Canlyniadau Chwilio - Bernard Jost

Mireinio'r Canlyniadau
  1. 1
    Dietary vitamins and selenium diminish the development of mechanically induced osteoarthritis and increase the expression of antioxidative enzymes in the knee joint of STR/1N mice

    Dietary vitamins and selenium diminish the development of mechanically induced osteoarthritis and increase the expression of antioxidative enzymes in the knee joint of STR/1N mice gan Bodo Kurz, Bernard Jost, Michael Schünke

    Cyhoeddwyd 2002
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  2. 2
    Ikaros mediates gene silencing in T cells through Polycomb repressive complex 2

    Ikaros mediates gene silencing in T cells through Polycomb repressive complex 2 gan Attila Oravecz, A Apostolov, Katarzyna Polak, Bernard Jost, Stéphanie Le Gras, Susan Chan, Philippe Kastner

    Cyhoeddwyd 2015
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  3. 3
    Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation

    Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation gan Ataaillah Benhaddou, Céline Keime, Tao Ye, Aurore Morlon, Isabelle Michel, Bernard Jost, Gabrielle Mengus, Irwin Davidson

    Cyhoeddwyd 2011
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  4. 4
    Cell-Specific Interaction of Retinoic Acid Receptors with Target Genes in Mouse Embryonic Fibroblasts and Embryonic Stem Cells

    Cell-Specific Interaction of Retinoic Acid Receptors with Target Genes in Mouse Embryonic Fibroblasts and Embryonic Stem Cells gan Laurence Delacroix, Emmanuel Moutier, Gioia Altobelli, Stéphanie Le Gras, Olivier Poch, Mohamed-Amin Choukrallah, Isabelle Bertin, Bernard Jost, Irwin Davidson

    Cyhoeddwyd 2009
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    Artigo
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  5. 5
    Combinatorial DNA methylation codes at repetitive elements

    Combinatorial DNA methylation codes at repetitive elements gan Christophe Papin, Abdulkhaleg Ibrahim, Stéphanie Le Gras, Amandine Velt, Isabelle Stoll, Bernard Jost, Hervé Menoni, Christian Bronner, Stéfan Dimitrov, Ali Hamiche

    Cyhoeddwyd 2017
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  6. 6
    Mitotic chromosome condensation resets chromatin to safeguard transcriptional homeostasis during interphase

    Mitotic chromosome condensation resets chromatin to safeguard transcriptional homeostasis during interphase gan Lucía Ramos-Alonso, Petter Holland, Stéphanie Le Gras, Xu Zhao, Bernard Jost, Magnar Bjørås, Yves Barral, Jorrit M. Enserink, Pierre Chymkowitch

    Cyhoeddwyd 2023
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  7. 7
    Bcl11b represses a mature T‐cell gene expression program in immature CD4<sup>+</sup>CD8<sup>+</sup> thymocytes

    Bcl11b represses a mature T‐cell gene expression program in immature CD4<sup>+</sup>CD8<sup>+</sup> thymocytes gan Philippe Kastner, Susan Chan, W. Vogel, Ling‐juan Zhang, Acharawan Topark‐Ngarm, Olga Golonzhka, Bernard Jost, Stéphanie Le Gras, Michael Groß, Mark Leid

    Cyhoeddwyd 2010
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  8. 8
    SOX2 Is an Oncogene Activated by Recurrent 3q26.3 Amplifications in Human Lung Squamous Cell Carcinomas

    SOX2 Is an Oncogene Activated by Recurrent 3q26.3 Amplifications in Human Lung Squamous Cell Carcinomas gan Thomas Hussenet, Soraya Dali, Exinger Julien, Ben Monga, Bernard Jost, Doulaye Dembélé, Nadine Martinet, Christelle Thibault-Carpentier, Joerg Huelsken, Élisabeth Brambilla, Stanislas du Manoir

    Cyhoeddwyd 2010
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  9. 9
    Cell-specific occupancy of an extended repertoire of CREM and CREB binding loci in male germ cells

