TAF9b (Formerly TAF9L) Is a Bona Fide TAF That Has Unique and Overlapping Roles with TAF9

Por Frontini, Mattia, Soutoglou, Evi, Argentini, Manuela, Bole-Feysot, Christine, Jost, Bernard, Scheer, Elisabeth, Tora, Làszlò
Publicado em 2005

Ikaros mediates gene silencing in T cells through Polycomb repressive complex 2

Por Oravecz, Attila, Apostolov, Apostol, Polak, Katarzyna, Jost, Bernard, Le Gras, Stéphanie, Chan, Susan, Kastner, Philippe
Publicado no Nat Commun (2015)

Cell-Specific Interaction of Retinoic Acid Receptors with Target Genes in Mouse Embryonic Fibroblasts and Embryonic Stem Cells

Por Delacroix, Laurence, Moutier, Emmanuel, Altobelli, Gioia, Legras, Stephanie, Poch, Olivier, Choukrallah, Mohamed-Amin, Bertin, Isabelle, Jost, Bernard, Davidson, Irwin
Publicado em 2010

Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription Regulatory Networks

Por de Taffin, Mathilde, Carrier, Yannick, Dubois, Laurence, Bataillé, Laetitia, Painset, Anaïs, Le Gras, Stéphanie, Jost, Bernard, Crozatier, Michèle, Vincent, Alain
Publicado no PLoS One (2015)

Cyclin K and cyclin D1b are oncogenic in myeloma cells

Por Marsaud, Véronique, Tchakarska, Guergana, Andrieux, Geoffroy, Liu, Jian-Miao, Dembele, Doulaye, Jost, Bernard, Wdzieczak-Bakala, Joanna, Renoir, Jack-Michel, Sola, Brigitte
Publicado em 2010

Cell-specific occupancy of an extended repertoire of CREM and CREB binding loci in male germ cells

Por Sassone-Corsi Paolo, Jost Bernard, Van Ijcken Wilfred, Rijkers Erikjan, Legras Stephanie, Ye Tao, Krebs Arnaud, Choukrallah Mohamed-Amin, Martianov Igor, Davidson Irwin
Publicado em 2010-09-01

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

Cell-specific occupancy of an extended repertoire of CREM and CREB binding loci in male germ cells

Por Martianov, Igor, Choukrallah, Mohamed-Amin, Krebs, Arnaud, Ye, Tao, Legras, Stephanie, Rijkers, Erikjan, Van Ijcken, Wilfred, Jost, Bernard, Sassone-Corsi, Paolo, Davidson, Irwin
Publicado em 2010

Genome Sequence of Halomonas sp. Strain A3H3, Isolated from Arsenic-Rich Marine Sediments

Por Koechler, Sandrine, Plewniak, Frédéric, Barbe, Valérie, Battaglia-Brunet, Fabienne, Jost, Bernard, Joulian, Catherine, Philipps, Muriel, Vicaire, Serge, Vincent, Stéphanie, Ye, Tao, Bertin, Philippe N.
Publicado em 2013

Bcl11b represses a mature T-cell gene expression program in immature CD4(+)CD8(+) thymocytes

Por Kastner, Philippe, Chan, Susan, Vogel, Walter K., Zhang, Ling-Juan, Topark-Ngarm, Acharawan, Golonzhka, Olga, Jost, Bernard, Le Gras, Stéphanie, Gross, Michael K., Leid, Mark
Publicado em 2010

Extensive Regulation of Diurnal Transcription and Metabolism by Glucocorticoids

Por Weger, Benjamin D., Weger, Meltem, Görling, Benjamin, Schink, Andrea, Gobet, Cédric, Keime, Céline, Poschet, Gernot, Jost, Bernard, Krone, Nils, Hell, Rüdiger, Gachon, Frédéric, Luy, Burkhard, Dickmeis, Thomas
Publicado no PLoS Genet (2016)

Abnormal Wnt and PI3Kinase Signaling in the Malformed Intestine of lama5 Deficient Mice

Por Ritié, Léa, Spenlé, Caroline, Lacroute, Joël, Bolcato-Bellemin, Anne-Laure, Lefebvre, Olivier, Bole-Feysot, Christine, Jost, Bernard, Klein, Annick, Arnold, Christiane, Kedinger, Michèle, Bagnard, Dominique, Orend, Gertraud, Simon-Assmann, Patricia
Publicado em 2012

