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Equipe TROLLET/MOULY

Orchestration cellulaire et moléculaire en régénération musculaire, pendant le vieillissement et en pathologies

L’équipe s’intéresse aux acteurs moléculaires et cellulaires impliqués chez l’homme dans la régénération musculaire, lors du vieillissement musculaire et dans les dystrophies musculaires, particulièrement la dystrophie musculaire oculo-pharyngée (OPMD) et la dystrophie musculaire de Duchenne (DMD).
Nos approches concernent plus particulièrement le métabolisme de l’ARN, la régénération musculaire, les cellules souches musculaires, et la fibrose, afin de développer des approches à visée thérapeutique.
L’équipe a développé une expertise solide sur les modèles cellulaires (y compris la plateforme d’immortalisation MyoLine que nous avons mise en place) et dans le domaine des xénotransplantation utilisant plusieurs modèles de souris immunodéficientes et plusieurs types de greffe).

Thèmes de recherche actuellement développés en parallèle et en synergie

  • Mécanismes moléculaires impliqués dans l’OPMD et dans le vieillissement musculaire
  • Communications inter-cellulaires lors de la régénération musculaire, du vieillissement, et de la fibrose
  • Développement d’approches thérapeutiques.

Laboratoire International Associé France-Brésil

Un autre aspect spécifique de notre équipe concerne le développement de collaborations internationales. En plus des nombreuses collaborations établies depuis de nombreuses années, nous avons mis en place un Laboratoire International Associé entre l’INSERM et Sorbonne Université pour la France et la FIOCRUZ et l’Université Fédérale de Rio-de-Janeiro pour le Brésil.

Ce LIA a pour but de mettre en synergie les expertises concernant le muscle et les pathologies neuromusculaires des équipes françaises et l’immunologie et l’inflammation des équipes brésiliennes.

Ce LIA a été déjà renouvelé une fois, a déjà donné lieu à 14 publications et un brevet commun, ainsi qu’à l’échange de 3 post-docs de longue durée, 5 thèses en co-direction, et de nombreux échanges de courte durée, y compris des postes de professeurs invités dans les deux pays. Un volet formation commune (master et/ou programme doctoral) est en cours d’élaboration et concernera les Biothérapies innovantes en environnement musculaire.

Capucine Trollet et Vincent Mouly

Capucine Trollet et Vincent Mouly

Contacts :

