
Publications
Articles et résultats scientifiques des équipes et collaborateurs du PGNM.
À propos
Les publications du PGNM reflètent la production scientifique des équipes et des collaborateurs du laboratoire, couvrant les mécanismes fondamentaux, les modèles de maladies, les technologies et la recherche translationnelle.
2017
Cockayne’s Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation.,
Mol Cell 2017 Dec; 68(6): 1054-1066.e6.
2017
Impaired excitation-contraction coupling in muscle fibres from the dynamin2R465W mouse model of centronuclear myopathy.,
J Physiol 2017 Dec; 595(24): 7369-7382.
2017
Na leak with gating pore properties in hypokalemic periodic paralysis V876E mutant muscle Ca channel.,
J Gen Physiol 2017 Dec; 149(12): 1139-1148.
2017
Elevated resting H+ current in the R1239H type 1 hypokalaemic periodic paralysis mutated Ca2+ channel.,
J Physiol 2017 Oct; 595(20): 6417-6428.
2017
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression.,
Hum Mol Genet 2017 Jun; 26(11): 2062-2075.
2017
LSD1 Controls Timely MyoD Expression via MyoD Core Enhancer Transcription.,
Cell Rep 2017 Feb; 18(8): 1996-2006.
2017
Effects of Macrophage Conditioned-Medium on Murine and Human Muscle Cells: Analysis of Proliferation, Differentiation, and Fusion.,
Methods Mol Biol 2017 ; 1556(): 317-327.
2017
Isolation of Exosomes and Microvesicles from Cell Culture Systems to Study Prion Transmission.,
Methods Mol Biol 2017 ; 1545(): 153-176.
2016
Phosphatidylinositol 3-kinase inhibition restores Ca2+ release defects and prolongs survival in myotubularin-deficient mice.,
Proc Natl Acad Sci U S A 2016 Dec; 113(50): 14432-14437.
2016
Macrophage PPARγ, a Lipid Activated Transcription Factor Controls the Growth Factor GDF3 and Skeletal Muscle Regeneration.,
Immunity 2016 Nov; 45(5): 1038-1051.
2016
[NeuroMyoGene Institute: a Franco-Canadian partnership promoting research in neuromuscular disorders].,
Med Sci (Paris) 2016 Nov; 32 Hors série n°2(): 55-56.
2016
Real-Time Tracking of Parental Histones Reveals Their Contribution to Chromatin Integrity Following DNA Damage.,
Mol Cell 2016 Oct; 64(1): 65-78.
2016
Latency Entry of Herpes Simplex Virus 1 Is Determined by the Interaction of Its Genome with the Nuclear Environment.,
PLoS Pathog 2016 Sep; 12(9): e1005834.
2016
mTOR inactivation in myocardium from infant mice rapidly leads to dilated cardiomyopathy due to translation defects and p53/JNK-mediated apoptosis.,
J Mol Cell Cardiol 2016 Aug; 97(): 213-25.
2016
A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia.,
Hum Mol Genet 2016 Aug; 25(15): 3341-3360.
2016
A ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repair.,
Nucleic Acids Res 2016 Jun; 44(11): 5246-55.
2016
Time-lapse scanning surface plasmon microscopy of living adherent cells with a radially polarized beam.,
Appl Opt 2016 Feb; 55(6): 1216-27.
2016
Notch Stimulates Both Self-Renewal and Lineage Plasticity in a Subset of Murine CD9High Committed Megakaryocytic Progenitors.,
PLoS One 2016 ; 11(4): e0153860.
2015
PAK1 and CtBP1 Regulate the Coupling of Neuronal Activity to Muscle Chromatin and Gene Expression.,
Mol Cell Biol 2015 Dec; 35(24): 4110-20.
2015
Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA.,
Appl Transl Genom 2015 Dec; 7(): 19-25.