Interplay between PML NBs and HIRA for H3.3 dynamics following type I interferon stimulus

por Kleijwegt, Constance, Bressac, Florent, Seurre, Coline, Bouchereau, Wilhelm, Cohen, Camille, Texier, Pascale, Simonet, Thomas, Schaeffer, Laurent, Lomonte, Patrick, Corpet, Armelle
Publicado 2023

Dynamic persistence of UPEC intracellular bacterial communities in a human bladder-chip model of urinary tract infection

por Sharma, Kunal, Dhar, Neeraj, Thacker, Vivek V, Simonet, Thomas M, Signorino-Gelo, Francois, Knott, Graham W, McKinney, John D
Publicado 2021

H2A.Z is dispensable for both basal and activated transcription in post-mitotic mouse muscles

por Belotti, Edwige, Lacoste, Nicolas, Simonet, Thomas, Papin, Christophe, Padmanabhan, Kiran, Scionti, Isabella, Gangloff, Yann-Gaël, Ramos, Lorrie, Dalkara, Defne, Hamiche, Ali, Dimitrov, Stefan, Schaeffer, Laurent
Publicado 2020

Performances of Targeted RNA Sequencing for the Analysis of Fusion Transcripts, Gene Mutation, and Expression in Hematological Malignancies

por Hayette, Sandrine, Grange, Béatrice, Vallee, Maxime, Bardel, Claire, Huet, Sarah, Mosnier, Isabelle, Chabane, Kaddour, Simonet, Thomas, Balsat, Marie, Heiblig, Maël, Tigaud, Isabelle, Nicolini, Franck E., Mareschal, Sylvain, Salles, Gilles, Sujobert, Pierre
Publicado 2021

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy

por Jacquier, Arnaud, Theuriet, Julian, Fontaine, Fanny, Mosbach, Valentine, Lacoste, Nicolas, Ribault, Shams, Risson, Valérie, Carras, Julien, Coudert, Laurent, Simonet, Thomas, Latour, Philippe, Stojkovic, Tanya, Piard, Juliette, Cosson, Anne, Lesca, Gaëtan, Bouhour, Françoise, Allouche, Stéphane, Puccio, Hélène, Pegat, Antoine, Schaeffer, Laurent
Publicado 2022

Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA

por Dimassi, Sarra, Simonet, Thomas, Labalme, Audrey, Boutry-Kryza, Nadia, Campan-Fournier, Amandine, Lamy, Raphaelle, Bardel, Claire, Elsensohn, Mad-Hélénie, Roucher-Boulez, Florence, Chatron, Nicolas, Putoux, Audrey, de Bellescize, Julitta, Ville, Dorothée, Schaeffer, Laurent, Roy, Pascal, Mougou-Zerelli, Soumaya, Saad, Ali, Calender, Alain, Sanlaville, Damien, Lesca, Gaetan
Publicado 2015

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons

por Jacquier, Arnaud, Risson, Valérie, Simonet, Thomas, Roussange, Florine, Lacoste, Nicolas, Ribault, Shams, Carras, Julien, Theuriet, Julian, Girard, Emmanuelle, Grosjean, Isabelle, Le Goff, Laure, Kröger, Stephan, Meltoranta, Julia, Bauché, Stéphanie, Sternberg, Damien, Fournier, Emmanuel, Kostera-Pruszczyk, Anna, O’Connor, Emily, Eymard, Bruno, Lochmüller, Hanns, Martinat, Cécile, Schaeffer, Laurent
Publicado 2022