Vincent Mouly
Capucine Trollet

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225 documents

Articles dans une revue147 document

  • Baptiste Bogard, Hélène Bonnet, Ekaterina Boyarchuk, Gilles Tellier, Denis Furling, et al.. Small nucleolar RNAs promote the restoration of muscle differentiation defects in cells from myotonic dystrophy type 1. Nucleic Acids Research, 2025, 53 (6), ⟨10.1093/nar/gkaf232⟩. ⟨hal-05057978⟩
  • Léna d'Agata, Phoebe Rassinoux, Céline Gounou, Flora Bouvet, Dounia Bouragba, et al.. A Novel Assay Reveals the Early Setting‐Up of Membrane Repair Machinery in Human Skeletal Muscle Cells. Journal of Cellular Biochemistry, 2024, 126 (1), pp.e30662. ⟨10.1002/jcb.30662⟩. ⟨hal-04884353⟩
  • Eden Engal, Aveksha Sharma, Uria Aviel, Nadeen Taqatqa, Sarah Juster, et al.. DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis. Science Advances , 2024, 10 (22), pp.eadn7732. ⟨10.1126/sciadv.adn7732⟩. ⟨hal-04603956⟩
  • Paul Dowling, Capucine Trollet, Laura Muraine, Elisa Negroni, Dieter Swandulla, et al.. The potential of proteomics for in-depth bioanalytical investigations of satellite cell function in applied myology. Expert Review of Proteomics, 2024, pp.1-7. ⟨10.1080/14789450.2024.2356578⟩. ⟨inserm-04603178⟩
  • Judit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, Eduard Juanola, Jovan Pesovic, et al.. Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity. iScience, 2024, 27 (6), pp.109930. ⟨10.1016/j.isci.2024.109930⟩. ⟨hal-04603947⟩
  • Alice Granados, Maeva Zamperoni, Roberta Rapone, Maryline Moulin, Ekaterina Boyarchuk, et al.. SETDB1 modulates the TGFβ response in Duchenne muscular dystrophy myotubes. Science Advances , 2024, 10 (18), pp.eadj8042. ⟨10.1126/sciadv.adj8042⟩. ⟨hal-04601015⟩
  • Paul Dowling, Capucine Trollet, Elisa Negroni, Dieter Swandulla, Kay Ohlendieck. How Can Proteomics Help to Elucidate the Pathophysiological Crosstalk in Muscular Dystrophy and Associated Multi-System Dysfunction?. Proteomes, 2024, 12 (1), pp.4. ⟨10.3390/proteomes12010004⟩. ⟨inserm-04603208⟩
  • Julia Pereira Lemos, Liliane Patrícia Gonçalves Tenório, Vincent Mouly, Gillian Butler-Browne, Daniella Arêas Mendes-Da-Cruz, et al.. T cell biology in neuromuscular disorders: a focus on Duchenne Muscular Dystrophy and Amyotrophic Lateral Sclerosis. Frontiers in Immunology, 2023, 14, pp.120283. ⟨10.3389/fimmu.2023.1202834⟩. ⟨hal-04603915⟩
  • Barbara Tedesco, Leen Vendredy, Elias Adriaenssens, Marta Cozzi, Bob Asselbergh, et al.. HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies. Autophagy, 2023, 19 (8), pp.2217-2239. ⟨10.1080/15548627.2023.2179780⟩. ⟨hal-04253799⟩
  • Willem de Ridder, Geert de Vries, Kristof van Schil, Tine Deconinck, Vincent Mouly, et al.. A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotype. Neuromuscular Disorders, 2023, 33 (5), pp.432-439. ⟨10.1016/j.nmd.2023.04.003⟩. ⟨hal-04253823⟩
  • Eline Lemerle, Jeanne Lainé, Marion Benoist, Gilles Moulay, Anne Bigot, et al.. Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation. eLife, 2023, 12, ⟨10.7554/eLife.84139⟩. ⟨hal-04094370⟩
  • Luca Pinton, Moustafa Khedr, Valentina Lionello, Shilpita Sarcar, Sara Maffioletti, et al.. 3D human induced pluripotent stem cell–derived bioengineered skeletal muscles for tissue, disease and therapy modeling. Nature Protocols, 2023, 18 (4), pp.1337-1376. ⟨10.1038/s41596-022-00790-8⟩. ⟨inserm-04603284⟩
  • Laura Muraine, Mona Bensalah, Gillian Butler-Browne, Anne Bigot, Capucine Trollet, et al.. Update on anti-fibrotic pharmacotherapies in skeletal muscle disease. Current Opinion in Pharmacology, 2023, 68, pp.102332. ⟨10.1016/j.coph.2022.102332⟩. ⟨hal-04253789⟩
  • Laura Muraine, Mona Bensalah, Gillian Butler-Browne, Anne Bigot, Capucine Trollet, et al.. Update on anti-fibrotic pharmacotherapies in skeletal muscle disease. Current Opinion in Pharmacology, 2022, 68, pp.102332. ⟨10.1016/j.coph.2022.102332⟩. ⟨hal-03997340⟩
  • Alexis Boulinguiez, Fany Roth, Hadidja Rose Mouigni, Gillian Butler-Browne, Vincent Mouly, et al.. Les agrégats nucléaires dans la dystrophie musculaire oculopharyngée. Médecine/Sciences, 2022, 38, pp.13 - 16. ⟨10.1051/medsci/2022175⟩. ⟨hal-03997379⟩
  • Alexandra Monceau, Dylan Moutachi, Mégane Lemaitre, Luis Garcia, Capucine Trollet, et al.. Dystrophin Restoration after Adeno-Associated Virus U7–Mediated Dmd Exon Skipping Is Modulated by Muscular Exercise in the Severe D2-Mdx Duchenne Muscular Dystrophy Murine Model. American Journal of Pathology, 2022, 192 (11), pp.1604-1618. ⟨10.1016/j.ajpath.2022.07.016⟩. ⟨hal-04308024⟩
  • Fanny Roth, Jamila Dhiab, Alexis Boulinguiez, Hadidja-Rose Mouigni, Saskia Lassche, et al.. Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy. Acta Neuropathologica, 2022, ⟨10.1007/s00401-022-02503-7⟩. ⟨hal-03832636⟩
