RNDr. Silvia Borecká, PhD.
International
Current
- European Network for Sigma-1 Receptor as a Therapeutic OpportunityProgram: COSTDuration: 25. 10. 2024 – 24. 10. 2028
National
Current
- Genetic causes of rare inherited metabolic diseases with emphasis on functional studies of novel variantsProgram: SRDADuration: 1. 7. 2023 – 30. 6. 2027
- Mitochondrial disease in heart failureProgram: SRDADuration: 1. 7. 2022 – 30. 6. 2026
- Mutations associated with Wolfram syndrome: alternative signaling pathways for calcium and mitochondrial physiologyProgram: SRDADuration: 1. 7. 2022 – 30. 6. 2026
Finished
- Identification of novel genetic variants in syndromic hearing loss by whole exome sequencingProgram: SRDADuration: 1. 7. 2021 – 30. 6. 2025
- Genetics of rare forms of diabetes with focus on functional characterization of new variantsProgram: VEGADuration: 1. 1. 2021 – 31. 12. 2024
- Identification of etiology in sporadic forms of hereditary hearing loss by whole exome sequencingProgram: VEGADuration: 1. 1. 2021 – 31. 12. 2024
- Cell-in-cell phenomena as microevolutionary processes in cancer progression: a role for hypoxia-induced carbonic anhydrase IXProgram: SRDADuration: 1. 7. 2020 – 30. 6. 2024
- Comprehensive innovative diagnostics and personalized treatment of diabetes mellitus in childrenProgram: Other projectsDuration: 1. 10. 2019 – 31. 3. 2022