Tripartite Motif 24 (Trim24/Tif1α) Tumor Suppressor Protein Is a Novel Negative Regulator of Interferon (IFN)/Signal Transducers and Activators of Transcription (STAT) Signaling Pa...

Por Tisserand, Johan, Khetchoumian, Konstantin, Thibault, Christelle, Dembélé, Doulaye, Chambon, Pierre, Losson, Régine
Publicado em 2011

TAF4 inactivation in embryonic fibroblasts activates TGFβ signalling and autocrine growth

Por Mengus, Gabrielle, Fadloun, Anas, Kobi, Dominique, Thibault, Christelle, Perletti, Lucia, Michel, Isabelle, Davidson, Irwin
Publicado em 2005

Transcriptomic Analysis of the Sulfate Starvation Response of Pseudomonas aeruginosa

Por Tralau, Tewes, Vuilleumier, Stéphane, Thibault, Christelle, Campbell, Barry J., Hart, C. Anthony, Kertesz, Michael A.
Publicado em 2007

Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculature

Por Fouillade, Charles, Baron-Menguy, Céline, Domenga-Denier, Valérie, Thibault, Christelle, Takamiya, Kogo, Huganir, Richard, Joutel, Anne
Publicado em 2012

Profiling target genes of FGF18 in the postnatal mouse lung: possible relevance for alveolar development

Por Franco-Montoya, Marie-Laure, Boucherat, Olivier, Thibault, Christelle, Chailley-Heu, Bernadette, Incitti, Roberto, Delacourt, Christophe, Bourbon, Jacques R.
Publicado em 2011

Distinct Mutations in Yeast TAF(II)25 Differentially Affect the Composition of TFIID and SAGA Complexes as Well as Global Gene Expression Patterns

Por Kirschner, Doris B., vom Baur, Elmar, Thibault, Christelle, Sanders, Steven L., Gangloff, Yann-Gaël, Davidson, Irwin, Weil, P. Anthony, Tora, Làszlò
Publicado em 2002

SOX2 Is an Oncogene Activated by Recurrent 3q26.3 Amplifications in Human Lung Squamous Cell Carcinomas

Por Hussenet, Thomas, Dali, Soraya, Exinger, Julien, Monga, Ben, Jost, Bernard, Dembelé, Doulaye, Martinet, Nadine, Thibault, Christelle, Huelsken, Joerg, Brambilla, Elisabeth, du Manoir, Stanislas
Publicado em 2010

Transcriptome analysis identifies genes with enriched expression in the mouse central Extended Amygdala

Por Becker, Jérôme A. J., Befort, Katia, Blad, Clara, Filliol, Dominique, Ghate, Aditee, Dembele, Doulaye, Thibault, Christelle, Koch, Muriel, Muller, Jean, Lardenois, Aurélie, Poch, Olivier, Kieffer, Brigitte L.
Publicado em 2008

Notch Activation Is an Early and Critical Event during T-Cell Leukemogenesis in Ikaros-Deficient Mice

Por Dumortier, Alexis, Jeannet, Robin, Kirstetter, Peggy, Kleinmann, Eva, Sellars, MacLean, dos Santos, Nuno R., Thibault, Christelle, Barths, Jochen, Ghysdael, Jacques, Punt, Jennifer A., Kastner, Philippe, Chan, Susan
Publicado em 2006

Novel insights into the relationships between dendritic cell subsets in human and mouse revealed by genome-wide expression profiling

Por Robbins, Scott H, Walzer, Thierry, Dembélé, Doulaye, Thibault, Christelle, Defays, Axel, Bessou, Gilles, Xu, Huichun, Vivier, Eric, Sellars, MacLean, Pierre, Philippe, Sharp, Franck R, Chan, Susan, Kastner, Philippe, Dalod, Marc
Publicado em 2008

Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome

Por Sellier, Chantal, Freyermuth, Fernande, Tabet, Ricardos, Tran, Tuan, He, Fang, Ruffenach, Frank, Alunni, Violaine, Moine, Herve, Thibault, Christelle, Page, Adeline, Tassone, Flora, Willemsen, Rob, Disney, Matthew D., Hagerman, Paul J., Todd, Peter K., Charlet-Berguerand, Nicolas
Publicado em 2013

Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome

Por Koutsopoulos, Olga S, Kretz, Christine, Weller, Claudia M, Roux, Aurelien, Mojzisova, Halina, Böhm, Johann, Koch, Catherine, Toussaint, Anne, Heckel, Emilie, Stemkens, Daphne, ter Horst, Simone A J, Thibault, Christelle, Koch, Muriel, Mehdi, Syed Q, Bijlsma, Emilia K, Mandel, Jean-Louis, Vermot, Julien, Laporte, Jocelyn
Publicado em 2013

Identification of a Novel BBS Gene (BBS12) Highlights the Major Role of a Vertebrate-Specific Branch of Chaperonin-Related Proteins in Bardet-Biedl Syndrome

Por Stoetzel, Corinne, Muller, Jean, Laurier, Virginie, Davis, Erica E., Zaghloul, Norann A., Vicaire, Serge, Jacquelin, Cécile, Plewniak, Frédéric, Leitch, Carmen C., Sarda, Pierre, Hamel, Christian, de Ravel, Thomy J. L., Lewis, Richard Alan, Friederich, Evelyne, Thibault, Christelle, Danse, Jean-Marc, Verloes, Alain, Bonneau, Dominique, Katsanis, Nicholas, Poch, Olivier, Mandel, Jean-Louis, Dollfus, Hélène
Publicado em 2007

ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q(10) Deficiency

Por Lagier-Tourenne, Clotilde, Tazir, Meriem, López, Luis Carlos, Quinzii, Catarina M., Assoum, Mirna, Drouot, Nathalie, Busso, Cleverson, Makri, Samira, Ali-Pacha, Lamia, Benhassine, Traki, Anheim, Mathieu, Lynch, David R., Thibault, Christelle, Plewniak, Frédéric, Bianchetti, Laurent, Tranchant, Christine, Poch, Olivier, DiMauro, Salvatore, Mandel, Jean-Louis, Barros, Mario H., Hirano, Michio, Koenig, Michel
Publicado em 2008

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Por Freyermuth, Fernande, Rau, Frédérique, Kokunai, Yosuke, Linke, Thomas, Sellier, Chantal, Nakamori, Masayuki, Kino, Yoshihiro, Arandel, Ludovic, Jollet, Arnaud, Thibault, Christelle, Philipps, Muriel, Vicaire, Serge, Jost, Bernard, Udd, Bjarne, Day, John W., Duboc, Denis, Wahbi, Karim, Matsumura, Tsuyoshi, Fujimura, Harutoshi, Mochizuki, Hideki, Deryckere, François, Kimura, Takashi, Nukina, Nobuyuki, Ishiura, Shoichi, Lacroix, Vincent, Campan-Fournier, Amandine, Navratil, Vincent, Chautard, Emilie, Auboeuf, Didier, Horie, Minoru, Imoto, Keiji, Lee, Kuang-Yung, Swanson, Maurice S., de Munain, Adolfo Lopez, Inada, Shin, Itoh, Hideki, Nakazawa, Kazuo, Ashihara, Takashi, Wang, Eric, Zimmer, Thomas, Furling, Denis, Takahashi, Masanori P., Charlet-Berguerand, Nicolas
Publicado no Nat Commun (2016)