  • Alexandrine Mahoudeau, Céline Anquetil, Nozomu Tawara, Hossein Khademian, Damien Amelin, et al.. Myostatin in idiopathic inflammatory myopathies: Serum assessment and disease activity. Neuropathology and Applied Neurobiology, 2022, ⟨10.1111/nan.12849⟩. ⟨hal-03830849⟩
  • Elisa Negroni, Maria Kondili, Laura Muraine, Mona Bensalah, Gillian Sandra Butler-Browne, et al.. Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their “virtual” secretome. Frontiers in Cell and Developmental Biology, 2022, 10, ⟨10.3389/fcell.2022.952041⟩. ⟨hal-03830589⟩
  • Alexandra Monceau, Dylan Moutachi, Mégane Lemaitre, Luis Garcia, Capucine Trollet, et al.. Dystrophin Restoration after Adeno-Associated Virus U7–Mediated Dmd Exon Skipping Is Modulated by Muscular Exercise in the Severe D2-Mdx Duchenne Muscular Dystrophy Murine Model. American Journal of Pathology, 2022, ⟨10.1016/j.ajpath.2022.07.016⟩. ⟨hal-03830848⟩
  • Alexis Boulinguiez, Christian Duhem, Alicia Mayeuf-Louchart, Benoit Pourcet, Yasmine Sebti, et al.. NR1D1 controls skeletal muscle calcium homeostasis through myoregulin repression. JCI Insight, 2022, 7 (17), ⟨10.1172/jci.insight.153584⟩. ⟨hal-03828260⟩
  • Eunhye Kim, Fang Wu, Danbi Lim, Christopher Zeuthen, Yiming Zhang, et al.. Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion. Frontiers in Cell and Developmental Biology, 2022, 10, ⟨10.3389/fcell.2022.875209⟩. ⟨hal-03820132⟩
  • Laura Le Gall, William J Duddy, Cecile Martinat, Virginie Mariot, Owen Connolly, et al.. Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles. Journal of Cachexia, Sarcopenia and Muscle, 2022, 13 (2), pp.1385 - 1402. ⟨10.1002/jcsm.12945⟩. ⟨hal-04767184⟩
  • Ingo Riederer, Daniella Arêas Mendes-Da-Cruz, Guilherme Cordenonsi da Fonseca, Mariela Natacha González, Otavio Brustolini, et al.. Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection. PLoS Neglected Tropical Diseases, 2022, 16 (2), pp.e0010166. ⟨10.1371/journal.pntd.0010166⟩. ⟨hal-03832616⟩
  • M Bensalah, L Muraine, A Boulinguiez, Lorenzo Giordani, V Albert, et al.. A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis.. Journal of Cachexia, Sarcopenia and Muscle, In press, ⟨10.1002/jcsm.12974⟩. ⟨hal-03618341⟩
  • Celine Bruge, Marine Geoffroy, Manon Benabides, Emilie Pellier, Evelyne Gicquel, et al.. Skeletal Muscle Cells Derived from Induced Pluripotent Stem Cells: A Platform for Limb Girdle Muscular Dystrophies. Biomedicines, 2022, 10 (6), pp.1428. ⟨10.3390/biomedicines10061428⟩. ⟨hal-03858917⟩
  • Francesco Galli, Vincent Mouly, Gillian Butler-Browne, Giulio Cossu. Challenges in cell transplantation for muscular dystrophy. Experimental Cell Research, 2021, 409 (1), pp.112908. ⟨10.1016/j.yexcr.2021.112908⟩. ⟨hal-03832578⟩
  • Dorian Culié, Alexandra Rousseau, Jean-Luc Pretet, Jean Lacau Saint Guily. HPV status and therapeutic initial strategy impact on survival and oncologic outcomes: 5-year results from the multicentric prospective cohort of oropharyngeal cancers Papillophar. European Archives of Oto-Rhino-Laryngology, 2021, 279 (6), pp.3071-3078. ⟨10.1007/s00405-021-07117-5⟩. ⟨hal-04602302⟩
  • Xavier Suárez‐calvet, Esther Fernández‐simón, Patricia Piñol‐jurado, Jorge Alonso‐pérez, Ana Carrasco‐rozas, et al.. Isolation of human fibroadipogenic progenitors and satellite cells from frozen muscle biopsies. FASEB Journal, 2021, 35 (9), ⟨10.1096/fj.202100588r⟩. ⟨hal-03350045⟩
  • Marco Narici, Jamie Mcphee, Maria Conte, Martino V Franchi, Kyle Mitchell, et al.. Age‐related alterations in muscle architecture are a signature of sarcopenia: the ultrasound sarcopenia index. Journal of Cachexia, Sarcopenia and Muscle, 2021, ⟨10.1002/jcsm.12720⟩. ⟨hal-03256174⟩
  • Vanessa Strings-Ufombah, Alberto Malerba, Shih-Chu Kao, Sonal Harbaran, Fanny Roth, et al.. BB-301: a silence and replace AAV-based vector for the treatment of oculopharyngeal muscular dystrophy. Molecular Therapy - Nucleic Acids, 2021, 24, pp.67 - 78. ⟨10.1016/j.omtn.2021.02.017⟩. ⟨hal-03176223⟩
  • Capucine Trollet, Arthur J Cheng, Lykke Sylow, Miguel L Batista, Nicolas J Pillon. Editorial: Skeletal Muscle Immunometabolism. Frontiers in Physiology, 2021, 12, ⟨10.3389/fphys.2021.683088⟩. ⟨hal-03229646⟩
  • Jasdeep Saini, Alessandro Faroni, Adam J Reid, Vincent Mouly, Gillian Butler-Browne, et al.. Cross‐talk between motor neurons and myotubes via endogenously secreted neural and muscular growth factors. Physiological Reports, 2021, 9 (8), pp.e14791. ⟨10.14814/phy2.14791⟩. ⟨hal-03215215⟩
  • Aline Bamia, Maha Sinane, Rima Naït-Saïdi, Jamila Dhiab, Marc Keruzoré, et al.. Anti-prion Drugs Targeting the Protein Folding Activity of the Ribosome Reduce PABPN1 Aggregation. Neurotherapeutics, 2021, 18 (2), pp.1137-1150. ⟨10.1007/s13311-020-00992-6⟩. ⟨hal-03158577⟩
  • Olivier Boyer, Gillian Butler-Browne, Hector Chinoy, Giulio Cossu, Francesco Galli, et al.. Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle. Frontiers in Genetics, 2021, 12, pp.702547. ⟨10.3389/fgene.2021.702547⟩. ⟨hal-03345371⟩
