Sfoglia per Autore
Critical involvement of calcium-dependent cytosolic phospholipase A2α in aortic valve interstitial cell calcification
2020-01-01 Bonetti, A.; Allegri, L.; Baldan, F.; Contin, M.; Battistella, C.; Damante, G.; Marchini, M.; Ortolani, F.
Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study
2020-01-01 Lazarevic, M.; Milosevic, M.; Jelovac, D.; Milenkovic, S.; Tepavcevic, Z.; Baldan, F.; Suboticki, T.; Toljic, B.; Trisic, D.; Dragovic, M.; Damante, G.; Milasin, J.
NKX2.1 run-on mutation associated to familial brain–lung–thyroid syndrome
2021-01-01 Cavaliere, E.; Gortan, A. J.; Passon, N.; Fabbro, D.; Marin, D.; Carecchio, M.; Baldan, F.; Credendino, S. C.; Gallo, R.; Cogo, P.; Damante, G.; De Vita, G.
Effects of dihydrotanshinone I on proliferation and invasiveness of paclitaxel-resistant anaplastic thyroid cancer cells
2021-01-01 Allegri, L.; Capriglione, F.; Maggisano, V.; Damante, G.; Baldan, F.
Spontaneous coronary artery dissection: Role of prognostic markers and relationship with genetic analysis
2021-01-01 Antonutti, M.; Baldan, F.; Lanera, C.; Spedicato, L.; Zanuttini, D.; Bisceglia, T.; Favaretto, E.; Poli, S.; Tioni, C.; Sut, D.; Gregori, D.; Damante, G.; Proclemer, A.
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation
2022-01-01 Baldan, F; Cavaliere, E; Gortan, Aj; Passon, N; Fabbro, D; Marin, D; Carecchio, M; Credendino, Sc; Gallo, R; Cogo, P; Damante, G; De Vita, G
GSK2801 Reverses Paclitaxel Resistance in Anaplastic Thyroid Cancer Cell Lines through MYCN Downregulation
2023-01-01 Molteni, E.; Baldan, F.; Damante, G.; Allegri, L.
Somatic genomic imbalances in ‘tumour-free’ surgical margins of oral cancer
2023-01-01 Baldan, F.; Gnan, C.; Lazarevic, M.; Nikolic, N.; Mio, C.; Tepavcevic, Z.; Robiony, M.; Milasin, J.; Damante, G.
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases
2024-01-01 Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Critical involvement of calcium-dependent cytosolic phospholipase A2α in aortic valve interstitial cell calcification | 1-gen-2020 | Bonetti, A.; Allegri, L.; Baldan, F.; Contin, M.; Battistella, C.; Damante, G.; Marchini, M.; Ortolani, F. | |
| Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study | 1-gen-2020 | Lazarevic, M.; Milosevic, M.; Jelovac, D.; Milenkovic, S.; Tepavcevic, Z.; Baldan, F.; Suboticki, T.; Toljic, B.; Trisic, D.; Dragovic, M.; Damante, G.; Milasin, J. | |
| NKX2.1 run-on mutation associated to familial brain–lung–thyroid syndrome | 1-gen-2021 | Cavaliere, E.; Gortan, A. J.; Passon, N.; Fabbro, D.; Marin, D.; Carecchio, M.; Baldan, F.; Credendino, S. C.; Gallo, R.; Cogo, P.; Damante, G.; De Vita, G. | |
| Effects of dihydrotanshinone I on proliferation and invasiveness of paclitaxel-resistant anaplastic thyroid cancer cells | 1-gen-2021 | Allegri, L.; Capriglione, F.; Maggisano, V.; Damante, G.; Baldan, F. | |
| Spontaneous coronary artery dissection: Role of prognostic markers and relationship with genetic analysis | 1-gen-2021 | Antonutti, M.; Baldan, F.; Lanera, C.; Spedicato, L.; Zanuttini, D.; Bisceglia, T.; Favaretto, E.; Poli, S.; Tioni, C.; Sut, D.; Gregori, D.; Damante, G.; Proclemer, A. | |
| A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation | 1-gen-2022 | Baldan, F; Cavaliere, E; Gortan, Aj; Passon, N; Fabbro, D; Marin, D; Carecchio, M; Credendino, Sc; Gallo, R; Cogo, P; Damante, G; De Vita, G | |
| GSK2801 Reverses Paclitaxel Resistance in Anaplastic Thyroid Cancer Cell Lines through MYCN Downregulation | 1-gen-2023 | Molteni, E.; Baldan, F.; Damante, G.; Allegri, L. | |
| Somatic genomic imbalances in ‘tumour-free’ surgical margins of oral cancer | 1-gen-2023 | Baldan, F.; Gnan, C.; Lazarevic, M.; Nikolic, N.; Mio, C.; Tepavcevic, Z.; Robiony, M.; Milasin, J.; Damante, G. | |
| A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases | 1-gen-2024 | Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C. |
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