- Grants since 2016
- 611
- Awarded, last 5 years (where amounts are published)
- €94.6M
- Funded works, last 5 years
- 5 837
- Funded works, all time
- 8 569
Grants
2023–2026 · grant
Role of myeloperoxidase-mediated neuroinflammation in aceruloplasminemia
Massimo Alessio · Vita-Salute San Raffaele University
2023–2026 · grant
Molecular mechanisms underlying Joubert syndrome
Daniele Guardavaccaro · University of Verona
2023–2024 · grant
Functional study on a new pharmacological approach in the Rett Syndrome
Flavia Antonucci · University of Milan
2023–2025 · grant
Treating autosomal dominant polycystic kidney disease by using inhalable thyroid hormone-nanocarriers
Christodoulos Xinaris · Mario Negri Institute for Pharmacological Research
2023–2025 · grant
Generation and morpho-functional characterization of zebrafish models of piga deficiency: new tools to investigate the molecular underpinnings of MCAHS2 and explore potential rescue strategies.
Dario Finazzi · University of Brescia
2023–2026 · grant
Exploring a new therapeutic target for Niemann-Pick C1 disease: the BET proteins
Valentina Pallottini · Roma Tre University
2023–2025 · grant
Toler8: Uncovering the dynamics of cellular and molecular pathways for immune tolerance in hemophilia A
Francesca Fallarino · University of Perugia
2023–2026 · grant
Unravelling the role of DNA on its own instability within the Huntington’s disease locus
Elena Cattaneo · University of Milan
2023–2026 · grant
Role of Cl- homeostasis in aberrant brain rhythms, from oscillations to sleep-wake cycles, in a mouse model of intellectual disability and autism spectrum disorder.
Claudia Lodovichi · National Research Council
2023–2026 · grant
Mechanisms of cardiopharyngeal differentiation
Antonio Baldini · University of Naples Federico II
2023–2024 · grant
Repurposing CFTR correctors in Allan Herndon Dudley syndrome
Dorianna Sandonà · University of Padua
2023–2026 · grant
Mechanisms and therapeutic targets of NEDAMSS, a novel regressive neurodevelopmental syndrome
Ferdinando Fiumara · University of Turin
2023–2025 · grant
Disease-Modifying Therapeutic Approaches in a Gene-Edited Model of Timothy Syndrome
Andrea Mazzanti · University of Pavia
2023–2025 · grant
The long tail of a STAR: a matter of cell differentiation impairment and aberrant cytoskeletal dynamics to explain STAR syndrome phenotype
Luca Proietti De Santis · Università degli Studi della Tuscia
2023–2026 · grant
Understanding the role of CNBP-eIF5A-polyamine metabolism in DM2 pathogenesis
Gianluca Canettieri · Sapienza University of Rome
2023–2026 · grant
Deciphering the role of the maternal-effect gene PADI6 in the etiology of genomic imprinting defects
Andrea Riccio · National Research Council
2023–2026 · grant
Dissecting the role of Sox2 in neurons of the visual thalamus: insights into developmental visual disorders
Sara Mercurio · University of Milano-Bicocca
2023–2026 · grant
Studies on PRPF40B/MECP2 crosstalk in Rett syndrome
Cecilia Mannironi · National Research Council
2023–2026 · grant
Disease mechanism and pharmacological approaches for TBC1D8B-induced steroid resistant nephrotic syndrome
Carlo Cosimo Campa · Italian institute for Genomic Medicine
2023–2024 · grant
An in vivo model of intractable R257C-ACTG2 Visceral Myopathy to study pathogenesis and to identify new disease targets
Thomas Vaccari · University of Milan
2023–2025 · grant
Harnessing the Sirtuin 6-Thyroid Hormone cross talk to counteract the progression of the Duchenne Muscular Dystrophy
Monica Dentice · University of Naples Federico II
2023–2026 · grant
Role of astrocyte Ca2+ signaling for hippocampal spatial memory in a mouse model of familial Alzheimer's Disease
Letizia Mariotti · National Research Council
2023–2025 · grant
Emerging pathways of neurodegeneration in Sanfilippo syndrome
Elvira De Leonibus · Telethon Institute Of Genetics And Medicine (tigem)
2023–2025 · grant
The Contribution of Schwann cell TRPA1 to familial episodic pain syndrome
Francesco De Logu · University of Florence
2023–2024 · grant
Mechanisms and disease models of neurodevelopmental disorders involving CLC anion transporters
Michael Pusch · National Research Council
2023–2024 · grant
Connecting craniofacial malformations with neural crest splicing defects by defining the role of nuclear cyclophilin NKTR
Anna Maria Cariboni · University of Milan
2023–2025 · grant
Structure-function characterization of TANC2, a novel postsynaptic candidate associated to neuropsychiatric disorders
Ivan De Curtis · Vita-Salute San Raffaele University
2023–2026 · grant
Dissecting the role of cytoplasmic signaling metabolites in Niemann-Pick disease type C
Alessandro Carrer · Veneto Institute of Molecular Medicine
2023–2025 · grant
Compose LI(L)RA1 ballad: enlighten its role in cutaneous lupus erithematosus
Jens Geginat · University of Milan
2023–2025 · grant
MAU2: the (T)dark side of Cornelia de Lange syndrome
Valentina Massa · University of Milan
2023–2025 · grant
Modeling Pitt-Hopkins syndrome and new pathogenetic variants of TCF4 by gene editing: a step forward toward personalized medicine (HOPeFOR)
Michela Ori · University of Pisa
2023–2025 · grant
Exploring the role of MLIP in LMNA-Cardiomyopathy in iPSC-based human cardiac models
Elisa Di Pasquale · National Research Council
2023–2024 · grant
Pharmacological and gene therapy approaches to restore mitochondrial quality control and frataxin processing in the PITRM1-dependent SCA
Dario Brunetti · Fondazione Istituto Neurologico Carlo Besta - Irccs
2023–2026 · grant
Correcting FOXG1 activity levels by small RNA-analogs modulating the corresponding mRNA levels and their translation rates
Antonello Mallamaci · Scuola Internazionale Superiore di Studi Avanzati
2023–2026 · grant
Selective control of DNA damage response at telomeres as an innovative therapeutic approach for Dyskeratosis Congenita
Fabrizio D'Adda Di Fagagna · Ifom Ets - Istituto Fondazione Di Oncologia Molecolare
2023–2026 · grant
Development and application of novel membrane-targeted photoswitches for restoration of the physiological retinal processing in Retinitis pigmentosa (LIGHTSWITCH)
Fabio Benfenati · Italian Institute of Technology
2023–2025 · grant
Understanding the basis of tubular aggregate myopathy
Armando Genazzani · University of Turin
2023–2024 · grant
Exploring pathogenetic mechanisms of Jamuar Syndrome: focus on transcriptomics and brain extracellular matrix changes
Emanuela Bottani · University of Verona
2023–2025 · grant
Role of Kctd20 gene in the pathogenesis of Phelan McDermid syndrome
Chiara Verpelli · National Research Council
2023–2025 · grant
Functional properties, localization and physiopathology of putative glucose transporter SLC45A1 involved in epilepsy and intellectual disability
Michael Pusch · National Research Council