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

VulneraBAP1 · Mechanism and vulnerability of BAP1 loss in tumor metastasis