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Structure: Internal structure identifier : 11974

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

Sim2 prevents entry into the myogenic program by repressing MyoD transcription during limb embryonic myogenesis.

Emmanuelle Havis , Pascal Coumailleau , Aline Bonnet , Keren Bismuth , Marie-Ange Bonnin et al.
Development (Cambridge, England), 2012, 139 (11), pp.1910-20. ⟨10.1242/dev.072561⟩
Journal articles hal-01122082v1