srikumar, Bettadapura N., Gastrein, Philippe, Lepleux, Marilyn, Zhang, Chun-Lei, Kneib, Marie, Poulain, Bernard, Reibel-Foisset, Sophie, Vitale, Nicolas, Chelly, Jamel, Billuart, Pierre, Lüthi, Andreas, Humeau, Yann
Publicado em 2014

Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis

Por Ramos-Brossier, Mariana, Montani, Caterina, Lebrun, Nicolas, Gritti, Laura, Martin, Christelle, Seminatore-Nole, Christine, Toussaint, Aurelie, Moreno, Sarah, Poirier, Karine, Dorseuil, Olivier, Chelly, Jamel, Hackett, Anna, Gecz, Jozef, Bieth, Eric, Faudet, Anne, Heron, Delphine, Kooy, Frank, Loeys, Bart, Humeau, Yann, Sala, Carlo, Billuart, Pierre
Publicado no Hum Mol Genet (2015)