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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 diseaseHuman Molecular Genetics, 2016, 25 (8), pp.1559--1573. ⟨10.1093/hmg/ddw033⟩
Journal articles
hal-01295646v1
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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 myogenesisNeuromuscular Disorders, 2016, 26 (suppl 2), pp.S118--S119. ⟨10.1016/j.nmd.2016.06.121⟩
Journal articles
hal-01415936v1
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Robust simplifications of multiscale biochemical networksBMC Systems Biology, 2008, 2:86
Journal articles
inria-00331212v1
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