Projects funded by the NCN


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8 projects found matching your search criteria :

  1. Identification of novel genetic factors involved in congenital disorders of endocrine gland using advanced methods of ge...

    Call: SONATA 2 , Panel: NZ5

    Principal investigator: dr Bartłomiej Budny

    Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski II

  2. Identification on novel copy-number variations (CNVs) in patients affected by bilateral congenital limb malformations by...

    Call: SONATA 2 , Panel: NZ2

    Principal investigator: dr hab. Aleksander Jamsheer

    Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski I, Katedra i Zakład Genetyki Medycznej

  3. Array-based genomic and transcriptomic profiling in pediatric acute myeloblastic leukemia in search of genes resposible ...

    Call: SONATA 2 , Panel: NZ5

    Principal investigator: dr Joanna Szczepanek

    Uniwersytet Mikołaja Kopernika

  4. Application of array comparative genomic hybridization (aCGH) to identify submicroscopic aberration and lethal genes in ...

    Call: PRELUDIUM 12 , Panel: NZ2

    Principal investigator: Katarzyna Kowalczyk

    Instytut Matki i Dziecka

  5. Identification of novel genetics variants as the cause of the premature closure of the cranial sutures in children using...

    Call: PRELUDIUM 12 , Panel: NZ5

    Principal investigator: Ewelina Bukowska-Olech

    Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

  6. Identification of novel structural variants in patients presenting with congenital limb malformations by means of the ge...

    Call: PRELUDIUM 12 , Panel: NZ2

    Principal investigator: dr Magdalena Socha

    Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

  7. Studies on non-coding regulatory copy-number variations as a cause of bilateral limb malformations in humans

    Call: SONATA BIS 6 , Panel: NZ5

    Principal investigator: prof. Aleksander Jamsheer

    Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

  8. Investigation of genetic variants underlying variability in patients with 22q11 Deletion Syndrome.

    Call: OPUS 9 , Panel: NZ5

    Principal investigator: dr Beata Nowakowska

    Instytut Matki i Dziecka