Oncogenic activation of the Notch1 gene by deletion of its promoter in Ikaros-deficient T-ALL

Por Jeannet, Robin, Mastio, Jérôme, Macias-Garcia, Alejandra, Oravecz, Attila, Ashworth, Todd, Geimer Le Lay, Anne-Solen, Jost, Bernard, Le Gras, Stéphanie, Ghysdael, Jacques, Gridley, Thomas, Honjo, Tasuku, Radtke, Freddy, Aster, Jon C., Chan, Susan, Kastner, Philippe
Publicado em 2010

Next generation sequencing for molecular diagnosis of neuromuscular diseases

Por Vasli, Nasim, Böhm, Johann, Le Gras, Stéphanie, Muller, Jean, Pizot, Cécile, Jost, Bernard, Echaniz-Laguna, Andoni, Laugel, Vincent, Tranchant, Christine, Bernard, Rafaelle, Plewniak, Frédéric, Vicaire, Serge, Levy, Nicolas, Chelly, Jamel, Mandel, Jean-Louis, Biancalana, Valérie, Laporte, Jocelyn
Publicado em 2012

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Por Redin, Claire, Le Gras, Stéphanie, Mhamdi, Oussema, Geoffroy, Véronique, Stoetzel, Corinne, Vincent, Marie-Claire, Chiurazzi, Pietro, Lacombe, Didier, Ouertani, Ines, Petit, Florence, Till, Marianne, Verloes, Alain, Jost, Bernard, Chaabouni, Habiba Bouhamed, Dollfus, Helene, Mandel, Jean-Louis, Muller, Jean
Publicado em 2012

An Integrated Diagnosis Strategy for Congenital Myopathies

Por Böhm, Johann, Vasli, Nasim, Malfatti, Edoardo, Le Gras, Stéphanie, Feger, Claire, Jost, Bernard, Monnier, Nicole, Brocard, Julie, Karasoy, Hatice, Gérard, Marion, Walter, Maggie C., Reilich, Peter, Biancalana, Valérie, Kretz, Christine, Messaddeq, Nadia, Marty, Isabelle, Lunardi, Joël, Romero, Norma B., Laporte, Jocelyn
Publicado em 2013

An open-access long oligonucleotide microarray resource for analysis of the human and mouse transcriptomes

Por Brigand, Kévin Le, Russell, Roslin, Moreilhon, Chimène, Rouillard, Jean-Marie, Jost, Bernard, Amiot, Franck, Magnone, Virginie, Bole-Feysot, Christine, Rostagno, Philippe, Virolle, Virginie, Defamie, Virginie, Dessen, Philippe, Williams, Gary, Lyons, Paul, Rios, Géraldine, Mari, Bernard, Gulari, Erdogan, Kastner, Philippe, Gidrol, Xavier, Freeman, Tom C., Barbry, Pascal
Publicado em 2006

20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

Por Piton, Amélie, Poquet, Hélène, Redin, Claire, Masurel, Alice, Lauer, Julia, Muller, Jean, Thevenon, Julien, Herenger, Yvan, Chancenotte, Sophie, Bonnet, Marlène, Pinoit, Jean-Michel, Huet, Frédéric, Thauvin-Robinet, Christel, Jaeger, Anne-Sophie, Le Gras, Stéphanie, Jost, Bernard, Gérard, Bénédicte, Peoc'h, Katell, Launay, Jean-Marie, Faivre, Laurence, Mandel, Jean-Louis
Publicado em 2014

Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome

Por Quartier, Angélique, Poquet, Hélène, Gilbert-Dussardier, Brigitte, Rossi, Massimiliano, Casteleyn, Anne-Sophie, Portes, Vincent des, Feger, Claire, Nourisson, Elsa, Kuentz, Paul, Redin, Claire, Thevenon, Julien, Mosca-Boidron, Anne-Laure, Callier, Patrick, Muller, Jean, Lesca, Gaetan, Huet, Frédéric, Geoffroy, Véronique, El Chehadeh, Salima, Jung, Matthieu, Trojak, Benoit, Le Gras, Stéphanie, Lehalle, Daphné, Jost, Bernard, Maury, Stéphanie, Masurel, Alice, Edery, Patrick, Thauvin-Robinet, Christel, Gérard, Bénédicte, Mandel, Jean-Louis, Faivre, Laurence, Piton, Amélie
Publicado no Eur J Hum Genet (2017)

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)