L
Lucile Revillod
Researcher at University of Paris
Publications - 5
Citations - 246
Lucile Revillod is an academic researcher from University of Paris. The author has contributed to research in topics: Myotonic dystrophy & Genotype. The author has an hindex of 5, co-authored 5 publications receiving 197 citations. Previous affiliations of Lucile Revillod include Paris Descartes University.
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Journal ArticleDOI
Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour
Oscar Hernández-Hernández,Céline Guiraud-Dogan,Géraldine Sicot,Aline Huguet,Sabrina Luilier,Esther Steidl,Stefanie Saenger,Elodie Marciniak,Hélène Obriot,Caroline Chevarin,Annie Nicole,Lucile Revillod,Konstantinos Charizanis,Kuang-Yung Lee,Kuang-Yung Lee,Yasuhiro Suzuki,Takashi Kimura,Tohru Matsuura,Bulmaro Cisneros,Maurice S. Swanson,F. Trovero,Bruno Buisson,Jean-Charles Bizot,Michel Hamon,Sandrine Humez,Guillaume Bassez,Friedrich Metzger,Luc Buée,Arnold Munnich,Nicolas Sergeant,Geneviève Gourdon,Mário Gomes-Pereira +31 more
TL;DR: A novel connection between physiological phenotypes and synaptic protein dysregulation, indicative of synaptic dysfunction in myotonic dystrophy type 1 brain pathology is found.
Journal ArticleDOI
Peptide-conjugated oligonucleotides evoke long-lasting myotonic dystrophy correction in patient-derived cells and mice
Arnaud F. Klein,Miguel A. Varela,Ludovic Arandel,Ashling Holland,Ashling Holland,Naira Naouar,A Arzumanov,A Arzumanov,David Seoane,David Seoane,Lucile Revillod,Guillaume Bassez,Arnaud Ferry,Arnaud Ferry,Dominic Jauvin,Geneviève Gourdon,Jack Puymirat,Michael J. Gait,Denis Furling,Matthew J.A. Wood,Matthew J.A. Wood +20 more
TL;DR: It is demonstrated that low-dose treatment with Pip6a-PMO-CAG induces long-lasting correction with high efficacy of DM1-associated phenotypes at both molecular and functional levels, and strongly support the use of advanced peptide conjugates for systemic corrective therapy in DM1.
Journal ArticleDOI
Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis.
Philippe Dieudé,Mickaël Guedj,Marie-Elise Truchetet,Julien Wipff,Lucile Revillod,G. Riemekasten,Marco Matucci-Cerinic,Inga Melchers,Eric Hachulla,Paolo Airò,E. Diot,Nicolas Hunzelmann,Luc Mouthon,J. Cabane,J.L. Cracowski,Valeria Riccieri,J. H. W. Distler,Zahir Amoura,Gabriele Valentini,P. Camaraschi,Ingo H. Tarner,Camille Francès,Patrick H. Carpentier,Nicolò Costantino Brembilla,Olivier Meyer,André Kahan,Carlo Chizzolini,Catherine Boileau,Yannick Allanore +28 more
TL;DR: CD226 is established as a new SSc genetic susceptibility factor underlying the contribution of costimulation pathways in the pathogenesis of SSc.
Journal ArticleDOI
A genetic variation located in the promoter region of the UPAR (CD87) gene is associated with the vascular complications of systemic sclerosis.
Mirko Manetti,Yannick Allanore,Lucile Revillod,Cinzia Fatini,Serena Guiducci,Giovanna Cuomo,Claudia Bonino,Valeria Riccieri,Laura Bazzichi,Vasiliki Liakouli,Paola Cipriani,Roberto Giacomelli,Rosanna Abbate,Stefano Bombardieri,Guido Valesini,Carlomaurizio Montecucco,Gabriele Valentini,Lidia Ibba-Manneschi,Marco Matucci-Cerinic +18 more
TL;DR: The UPAR rs344781 gene variant is associated with the SSc vascular phenotype, and in a multivariate logistic regression analysis model including the above associated phenotypes of SSc patients, thers344781 GG genotype remained an independent risk factor for SSc-related digital ulceration.
Journal ArticleDOI
TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients
Eugénie Koumakis,Julien Wipff,Philippe Dieudé,Barbara Ruiz,Matthieu Bouaziz,Lucile Revillod,Mickaël Guedj,Jörg H W Distler,Marco Matucci-Cerinic,Marc Humbert,G. Riemekasten,G. Riemekasten,Paolo Airò,Inga Melchers,Eric Hachulla,Daniele Cusi,H.-Erich Wichmann,Nicolas Hunzelmann,Kiet Tiev,Paola Caramaschi,Elisabeth Diot,Otylia Kowal-Bielecka,Giovanna Cuomo,Ulrich A. Walker,László Czirják,Nemanja Damjanov,Sara Lupoli,Costanza Conti,Martina Müller-Nurasyid,Ulf Müller-Ladner,Valeria Riccieri,Jean-Luc Cracowski,Franco Cozzi,Vasiliki Kalliopi Bournia,P. G. Vlachoyiannopoulos,Gilles Chiocchia,Catherine Boileau,Yannick Allanore +37 more
TL;DR: This study demonstrates the lack of association between these TGFβ receptor gene polymorphisms and SSc–PAH using both sequencing and genotyping methods.