Sfoglia per Autore
Cationic carboxylate and thioacetate ruthenium(ii) complexes: Synthesis and cytotoxic activity against anaplastic thyroid cancer cells
2020-01-01 Lovison, D.; Allegri, L.; Baldan, F.; Ballico, M.; Damante, G.; Jandl, C.; Baratta, W.
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.
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.
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.
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
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.
GSK2801 Reverses Paclitaxel Resistance in Anaplastic Thyroid Cancer Cell Lines through MYCN Downregulation
2023-01-01 Molteni, E.; Baldan, F.; Damante, G.; Allegri, L.
Using the AlphaFold system to the interpretation of variants of uncertain significance
2023-01-01 Franzoni, A; Driul, D; Passon, N; Fabbro, D; Baldan, F; Cogo, P; Fogolari, F; 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.
Longitudinal detection of somatic mutations in the saliva of head and neck squamous cell carcinoma–affected patients: a pilot study
2024-01-01 Dal Secco, C.; Tel, A.; Allegri, L.; Baldan, F.; Curcio, F.; Sembronio, S.; Faletra, F.; Robiony, M.; Damante, G.; Mio, C.
Dihydrotanshinone I exhibits antitumor effects via β-catenin downregulation in papillary thyroid cancer cell lines
2024-01-01 Molteni, E.; Baldan, F.; Damante, G.; Allegri, L.
The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases
2024-01-01 Mio, C.; Zucco, J.; Fabbro, D.; Bregant, E.; Baldan, F.; Allegri, L.; D'Elia, A. V.; Collini, V.; Imazio, M.; Damante, G.; Faletra, F.
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance
2025-01-01 Baldan, F.; Demori, E.; Gnan, C.; Passon, N.; Damante, G.; Mio, C.; Allegri, L.; Morgan, A.; Girotto, G.; De Paoli, F.; Limongelli, I.; Zucca, S.; Faletra, F.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Cationic carboxylate and thioacetate ruthenium(ii) complexes: Synthesis and cytotoxic activity against anaplastic thyroid cancer cells | 1-gen-2020 | Lovison, D.; Allegri, L.; Baldan, F.; Ballico, M.; Damante, G.; Jandl, C.; Baratta, W. | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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. | |
| GSK2801 Reverses Paclitaxel Resistance in Anaplastic Thyroid Cancer Cell Lines through MYCN Downregulation | 1-gen-2023 | Molteni, E.; Baldan, F.; Damante, G.; Allegri, L. | |
| Using the AlphaFold system to the interpretation of variants of uncertain significance | 1-gen-2023 | Franzoni, A; Driul, D; Passon, N; Fabbro, D; Baldan, F; Cogo, P; Fogolari, F; 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. | |
| Longitudinal detection of somatic mutations in the saliva of head and neck squamous cell carcinoma–affected patients: a pilot study | 1-gen-2024 | Dal Secco, C.; Tel, A.; Allegri, L.; Baldan, F.; Curcio, F.; Sembronio, S.; Faletra, F.; Robiony, M.; Damante, G.; Mio, C. | |
| Dihydrotanshinone I exhibits antitumor effects via β-catenin downregulation in papillary thyroid cancer cell lines | 1-gen-2024 | Molteni, E.; Baldan, F.; Damante, G.; Allegri, L. | |
| The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases | 1-gen-2024 | Mio, C.; Zucco, J.; Fabbro, D.; Bregant, E.; Baldan, F.; Allegri, L.; D'Elia, A. V.; Collini, V.; Imazio, M.; Damante, G.; Faletra, F. | |
| Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance | 1-gen-2025 | Baldan, F.; Demori, E.; Gnan, C.; Passon, N.; Damante, G.; Mio, C.; Allegri, L.; Morgan, A.; Girotto, G.; De Paoli, F.; Limongelli, I.; Zucca, S.; Faletra, F. |
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