Restoring wild-type-like CA1 network dynamics and behavior during adulthood in a mouse model of schizophrenia

T Marissal, RF Salazar, C Bertollini, S Mutel… - Nature …, 2018 - nature.com
Schizophrenia is a severely debilitating neurodevelopmental disorder. Establishing a
causal link between circuit dysfunction and particular behavioral traits that are relevant to …

Lateral allosterism in the glucagon receptor family: glucagon-like peptide 1 induces G-protein-coupled receptor heteromer formation

…, F Joly, S Mutel, C Hampe, B Breton, V Mutel… - Molecular …, 2012 - ASPET
Activation of G-protein-coupled receptors (GPCRs) results in a variety of cellular responses,
such as binding to the same receptor of different ligands that activate distinct downstream …

The claustrum-medial prefrontal cortex network controls attentional set-shifting

L Fodoulian, O Gschwend, C Huber, S Mutel… - BioRxiv, 2020 - biorxiv.org
In various mental disorders, dysfunction of the prefrontal cortex contributes to cognitive deficits.
Here we studied how the claustrum (CLA), a nucleus sharing reciprocal connections with …

[HTML][HTML] Effect of the Metabotropic Glutamate Receptor Type 5 Negative Allosteric Modulator Dipraglurant on Motor and Non-Motor Symptoms of Parkinson's Disease

MP Epping-Jordan, F Girard, AS Bessis, V Mutel… - Cells, 2023 - mdpi.com
Parkinson’s disease (PD) patients suffer not only from the primary motor symptoms of the
disease but also from a range of non-motor symptoms (NMS) that cause disability and low …

NADPH oxidase and extracellular regulated kinases 1/2 are targets of prion protein signaling in neuronal and nonneuronal cells

B Schneider, V Mutel, M Pietri… - Proceedings of the …, 2003 - National Acad Sciences
Putative functions of the cellular prion protein, PrP C , include resistance to oxidative stress,
copper uptake, cell adhesion, and cell signaling. Here, we report NADPH oxidase-…

DAPK2 downregulation associates with attenuated adipocyte autophagic clearance in human obesity

H Soussi, S Reggio, R Alili, C Prado, S Mutel, M Pini… - Diabetes, 2015 - Am Diabetes Assoc
Adipose tissue dysfunction in obesity has been linked to low-grade inflammation causing
insulin resistance. Transcriptomic studies have identified death-associated protein kinase 2 (…

Targeted deletion of liver glucose-6 phosphatase mimics glycogen storage disease type 1a including development of multiple adenomas

E Mutel, A Abdul-Wahed, N Ramamonjisoa… - Journal of …, 2011 - Elsevier
BACKGROUND AND AIMS: Glycogen storage disease type 1a (GSD1a) is an inherited
disease caused by a deficiency in the catalytic subunit of the glucose-6 phosphatase enzyme (…

Reactive oxygen species‐dependent TNF‐α converting enzyme activation through stimulation of 5‐HT2B and α1D autoreceptors in neuronal cells

…, S Mouillet‐Richard, M Ermonval, V Mutel… - The FASEB …, 2005 - Wiley Online Library
A major determinant of neuronal homeostasis is the proper integration of cell signaling
pathways recruited by a variety of neuronal and non‐neuronal factors. By taking advantage of a …

Hepatic lentiviral gene transfer prevents the long-term onset of hepatic tumours of glycogen storage disease type 1a in mice

J Clar, E Mutel, B Gri, A Creneguy… - Human molecular …, 2015 - academic.oup.com
Glycogen storage disease type 1a (GSD1a) is a rare disease due to the deficiency in the
glucose-6-phosphatase (G6Pase) catalytic subunit (encoded by G6pc), which is essential for …

Cellular prion protein signaling in serotonergic neuronal cells

…, J Grassi, JG Richards, V Mutel… - Annals of the New …, 2007 - Wiley Online Library
The cellular prion protein PrP C is the normal counterpart of the scrapie prion protein PrP Sc
, the main component of the infectious agent of transmissible spongiform encephalopathies (…