- 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
The natural antisense lncRNA PHOX2B-AS1 in the pathogenesis and as potential drug target in Congenital Central Hypoventilation Syndrome (CCHS)
Diego Maria Michele Fornasari · University of Milan
2023–2026 · grant
Study of the amyloidogenic conversion of V30M, S52P and V122I transthyretin variants by real-time Nuclear Magnetic Resonance: elucidation of the molecular mechanisms leading to different ATTR amyloidosis severity and different drug response.
Alessandra Corazza · University of Udine
2023–2026 · grant
Dissecting the role of the KLHL17 gene in the molecular pathogenesis of the West syndrome
Matteo Fossati · Fondazione Humanitas per la Ricerca
2023–2026 · grant
Deciphering Cholesterol efficacy on cognition in prodromal Huntington’s disease
Marta Valenza · University of Milan
2023–2024 · grant
Contribution of vascular abnormalities to gastrointestinal bleeding in patients with Glanzmann Thrombasthenia: mechanistic studies using endothelial colony forming cells (ECFCs)
Loredana Bury · University of Perugia
2023–2026 · grant
Neuronal activity control by products of Foxg1-responsive, Tdark Rnf genes
Antonello Mallamaci · Scuola Internazionale Superiore di Studi Avanzati
2023–2026 · grant
Posterior Column Ataxia and Retinitis Pigmentosa: new pathogenetic insights from the study of mitochondria-associated membranes
Deborah Chiabrando · University of Turin
2023–2026 · grant
Molecular interactions and functional dissection of TMEM65: relevance for mitochondrial diseases
Maria Eugenia Soriano · University of Padua
2023–2025 · grant
Identification of possible therapeutic targets to rescue neuronal and synaptic dysfunctions caused by deletions and mutations of the TCF20 intellectual disability gene
Carlo Sala · National Research Council
2023–2025 · grant
PLVAP as a novel player for lymphatic malformations in the SOX18-VEGFC regulatory network
Monica Beltrame · University of Milan
2023–2025 · grant
Understanding the causes and consequences of inflammation in FSHD muscular dystrophy to develop a possible treatment
Davide Gabellini · Vita-Salute San Raffaele University
2022–2027 · grant
Flow Cytrometry Facility - FACS - CITOFLUORIMETRIA
Stefano Pepe · Telethon Institute Of Genetics And Medicine (tigem)
2022–2024 · grant
The role of microglia in Lafora disease: characterisation of microglial signatures and screening of anti-inflammatory molecules in a novel zebrafish model
Stefania Della Vecchia · Fondazione Stella Maris - Irccs
2022–2023 · grant
Corticospinal tract microstructural integrity and its correlation with clinical and molecular biomarkers: a profilometry MRI study to identify in-vivo biomarkers of disease severity in ARSACS
Sirio Cocozza · University of Naples Federico II
2022–2025 · grant
Delving into the mechanisms underlying HPDL-related disorders with a multi-model approach
Filippo Maria Santorelli · Fondazione Stella Maris - Irccs
2022–2027 · grant
Therapeutic induction of cell clearance to cure Inherited Retinal Dystrophies
Ivan Conte · Telethon Institute Of Genetics And Medicine (tigem)
2022–2026 · grant
Cellular aging of hematopoietic stem cells in physiology and disease.
Raffaella Di Micco · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2022–2026 · grant
A human pluripotent stem cell-based approach to study human hematopoietic stem cell development
Andrea Ditadi · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2022–2027 · grant
Systems Biology approaches for the identification of biomarker genes of drug response and the study of genetic diseases
Gennaro Gambardella · Telethon Institute Of Genetics And Medicine (tigem)
2022–2027 · grant
Targeting mitochondria to treat rare and common neurodegenerative disorders
Alessia Indrieri · Telethon Institute Of Genetics And Medicine (tigem)
2022–2027 · grant
The molecular mechanisms behind membrane trafficking
Maria Antonietta De Matteis · Telethon Institute Of Genetics And Medicine (tigem)
2022–2026 · grant
GLP Test Facility
Luigi Naldini · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2022–2026 · grant
Elucidating the significance of osteopetrotic bone marrow niche in hematopoietic stem and progenitor cells, and its implications for stem cell therapy
Anna Villa · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2022–2024 · grant
Pathological molecular mechanisms underlying APOPT1 loss of function
Erika Fernandez-Vizarra · Fondazione Per La Ricerca Biomedica Avanzata Onlus - Istituto Veneto Di Medicina Molecolare (vimm)
2022–2025 · grant
The interplay between HPCAL4 and MeCP2: identification and characterization of a novel putative target for Rett syndrome therapy
Nicoletta Landsberger · University of Milan
2022–2025 · grant
Use of the national registry of muscular dystrophies and congenital myopathies to collect clinical data of patients with Collagen VI-related myopathies for feasibility studies
Adele D'Amico · Ospedale Pediatrico Bambino Gesù - Irccs
2022–2024 · grant
Mitochondrial myopathy associated to FDX2 mutations: a crossroad of FeS protein biogenesis and Coenzyme Q biosynthesis
Paola Costantini · University of Padua
2022–2027 · grant
New therapies for inborn errors of metabolism and Alpha1 antitrypsin deficiency
Nicola Brunetti-Pierri · Telethon Institute Of Genetics And Medicine (tigem)
2022–2025 · grant
Centriolar distal appendage: one nanoscopic structure, many diseases
Luca Fava · University of Trento
2022–2025 · grant
Assessing the consequences of AMPARs defective transport in an AP4 deficiency mouse model
Maria Passafaro · National Research Council
2022–2027 · grant
Gene-dependent and -independent approaches for therapy of retinal diseases which are inaccessible to conventional gene therapy
Ivana Trapani · Telethon Institute Of Genetics And Medicine (tigem)
2022–2024 · grant
Unveiling (epi)genetic variants for Atypical Hemolytic Uremic Syndrome (aHUS) beyond current knowledge: idiopathic cases, familial occurrence and auto-antibody development
Ilaria Bestetti · Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
2022–2027 · grant
Modulation of autophagy in human disorders
Carmine Settembre · Telethon Institute Of Genetics And Medicine (tigem)
2022–2023 · grant
Leading GLUT1 towards the plasma membrane
Paolo Grumati · Telethon Institute Of Genetics And Medicine (tigem)
2022–2027 · grant
The lysosome in health and disease
Andrea Ballabio · Telethon Institute Of Genetics And Medicine (tigem)
2022–2023 · grant
Modulation of selective autophagy to treat Vascular Ehlers Danlos Syndrome
Carmine Settembre · Telethon Institute Of Genetics And Medicine (tigem)
2022–2024 · grant
Functional characterization of FSD1L: a novel "master regulator" of neurodevelopment?
Enza Maria Valente · University of Pavia
2022–2027 · grant
Tackling the biological complexity of AATD
Nunzia Pastore · Telethon Institute Of Genetics And Medicine (tigem)
2022–2026 · grant
Understanding the pathogenesis and developing better therapies for adenosine deaminase 2 deficiency
Alessandra Mortellaro · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2022–2025 · grant
Characterization of the phenotypic diversity in DupEx2 Duchenne Muscular Dystrophy and identification of predictive/prognostic markers
Stefano Previtali · Fondazione Centro San Raffaele