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Hyperinsulinemia affects 72% of Fanconi anemia (FA) patients and an additional 25% experience lowered glucose tolerance or frank diabetes. The underlying molecular mechanisms contributing to the dysfunction of FA pancreas β cells is unknown. These experiments were performed in 293FT HEK cells as a p...
ORGANISM(S): Homo sapiens (Human) 
2019-07-25 | PXD010570 | Pride
CCH-SCC-FA1 FANCA-essentiality screen
Hyperinsulinemia affects 72% of Fanconi anemia (FA) patients and an additional 25% experience lowered glucose tolerance or frank diabetes. The underlying molecular mechanisms contributing to the dysfunction of FA pancreas β cells is unknown. Therefore, we sought to identify previously unexplored rol...
ORGANISM(S): Homo sapiens (Human) 
2019-07-25 | PXD010589 | Pride
The purpose of this screen was to identify synthetic lethal targets in FANCA-deficient cells.
ORGANISM(S): Homo sapiens 
Alisertib treatment in FANCA-deficient cell lines
The objective of the project is to determine the interactome of FANCA in order to identify the partners and the biochemical and molecular pathways to which it contributes, which will be successively functionally analyzed by bioinformatics approaches and in living cells.
ORGANISM(S): Homo sapiens (Human) 
2026-08-05 | PXD068730 | Pride
Kinome-wide shRNA screen for synthetic lethality in patient-derived FANCA-deficient fibroblasts.
Leukaemia is caused by the clonal evolution of a cell that accumulates mutations/genomic rearrangements, allowing unrestrained cell growth. However, recent identification of leukaemic mutations in the blood cells of healthy individuals revealed that additional events are required to expand the mutat...
ORGANISM(S): Mus musculus 
2023-08-31 | GSE164411 | GEO
FANCA deficiency promotes leukemic progression by allowing emergence of cells carrying oncogenic driver mutations
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