  • Daniel J Owens, Julien Messéant, Sophie Moog, Mark Viggars, Arnaud Ferry, et al.. Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth. International Journal of Molecular Sciences, 2020, 22 (1), pp.306. ⟨10.3390/ijms22010306⟩. ⟨hal-03146374⟩
  • Cara A. Timpani, Kamel Mamchaoui, Gillian Butler-Browne, Emma Rybalka. Nitric oxide (NO) and Duchenne Muscular Dystrophy: NO way to go?. Antioxidants , 2020, 9 (12), pp.1268. ⟨10.3390/antiox9121268⟩. ⟨hal-03276089⟩
  • Apostolos Malatras, Ioannis Michalopoulos, Stéphanie Duguez, Gillian Butler-Browne, Simone Spuler, et al.. MyoMiner: explore gene co-expression in normal and pathological muscle. BMC Medical Genomics, 2020, 13 (1), pp.67. ⟨10.1186/s12920-020-0712-3⟩. ⟨hal-02746400⟩
  • Jasdeep Saini, Alessandro Faroni, Adam J Reid, Kamel Mamchaoui, Vincent Mouly, et al.. A Novel Bioengineered Functional Motor Unit Platform to Study Neuromuscular Interaction. Journal of Clinical Medicine, 2020, 9 (10), pp.3238. ⟨10.3390/jcm9103238⟩. ⟨hal-03018813⟩
  • Adriana C. Bonomo, Fernanda Pinto-Mariz, Ingo Riederer, Claudia F. Benjamim, Gillian Butler-Browne, et al.. Crosstalk Between Innate and T Cell Adaptive Immunity With(in) the Muscle. Frontiers in Physiology, 2020, 11, pp.573347. ⟨10.3389/fphys.2020.573347⟩. ⟨hal-02978746⟩
  • Laura Le Gall, Zamalou Gisele Ouandaogo, Ekene Anakor, Owen Connolly, Gillian Butler Browne, et al.. Optimized method for extraction of exosomes from human primary muscle cells. Skeletal Muscle, 2020, 10 (1), ⟨10.1186/s13395-020-00238-1⟩. ⟨hal-03276085⟩
  • Maud Wurmser, Nathalie Chaverot, Rouba Madani, Hiroshi Sakai, Elisa Negroni, et al.. SIX1 and SIX4 homeoproteins regulate PAX7+ progenitor cell properties during fetal epaxial myogenesis. Development (Cambridge, England), 2020, pp.dev.185975. ⟨10.1242/dev.185975⟩. ⟨hal-02905565⟩
  • Claudia Filippone, Vincent Legros, Patricia Jeannin, Valérie Choumet, Gillian Butler-Browne, et al.. Arboviruses and Muscle Disorders: From Disease to Cell Biology. Viruses, 2020, 12 (6), pp.E616. ⟨10.3390/v12060616⟩. ⟨hal-02905586⟩
  • Daniel J Owens, Martina Fischer, Saline Jabre, Sophie Moog, Kamel Mamchaoui, et al.. Lamin Mutations Cause Increased YAP Nuclear Entry in Muscle Stem Cells. Cells, 2020, 9 (4), pp.E816. ⟨10.3390/cells9040816⟩. ⟨inserm-02538651⟩
  • Cara A Timpani, Craig A Goodman, Christos G Stathis, Jason D White, Kamel Mamchaoui, et al.. Adenylosuccinic acid therapy ameliorates murine Duchenne Muscular Dystrophy. Scientific Reports, 2020, 10 (1), pp.1125. ⟨10.1038/s41598-020-57610-w⟩. ⟨inserm-02486207⟩
  • Stéphane M Camus, Marine Camus, Carmen Figueras-Novoa, Gaelle Boncompain, L. Amanda Sadacca, et al.. CHC22 clathrin mediates traffic from early secretory compartments for human GLUT4 pathway biogenesis. Journal of Cell Biology, 2020, 219 (1), ⟨10.1083/jcb.201812135⟩. ⟨hal-02555498⟩
  • Vincent Legros, Patricia Jeannin, Julien Burlaud-Gaillard, Thibault Chaze, Quentin Giai Gianetto, et al.. Differentiation-dependent susceptibility of human muscle cells to Zika virus infection. PLoS Neglected Tropical Diseases, 2020, 14 (8), pp.e0008282. ⟨10.1371/journal.pntd.0008282⟩. ⟨hal-03184236⟩
  • Ximena Baez-Matus, Cindel Figueroa-Cares, Arlek Gonzalez-Jamett, Hugo Almarza-Salazar, Christian Arriagada, et al.. Defects in G-Actin Incorporation into Filaments in Myoblasts Derived from Dysferlinopathy Patients Are Restored by Dysferlin C2 Domains. International Journal of Molecular Sciences, 2020, 21 (1), pp.37. ⟨10.3390/ijms21010037⟩. ⟨hal-02512306⟩
  • Laura Muraine, Mona Bensalah, Jamila Dhiab, Gonzalo Cordova, Ludovic Arandel, et al.. Transduction Efficiency of Adeno-Associated Virus Serotypes After Local Injection in Mouse and Human Skeletal Muscle. Human Gene Therapy, In press, ⟨10.1089/hum.2019.173⟩. ⟨hal-02472542⟩
  • Alberto Malerba, Pierre Klein, Ngoc Lu-Nguyen, Ornella Cappellari, Vanessa Strings-Ufombah, et al.. Established PABPN1 intranuclear inclusions in OPMD muscle can be efficiently reversed by AAV-mediated knockdown and replacement of mutant expanded PABPN1. Human Molecular Genetics, 2019, 28 (19), pp.3301-3308. ⟨10.1093/hmg/ddz167⟩. ⟨hal-02466975⟩
  • Jessica Vargas, Frida Loria, Yuan‐ju Wu, Gonzalo Córdova, Takashi Nonaka, et al.. The Wnt/Ca 2+ pathway is involved in interneuronal communication mediated by tunneling nanotubes. EMBO Journal, 2019, 38 (23), ⟨10.15252/embj.2018101230⟩. ⟨hal-02466969⟩
  • Pradeep Harish, Alberto Malerba, Ngoc Lu‐nguyen, Leysa Forrest, Ornella Cappellari, et al.. Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD). Journal of Cachexia, Sarcopenia and Muscle, 2019, 10 (5), pp.1016-1026. ⟨10.1002/jcsm.12438⟩. ⟨hal-02466979⟩
  • Alberto Malerba, Fanny N Roth, Pradeep Harish, Jamila Dhiab, Ngoc Lu-Nguyen, et al.. Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy. Human Molecular Genetics, 2019, ⟨10.1093/hmg/ddz007⟩. ⟨hal-02364803⟩