    Cell-specific occupancy of an extended repertoire of CREM and CREB binding loci in male germ cells gan Igor Martianov, Mohamed-Amin Choukrallah, Arnaud R. Krebs, Ye Tao, Stéphanie Le Gras, Erikjan Rijkers, Wilfred F. J. van IJcken, Bernard Jost, Paolo Sassone–Corsi, Irwin Davidson

    Cyhoeddwyd 2010
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  10. 10
    Extensive Regulation of Diurnal Transcription and Metabolism by Glucocorticoids

    Extensive Regulation of Diurnal Transcription and Metabolism by Glucocorticoids gan Benjamin D. Weger, Meltem Weger, Benjamin Görling, Andrea Schink, Cédric Gobet, Céline Keime, Gernot Poschet, Bernard Jost, Nils Krone, Rüdiger Hell, Frédéric Gachon, Burkhard Luy, Thomas Dickmeis

    Cyhoeddwyd 2016
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  11. 11
    RNA profiling of human testicular cells identifies syntenic lncRNAs associated with spermatogenesis

    RNA profiling of human testicular cells identifies syntenic lncRNAs associated with spermatogenesis gan Antoine D. Rolland, Bertrand Evrard, Thomas Darde, Céline Le Béguec, Yvan Le Bras, Karim Bensalah, Sylvain Lavoué, Bernard Jost, Michael Primig, Nathalie Dejucq‐Rainsford, Frédéric Chalmel, Bernard Jégou

    Cyhoeddwyd 2019
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    Artigo
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  12. 12
    Extensive NEUROG3 occupancy in the human pancreatic endocrine gene regulatory network

    Extensive NEUROG3 occupancy in the human pancreatic endocrine gene regulatory network gan Valérie Schreiber, Reuben Mercier, Sara Jiménez, Tao Ye, Emmanuel García-Sánchez, Annabelle Klein, A. Meunier, Sabitri Ghimire, Catherine Birck, Bernard Jost, Kristian Honnens de Lichtenberg, Christian Honoré, Palle Serup, Gérard Gradwohl

    Cyhoeddwyd 2021
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  13. 13
    Oncogenic activation of the Notch1 gene by deletion of its promoter in Ikaros-deficient T-ALL

    Oncogenic activation of the Notch1 gene by deletion of its promoter in Ikaros-deficient T-ALL gan Robin Jeannet, Jérôme Mastio, Alejandra Macias-Garcia, Attila Oravecz, Todd Ashworth, Anne-Solen Geimer Le Lay, Bernard Jost, Stéphanie Le Gras, Jacques Ghysdael, Thomas Gridley, Tasuku Honjo, Freddy Radtke, Jon C. Aster, Susan Chan, Philippe Kastner

    Cyhoeddwyd 2010
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  14. 14
    Next generation sequencing for molecular diagnosis of neuromuscular diseases

    Next generation sequencing for molecular diagnosis of neuromuscular diseases gan Nasim Vasli, Johann Böhm, Stéphanie Le Gras, Jean Muller, Cécile Pizot, Bernard Jost, Andoni Echaniz‐Laguna, Vincent Laugel, Christine Tranchant, Rafaëlle Bernard, Frédéric Plewniak, Serge Vicaire, Nicolas Lévy, Jamel Chelly, Jean‐Louis Mandel, Valérie Biancalana, Jocelyn Laporte

    Cyhoeddwyd 2012
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  15. 15
    Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

    Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes gan Claire Redin, Stéphanie Le Gras, O. M'hamdi, Véronique Geoffroy, Corinne Stoetzel, Marie‐Claire Vincent, Pietro Chiurazzi, Didier Lacombe, Inès Ouertani, Florence Petit, Marianne Till, Alain Verloès, Bernard Jost, Habiba Chaâbouni, Hélène Dollfus, Jean‐Louis Mandel, Jean Muller

    Cyhoeddwyd 2012
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  16. 16
    An Integrated Diagnosis Strategy for Congenital Myopathies

