Projects funded by the NCN


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4 projects found matching your search criteria :

  1. Functional studies of TPM2 gene mutation responsible for the hereditary form of clubfoot disease

    Call: PRELUDIUM 23 , Panel: NZ5

    Principal investigator: Akshaya Ramanujam

    Uniwersytet Medyczny w Lublinie

  2. Molecular basis of hereditary Clubfoot disease

    Call: PRELUDIUM 14 , Panel: NZ5

    Principal investigator: Ewa Zuzanna Hordyjewska-Kowalczyk

    Uniwersytet Medyczny w Lublinie, II Wydział Lekarski z Oddziałem Anglojęzycznym

  3. Molecular variation of RAS-MAPK pathway genes and phenotypic expression of Noonan syndrome

    Call: SONATA 1 , Panel: NZ5

    Principal investigator: dr Jakub Klapecki

    Instytut Matki i Dziecka

  4. Searching for genomic regions responsible for the observed divergence in the outcome of multiple endocrine neoplasia typ...

    Call: PRELUDIUM 9 , Panel: NZ5

    Principal investigator: dr Anna Elżbieta Skalniak

    Uniwersytet Jagielloński- Collegium Medicum, Collegium Medicum; Wydział Lekarski