  • Mona Bensalah, Pierre Klein, Ingo Riederer, Soraya Chaouch, Laura Muraine, et al.. Combined methods to evaluate human cells in muscle xenografts. PLoS ONE, 2019, 14 (5), pp.e0211522. ⟨10.1371/journal.pone.0211522⟩. ⟨hal-02147551⟩
  • Lorenzo Giordani, Gary He, Elisa Negroni, Hiroshi Sakai, Justin Y.C. Law, et al.. High-Dimensional Single-Cell Cartography Reveals Novel Skeletal Muscle-Resident Cell Populations. Molecular Cell, 2019, 74 (3), pp.609-621.e6. ⟨10.1016/j.molcel.2019.02.026⟩. ⟨hal-02376541⟩
  • Jennifer Morgan, Gillian Butler-Browne, Francesco Muntoni, Ketan Patel, Helge Amthor, et al.. 240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands. Neuromuscular Disorders, 2019, 29 (9), pp.704-715. ⟨10.1016/j.nmd.2019.07.003⟩. ⟨hal-03201551⟩
  • Paloma de Carvalho Vieira, Mariana Caldas Waghabi, Daniela Gois Beghini, Danilo Predes, Jose Garcia Abreu, et al.. Toxoplasma gondii Impairs Myogenesis in vitro, With Changes in Myogenic Regulatory Factors, Altered Host Cell Proliferation and Secretory Profile. Frontiers in Cellular and Infection Microbiology, 2019, 9, pp.395. ⟨10.3389/fcimb.2019.00395⟩. ⟨hal-02443970⟩
  • Apostolos Malatras, Stéphanie Duguez, William Duddy. Muscle Gene Sets: a versatile methodological aid to functional genomics in the neuromuscular field. Skeletal Muscle, 2019, 9, pp.10. ⟨10.1186/s13395-019-0196-z⟩. ⟨hal-02136675⟩
  • Melissa Dewulf, Darius Vasco Köster, Bidisha Sinha, Christine C. Viaris de Lesegno, Valérie Chambon, et al.. Dystrophy-associated caveolin-3 mutations reveal that caveolae couple IL6/STAT3 signaling with mechanosensing in human muscle cells. Nature Communications, 2019, 10, pp.1974. ⟨10.1038/s41467-019-09405-5⟩. ⟨hal-02129168⟩
  • Jessica González-Sánchez, Agustín Sánchez-Temprano, Tania Cid-Díaz, Regina Pabst-Fernández, Carlos S. Mosteiro, et al.. Improvement of Duchenne muscular dystrophy phenotype following obestatin treatment. Journal of Cachexia, Sarcopenia and Muscle, 2018, 9 (6), pp.1063-1078. ⟨10.1002/jcsm.12338⟩. ⟨hal-01945902⟩
  • Ghizlane Maarifi, Juliette Fernandez, Débora Portilho, Aude Boulay, Jacques Dutrieux, et al.. RanBP2 regulates the anti-retroviral activity of TRIM5α by SUMOylation at a predicted phosphorylated SUMOylation motif. Communications Biology, 2018, 1 (1), pp.193. ⟨10.1038/s42003-018-0198-0⟩. ⟨hal-01930335⟩
  • Hila Barzilai-Tutsch, Melissa Dewulf, Christophe Lamaze, Gillian Butler Browne, Mark Pines, et al.. A promotive effect for halofuginone on membrane repair and synaptotagmin-7 levels in muscle cells of dysferlin-null mice. Human Molecular Genetics, 2018, 27 (16), pp.2817-2829. ⟨10.1093/hmg/ddy185⟩. ⟨hal-03832441⟩
  • Aurore L'Honoré, Pierre-Henri Commère, Elisa Negroni, Giorgia Pallafacchina, Bertrand Friguet, et al.. The role of Pitx2 and Pitx3 in muscle stem cells gives new insights into P38α MAP kinase and redox regulation of muscle regeneration. eLife, 2018, 7, pp.e32991. ⟨10.7554/eLife.32991⟩. ⟨hal-01908415⟩
  • Suey S.Y. Yeung, Esmee Reijnierse, Marijke Trappenburg, Jean-Yves Hogrel, Jamie Mcphee, et al.. Handgrip Strength Cannot Be Assumed a Proxy for Overall Muscle Strength. Journal of the American Medical Directors Association, 2018, 19 (8), pp.703-709. ⟨10.1016/j.jamda.2018.04.019⟩. ⟨hal-03842068⟩
  • Leandro Ladislau, Xavier Suárez-Calvet, Ségolène Toquet, Océane Landon-Cardinal, Damien Amelin, et al.. JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis. Brain - A Journal of Neurology , 2018, 141 (6), pp.1609 - 1621. ⟨10.1093/brain/awy105⟩. ⟨pasteur-01819244⟩
  • Leandro Ladislau, Débora M. Portilho, Tristan Courau, Alhondra Solares-Pérez, Elisa Negroni, et al.. Activated dendritic cells modulate proliferation and differentiation of human myoblasts. Cell Death and Disease, 2018, 9 (5), pp.551. ⟨10.1038/s41419-018-0426-z⟩. ⟨hal-03273530v2⟩
  • Gonzalo Cordova, Elisa Negroni, Claudio Cabello-Verrugio, Vincent Mouly, Capucine Trollet. Combined Therapies for Duchenne Muscular Dystrophy to Optimize Treatment Efficacy. Frontiers in Genetics, 2018, 9, ⟨10.3389/fgene.2018.00114⟩. ⟨hal-03273538⟩
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  • V Jacquemin, D Furling, Anne Bigot, G.S Butler-Browne, V Mouly. IGF-1 induces human myotube hypertrophy by increasing cell recruitment. Experimental Cell Research, 2004, 299 (1), pp.148-158. ⟨10.1016/j.yexcr.2004.05.023⟩. ⟨hal-03833701⟩
  • Ana Buj-Bello, Furling D, Helene Tronchere, Jocelyn Laporte, Thierry Lerouge, et al.. Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells. Human Molecular Genetics, 2002, 11 (19), pp.2297-2307. ⟨10.1093/hmg/11.19.2297⟩. ⟨hal-04481805⟩
  • V. Mouly, M. Lemonnier, D. Libri, Fiszman M.Y.. TRANSFORMATION ET CLONAGE DES MYOBLASTES AU COURS DU DEVELOPPEMENT CHEZ LES OISEAUX. Reproduction Nutrition Development, 1989, 29 (Suppl), pp.32-32. ⟨hal-00899158⟩
  • V. Mouly, M. Y. Fiszman. Plusieurs classes de myoblastes participent à la formation des muscles du squelette chez les oiseaux. Reproduction Nutrition Développement, 1988, 28 (3B), pp.687-692. ⟨hal-00898863⟩

