Projects funded by the NCN


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12 projects found matching your search criteria :

  1. Clinical, molecular and cytogenetic evaluation of genome imbalances in patients with clinical features of microdeletion ...

    Call: SONATA 1 , Panel: NZ2

    Principal investigator: dr hab. Beata Lipska-Ziętkiewicz

    Gdański Uniwersytet Medyczny, Wydział Lekarski

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. Cytogenetic and molecular characterization of chromosomal alterations in T-cell large garnular lymphocyte leukemia.

    Call: PRELUDIUM 1 , Panel: NZ2

    Principal investigator: dr Katarzyna Iżykowska

    Instytut Genetyki Człowieka PAN

  11. Genome abberations, p53 status and nitrosative-oxidative stress manifestation during establishment of methotrexate-induc...

    Call: OPUS 1 , Panel: NZ4

    Principal investigator: dr hab. Magdalena Dąbrowska

    INSTYTUT BIOLOGII DOŚWIADCZALNEJ PAN IM.M.NENCKIEGO

  12. 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