
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.
2023
Probenecid affects muscle Ca2+ homeostasis and contraction independently from pannexin channel block.,
J Gen Physiol 2023 Apr; 155(4): .
2023
PCYT2-regulated lipid biosynthesis is critical to muscle health and ageing.,
Nat Metab 2023 Mar; 5(3): 495-515.
2023
MBNL-dependent impaired development within the neuromuscular system in myotonic dystrophy type 1.,
Neuropathol Appl Neurobiol 2023 Feb; 49(1): e12876.
2023
Chromodomain on Y-like 2 (CDYL2) implicated in mitosis and genome stability regulation via interaction with CHAMP1 and POGZ.,
Cell Mol Life Sci 2023 Jan; 80(2): 47.
2023
Nucleolar reorganization after cellular stress is orchestrated by SMN shuttling between nuclear compartments,
Nat Commun 2023 Nov; 14(1): 7384.
2023
Repurposing pentamidine using hyaluronic acid-based nanocarriers for skeletal muscle treatment in myotonic dystrophy.,
Nanomedicine 2023 Jan; 47(): 102623.
2023
SMA-linked SMN mutants prevent phase separation properties and SMN interactions with FMRP family members.,
Life Sci Alliance 2023 Jan; 6(1): .
2023
Disrupted T-tubular network accounts for asynchronous calcium release in MTM1-deficient skeletal muscle.,
J Physiol 2023 Jan; 601(1): 99-121.
2022
Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy.,
Hum Mutat 2022 Dec; 43(12): 1898-1908.
2022
Pharmacological inhibition of HDAC6 improves muscle phenotypes in dystrophin-deficient mice by downregulating TGF-β via Smad3 acetylation.,
Nat Commun 2022 Nov; 13(1): 7108.
2022
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.,
Acta Neuropathol 2022 Oct; 144(4): 707-731.
2022
Superfast excitation-contraction coupling in adult zebrafish skeletal muscle fibers.,
J Gen Physiol 2022 Sep; 154(9): .
2022
XAB2 dynamics during DNA damage-dependent transcription inhibition,
Elife 2022 Jul; 11(): .
2022
A stable XPG protein is required for proper ribosome biogenesis: Insights on the phenotype of combinate Xeroderma Pigmentosum/Cockayne Syndrome patients,
PLoS One 2022 ; 17(7): e0271246.
2022
Simple Methods for Permanent or Transient Denervation in Mouse Sciatic Nerve Injury Models.,
Bio Protoc 2022 Jun; 12(11): .
2022
Hypothalamic-pituitary-adrenal axis activation and glucocorticoid-responsive gene expression in skeletal muscle and liver of Apc mice.,
J Cachexia Sarcopenia Muscle 2022 Jun; 13(3): 1686-1703.
2022
Involvement of Type I Interferon Signaling in Muscle Stem Cell Proliferation During Dermatomyositis.,
Neurology 2022 May; 98(21): e2108-e2119.
2022
Mice with muscle-specific deletion of Bin1 recapitulate centronuclear myopathy and acute downregulation of dynamin 2 improves their phenotypes.,
Mol Ther 2022 Feb; 30(2): 868-880.
2022
Epigenetic Control of Muscle Stem Cells: Focus on Histone Lysine Demethylases.,
Front Cell Dev Biol 2022 ; 10(): 917771.
2022
Development of a high-throughput tailored imaging method in zebrafish to understand and treat neuromuscular diseases.,
Front Mol Neurosci 2022 ; 15(): 956582.