Communications dans un congrès34 document

  • L. Benarroch, I. Nelson, T. Stojkovic, B Mohand Oumoussa, H. Madry, et al.. P166 Deciphering the genetic cause of oculopharyngodistal myopathy in a French cohort using Cas9-targeted long-read sequencing. 28th International Annual Congress of the World Muscle Society, Oct 2023, Charleston SC, United States. pp.S141, ⟨10.1016/j.nmd.2023.07.298⟩. ⟨hal-04280249⟩
  • Mona Bensalah, Laura Muraine, Alexis Boulinguiez, Lorenzo Giordani, Victorine Albert, et al.. A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis. 12th French-Japanese workshop, Sep 2022, Giverny, France. ⟨hal-04011411⟩
  • Mona Bensalah, Laura Muraine, Alexis Boulinguiez, Lorenzo Giordani, Victorine Albert, et al.. Muscle fibrosis: a vicious circle between human fibroadipogenic progenitors and muscle fibers. Myology 2022, Sep 2022, Nice, France. ⟨hal-04011420⟩
  • Capucine Trollet. Where are we now on Oculopharyngeal muscular dystrophy? -update on protein aggregation and fibrosis. Centre d'Immunologie et des Maladies Infectieuses, 2022, Paris, France. ⟨hal-04012485⟩
  • Alexis Boulinguiez. Endoplasmic reticulum implication in oculopharyngeal muscular dystrophy. Club Muscle, 2022, Paris, France. ⟨hal-04011426⟩
  • Negroni Elisa. Cellular and moleculars actors of human muscular fibrosis in muscular disorders. 19èmes Journées de la Société Française de Myologie, 2022, Toulouse, France. ⟨hal-04011428⟩
  • Mona Bensalah. Muscle fibrosis: a vicious circle between human fibroadipogenic progenitors and muscle fibers. Colloque Reseau 'Cellules Souches et Medecine Regeneratrice', 2022, Paris, France. ⟨hal-04011445⟩
  • Alexis Boulinguiez, Fanny Roth, Jamila Dhiab, Hadidja Rose Mouigni, Saskia Lassche, et al.. Status and role of PABPN1 nuclear aggregates in Oculopharyngeal Muscular Dystrophy. 19èmes Journées de la Société Française de Myologie, 2022, Toulouse, France. ⟨hal-04011442⟩
  • Capucine Trollet. « Where are we now on Oculopharyngeal muscular dystrophy? ». Institut NeuroMyoGène, 2022, Lyon, France. ⟨hal-04011423⟩
  • Fanny Roth, Alexis Boulinguiez, Jamila Dhiab, Negroni Elisa, Vincent Mouly, et al.. Targeting UPR to resolve aggresome accumulation in OPMD muscle. 18èmes Journées de la Société Française de Myologie, Nov 2021, Saint Etienne, France. ⟨hal-04011367⟩
  • Laura Muraine, Mona Bensalah, Jean Lacau St Guily, Aurélien Corneau, Gillian S. Butler-Browne, et al.. Muscle fibrosis: a vicious circle between human fibroadipogenic progenitors and muscle fibers. 18èmes Journées de la Société Française de Myologie, Nov 2021, Saint Etienne, France. ⟨hal-04011352⟩
  • Capucine Trollet. OPMD: agregats and stem cell dysfunction. 1º Simpósio Brasileiro de Biologia Muscular, 2021, Virtual conference, France. ⟨hal-04011389⟩
  • Capucine Trollet, Gillian S. Butler-Browne. Therapeutic approaches for oculopharyngeal muscular dystrophy: where are we now?. Padua Days of Muscle and Mobility Medicine, 2021, Virtual conference, France. ⟨hal-04011383⟩
  • Laura Muraine, Ludovic Gaut, Mona Bensalah, Gillian S. Butler-Browne, Vincent Mouly, et al.. Intercellular communication in fibrotic and aged human skeletal muscle. Workshop « Inflamaging and Regeneration: Pain or Partnership? », 2021, Virtual conference, France. ⟨hal-04011377⟩
  • Laura Muraine, Mona Bensalah, Jean Lacau St Guily, Aurélien Corneau, Gillian S. Butler-Browne, et al.. Muscle fibrosis: a vicious circle between human fibroadipogenic progenitors and muscle fibers. British Society for Matrix Biology online Spring meeting, 2021, Virtual, France. ⟨hal-04011396⟩
  • E. Cohen, I. Nelson, C. Gartioux, M. Beuvin, Z. Mezdari, et al.. Whole exome sequencing identifies compound heterozygous missense variants in the LOXL4 gene: a novel candidate cause of contractural myopathy. 25th International Congress of the World-Muscle-Society (WMS), Sep 2020, ELECTR NETWORK, France. pp.S47, ⟨10.1016/j.nmd.2020.08.007⟩. ⟨hal-03867603⟩
  • Capucine Trollet. OPMD: agregats and stem cell dysfunction. Muscle SCience Talk, 2020, Virtual conference, France. ⟨hal-04011311⟩
  • Gillian S. Butler-Browne, Capucine Trollet. Towards therapy for OPMD. Advances in Skeletal Muscle Biology in Health and Disease, 2019, Gainsville, United States. ⟨hal-04011190⟩
  • Gillian S. Butler-Browne, Fanny Roth, Negroni Elisa, Vincent Mouly, Capucine Trollet. 240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands. 240th ENMC workshop, 2019, Amsterdam, Netherlands. pp.704-715, ⟨10.1016/j.nmd.2019.07.003⟩. ⟨hal-04011177⟩
  • Laura Muraine, Jamila Dhiab, Mona Bensalah, Gonzalo Cordova, Alison Oliver, et al.. Transduction efficiency of AAV1 to 10 serotypes after local intramuscular injetion in mouse and in human xenograft. The European Society of Gene and Cell Therapy "Thematic day on viral vectors", 2019, Paris, France. ⟨hal-04011282⟩
  • Capucine Trollet. Intranuclear aggregates and muscle stem cell dysfunction in Oculopharyngeal Muscular Dystrophy. Max Delbrück Center, 2019, Berlin, Germany. ⟨hal-04011264⟩
  • Capucine Trollet. Gene therapy for Oculopharyngeal muscular dystrophy. 11th Japanese-French Workshop “New insights in personalized medicine for neuromuscular diseases: From Basic to Applied Myology”, Jun 2018, Tokyo, Japan. ⟨hal-04011201⟩
  • Vanessa Strings-Ufombah, Alberto Malerba, Sonal Harbaran, Fanny Roth, O Cappellari, et al.. BB-301: a single “silence and replace” AAV-based vector for the treatment of oculopharyngeal muscular dystrophy (OPMD). The European Society of Gene and Cell Therapy, 2018, Lausanne, Switzerland. ⟨hal-04011134⟩
  • Gillian S. Butler-Browne, Vincent Mouly, Capucine Trollet. Oculopharyngeal muscular dystrophy: from bench to bedside and back again. XIII Congress of Mediterranean Society of Myology, 2018, Avanos, Cappadocia, Turkey. ⟨hal-04011212⟩
  • Capucine Trollet, Fanny Roth, Gillian S. Butler-Browne. Update on PABPN1 aggregates in Oculopharyngeal muscular dystrophy. 16èmes Journées de la Société Française de Myologie, 2018, Brest, France. ⟨hal-04011143⟩
  • Negroni Elisa. Nature and role of interstitial non myogenic cells in human fibrotic muscle. Interuniversity Institute of Myology Meeting, 2018, Assisi, Italy. ⟨hal-04012478⟩
  • Fanny Roth, Capucine Trollet, Gillian S. Butler-Browne. Deciphering the nature and role of PABPN1 nuclear aggregates in OPMD. 15èmes Journées de la Société Française de Myologie, Nov 2017, Colmar, France. ⟨hal-04011091⟩
  • Mona Bensalah, Victorine Albert, Gonzalo Cordova, Alison Oliver, Laura Muraine, et al.. Peculiar behavior of interstitial non myogenic cells from human fibrotic muscle. 15èmes Journées de la Société Française de Myologie, Nov 2017, Colmar, France. ⟨hal-04011082⟩
  • Alberto Malerba, Pierre Klein, Houria Bachtarzi, Arnaud Ferry, Michael Graham, et al.. Gene replacement therapy as a novel approach for the treatment of oculopharyngeal muscular dystrophy. 45th European Muscle Conference, 2017, Montpellier, France. ⟨hal-04011108⟩
  • Capucine Trollet. Oculopharyngeal muscular Dystrophy. European Academy of Neurology, 2017, Amsterdam, Netherlands. ⟨hal-04011059⟩
  • B. Kalman, C. Monge, Anne Bigot, Vincent Mouly, C. Picart, et al.. Engineering human 3D micromuscles with co-culture of fibroblasts and myoblasts.. Congress of the French Society of Biomechanics., Oct 2015, Paris, France. ⟨hal-02112199⟩
  • Vanessa E. Jahnke, Jerôme Lecardonnel, Marco Moroldo, V. Mouly, V. Mamchaoui, et al.. Mitochondrial microARN profiling in Duchenne muscular dystrophy, Limb girdle muscular dystrophy and collagene VI related myopathies. EMBO Workshop Modern DNA concepts and tools for safe gene transfer and modification, Mar 2015, Evry, France. ⟨hal-02738918⟩
  • Capucine Trollet, Aymeric Chartier, Pierre Klein, Nicolas Barbezier, Teresa Gidaro, et al.. Mitochondrial dysfunction reveals defective poly(A) tail regulation of specific mRNAs as a primary defect in oculopharyngeal muscular dystrophy. 19. International Congress of the World Muscle Society, Oct 2014, Berlin, Germany. pp.793-794. ⟨hal-02740677⟩
  • M Ferreboeuf, V. Mariot, B. Bessières, A Vasiljevic, Tania Attié-Bitach, et al.. DUX 4 and DUX4 downstream target genes are expressed in fetal FSHD muscles. 18th International Congress of The World Muscle Society, Oct 2013, Pacific Grove, CA, United States. pp.823, ⟨10.1016/j.nmd.2013.06.640⟩. ⟨hal-01907613⟩

