Publications
Scientific articles and outputs from PGNM teams and collaborators.
About
PGNM publications reflect the scientific output of the laboratory’s teams and collaborators, spanning fundamental mechanisms, disease models, technologies and translational research.
2024
Hereditary Ataxias: From Bench to Clinic, Where Do We Stand?,
Cells.
2024
Omaveloxolone: a groundbreaking milestone as the first FDA-approved drug for Friedreich ataxia,
Trends in Molecular Medicine.
2024
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
Impaired skeletal muscle regeneration in diabetes: From cellular and molecular mechanisms to novel treatments,
Cell Metabolism.
2024
Combining doxorubicin and miR-218-5p: a new strategy to fight breast cancer?,
Autophagy Reports.
2023
[Microtubular network and functionality of the striated skeletal muscle].
Réseau microtubulaire et fonctionnalité du muscle strié squelettique,
Médecine/Sciences.
2023
AMBRA1 phosphorylation by CDK1 and PLK1 regulates mitotic spindle orientation,
Cellular and Molecular Life Sciences.
2023
Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD,
Cell Death Discovery.
2023
Apoptotic cell death in disease—Current understanding of the NCCD 2023,
Cell Death and Differentiation.
2023
Mitochondrial Bcl-xL promotes brain synaptogenesis by controlling non-lethal caspase activation,
iScience.
2023
Kinetics of skeletal muscle regeneration after mild and severe muscle damage induced by electrically‐evoked lengthening contractions,
FASEB Journal.
2022
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy,
Brain - A Journal of Neurology.
2022
Initial TK-deficient HSV-1 infection in the lip alters contralateral lip challenge immune dynamics,
Sci Rep 2022 May; 12(1): 8489.
2022
Cobalt chloride has beneficial effects across species through a hormetic mechanism,
Frontiers in Cell and Developmental Biology.
2022
Monocyte Phenotypes and Physical Activity in Patients with Carotid Atherosclerosis,
Antioxidants.
2022
Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies,
Front Cell Neurosci 2022 ; 16(): 896854.
2022
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy,
Brain 2023 Aug; 146(8): 3470-3483.
2022
ERRα coordinates actin and focal adhesion dynamics,
Cancer Gene Therapy.
2022
Fluorescent Polymer-AS1411-Aptamer Probe for dSTORM Super-Resolution Imaging of Endogenous Nucleolin,
Biomacromolecules.
2021
The TeloDIAG: how telomeric parameters can help in glioma rapid diagnosis and liquid biopsy approaches,
Annals of Oncology.