
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.
2022
Initial TK-deficient HSV-1 infection in the lip alters contralateral lip challenge immune dynamics,
Sci Rep 2022 May; 12(1): 8489.
2022
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy,
Brain - A Journal of Neurology.
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
[HDAC6, a very specific deacetylase with a potential therapeutic role].,
Med Sci (Paris) 2022 Dec; 38 Hors série n° 1(): 6-12.
2022
Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report.,
Genes (Basel) 2022 Nov; 13(12): .
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
SMA-linked SMN mutants prevent phase separation properties and SMN interactions with FMRP family members,
Life Science Alliance.
2022
Nucleolar Reorganization After Cellular Stress is Orchestrated by SMN Shuttling Between Nuclear Compartments,
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2022
β-Actin and Nuclear Myosin I are responsible for nucleolar reorganization during DNA Repair,
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2022
Cobalt chloride has beneficial effects across species through a hormetic mechanism,
Frontiers in Cell and Developmental Biology.
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
Monocyte Phenotypes and Physical Activity in Patients with Carotid Atherosclerosis,
Antioxidants.
2022
XAB2 dynamics during DNA damage-dependent transcription inhibition,
eLife.
2022
ESTABLISHMENT OF AN OPTIMIZED AND AUTOMATED WORKFLOW FOR WHOLE BRAIN PROBING OF NEURONAL ACTIVITY PATTERNS IN TRAP MICE,
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2022
ALTERATIONS OF CORTICAL CONNECTIVITY IN A MOUSE MODEL OF PREMATURE BRAIN INJURY,
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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
Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies,
Front Cell Neurosci 2022 ; 16(): 896854.
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
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.