mutation
616 проекта
H2020Индивидуална стипендия2019–2021Австрия
MiniBRAIN · Investigating the pathogenic mechanisms underlying TUBB2B-related brain malformations using induced pluripotent stem cells and cerebral organoids.
H2020Индивидуална стипендия2019–2020Норвегия
GEMZ · Genetic Epilepsy Models in Zebrafish
H2020Индивидуална стипендия2019–2021Обединеното кралство
P-MaleReg · Establishment of P-element silencing in Drosophila simulans dysgenic males
H2020Индивидуална стипендия2019–2021Франция
AvINFLUENZA · Molecular basis of avian influenza polymerase adaptation to human hosts
H2020Индивидуална стипендия2019–2021Италия
LEUKEYOLK · Uncovering the origin and mechanisms of Down syndrome-associated leukaemia through human induced pluripotent stem cell-derived haemopoiesis
H2020Индивидуална стипендия2019–2021Обединеното кралство
OESOPHAGEAL FATE · Epithelial/Mesenchymal Cross-talk in response to injury and early tumorigenesis; a spatiotemporal perspective
H2020Индивидуална стипендия2019–2021Испания
SHINE · Self-Healthcare for breast cancer detection using an INtegrated paper-based Electrochemical device
H2020Индивидуална стипендия2019–2021Франция
FABA-SHAPE · Unveiling the Origins of the Faba Bean by means of Shape and Stable Carbon Isotope Analyses of Archaeological Remains
H2020Индивидуална стипендия2019–2021Германия
Stress Granules · Using Reconstituted Stress Granules to Gain Insight into the Molecular Pathology of Neurodegenerative Diseases
H2020Индивидуална стипендия2019–2021Германия
PrunMut · Candidate mutation discovery in early-flowering mutants 'Rojo Pasión Precoz' and 'Bulida Precoz'
H2020Индивидуална стипендия2019–2021Нидерландия
HGB-StIC · Human Genetic Basis of Severe Staphylococcal Infections in Childhood
2 партньори · 2 държави
H2020Индивидуална стипендия2019–2021Нидерландия
PSR · Photometabolic Self-Replication
H2020Индивидуална стипендия2019–2020Швеция
CL_Exocytosis · “Molecular dissection of cytotoxic lymphocyte exocytosis
H2020Докторантска мрежа2018–2023Белгия
StarT · European Training Network to Diagnose, Understand and Treat Stargardt Disease, a Frequent Inherited Blinding Disorder
16 партньори · 8 държави
H2020Докторантска мрежа2018–2023Германия
pHioniC · pH and Ion Transport in Pancreatic Cancer
17 партньори · 7 държави
H2020Докторантска мрежа2018–2023Обединеното кралство
EVOdrops · directed EVOlution in DROPS
19 партньори · 9 държави
H2020Индивидуална стипендия2018–2020Швейцария
PLEVOCON · Pleiotropy and Evolutionary Constraint
H2020Индивидуална стипендия2018–2022Германия
BSLchlamy · Understanding the essential function of the conserved plant-specific protein phosphatase family BSL
2 партньори · 2 държави
H2020Индивидуална стипендия2018–2020Обединеното кралство
PCDfert · Identification of novel genes and mechanisms for PCD and male infertility
H2020Индивидуална стипендия2018–2020Обединеното кралство
ProMeta · Non-histone protein acetylation targets of KAT2A in AML
H2020Индивидуална стипендия2018–2020Нидерландия
NINTCORDEV · NIPBL and Integrator function and dysfunction in human cortical development
H2020Индивидуална стипендия2018–2020Франция
HiMIN · Histone H3.3 oncogenic mutations: a role in genome instability through altered DNA repair and replication fork stability?
H2020Индивидуална стипендия2018–2020Нидерландия
KILNEV · Killing Senescent Cells as a Novel Method to Eliminate Nevi
H2020Индивидуална стипендия2018–2020Германия