Projects funded by the NCN
Identification of novel genetic factors involved in congenital disorders of endocrine gland using advanced methods of genome screening
2011/03/D/NZ5/06142
Keywords:
combined pituitary hormone deficiency thyroid dysgenesis thyroid ectopy hypogonadotropic hypogonadism microarrays SNP comparative genomic hybrydisation CGH array-CGH next generation sequencing NGS
Descriptors:
- NZ5_1: Etiology of human diseases
- NZ2_2: Genomics, transcriptomics, epigenomics
- NZ2_7: Bioinformatics
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, Wydział Lekarski II
woj. wielkopolskie
Principal investigator (from the host institution):
Number of co-investigators in the project: 4
Call: SONATA 2 - announced on 2011-09-15
Amount awarded: 568 216 PLN
Project start date (Y-m-d): 2012-09-19
Project end date (Y-m-d): 2016-09-18
Project duration:: 48 months (the same as in the proposal)
Project status: Project settled