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Structure: Internal structure identifier : 247291
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Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

Frédérique Rau , Jeanne Lainé , Laetitita Ramanoudjame , Arnaud Ferry , Ludovic Arandel et al.
Nature Communications, 2015, 6 (1), pp.7205. ⟨10.1038/ncomms8205⟩
Journal articles hal-01162385v1

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

Laurianne Davignon , Claire Chauveau , Cédric Julien , Corinne Dill , Isabelle Duband-Goulet et al.
Human Molecular Genetics, 2016, 25 (8), pp.1559--1573. ⟨10.1093/hmg/ddw033⟩
Journal articles hal-01295646v1
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Implication of the SMN complex in the biogenesis and steady state level of the Signal Recognition Particle

Nathalie Piazzon , Florence Schlotter , Suzie Lefebvre , Maxime Dodre , Agnes Mereau et al.
Nucleic Acids Research, 2013, 41 (2), pp.1255-1272. ⟨10.1093/nar/gks1224⟩
Journal articles hal-01064047v1
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Infliximab versus adalimumab in the treatment of refractory inflammatory uveitis: Multicenter study from the french uveitis network

Hélène Vallet , Pascal Seve , Lucie Biard , Jean-Baptiste Fraison , Philip Bielefeld et al.
Arthritis & rheumatology, 2016, 66 (6), pp.1522-1530. ⟨10.1002/art.39667⟩
Journal articles hal-01301142v1

Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis

L. Davignon , C. Chauveau , C. Julien , C. Dill , L. Duband-Goulet et al.
Neuromuscular Disorders, 2016, 26 (suppl 2), pp.S118--S119. ⟨10.1016/j.nmd.2016.06.121⟩
Journal articles hal-01415936v1

Clinical phenotypes as predictors of DMD exon 51 skipping therapy: a systematic review

Megan A. Waldrop , Rabah Ben Yaou , Karin K. Lucas , Ann Martin , Erin O’rourke et al.
2018 New Directions in Biology and Disease of Skeletal Muscle Conference, Jun 2018, New Orleans, Louisiane, United States
Conference poster hal-04015230v1