muscular dystrophies
25 projects
HEIndividual fellowship2026–2028France
SKM-REFORMAT · SKeletal Muscle - REgulation of FORce and Maturation through Tubulin isotypes
HEDoctoral network2025–2029France
ENTRY-DM · Interdisciplinary doctoral training on oligonucleotide-based therapies for myotonic dystrophy
29 partners · 9 countries
HEIndividual fellowship2024–2027Italy
MyoPALM · Deciphering the role of protein S-palmitoylation in skeletal muscle physiopathology
2 partners · 2 countries
H2020Individual fellowship2021–2024Italy
Myo_LysoZOOM · An insight into lysosomal signature in muscle wasting
2 partners · 2 countries
H2020Individual fellowship2021–2023France
MUMDUPSC · Modelling undiagnosed muscular dystrophies using patients's stem cells
H2020Individual fellowship2021–2025France
DYSTROPHIC-ECM · Active role of skeletal muscle extracellular matrix in muscular dystrophies
H2020Individual fellowship2021–2023Italy
DREAM · Dux4-Regulated Expression and Activity by an inhibitor Molecule
H2020Individual fellowship2020–2022United Kingdom
RE-GENESis · GENome Editing and delivery Strategies for REcoding the mammalian genome
H2020Individual fellowship2019–2022Greece
MechanoGenetic · Role of mechanical forces in cell-matrix adhesion sites
H2020Individual fellowship2018–2020Netherlands
DUX4 · Function of DUX4 in skeletal muscle and non-muscle tissues
H2020Individual fellowship2017–2019Switzerland
MuSCel Genome · Muscle Specific C. elegans Genome in health and disease: finding novel factors in 3D organization
H2020Individual fellowship2017–2019Germany
VGAP · The Viral Genome Associated Proteome
H2020Individual fellowship2017–2019France
DMD2CURE · Correction of duplications in the DMD gene by a CRISPR/Cas9 approach
H2020Individual fellowship2016–2018Israel
channelopathies · Type 1 reyanodine receptor Structure and regulation by post-translational modifications and small molecules.
H2020Individual fellowship2016–2017United Kingdom
Subpopulations · Investigating Fibrotic and Regenerative Fibroblast Populations in Muscular Dystrophy
H2020Individual fellowship2016–2017United Kingdom
DYS_FUNCTION · Novel use of exon skipping technology to study structure-function relationship of dystrophin
H2020Individual fellowship2016–2018United Kingdom
INAME · Imaging nucleic acid metabolism in cells
H2020Individual fellowship2015–2017Denmark
PIOMES · Pbx proteins as pioneer factors promoting signal specificity in mesodermal differentiation
FP7Reintegration grant2013–2017Spain
ANTES · Accelerating Neuromuscular Treatment Selection
FP7Reintegration grant2010–2014Spain
LGMD2A · Development of a strategy to treat limb-girdle muscular dystrophy (LGMD2A) using combined cell and gene therapy strategies
2 partners
FP7Individual fellowship2010–2012Spain
STROKECELLFUSION · Cell fusion as regenerative tool for stroke treatment
FP6Reintegration grant2006–2008Italy
FSHD ANIMAL MODEL. · An animal model to develop therapeutic strategies for facioscapulohumeral muscular dystrophy, FSHD
FP6Individual fellowship2005–2007France
DM BRAIN · Dissecting the molecular pathways of brain dysfunction in myotonic dystrophy
FP5Individual fellowship2002–2003Italy