    An Integrated Diagnosis Strategy for Congenital Myopathies gan Johann Böhm, Nasim Vasli, Edoardo Malfatti, Stéphanie Le Gras, Claire Feger, Bernard Jost, Nicole Monnier, Julie Brocard, Hatice Karasoy, Marion Gérard, Maggie C. Walter, Peter Reilich, Valérie Biancalana, Christine Kretz, Nadia Messaddeq, Isabelle Marty, Joël Lunardi, Norma B. Romero, Jocelyn Laporte

    Cyhoeddwyd 2013
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  17. 17
    An open-access long oligonucleotide microarray resource for analysis of the human and mouse transcriptomes

    An open-access long oligonucleotide microarray resource for analysis of the human and mouse transcriptomes gan Kévin Le Brigand, Roslin Russell, Chimène Moreilhon, Jean-Marie Rouillard, Bernard Jost, Franck Amiot, Virginie Magnone, Christine Bôle‐Feysot, Philippe Rostagno, Virginie Virolle, Virginie Defamie, Philippe Dessen, Gary W. Williams, Paul Lyons, Géraldine Rios, Bernard Mari, Erdoḡan Gülari, Philippe Kastner, Xavier Gidrol, Tom C. Freeman, Pascal Barbry

    Cyhoeddwyd 2006
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  18. 18
    20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

    20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition gan Amélie Piton, Hélène Poquet, Claire Redin, Alice Masurel, Julia Lauer, Jean Muller, Julien Thévenon, Yvan Herenger, Sophie Chancenotte, Marlène Bonnet, Jean‐Michel Pinoit, Frédéric Huet, Christel Thauvin‐Robinet, Anne-Sophie Jaeger, Stéphanie Le Gras, Bernard Jost, Bénédicte Gérard, Katell Peoc’h, Jean‐Marie Launay, Laurence Faivre, Jean‐Louis Mandel

    Cyhoeddwyd 2013
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  19. 19
    Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome

    Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome gan Angélique Quartier, Hélène Poquet, Brigitte Gilbert‐Dussardier, Massimiliano Rossi, Anne-Sophie Casteleyn, Vincent des Portes, Claire Feger, Elsa Nourisson, Paul Kuentz, Claire Redin, Julien Thévenon, Anne‐Laure Mosca‐Boidron, Patrick Callier, Jean Muller, Gaëtan Lesca, Frédéric Huet, Véronique Geoffroy, Salima El Chehadeh, Matthieu Jung, Benoît Trojak, Stéphanie Le Gras, Daphné Lehalle, Bernard Jost, Stéphanie Maury, Alice Masurel, Patrick Edery, Christel Thauvin-Robinet, Bénédicte Gérard, Jean‐Louis Mandel, Laurence Faivre, Amélie Piton

    Cyhoeddwyd 2017
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    Revisão
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  20. 20
    Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

    Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy gan Fernande Freyermuth, Fredérique Rau, Yosuke Kokunai, Thomas Linke, Chantal Sellier, Masayuki Nakamori, Yoshihiro Kino, Ludovic Arandel, Arnaud Jollet, Christelle Thibault-Carpentier, Muriel Philipps, Serge Vicaire, Bernard Jost, Bjarne Udd, John Day, Denis Duboc, Karim Wahbi, Tsuyoshi Matsumura, Harutoshi Fujimura, Hideki Mochizuki, François Deryckère, Takashi Kimura, Nobuyuki Nukina, Shoichi Ishiura, Vincent Lacroix, Amandine Campan-Fournier, Vincent Navratil, Émilie Chautard, Didier Auboeuf, Minoru Horie, Keiji Imoto, Kuang‐Yung Lee, Maurice S. Swanson, Adolfo López de Munaín, Shin Inada, Hideki Itoh, Kazuo Nakazawa, Takashi Ashihara, Eric T. Wang, Thomas Zimmer, Denis Furling, Masanori Takahashi, Nicolas Charlet‐Berguerand

    Cyhoeddwyd 2016
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