Poster de conférence34 document

  • Alexis Boulinguiez, Jamila Dhiab, Fanny Roth, Ludovic Gaut, Valentine Hanique, et al.. ER stress participates to aggresome accumulation in oculopharyngeal muscular dystrophy. Myology 2022, Sep 2022, Nice, France. ⟨hal-04010927⟩
  • Laura Muraine, Mona Bensalah, Jamila Dhiab, Stephen Gargan, Paul Dowling, et al.. Molecular and cellular actors of human muscle fibrosis among different muscular disorders. Myology 2022, Sep 2022, Nice, France. ⟨hal-04010959⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Control of PABPN1 expression in skeletal muscle. Myology 2022, Sep 2022, Nice, France. ⟨hal-04010967⟩
  • Samuel Horita, Mona Bensalah, Anne Bigot, Kamel Mamchaoui, Negroni Elisa, et al.. Laminin-111 derived peptide promotes adhesion, proliferation, differentiation and migration in human muscle cells.. Myology 2022, Sep 2022, Nice, France. ⟨hal-04010988⟩
  • Ohana Jessica, Kamel Mamchaoui, Mona Bensalah, Negroni Elisa, Capucine Trollet, et al.. Immortalized human muscle cells: easy-to-use models to study neuromuscular diseases. Myology 2022, Sep 2022, Nice, France. ⟨hal-04010975⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Control of PABPN1 expression in human skeletal muscle. Post-transcriptional Control of Gene Expression Conference: Mechanisms of RNA Decay, 2022, Jupiter, United States. ⟨hal-04011417⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Control of PABPN1 expression in skeletal muscle. 19èmes Journées de la Société Française de Myologie, 2022, Toulouse, France. ⟨hal-04010992⟩
  • Laura Muraine, Mona Bensalah, Jamila Dhiab, Stephen Gargan, Paul Dowling, et al.. Molecular and cellular actors of human muscle fibrosis among different muscular disorders. Journées Boris Ephrussi, 2022, Paris, France. ⟨hal-04011029⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Regulation of PABPN1 expression in skeletal muscle. Journées Boris Ephrussi, 2022, Paris, France. ⟨hal-04011407⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Regulation of PABPN1 expression in skeletal muscle. 18èmes Journées de la Société Française de Myologie, Nov 2021, Saint-etienne, France. ⟨hal-04010908⟩
  • Alexis Boulinguiez, Capucine Trollet. Reducing ER stress to resolve aggresome accumulation in oculopharyngeal muscular dystrophy. Frontiers in Myogenesis Conference, Nov 2021, Herradura, Costa Rica. ⟨hal-04010913⟩
  • Laura Muraine, Mona Bensalah, Jean Lacau St Guily, Kay Ohlendieck, Aurélien Corneau, et al.. Molecular and cellular actors of human muscle fibrosis among muscular disorders. Journées Boris Ephrussi, 2021, Virtual conference, France. ⟨hal-04011015⟩
  • Fanny Roth, Alexis Boulinguiez, Jamila Dhiab, Negroni Elisa, Vincent Mouly, et al.. Targeting the UPR to resolve ER stress in human OPMD skeletal muscle. Endoplasmic Reticulum 2019, Oct 2019, Paris, France. ⟨hal-04010900⟩
  • Daniel J. Owens, Martina Fischer, Kamel Mamchaoui, Sophie Moog, Gisèle Bonne, et al.. Nuclear export of YAP requires functional LINC complexes in skeletal muscle. Satellite Meeting​ European Network for Laminopathies Meeting, Sep 2019, London, United Kingdom. ⟨hal-03986932⟩
  • Elisa Negroni, Anne Bigot, Kamel Mamchaoui, Mona Bensalah, Laura Muraine, et al.. Human models to test therapeutic strategies for neuromuscular disorders. Myology 2019, Mar 2019, Bordeaux, France. ⟨hal-04010095⟩
  • Fanny Roth, Alberto Malerba, Jamila Dhiab, Gillian S. Butler-Browne, Cécile Voisset, et al.. Guanabenz acetate treatment improves oculopharyngeal muscular dystrophy, a protein aggregate disease.. Myology 2019, Mar 2019, Bordeaux, France. ⟨hal-04010884⟩
  • Laura Muraine, Jamila Dhiab, Mona Bensalah, Gonzalo Cordova, Alison Oliver, et al.. Transduction efficiency of AAV1 to 10 serotypes after local intramuscular injetion in mouse and in human xenograft. Myology 2019, Mar 2019, Bordeaux, France. ⟨hal-04010878⟩
  • Fanny Roth, Jamila Dhiab, Saskia Lassche, Alison Oliver, Jeanne Lainé, et al.. PABPN1 nuclear aggregates in oculopharyngeal muscular dystrophy: does age and genotype matters?. Myology 2019, Mar 2019, Bordeaux, France. ⟨hal-04010890⟩
  • Mona Bensalah, Laura Muraine, Victorine Albert, Alison Oliver, Teresa Gidaro, et al.. Deciphering the nature and role of interstitial non-myogenic cells in fibrotic and dystrophic human muscles. Myology 2019, Mar 2019, Bordeaux, France. ⟨hal-04010080⟩
  • Mona Bensalah, Laura Muraine, Victorine Albert, Gonzalo Cordova, Alison Oliver, et al.. Peculiar behavior of interstitial non myogenic cells from human fibrotic muscle. 11th Japanese-French Workshop “New insights in personalized medicine for neuromuscular diseases: From Basic to Applied Myology”, Jun 2018, Tokyo, Japan. ⟨hal-04010053⟩
  • Mona Bensalah, Laura Muraine, Victorine Albert, Gonzalo Cordova, Alison Oliver, et al.. Peculiar behavior of interstitial non myogenic cells from human fibrotic muscle. Journée Boris Ephrussi, May 2018, Paris, France. ⟨hal-04010008⟩
  • Fanny Roth, Gillian S. Butler-Browne, Capucine Trollet. Guanabenz acetate treatment improves oculopharyngeal muscular dystrophy, a protein aggregate disease. Journée Boris Ephrussi, May 2018, Paris, France. ⟨hal-04010019⟩
  • Mona Bensalah, Laura Muraine, Victorine Albert, Gonzalo Cordova, Alison Oliver, et al.. Peculiar behavior of interstitial non myogenic cells from human fibrotic muscle. Muscle Development, Regeneration and Disease, Apr 2018, Berlin, Germany. ⟨hal-04009925⟩
  • Laura Muraine, Jamila Dhiab, Mona Bensalah, Gonzalo Cordova, Alison Oliver, et al.. Transduction efficiency of AAV serotypes after intramuscular injection. Muscle Development, Regeneration and Disease, Apr 2018, Berlin, Germany. ⟨hal-04009953⟩
  • Anne Bigot, Kamel Mamchaoui, Mona Bensalah, Capucine Trollet, Vincent Mouly, et al.. Human models to test therapeutic strategies for neuromuscular diseases. Muscle Development, Regeneration and Disease, Apr 2018, Berlin, Germany. ⟨hal-04009959⟩
  • Mona Bensalah, Laura Muraine, Fanny Roth, Victorine Albert, Alison Oliver, et al.. Nature and role of interstitial non myogenic cells in human fibrotic muscles. Muscle Wasting Conference, 2018, Ascona, Italy. ⟨hal-04009745⟩
  • Daniel Owens, Julien Messeant, G Herledan, Arnaud Ferry, Anne Bertrand, et al.. Nuclear envelope protein lamin A/C is a crucial mechanosensory component for skeletal muscle plasticity. International Congress of Neuromuscular Disorders, Sep 2017, Ottawa, Canada. 2017. ⟨hal-03968419⟩
  • Capucine Trollet, Fanny Roth, Gillian S. Butler-Browne. PABPN1 aggregate and RNA: from molecular interactions to muscle cell dysfunction. RNA localization and local translation - EMBO, Jul 2017, Barga, Italy. ⟨hal-04009547⟩
  • Gonzalo Cordova, Ludovic Arandel, Negroni Elisa, Fanny Roth, Alison Oliver, et al.. Model of human skeletal muscle in immunodeficient mice for the study of human muscle regeneration and therapies for muscle disorders. Colloque Jeunes Chercheurs 2017 - Journées des familles, Jun 2017, Paris, France. ⟨hal-04012483⟩
  • Fanny Roth, Gillian S. Butler-Browne, Capucine Trollet. PolyA in OPMD : Alanine, Aggregates and Ageing. Colloque Jeunes Chercheurs 2017 - Journées des familles, Jun 2017, Paris, France. ⟨hal-04009714⟩
  • Mona Bensalah, Victorine Albert, Gonzalo Cordova, Alison Oliver, Teresa Gidaro, et al.. Cellules non-myogéniques du muscle fibrotique humain. colloque Jeunes Chercheurs 2017 - Journées des familles, Jun 2017, Paris, France. ⟨hal-04009730⟩
  • Mona Bensalah, Victorine Albert, Gonzalo Cordova, Alison Oliver, Teresa Gidaro, et al.. Peculiar behavior of interstitial non myogenic cells from human fibrotic muscle. Advances in Skeletal Muscle Biology in Health and Disease, Mar 2017, gainsville, United States. ⟨hal-04009529⟩
  • Mona Bensalah, Victorine Albert, Gonzalo Cordova, Alison Oliver, Teresa Gidaro, et al.. Peculiar behavior of interstitial non myogenic cells from human fibrotic muscles. Journée Boris Ephrussi, 2017, Paris, France. ⟨hal-04009572⟩
  • Fanny Roth, Alison Oliver, Jean Lacau St Guily, Sophie Périé, Gillian S. Butler-Browne, et al.. PolyA in OPMD : Alanine, Aggregates and Aging. Journée Boris Ephrussi, 2017, Paris, France. ⟨hal-04011044⟩

