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authIdHal_s : valerie-allamand
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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

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
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A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies

Véronique Bolduc , A. Reghan Reghan Foley , Herimela Solomon-Degefa , Apurva Sarathy , Sandra Donkervoort et al.
JCI Insight, 2019, 4 (6), ⟨10.1172/jci.insight.124403⟩
Journal articles hal-03285227v1