Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy von Nguyen, Karine, Puppo, Francesca, Roche, Stéphane, Gaillard, Marie‐Cécile, Chaix, Charlène, Lagarde, Arnaud, Pierret, Marjorie, Vovan, Catherine, Olschwang, Sylviane, Salort‐Campana, Emmanuelle, Attarian, Shahram, Bartoli, Marc, Bernard, Rafaëlle, Magdinier, Frédérique, Levy, Nicolas

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SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophy von Robin, Jérôme D, Ludlow, Andrew T, Batten, Kimberly, Gaillard, Marie-Cécile, Stadler, Guido, Magdinier, Frédérique, Wright, Woodring E, Shay, Jerry W

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Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers von Gaillard, Marie-Cécile, Roche, Stéphane, Dion, Camille, Tasmadjian, Armand, Bouget, Gwenaëlle, Salort-Campana, Emmanuelle, Vovan, Catherine, Chaix, Charlene, Broucqsault, Natacha, Morere, Julia, Puppo, Francesca, Bartoli, Marc, Levy, Nicolas, Bernard, Rafaëlle, Attarian, Shahram, Nguyen, Karine, Magdinier, Frédérique

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Identification of Variants in the 4q35 Gene FAT1 in Patients with a Facioscapulohumeral Dystrophy-Like Phenotype von Puppo, Francesca, Dionnet, Eugenie, Gaillard, Marie-Cécile, Gaildrat, Pascaline, Castro, Christel, Vovan, Catherine, Bertaux, Karine, Bernard, Rafaelle, Attarian, Shahram, Goto, Kanako, Nishino, Ichizo, Hayashi, Yukiko, Magdinier, Frédérique, Krahn, Martin, Helmbacher, Françoise, Bartoli, Marc, Lévy, Nicolas

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Analysis of the 4q35 chromatin organization reveals distinct long-range interactions in patients affected with Facio-Scapulo-Humeral Dystrophy von Gaillard, Marie-Cécile, Broucqsault, Natacha, Morere, Julia, Laberthonnière, Camille, Dion, Camille, Badja, Cherif, Roche, Stéphane, Nguyen, Karine, Magdinier, Frédérique, Robin, Jérôme D.

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Design on a Rational Basis of High-Affinity Peptides Inhibiting the Histone Chaperone ASF1 von Bakail, May, Gaubert, Albane, Andreani, Jessica, Moal, Gwenaëlle, Pinna, Guillaume, Boyarchuk, Ekaterina, Gaillard, Marie-Cécile, Courbeyrette, Regis, Mann, Carl, Thuret, Jean-Yves, Guichard, Bérengère, Murciano, Brice, Richet, Nicolas, Poitou, Adeline, Frederic, Claire, Le Du, Marie-Hélène, Agez, Morgane, Roelants, Caroline, Gurard-Levin, Zachary A., Almouzni, Geneviève, Cherradi, Nadia, Guerois, Raphael, Ochsenbein, Françoise

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Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy von Broucqsault, Natacha, Morere, Julia, Gaillard, Marie-Cécile, Dumonceaux, Julie, Torrents, Julia, Salort-Campana, Emmanuelle, Maues De Paula, André, Bartoli, Marc, Fernandez, Carla, Chesnais, Anne Laure, Ferreboeuf, Maxime, Sarda, Laure, Dufour, Henry, Desnuelle, Claude, Attarian, Shahram, Levy, Nicolas, Nguyen, Karine, Magdinier, Frédérique, Roche, Stéphane

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Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report von Gaillard, Marie-Cécile, Puppo, Francesca, Roche, Stéphane, Dion, Camille, Campana, Emmanuelle Salort, Mariot, Virginie, Chaix, Charlene, Vovan, Catherine, Mazaleyrat, Killian, Tasmadjian, Armand, Bernard, Rafaelle, Dumonceaux, Julie, Attarian, Shahram, Lévy, Nicolas, Nguyen, Karine, Magdinier, Frédérique, Bartoli, Marc

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SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite von Dion, Camille, Roche, Stéphane, Laberthonnière, Camille, Broucqsault, Natacha, Mariot, Virginie, Xue, Shifeng, Gurzau, Alexandra D, Nowak, Agnieszka, Gordon, Christopher T, Gaillard, Marie-Cécile, El-Yazidi, Claire, Thomas, Morgane, Schlupp-Robaglia, Andrée, Missirian, Chantal, Malan, Valérie, Ratbi, Liham, Sefiani, Abdelaziz, Wollnik, Bernd, Binetruy, Bernard, Salort Campana, Emmanuelle, Attarian, Shahram, Bernard, Rafaelle, Nguyen, Karine, Amiel, Jeanne, Dumonceaux, Julie, Murphy, James M, Déjardin, Jérôme, Blewitt, Marnie E, Reversade, Bruno, Robin, Jérôme D, Magdinier, Frédérique

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Epigenetic Factors in Normal and Pathological Neuronal Development von Broucqsault, Natacha, Badja, Cherif, Gaillard, Marie-Cécile, Magdinier, Frédérique

