mutation
616 projects
H2020Individual fellowship2019–2021Austria
MiniBRAIN · Investigating the pathogenic mechanisms underlying TUBB2B-related brain malformations using induced pluripotent stem cells and cerebral organoids.
H2020Individual fellowship2019–2020Norway
GEMZ · Genetic Epilepsy Models in Zebrafish
H2020Individual fellowship2019–2021United Kingdom
P-MaleReg · Establishment of P-element silencing in Drosophila simulans dysgenic males
H2020Individual fellowship2019–2021France
AvINFLUENZA · Molecular basis of avian influenza polymerase adaptation to human hosts
H2020Individual fellowship2019–2021Italy
LEUKEYOLK · Uncovering the origin and mechanisms of Down syndrome-associated leukaemia through human induced pluripotent stem cell-derived haemopoiesis
H2020Individual fellowship2019–2021United Kingdom
OESOPHAGEAL FATE · Epithelial/Mesenchymal Cross-talk in response to injury and early tumorigenesis; a spatiotemporal perspective
H2020Individual fellowship2019–2021Spain
SHINE · Self-Healthcare for breast cancer detection using an INtegrated paper-based Electrochemical device
H2020Individual fellowship2019–2021France
FABA-SHAPE · Unveiling the Origins of the Faba Bean by means of Shape and Stable Carbon Isotope Analyses of Archaeological Remains
H2020Individual fellowship2019–2021Germany
Stress Granules · Using Reconstituted Stress Granules to Gain Insight into the Molecular Pathology of Neurodegenerative Diseases
H2020Individual fellowship2019–2021Germany
PrunMut · Candidate mutation discovery in early-flowering mutants 'Rojo Pasión Precoz' and 'Bulida Precoz'
H2020Individual fellowship2019–2021Netherlands
HGB-StIC · Human Genetic Basis of Severe Staphylococcal Infections in Childhood
2 partners · 2 countries
H2020Individual fellowship2019–2021Netherlands
PSR · Photometabolic Self-Replication
H2020Individual fellowship2019–2020Sweden
CL_Exocytosis · “Molecular dissection of cytotoxic lymphocyte exocytosis
H2020Doctoral network2018–2023Belgium
StarT · European Training Network to Diagnose, Understand and Treat Stargardt Disease, a Frequent Inherited Blinding Disorder
16 partners · 8 countries
H2020Doctoral network2018–2023Germany
pHioniC · pH and Ion Transport in Pancreatic Cancer
17 partners · 7 countries
H2020Doctoral network2018–2023United Kingdom
EVOdrops · directed EVOlution in DROPS
19 partners · 9 countries
H2020Individual fellowship2018–2020Switzerland
PLEVOCON · Pleiotropy and Evolutionary Constraint
H2020Individual fellowship2018–2022Germany
BSLchlamy · Understanding the essential function of the conserved plant-specific protein phosphatase family BSL
2 partners · 2 countries
H2020Individual fellowship2018–2020United Kingdom
PCDfert · Identification of novel genes and mechanisms for PCD and male infertility
H2020Individual fellowship2018–2020United Kingdom
ProMeta · Non-histone protein acetylation targets of KAT2A in AML
H2020Individual fellowship2018–2020Netherlands
NINTCORDEV · NIPBL and Integrator function and dysfunction in human cortical development
H2020Individual fellowship2018–2020France
HiMIN · Histone H3.3 oncogenic mutations: a role in genome instability through altered DNA repair and replication fork stability?
H2020Individual fellowship2018–2020Netherlands
KILNEV · Killing Senescent Cells as a Novel Method to Eliminate Nevi
H2020Individual fellowship2018–2020Germany
