Publications

2013

S. Mourgues, V. Gautier, A. Lagarou, C. Bordier, A. Mourcet, J. Slingerland, L. Kaddoum, Frédéric ..., ELL, a novel TFIIH partner, is involved in transcription restart after DNA repair, Proceedings of the National Academy of Sciences of the United States of America.

2013

M. Sabra, P. Texier, J. El Maalouf, P. Lomonte, The Tudor protein survival motor neuron (SMN) is a chromatin-binding protein that interacts with methylated lysine 79 of histone H3, J Cell Sci 2013 Aug; 126(Pt 16): 3664-77.

2013

Bruneteau G, Simonet T, Bauché S, Mandjee N, Malfatti E, Girard E, Tanguy ML, Behin A, Khiami F, Sa..., Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression., Brain 2013 Aug; 136(Pt 8): 2359-68.

2013

Julie Nonnekens, Jorge Perez-Fernandez, Arjan F Theil, Olivier Gadal, Chrystelle Bonnart, Giuseppina..., Mutations in TFIIH causing trichothiodystrophy are responsible for defects in ribosomal RNA production and processing, Human Molecular Genetics.

2013

Marion Maisonobe, Giuseppina Giglia-Mari, Denis Eckert, DNA Repair: A changing geography? (1964–2008), DNA Repair.

2013

Jorquera G, Altamirano F, Contreras-Ferrat A, Almarza G, Buvinic S, Jacquemond V, Jaimovich E, Casas..., Cav1.1 controls frequency-dependent events regulating adult skeletal muscle plasticity., J Cell Sci 2013 Mar; 126(Pt 5): 1189-98.

2013

Lara Kaddoum, Nicolas Panayotis, Honoré Mazarguil, Giuseppina Giglia-Mari, Jean Christophe Roux, Et..., Isoform-specific anti-MeCP2 antibodies confirm that expression of the e1 isoform strongly predominates in the brain, F1000Research.

2013

Lefebvre R, Legrand C, Groom L, Dirksen RT, Jacquemond V, Ca2+ release in muscle fibers expressing R4892W and G4896V type 1 ryanodine receptor disease mutants., PLoS One 2013 ; 8(1): e54042.

2013

Ben Ammar A, Soltanzadeh P, Bauché S, Richard P, Goillot E, Herbst R, Gaudon K, Huzé C, Schaeffer ..., A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia., PLoS One 2013 ; 8(1): e53826.