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  1. Article

    Open Access

    A conformational switch controlling the toxicity of the prion protein

    Prion infections cause conformational changes of the cellular prion protein (PrPC) and lead to progressive neurological impairment. Here we show that toxic, prion-mimetic ligands induce an intramolecular R208-H14...

    Karl Frontzek, Marco Bardelli, Assunta Senatore in Nature Structural & Molecular Biology (2022)

  2. Article

    Open Access

    Author Correction: Brain aging is faithfully modelled in organotypic brain slices and accelerated by prions

    Yingjun Liu, Assunta Senatore, Silvia Sorce, Mario Nuvolone in Communications Biology (2022)

  3. Article

    Open Access

    Brain aging is faithfully modelled in organotypic brain slices and accelerated by prions

    Mammalian models are essential for brain aging research. However, the long lifespan and poor amenability to genetic and pharmacological perturbations have hindered the use of mammals for dissecting aging-regul...

    Yingjun Liu, Assunta Senatore, Silvia Sorce, Mario Nuvolone in Communications Biology (2022)

  4. Article

    Open Access

    The Epidemiology of Persons Living with Fontan in 2020 and Projections for 2030: Development of an Epidemiology Model Providing Multinational Estimates

    Fontan surgery is a palliative procedure performed in children with a functionally univentricular heart. Improvements in surgical technique over the past 30 years have increased life expectancy in this rare po...

    Leandra Plappert, Susan Edwards, Assunta Senatore, Angela De Martini in Advances in Therapy (2022)

  5. Article

    Open Access

    PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

    Recently, several genome-wide association studies identified PHACTR1 as key locus for five diverse vascular disorders: coronary artery disease, migraine, fibromuscular dysplasia, cervical artery dissection and hy...

    Clemens Messerschmidt, Marco Foddis, Sonja Blumenau, Susanne Müller in Scientific Reports (2021)

  6. Article

    Open Access

    The biological function of the cellular prion protein: an update

    The misfolding of the cellular prion protein (PrPC) causes fatal neurodegenerative diseases. Yet PrPC is highly conserved in mammals, suggesting that it exerts beneficial functions preventing its evolutionary eli...

    Marie-Angela Wulf, Assunta Senatore, Adriano Aguzzi in BMC Biology (2017)

  7. No Access

    Article

    The prion protein is an agonistic ligand of the G protein-coupled receptor Adgrg6

    The cellular prion protein PrPC promotes peripheral myelin homeostasis by acting on a G protein-coupled receptor to increase levels of cyclic AMP in Schwann cells.

    Alexander Küffer, Asvin K. K. Lakkaraju, Amit Mogha, Sarah C. Petersen in Nature (2016)