Chapitres d'ouvrage2 document

  • C Trollet, Alexis Boulinguiez, Fanny Roth, Tanya Stojkovic, Gillian S. Butler-Browne, et al.. Oculopharyngeal Muscular Dystrophy. GeneReviews, 2020. ⟨hal-03836527⟩
  • Wilson Savino, Fernanda Pinto-Mariz, Vincent Mouly. Flow Cytometry-Defined CD49d Expression in Circulating T-Lymphocytes Is a Biomarker for Disease Progression in Duchenne Muscular Dystrophy. Duchenne Muscular Dystrophy, 1687, Springer New York, pp.219-227, 2018, Methods in Molecular Biology, ⟨10.1007/978-1-4939-7374-3_16⟩. ⟨hal-03832501⟩

Brevets2 document

  • David Suhy, Michael Graham, Capucine Trollet, Alberto Malerba, George Dickson. Reagents for treatment of oculopharyngeal muscular dystrophy (OPMD) and use thereof. France, Patent n° : 11234994. 2022. ⟨hal-04012488⟩
  • Martine Simonelig, Frédéric Bihel, Cécile Voisset, Capucine Trollet. NOVEL PFAR-INHIBITING COMPOUNDS. France, Patent n° : 20220273637. 2022. ⟨hal-04012493⟩

Thèses6 document

  • Laura Le Gall. Secretion of neurotoxic vesicles by muscle cells of ALS patients. Human health and pathology. Sorbonne Université; University of Ulster, 2019. English. ⟨NNT : 2019SORUS210⟩. ⟨tel-03337418⟩
  • Mona Bensalah. Fibrose musculaire : acteurs cellulaires et stratégies thérapeutiques. Médecine humaine et pathologie. Sorbonne Université, 2019. Français. ⟨NNT : 2019SORUS031⟩. ⟨tel-03718899⟩
  • Fanny Roth. Les agrégats de PABPN1 dans la dystrophie musculaire oculopharyngée. Biologie moléculaire. Sorbonne Université, 2019. Français. ⟨NNT : 2019SORUS342⟩. ⟨tel-03162426⟩
  • Apostolos Malatras. Bioinformatics tools for the systems biology of dysferlin deficiency. Quantitative Methods [q-bio.QM]. Université Pierre et Marie Curie - Paris VI; Freie Universität (Berlin), 2017. English. ⟨NNT : 2017PA066627⟩. ⟨tel-01996499⟩
  • Anne-Charlotte Marsollier. Développement d'une stratégie thérapeutique pour la dystrophie facio-scapulo-humérale. Biologie cellulaire. Université Pierre et Marie Curie - Paris VI, 2017. Français. ⟨NNT : 2017PA066035⟩. ⟨tel-02151743⟩
  • Capucine Trollet. Transfert de gène in vivo:
    étude, régulation et application de l'électrotransfert. Biochimie [q-bio.BM]. Chimie ParisTech, 2005. Français. ⟨NNT : ⟩. ⟨tel-00011410⟩

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