检索结果 - Thomas Voit
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Antisense targeting of 3′ end elements involved in<i>DUX4</i>mRNA processing is an efficient therapeutic strategy for facioscapulohumeral dystrophy: a new gene-silencing approach 由 Anne-Charlotte Marsollier, Lukasz Ciszewski, Virginie Mariot, Linda Popplewell, Thomas Voit, George Dickson, Julie Dumonceaux
出版 2016Artigo -
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Repair of Rhodopsin mRNA by Spliceosome-Mediated RNA Trans -Splicing: A New Approach for Autosomal Dominant Retinitis Pigmentosa 由 Adeline Berger, Stéphanie Lorain, Charlène Joséphine, Mélissa Desrosiers, Cécile Peccate, Thomas Voit, Luis Garcı́a, José‐Alain Sahel, Alexis‐Pierre Bemelmans
出版 2015Artigo -
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Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; Report of three expert workshops: TREAT-NMD/ENMC Workshop on outcome measures, 12th–13th May 2007, Naard... 由 Eugenio Mercuri, Anna Mayhew, Francesco Muntoni, Sonia Messina, Volker Straub, G J van Ommen, Thomas Voit, Enrico Bertini, Kate Bushby
出版 2008Artigo -
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Acute Fluid Intake Impacts Assessment of Body Composition via Bioelectrical Impedance Analysis. A Randomized, Controlled Crossover Pilot Trial 由 Janis Schierbauer, Svenja Günther, Sandra Haupt, Rebecca T. Zimmer, Daniel Herz, Thomas Voït, Paul Zimmermann, Nadine Wachsmuth, Felix Aberer, Othmar Moser
出版 2023Artigo -
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A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and <i>mdx</i> mice Immunological evidence 由 F. Pons, N Augier, Jocelyne Léger, Aude Robert, F.M.S. Tomé, Michel Fardeau, Thomas Voit, L. V. B. Nicholson, Dominique Mornet, J. Léger
出版 1991Artigo -
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A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment 由 Anne‐Gaëlle Le Moing, A. Seferian, A. Moraux, M. Annoussamy, Éric Dorveaux, E. Gasnier, Jean‐Yves Hogrel, Thomas Voit, David Vissière, Laurent Servais
出版 2016Artigo -
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Serum Profiling Identifies Novel Muscle miRNA and Cardiomyopathy-Related miRNA Biomarkers in Golden Retriever Muscular Dystrophy Dogs and Duchenne Muscular Dystrophy Patients 由 Laurence Jeanson-Leh, Julie Lameth, Soraya Krimi, Julien Buisset, Fatima Amor, Caroline Le Guiner, Inès Barthélémy, Laurent Servais, Stéphane Blot, Thomas Voit, David Israeli
出版 2014Artigo -
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A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model 由 Maria Grazia Biferi, Mathilde Cohen-Tannoudji, Ambra Cappelletto, Benoit Giroux, Marianne Roda, Stéphanie Astord, Thibaut Marais, Corinne Bos, Thomas Voit, Arnaud Ferry, Martine Barkats
出版 2017Artigo
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Medicine
Biology
Genetics
Internal medicine
Gene
Duchenne muscular dystrophy
Muscular dystrophy
Cell biology
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Physical therapy
Dystrophin
Endocrinology
Biochemistry
Phenotype
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Pediatrics
Physical medicine and rehabilitation
Skeletal muscle
Laminin
Missense mutation
Myocyte
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Cell
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Congenital muscular dystrophy
Dystroglycan
Exon
Genetic enhancement