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Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism von Roche, Stéphane, Dion, Camille, Broucqsault, Natacha, Laberthonnière, Camille, Gaillard, Marie-Cécile, Robin, Jérôme D, Lagarde, Arnaud, Puppo, Francesca, Vovan, Catherine, Chaix, Charlene, Campana, Emmanuelle Salort, Attarian, Shahram, Bartoli, Marc, Bernard, Rafaelle, Nguyen, Karine, Magdinier, Frédérique

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A score for measurement of the role of social vulnerability in decisions on abortion von Combes, Philippe, Gaillard, Marie-Cécile, Pellet, Jacques, Demongeot, Jacques

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Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy: NGUYEN et al von Nguyen, Karine, Puppo, Francesca, Roche, Stéphane, Gaillard, Marie-Cécile, Chaix, Charlène, Lagarde, Arnaud, Pierret, Marjorie, Vovan, Catherine, Olschwang, Sylviane, Salort-Campana, Emmanuelle, Attarian, Shahram, Bartoli, Marc, Bernard, Rafaëlle, Magdinier, Frédérique, Levy, Nicolas

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SMCHD1 is involved in de novo methylation of theDUX4-encoding D4Z4 macrosatellite von Dion, Camille, Roche, Stéphane, Laberthonnière, Camille, Broucqsault, Natacha, Mariot, Virginie, Xue, Shifeng, Gurzau, Alexandra D, Nowak, Agnieszka, Gordon, Christopher T, Gaillard, Marie-Cécile, El-Yazidi, Claire, Thomas, Morgane, Robaglia-Schlupp, Andrée, Missirian, Chantal, Malan, Valérie, Ratbi, Liham, Sefiani, Abdelaziz, Wollnik, Bernd, Salort-Campana, Emmanuelle, Binétruy, Bernard, Attarian, Shahram, Bernard, Rafaelle, Nguyen, Karine, Amiel, Jeanne, Dumonceaux, Julie, Murphy, James M, Déjardin, Jérôme, Blewitt, Marnie E, Reversade, Bruno, Robin-Ducellier, Jérôme, Magdinier, Frédérique

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Differential DNA methylation of the D sub(4) Z sub(4) repeat in patients with FSHD and asymptomatic carriers von Gaillard, Marie-Cecile, Roche, Stephane, Dion, Camille, Tasmadjian, Armand, Bouget, Gwenaelle, Salort-Campana, Emmanuelle, Vovan, Catherine, Chaix, Charlene, Broucqsault, Natacha, Morere, Julia

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Additional file 1: Figure S1. of Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report von Marie-Cécile Gaillard, Puppo, Francesca, Roche, Stéphane, Dion, Camille, Campana, Emmanuelle, Mariot, Virginie, Chaix, Charlene, Vovan, Catherine, Mazaleyrat, Killian, Tasmadjian, Armand, Bernard, Rafaelle, Dumonceaux, Julie, Attarian, Shahram, Lévy, Nicolas, Nguyen, Karine, Magdinier, Frédérique, Bartoli, Marc

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Additional file 3: Figure S2. of Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report von Marie-Cécile Gaillard, Puppo, Francesca, Roche, Stéphane, Dion, Camille, Campana, Emmanuelle, Mariot, Virginie, Chaix, Charlene, Vovan, Catherine, Mazaleyrat, Killian, Tasmadjian, Armand, Bernard, Rafaelle, Dumonceaux, Julie, Attarian, Shahram, Lévy, Nicolas, Nguyen, Karine, Magdinier, Frédérique, Bartoli, Marc

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Additional file 2: Table S1. of Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report von Marie-Cécile Gaillard, Puppo, Francesca, Roche, Stéphane, Dion, Camille, Campana, Emmanuelle, Mariot, Virginie, Chaix, Charlene, Vovan, Catherine, Mazaleyrat, Killian, Tasmadjian, Armand, Bernard, Rafaelle, Dumonceaux, Julie, Attarian, Shahram, Lévy, Nicolas, Nguyen, Karine, Magdinier, Frédérique, Bartoli, Marc

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The endocytic recycling compartment serves as a viral factory for hepatitis E virus von Bentaleb, Cyrine, Hervouet, Kévin, Montpellier, Claire, Camuzet, Charline, Ferrié, Martin, Burlaud-Gaillard, Julien, Bressanelli, Stéphane, Metzger, Karoline, Werkmeister, Elisabeth, Ankavay, Maliki, Janampa, Nancy Leon, Marlet, Julien, Roux, Julien, Deffaud, Clarence, Goffard, Anne, Rouillé, Yves, Dubuisson, Jean, Roingeard, Philippe, Aliouat-Denis, Cécile-Marie, Cocquerel, Laurence

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Human Mus81-Associated Endonuclease Cleaves Holliday Junctions In Vitro von Chen, Xiao-Bo, Melchionna, Roberta, Denis, Cecile-Marie, Gaillard, Pierre-Henri L., Blasina, Alessandra, Van de Weyer, Inez, Boddy, Michael N., Russell, Paul, Vialard, Jorge, McGowan, Clare H.

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