Projects funded by the NCN

Effect of Embryonic Diapause on mitochondrial mutations inheritance in the mouse model of obesity.

Call: PRELUDIUM 18 , Panel: NZ3

Principal investigator: Łukasz Józef Gąsior

Uniwersytet Jagielloński, Małopolskie Centrum Biotechnologii Uniwersytetu Jagiellońskiego

How activation of the Mec1/Tel1 kinase (human ATR/ATM) pathway in response to the nuclear genome damage influences the s...

Call: OPUS 13 , Panel: NZ3

Principal investigator: dr Aneta Edyta Kaniak-Golik

Instytut Biochemii i Biofizyki PAN

Understanding of the functioning of mitochondrial ATP synthase by studying in yeast the phenotype of human pathology rel...

Call: OPUS 12 , Panel: NZ3

Principal investigator: dr hab. Róża Kucharczyk

Instytut Biochemii i Biofizyki PAN

The molecular effects of human mitochondrial cytochrome b mutations studied in bacterial Rhodobacter capsulatus cytochro...

Call: OPUS 11 , Panel: NZ1

Principal investigator: dr Arkadiusz Borek

Uniwersytet Jagielloński, Wydział Biochemii, Biofizyki i Biotechnologii

Mutations in mitochondrial ATP6 gene, identified in cancer and myopathies, and their impact on ATP synthase and cell met...

Call: OPUS 6 , Panel: NZ1

Principal investigator: dr hab. Róża Kucharczyk

Instytut Biochemii i Biofizyki PAN

Searching for the mutations in whole mitochondrial DNA among patients with hearing loss using Next Generation Sequencing...

Call: PRELUDIUM 3 , Panel: NZ5

Principal investigator: dr Urszula Agnieszka Lechowicz

Instytut Fizjologii i Patologii Słuchu

Epidemiology of recurrent POLG mutations in the Polish population and their role in the etiology of mitochondrial diseas...

Call: OPUS 3 , Panel: NZ2

Principal investigator: dr Dorota Maria Piekutowska-Abramczuk

INSTYTUT - POMNIK - CENTRUM ZDROWIA DZIECKA

A cellular model for understanding gender differences in Leber's Hereditary Optic Neuropathy

Call: PRELUDIUM 2 , Panel: NZ3

Principal investigator: Agata Krystyna Kodroń

Uniwersytet Warszawski