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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.

2024
Flück M, Sanchez C, Jacquemond V, Berthier C, Giraud MN, Jacko D, Bersiner K, Gehlert S, Baan G, Ja..., Enhanced capacity for CaMKII signaling mitigates calcium release related contractile fatigue with high intensity exercise., Biochim Biophys Acta Mol Cell Res 2024 Feb; 1871(2): 119610.
2024
Sutcu HH, Rassinoux P, Donnio LM, Neuillet D, Vianna F, Gabillot O, Mari PO, Baldeyron C, Giglia-Mar..., Decline of DNA damage response along with myogenic differentiation., Life Sci Alliance 2024 Feb; 7(2): .
2024
Federica Pilotto, Deepika Chellapandi, Hélène Puccio, Omaveloxolone: a groundbreaking milestone as the first FDA-approved drug for Friedreich ataxia, Trends in Molecular Medicine.
2024
Liénard C, Pintart A, Bomont P, Neuronal Autophagy: Regulations and Implications in Health and Disease., Cells 2024 Jan; 13(1): .
2024
Francesco Davide Naso, Flavie Strappazzon, Combining doxorubicin and miR-218-5p: a new strategy to fight breast cancer?, Autophagy Reports.
2024
Ever Espino-Gonzalez, Emilie Dalbram, Rémi Mounier, Julien Gondin, Jean Farup, Niels Jessen, Jonas ..., Impaired skeletal muscle regeneration in diabetes: From cellular and molecular mechanisms to novel treatments, Cell Metabolism.
2024
Hélène Puccio, Valentine Mosbach, A multiple animal and cellular models approach to study frataxin deficiency in Friedreich Ataxia, Biochim Biophys Acta Mol Cell Res 2024 Oct; 1871(7): 119809.
2024
Theuriet J, Fernandez-Eulate G, Latour P, Stojkovic T, Masingue M, Vidoni L, Bernard E, Jacquier A, ..., Genetic characterization of non-5q proximal spinal muscular atrophy in a French cohort: the place of whole exome sequencing., Eur J Hum Genet 2024 Jan; 32(1): 37-43.
2023
Sandoz J, Cigrang M, Zachayus A, Catez P, Donnio LM, Elly C, Nieminuszczy J, Berico P, Braun C, Alek..., Active mRNA degradation by EXD2 nuclease elicits recovery of transcription after genotoxic stress, Nat Commun 2023 Jan; 14(1): 341.
2023
Lequain H, Dégletagne C, Streichenberger N, Valantin J, Simonet T, Schaeffer L, Sève P, Leblanc P, Spatial Transcriptomics Reveals Signatures of Histopathological Changes in Muscular Sarcoidosis., Cells 2023 Nov; 12(23): .
2023
Léa Castellano, Vincent Gache, [Microtubular network and functionality of the striated skeletal muscle]. Réseau microtubulaire et fonctionnalité du muscle strié squelettique, Médecine/Sciences.
2023
Sébastien Cabrera, Renato Maciel, Nicolas Vachoud, Stevenson Desmercieres, Marine Breuilly, Gérald..., Establishment of an optimized and automated workflow for whole brain probing of neuronal activity patterns in TRAP mice., .
2023
Idoux R, Exbrayat-Héritier C, Sohm F, Jaque-Fernandez F, Vaganay E, Berthier C, Bretaud S, Jacquemo..., A mechano- and heat-gated two-pore domain K+ channel controls excitability in adult zebrafish skeletal muscle., Proc Natl Acad Sci U S A 2023 Nov; 120(45): e2305959120.
2023
Eleanor Seaby, Annie Godwin, Valentine Clerc, Géraldine Meyer-Dilhet, Xavier Grand, Tia Fletcher, L..., Monoallelic de novo variants in DDX17 cause a novel neurodevelopmental disorder, .
2023
Cloé Paret, Vincent Gache, J. Sohier, Injectable and porous hydrogel fate as scaffold in Volumetric Muscle Loss context, .
2023
Fiorella Faienza, Federica Polverino, Girish Rajendraprasad, Giacomo Milletti, Zehan Hu, Barbara Col..., AMBRA1 phosphorylation by CDK1 and PLK1 regulates mitotic spindle orientation, Cellular and Molecular Life Sciences.
2023
Lequain H, Gerfaud-Valentin M, Emile JF, Gangloff YG, Boursier G, Deligny C, Le Guenno G, Tantot J, ..., H syndrome mimicking Erdheim Chester disease: new entity and therapeutic perspectives., Haematologica 2023 Aug; 108(8): 2255-2260.
2023
Lescouzères L, Hassen-Khodja C, Baudot A, Bordignon B, Bomont P, A multilevel screening pipeline in zebrafish identifies therapeutic drugs for GAN., EMBO Mol Med 2023 Jul; 15(7): e16267.
2023
Davi a G Mázala, Ravi Hindupur, Young Jae Moon, Fatima Shaikh, Iteoluwakishi H Gamu, Dhruv Alladi, ..., Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD, Cell Death Discovery.
2023
Binda O, Kimenyi Ishimwe AB, Galloy M, Jacquet K, Corpet A, Fradet-Turcotte A, Côté J, Lomonte P, The TUDOR domain of SMN is an H3K79me1 histone mark reader., Life Sci Alliance 2023 Jun; 6(6): .