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authIdHal_s : alain-lilienbaum

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

Robust simplifications of multiscale biochemical networks

Ovidiu Radulescu , Alexander N. Gorban , Andrei Zinovyev , Alain Lilienbaum
BMC Systems Biology, 2008, 2:86
Journal articles inria-00331212v1