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PGNM publications reflect the scientific output of the laboratory’s teams and collaborators, spanning fundamental mechanisms, disease models, technologies and translational research.

2015
Ratti F, Ramond F, Moncollin V, Simonet T, Milan G, Méjat A, Thomas JL, Streichenberger N, Gilquin ..., Histone deacetylase 6 is a FoxO transcription factor-dependent effector in skeletal muscle atrophy., J Biol Chem 2015 Feb; 290(7): 4215-24.
2015
Frecha C, Chevalier SA, van Uden P, Rubio I, Siouda M, Saidj D, Cohen C, Lomonte P, Accardi R, Tomma..., Expression of the epidermodysplasia verruciformis-associated genes EVER1 and EVER2 is activated by exogenous DNA and inhibited by LMP1 oncoprotein from Epstein-Barr virus., J Virol 2015 Jan; 89(2): 1461-7.
2015
Xavier Gaume, Anne-Marie Tassin, Iva Ugrinova, Fabien Mongelard, Karine Monier, Philippe Bouvet, Centrosomal nucleolin is required for microtubule network organization, Cell Cycle.
2014
Gallot YS, Durieux AC, Castells J, Desgeorges MM, Vernus B, Plantureux L, Rémond D, Jahnke VE, Lefa..., Myostatin gene inactivation prevents skeletal muscle wasting in cancer., Cancer Res 2014 Dec; 74(24): 7344-56.
2014
S. Cavallero, N. Huot, L. Francelle, P. Lomonte, T. Naas, M. Labetoulle, Biological Features of Herpes Simplex Virus Type 1 Latency in Mice According to Experimental Conditions and Type of Neurones, Invest Ophthalmol Vis Sci 2014 Oct; 55(12): 7761-74.
2014
Morel V, Lepicard S, Rey AN, Parmentier ML, Schaeffer L, Drosophila Nesprin-1 controls glutamate receptor density at neuromuscular junctions., Cell Mol Life Sci 2014 Sep; 71(17): 3363-79.
2014
Gasperi C, Melms A, Schoser B, Zhang Y, Meltoranta J, Risson V, Schaeffer L, Schalke B, Kröger S, Anti-agrin autoantibodies in myasthenia gravis., Neurology 2014 Jun; 82(22): 1976-83.
2014
Lomonte P, Corps nucléaires PML, centromères et contrôle de la latence du virus herpès simplex 1., Virologie (Montrouge) 2014 Jun; 18(3): 170-179.
2014
Nicot AS, Lo Verso F, Ratti F, Pilot-Storck F, Streichenberger N, Sandri M, Schaeffer L, Goillot E, Phosphorylation of NBR1 by GSK3 modulates protein aggregation., Autophagy 2014 Jun; 10(6): 1036-53.
2014
Rodríguez EG, Lefebvre R, Bodnár D, Legrand C, Szentesi P, Vincze J, Poulard K, Bertrand-Michel J,..., Phosphoinositide substrates of myotubularin affect voltage-activated Ca²⁺ release in skeletal muscle., Pflugers Arch 2014 May; 466(5): 973-85.
2014
Martinez-Torres C, Berguiga L, Streppa L, Boyer-Provera E, Schaeffer L, Elezgaray J, Arneodo A, Argo..., Diffraction phase microscopy: retrieving phase contours on living cells with a wavelet-based space-scale analysis., J Biomed Opt 2014 Mar; 19(3): 36007.
2014
Frédéric Catez, Antoine Rousseau, Marc Labetoulle, Patrick Lomonte, Detection of the Genome and Transcripts of a Persistent DNA Virus in Neuronal Tissues by Fluorescent In situ Hybridization Combined with Immunostaining, J Vis Exp 2014 Jan; (83): e51091.
2014
Lefebvre R, Pouvreau S, Collet C, Allard B, Jacquemond V, Whole-cell voltage clamp on skeletal muscle fibers with the silicone-clamp technique., Methods Mol Biol 2014 ; 1183(): 159-70.
2013
Mourgues S, Gautier V, Lagarou A, Bordier C, Mourcet A, Slingerland J, Kaddoum L, Coin F, Vermeulen ..., ELL, a novel TFIIH partner, is involved in transcription restart after DNA repair., Proc Natl Acad Sci U S A 2013 Oct; 110(44): 17927-32.
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
Nonnekens J, Cabantous S, Slingerland J, Mari PO, Giglia-Mari G, In vivo interactions of TTDA mutant proteins within TFIIH., J Cell Sci 2013 Aug; 126(Pt 15): 3278-83.
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
Theil AF, Nonnekens J, Steurer B, Mari PO, de Wit J, Lemaitre C, Marteijn JA, Raams A, Maas A, Verme..., Disruption of TTDA results in complete nucleotide excision repair deficiency and embryonic lethality., PLoS Genet 2013 Apr; 9(4): e1003431.