muscular dystrophies
25 проекта
HEИндивидуална стипендия2026–2028Франция
SKM-REFORMAT · SKeletal Muscle - REgulation of FORce and Maturation through Tubulin isotypes
HEДокторантска мрежа2025–2029Франция
ENTRY-DM · Interdisciplinary doctoral training on oligonucleotide-based therapies for myotonic dystrophy
29 партньори · 9 държави
HEИндивидуална стипендия2024–2027Италия
MyoPALM · Deciphering the role of protein S-palmitoylation in skeletal muscle physiopathology
2 партньори · 2 държави
H2020Индивидуална стипендия2021–2024Италия
Myo_LysoZOOM · An insight into lysosomal signature in muscle wasting
2 партньори · 2 държави
H2020Индивидуална стипендия2021–2023Франция
MUMDUPSC · Modelling undiagnosed muscular dystrophies using patients's stem cells
H2020Индивидуална стипендия2021–2025Франция
DYSTROPHIC-ECM · Active role of skeletal muscle extracellular matrix in muscular dystrophies
H2020Индивидуална стипендия2021–2023Италия
DREAM · Dux4-Regulated Expression and Activity by an inhibitor Molecule
H2020Индивидуална стипендия2020–2022Обединеното кралство
RE-GENESis · GENome Editing and delivery Strategies for REcoding the mammalian genome
H2020Индивидуална стипендия2019–2022Гърция
MechanoGenetic · Role of mechanical forces in cell-matrix adhesion sites
H2020Индивидуална стипендия2018–2020Нидерландия
DUX4 · Function of DUX4 in skeletal muscle and non-muscle tissues
H2020Индивидуална стипендия2017–2019Швейцария
MuSCel Genome · Muscle Specific C. elegans Genome in health and disease: finding novel factors in 3D organization
H2020Индивидуална стипендия2017–2019Германия
VGAP · The Viral Genome Associated Proteome
H2020Индивидуална стипендия2017–2019Франция
DMD2CURE · Correction of duplications in the DMD gene by a CRISPR/Cas9 approach
H2020Индивидуална стипендия2016–2018Израел
channelopathies · Type 1 reyanodine receptor Structure and regulation by post-translational modifications and small molecules.
H2020Индивидуална стипендия2016–2017Обединеното кралство
Subpopulations · Investigating Fibrotic and Regenerative Fibroblast Populations in Muscular Dystrophy
H2020Индивидуална стипендия2016–2017Обединеното кралство
DYS_FUNCTION · Novel use of exon skipping technology to study structure-function relationship of dystrophin
H2020Индивидуална стипендия2016–2018Обединеното кралство
INAME · Imaging nucleic acid metabolism in cells
H2020Индивидуална стипендия2015–2017Дания
PIOMES · Pbx proteins as pioneer factors promoting signal specificity in mesodermal differentiation
FP7Реинтеграция2013–2017Испания
ANTES · Accelerating Neuromuscular Treatment Selection
FP7Реинтеграция2010–2014Испания
LGMD2A · Development of a strategy to treat limb-girdle muscular dystrophy (LGMD2A) using combined cell and gene therapy strategies
2 партньори
FP7Индивидуална стипендия2010–2012Испания
STROKECELLFUSION · Cell fusion as regenerative tool for stroke treatment
FP6Реинтеграция2006–2008Италия
FSHD ANIMAL MODEL. · An animal model to develop therapeutic strategies for facioscapulohumeral muscular dystrophy, FSHD
FP6Индивидуална стипендия2005–2007Франция
DM BRAIN · Dissecting the molecular pathways of brain dysfunction in myotonic dystrophy
FP5Индивидуална стипендия2002–2003Италия