Publications en collaboration avec des chercheurs de Università di Urbino (13)

2024

  1. Melatonin Modulates Cell Cycle Dynamics and Promotes Hippocampal Cell Proliferation After Ischemic Injury in Neonatal Rats

    Molecular Neurobiology, Vol. 61, Núm. 9, pp. 6910-6919

2023

  1. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

    Movement Disorders, Vol. 38, Núm. 2, pp. 286-303

  2. The Endocannabinoid System as a Target for Neuroprotection/Neuroregeneration in Perinatal Hypoxic–Ischemic Brain Injury

    Biomedicines, Vol. 11, Núm. 1

2022

  1. Editorial: Neonatal Brain Injury and the Search for New Therapies

    Frontiers in Pediatrics

  2. The Synthetic Cannabinoid URB447 Exerts Antitumor and Antimetastatic Effect in Melanoma and Colon Cancer

    Pharmaceuticals, Vol. 15, Núm. 10

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

  2. Identification of sixteen novel candidate genes for late onset Parkinson’s disease

    Molecular Neurodegeneration, Vol. 16, Núm. 1

2020

  1. The Synthetic Cannabinoid URB447 Reduces Brain Injury and the Associated White Matter Demyelination after Hypoxia-Ischemia in Neonatal Rats

    ACS Chemical Neuroscience, Vol. 11, Núm. 9, pp. 1291-1299

2019

  1. Aging-Related Expression of Twinfilin-1 Regulates Cholangiocyte Biological Response to Injury

    Hepatology, Vol. 70, Núm. 3, pp. 883-898

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

2012

  1. Pretreatment with the monoacylglycerol lipase inhibitor URB602 protects from the long-term consequences of neonatal hypoxic-ischemic brain injury in rats

    Pediatric Research, Vol. 72, Núm. 4, pp. 400-406

1999

  1. The A1555G mutation in the 12S rRNA gene of human mtDNA: Recurrent origins and founder events in families affected by sensorineural deafness

    American Journal of Human Genetics, Vol. 65, Núm. 5, pp. 1349-1358