Projects funded by the NCN

Astrocytic Mitochondria in PACS2 Syndrome: Pathogenesis and Therapeutic Intervention

Call: PRELUDIUM 24 , Panel: NZ5

Principal investigator: Arkadiusz Franciszek Żbikowski

Uniwersytet Medyczny w Białymstoku

Metabolic disturbances involved in the pathogenesis of PACS2-related disorder

Call: OPUS 28 , Panel: NZ4

Principal investigator: prof. Mariusz Roman Więckowski

Instytut Biologii Doświadczalnej im. M. Nenckiego PAN

Rare genetic variants of complement components as etiologic factors of autoimmune diseases.

Call: OPUS 26 , Panel: NZ6

Principal investigator: dr hab. Marcin Sebastian Okrój

Gdański Uniwersytet Medyczny, Międzyuczelniany Wydział Biotechnologii Uniwersytetu Gdańskiego i Gdańskiego Uniwersytetu Medycznego

Use of comparative oncology approach to dissect the PD-1 intrinsic signalling in osteosarcoma. Can dog be the key for ne...

Call: PRELUDIUM 21 , Panel: NZ1

Principal investigator: Katarzyna Joanna Dziubek

Uniwersytet Gdański, Międzynarodowe Centrum Badań nad Szczepionkami Przeciwnowotworowymi

The interdisciplinary and holistic analysis of the functioning of families with the child with rare genetical disease

Call: PRELUDIUM 21 , Panel: HS6

Principal investigator: dr Paulina Anikiej-Wiczenbach

Uniwersytet Gdański, Wydział Nauk Społecznych

Investigation of copper homeostasis disturbances in yeast model of rare neurodegenerative diseases associated with VPS13...

Call: PRELUDIUM 16 , Panel: NZ3

Principal investigator: Piotr Soczewka

Instytut Biochemii i Biofizyki PAN

An Anthropology of Rare Diseases: A Study of the Baltic Sea Region

Call: SONATA BIS 7 , Panel: HS3

Principal investigator: dr hab. Małgorzata Rajtar

Instytut Filozofii i Socjologii Polskiej Akademii Nauk

Development of novel bioinformatics software for analysis of genetic variation in non-coding elements of the human genom...

Call: POLONEZ 3 , Panel: NZ2

Principal investigator: dr Paweł Szymon Sztromwasser

Uniwersytet Medyczny w Łodzi, I Katedra Pediatrii

Decoding genetic presisposition to rare neurodevelopmental diseases: Integration of genome, transcriptome and methylome ...

Call: HARMONIA 8 , Panel: NZ2

Principal investigator: dr hab. Paweł Lisowski

Instytut Genetyki i Hodowli Zwierząt PAN

Molecular bases of a therapy of rare genetic diseases caused by impaired activity of nucleotide sugar transporters

Call: OPUS 11 , Panel: NZ5

Principal investigator: prof. Mariusz Olczak

Uniwersytet Wrocławski, Wydział Biotechnologii

Yeast model to study function of Vps13 proteins involved in pathogenesis of rare genetic neurodegenerative diseases.

Call: OPUS 10 , Panel: NZ3

Principal investigator: prof. Teresa Grażyna Żołądek

Instytut Biochemii i Biofizyki PAN

Socio-cultural dimensions of rare diseases: the case of LCHAD deficiency. A comparative study of Poland and Finland

Call: OPUS 9 , Panel: HS3

Principal investigator: dr hab. Małgorzata Rajtar

Uniwersytet im. Adama Mickiewicza w Poznaniu, Wydział Historyczny

FUNCTIONAL STUDIES OF RARE GENETIC VARIANTS OF GENES CAUSSALLY CONNECTED WITH ALZHEIMER'S DISEASE IN THE POLISH POPULATI...

Call: SONATA 5 , Panel: NZ3

Principal investigator: dr Michalina Maria Wężyk

Instytut Medycyny Doświadczalnej i Klinicznej im. Mirosława Mossakowskiego PAN

Changes in the level of expression of genes involved in the pathogenic mechanisms in rare, inherited metabolic diseases.

Call: OPUS 4 , Panel: NZ1

Principal investigator: dr hab. Agnieszka Ługowska

Instytut Psychiatrii i Neurologii