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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.
Journal articles
hal-01162385v1
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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.
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.
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.
Journal articles
hal-01301142v1
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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.
Journal articles
hal-01415936v1
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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
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