mutation
616 projects
HEIndividual fellowship2022–2024Denmark
SynDrops · Understanding the physiological and pathological relevance of liquid-liquid phase separation by synuclein family of proteins
HEIndividual fellowship2022–2024Germany
3-D Cardioid · Decoding enhancer usage and gene expression of human heart development in 3-D cardioids
HEIndividual fellowship2022–2024Italy
Edit-hCOs · Precise Genome Editing to Correct Cardiomyopathies in Human Cardiac Organoids
2 partners · 2 countries
H2020Individual fellowship2022–2025Denmark
FBXW7-InReg · Defining the role of FBXW7 in intestinal epithelium regeneration
H2020Individual fellowship2022–2024Spain
DeciphGYG · Deciphering the Molecular Mechanism of an Enzymatic Machinery for Glycogen Biosynthesis
H2020Individual fellowship2022–2025Italy
HodgkINsights · Hodgkin Lymphoma: Insights from genomic studies of mutations in coding and non-coding regions
H2020Individual fellowship2022–2024Switzerland
EGR · The role of genetic redundancy in adaptive evolution of efflux pumps
H2020Individual fellowship2022–2024United Kingdom
POLYGARCH · Impact of whole-genome duplications on the genetic and genomic architecture of adaptation
H2020Individual fellowship2022–2024Italy
NECESSITY · New prECision thErapieS for uveal melanoma (targeting the Gαq/GNAQ oncogenic Signaling cIrcuiTrY)
2 partners · 2 countries
H2020Individual fellowship2022–2023Germany
TITINmap · Towards Uncovering the Splicing Code of the Gigantic Gene Titin in Familial Dilated Cardiomyopathy
2 partners · 2 countries
H2020Individual fellowship2022–2024Spain
DEEPCONSTRUCT · Understanding epigenetic inheritance and the structures of non-amyloid prion condensates using deep mutagenesis scans
H2020Individual fellowship2022–2024Spain
RiboEscapers · A Riboescaper study: Protein synthesis driven by deficiently assembled ribosomes
H2020Individual fellowship2022–2024Denmark
Iso-Proline CTD · Hidden in plain sight: Masking RNA Pol II phosphorylation via proline isomerization during gene expression
H2020Doctoral network2021–2025Spain
PIPgen · PI3K/PTEN-related monogenic disease to understand cancer
11 partners · 5 countries
H2020Individual fellowship2021–2023Spain
PROBYDE · Probing the bypassability of genetic constraints in drug-resistance enzymes
H2020Individual fellowship2021–2023Sweden
RET-TRAF · RET Trafficking
H2020Individual fellowship2021–2023Spain
MITORett · Deciphering cerebellar mitochondrial alterations in Rett Syndrome
H2020Individual fellowship2021–2023France
MUMDUPSC · Modelling undiagnosed muscular dystrophies using patients's stem cells
H2020Individual fellowship2021–2025Belgium
NotSOSTRESSED · The Neurobiology of Social Context-Dependent Stress Responses
H2020Individual fellowship2021–2023Portugal
GENMAINEVO · Genome maintenance and evolution
H2020Individual fellowship2021–2023Denmark
InMIND · Intervention in Neurodegenerative disorders via Mechanistic INsight into liquid-like Droplets
H2020Individual fellowship2021–2023United Kingdom
TxImmuneOrganoids · Divide and conquer: using patient-derived tumour organoids to dissect intra-tumour immune heterogeneity of non-small cell lung cancer
H2020Individual fellowship2021–2023France
PERTURBATIONS · Large scale perturbations of the gene regulatory networks of E. coli
H2020Individual fellowship2021–2024Cyprus
