Projects funded by the NCN
Towards an understanding of the molecular basis of osseous structural vertebral malformations in humans
2020/37/B/NZ5/03693
Keywords:
vertebral malformations osseous malformations osseous vertebral defects Klippel-Feil syndrome congenital developmental defects the etiopathogenesis of human birth defects clinical genetics medical genetics developmental biology WGS,
Descriptors:
- NZ5_003:
- NZ2_002:
- NZ4_012:
Panel:
NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)
Host institution :
Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu
woj. wielkopolskie
Principal investigator (from the host institution):
prof. Aleksander Marian Jamsheer
Number of co-investigators in the project: 4
Call: OPUS 19 - announced on 2020-03-16
Amount awarded: 1 048 200 PLN
Project start date (Y-m-d): 2021-01-22
Project end date (Y-m-d): 2026-01-21
Project duration:: 60 months (the same as in the proposal)
Project status: Pending project
Project description
Download the project description in a pdf file
Note - project descriptions were prepared by the authors of the applications themselves and placed in the system in an unchanged form.
Information in the final report
- Publication in academic press/journals (1)
- Molecular landscape of congenital vertebral malformations: recent discoveries and future directionsAuthors:Anna Szoszkiewicz, Ewelina Bukowska-Olech, Aleksander JamsheerAcademic press:Orphanet Journal of Rare Diseases (rok: 2024, tom: 19, strony: 32), Wydawca: BMCStatus:PublishedDOI:10.1186/s13023-024-03040-0 - link to the publication