- 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
2018–2020 · grant
Extracellular ATP and T regulatory cells: new therapeutics targets in alpha-sarcoglycan deficient muscular dystrophy (LGMD2D)
Claudio Bruno · Irccs - Istituto Giannina Gaslini
2018–2022 · grant
A silk-based bone marrow model to predict individual response to old and new drugs for increasing platelet count in inherited thrombocytopenias
Alessandro Pecci · Policlinico San Matteo Fondazione - Irccs
2018–2022 · grant
Rescuing epilepsy associated with SYN1 gene mutations by inhibiting eEF2K/eEF2 pathway
Carlo Sala · National Research Council
2017–2020 · grant
The ciliopathy-related traffic machinery: a new player in immune synapse assembly in T lymphocytes and a disease target in common variable immunodeficiency (CVID)
Cosima T. Baldari · University of Siena
2017–2019 · grant
Excitatory/Inhibitory unbalance in Ataxia telangiectasia and perspective therapeutical interventions
Flavia Antonucci · University of Milan
2017–2020 · grant
Designing therapeutic strategies to rescue epidermal defects in AEC syndrome
Caterina Missero · University of Campania "Luigi Vanvitelli"
2017–2021 · grant
SAP-mediated DGKa inhibition triggers a novel cell fate switch in antigen-activated T cells: implications for XLP1 therapy
Andrea Graziani · Vita-Salute San Raffaele University
2017–2021 · grant
Targeting lipids in CLN8-associated NCL diseases: structural and functional interaction of CLN8 with vesicle-associated membrane protein-associated protein A (VAPA), and genotype-phenotype correlations
Patrizia Guarneri · National Research Council
2017–2021 · grant
Dissecting dendritic cell subsets as key to installing tolerance to FVIII in hemophilia A
Francesca Fallarino · University of Perugia
2017–2021 · grant
Cone dystrophies and retinal degeneration from protein structures to biological networks. Toward the design of therapeutic molecules
Daniele Dell'Orco · Ospedale Policlinico G.b. Rossi
2017–2021 · grant
Development of a liver-based epigenetic silencing strategy to treat familiar hypercholesterolemia
Angelo Lombardo · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2017–2021 · grant
Identification of new druggable targets and potential therapeutic compounds for Spinal Muscular Atrophy, using a C.elegans model of neurodegeneration
Elia Di Schiavi · National Research Council
2017–2020 · grant
RNA-based studies of Duchenne Muscular Dystrophy: post-transcriptional control and role of non coding RNAs in normal and dystrophic muscle development
Irene Bozzoni · Sapienza University of Rome
2017–2021 · grant
A novel comprehensive strategy for the study of the molecular basis of Familial Hemiplegic Migraine 3
Paola Gavazzo · National Research Council
2017–2025 · grant
PROCESS DEVELOPMENT LAB
Luigi Naldini · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2017–2021 · grant
Impairment of GABAergic signaling and synaptic plasticity as key determinants for neurodevelopmental disorders: a study from NL3R451C knock-in mice, an animal model of autism
Enrico Cherubini · Fondazione Ebri Rita Levi Montalcini
2017–2023 · grant
Role of the Coiled-coil structure of the Huntingtin protein in the intercellular propagation of polyQ aggregates and in the progression of the disease
Luana Fioriti · Mario Negri Institute for Pharmacological Research
2017–2021 · grant
Developing tools for trial readiness in primary mitochondrial myopathies of the adulthood
Michelangelo Mancuso · Azienda Ospedaliera Universitaria Pisana
2017–2021 · grant
Implementation of human neuronal cultures and mouse models of Pantothenate kinase 2 deficiency to investigate pathogenic mechanisms of iron-related neurodegeneration and evaluate Coenzyme A therapeutic efficacy
Sonia Levi · Vita-Salute San Raffaele University
2017–2020 · grant
Neuronal dysfunctions underlying Phelan-McDermid syndrome and theirs rescue by genetic and pharmacological modulation of mGlu5 signaling
Chiara Verpelli · National Research Council
2017–2021 · grant
A mitochondrial therapy for muscular dystrophies
Paolo Bernardi · University of Padua
2017–2018 · grant
Hereditary spastic paraplegia: investigations on the regulation of spastin protein mediated by the kinase HIPK2 in proliferating cells and in neurons
Cinzia Rinaldo · National Research Council
2017–2021 · grant
Charcot-Marie-Tooth type 2B: Role of the Rab7 GTPase and of Rab7 interacting proteins
Cecilia Bucci · University of Salento
2017–2021 · grant
Neuroserpin misfolding and FENIB neurodegeneration: mechanism and inhibition processes
Martino Bolognesi · University of Milan
2017–2021 · grant
Unravelling the role of PAX2 mutations in human Focal Segmental Glomerulosclerosis
Ariela Benigni · Mario Negri Institute for Pharmacological Research
2017–2021 · grant
Targeting mitochondria in myopathies with RyR1 and MICU1 mutations
Gyorgy Szabadkai · University of Padua
2017–2020 · grant
Observational longitudinal study of growth patterns, body composition, energy expenditure and dietary intake in Italian infants and children with spinal muscular atrophy type I and II
Simona Bertoli · University of Milan
2017–2020 · grant
Contribution of lipids and their oxidized metabolites on Arrhythmogenic Cardiomyopathy pathogenesis
Giulio Pompilio · Centro Cardiologico Monzino
2017–2020 · grant
A novel in vitro Duchenne Muscular Dystrophy cardiomyopathy model: human iPSC-derived cardiomyocytes for mechanistic studies
Cecilia Ferrantini · University of Florence
2017–2021 · grant
Mitochondrial Ca2+ uptake in the pathogenesis of familial Alzheimer’s disease
Rosario Rizzuto · University of Padua
2016–2021 · grant
Tigem Vector Core
Alberto Auricchio · Telethon Institute Of Genetics And Medicine (tigem)
2016–2021 · grant
Mendelian Disorders of Membrane Trafficking: Molecular Mechanisms and Drug Target Identification
Maria Antonietta De Matteis · Telethon Institute Of Genetics And Medicine (tigem)
2016–2021 · grant
Genomic mechanisms of human myelopoiesis: implications for bone marrow reconstitution after gene therapy
Renato Ostuni · Fondazione Centro San Raffaele
2016–2021 · grant
Mechanisms of Neurodegeneration and CNS therapy in Lysosomal Storage Disorders
Alessandro Fraldi · Telethon Institute Of Genetics And Medicine (tigem)
2016–2018 · grant
Novel pharmacologic approaches to hepcidin genetic disorders
Maura Poli · University of Brescia
2016–2021 · grant
Fabry Disease
Maria Antonietta De Matteis · Telethon Institute Of Genetics And Medicine (tigem)
2016–2021 · grant
Therapeutic induction of cell clearance to cure Inherited Retinal Dystrophies
Ivan Conte · Telethon Institute Of Genetics And Medicine (tigem)
2016–2021 · grant
Tigem Cell Culture and Cytogenetics Core
Luis Juan Vicente Galietta · Telethon Institute Of Genetics And Medicine (tigem)
2016–2021 · grant
Lentiviral-mediated gene transfer of TCIRG1 to correct osteoclast function in autosomal recessive osteopetrosis: a pilot study
Anna Villa · Fondazione Centro San Raffaele
2016–2021 · grant
Towards a Clinical Trial of Gene Therapy for Mucopolysaccharidosis VI
Alberto Auricchio · Telethon Institute Of Genetics And Medicine (tigem)